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isis
poster session
program information / abstracts
Congratulations to our poster session winners, who have
been awarded a
$50 gift certificate to the UCI Bookstore! See photos of winners
and participants below!
Poster Session Award Recipients:
14.
Author(s)::
R. J. Lazarowich and P. Taborek (1); N. V. Myung (2)
(1) Department of Physics and Astronomy, UC Irvine
(2) Department of Chemical and Environmental Engineering, U C Riverside
TITLE:: FABRICATION OF HUMIDITY SENSORS USING POROUS
ALUMINA
....................................................................................................................................................................
17.
Author(s)::
A. A. Shinde C. Jo J.P. You J. Choi R. Wu R. Ragan
Department of Physics and Astronomy / ChEMS, UC Irvine
TITLE:: FABRICATION, OPTIMIZATION AND MODELING OF
HIGHLY ORDERED ASSEMBLIES OF MONODISPERSE METALLIC NANOSTRUCTURE ARRAYS
....................................................................................................................................................................
18.
Author(s)::
I. Vlassiouk, Z. Siwy
Department of Physics and Astronomy, UC Irvine
TITLE:: NANOFLUIDIC DIODE
....................................................................................................................................................................
20.
Author(s)::
C. Xiang, M.A. Thompson, A.G. Güell, E.J. Menke, R. M.
Penner
Department of Chemistry, U C Irvine
TITLE:: LITHOGRAPHICALLY PATTERNED NANOWIRE
ELECTRODEPOSITION
POSTER SESSION WINNERS
December 8, 2006
5:00 -
7:00 p.m.
Location:
1201 Natural Sciences II
ISIS (the
Institute of
Surface and Interface Science) is one of 16 Organized
Research
Units (ORUs) on the University of California, Irvine (UCI) campus.
Through collaborative projects it brings together faculty and
researchers in:
:: Chemistry
:: Physics
:: Developmental
and
Cell Biology
:: Chemical
Engineering and
Materials Science
:: INRF
::
Electrical
Engineering and
Computer Science
This
poster session is informal
in nature, and it provides an opportunity to learn
about
current
ISIS member research projects. This is
also a social occasion
for ISIS members to get together to interact - students, postdocs and
other
group members are especially welcome!
Posters
for the session
can be composed of papers presented at recent conferences, or just a
few
figures interspersed with brief explanatory prose.
Please
submit abstract and presentation using the ONLINE
SUBMISSION FORM:
http://forms5.createforms.com/11061/form_3_1.html
If
your abstract exceeds 250 characters, please forward it to Alison Lara:
For
additional information, please contact:
Anne
Taub (annetaub@uci.edu)
or Diane
Stathakis (destatha@uci.edu).
....................................................................................................................................................................
Program Information (updated 12-11-2006 10:00 a.m.)
.........................................................................................................................................
1
|
|
|
|
Author(s)::
|
M.
G. Aggleton, J. C. Burton, D. A. Hook, P. Taborek, J. E. Rutledge, M.
T. Dugger
(email: maggleton@gmail.com)
|
|
|
Affiliation(s)::
|
Chemical
& Material Physics, U C Irvine
|
|
|
Title::
|
Cryotribology
in Micro and Macroscale Setups
|
|
|
Abstract::
|
An overview
of current and recent cryo-tribological studies
performed
at UCI with support from NCSU and Sandia Nationa
Laboratories. We focus on two systems: a sliding block
tribometer and a MEMS tribometer. Measurements of static and
kinetic friction are taken from room temperature to 4K. This
work is supported by
Extreme Friction: MURI AFOSR # FA9550-04-1-0381.
|
|
|
2
|
|
|
|
Author(s)::
|
J.
