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Using plasmonically generated carriers as redox equivalents

Published online by Cambridge University Press:  10 January 2020

Sungju Yu ,
Varun Mohan  and
Prashant K. Jain
Sungju Yu
Affiliation:
Department of Chemistry, University of Illinois at Urbana-Champaign, USA; yus@illinois.edu
Varun Mohan
Affiliation:
Department of Materials Science and Engineering, University of Illinois at Urbana-Champaign, USA; vmohan8@illinois.edu
Prashant K. Jain
Affiliation:
Department of Chemistry, Materials Research Laboratory, Department of Physics, and Beckman Institute of Advanced Science and Technology, University of Illinois at Urbana-Champaign, USA; jain@illinois.edu
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Abstract

Nanostructures of plasmonic metals naturally combine strong light–matter interactions with catalytic activity, enabling new opportunities for light harvesting, catalytic chemistry, and artificial photosynthesis. Numerous studies have demonstrated that the optical excitation of localized surface plasmons generates hot electrons that can activate adsorbates triggering or facilitating chemical reactions on the surface of the nanoparticle. Going beyond such hot-electron-activated chemistry, a body of studies has shown that electron and hole carriers can be harvested from a plasmonically excited nanoparticle and utilized as redox equivalents for driving chemical reactions involving charge transfer. This article reviews such photoredox chemistry driven by plasmonic excitation of metal nanoparticles. Under certain conditions, a plasmonically excited nanoparticle can catalyze multielectron, multiproton transformations such as the photosynthesis of CO2 to hydrocarbons. We describe how the free energy of plasmonically generated charge carriers can be harvested and utilized for thermodynamically uphill reactions involving the formation of energy-rich chemical bonds or the development of molecular complexity. We end with a discussion of future opportunities in plasmon-excitation-driven photoredox chemistry.

Type
Materials for Hot-Carrier Chemistry
Information
MRS Bulletin , Volume 45 , Issue 1: Materials for Hot-Carrier Chemistry , January 2020 , pp. 43 - 48
Copyright
Copyright © Materials Research Society 2020

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