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Note: Poster Registration Ended March 21st.
Posters Being Presented::
Please put your posters up as soon as
possible in the morning Authors are expected to be by their
posters, Even number posters are in the morning session and
odd number posters are in the afternoon session.
Poster 1
Seed-Mediated Growth of Uniform Arrays of Metal
Nanoparticles on Silicon Wafer
Deok-im Jean, Sachin Kumar, and Shouzhong Zou*, Miami University
Center for Nanotechnology, Department of Chemistry & Biochemistry,
Oxford, Ohio
Fabrication of metal nanoparticle arrays with
controlled particle size, shape, and distribution has been attracting
a lot of research interests in recent years, due to their potential
applications in catalysis, information storage, sensors, and
photonics. Although excellent progress has been made towards
shape and size control of nanoparticles in the solution phase,
research on the growth of particles supported on solid substrate
is still evolving. A common limitation in previous studies has
been the lack of control over particle size and distribution.
In this work, we demonstrate a simple synthetic
route to fabricate arrays of Au nanoparticles with controlled
size and spacing on silicon wafer substrates; following which
the nanoparticles are grown to form different shapes utilizing
a seed-mediated growth method. Au and Pd growth on Au seeds
are achieved utilizing this approach. The grown particle size,
shape, and interparticle distance can be tuned by varying the
growth solution concentration, growth time, and using different
Au seed arrays. These grown arrays of metal nanoparticles are
excellent substrates for surface enhanced Raman spectroscopy
(SERS). 1,4-phenylene diisocyanide (PDI) is used as a probe
molecule to illustrate the application of these grown particle
arrays in SERS.
Poster 2
O2 Reduction on Uniform Pt Nanoparticle Array
Electrodes, Hongzhou Yang, Sachin Kumar and Shouzhong Zou*,
Miami University Center for Nanotechnology, Department of Chemistry
& Biochemistry, Oxford, Ohio
Oxygen reduction reaction (ORR) is one of the
most extensively studied electrochemical reactions due to its
important role in fuel cells. A long-standing debate on the
ORR is whether the reaction kinetics depends on the particle
size. In the past decades, controversial observations have been
reported by different research groups. One conceivable reason
for the disagreement between different authors is the lack of
a good control of particle size and interparticle distance.
Recent advancement in the nanoparticle synthesis
and fabrication offers new opportunities for exploring the particle
size and other structural dependence of reactivity. In the present
work, uniform arrays of Pt nanoparticles with controlled size
and interparticle distance supported on glassy carbon electrodes
were formed by using polystyrene-poly(2-vinylpyridine) diblock
copolymers as the template. Electroreducion of O2 on these Pt
nanoparticle arrays was studied using rotating disk (RDE) and
rotating ring-disk electrode (RRDE) voltammetry. The obtained
results indicated that the specific activity of O2 reduction
increased with increasing particle size and the extent of H2O2
formation increases as the particle size decreases.
Poster 3
Effect of Dye Adsorption on Nanostructured TiO2
and ZnO based Dye Sensitized Solar Cells, Jie Pan and Lei L.
Kerr, Miami University Center for Nanotechnology, Department
of Paper and Chemical Engineering, Oxford, Ohio
Very recently, there is a growing interest in
using ZnO as an alternative electrode. However, the efficiency
of ZnO based-DSSC is much lower than that based on TiO2. The
interface between the ZnO/dye directly impacts the DSSC performance.
Nanostructured porous ZnO film was developed by a simple chemical
solution process. Nanostructured TiO2 was grown by dip coating.
The films of ZnO and TiO2 were controlled at similar thickness.
Adsorption studies were conducted at 25ºC and 40ºC.
The results showed that the Both TiO2 and ZnO based solar cell
performance were significantly influenced by the dye adsorption
temperatures. At higher adsorption temperature, the overall
cell efficiency of ZnO based solar cells is improved by 30%
(from 0.552% to 0.736%). Moreover, the problem of the dye aggregation
on the ZnO surface was reduced at higher adsorption temperatures.
The adsorption temperature has the adverse effect on TiO2 based
solar cell. At higher temperature, the overall cell efficiency
of TiO2 solar cell is decreased from 0.856% to 0.602%. The adsorption
mechanism and the opposite effect of dye adsorption temperature
on TiO2 and ZnO electrode is investigation.
Poster 4
CO and methanol electrooxidation on uniform
Au nanoparticle arrays in alkaline media – Role of particle
size and interparticle distance, Sachin Kumar and Shouzhong
Zou* Miami University Center for Nanotechnology, Department
of Chemistry and Biochemistry, Oxford, Ohio
In fuel cell research, the role of catalyst
particle structure, including size, surface atomic arrangement,
and composition towards catalyst performance have eluded researchers
for a long time. A common limitation in the previous studies
of nanoparticle electrocatalysis is the poor control over particle
size and distribution. Particle aggregation along with other
issues such as the presence of surfactant complicates the experimental
results. CO and methanol electrooxidation are two most studied
reactions in nanoparticle catalysis. This is primarily due to
their importance in fuel cell development. Typically, Pt and
Pt-based alloy particles are used for methanol oxidation. CO
poisoning effect along with the high cost of Pt has encouraged
researchers to find alternative catalyst materials. Au is one
of such alternative materials. Although Au is traditionally
considered as a poor catalyst for methanol oxidation, it has
been demonstrated by various researchers that after undergoing
activation steps, Au can possess unusually high catalytic activity.
Another advantage is that during methanol oxidation, in contrast
to the reaction on Pt, CO is not formed on Au. In addition,
in gas phase, supported Au nanoparticles show unexpectedly high
catalytic activity towards CO oxidation and the reactivity is
size dependent. Corresponding reaction in electrochemical environment
has not been systematically studied. In this presentation we
will demonstrate a simple route to synthesize arrays of Au nanoparticles
where the size and interparticle distance between nanoparticles
are well controlled. CO and methanol electrooxidation in alkaline
media on these Au nanoparticles will be used to explicate the
relationship between particle size, interparticle spacing and
reactivity. Comparison between gas phase and electrochemical
CO oxidation will be discussed as well.
Poster 5
Polymer thin film Modeling with Silica Substrate
in presence of Carbon Dioxide, Anand Srivastava, Coleman Alleman,
Somnath Ghosh, Jintao Yang, L J Lee Department of Mechanical
Engineering, The Ohio State University, Columbus, Ohio.
The classical processing and fabrication technologies
that produce stable macro and micro level polymer structures
cannot be used for fabrication of nanostructures because of
the length scale dependence of critical properties like Glass
Transition Temperature (Tg). Novel methods of fabricating polymers
nanostructures without introducing either organic solvents or
higher processing temperatures are being explored. One of the
methods is the use of sub critical CO2 as an intermediate processing
agent in the Polymer. In presence of CO2, there is Tg depression,
reduced viscosity and reduced interfacial tension, all of which
felicitate processing. However, because of the absence of any
understanding of the underlying molecular level mechanisms involved,
fabrication of stable structure is still questionable.
An objective of this research is to develop a molecular dynamics
(MD) based multi-scale computational model to understand these
mechanisms on polymer thin film due to the film size, free surface,
effect of CO2 and the type of substrate used. The models are
being developed based on related experimental work that is going
on in other polymer groups at NSEC.
Poster 6
Low-Cost Nanocomposite Tooling for Agile Manufacturing,
Richard Garozzo, Tom Glenchur, Derek Johnson, Ken Han, University
of Dayton Research Institute, Dayton, Ohio
"Low-Cost Nanocomposite Tooling for Agile Manufacturing,"
focuses on developing low-cost tooling solutions based on newly-commercialized
polymer nanocomposites. Conventional tooling materials such
as steel and aluminum are costly and time consuming to machine.
Often the cost of tooling negates business opportunities for
limited production runs which could lead to major new markets
and commercial products. While other tooling materials exist
for prototyping they are not suitable for production. The recent
commercialization of affordable polymer nanocomposite thermoset
molding compounds has created a new opportunity to make low
cost production tools with tailored mechanical, thermal, and
electrical properties. Tooling applications include injection
molding, compression molding, pultrusion, extrusion, filament
winding, resin transfer molding, blow molding, vacuum forming,
autoclave, resin film infusion, resin transfer molding, and
sheet metal stamping.
The goal of developing Low Cost Nanocomposite Tooling is to
protect Ohio manufacturers against international competition
from developing countries. In 1998, Dayton, Cleveland, Akron,
Toledo and Cincinnati were among the largest tooling and machining
centers in the United States. Over the past ten years, Ohio’s
tooling and machining capabilities have been dramatically reduced
due to the increased outsourcing of work to countries that have
lower labor costs. Outsourcing tooling not only is a problem
for the Ohio’s tool and die industry, but also for the
rest of Ohio’s industry, due to a cascade effect. For
example, when tool and dies are made in other countries, eventually
the part manufacturing and assembly work will also be outsourced.
We are seeking a technology that would result in significantly
lower tool and die costs and drastically shorter lead times.
The total time to make large production tools from this process
could mean a reduction from 26 weeks for metal tooling to 4
weeks for hybrid non-metal-nanopolymer tooling, with an accompanying
cost saving of 75%. This could be the competitive advantage
that will allow Ohio to successfully compete in the 21st century
economy.
The limitation of currently used filled-polymer tooling is lack
of hardness, toughness, thermal and electrical conductivity,
and inability to hold threaded holes for hardware attachment.
If a polymer material could be made electrically conductive
through the utilization of nanomaterials, metal coating processes
could be used to deposit a metal surface coating for hardness
and durability. Improvements in thermal conductivity would also
be valuable for heat transfer issues and improved physical properties
will provide improved machineability and durability.
UDRI is interested in developing the improvements to the existing
filled polymer material using available nanomaterials and processing
technology. Throughout the program, UDRI is providing expertise
in materials testing, analysis, and basic understanding of the
nanomaterials. Subsequent work could be funded directly by the
collaborators for transition into their own industrial applications.
This project directly leverages off UD's existing Third Frontier
projects which support commercialization of carbon nanoparticles,
dispersion of nanoparticles into polymers, and manufacturing
of components produced from polymer nanocomposites.
Poster 7
Development of Carbon Nanofiber-Reinforced Polyimide Films and
Composites”, Don Klosterman, Rob McKellar, Bill Price,
University of Dayton Research Institute (UDRI), Dayton, Ohio
This poster will highlight three areas of achievement
and capability relating to the production of polyimide materials
with enhanced properties via addition of carbon nanofibers.
The first area involves organic functionalization of carbon
nanofibers for improved compatibility with polyimide resin systems.