A. Abbondondola, K. Janda
(email: jabbondo@uci.edu)
|
|
|
Affiliation(s)::
|
Chemical
& Material Physics, U C Irvine
|
|
|
Title::
|
Hydrogen
and Argon Uptake into a Propane Hydrate
|
|
|
Abstract::
|
It
has been proposed that clathrate hydrates can be a possible storage
medium for alternative fuels, such as hydrogen. However, pure
hydrogen clathrate requires extremely high pressure (220MPa) and low
temperature (249K) for production, resulting in a costly hydrate to
produce and use in commercial applications. The sII natural gas
hydrate is an alternative to a pure hydrogen clathrate. The
larger cavities are filled by a relatively large guest molecule (e.g.,
propane), the small cavities are available for hydrogen storage.
Our objective is to determine whether hydrogen diffuses into the sII
propane hydrate at near-ambient conditions and quantify the uptake
rate.
We investigated hydrogen and argon gas uptake into a propane hydrate
and into ice grains at 0.68 MPa and 263 K. The data showed that
there is an average of 19 times more total gas uptake into the propane
hydrate, as compared to the ice grain samples. A review of the physical
processes involved in gas adsorption and absorption into a solid
suggests that the dominant process involved in hydrate-uptake is bulk
or lattice diffusion. The ice grain-uptake is very small and
saturates very quickly which is indicative of surface adsorption.
The propane hydrate occupancy yields for the total hydrogen and argon
uptake were estimated at 1.3 % and 1.8 %; respectively. The
average argon initial hydrate-uptake rate is 8.7 x 10-6 Mol/g-hr, which
is less than the average hydrogen initial hydrate-uptake rate of 2.7 x
10-4 Mol/g-hr. Initially, the hydrogen uptake rate into a propane
hydrate is faster than the argon hydrate-uptake rate, but this hydrogen
uptake rate decreases within 10 minutes to near-equilibrium. The
argon hydrate-uptake rate does not reach equilibrium even at the end of
a 90 hour experimental run. This results in a total argon uptake
into a propane hydrate which is larger than the hydrogen uptake over
the long-time period.
|
|
|
3
|
|
|
|
Author(s)::
|
M.
Bourg, R. M. Penner
(email: mbourg@uci.edu)
|
|
|
Affiliation(s)::
|
Department
of Chemistry, UC Irvine |
|
|
Title::
|
Towards
Nanowire-Based Thermocouples
|
|
|
Abstract::
|
The
ability to accurately measure temperature on the same time scale as a
thermal process under investigation is important in many industrial
processes. A thermocouple, which consists of a junction between
two dissimilar metals, is most often the device used for such
measurements. As the thermal mass of the junction decreases, the
response time decreases and the spatial resolution increases.
Therefore, junctions containing nanowires should lead to faster
response times and increased spatial resolution. In order to
initally investigate this, we prepared nanowire-thin film (NWTF)
junctions consisting of electrodeposited nanowires and an evaporated
film. These devices measure temperature accurately and
reproducibly, and have a response time of 1.9ms.
For comparison, the response time of a 125μm type J thermocouple was
5.7ms. To improve upon the enhancements shown by NWTF devices,
nanowire-nanowire (NWNW) junctions were also fabricated. NWNW
thermocouples measure temperature accurately and reproducibly, and have
a response time of 0.7ms. Neither type of nanowire- based
thermocouple show a decrease in sensitivity. The
characterization of these thermocouple arrays by SEM, EDS, and thermal
measurements will be presented.
|
|
|
4
|
|
|
|
Author(s)::
|
K.
Callahan, M. Roeselova, D.J. Tobias
(email:
callahak@uci.edu)
|
|
|
Affiliation(s)::
|
Department
of Chemistry, UC Irvine |
|
|
Title::
|
Molecular
Dynamics Simulations of the Influence of Magnesium Dication on Aqueous
Salt Solutions
|
|
|
Abstract::
|
Field
studies and laboratory measurements have demonstrated that molecular
chlorine is produced via oxidation of sea salt aerosol by hydroxyl
radical. A surface mechanism for chloride production was proposed
based on molecular dynamics simulations of concentrated sodium chloride
solutions, which predicted that chloride anions adsorb to the
solution-air interface. Sea water contains a substantial amount
of magnesium chloride
in addition to sodium chloride. The present study seeks to
quantify the effects of magnesium dications on the interfacial
propensity and reactivity of chloride anion. To this end,
molecular dynamics simulations of concentrated magnesium chloride and
sodium chloride solutions, as well as a model of sea water containing
85 mol% sodium chloride and 15 mol%
magnesium chloride, were performed. Structural and thermodynamic
properties were calculated from the simulations and compared to
available
experimental data. The simulations show that the presence of magnesium
dications does not effect the interfacial distribution of chloride
anions. In addition, the simulations predict that magnesium
dications displace sodium cations in the model sea water system, and
the presence of magnesium dications in the subsurface layer induces
changes of the
solvent structure in the interfacial region that could influence the
surface reactivity of chloride anion.
