Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Au-Pt-Ni nanochains as dopamine catalysts: role of elements and their spatial distribution.

ABSTRACT: Multi-element materials can improve biosensing ability as each element can catalyze different steps in a reaction pathway. By combining Pt and Ni on self-assembled 1D gold nanochains and controlling their spatial distribution, a detailed understanding of each element's role in dopamine oxidation is developed. In addition, the developed synthesis process provides a simple way to fabricate multi-element composites for electrocatalytic applications based on electrical double-layer formation on the surface of charged nanoparticles. The performance parameters of the catalyst, such as its sensitivity, limit of detection, and range of operation for dopamine sensing, are optimized by changing the relative ratios of Pt : Ni and the morphology of the Pt and Ni domains, using the developed understanding. The morphology of the domains also affects the oxidation state of Ni, which is crucial to the performance of the electrocatalyst.

SUBMITTER: Fan H

PROVIDER: S-EPMC10089120 | biostudies-literature | 2023 Apr

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Au-Pt-Ni nanochains as dopamine catalysts: role of elements and their spatial distribution.

Fan Hua H Le Boeuf William W Maheshwari Vivek V

Nanoscale advances 20230307 8

Multi-element materials can improve biosensing ability as each element can catalyze different steps in a reaction pathway. By combining Pt and Ni on self-assembled 1D gold nanochains and controlling their spatial distribution, a detailed understanding of each element's role in dopamine oxidation is developed. In addition, the developed synthesis process provides a simple way to fabricate multi-element composites for electrocatalytic applications based on electrical double-layer formation on the ...[more]

PMID: 37056628

Similar Datasets

Oxidation of Dichloromethane over Au, Pt, and Pt-Au Containing Catalysts Supported on γ-Al2O3 and CeO2-Al2O3.

Project description:Au, Pt, and Pt-Au catalysts supported on Al2O3 and CeO2-Al2O3 were studied in the oxidation of dichloromethane (DCM, CH2Cl2). High DCM oxidation activities and HCl selectivities were seen with all the catalysts. With the addition of Au, remarkably lower light-off temperatures were observed as they were reduced by 70 and 85 degrees with the Al2O3-supported and by 35 and 40 degrees with the CeO2-Al2O3-supported catalysts. Excellent HCl selectivities close to 100% were achieved with the Au/Al2O3 and Pt-Au/Al2O3 catalysts. The addition of ceria on alumina decreased the total acidity of these catalysts, resulting in lower performance. The 100-h stability test showed that the Pt-Au/Al2O3 catalyst was active and durable, but the selectivity towards the total oxidation products needs improvement. The results suggest that, with the Au-containing Al2O3-supported catalysts, DCM decomposition mainly occurs via direct DCM hydrolysis into formaldehyde and HCl followed by the oxidation of formaldehyde into CO and CO2.

| S-EPMC7587384 | biostudies-literature

Interfacial nanodroplets guided construction of hierarchical Au, Au-Pt, and Au-Pd particles as excellent catalysts.

Project description:Interfacial nanodroplets were grafted to the surfaces of self-sacrificed template particles in a galvanic reaction system to assist the construction of 3D Au porous structures. The interfacial nanodroplets were formed via direct adsorption of surfactant-free emulsions onto the particle surfaces. The interfacial nanodroplets discretely distributed at the template particle surfaces and served as soft templates to guide the formation of porous Au structures. The self-variation of footprint sizes of interfacial nanodroplets during Au growth gave rise to a hierarchical pore size distribution of the obtained Au porous particles. This strategy could be easily extended to synthesize bimetal porous particles such as Au-Pt and Au-Pd. The obtained porous Au, Au-Pt, and Au-Pd particles showed excellent catalytic activity in catalytic reduction of 4-nitrophenol.

| S-EPMC4010925 | biostudies-literature

Topographical and compositional engineering of core-shell Ni@Pt ORR electro-catalysts.

Project description:Complex faceted geometries and compositional anisotropy in alloy nanoparticles (NPs) can enhance catalytic performance. We report on the preparation of binary PtNi NPs via a co-thermolytic approach in which we optimize the synthesis variables, which results in significantly improved catalytic performance. We used scanning transmission electron microscopy to characterise the range of morphologies produced, which included spherical and concave cuboidal core-shell structures. Electrocatalytic activity was evaluated using a rotating disc electrode (1600 rpm) in 0.1 M HClO4; the electrocatalytic performance of these Ni@Pt NPs showed significant (∼11-fold) improvement compared to a commercial Pt/C catalyst. Extended cycling revealed that electrochemical surface area was retained by cuboidal PtNi NPs post 5000 electrochemical cycles (0.05-1.00 V, vs. SHE). This is attributed to the enclosure of Ni atoms by a thick Pt shell, thus limiting Ni dissolution from the alloy structures. The novel synthetic strategy presented here results in a high yield of Ni@Pt NPs which show excellent electro-catalytic activity and useful durability.

| S-EPMC9055937 | biostudies-literature

Novel continuous flow synthesis of Pt NPs with narrow size distribution for Pt@carbon catalysts.