The second area is production of thermoplastic polyimide films
with well dispersed nanofibers for enhanced mechanical and electrical
properties. The third area is addition of carbon nanofibers
to thermosetting polyimide resins for improved mechanical and
thermooxidative stability. The poster will highlight not only
the material properties but the scaleable processing techniques
used to produce these materials.
Poster 8
Carbon Nano Fiber (CNF) Modified Thermoplastic
Polymer Process and Property Study, Jared Stonecash, James Hartings,
University of Dayton Research Institute, Multiscale Composites
and Polymers Division, Dayton, Ohio
Abstract: Several thermoplastic + carbon nanofiber
(CNF) nanocomposites were prepared by melt compounding and extrusion.
These materials were then injection molded into tensile bar
test specimens (ASTM D638) for material property evaluation.
Injection molding process conditions were varied for the baseline
thermoplastic polymers as well as for the polymer nanocomposites
to determine molding condition affects on final part properties.
CNF concentration was varied by diluting the base nanocomposite
with more polymer to yield the desired nanofiber loading level.
All of the final parts were evaluated for tensile properties,
CNF dispersion and electrical properties to provide structure-property
relationships for this new class of multi-functional materials.
Poster 9
Nanophotonic Device Engineering, Scott A. Masturzo1,
Joseph T. Boyd1, Howard E. Jackson2, Jan M. Yarrison-Rice3,
Robert L. Ewing4, 1 Department of Electrical & Computer
Engineering, University of Cincinnati, 2 Department of Physics,
University of Cincinnati, 3 Department of Physics, Miami University,
4 Air Force Research Laboratories, WPAFB
Design, fabrication, and characterization of
nanophotonic devices including grating couplers, planar solid
immersion lenses, and photonic crystals is presented. Integration
of optically active materials with silicon-on-insulator photonic
crystals for optically tunable devices is discussed.
Poster 10
Super-Long Multiwall Carbon Nanotube Arrays for Spinning Yarn,
Chaminda Jayasinghe*, Pravahan Salunke*, Lucy Lee*, Emily Head*,
Nilanjan Mallik**, YeoHeung Yun**, Chandrashekhar Pendyala***,
Mark J. Schulz** and Vesselin N. Shanov* * Department of Chemical
and Material Engineering, University of Cincinnati, Cincinnati,
Ohio, ** Department of Mechanical Engineering, University of
Cincinnati, Cincinnati, Ohio, *** Department of Chemical Engineering,
University of Louisville, Louisville, Kentucky
Centimeter long Multiwall Carbon Nanotube (MWCNT) arrays have
been grown by Chemical Vapor Deposition (CVD) from H2-C2H4-H20-Ar
gas mixture at 750° C in an EasyTubeTM furnace from First
Nano Inc. The arrays were characterized by Atomic Force Microscopy
(AFM), Scanning Electron Microscopy (SEM), Transmission Electron
Microscopy (TEM) and Raman spectroscopy. The diameter of the
CNT was found to be affected by the substrate design. The catalyst
thickness and the catalyst annealing temperature had great impact
on the nanotube diameter. The CVD growth has been optimized
with respect to the length and the purity of the CNT. It was
found that the carbon partial pressure in the CVD gas phase
and the growth temperature affect dramatically the quality of
the arrays. Base on the optimized process 15 mm long CNT arrays
were synthesized and preliminary data were obtained on spinning
them into yarns.
Poster 11
Substrate Preparation by Magnetron Sputtering
for Chemical Vapor Deposition Growth of Long Carbon Nanotube
Arrays, Pravahan Salunkea, Sergei Yarmolenkoc, Sudhir Nerallac,
Svetlana Fialkovac , Jaganathan Sankarc, Kyle Fischbacha, Ge
Lia, Chaminda Jayasinghea, Wondong Choa, Emily Heada, Yeo-Heung
Yunb, Mark Schulzb and Vesselin Shanova*, aDepartment of Chemical
and Materials Engineering, University of Cincinnati, Cincinnati,
Ohio, bDepartment of Mechanical, Industrial and Nuclear Engineering,
University of Cincinnati, Cincinnati, Ohio, c Department of
Mechanical and Chemical Engineering, North Carolina Agricultural
and Technological State University, Greensboro, NC
In this study we explored the use of magnetron
sputtering as an alternative to e-beam deposition for preparation
of the alumina intermediate layer and of the metal catalyst
on an oxidized Si wafer. This approach offers large area deposition
of the layered substrate which is promising for scaling up the
process. The effects of the substrate design on the growth of
long multi-wall carbon nanotube (MWCNT) arrays by CVD (Chemical
Vapor Deposition) were also explored. The CNT synthesis was
carried on in a hydrogen/ethylene/water/argon environment at
750 °C for different periods of deposition time. Atomic
Force Microscopy (AFM), Scanning Electron Microscopy (SEM),
X-Ray Diffraction (XRD), Thermal Gravimetric Analysis (TGA)
and Transmission Electron Microscopy (TEM) were employed to
characterize the substrates and the CNT arrays. The study showed
that for specific processing conditions the length of highly
oriented CNTs strongly depends on the thickness of Al2O3 intermediate
layer and on the catalyst film. The obtained results confirm
that magnetron sputtering can be successfully employed as a
tool for substrate preparation which was used to grow up to
10 mm long CNT arrays with high purity. The aligned nanotubes
do not suffer from limitations typical for powdered (spaghetti
type nanotubes) which opens up possibilities for new applications.
Poster 12
Carbon nanoadditives to enhance latent energy
storage of phase change materials, Shadab Shaikh, Khalid Lafdi,
Kevin Hallinan. Mechanical Engineering, University of Dayton,
Dayton, Ohio
The present work focus on analyzing the energy
storage capacity of a PCM based nanocomposites. It is perceived
that by the intimate inclusion of carbon nanotubes (CNT) in
the PCMs their thermal properties can be changed. For a matrix
with nano-scale CNT the surface to volume ratio is very high
and consequently the molecular interaction between the nanotube
surface and PCM can change the heat of fusion and melting point
of the original PCM. By optimizing the amount of CNT inside
the PCM, the properties of the PCM can be altered to improve
their thermal performance based on a specific application.
Poster 13
An assay for metallic/semiconducting carbon
nanotube contents in mixtures, Wei Lu, Yao Xiong, and Liwei
Chen, Ohio University, Nanoscale and Quantum Phenomena Institute
(NQPI), Athens, Ohio
An assay for metallic/semiconducting carbon
nanotube contents in mixtures, Ohio University, Nanoscale and
Quantum Phenomena Institute (NQPI), As prepared single-walled
carbon nanotube samples are mixture of metallic and semiconducting
species. Although electric transport measurements and resonance
Raman spectroscopy can give some information about the metallic
or semiconducting nature of the tubes, a quantitative assay
for the content of these two categories is lacking. Here we
report a scanning force microscopy based assay.
Poster 14
Smart Nanocomposites for Industrial Health Monitoring,
Gunjan Maheshwari1, Wondong Cho2, Jandro Abot3, Nilanjan Mallik1,
Surya Narayanan Sundaramurthy1, Emily Head2, Mitul Dadhania1,
Weifeng Li1, Vesselin Shanov2, Chaminda Jayasinghe2, Pravahan
Salunke2, Lucy Lee2, Douglas Hurd1, YeoHeung Yun1, Sergey Yarmolenko4,
Jag Sankar4, Mark J. Schulz1, 1-University of Cincinnati, Mechanical
Engineering, Cincinnati, OH, 2-University of Cincinnati, Chemical
and Materials Engineering, Cincinnati, OH, 3-University of Cincinnati,
Aerospace Engineering, Cincinnati, OH, 4-Department of Chemical
and Mechanical Engineering, Center for Advanced Materials and
Smart Structures, North Carolina A&T State University, Greensboro,
NC
There is a need for new smart materials for
use in large industrial health monitoring applications. This
paper explores the use of Carbon Nanotubes (CNT) and Carbon
Nanosphere Chains (CNSC) to develop nanocomposite smart materials
having electrochemical impedance, piezoresistive, and magnetic
properties for sensing. These responsive nanocomposites exhibit
a change in electrical conductivity due to strain that can be
used for detection of structural damage and abnormalities. Along
with excellent mechanical, thermal, and electrical properties,
CNSC have shown weak magnetic properties obtained by post processing
the material. This novel material might be used to replace iron
thereby reducing sensor weight and cost, which can be crucial
for industrial applications. Nanocomposites based on host materials
like epoxy, elastomers, cement, and ice have shown a change
in electrical properties when subjected to stress. Distributed
sensors based on “spray-on nanocomposites” on complex
structures change electrical impedance when subjected to external
loading. Fabrication, characterization and testing of carbon
nanocomposite materials will be discussed in the paper. Electrochemical
Impedance Spectroscopy (EIS) and piezoresistivity testing will
be discussed to characterize the electrical properties of the
nanocomposite. Since the nanocomposite has piezoresistivity
and electrochemical properties, it can monitor the health of
a structure and detect changes due to deterioration of large
complex structures. Also, a novel application of CNT arrays
is improving the interlaminar shear strength and enhancing the
transverse elastic modulus of aligned fiber composites. This
can be crucial for the automotive and aerospace industries because
there is a need to improve the transverse properties and toughness
of lightweight fiber composites.
Poster 15
CAE Applications in Product and Process Developments
of Nano-Composites, Ken Han and Brian Rice, Multiple Scale Composite
& Polymer Division, UDRI, Dayton, Ohio
Computer Aided Engineering (CAE) plays a key role in nano-material
product and process developments. CAE tools were used in Injection
molding, co-injection molding and manufacturing of injection
mold with nano-materials developments at UDRI. The poster shows
the CAE tool capabilities and applications in the nano-material
product and process developments.
Poster 16
A CNT hierarchical reinforcement approach for
superior matrix-dominated properties in fiber reinforced polymeric
composites. Mandar Kulkarni1, Gunjan Maheshwari2 , D. Qian2
,J. L. Abot1, 1Department of Aerospace Engineering & Engineering
Mechanics, University of Cincinnati, 745 Baldwin Hall, Cincinnati,
OH, 2 Department of Mechanical Engineering, University of Cincinnati,
Cincinnati, OH
Fiber composite materials are ideal engineered
materials to carry loads and stresses in the fiber direction
due to their high in-plane specific mechanical properties. However,
premature failure due to low transverse ultimate material composite
properties constitutes a fundamental weakness of composites.