|
|
|
5
|
|
|
|
Author(s)::
|
J.
X. Cao (Juexian Cao) and R. Q. Wu
(email:
uexianc@uci.edu)
|
|
|
Affiliation(s)::
|
Department
of Physics and Astronomy, UC Irvine
|
|
|
Title::
|
High
piezoresistance effect in silicon nanowires
|
|
|
Abstract::
|
The silicon
nanowires possess an unusually large piezoresistance effects compared
with Si bulk (Nature nanotechnology, 1(2006), 42). Using first
principle technique, we found that the high piezoresistance coefficient
was traceable from the effective mass change effect with compressive
strain. It is found that compressive strain would induce the change of
the heavy effective mass band with a light effective mass band. The
difference between the effective mass of those band is rather large
compared with the valance band in p-type Si bulk. Due to those bands
are surface states, the
surface modification would play a vital role on the piezoresistance
effects.
|
|
|
6
|
|
|
|
Author(s)::
|
P.
Chu, D.L. Mills
(email: pingc@uci.edu)
|
|
|
Affiliation(s)::
|
Department
of Physics and Astronomy, UC Irvine
|
|
|
Title::
|
Laser
Induced Forces Between Metallic Nanospheres; The Role of Collective
Plasmon Resonances
|
|
|
Abstract::
|
We
explore the theory of laser induced attractive forces between
conducting nanospheres. Emphasis is placed on the influence of
collective mode resonances on this force. As two spheres approach each
other, the dipole active plasmon resonances drop in frequency and can
pass through the laser frequency. This produces a dramatic enhancement
of the force. We present explicit calculation for Ag nanospheres in
solution. We compare the amplitude of the laser induced attractive
force with the van der Waals forece.
Research supported by the U.S. Department of Energy
through Grant No.
DE-FG03-84ER-45083.
|
|
|
7
|
|
|
|
Author(s)::
|
B.
Goldsmith, J. Mannik, J.G. Coroneus A.A. Kane G.A. Weiss P.G. Collins
(email: bgoldsmi@uci.edu)
|
|
|
Affiliation(s)::
|
Department of
Physics and Astronomy, UC Irvine
|
|
|
Title::
|
Fabrication
of Single-Biomolecule Electronic Devices
|
|
|
Abstract::
|
New
inventions in nanotechnology are likely to enable the investigation of
biochemical reactions with single molecule precision. One
promising
approach is the integration of bioactive molecules into electronic
devices. We present a two step method to build single protein
sensors
from carbon nanotube circuits. In the first, feedback-controlled
step,
a single attachment site is introduced to the nanotube sidewall using
electrochemical oxidation. In the second step, the site is
covalently
linked to a protein's amide termination. The resulting circuits
incorporate a single functional molecule and allow interrogation under
various environments and biochemical conditions
|
|
|
8
|
|
|
|
Author(s)::
|
Y.
