Localized surface plasmon-enhanced photoelectrochemical water oxidation by inorganic/organic nano-heterostructure...

This research article reports the visible-light-driven photoelectrochemical water oxidation performances of the plasmonic Au-Pd nanoparticle-decorated inorganic/organic nano-heterostructures (NHs)-B-TiO₂/NDIEHTh@Au-Pd. The inorganic constituent of the NHs consists of boron-doped TiO₂ nanorods (NRs) grown on fluorine-doped tin oxide (FTO) coated glass substrate. The organic part (NDIEHTh) consists of an acceptor naphthalene diimide (NDI)-based donor-acceptor-donor (D-A-D) type small molecule, in which thiophene serves as the donor. Because of the benefits of the localized surface plasmon resonance (LSPR) effect, the Au-Pd binary alloy nanoparticles substantially ameliorate the visible-light-driven photoelectrochemical performances of the B-TiO₂/NDIEHTh@Au-Pd NHs photoanode compared to the B-TiO₂/NDIEHTh NHs photoanode. The photocurrent densities exhibited by the B-TiO₂/NDIEHTh NHs, and B-TiO₂/NDIEHTh@Au-Pd NHs photoanodes at 1 V vs Ag/AgCl are 0.68 mA/cm² and 1.59 mA/cm², respectively, manifesting 209% and 623% increments in the photocurrent density compared to that shown by B-TiO₂ NRs photoanode. Besides, the B-TiO₂/NDIEHTh@Au-Pd NHs photoanode offers a significantly cathodically shifted water oxidation potential, reduced charge transfer resistance, better surface injection efficiency, and most importantly, superior photostability compared to the B-TiO₂/NDIEHTh NHs photoanode. The enhancement in the different photoelectrochemical performances could be attributed to the various advantages of LSPR, such as enhanced light absorbance, light concentration, hot electron injection, and plasmon-induced resonance energy transfer.