12 research outputs found
MOESM1 of Raman Spectroscopic Characterizations of Self-Catalyzed InP/InAs/InP One-Dimensional Nanostructures on InP(111)B Substrate using a Simple Substrate-Tilting Method
Additional file 1: Figure S1. InP(111)B “nanoisland” reference substrate, treated with high temperature deposition of InP nanostructure, exhibiting preferred lateral growth to vertical growth. Figure S2. Effect of excitation power on Raman spectra of InP/InAs/InP nanopillar and nanocone for two substrate tilting angles (0 and 30 degrees)
Additional file 1: Figure S1. of Self-Catalyzed Growth and Characterization of In(As)P Nanowires on InP(111)B Using Metal-Organic Chemical Vapor Deposition
45° tilted SEM image of InP nanowires on InP(111)B substrate grown at 365 °C for 300 s using TMIn (5.0 × 10−5 mol/s) and TBP (7.4 × 10−6 mol/s) precursors with the molar ratio of V/III = 29. Mechanically exfoliated InP nanowires are used as the reference for Raman spectroscopy measurements. (PNG 215 kb
Supplementary document for Easy-to-make-and-use gold nanotrench arrays for surface-enhanced Raman scattering - 5367773.pdf
Experimental details of microRNA measurement
Supplementary document for Easy-to-make-and-use gold nanotrench arrays for surface-enhanced Raman scattering - 5427738.pdf
Details of SERS measurement
Suppressed Formation of Conductive Phases in One-Pot Electrodeposited CuInSe<sub>2</sub> by Tuning Se Concentration in Aqueous Electrolyte
The single-bath electrochemical
deposition of CuInSe<sub>2</sub> often leads to short-circuit behavior
of the resulting solar cells due to the high shunt conductance. In
this study, in an attempt to resolve this problem, the influence of
the Se precursor concentration (<i>C</i><sub>Se</sub>) on
electrodeposited CuInSe<sub>2</sub> films and solar cell devices is
examined in the <i>C</i><sub>Se</sub> range of 4.8 to 12.0
mM in selenite-based aqueous solutions containing Cu and In chlorides
along with sulfamic acid (H<sub>3</sub>NSO<sub>3</sub>) and potassium
hydrogen phthalate (C<sub>8</sub>H<sub>5</sub>KO<sub>4</sub>) additives.
As <i>C</i><sub>Se</sub> increases, the CuInSe<sub>2</sub> layers become porous, and the grain growth of the CuInSe<sub>2</sub> phase is restricted, while the parasitic shunting problem was markedly
alleviated, as unambiguously demonstrated by measurements of the local
current distribution. Due to these ambivalent influences, an optimal
value of <i>C</i><sub>Se</sub> that achieves the best quality
of the films for high-efficiency solar cells is identified. Thus,
the device prepared with 5.2 mM Se exhibits a power-conversion efficiency
exceeding 10% with greatly improved device parameters, such as the
shunt conductance and the reverse saturation current. The rationale
of the present approach along with the physicochemical origin of its
conspicuous impact on the resulting devices is discussed in conjunction
with the electro-crystallization mechanism of the CuInSe<sub>2</sub> compound
Nanoscale Joule Heating and Electromigration Enhanced Ripening of Silver Nanowire Contacts
Solution-processed metallic nanowire thin film is a promising candidate to replace traditional indium tin oxide as the next-generation transparent and flexible electrode. To date however, the performance of these electrodes is limited by the high contact resistance between contacting nanowires; so improving the point contacts between these nanowires remains a major challenge. Existing methods for reducing the contact resistance require either a high processing power, long treatment time, or the addition of chemical reagents, which could lead to increased manufacturing cost and damage the underlying substrate or device. Here, a nanoscale point reaction process is introduced as a fast and low-power-consumption way to improve the electrical contact properties between metallic nanowires. This is achieved <i>via</i> current-assisted localized joule heating accompanied by electromigration. Localized joule heating effectively targets the high-resistance contact points between nanowires, leading to the automatic removal of surface ligands, welding of contacting nanowires, and the reshaping of the contact pathway between the nanowires to form a more desirable geometry of low resistance for interwire conduction. This result shows the interplay between thermal and electrical interactions at the highly reactive nanocontacts and highlights the control of the nanoscale reaction as a simple and effective way of turning individual metallic nanowires into a highly conductive interconnected nanowire network. The temperature of the adjacent device layers can be kept close to room temperature during the process, making this method especially suitable for use in devices containing thermally sensitive materials such as polymer solar cells
Fused Silver Nanowires with Metal Oxide Nanoparticles and Organic Polymers for Highly Transparent Conductors