He, Z. Siwy
(email:
zsiwy@uci.edu)
|
|
|
Affiliation(s)::
|
Department
of Physics and Astronomy, UC Irvine
|
|
|
Title::
|
Preparation
of Synthetic Nanopores Selective for Calcium Channels
|
|
|
Abstract::
|
Ion
channels in biological membranes are nanodevices selectively
transporting one type of ion and excluding other ions. We have studied
mechanism of calcium channel selectivity and have tested predictions of
a particular theoretical model. The model suggests that if there
is a high density of carboxylate groups on walls of a nanometric
channel, which ensures a high binding affinity for calcium ions, these
groups will preferentially bind doubly charged calcium ions rather than
monovalent ions like sodium. Predictions of this model have been tested
with polymer nanopores of high suface charge density of COOH groups.
|
|
|
9
|
|
|
|
Author(s)::
|
C.
Jo, R. Wu
(email:cjo@uci.edu)
|
|
|
Affiliation(s)::
|
Department
of Physics and Astronomy, UC Irvine
|
|
|
Title::
|
Interface
Configuration in Fe/GaAs(001) and Induced Spin Polarization
|
|
|
Abstract::
|
We have
calculated x-ray absorption spectroscopy (XAS) and x-ray magnetic
circular dichroism (XMCD) of the interface in Fe/GaAs(001) by using the
density functional full-potential linearized augmented plane wave
method. Intermixing interface with As and substitutional Ga plausibly
reproduces the experimental XAS/XMCD data of As and Ga. The XAS/XMCD
curves are highly sensitive to the change of interface configurations,
and thus
provide a clue to determine the atomic structure of the interface
between Fe and GaAs. The significant spin polarizations on As and Ga
atoms are induced, which is the key factor for the carrier-induced
magnetic ordering.
|
|
|
10
|
|
|
|
Author(s)::
|
E.
Kalman, Z. Siwy
(email: zsiwy@uci.edu)
|
|
|
Affiliation(s)::
|
Department
of Physics and Astronomy, UC Irvine
|
|
|
Title::
|
Tuning
of Ion Current Rectification in Asymmetric Nanopores by Signal Mixing
|
|
|
Abstract::
|
Transport
properties of asymmetric and rectifying single nanopores in polymer
films were studied in the presence of two periodic, rectangular voltage
signals. We show that tuning the ratio of frequencies, the phase
difference and amplitude of the two voltage inputs gives a new
possibility to enhance, hinder or cancel the rectifying properties of
the nanoporous system.
|
|
|
11
|
|
|
|
Author(s)::
|
A.
Kane, B. Goldsmith, P.G. Collins
(email: akane@uci.edu)
|
|
|
Affiliation(s)::
|
Department of
Physics and Astronomy, UC Irvine |
|
|
Title::
|
High
Temperature Resistance and Reactivity of Carbon Nanotube Electronic
Circuits
|
|
|
Abstract::
|
At
sufficiently high temperatures, carbon nanotubes (CNTs) begin to react
with their immediate environment. For example, adsorbates first desorb,
then the carbon may react with connective electrodes, and ultimately
Stone-Wales defects become mobile and can be annealed. We have designed
and built an apparatus to study electronic transport in individual CNTs
under these extreme conditions. Our apparatus provides continuous, four
probe measurements of impedance and transimpedance from room
temperature to 1500 K in an ultrahigh vacuum (UHV) system.
By heating the devices to such temperatures, we are able to study the
onset and progress of reactions, and the UHV environment allows for
precise control of the local surface chemistry. Furthermore, the
devices can be heated either resistively or radiatively at rates
exceeding 100 K/min, allowing for pulsed thermal processing and an
investigation of photoinduced chemistries.We will present results on
the high temperature resistance of CNT devices in a UHV environment,
and preliminary results indicating irreversible chemical changes which
occur at high temperatures.
|
|
|
12
|
|
|
|
Author(s)::
|
V.
Khalap, A. Kane, P. G. Collins
(email: vkhalap@uci.edu)
|
|
|
Affiliation(s)::
|
Department
of Physics and Astronomy, UC Irvine
|
|
|
Title::
|
Chemoresistance
of carbon nanotube circuits incorporating electrochemically-decorated
defects
|
|
|
Abstract::
|
We
specifically investigate SWNT devices with single point
functionalizations. Standard fabrication techniques are supplemented by
an electrochemical point-oxidation process that creates insulating
defects into otherwise pristine SWNTs. Selective electrochemistry
subsequently deposits metal onto the insulating site(s) and restores
the device conductivity. Furthermore, the resulting circuits
inherit the chemicalsensitivity of the metal deposits.
|
|
|
13
|
|
|
|
Author(s)::
|
M.
