Solar-driven electrochemical NH3 splitting into H2 and N2 on BiVO4-based photoanodes

From the viewpoints of energy and the environment, NH3 splitting into N-2 and H-2 is an important challenge in chemistry, and we have found that BiVO4 is a highly promising base photoanode material for it. Semiconductor films (TiO2 and BiVO4) were formed on a fluorine-doped tin oxide (FTO) electrode, and three-electrode photoelectrochemical (PEC) cells using them as the photoanodes were fabricated. The photocurrent in the TiO2/FTO photoanode cell is saturated at similar to 0.1 mA cm(-2) in the range of electrode potential (E) more positive than +0.3 V vs. the standard hydrogen electrode (SHE) in an electrolyte solution containing NH3 (pH 11) under illumination of simulated sunlight (AM 1.5, 100 mW cm(-2), one sun). In contrast, the photocurrent in the BiVO4/FTO photoanode cell increases with increasing anodic polarization to reach 1.78 mA cm(-2) at E = +1 V vs. SHE. This PEC cell produces H-2 from NH3 with a selectivity of 92% under the same irradiation conditions, and the incident photon-to-current conversion efficiency reaches 11.7% at a wavelength of excitation light = 365 nm. Provision of an SnO2 interlayer between the BiVO4 and FTO films effectively suppresses the recombination at the interface to enhance the photocurrent under weak anodic polarization at E < +0.5 V vs. SHE.