A solution to this problem is being addressed through the creation
of a nanoreinforced composite material where carbon nanotubes
are grown in the surface of the fiber filaments to increase
the matrix-dominated properties. The carbon nanotubes increase
the effective diameter of the fiber and provide a much larger
interface area for the polymeric matrix to wet the fiber.. These
nanoreinforced composite materials are presently being fabricated
and characterized under quasi-static mechanical loading in the
transverse direction to the fiber. A study is now being carried
out to numerically predict the elastic properties of these nanoreinforced
composites. A fully three-dimensional (3D) Finite Element (FEA)
is being developed considering perfect bonding between the phases
of the composites. Preliminary studies were conducted on a representative
volume element of a non-reinforced composite and the results
were correlated with micromechanical models. The numerical results
from this study will be correlated with those of the experiments
for the nanoreinforced polymeric composites. These composites
could prove critical for many automotive and aerospace industries
where there is a need to improve the transverse properties and
toughness of lightweight fiber composites.
Poster 17
Electrodeposited Perpendicularly Oriented Mesoporous
Materials, Aleksey N Pisarenko, Wolfgang U. Spendel, Richard
T. Taylor, Jordan D. Brown, James.A. Cox, and Gilbert E. Pacey,
Miami University Center for Nanotechnology, Department of Chemistry
and Biochemistry, Oxford, Ohio
Mesostructured supported films have been synthesized
to produce new electrodeposited perpendicularly oriented mesoporous
materials (EPOM’s). The principle demonstrated here is
electrochemically induced self-assembly of CTAB (cetyl trimethylammonium
bromide) surfactant at the solid-liquid interface and electrochemical
catalysis method to produce sol-gel EPOM. A substituted coumarin
4 molecule was incorporated into the sol gel material and was
used to study the various characteristics of the EPOM.
Poster 18
Synthesis of ZnO Nanoparticles By Microwave
Radiation, Sasha A. Ivanov, Aleksey N Pisarenko, Wolfgang U.
Spendel, and Gilbert E Pacey, Miami University Center for Nanotechnology,
Department of Chemistry and Biochemistry, Oxford, Ohio
Zinc oxide (ZnO) nanoparticles were synthesized
in aqueous / glycerin solutions using microwave radiation. The
reported method is faster, less costly, and comparatively selective
as compared to hotplate or oven synthesis methods. Different
sizes and shapes are controlled by varying the water to glycerin
ratio in sample solutions. Spheres, rods, and cones are obtained.
Particles sizes of 25-500 nm are produced. This allows us to
tune optical properties of the nanoparticles.
Poster 19
Dynamic Covalent Assembly of 2D Organic Nanostructures,
C. Scott Hartley,1,2 Erin L. Elliott,2 and Jeffrey S. Moore2
1Miami University Center for Nanotechnology, Department of Chemistry
and Biochemistry, Miami University, Oxford, Ohio 2Department
of Chemistry, University of Illinois at Urbana-Champaign, Urbana,
Illinois
The construction of atomically-precise organic
nanostructures represents a current challenge for organic materials
synthesis. Dynamic covalent chemistry has established itself
as an attractive route to the self-assembly of nanoscale organic
compounds, allowing the formation of multiple covalent bonds
in a single step in high yield. Here we demonstrate that imine
formation/metathesis can be used to crosslink m-phenylene ethynylene
oligomers to give two dimensional shape-persistent nanostructures.
The resulting structures are simple [n]-rung molecular ladders
with dimensions of up to ~1.6 × 6.2 nm (n = 6). These
materials represent the first step in the synthesis of larger
grids with potential use as high precision nanofiltration membranes
or “smart matrix” grids to position units for solar
energy harvesting. We also demonstrate that the directionality
of the imine bond can be used to program covalent self-assembly,
much in the same way that the directionality of the hydrogen
bond is used to direct the assembly of non-covalent structures.
Specifically, we have prepared a series of unsymmetrical shape-persistent
macrocycles with a variety of side-chain substitution patterns.
Poster 20
EMI Shielding Properties of Exfoliated Graphite
Based Nanocomposites, Matt Boehle, Elizabeth Zinsser, Khalid
Lafdi, Peter Collins, 1. University of Dayton, 300 College Park
Dayton Ohio, 2. Air Force Institute of Technology, 2950 Hobson
Way Wright-Patterson AFB, Ohio
The increasing density of electronic devices
in industrial and military applications has lead to a need for
enhanced electromagnetic shielding properties. Plastics have
also become a major component in most electronic devices. Polymer
composite shielding materials utilizing carbon nanotechnology
merge these requirements into a device with reduced cost, higher
performance and lower weight. In this study, the relationship
between EMI shielding effectiveness and resistivity of epoxy
composites was examined. Test specimens were prepared with varying
concentrations and sizes of exfoliated graphite used as an additive.
Exfoliated graphite is an ideal choice as it possesses high
conductivity, light weight and low cost. After testing the composite
panels, a strong correlation between electrical properties and
EMI shielding was found. The end goal of this work is to characterize
the EMI shielding performance of carbon nanocomposites in order
to design a material which can be optimized for a given application.
Poster 21
SiO2 Thin Film Deposition Techniques and Low
Index SiO2 Thin Film, Mengshu Pan, Andrew Sarangan University
of Dayton
Three common SiO2 thin film deposition techniques
are presented here, which are Radio Frequency Sputtering, Electron-Beam
Evaporation and Plasma Enhanced Chemical Vapor Deposition. The
fabrication of ultra-low index nano-porous glass film using
oblique angled e-beam evaporation and the experimental results
are also presented.
Poster 22
Nanostructured Carbon Containing Nitrogen as
Cathode Catalysts in the PEM Fuel Cells, Elizabeth J. Biddinger,
Paul H. Matter, Dieter von Deak, Umit S. Ozkan, Chemical and
Biomolecular Engineering, The Ohio State University, Columbus,
Ohio
Less expensive nitrogen containing carbon nanostructured
(CNx) catalysts have been studied as an alternative to the current
oxygen reduction reaction (ORR) Pt catalysts for the cathode
catalyst of PEM and Direct Methanol Fuel Cells. These CNx catalysts
have been shown to be active for ORR in acidic media. The nature
of the active site for nitrogen-carbon ORR catalysts has been
debated in the literature. Previous studies at Ohio State have
revealed that a transition metal is not required on the CNx
catalyst for it to reduce oxygen. Activity increased with graphitic
edge plane exposure and pyridinic-Nitrogen content (found on
the edge plane) determined by X-ray photoelectron spectroscopy
(XPS). Nano-structure morphology appeared to affected ORR activity
and selectivity. These CNx catalysts have been extensively characterized
and tested for activity and selectivity by the rotating ring
disk method (RRDE).
Poster 23
Bottom-Up Synthesis of Graphene Nanoribbons, Jason L. Crase,
Benjamin R. Wiechmann, and C. Scott Hartley* Miami University
Center for Nanotechnology, Department of Chemistry and Biochemistry,
Miami University, Oxford, Ohio
There has been recent and growing interest in
graphene, a two-dimensional sheet of benzenoid carbon atoms
(the basic unit of graphite), for use in nanoscale electronics
and other areas (e.g., hydrogen storage, organic magnetism).
Here we discuss our efforts toward the bottom-up synthesis of
one-dimensional (board-like) graphene oligomers. Our strategy
is to synthesize an o-phenylene oligomer, which will be planarized
by oxidative cyclodehydrogenation (the Scholl reaction). We
expect these materials to compliment the behavior of the existing
graphene nanostructures prepared by organic synthesis (e.g.,
hexabenzocoronenes). Specifically, we believe they will be predisposed
to lamellar (as opposed to columnar) self-assembly, and will
better maintain solubility as their size is increased.
Poster 24
Novel Materials Based on Tubular Discotic Liquid
Crystals, Amanda E. Ponsot, Katherine M. Digianantonio, and
C. Scott Hartley*, Miami University Center for Nanotechnology,
Department of Chemistry and Biochemistry, Miami University,
Oxford, Ohio
The synthesis of materials exhibiting unusual nanoscale features
is one of the major challenges facing chemists today. We are
currently interested in developing the tubular discotic liquid
crystal phase as a component for new materials. This phase is
similar to the well-known columnar discotic liquid crystal phases,
but rather than plate-like molecules stacked into columns it
consists of shape-persistent macrocycles stacked into tubes
(with the tubes further organized into a hexagonal lattice).
Because these tubes are, in principle, empty, this material
is (effectively) the liquid crystalline analogue of a porous
crystal (i.e., a porous fluid). This behavior is rare, but a
few examples of macrocycles exhibiting columnar phases have
been reported. We are interested in studying the use of these
materials as hosts for organic guest molecules. Our goal is
to develop hybrid materials which combine the properties of
the liquid crystalline host (e.g., self-assembling order, fluidity)
with new properties due to the guest molecules (e.g., ferroelectricity).
Poster 25
Nanotube Hairy Fibers and Vertically Aligned Nanotube Films
(Nanotube Grass), Lingchuan and Khalid Lafdi , Mechanical Engineering,
University of Dayton, 300 College Park Dayton Ohio
For exploring applications of nanocarbon in producing polymeric
composites, energy conversion and storage, and thermal management,
two efforts were carried out. One involves growing carbon nanotubes
(CNTs) on carbon fibers (bundle, veil, fabric), while another
involves producing nanocarbon films. Our studies have showed
that uniform CNTs with good adhesion, controllable CNT density
and length could be grown on carbon fibers, giving promising
potential uses of the carbon nano-architecture. Large CNT-polymer
and free-standing carbon nanofiber films could also be produced.
Poster 26
Growth of Carbon Nanotubes on Porous Microcellular
Carbon Substrates I.T. Barney, A.G. Jackson, and S.M. Mukhopadhyay
Department of Mechanical and Materials Engineering, Wright State
University
This project focuses on the growth of carbon
nanotubes (CNTs) over larger engineering structures, including
microcellular porous material. The goal is to create multi-scale
materials with significantly increased surface area for advanced
thermal, catalytic and electrochemical applications. Nanotubes
have been fabricated on various graphitic substrates (microcellular
foams, fibers, and flat model surfaces ) using chemical vapor
deposition (CVD). Structure and morphology of CNT growth has
been characterized using Field Emission Scanning Electron Microscopy
(FE-SEM) and analyses of chemical states have been preformed
using x-ray photoelectron spectroscopy (XPS) It is seen that
a plasma enhanced nano-coating on the uneven surface significantly
enhances its catalytic activity, and improves CNT growth. Other
factors influencing growth kinetics are gas flow and pore geometry.
BET surface area analysis and thermal transport measurements
have been performed to understand structure- property relationships.
These results will be presented in light of understanding and
controlling growth mechanisms for future applications.