Krisch, R. D’Auria, M.A. Brown, D.J. Tobias, J.C. Hemminger
(email: mkrisch@uci.edu)
|
|
|
Affiliation(s)::
|
Department
of Chemistry, UC Irvine |
|
|
Title::
|
The
effect of an organic on the interfacial structure of an electrolyte
solution
|
|
|
Abstract::
|
The
addition of 1-butanol to an aqueous potassium iodide solution modifies
the interfacial profile of ions at the liquid - vapor interface.
Our experiments probe atomic composition at the liquid surface with
ambient
pressure x-ray photoelectron spectroscopy at beamline 11.0.2 of the
Advanced Light Source. Photoelectron kinetic energies are varied
to produce a depth profile of the liquid - vapor interface.
Surface enhancement of iodide anions, an effect observed in aqueous
potassium
iodide solution, disappears in the presence of 1-butanol, a surface
active alcohol. Molecular dynamics simulations of butanol in an
aqueous electrolyte solution observe the same effect. Radial
distribution functions show that butanol appears to interact with both
the anion and
the cation; this is likely to be the basis for the observed changes in
the ion distribution in the presence of the organic. Insight into
ion behavior at mixed liquid surfaces is crucial for understanding the
chemistry of atmospheric aerosols, which frequently contain mixtures of
water, electrolytes, and organics.
|
|
|
|
Markus
Ammann
Laboratory of Radio- and Environmental Chemistry, Paul Scherrer
Institute, CH-5232 Villigen, Switzerland
David E. Starr, Hendrik Bluhm
Lawrence Berkeley National Laboratory, Mail Stop 6R2100, One Cyclotron
Road, Berkeley, CA 94720
|
|
|
14
|
|
|
|
Author(s)::
|
R.
J. Lazarowich and P. Taborek (1); N. V. Myung (2)
(email:
rlazarowich@gmail.com) |
|
|
Affiliation(s)::
|
(1)
Department
of Physics and Astronomy, UC Irvine
(2) Department of Chemical and
Environmental Engineering, U C Riverside |
|
|
Title::
|
Fabrication
of Humidity Sensors Using Porous Alumina |
|
|
Abstract::
|
Nanoporous
alumina structures were fabricated
on quartz crystal microbalances (QCMs) by electrochemically anodizing
aluminum electrodes which had a typical thickness of 10-15 microns. By
varying the temperature and voltage of anodization, the diameter of the
cylindrical pores could be controlled in the range
of 12 to 40 nm. Properties of the porous films were determined from SEM
images and by analyzing isotherms of N$2$, O$2$, C$3$H$8$, and H$2$O.
The sensitivity increased up to 120 times that of a conventional QCM
with flat electrodes. With a long-range order of
cylindrical pores and enhanced sensitivity, these devices are prime
candidates for use as sensors and templates. A subsequent experiment
under constant flow of N$2$ near room temperature shows that QCMs with
porous alumina electrodes are very sensitive to the condensation of
water, therefore, making them excellent humidity sensors.
|
|
|
15
|
|
|
|
Author(s)::
|
J.
Loussaert
(email:jloussae@uci.edu)
|
|
|
Affiliation(s)::
|
Department
of Chemistry, UC Irvine |
|
|
Title::
|
The
Characterization and Functionalization of Polymer Optical Waveguide
Layers for Bio-Affinity Sensing
|
|
|
Abstract::
|
The
technique of Optical Waveguide Layer Spectroscopy (OWLS) is
demonstrated as new methodology for surface bioaffinity
sensing. OWLS uses a combination of a thin metal film and a
thin polymer overlayer to create enhanced TE and TM-polarized
electromagnetic fields within the film and at the biosensor surface.