Project description:In this work, we report a novel continuous flow synthesis method to achieve ultra-small Pt NPs (2.3 to 2.5 nm) with narrow size distribution. This method expedited the synthesis of Pt NPs without any harsh reducing agent or capping agent. Further these Pt NPs were immobilized on a carbon support in a single step procedure for its application as an electrocatalyst for fuel cells. The synthesized Pt NPs and Pt NPs supported on carbon were analyzed using transmission electron microscopy affirming uniform distribution of Pt NPs throughout the carbon support without aggregation.

| S-EPMC9047455 | biostudies-literature

Fabrication of vertical GaN/InGaN heterostructure nanowires using Ni-Au bi-metal catalysts.

Project description:We have fabricated the vertically aligned coaxial or longitudinal heterostructure GaN/InGaN nanowires. The GaN nanowires are first vertically grown by vapor-liquid-solid mechanism using Au/Ni bi-metal catalysts. The GaN nanowires are single crystal grown in the [0001] direction, with a length and diameter of 1 to 10 μm and 100 nm, respectively. The vertical GaN/InGaN coaxial heterostructure nanowires (COHN) are then fabricated by the subsequent deposition of 2 nm of InxGa1-xN shell on the surface of GaN nanowires. The vertical GaN/InGaN longitudinal heterostructure nanowires (LOHN) are also fabricated by subsequent growth of an InGaN layer on the vertically aligned GaN nanowires using the catalyst. The photoluminescence from the COHN and LOHN indicates that the optical properties of GaN nanowires can be tuned by the formation of a coaxial or longitudinal InGaN layer. Our study demonstrates that the bi-metal catalysts are useful for growing vertical as well as heterostructure GaN nanowires. These vertically aligned GaN/InGaN heterostructure nanowires may be useful for the development of high-performance optoelectronic devices.

| S-EPMC3720202 | biostudies-literature

Low Metal Loading (Au, Ag, Pt, Pd) Photo-Catalysts Supported on TiO2 for Renewable Processes.

Project description:Photo-catalysts based on titanium dioxide, and modified with highly dispersed metallic nanoparticles of Au, Ag, Pd and Pt, either mono- or bi-metallic, have been analyzed by multiple characterization techniques, including XRD, XPS, SEM, EDX, UV-Vis and N2 adsorption/desorption. Mono-metallic photo-catalysts were prepared by wet impregnation, while bi-metallic photocatalysts were obtained via deposition-precipitation (DP). The relationship between the physico-chemical properties and the catalyst's behavior for various photo-synthetic processes, such as carbon dioxide photo-reduction to liquid products and glucose photo-reforming to hydrogen have been investigated. Among the tested materials, the catalysts containing platinum alone (i.e., 0.1 mol% Pt/TiO2) or bi-metallic gold-containing materials (e.g., 1 wt% (AuxAgy)/TiO2 and 1 wt% (AuxPtz)/TiO2) showed the highest activity, presenting the best results in terms of productivity and conversion for both applications. The textural, structural and morphological properties of the different samples being very similar, the main parameters to improve performance were function of the metal as electron sink, together with optoelectronic properties. The high activity in both applications was related to the low band gap, that allows harvesting more energy from a polychromatic light source with respect to the bare TiO2. Overall, high selectivity and productivity were achieved with respect to most literature data.

| S-EPMC9031976 | biostudies-literature

Synergistic Effect of Pt and Dual Ni/Co Cations in Hydrotalcite-Derived Pt/Ni<sub>1.5</sub>Co<sub>0.5</sub>AlO Catalysts for Promoting Soot Combustion.