Poster 27
Two Photon absoption and nonlinear refraction
in PTCDA films, *A.M. Ajward, V.R. Gangilenka, #H. Schmitzer,
*H.P. Wagner, *Department of Physics, University of Cincinnati,
Ohio, #Department of Physics, Xavier University, Cincinnati,
Ohio
The two-photon absorption coefficient of a polycrystalline
PTCDA (perylene-3,4,9,10-tetracarboxylic-3,4,9,10-dianhydride)
thin film was measured at 880 nm using the z-scan technique.
The 2 µm thick PTCDA film was grown by organic molecular
beam deposition (OMBD) on Pyrex. For the z-scan measurements
~1 ps pulses were focused onto the thin film using a microscope
objective lens (100x) of numerical aperture 0.55 and a beam
waist of 1 µm. The films have been moved by a translation
stage with a travel range of 100 µm and with a step size
of 0.5 µm. The two-photon absorption coefficient of PTCDA
obtained from a fit with open aperture measurements at different
intensities results to ~20 cm GW-1 and the nonlinear refraction
coefficient obtained from a fit to closed aperture measurements
results to ~-1.4x10-12 cm2/W. The z-scan measurements demonstrate
that crystalline PTCDA films possess strong nonlinear optical
properties that might be utilized for optical applications.
Poster 28
Effect of Catalysts, Contaminants and Surface
Area on Toxicity of Carbon Bases Nanomaterials, K. Lafdi, C.
Grabinski, M. Gamble and P. Tsonis, Center for Tissue Regeneration
and Engineering at Dayton, University of Dayton, 300 College
Park, Dayton, Ohio.
Previous studies have shown that the presence
of metal impurities plays an important role in the toxicity
of carbon nanotubes (CNT). Specifically, the metal impurity
content correlated to the level of oxidative stress in the cells,
marked by the production of reactive oxygen species (ROS). However,
the viability of the cells, measured by their mitochondrial
function, did not correlate directly with the metal impurity
content in CNT, so there must be additional factors that affect
the toxicity of carbon-based nanomaterials. Many studies have
suggested that high surface area per mass may play a role in
nanomaterial toxicity. Therefore, further studies were carried
out to test the effect of surface area on cell viability and
oxidative stress in vitro. Results showed that CNT with low
impurities and low surface area did not significantly reduce
cell viability or induce oxidative stress in cells. However,
nanographite, induced the production of ROS nearly 10 times
greater than that induced by CNT with high impurities. Because
nanographite lacks impurities, this effect must be due to the
exceptionally high surface area. To compliment these results,
the relative toxicity of metal catalysts commonly used in the
synthesis of CNT was investigated, including aluminum oxide
coated and uncoated iron, nickel, and cobalt. It was found that
aluminum oxide-coated nanoparticles produced less toxicity than
those that were not coated. The results of these studies reveal
that carbon-based nanomaterial toxicity is a function of both
impurity content and surface area, and that toxicity of metal
catalysts is reduced with the addition of an aluminum oxide
coating.
Poster 29
Thermo-optical Properties and Characterization
of Heat Generation of Single Gold Nanoparticles Embedded in
Ice, Thomas, A. C.1, Richardson, H. H.1, Carlson, M. C.1, and
Govorov, A. O.2, 1Ohio University, Chemistry and Biochemistry,
Athens, Ohio, 2Ohio University, Physics and Astronomy, Athens,
Ohio
We have previously investigated the thermo-optical
properties of gold nanoparticles (Au NPs) embedded in an ice
matrix.1 Resonant laser light of relatively weak intensity is
able to melt ice with embedded Au NPs, whereas even a very intense
laser beam does not melt ice alone. We have also theoretically
determined that the local temperature in and around a NP complex
is dependent on its geometry and large scattering in melting
power is observed for aggregated complexes.2 By immobilizing
the NPs on a glass surface, we are able to characterize them
by atomic force microscopy (AFM) and single particle spectroscopy.
Using both techniques, we are able to determine the heat generation
of single NPs embedded in an ice matrix as a function of laser
intensity and matrix temperature.
1 Richardson, H. H.; Hickman, Z. N.; Govorov,
A. O.; Thomas, A. C.; Zhang, W.; Kordesch, M. E., Thermooptical
properties of gold nanoparticles embedded in ice: Characterization
of heat generation and melting. Nano Letters 2006, 6, 783-788.
2 Govorov, A. O.; Zhang, W.; Skeini, T.; Richardson, H.; Lee,
J.; Kotov, N. A., Gold nanoparticle ensembles as heaters and
actuators: melting and collective plasmon resonances. Nanoscale
Research Letters 2006, 1, 84-90.
Poster 30
Single CdS Nanosheets: Spatially-resolved Photoluminescence
Mapping, M. Fickenscher, T. B. Hoang, L. V. Titova, A. Mishra,
L. M. Smith, H. E. Jackson, Department of Physics, University
of Cincinnati, Cincinnati, OH 45221, J. M. Yarrison-Rice, Physics
Department, Miami University, Oxford, OH 45056, H. Rho, K. -Y.
Lee
Department of Physics, Chonbuk National University, Jeonju 561-756,
Korea, Y. -J. Choi, K. J. Choi, and J. -G. Park, Nano Materials
Research Center, Korea Institute of Science and Technology,
Seoul 130-650, Korea
Results of spatially-resolved low temperature
photoluminescence of single 5 micron wide, 30 micron long and
50 nm thick CdS nanosheets are presented. The sheets, grown
by pulsed laser deposition using vapor-phase transport, are
uniform in size and shape and exhibit a hexagonal wurtzite structure.
The orientation of the c-axis determined by PL polarization
analysis and HR TEM varies from sheet to sheet. A method for
determining the c-axis direction from the polarized PL is demonstrated.
The spatially-resolved PL reveals spectral variation across
the sheet, with A-like excitons at the edges showing a spectral
peak at 2.547eV, and B like excitons at the center showing a
peak at 2.563eV. Exciton lifetimes of ~200 ps are observed,
which are significantly longer than CdS nanowires of identical
diameter, but shorter than measured in bulk CdS.
Support provided by NSF (#0701703), Korea Research
Foundation and KIST.
Poster 31
Synthesis and Chemistry of Size-Constrained
Cadmium Sulfide Quantum Dots in Microporous Materials, Jeremy
White, Prabir K. Dutta, Department of Chemistry, The Ohio State
University, 120 W 18th Avenue, Columbus, Ohio
Attention to the synthesis and characterization of semiconductor
quantum dots (QDs) from 2-10 nanometers has greatly increased
due to their interesting optical properties and applications
in photovoltaics and biological imaging. Cadmium sulfide (CdS)
is one example of these II-VI type semiconductors; however,
the solution based synthesis of CdS QDs with sizes smaller than
2 nm is extremely difficult. The microporous framework of zeolites
have been considered as ideal hosts for generating highly uniform
QDs. Because of its geometric properties, zeolite Y limits the
size of incorporated nanoparticles to 1.5 nm due to the limited
pore size. Motivated by these findings, the current research
is aimed at the characterization and isolation of uniform CdS
quantum dots of 1.5 nm or smaller synthesized within the framework
of zeolite Y. It was found that under anhydrous conditions,
the zeolite framework helps to organize the CdS QDs into regularly
spaced 3D arrays, as well as prevents them from aggregating
into larger particles. However, upon exposure to moisture the
CdS QDs become larger than the zeolite pores, thus forcing them
to the exterior of the zeolite. Strategies are currently being
developed to isolate the CdS quantum dots from the zeolites,
while maintaining their small particle size. The structural
and optical properties of the as-synthesized quantum dots were
characterized by electron microscopy, Raman spectroscopy, ultrafast
time-resolved spectroscopy, as well as absorption and fluorescence
based assays.
Poster 32
Polymer-Fullerene Bulk Heterojunction Photovoltaic Devices for
Efficient Solar Energy Conversion on a Low-Cost, Flexible Substrate,
Woo-Jun Yoon and Paul R. Berger*, Department of Physics, The
Ohio State University, Columbus, Ohio
Polymer-fullerene bulk heterojunction photovoltaic
(PV) devices are of tremendous interest for their potential
societal benefits and the opportunity for relatively low cost
production on flexible substrates. We will discuss the interface
engineering, the low-bandgap absorber toward for spectral expansion,
and hermetic packaging for highly efficient polymer-fullerene
bulk heterojunction PV devices.
Poster 33 e-mail sent
Ceramic Nano-Structures without Lithography:
Platforms for Chemical Sensing and Catalysis, B. Dinan, S. Yoo,
C. Carney, M. Rauscher, H. Lee, S. Dregia and S. Akbar, Material
Science, The Ohio State University, Columbus, Ohio
Due to their enhanced properties nanostructures
have been widely researched. One way to produce nanostructures
is by a gas phase reaction brought about by a thermal treatment
process. Using this method we have developed several different
ceramic nanostructures from a wide range of materials including
SnO2, TiO2, Ti, and Gd-doped CeO2. Some potential applications
for these materials include platforms for chemical sensing,
catalysis, photo-catalysis, bio-medical, and nano-fluidics.
Poster 34
Impact of Near-Surface Native Point Defects,
Chemical Reactions and Surface Morphology on ZnO Interfaces,
D. Doutt,1 M. Kramer,1 D. Tayim,2 C. Zgrabik,1 Z.Q.Fang,3 D.C.
Look,3 G. Cantwell,4 J. Zhang,4 J.J. Song,4 H.L. Mosbacker,1
L.J. Brillson1,5 1Department of Physics, The Ohio State University,
Columbus, Ohio 2Columbus School for Girls, Bexley, Ohio, 3Z.Q.Fang
and D.C. Look, Wright State University, Dayton, OH 45433, 4ZN
Technology, Inc., La Brea, California, 5Dept. of Electrical
& Computer Engineering, Ohio State University, Columbus,
Ohio
ZnO has been studied actively for over 50 years, yet it is only
in the past few years with greater control of its crystal quality
and doping that its outstanding optoelectronic, microelectronic,
and chemical sensing properties have emerged. Central to all
these applications is the understanding and control of ZnO surface
and interface electronic properties, yet these have until recently
remained largely unexplored. We have used a complement of depth-resolved
cathodoluminescence spectroscopy (DRCLS), temperature-dependent
charge transport, deep level transient spectroscopy (DLTS),
atomic force microscopy (AFM), and Kelvin probe force microscopy
(KPFM) to correlate the formation of native point defects with
interface chemical reactions as well as surface morphology and
their impact on charge transport at metal-ZnO junctions. Previously,
we showed that surface adsorbates, hydrogen donors, and subsurface
native point defects each contribute independently to interface
charge transport and Schottky barrier formation (1). Furthermore,
metal deposition (2) and subsequent annealing (3) induce additional
native point defects extending tens of nanometers or more below
the free ZnO surface that increase tunneling, recombination
and hopping transport.
