Abstract
Plasmonic nanoparticles have been demonstrated to enhance photocatalysis due to their strong photon absorption and efficient hot-carrier generation. However, plasmonic photocatalysts suffer from a short lifetime of plasmon-generated hot carriers that decay through internal relaxation pathways before being harnessed for chemical reactions. Here, we demonstrate the enhanced photocatalytic reduction of gold ions on gold nanorods functionalized with polyvinylpyrrolidone. The catalytic activities of the reaction are quantified by in situ monitoring of the spectral evolution of single nanorods using a dark-field scattering microscope. We observe a 13-fold increase in the reduction rate with the excitation of d-sp interband transition compared to dark conditions, and a negligible increase in the reduction rate when excited with intraband transition. The hole scavenger only plays a minor role in the photocatalytic reduction reaction. We attribute the enhanced photocatalysis to an efficient charge separation at the gold-polyvinylpyrrolidone interface, where photogenerated d-band holes at gold transfer to the HOMO of polyvinylpyrrolidone, leading to the prolonged lifetime of the electrons that subsequently reduce gold ions to gold atoms. These results provide new insight into the design of plasmonic photocatalysts with capping ligands.