Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Metal Nanoparticle-Decorated Two-Dimensional Molybdenum Sulfide for Plasmonic-Enhanced Polymer Photovoltaic Devices.

ABSTRACT: Atomically thin two-dimensional (2D) transition metal dichalcogenides have also attracted immense interest because they exhibit appealing electronic, optical and mechanical properties. In this work, we prepared gold nanoparticle-decorated molybdenum sulfide (AuNP@MoS2) through a simple spontaneous redox reaction. Transmission electron microscopy, UV-Vis spectroscopy, and Raman spectroscopy were used to characterize the properties of the AuNP@MoS2 nanomaterials. Then we employed such nanocomposites as the cathode buffer layers of organic photovoltaic devices (OPVs) to trigger surface plasmonic resonance, leading to noticeable enhancements in overall device efficiencies. We attribute the primary origin of the improvement in device performance to local field enhancement induced by the effects of localized surface plasmonic resonance. Our results suggest that the metal nanoparticle-decorated two-dimensional materials appear to have great potential for use in high-performance OPVs.

SUBMITTER: Chuang MK

PROVIDER: S-EPMC5455522 | biostudies-other | 2015 Aug

REPOSITORIES: biostudies-other

ACCESS DATA

Json Xml

Similar Datasets

Polypyrrole decorated metal-organic frameworks for supercapacitor devices.

Project description:Due to their large specific surface areas and porosity, metal-organic frameworks (MOFs) have found many applications in catalysis, gas separation, and gas storage. However, their use as electronic components such as supercapacitors is stunted due to their poor electrical conductivity. We report a remedy for this by combining the MOF structure with polypyrrole (PPy), a well-known conductive polymer. Three MOFs are studied for modification to this end: CPO-27-Ni and CPO-27-Co (M2DOBDC, M = Ni2+, Co2+, DOBDC = 2,5-dihydroxy-1,4-benzenedicarboxylate) and HKUST-1 (Cu3(BTC)2, BTC = 1,3,5 benzenetricarboxylate). The gravimetric capacitance of pure MOFs is boosted several orders of magnitude after reinforcement of PPy (e.g., from 0.679 to 185 F g-1 for HKUST-1 and PPy-HKUST-1, respectively), and is much higher than reported for pure PPy. In total, these PPy-d-MOFs exhibit specific capacitances up to 354 F g-1, retaining 70% of this value even after 2500 cycles. Among them, the highest capacitance is found for PPy-CPO-27-Ni (354 F g-1), followed by PPy-CPO-27-Co (263 F g-1) and PPy-HKUST-1 (185 F g-1). The maximum operating potential for these electrodes is 0.5 V, which is restricted by the contact of MOF with aqueous electrolyte and with extremely low PPy content. As a solution, higher PPy loading and rational adjustment of particle size and porosity of both MOF and PPy are recommended so that the MOF/electrolyte interface is limited, leading to more robust electrode. The work completed here describes a highly promising approach to tackling the electrically insulating nature of MOFs, paving the way for their use in electrochemical energy storage devices.

| S-EPMC9054202 | biostudies-literature

Metal-Polymer Heterojunction in Colloidal-Phase Plasmonic Catalysis.

Project description:Plasmonic catalysis in the colloidal phase requires robust surface ligands that prevent particles from aggregation in adverse chemical environments and allow carrier flow from reagents to nanoparticles. This work describes the use of a water-soluble conjugated polymer comprising a thiophene moiety as a surface ligand for gold nanoparticles to create a hybrid system that, under the action of visible light, drives the conversion of the biorelevant NAD+ to its highly energetic reduced form NADH. A combination of advanced microscopy techniques and numerical simulations revealed that the robust metal-polymer heterojunction, rich in sulfonate functional groups, directs the interaction of electron-donor molecules with the plasmonic photocatalyst. The tight binding of polymer to the gold surface precludes the need for conventional transition-metal surface cocatalysts, which were previously shown to be essential for photocatalytic NAD+ reduction but are known to hinder the optical properties of plasmonic nanocrystals. Moreover, computational studies indicated that the coating polymer fosters a closer interaction between the sacrificial electron-donor triethanolamine and the nanoparticles, thus enhancing the reactivity.

| S-EPMC8935371 | biostudies-literature

Plasmonic Characterization of 3D Printable Metal–Polymer Nanocomposites

Project description: Not available

| S-EPMC11240405 | biostudies-literature

Coordination polymer structure and revisited hydrogen evolution catalytic mechanism for amorphous molybdenum sulfide.

