Plasmonic Control of Multi-Electron Transfer and C–C Coupling in Visible-Light-Driven CO₂ Reduction on Au Nanoparticles

Abstract

Artificial photosynthesis relies on the availability of synthetic photocatalysts that can drive CO₂ reduction in the presence of water and light. From the standpoint of solar fuel production, it is desirable that these photocatalysts perform under visible light and produce energy-rich hydrocarbons from CO₂ reduction. However, the multistep nature of CO₂-to-hydrocarbon conversion poses a significant kinetic bottleneck when compared to CO production and H₂ evolution. Here, we show that plasmonic Au nanoparticle photocatalysts can harvest visible light for multielectron, multiproton reduction of CO₂ to yield C₁ (methane) and C₂ (ethane) hydrocarbons. The light-excitation attributes influence the C₂ and C₁ selectivity. The observed trends in activity and selectivity follow Poisson statistics of electron harvesting. Higher photon energies and flux favor simultaneous harvesting of more than one electron from the photocharged Au nanoparticle catalyst, inducing the C-C coupling required for C₂ production. These findings elucidate the nature of plasmonic photocatalysis, which involves strong light-matter coupling, and set the stage for the controlled chemical bond formation by light excitation.