Dewetted Au Nanoparticles on TiO2 Surfaces: Evidence of a Size-Independent Plasmonic Photoelectrochemical Response

Abstract

We induce solid-state dewetting of thin Au films (nominal thickness of 0.5-10 nm) on flat TiO2 surfaces to produce Au nanoparticles with an average size tunable in the 3-200 nm range. Such Au-decorated TiO2 surfaces enable plasmonic photoelectrochemical water splitting under visible light illumination (450-750 nm), with a photon-to-current conversion efficiency that reaches a maximum for TiO2 surfaces decorated with ∼30 nm sized Au particles. Optical measurements show, as expected, a red shift of the plasmon resonance with the increasing Au nanoparticle size. More interestingly, the photocurrent is found to peak for every photoanode at ∼600 nm regardless of the Au nanoparticle size, i.e., the wavelength of maximum photocurrent is size-independent. Such a remarkable observation can be ascribed to a hot electron injection cutoff effect, i.e., can be explained in terms of the interband versus intraband transition scenario.