Project description:Molybdenum sulfides are very attractive noble-metal-free electrocatalysts for the hydrogen evolution reaction (HER) from water. The atomic structure and identity of the catalytically active sites have been well established for crystalline molybdenum disulfide (c-MoS2) but not for amorphous molybdenum sulfide (a-MoSx), which exhibits significantly higher HER activity compared to its crystalline counterpart. Here we show that HER-active a-MoSx, prepared either as nanoparticles or as films, is a molecular-based coordination polymer consisting of discrete [Mo3S13](2-) building blocks. Of the three terminal disulfide (S2(2-)) ligands within these clusters, two are shared to form the polymer chain. The third one remains free and generates molybdenum hydride moieties as the active site under H2 evolution conditions. Such a molecular structure therefore provides a basis for revisiting the mechanism of a-MoSx catalytic activity, as well as explaining some of its special properties such as reductive activation and corrosion. Our findings open up new avenues for the rational optimization of this HER electrocatalyst as an alternative to platinum.

| S-EPMC5495159 | biostudies-literature

Two-dimensional, conductive niobium and molybdenum metal-organic frameworks.

Project description:The incorporation of second-row transition metals into metal-organic frameworks could greatly improve the performance of these materials across a wide variety of applications due to the enhanced covalency, redox activity, and spin-orbit coupling of late-row metals relative to their first-row analogues. Thus far, however, the synthesis of such materials has been limited to a small number of metals and structural motifs. Here, we report the syntheses of the two-dimensional metal-organic framework materials (H2NMe2)2Nb2(Cl2dhbq)3 and Mo2(Cl2dhbq)3 (H2Cl2dhbq = 3,6-dichloro-2,5-dihydroxybenzoquinone), which feature mononuclear niobium or molybdenum metal nodes and are formed through reactions driven by metal-to-ligand electron transfer. Characterization of these materials via X-ray absorption spectroscopy suggests a local trigonal prismatic coordination geometry for both niobium and molybdenum, consistent with their increased covalency relative to related first-row transition metal compounds. A combination of vibrational spectroscopy, magnetic susceptibility, and electronic conductivity measurements reveal that these two frameworks possess distinct electronic structures. In particular, while the niobium compound displays evidence for redox-trapping and strong magnetic interactions, the molybdenum phase is valence-delocalized with evidence of large polaron formation. Weak interlayer interactions in the neutral molybdenum phase enable solvent-assisted exfoliation to yield few-layer hexagonal nanosheets. Together, these results represent the first syntheses of metal-organic frameworks containing mononuclear niobium and molybdenum nodes, establishing a route to frameworks incorporating a more diverse range of second- and third-row transition metals with increased covalency and the potential for improved charge transport and stronger magnetic coupling.

| S-EPMC7481840 | biostudies-literature

Enhanced Photovoltaic Properties of Bulk Heterojunction Organic Photovoltaic Devices by an Addition of a Low Band Gap Conjugated Polymer.

Project description:In this study, we fabricated organic photovoltaics (OPVs) by introducing the polymer additive HTh6BT into the photoactive layer of a poly(3-hexylthiophene):phenyl-C61-butyric acid methyl ester (P3HT:PCBM) system. The HTh6BT had a relatively low band gap energy of 1.65 eV and a molecular and crystalline structure similar to that of P3HT. In the photoactive layer, the HTh6BT and P3HT can both act as donors. In such parallel-type bulk heterojunctions, each donor can form excitons and generate charges while being separated from the donor/acceptor interface. Changes in the photovoltaic property of the OPV device by the addition of HTh6BT were evaluated, and the optical characteristics of the photoactive layer, as well as the surface morphology, polymer ordering, and crystallinity of the P3HT:PCBM film were analyzed. Compared to a device without HTh6BT, all short-circuit current densities, open-circuit voltages, and fill factors were enhanced, leading to the enhancement of the power conversion efficiency by 36%.

| S-EPMC5456957 | biostudies-literature

Printable Metal-Polymer Conductors for Highly Stretchable Bio-Devices.

