Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9153
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dc.contributor.authorDHANKHAR, ANKITen_US
dc.contributor.authorPILLAI, PRAMOD P.en_US
dc.date.accessioned2024-10-29T06:44:56Z
dc.date.available2024-10-29T06:44:56Z
dc.date.issued2024-10en_US
dc.identifier.citationChemistry of Materials, 36(20), 10227–10237.en_US
dc.identifier.issn0897-4756en_US
dc.identifier.issn1520-5002en_US
dc.identifier.urihttps://doi.org/10.1021/acs.chemmater.4c01966en_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/9153
dc.description.abstractThe 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.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectEpitaxyen_US
dc.subjectGolden_US
dc.subjectPhotocatalysisen_US
dc.subjectPhotocatalystsen_US
dc.subjectPlasmonicsen_US
dc.subject2024en_US
dc.subject2024-OCT-WEEK2en_US
dc.subjectTOC-OCT-2024en_US
dc.titlePlasmonic Antenna-Reactor Photocatalysts Based on Anisotropic Gold-Rhodium Superstructures for Biological Cofactor Regenerationen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Chemistryen_US
dc.identifier.sourcetitleChemistry of Materialsen_US
dc.publication.originofpublisherForeignen_US
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