Chemical modification of the interface with bioaffinity probe molecules
lead to the formation of biosensors for DNA, RNA, proteins and
antibodies.
|
|
|
16
|
|
|
|
Author(s)::
|
Gang
Qiu, M.M. Kobayashi, C.S. Tsai
(email:
cstsai@uci.edu)
|
|
|
Affiliation(s)::
|
Department
of Electrical Engineering & Computer Science |
|
|
Title::
|
Enhanced
Microwave FMR Absorption in a
YIG/GGG-GaAs Flip-Chip Layer Structure Using
Microstrip Step-Impedance Low-Pass Filter |
|
|
Abstract::
|
Enhanced
microwave ferromagnetic resonance (FMR) absorptions in
yttrium iron garnet / gadolinium gallium garnet-gallium arsenide
(YIG/GGG-GaAs) flip-chip layer structures using a microstrip
step-impedance low-pass filter (LPF) are reported. The field
simulations of the step-impedance LPF show clearly that, in contrast to
a 50 microstrip, the ac magnetic fields of the propagating
microwaves are heavily concentrated in its inductive elements. Stronger
local ac magnetic fields at each inductive element of the
step-impedance LPF facilitate enhanced coupling into the magnetic
over-layer and, thus, significantly increase the microwave power
absorptions at the FMR frequencies. The measured transmission loss
(S21) and return loss (S11) of –25.0 dB and –8.7 dB using the
microstrip step-impedance LPF, at FMR frequency of 8.5 GHz, show a
higher level of microwave FMR absorption in the YIG/GGG-GaAs layer
structure as compared to a 50 microstrip with the measured
S21 and S11 of –20.8 dB and –5.8 dB. The microwave transmission
characteristics of the magnetic over-layer in a large base band of
2.0-20.0 GHz, using both the step-impedance LPF and the 50
microstrip, were also measured and compared.
Sponsor: This work was supported in part by the UC
Discovery Program
|
|
|
17 |
|
|
|
Author(s)::
|
A.
A. Shinde C. Jo J.P. You J. Choi R. Wu R. Ragan
(email: ashinde@uci.edu)
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Affiliation(s)::
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Department
of Physics and Astronomy / ChEMS
UC Irvine |
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Title::
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Fabrication,
Optimization and Modeling of Highly Ordered Assemblies of Monodisperse
Metallic Nanostructure Arrays
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Abstract::
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Metal
nanostructures have demonstrated extraordinary properties: the capacity
for single molecule detection in plasmon resonance biosensors, chemical
sensitivity and higher performance in catalytic processes than their
bulk counterparts, and the transport of electromagnetic energy along
particle chains in optical circuits. One of the most significant
challenges to technical developments that capitalize on unique
properties of metal nanostructures is the fabrication of nanostructure
arrays with monodisperse size, shape and high density using low cost
and high throughput technique.
We will present a unique Si-compatible fabrication process for dense
ordered arrays (~1011 cm 2) of metal nanostructures with monodisperse
size and shape, over large area ( >1mm2), and having feature size
and inter-particle spacing unattainable with state of the art electron
beam lithography.
Noble metal deposited via physical vapor deposition on a nanowire
template combined with reactive ion etching produced noble metal
core-shell nanowire and nanoparticle arrays with mean feature size of
approximately 8 nm. Hexagonal rare earth disilicide nanowires,
such as DySi2 and ErSi2, are used as self-assembled nanowire templates
on Si(001). Dense arrays of parallel DySi2 and ErSi2 nanowires
having lengths greater than 1 micron and widths less than 5 nm have
been fabricated and characterized on vicinal Si(001) previously.
Scanning tunneling microscopy has shown than platinum (gold) forms
clusters on the ErSi2 (DySi2) nanowire surfaces, and scanning electron
microscopy backscattered images have shown that noble metal
preferentially aggregates on the nanowire surfaces as opposed to the Si
substrate.
