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Volume 214, 2019
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Direct hot-carrier transfer in plasmonic catalysis

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Abstract

Plasmonic metal nanoparticles can concentrate optical energy and enhance chemical reactions on their surfaces. Plasmons can interact with adsorbate orbitals and decay by directly exciting a carrier from the metal to the adsorbate in a process termed the direct-transfer process. Although this process could be useful for enhancing the efficiency of a chemical reaction, it remains poorly understood. Here, we report a preliminary investigation employing time-dependent density-functional theory (TDDFT) calculations to capture this process at a model metal–adsorbate interface formed by a silver nanoparticle (Ag147) and a carbon monoxide molecule (CO). Direct hot-electron transfer is observed to occur from the occupied states of Ag to the unoccupied molecular orbitals of CO. We determine the probability of this process and show that it depends on the adsorption site of CO. Our results are expected to aid the design of more efficient metal–molecule interfaces for plasmonic catalysis.

Graphical abstract: Direct hot-carrier transfer in plasmonic catalysis

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Publication details

The article was received on 16 Oct 2018, accepted on 15 Nov 2018 and first published on 27 Feb 2019


Article type: Paper
DOI: 10.1039/C8FD00154E
Faraday Discuss., 2019,214, 189-197

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    Direct hot-carrier transfer in plasmonic catalysis

    P. V. Kumar, T. P. Rossi, M. Kuisma, P. Erhart and D. J. Norris, Faraday Discuss., 2019, 214, 189
    DOI: 10.1039/C8FD00154E

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