Silver nanowire (AgNW) networks are promising candidates to replace indium–tin–oxide (ITO) as transparent conductors. However, complicated treatments are often required to fuse crossed AgNWs to achieve low resistance and good substrate adhesion. In this work, we demonstrate a simple and effective solution method to achieve highly conductive AgNW composite films with excellent optical transparency and mechanical properties. These properties are achieved via sequentially applying TiO2 sol–gel and PEDOT:PSS solution to treat the AgNW film. TiO2 solution volume shrinkage and the capillary force induced by solvent evaporation result in tighter contact between crossed AgNWs and improved film conductivity. The PEDOT:PSS coating acts as a protecting layer to achieve strong adhesion. Organic photovoltaic devices based on the AgNW–TiO2–PEDOT:PSS transparent conductor have shown comparable performance to those based on commercial ITO substrates
Photoreaction of Matrix-Isolated Dihydroazulene-Functionalized Molecules on Au{111}
Dihydroazulenes are photochromic molecules that reversibly
switch
between two distinct geometric and conductivity states. Molecular
design, surface attachment, and precise control over the assembly
of such molecular machines are critical in order to understand molecular
function and motion at the nanoscale. Here, we use surface-enhanced
Raman spectroscopy on special atomically flat, plasmonically enhanced
substrates to measure the photoreaction kinetics of isolated dihydroazulene-functionalized
molecules assembled on Au{111}, which undergo a ring-opening reaction
upon illumination with UV light and switch back to the initial isomer
via thermal relaxation. Photokinetic analyses reveal the high efficiency
of the dihydroazulene photoreaction on solid substrates compared to
other photoswitches. An order of magnitude decrease in the photoreaction
cross section of surface-bound dihydroazulenes was observed when compared
with the cross sections of these molecules in solution
Electrodeposited Silver Nanowire Transparent Conducting Electrodes for Thin-Film Solar Cells
Silver
nanowire (AgNW) networks have demonstrated high optical
and electrical properties, even better than those of indium tin oxide
thin films, and are expected to be a next-generation transparent conducting
electrode (TCE). Enhanced electrical and optical properties are achieved
when the diameter of the AgNWs in the network is fairly small, that
is, typically less than 30 nm. However, when AgNWs with such small
diameters are used in the network, stability issues arise. One method
to resolve the stability issues is to increase the diameter of the
AgNWs, but the use of AgNWs with large diameters has the disadvantage
of causing a rough surface morphology. In this work, we resolve all
of the aforementioned issues with AgNW TCEs by the electrodeposition
of Ag onto as-spin-coated thin AgNW TCEs. The electrodeposition of
Ag offers many advantages, including the precise adjustment of the
AgNW diameter and wire-to-wire welding to improve the junction conductance
while minimizing the increase in protrusion height because of the
overlap of AgNWs upon increasing the diameter. In addition, Ag electrodeposition
on AgNW TCEs can provide higher conductance than that of as-spin-coated
AgNW TCEs at the same transparency because of the reduced junction
resistance, which generates a superior figure of merit. We applied
the electrodeposited (ED) AgNW network to a Cu(In,Ga)Se2 thin-film solar cell and compared the device performance to a device
with a standard sputtered transparent conducting oxide (TCO). The
cell fabricated by the electrodeposition method showed nearly equal
performance to that of a cell with the sputtered TCO. We expect that
ED AgNW networks can be used as high-performance and robust TCEs for
various optoelectronic applications
Dispersal State of Multiwalled Carbon Nanotubes Elicits Profibrogenic Cellular Responses That Correlate with Fibrogenesis Biomarkers and Fibrosis in the Murine Lung
We developed a dispersal method for multiwalled carbon nanotubes (MWCNTs) that allows quantitative assessment of dispersion on profibrogenic responses in tissue culture cells and in mouse lung. We demonstrate that the dispersal of as-prepared (AP), purified (PD), and carboxylated (COOH) MWCNTs by bovine serum albumin (BSA) and dipalmitoylphosphatidylcholine (DPPC) influences TGF-β1, PDGF-AA, and IL-1β production in vitro and in vivo. These biomarkers were chosen based on their synergy in promoting fibrogenesis and cellular communication in the epithelial–mesenchymal cell trophic unit in the lung. The effect of dispersal was most noticeable in AP- and PD-MWCNTs, which are more hydrophobic and unstable in aqueous buffers than hydrophilic COOH-MWCNTs. Well-dispersed AP- and PD-MWCNTs were readily taken up by BEAS-2B, THP-1 cells, and alveolar macrophages (AM) and induced more prominent TGF-β1 and IL-1β production in vitro and TGF-β1, IL-1β, and PDGF-AA production in vivo than nondispersed tubes. Moreover, there was good agreement between the profibrogenic responses in vitro and in vivo as well as the ability of dispersed tubes to generate granulomatous inflammation and fibrosis in airways. Tube dispersal also elicited more robust IL-1β production in THP-1 cells. While COOH-MWCNTs were poorly taken up in BEAS-2B and induced little TGF-β1 production, they were bioprocessed by AM and induced less prominent collagen deposition at sites of nongranulomatous inflammation in the alveolar region. Taken together, these results indicate that the dispersal state of MWCNTs affects profibrogenic cellular responses that correlate with the extent of pulmonary fibrosis and are of potential use to predict pulmonary toxicity