We have now studied a wide array of ZnO crystals grown by vapor-phase
transport, melt, and hydrothermal growth methods. These crystals
display orders-of-magnitude variation in 2.1, 2.5, and 3.0 eV
native point defect optical transitions at their free surface
and as a function of depth on a nanometer scale. DLTS within
50-200 nm depths confirms such variations along with the production
of new defects and higher carrier concentrations that reduce
effective barriers. Our melt-grown and vapor-phase ZnO exhibit
uniformly distributed defect emission from the surface to the
bulk, whereas hydrothermal ZnO displays up to 100x increase
in defect density from <5nm to 1000 nm below the surface.
AFM using a Park Systems XE-70 reveals large variations in surface
morphology related to the growth method and subsequent processing.
Significantly, when the DRCLS defect emission is low, surface
roughness is low and morphology matches the KPFM potential images.
When DRCLS emissions vary with depth, AFM and KPFM potential
maps do not correlate. Indeed, the latter can vary by hundreds
of meV across micron square areas. We are now correlating specific
potential variations within these inhomogeneous regions with
DRCLS defect emissions localized on a nanometer scale. Measurement
of these near-surface states associated with native point defects
and those induced by interface chemical bonding can provide
a guide to understanding and controlling ZnO electronic contacts.
Supported by National Science Foundation Grant DMR-0513968 (Verne
Hess) and AFRL under Contract No.FA8650-06-D5401 (J. Zetts).
1. Y.M. Strzhemechny et al., Appl. Phys. Lett. 84, 2545 (2004);
H.L. Mosbacker et al., ibid. 87, 012102 (2005).
2. L.J. Brillson et al., Appl. Phys. Lett. 90, 1 (2007).
3. H.L. Mosbacker et al., Appl. Phys. Lett., 91, 072102 (2007).
Poster 35
Phonon-assisted charge hopping and its role
in odor recognition models, Edson Vernek and Sergio Ulloa, Department
of Physics and Astronomy, and Nanoscale and Quantum Phenomena
Institute, Ohio University, Athens, Ohio
How humans recognize odors is a very interesting
subject. Although attempts to explain how we recognize several
odors from different molecules at different concentrations have
been published, the models are still unable to fully explain
the molecular selectivity of odorants and other characteristics
of the olfactory process. One recent attractive model was proposed
by Luca Turin in the last decade [1].
Turin's ideas were based on exploring the role
of quantum mechanical vibrations (phonons) in the activation
mechanism that triggers odorant detection. One of the advantages
of his model compared to the “/lock and key”/ model
[2] is that he was able to explain why different molecules may
smell alike while other very similar molecules smell different.
Turin suggested that the size and shape argument
implied in the “/lock and key” /mechanism may be
important but it is not enough to explain odor recognition.
Recently a Hamiltonian model was proposed by Brookes et al.
[3], which took steps to quantitatively confirm the viability
of Turin's ideas. The model is based on a two level system (/donor/
and /acceptor/ levels) with a /local/ electron-phonon interaction,
which produces inelastic (phonon-assisted) tunneling between
the /donor/ and /acceptor/ levels.
Realistic systems, however, may include not
only local but /non-local/ electron-phonon interactions, where
electron can relax from the /donor/ to the /acceptor/ level
by emitting a phonon. We propose a Hamiltonian which includes
this mechanism and study the consequences of their presence
for the Turin's mechanism. Preliminary results show that for
almost the entire range of /non-local/ electron-phonon coupling
the model still contains the proper conditions of validity of
Turin's model. However, we find that for a narrow range of coupling
values, odor recognition is not possible and the model breaks
down.
References:
[1] L. Turin, Chem. Senses *21*, 773 (1996).
[2] R. B. Silverman, “The Organic Chemistry of Enzime-Catalyzed
Reactions” (Elsevier, New York, 2002).
[3] J. C. Brookes et al, Phys. Rev. Lett. *98*, 038101 (2007).
Poster 36
Cavity Resonances of Metal-Dielectric-Metal
Nanoantennas, Bhuwan P. Joshi and Qi-Huo Wei, Liquid Crystal
Institute, Kent State University, Kent, Ohio
We numerically study the optical properties
of nanaoantennas consisting of two metal nanorods stacked vertically
with a dielectric disk spacer. In addition to antenna resonances,
these new nanoantennas show interesting cavity resonance behaviors
when the spacer thickness is below 5nm and the diameter of the
dielectric disk is smaller than the diameter of the metal rods.
The antenna resonance generates a peak in far-field scattering
spectra, while the cavity resonances generate multiple dips
in the scattering spectra. The cavity and antenna resonant frequencies
are widely tunable through varying the size of the dielectric
disk. Cavity resonances result strong local field enhancements
inside the nanocavity, and the enhancement factors are much
higher than those resulting from only antenna resonances. This
new nanoantenna promises applications in single molecule surface
enhanced Raman spectroscopy (SERS) due to its high local field
enhancements and large scale manufacturability.
Poster 37
Ordered Manganese Atom Structure on Semiconducting
Wurtzite Gallium Nitride, Abhijit Chinchore, Kangkang Wang,
Wenzhi Lin, Jeonghim Pak, Arthur Smith, Nanoscale and Quantum
Phenomena Institute ; Physics and Astronomy Department.
Ohio University, Athens OH-45701.
An important technological challenge of nanoscience
is to bring together magnetism and electronics under a single
material system or combination. This can lead to novel data
storage and device functionality based on use of the electron's
spin degree of freedom. Efforts to introduce transition metal
atoms into III-V semiconductor host materials have been difficult,
due particularly to solubility issues. Still, there is much
interest in achieving transition metal atoms dispersed uniformly
in gallium nitride, due to the possibility of forming room-temperature
operating dilute magnetic semiconductors.[1] In this project,
we investigate the formation of an ordered array of manganese
atoms on the gallium nitride surface. The manganese atom layer
is formed by evaporation of Mn onto the prepared GaN substrate
surface in sub-monolayer doses. High energy electron diffraction
is used to monitor the evolution of the surface in real time.
After depositing less than 1 monolayer Mn, we observe the formation
of a highly ordered surface consisting of Mn atoms spaced at
equal nano-scale intervals. Such a well- ordered Mn structure
may have interesting nanoscale magnetic properties which can
be studied using surface-sensitive magnetic probes. The project
is supported by DOE and NSF.
[1] T. Dietl, Science 287 (2000) 1019.
Poster 38
Polyimide Nanocomposites with Tunable Coefficient
of Thermal Expansion, Gayathri R Sharma1, Maria R Coleman1 and
Cora Lind2 , 1 Department of Chemical and Environmental Engineering,
The University of Toledo, Ohio, 2 Department of Chemistry, The
University of Toledo, Ohio
Polyimides are widely used in industry for applications like
microelectronics, optoelectronics and aerospace applications.
Low coefficient of thermal expansion (CTE) is a pre-requisite
for the use of polyimides in these applications, as it helps
in achieving the dimensional stability in polymer comparable
to that of the adjoining metals or ceramics used. Polyimides
with tunable CTEs were prepared by incorporating cubic zirconium
tungstate (ZrW2O8) as the nanofiller. Cubic ZrW2O8 is well known
for its isotropic negative thermal expansion (NTE) over a wide
temperature range from -272.7 to 777 °C. The increase in
the rigidity of polymer due to the addition of cubic ZrW2O8
and the NTE property result in a reduction in the CTE of polymer.
A modified hydrothermal method was used to synthesize ZrW2O8
nanoparticles. Polyimide-ZrW2O8 interface interaction was enhanced
by using suitable surface chemistries ranging from short chain
linker molecules to flexible oligomer chains. Better interfacial
interaction improves polymer wetting and allows for physical
wrapping or chemical interactions between polyimide and ZrW2O8.
Different processing techniques including direct blending and
reprecipitation blending were explored for the formation of
nanocomposites. The impact of surface modification and processing
techniques on the dispersion and wetting property of ZrW2O8
were explored using scanning electron microscopy (SEM). Preliminary
studies on the bulk properties of polyimide-ZrW2O8 nanocomposites
including thermal stability and CTE will be presented.
Poster 39
Imaging charge transfer molecular orbitals,
U.G.E. Perera1, F. Jäckel1, 2, V. Iancu1, K.-F. Braun1,
N. Koch2, J. P. Rabe2, S.-W. Hla1, 1Ohio University, Physics
& Astronomy Department, Athens, Ohio, 2Humboldt-Universität
zu Berlin, Institut f. Physik, Newtonstraße 15, 12489
Berlin, Germany.
A low temperature scanning tunneling microscope
(STM) and spectroscopy (STS) study under ultra-high vacuum conditions
of organic charge transfer complexes (CTCs) is presented. The
complexes are formed by self assembly from the electron donor
a- sexithiophene (6T) and the electron acceptor tetrafluro-tetracyano-quinodimethane
(F4TCNQ) on Au(111) surface. The formation of new hybrid molecular
orbitals in CTCs are indicated by differential conductance spectra
(dI/dV). The highest occupied molecular orbital of the CTC is
mainly located on the electron accepting F4TCNQ and the lowest
unoccupied molecular orbital is located on the electron donating
6T. Further, voltage dependent STM images and the dI/dV maps
of CTCs reveal the intensity changes of F4TCNQ locations based
on bias voltage. This work is financially supported by the US
Department of Energy Basic Energy Sciences grant no. DE-FG02-02ER46012
and OU-BNNT.
Poster 40
Well Width Dependence of the Phase Coherent
Photorefractive Effect in ZnSe Quantum Wells, Amin Kabir1, Alexander
Pawlis2, Marina Panfilova2, Klaus Lischka2 and Hans-Peter Wagner1,
1 Department of Physics, University of Cincinnati Cincinnati,
Ohio, 2 Department of Physics, University of Paderborn, Warburger
Str. 100, 33098 Paderborn, Germany
The large excitonic nonlinearities of quantum well (QW) structures
have been used to fabricate photorefractive (PR) devices that
open new possibilities for optical data storage and optical
computation. In contrast to present III-V PR QWs, ZnSe based
PR devices do not require externally applied electric fields
but use the coherence of excitons to generate an electron grating
in the QW which causes an efficient all-optical PR effect.