Project description:In this article, the catalysts of hydrotalcite-derived Ni1.5Co0.5AlO nanosheet-supported highly dispersed Pt nanoparticles (Ptn/Ni1.5Co0.5AlO, where n% is the weigh percentage of the Pt element in the catalysts) were elaborately fabricated by the gas-bubble-assisted membrane--reduction method. The specific porous structure formed by the stack of hydrotalcite-derived Ni1.5Co0.5AlO nanosheets can increase the transfer mass efficiency of the reactants (O2, NO, and soot) and the strong Pt-Ni1.5Co0.5AlO interaction can weaken the Ni/Co-O bond for promoting the mobility of lattice oxygen and the formation of surface-oxygen vacancies. The Ptn/Ni1.5Co0.5AlO catalysts exhibited excellent catalytic activity and stability during diesel soot combustion under the loose contact mode between soot particles and catalysts. Among all the catalysts, the Pt2/Ni1.5Co0.5AlO catalyst showed the highest catalytic activities for soot combustion (T50 = 350 °C, TOF = 6.63 × 10-3 s-1). Based on the characterization results, the catalytic mechanism for soot combustion is proposed: the synergistic effect of Pt and dual Ni/Co cations in the Pt/Ni1.5Co0.5AlO catalysts can promote the vital step of catalyzing NO oxidation to NO2 in the NO-assisted soot oxidation mechanism. This insight into the synergistic effect of Pt and dual Ni/Co cations for soot combustion provides new strategies for reducing the amounts of noble metals in high-efficient catalysts.

| S-EPMC9965507 | biostudies-literature

Pt-Ni/ZnO-rod catalysts for hydrogen production by steam reforming of methanol with oxygen.

Project description:Ni, Pt and a mixture of Ni and Pt supported on ZnO-rods were evaluated in autothermal steam reforming of methanol (ASRM) for hydrogen production as a function of the reaction temperature. The catalytic materials were characterized by SEM-EDS, XRD, TEM, HRTEM, TPR and BET. Analysis by SEM and TEM showed structural modifications on the surface of the ZnO rods after Ni impregnation. The reactivity of the catalytic materials in the range of 200-500 °C showed that the bimetallic sample had better catalytic activity among all the catalysts studied. This finding could be associated to PtZn and NiZn alloys present in this catalyst, which were identified by XRD and HRTEM analyses. Catalyst characterization by XRD after the catalytic testing showed that the intermetallic PtZn phase was stable during the reaction in the Pt/ZnO-rod sample. The cubic Ni0.75-Zn0.25 structure identified in the Ni/ZnO-rod sample was transformed to Zn0.1-Ni0.9-O and metallic Ni phases, respectively. On the bimetallic PtNi/ZnO-rod sample, the cubic Ni0.75-Zn0.25 structure remained, although the tetragonal NiZn structure is unstable and was destroyed during the ASRM reaction and then a new phase of Ni0.7Pt0.3 emerged. The promotion effect of Pt and/or Ni on the ZnO-rod was clearly shown.

| S-EPMC9057812 | biostudies-literature

Activity of Mono-, Bi-, and Trimetallic Catalysts Pt-Ni-Cr/C in the Bicyclohexyl Dehydrogenation Reaction.

Project description:The influence of metals with different redox properties and a carbon carrier on the activity of mono-, bi- and trimetallic Pt-Ni-Cr/C catalysts has been studied in the bicyclohexyl dehydrogenation reaction as the hydrogen release stage in hydrogen storage. An increase in the conversion (X > 62%) of bicyclohexyl and selectivity for biphenyl (S > 84%) was observed on trimetallic catalysts Pt-Ni-Cr/C compared with the monometallic catalyst Rt/C (X > 55%; S > 68%). It has been established that the increase in the conversion of bicyclohexyl and selectivity for biphenyl in the dehydrogenation reaction on trimetallic catalysts is due to an increase in the activity of Pt nanoparticles in the vicinity of local Cr-Ni clusters of solid substitution solutions.

| S-EPMC9737465 | biostudies-literature

Observation of spin Seebeck contribution to the transverse thermopower in Ni-Pt and MnBi-Au bulk nanocomposites.

Project description:Transverse thermoelectric devices produce electric fields perpendicular to an incident heat flux. Classically, this process is driven by the Nernst effect in bulk solids, wherein a magnetic field generates a Lorentz force on thermally excited electrons. The spin Seebeck effect also produces magnetization-dependent transverse electric fields. It is traditionally observed in thin metallic films deposited on electrically insulating ferromagnets, but the films' high resistance limits thermoelectric conversion efficiency. Combining Nernst and spin Seebeck effect in bulk materials would enable devices with simultaneously large transverse thermopower and low electrical resistance. Here we demonstrate experimentally that this is possible in composites of conducting ferromagnets (Ni or MnBi) containing metallic nanoparticles with strong spin-orbit interactions (Pt or Au). These materials display positive shifts in transverse thermopower attributable to inverse spin Hall electric fields in the nanoparticles. This more than doubles the power output of the Ni-Pt materials, establishing proof of principle that the spin Seebeck effect persists in bulk nanocomposites.

| S-EPMC5159888 | 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