Noble metal coverage is used to select nanoparticle versus nanowire
arrays after RIE. In the case of nanoparticles, a narrow size
distribution of less than than ±1 nm and inter-particle spacing
of approximately 10 nm is obtained by our process. Few studies
have been done on the theory behind the formation of the nanowire
templates as well as the phenomena of preferential aggregation of noble
metal on nanowire surfaces. Thus, theoretical modeling is
combined with scanning probe microscopy in order to gain a deeper
understanding of thermodynamics and kinetics driving nanostructure
formation. We will also present ongoing work that uses VASP, an
ab initio software package, to simulate RESi2 crystal structures as
well as metal atoms on nanowire surfaces. Our preliminary
calculations for bulk YSi2 have been found to be in close agreement
with experiment and other theoretical studies. Our goal is to
understand assembly mechanisms in order to optimize structure and make
our process applicable to other material systems.
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18 |
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Author(s)::
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I.
Vlassiouk, Z. Siwy
(email: zsiwy@uci.edu)
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Affiliation(s)::
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Department
of Physics and Astronomy, UC Irvine
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Title::
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Nanofluidic
diode
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Abstract::
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We present
a nanofluidic diode that at voltage range (-5 V, +5V) rectifies ion
current with degrees of rectification reaching several hundreds. The
diode is based on a single asymmetric nanopore whose surface was
patterned so that a sharp boundary between positively and negatively
charged regions is created. This boundary defines a zone that is
enriched with positive and negative ions or creates a depletion zone.
The principle of operation of the nanofluidic diode is analogues to
that of a bipolar semiconductor diode.
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19
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Author(s)::
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S. Wu (1),
N. Ogawa (2), W. Ho (1,3)
(email:
shiweiw@uci.edu)
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Affiliation(s)::
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1 Department
of Physics and Astronomy, UC Irvine
2 Research Center for Advanced Science and
Technology, The University
of Tokyo, Tokyo 153-8904, Japan,
3 Department
of Chemistry, UC Irvine |
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Title::
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Atomic-scale
coupling of photons to single-molecule junctions |
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Abstract::
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The study
of optical phenomena at the
atomic scale is expected to provide new understanding of molecules and
their chemical dynamics. The combination of lasers with a low
temperature scanning tunneling microscope (STM) has led to the
observation of photo-induced resonant tunneling with sub-molecular
spatial resolution for electron transfer to a single molecule adsorbed
on a solid surface [Science 312, 1362, (2006)]. Furthermore,
irradiation of femtosecond laser pulses into this single-molecule
junction defined by STM results in non-linear coupling by two-photon
excitation, rather than the single-photon coupling in the case of
continuous wave (CW) lasers. These experiments lead to new
opportunities by tapping into the unique properties of lasers and the
STM. |
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20 |
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Author(s)::
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C.
Xiang, M.A. Thompson, A.G. Güell, E.J.
Menke, R. M. Penner
(email: cxiang@uci.edu)
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Affiliation(s)::
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Department
of Chemistry, U C Irvine |
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Title::
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Lithographically
Patterned Nanowire Electrodeposition
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Abstract::
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Nanowire
fabrication methods can be classified either as “top down”, involving
photo- or electron beam lithography, or “bottom-up”, involving the
synthesis of nanowires from molecular precursors. Lithographically
Patterned Nanowire Electrodeposition (LPNE) combines attributes of
photolithography with the versatility of bottom-up electrochemical
synthesis. Photolithography is employed to define the position of a
sacrificial nickel nanoband electrode that is recessed into a
horizontal trench defined by the substrate surface and photoresist.
This trench acts
as a “nanoform” to define the height of an incipient nanowire during
its electrodeposition. The width of the nanowire is determined by
the electrodeposition duration. Removal of the photoresist and
nickel reveals a nanowire - composed of gold, platinum or palladium –
with a rectangular cross section and a height and width that can be
independently controlled, and as small as 10 nm. The polycrystalline
nanowires synthesized by LPNE can be electrically continuous for 1 cm.
Application of LPNE synthesized nanowires including thermocouples,
crossed
wires, and bimetallic wire arrays are briefly explored.