We report on the well width dependence of this novel phase coherent
photorefractive (PCP) effect in ZnSe/ZnMgSe single QWs using
90 fs light pulses that do not overlap in time. The experiments
are performed in a four-wave-mixing configuration at temperatures
between 25 and 65 K. The ZnMgSe/ZnSe QWs with 10, 5 and 3 nm
well width have been grown on GaAs substrates using molecular
beam epitaxy. With decreasing QW thickness we observe a reduction
of the PCP diffraction efficiency. This is attributed to the
higher electron energy in small QWs due to the quantum size
effect which leads to a reduced electron density in the QW.
With increasing temperature the PCP signal further decreases
in all investigated ZnSe QWs which is attributed to an enhanced
thermal activation of the QW electrons back to the GaAs substrate.
The reduction of the electron density with increasing temperature
is also indicated by a longer exciton dephasing time in the
PCP signal trace due to reduced exciton-electron scattering.
Poster 41
Optical coherence imaging using novel phase
coherent photorefractive ZnSe quantum wells, A. Kabir, M. Ajward,
S. Tripathy, H. P. Wagner, Department of Physics, University
of Cincinnati, Cincinnati, Ohio
We have performed depth-resolved optical coherence
imaging (OCI) of both stationary and moving objects using the
exciton resonant phase coherent photorefractive (PCP) effect
in ZnSe quantum wells (QWs). PCP QWs operate without electrical
contacts thus avoiding elaborate sample processing and avoiding
sample destruction due to Joule heating. In addition, the PCP
effect exploits the coherence of excitons in OCI experiments
thus enabling 3D images of reflecting objects with a depth resolution
of ~15 ?m using 90 fs pulses. Due to the high diffraction efficiency
of ? = 5x10-4 in our PCP ZnSe QWs we are able to record still
images at very low intensities (~ 500 µW/cm-2). The OCI
movies of moving objects were recorded using a camcorder with
frame rates of 60 and 180 Hz. The shortest possible time resolution
in these experiments is determined by the decay time of the
PCP electron grating being in the ~10 ?s range.
Poster 42
Synthesis and Characterization of Metal-Oxide-Metal
Heterojunction Nanowires,
E.D. Herderick, N.P. Padture, Department of Materials Science
and Engineering, The Ohio State University, Columbus, Ohio
Oxide nanowires (nanoribbons, nanobelts, or
nanorods) are being used increasingly as 1-dimensional (1-D)
building blocks in “bottom up” multifunctional nanoelectronics,
taking advantage of the myriad size-dependent functional properties
of oxides. In this context, metal—oxide—metal (MOM)
heterojunction nanowires, where a nanoscale segment of a functional
oxide is sandwiched axially between two noble-metal nanowires,
are likely to have some distinct advantages over all-oxide nanowires
(where the entire nanowire is an oxide), including definition
of the functional segment of oxide and “end-on”
contacts.
In order to study piezoelectric and ferroelectric
properties of nanoscale oxides, a novel synthesis method is
developed to make MOM nanowires in the Au-BaTiO3-Au system.
The synthesis method is described in detail along with characterization
results of the MOM nanowire structure. Additionally, an approach
for fabricating electronic devices incorporating these nanowires
is presented.
Poster 43 e-mail sent
Precipitation anneals in the PbTe-PbS system*,
Christopher M. Jaworski1, Joseph P. Heremans1,2 Steven N. Girard3,
Mercouri Kanatzidis3, 1 Department of Mechanical Engineering,
The Ohio State University, 2 Department of Physics, The Ohio
State University, 3 Department of Chemistry, Northwestern University
Bulk samples of (Pb1-xSnxTe)1-y (PbS)y have
been prepared in the range 4%<y<30%1. There is a miscibility
gap in the pseudo-binary PbTe/PbS phase diagram that enables
the precipitation of a PbS-rich phase in a PbTe-rich matrix.
To that effect, the samples were compounded in the liquidus,
and then quenched, resulting in a supersaturated solution. Conditions
for precipitation anneals were then developed, and samples with
nano-precipitates of a PbS-rich phase in a PbTe-rich parent
phase have been obtained, as evidenced by X-ray diffractions.
This technique, previously applied to Pb-rich PbTe2, is aimed
at creating a bulk material containing a substantial fraction
of nanometer-sized particles in order to mimic the morphology
of quantum-dot superlattices that reached very high values of
the thermoelectric figure of merit.3 This material’s notably
low thermal conductivity will not be discussed here. Galvanomagnetic
and thermomagnetic data will be presented with the aim of identifying
the electronic properties of the materials.
[1] 1. Kanatzidis, et. al. J. AM. CHEM. SOC.
2007, 129, 9780-9788. [2] J. P. Heremans, C. M. Thrush and D.T.
Morelli, Thermopower enhancement in PbTe with b precipitates,
J.Appl. Phys. 98 063703 (2005 [3]T. C. Harman, M. P. Walsh,
B. E.LaForge, and G. W. Turner, J. Electron. Mater. 34, L19
(2005).
This work is supported by: Amerigon/BSST, Wright Center for
Photovoltaics Innovation and Commercialization, Office of Naval
Research: N00014-03-10789 MURI, N00014-06-10130
Poster 44
Novel Organic-Inorganic Hybrid Solar Cells Based
on Titania Nanotube Arrays and Metalloorganic/Polymer Blends,
Tengfei Jiang and Nitin P. Padture, Department of Materials
Science and Engineering, The Ohio State University, Columbus,
Ohio
Fabrication, structure, properties, and performance
of novel organic-inorganic hybrid solar cells based on titania
nanotube arrays and metallo-organic/polymer blends are presented.
Ordered arrays of amorphous nanotubes are formed on indium-tin-oxide
(ITO)-coated glass substrates using the anodization method,
and they are subsequently crystallized to rutile titania. The
nanotube dimensions are carefully tuned considering the exciton
diffusion lengths, for improved efficiency. Hole-conducting
polymers are blended with light-harvesting metallo-organic complexes
with broad absorption spectra for efficient capture of the solar
spectrum. These blends are impregnated into the titania nanotube
arrays, while providing electrodes, to create the solar cells.
The structure of these solar cells is discussed together with
the effect of the structure on the cell properties and performance.
Poster 45
Etch Rate and Profile Control in Silicon and
Lithium Niobate by a Fluorocarbon ICP Technique for Micro-Optic
Structures, Lirong Sun & Andrew Sarangan, University of
Dayton, Electro-optics Program, 300 College Park Drive, Dayton,
Ohio
Fluorocarbon plasma etching with arbitrary depth
and profile independent of crystal orientation opens up significant
capabilities for micro-optic and MOEMS designs. In this research,
we investigate the etch rate and sidewall profile using the
Inductively Coupled Plasma (ICP) etching technique. The materials
being investigated are silicon, silicon dioxide and lithium
niobate. Micro-optic structures using different etch chemistries
such as CF4, CHF3, SF6 and Argon have been explored to achieve
a wide range of etch rates, sidewall angles, and surface roughness.
The sidewall profiles are adjusted by gas composition, ICP power,
pressure, bias power and etching time.
In a fluorocarbon plasma, the substrate simultaneously experiences
polymer deposition, ion bombardment and free radical chemical
etching. The passivation caused by the fluorocarbon polymer
protects the sidewalls from any lateral etching, and an anisotropic
profile is achieved. The etch profiles in our study were characterized
by SEM. The CHF3 gas gave the best results for controlling the
sidewall angles and the surface smoothness on silicon and lithium
niobate due to its relatively high polymer deposition rate at
the zero bias. We also investigated the polymer film deposited
on the silicon by CHF3 gas at zero bias power. The deposition
thickness of the polymer was measured by a stylus profiler and
a refractive of index was obtained with a spectroscopic ellipsometer.
Poster 46
Selective excitation of excitonic transitions
in PTCDA crystals and thin films, V. R. Gangilenka, A. Desilva,
Lyubov V. Titova, L. M. Smith Department of Physics, University
of Cincinnati, Cincinnati, Ohio, R. Scholz Walter Schottky Institute,
Technical University of Munich, 80333 Munchen, Germany, H. P.
Wagner Department of Physics, University of Cincinnati, Cincinnati,
Ohio
We study various exciton transitions in PTCDA
crystals and in thin films at low temperatures (~5 K) by photoluminescence
excitation spectroscopy (PLE) using DCM and RG6 dyes. The investigated
PTCDA crystals are grown by sublimation and thin films are deposited
on Si substrate by organic molecular beam deposition (OMBD)
at high vacuum. The PLE excitation energy ranging from 1.878
to 2.172 eV enables the selective excitation of Frenkel excitons
and of charge transfer transitions between PTCDA molecules in
the same unit cell (CT1) as well as between stacked molecules
along the growth direction (CT2). The observed excitation energy
dependence of the emission bands supports the assignment of
the different recombination channels obtained from time resolved
PL measurements [1].
[1] A. Yu. Kobitski, R. Scholz, I Vragovic, H. P. Wagner, and
D. R. T. Zahn, Phys. Rev. B 66, 153204 (2002).
Poster 47
Coatings to Improve Surface Properties of Microcellular
and Fibrous Carbon Structures, A.Karumuri*, D.Sharma, and S.M.Mukhopadhyay,
Mechanical & Materials Engineering, Wright State University
Formation of continuous and adherent ceramic
coatings such as nitrides, carbides, and oxides on carbon structures
can enhance many surface properties such as high temperature
oxidation resistance, heat exchange, and bonding with other
phases. Most currently used coating methods use complex vapor
phase depositions involving toxic chemical precursors and undesirable
by-products.
The goal of this project is to investigate simple,
non-toxic thin film deposition techniques that use benign precursors
and/or nanoscale particles on uneven, high porosity graphite
structures with a variety of oxidation resistant compositions.
Carbon foams and fiber fabrics were coated with BN, SiC, Silica,
and mixed phases. The effectiveness of each coating in surface
property enhancements have been studied, and will be presented.
Microstructure, composition, and chemical states have been characterized
by Field Emission Scanning Electron Microscopy (FESEM) and X-Ray
Photoelectron Spectroscopy (XPS). The quality of films obtained
so far, and scope of future improvements will be discussed.