Project description:Stretchable, biocompatible devices can bridge electronics and biology. However, most stretchable conductors for such devices are toxic, costly, and regularly break/degrade after several large deformations. Here we show printable, highly stretchable, and biocompatible metal-polymer conductors by casting and peeling off polymers from patterned liquid metal particles, forming surface-embedded metal in polymeric hosts. Our printable conductors present good stretchability (2,316 S/cm at a strain of 500%) and repeatability (?R/R <3% after 10,000 cycles), which can satisfy most electrical applications in extreme deformations. This strategy not only overcomes large surface tension of liquid metal but also avoids the undesirable sintering of its particles by stress in deformations, such that stretchable conductors can form on various substrates with high resolution (15 ?m), high throughput (?2,000 samples/hour), and low cost (one-quarter price of silver). We use these conductors for stretchable circuits, motion sensors, wearable glove keyboards, and electroporation of live cells.

| S-EPMC6146547 | biostudies-literature

Gelation of plasmonic metal oxide nanocrystals by polymer-induced depletion attractions.

Project description:Gelation of colloidal nanocrystals emerged as a strategy to preserve inherent nanoscale properties in multiscale architectures. However, available gelation methods to directly form self-supported nanocrystal networks struggle to reliably control nanoscale optical phenomena such as photoluminescence and localized surface plasmon resonance (LSPR) across nanocrystal systems due to processing variabilities. Here, we report on an alternative gelation method based on physical internanocrystal interactions: short-range depletion attractions balanced by long-range electrostatic repulsions. The latter are established by removing the native organic ligands that passivate tin-doped indium oxide (ITO) nanocrystals while the former are introduced by mixing with small PEG chains. As we incorporate increasing concentrations of PEG, we observe a reentrant phase behavior featuring two favorable gelation windows; the first arises from bridging effects while the second is attributed to depletion attractions according to phase behavior predicted by our unified theoretical model. Our assembled nanocrystals remain discrete within the gel network, based on X-ray scattering and high-resolution transmission electron microscopy. The infrared optical response of the gels is reflective of both the nanocrystal building blocks and the network architecture, being characteristic of ITO nanocrystals' LSPR with coupling interactions between neighboring nanocrystals.

| S-EPMC6130341 | biostudies-literature

Sonochemical preparation of polymer-metal nanocomposites with catalytic and plasmonic properties.

Project description:Polymer-metal nanocomposites are of increasing interest for a wide range of applications; however, the preparation of these nanocomposites often requires the addition of external initiation and reducing agents for the synthesis of polymer and metal nanoparticles, respectively. Herein, we demonstrate the preparation of polymer-metal nanocomposites for improved catalytic performance by utilizing ultrasound as both the initiation and reducing source. Specifically, synthesis of the macro-RAFT agent containing poly[2-(dimethylamino)ethyl methacrylate], followed by ultrasound-initiated polymerization-induced self-assembly (sono-PISA), provides triblock copolymer nanoparticles containing tertiary amine groups. These polymer nanoparticles were further used as the scaffold for the in situ reduction of metal ions (Au and Pd ions) by radicals generated via sonolysis of water without additional reducing agents. The immobilization of metal nanoparticles has been confirmed by TEM and electron diffraction patterns. Polymer-Au nanocomposites with stepwise-grown AuNPs can be applied as surface-enhanced Raman scattering (SERS) substrates for 4-aminothiophenol (4-ATP) detection. Furthermore, the catalytic performances of these prepared polymer-Au and polymer-Pd nanocomposites were examined for aerobic alcohol oxidation and the Suzuki-Miyaura cross-coupling reaction, respectively. Overall, this strategy is expected to greatly expand the utility of ultrasound in the preparation of polymer-metal nanocomposites and promote the catalytic applications of these nanocomposites.

| S-EPMC9418413 | biostudies-literature

Importance of Plasmonic Heating on Visible Light Driven Photocatalysis of Gold Nanoparticle Decorated Zinc Oxide Nanorods.

Project description:Herein we explore the role of localized plasmonic heat generated by resonantly excited gold (Au) NPs on visible light driven photocatalysis process. Au NPs are deposited on the surface of vertically aligned zinc oxide nanorods (ZnO NRs). The localized heat generated by Au NPs under 532?nm continuous laser excitation (SPR excitation) was experimentally probed using Raman spectroscopy by following the phonon modes of ZnO. Under the resonant excitation the temperature at the surface of the Au-ZnO NRs reaches up to about 300?°C, resulting in almost 6 times higher apparent quantum yield (AQY) for photocatalytic degradation of methylene blue (MB) compared to the bare ZnO NRs. Under solar light irradiation the Au-ZnO NRs demonstrated visible light photocatalytic activity twice that of what was achieved with bare ZnO NRs, while significantly reduced the activation energy required for the photocatalytic reactions allowing the reactions to occur at a faster rate.

| S-EPMC4886257 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data