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21
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Author(s)::
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L.C.
Yang, P.Y. Tam, J. Diaz, T.M. McIntire,
B.J. Murray, C.M. Overstreet, G.A. Weiss,
R.M. Penner
(email:
lcyang@uci.edu) |
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Affiliation(s)::
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Department
of Chemistry, UC Irvine |
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Title::
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Electrodes
for Biodetection |
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Abstract::
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The
development of label-free biosensors for key biomolecules is an
objective that is shared by many research groups worldwide. We
present an approach involving the electrochemical detection of
biomolecules binding to electrode surfaces on which an engineered
bacteriophage, M13, has been covalently attached. This bacteriophage
has - on its surface - polypeptide receptors that form the basis for
molecular recognition. These phage particles are prepared using
the techniques of phage display.
We describe the preparation of the biosensor surface, the optimization
of the electrochemical impedance and quartz crystal microbalance
measurements, and the results of our experiments that involve the
detection of antibodies that are recognized and bound by the
immobilized phage particles, and “control” antibodies that are not
recognized. The response of this biosensor to the prostate cancer
marker, PMSA, is also reported. In all cases, the observed impedance
responses are “benchmarked” against the response of a quartz crystal
microbalance, on which the biosensor is constructed.
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22
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Author(s)::
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Donghyung
Lee, Kieron Burke
(email:
donghyul@uci.edu) |
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Affiliation(s)::
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Department
of Chemistry, UC Irvine
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Title::
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Negative
Ions in DFT |
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Abstract::
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The atomic
electron affinities and densities are investigated using density
functional methods (LDA, GGA) with both large basis sets and using OEP
densities on a numerical basis, and the results are compared. The
instability of negative ions in DFT is a well-known problem.[1,2] In
the case of negative ions such as H¯ and F¯, the incorrect
asymptotic single particle potential and density decay lead to unbound
systems. In this
work, we show the functional dependence of the extra electron density
behavior in asymptotic region and how the values of electron affinity
are significantly improved by using OEP densities.
[1] Galbraith, J.M., et al, J. Chem. Phys. 105, 862, 1996
[2] Rosch, N., et al, J. Chem. Phys. 105, 862, 199
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23
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Author(s)::
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Ilya
Goldshleger, Galina Kerenskaya, Vahan Senekerymian, V. Ara Apakarian,
and Kenneth C. Janda
(email:
igoldshl@uci.edu) |
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Affiliation(s)::
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Department
of Chemistry, UC Irvine
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Title::
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Bromine
Hydrate: Microscopy, Spectroscopy, and Ultrfast Dynamics
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Abstract::
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24
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Author(s)::
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L.
Pocivavsek, S. Frey, K. Krishan, H. Diamant. K.Y. Lee, M. Dennin
(email:
kkrishan@uci.edu) |
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Affiliation(s)::
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Department
of Physics & Astronomy, UC Irvine
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Title::
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Packing
in Biphasic Monolayers: Origins and Effects on Collapse.
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Abstract::
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One
of the inherent limitations of standard Langmuir monolayer troughs is
the rectangular geometry used. Here, one or two barriers are used to
reduce the area of the system with the other boundaries remaining
stationary. The compression in this geometry is anisotropic, and prone
to shear stresses and flows. Such influence of externally imposed
symmetries on microscopic dynamics in monolayers has not been
investigated
systematically. Our current experiments attempt to understand this in
relation to DPPC:POPG monolayers by subjecting them to circularly
symmetric compression. These monolayers are similar to those used as
lung surfactants, where monolayer compression and dilation are
essential. These surfactants also have a novel mechanism of collapse
through reversible folding. The folding seen in these surfactants
reflect the symmetries
of the compression in rectangular geometries. In addition, spatial
structure of domains have also been observed to have symmetries that
may be associated with the symmetry of compression. The use of
circularly symmetric compression contrasted with linear compression is
expected to
clarify aspects of spatial structure formation in monolayers that may
be associated with the geometry of compression.
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