Poster 48
Reversible Photoinduced Magnetism in V-Cr Prussian
blue analogues, K. Deniz Duman, Jung-Woo Yoo, N.P. Raju, Department
of Physics, The Ohio State University, Columbus, Ohio, Amber
C. McConnell, William W. Shum, Kendric J. Nelson, Joel S. Miller,
Department of Chemistry, University of Utah, A.J. Epstein Department
of Physics and Chemistry, The Ohio State University, Columbus,
Ohio
Prussian blue analogues display a broad range of interesting
photoinduced magnetic phenomena. A commonly studied example
is Fe-Co Prussian blue magnet, which has a low ordering temperature
(Tc ~ 25K) and exhibits light-induced changes in between magnetic
states together with glassy behavior [1,2]. Here, we report
reversible photoinduced magnetic phenomena in V-Cr Prussian
blue analogue K1.54VII0.77VIII0.08[CrIII(CN)6](SO4)0.16•3.1H2O,
one of the few room temperature molecule-based magnets. In this
analogue, illumination with UV light suppresses magnetization,
whereas subsequent illumination with green light partially recovers
from photoinduced state and increases magnetization. V-Cr Prussian
Blue fully recovers from its photoinduced state after annealing
above 250K. The photoinduced effect is stable for a long time
at low temperature ( T < 100 K) and have a high operating
temperature (T ~150K). Results of detailed magnetic studies
and the likely microscopic mechanisms will be discussed.
[1] Hashimoto et al. science 272, 5262 (1996); [2] Pejakovic,
et al. PRL 85, 1994 (2000)
Poster 49
Chemical Vapor Deposition of Carbon Nanotubes
on Copper Substrates, Ge Li1, Chaminda Jayasinghe1, Pravahan
Salunke1, Emily Head1, Wondong Cho1, YeoHeung Yun2, Mark J.
Schulz2, and Vesselin Shanov1, 1-University of Cincinnati, Chemical
and Materials Engineering, Cincinnati, Ohio, 2-University of
Cincinnati, Mechanical Engineering, Cincinnati, Ohio
Vertically aligned Carbon Nanotubes (CNTs) on
conducting substrates may find future applications in areas
from electronic chip cooling, cryogenic pumps to thermal management
in spacecrafts. The study is focused on advanced thermal interface
materials (TIMs) for cooling and thermal management of electronic
devices. The goal is to employ CNTs for enhanced thermal conduction
across the interfaces. Vertically aligned CNT arrays were grown
by Chemical Vapor Deposition (CVD) on copper substrates with
multilayered structure on top. Prior the synthesis the substrate
was studied by X-ray Photoelectron Spectroscopy (XPS) and Atomic
Force Microscopy (AFM) in order to understand the correlation
between the surface properties of the substrate and the CNT
growth. The CNTs were characterized by Scanning Electron Microscopy
(SEM), Transmission Electron Microscopy (TEM), Raman Spectroscopy,
and Thermal Gravimetric Analysis (TGA). The obtained results
demonstrated that CNTs can be successfully grown on thermally
and electrically conductive substrates.
Poster 50
Comparative Studies of the Optical Cross-Section
Spectra of the Rare Earth
Doped III-Nitride Thin Films and Nanosize-Particles, W. Jadwisienczak1,
A. Vemuru1, N. Hearpy1 and A. Anders2, 1School of EECS, Ohio
University, Athens, OH 45701, 2Plasma Applications Group, Lawrence
Berkeley, National Laboratory, University of California, Berkeley,
CA 94720
The integration of optics and microelectronics
on a single Silicon chip platform has been a dream for many
years. The most basic devices for the integration of optics
and electronics are the light sources, modulators, detectors
and waveguides [1]. There has been considerable interest in
recent years in using III-Nitride semiconductors doped with
rare earth ions for optoelectronics, phosphors and semiconductor
laser applications [2,3]. Trivalent rare earth ions (RE3+) were
successfully incorporated into GaN, AlN and their alloys resulting
in an efficient emission across the entire visible and near
IR spectral range. Among the most extensively studied were Eu,
Er and Tm doped different III-Nitride hosts. Although there
have been significant research efforts on the spectroscopic
and laser characterization of these materials, little work has
been performed on evaluating parameters like absorption and
emission cross sections for RE-doped III-Nitride thin films.
These parameters, which give the fictitious area interacting
with the electromagnetic radiation, are necessary to model the
devices with optimum efficiency [4]. The reduced dimension of
the active thin film layer, as is in the case of RE ions implanted
epilayers, has a much smaller number of the optically active
RE ions interacting with the radiation comparing with bulk counterparts
that makes absorption spectra measurement difficult in reflective
and transmission modes. Further, the rare earth doped nanosize
crystal hosts have even fewer active species when compared to
thin films making the measurement even tougher. In this presentation
the optical cross sections of the selected RE ions implanted
in GaN thin films and nanosize RE2O3 particles are calculated
from the measured luminescence spectra using Fuchtbauer-
Landenburg and McCumber theories [5,6]. Obtained results are
compared with the data on the optical cross sections for solid
state laser materials described in the literature [7].
[1] A. Steckl, J. Park, J.Ho and J. Zavada Prospects
for Rare Earth Doped GaN Lasers on Si, Materials Today,Vol.
10, pp.20-27 (2007).
[2] H. Lozykowski, W. M. Jadwisienczak, Thermal Quenching of
Luminescence and Isovalent Trap Model for Rare-Earth-Ion-Doped
AlN, phys. stat. sol. (b), Vol.244, pp. 2109 – 2126 (2007).
[3] J. H. Park and A. J. Steckl, Laser action in Eu-doped GaN
thin-film cavity at room temperature, Appl.Phys. Lett., Vol.
85, pp. 4588-4590 (2004).
[4] P. L. Pernas and E. Cantelar, Emission and Absorption Cross-Section
Calculation of Rare Earth Doped Materials for Applications to
Integrated Optic Devices, Phys. Scr. T118 pp.93-97 (2005).
[5] B. A. Aull, H. P. Jenssen, Vibronic Interactions in Nd:YAG
Resulting in Nonreciprocity of Absorption and Stimulated Emission
Cross Sections, IEEE J. Quantum. Electron. Vol..QE-18, pp.925-930
(1982).
[6] D. E. McCumber, Einstein relations connecting emission and
absorption spectra, Phy. Rev. Vol. 136, pp. 954-957 (1964).
[7] K. Dhiraj, K. L. Nash, R. M. Yow, J. B. Gruber, Absorption
Intensities and Emission Cross Section of Intermanifold Transition
of Er3+ in Er3+:Y2O3 Nanocrystals, J. Appl. Phys. Vol.101, pp.
113115 (2007).
Poster 51
Lightweight and Flexible Quantum Dot-Polymer
Composites: Synthesis and Applications, Raj Makote, Nonstructural
Materials Division, University of Dayton Research Institute
(UDRI), Dayton Ohio
When the size of the semiconductor crystalline
material becomes smaller than the Bhor exciton radius, it exhibits
a strong quantum confinement effect. The luminescence spectrum
of a quantum dot is tunable and strongly dependent on dot size.
We have investigated different pathways to synthesize quantum
dots in a polymer matrix. CdSe, ZnS and PbS quantum dots were
synthesized in transparent Sol-gel hybrid polymers as well as
in PMMA, PDMS and Polystyrene matrices. The effect of molecular
chain structure on the uniformity of quantum dot size and dispersion
in the polymer matrix have been studied.
Poster 52
Iron and Iron Nitrides on Wurtzite Gallium Nitride
(0001), Wenzhi Lin, Jeongihm Pak, David C. Ingram, and Arthur
R. Smith, Nanoscale & Quantum Phenomena Institute (NQPI),
Department of Physics and Astronomy, Ohio University, Athens,
Ohio
In this report, we study and compare the epitaxial
growth of iron and iron nitride on wurtzite (w)-GaN(0001) by
using reflection high energy electron diffraction (RHEED) and
other techniques. We have investigated the growth of ~ 1:1 (nominal
concentration) FeN on w-GaN(0001) using rf N2 plasma molecular
beam epitaxy (MBE) and monitored in-situ using RHEED; these
recent results indicate that FeN grows epitaxially with [111]-orientation
on w-GaN(0001) and that the film grows smoothly (two dimensional-like
mode) up to the first two monolayers, after which it begins
to relax while changing to a three-dimensional growth mode.
The in-plane epitaxial relationship with the GaN substrate was
determined to be [-110]FeN || [11-20]GaN and [11-2]FeN || [1-100]GaN,
and the FeN was determined to have zinc-blende crystal structure.
Fe metal on w-GaN(0001), as the end-point system
of the spectrum, is also being explored. Initial results for
Fe growth show a very streaky RHEED pattern, compared to the
FeN film. It is also apparent that a multi-domain film structure
arises in the growth process based on the multi-streak pattern.
The XRD and RHEED studies suggest the films has body-centered
cubic crystal structure, with epitaxial relationship of [110]
Fe || w-GaN [0001], and [001] Fe || GaN <11-20>. The multiple
streaks RHEED patterns are attributable to the multiple domains
under such an epitaxial relationship.
Poster 53
Photoluminescence Dynamics of GaAs/AlGaAs Core-shell
Nanowires, S. Perera, M. Fickenscher, T. B. Hoang, H. E. Jackson,
L. M. Smith, Department of Physics, University of Cincinnati
Ohio, J. M. Yarrison-Rice, Department of Physics, Miami University,
Oxford, Ohio, H. J. Joyce, Y. Kim, Q. Gao, H. H. Tan, C. Jagadish,
Australian National University, Canberra ACT 0200, Australia,
X. Zhang, J. Zou, University of Queensland, St. Lucia, QLD 4072,
Australia
We use time-resolved PL spectroscopy to study
the exciton dynamics of GaAs/AlGaAs core-shell nanowires (NWs)
at 20 K. NWs were prepared by Au catalyst-assisted MOCVD and
a titanium-Sapphire laser (780nm) was used to excite the nanowire
sample. PL emission from single NWs exhibits an excitonic peak
at ~1.515 eV. The exciton lifetime depends on the morphology
and crystallographic defect density of the GaAs core, which
are in turn dependent upon the growth conditions. Nanowires
cores grown at higher temperatures (450 C) give short exciton
lifetimes (<100 ps). We reduce twin defects within the nanowire
by using a new two temperature growth technique in which the
core is nucleated at a higher temperature (450 C) for 1 minute
and then grown at a low temperature (375 C) for 30 minutes.
In addition, we deposit a 5nm GaAs cap around the AlGaAs shell
which prevents oxidation of the shell. These twin-free minimally
tapered nanowires achieved using a low growth temperature (375
C) exhibit high quantum efficiency with an exciton lifetime
approaching 1.1 ns at 20 K.
Support for this work was provided by NSF (#0701703)
and the Australian Research Council.
Poster 54
Synthesis of Ultrastable, Highly Luminescent
CdTe/CdS Core/Shell Nanocrystals,
Yueran Yan, Mary E. Eberly, and P. Gregory Van Patten, Department
of Chemistry & Biochemistry and Nanoscience & Quantum
Phenomena Institute, Ohio University, Athens, Ohio,
Colloidal CdTe nanocrystals are of interest
for a variety of applications including bioimaging and diagnostics.
