dc.contributor.author |
DHANKHAR, ANKIT |
en_US |
dc.contributor.author |
PILLAI, PRAMOD P. |
en_US |
dc.date.accessioned |
2024-10-29T06:44:56Z |
|
dc.date.available |
2024-10-29T06:44:56Z |
|
dc.date.issued |
2024-10 |
en_US |
dc.identifier.citation |
Chemistry of Materials, 36(20), 10227–10237. |
en_US |
dc.identifier.issn |
0897-4756 |
en_US |
dc.identifier.issn |
1520-5002 |
en_US |
dc.identifier.uri |
https://doi.org/10.1021/acs.chemmater.4c01966 |
en_US |
dc.identifier.uri |
http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9153 |
|
dc.description.abstract |
The creation of antenna-reactor systems with a precise arrangement of reactor sites around an anisotropic plasmonic nanomaterial is essential to achieving a perfect balance between the charge generation, separation, and extraction processes in plasmonic photocatalysis. Here, we propose the formation and photocatalytic properties of gold-rhodium superstructures (AuNR-Rh SSs), wherein site-selective epitaxial growth of ordered rhodium islands is achieved on plasmonic gold nanorods (AuNR). Iodide ions play a crucial role in spatially controlling the nucleation and growth of reactor sites (Rh islands). The rational design of AuNR-Rh SSs led to the formation of uniform and spatially separated Rh islands with high-index facets on the surface of AuNR, ensuring efficient light excitation and hot charge carrier separation, as well as enhanced reactant adsorption and activation. These antenna-reactor superstructures are further used for plasmon-driven photoregeneration of biological nicotinamide cofactors (NADH and NADPH). A suitable functionalization of AuNR-Rh SSs with negatively charged surface ligands helped the electrostatic channeling of electron mediators toward the photocatalyst surface, thereby increasing the charge transfer and utilization processes. Both the antenna-reactor effect and favorable catalyst-reactant interaction collectively boost the photocatalytic activity of AuNR-Rh SSs in regenerating the enzymatically active 1,4-NAD(P)H cofactors in similar to 40% yield. A series of control experiments prove the role of each component, the precise arrangement of active sites, and appropriate surface functionalization in dictating the photocatalytic activity of anisotropic AuNR-Rh SSs antenna-reactor construct. Our work shows the need for a uniform but spatially separated deposition of reactor sites on the surface of an anisotropic nanoparticle to achieve the desired photocatalytic output from the corresponding antenna-reactor system. The anisotropic Au-Rh based antenna-reactor systems reported here could find applications in other plasmon-driven chemical transformations as well. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
American Chemical Society |
en_US |
dc.subject |
Epitaxy |
en_US |
dc.subject |
Gold |
en_US |
dc.subject |
Photocatalysis |
en_US |
dc.subject |
Photocatalysts |
en_US |
dc.subject |
Plasmonics |
en_US |
dc.subject |
2024 |
en_US |
dc.subject |
2024-OCT-WEEK2 |
en_US |
dc.subject |
TOC-OCT-2024 |
en_US |
dc.title |
Plasmonic Antenna-Reactor Photocatalysts Based on Anisotropic Gold-Rhodium Superstructures for Biological Cofactor Regeneration |
en_US |
dc.type |
Article |
en_US |
dc.contributor.department |
Dept. of Chemistry |
en_US |
dc.identifier.sourcetitle |
Chemistry of Materials |
en_US |
dc.publication.originofpublisher |
Foreign |
en_US |