The bulk band gap of CdTe is smaller than that of CdSe, making
it better suited for imaging in biological tissues. Unfortunately,
CdTe nanocrystals lose their fluorescence rapidly on exposure
to air. For this reason, most studies involving high quality
(i.e. highly luminescent and monodisperse) nanocrystals focus
on CdSe. In this work, high-quality, airstable, CdTe nanocrystals
were synthesized in a noncoordinating solvent, octadecene (ODE).
The simple procedure provided very good quality nanocrystals
with nearly monodisperse shape and size. Following preparation,
a protective shell of CdS was added to the CdTe to protect the
core from quenching by oxygen, water, or other reactive species.
These core/shell nanocrystals maintain very high luminescence
quantum yield after exposure to air and after transfer into
aqueous phase through ligand exchange.
Poster 55
Peptide Ligands for Shape Control and Directed
Assembly of Inorganic Nanocrystals, John D. Suter, Mary E. Eberly,
and P. Gregory Van Patten, Department of Chemistry & Biochemistry
and Nanoscience & Quantum Phenomena Institute, Ohio University,
Athens, Ohio
We describe a combinatorial panning procedure
aimed at discovering peptide chains that exhibit selective binding
to individual lattice planes of a given crystal with minimal
binding to other surfaces of the same crystal. This extraordinary
surface binding selectivity may allow for nanocrystal shape
control and/or bottom up nanocrystal-assembly.
Poster 56 e-mailed
Thermal Effects of Electromagnetic Stimulation of Nanoparticles,
Carlson, M. T.1, Richardson, H. H.1, Kordesch, M. E.2 , 1Ohio
University, Chemistry and Biochemistry, Athens, Ohio, 2Ohio
University, Physics and Astronomy, Athens, Ohio
Ohio University, Department of Chemistry and Biochemistry, Athens,
Ohio
The field of nanoparticle research has gained considerable momentum
over the past few years. Particularly, metal and magnetic nanoparticles
are increasingly becoming the focus of new research. Our current
work involves the characterization of thermal effects of metal
and magnetic nanoparticles subjected to electromagnetic stimulation.
Iron oxide nanoparticles in aqueous solutions were synthesized1.
Size-characterization of the iron oxide nanoparticles was conducted.
The thermal effects of iron oxide and gold nanoparticles were
then studied in the presence of electromagnetic stimulation.
(1) Kang, Y.S., Risbud, S., Rabolt, J.F., Stroeve, P. (1996)
Chem. Mater. 8, 2209 – 2211.
Poster 57
Experimental Evidence of Fermi-Luttinger Liquid
State via Coulomb Drag between Short 1D Wires., Mustafa Muhammad*,
Philippe Debray*, Steve Herbert**, Richard Newrock*,*Department
of Physics, University of Cincinnati, OH.
**Department of Physics, Xavier University, OH.
We have measured Coulomb drag between two parallel,
electrically isolated one-dimensional wires. The wires are spatially
separated and are fabricated with GaAs/AlGaAs heterostructure
with 2DEG in interface, using split-gate technique with the
use of e-beam lithography, metal deposition and lift-off and
various associated processing steps. Drag is measured between
wires with 500 and 300 nm lengths in the 1D transport regime,
in temperature range 28 mK – 1.2 K. We have observed both
positive and negative drag. The temperature dependence of both
drag types is in excellent agreement with that predicted by
the recently proposed Fermi-Luttinger liquid (FLL) theory that
takes into account of the curvature in the 1D dispersion. Positive
drag occurs when the curvature is positive and negative drag
occurs when it is negative.
Poster 58
Non-Linear Conductance of A Short Quantum Point
Contact, Tai-Min Liu, Maryam Torabi, Amir Maharjan and Andrei
Kogan(1), Steven Herbert( 2) Michael Melloch (3), (1) Department
of Physics, University of Cincinnati, Cincinnati, Ohio, 2Xavier
University, Cincinnati, Ohio, 3Purdue University, West Lafayette,
Indiana
Abstract: We have measured non-linear conductance
G of a very short, less than 80 nm lithographic length, quantum
point contact as a function of the source-drain voltage Vsd
and gate voltage Vg at the device lattice temperature T <
20 millikelvin. The lithographic width/length ratio of the QPC
is approximately 2.5. We observe several well-resolved plateaus
in G at Vds=0, but find no prominent zero-bias peak in G(Vds)
reported by several groups in longer, lower aspect ratio contacts
at near-opening gate voltage [1,2]. The peak is believed to
arise due to Kondo-like correlations between a quasi-local magnetic
state in the constriction [1,3] and the device "leads".
Our data suggest that the quasi-bound spin state does not form
in short QPCs and agree qualitatively with the recent predictions
[3].
1. S.M. Cronenwett et. al. "Low-temperature
fate of the 0.7 structure in a point contact: A kondo-like correlated
state in an open system". Physical Review Letters, 88(226805),
2002.
2. E.J. Koop et. al. "The influence of device geometry
on many-body effect in quantum point contact: Signatures of
the 0.7 anomaly,exchange and kondo". J Sup. Nov Magn.,
20:433, 2007.
3. Tomaz Rejec and Yigal Meir. "Magnetic impurity formation
in quantum point contacts". Nature, 442:900, 2006.
Poster 59
Hybrid Functional Nanomaterial: POSS Functionalized
Carbon Nanofiber, Javed A. Mapkar, Pallavi Iyer and Maria R.
Coleman, The University of Toledo, Chemical & Environmental
Engineering Department1, Toledo, Ohio
Hybrid nanomaterials are broadly described as
multi-component system where two or more nanomaterials are integrated
to form a new nanomaterial having attractive multifunctional
properties. In this paper we discuss the formation of one such
hybrid nanomaterial based on carbon nanofiber (CNF) and polyhedral
oligomeric silsesquioxane (POSS). The octaaminofunctional POSS
(OAPS) were covalently attached on the surface of CNF to increase
the level of surface functionality and provide a platform for
further modification. The CNF-POSS hybrids were designed to
improve their interaction with the polymer matrix and to form
nanocomposite with enhance multifunctional properties.
Functionalization of POSS was confirmed using x-ray photoelectron
spectroscopy (XPS), thermogravimetric analysis (TGA) and transmission
electron microscopy (TEM). In brief the effect of CNF-POSS on
the mechanical properties of polyimide nanocomposite will be
discussed.
Poster 60
Reconfigurable Threshold Logic Gates Using Nanoscale
DG-MOSFETs, Darwin T Ting & Savas Kaya, School of EE&CS,
Ohio University, Athens OH 45701
Reconfigurable logic systems carry a special
importance, especially in compact, low-power logic design, because
they can implement alternative or supplementary logic operations
without devoting additional resources in nanochips with already
dense layouts. Threshold logic gates (TLG) are one of the prime
examples of such reconfigurable logic systems with fine-grain
re-configurability without needing specialized programming hardware
or procedures. We designed very flexible and compact TLG circuits
using nanoscale DG-MOSFETs and verified their operations using
TCAD/SPICE mixed-signal simulations. We illustrate how input
weights as well as evaluation thresholds can be readily altered
in these novel TLG circuitry that can outperform the conventional
counterparts.
Poster 61
Novel Voltage & Current Controlled Oscillators
Based on Nanoscale DG-MOSFETs, Anish Kulkarni & Savas Kaya,
School of EE&CS, Ohio University, Athens OH 45701
Double-gate MOSFETs have intrinsic features
such as local and dynamic threshold control via back-gate biasing,
which make them ideally suited for voltage and/or current controlled
oscillator designs. In this work we utilize these nanoscale
transistors to design novel voltage-controlled (VCO and current-controlled
oscillators (ICO) with reduced complexity and improved performance
by using DG-MOSFETs in various innovative circuits and biasing
schemes. Besides the traditional applications, such ultra-compact
and highly-sensitive VCO and ICOs can become very efficient
nanosensors that can be integrated with conventional and evolutionary
CMOS platforms at the end of Silicon scaling.
Poster 62
Vacancy Electronic Structure of Ag(lll), Danda
P. Acharya', Kendal W. Clark, Kai-F. Braun, Saw-W. Hla, 0hio
University, Physics & Astronomy Department, Athens, Ohio
The surface electronic structure of Ag(lll)
is important for the various catalytic reaction processes. Here
we present the electronic structure of vacancies on Ag( 111)
studied by means of low temperature scanning tunneling microscopy
(STM) and spectroscopy at 4.6K. Vacancies with varying sizes
are created on Ag(lll) :surface via controlled tip-sample contact.
Then these vacancies are filled back with individual atoms which
are extracted locally using STM tip, until the vacancies are
completely filled. At each vacancy filling step, the conductance
tunneling spectra are acquired to determine the associated electronic
structure. We find that the depopulation of surface state occurs
with increasing vacancy size and depth. The surface state signal
is no longer detectable after 6 atomic layer deep vacancies.
Furthermore, a new vacancy state is discovered whose energy
decreases with the increasing vacancy size.
This work is financially supported by the United
States DOE, BES grant no. DE•FG02-02RR46012 and OU-BNNT.
Poster 63
Nanofocusing of Surface Plasmons in Metallic
Nanostructures, Weibin Chen and Qiwen Zhan,Electro-Optics Graduate
Program, University of Dayton, 300 College Park, Dayton, Ohio
45469-0245
Plasmonic focusing with metallic nanostructures
is an effective approach to confine optical field into nanometric
size, which breaks the diffraction limit of light. Owing to
strong spatial confinement and high field enhancement, plamonic
focusing has important applications in near field optical imaging
and sensing. Surface plasmon is an electromagnetic wave due
to the interaction of light and metallic structures. As a wave
phenomenon, surface plasmon can be focused using appropriate
excitation geometry and metallic structures. We explored three
different metallic structures for nanofocusing of surface plasmons
with radial polarization illumination. When radially polarized
beam is launched into these plasmonic structures, the entire
beam is TM polarized with respect to the dielectric/metal interface,
providing an efficient way to generate highly focused surface
plasmon through constructive interference and creating an enormously
enhanced local field. An evanescent nondiffracting Bessel beam
can be obtained with planar metallic/dielectric interface. Plasmonic
lens with conical shape and annular rings under radial polarization
illumination are numerically studied with a finite-element-method
model. The field distribution with a full-width-half-maximum
as small as 10 nm and intensity enhancement of five orders of
magnitude can be achieved with 633 nm optical excitation. We
coupled the radia |