Fabrication of an Efficient N, S Co-Doped WO₃ Operated in Wide-Range of Visible-Light for Photoelectrochemical Water Oxidation

Abstract

In this work, a highly efficient wide-visible-light-driven photoanode, namely, nitrogen and sulfur co-doped tungsten trioxide (S-N-WO3), was synthesized using tungstic acid (H2WO4) as W source and ammonium sulfide ((NH4)2S), which functioned simultaneously as a sulfur source and as a nitrogen source for the co-doping of nitrogen and sulfur. The EDS and XPS results indicated that the controllable formation of either N-doped WO3 (N-WO3) or S-N-WO3 by changing the nW:n(NH4)2S ratio below or above 1:5. Both N and S contents increased when increasing the nW:n(NH4)2S ratio from 1:0 to 1:15 and thereafter decreased up to 1:25. The UV-visible diffuse reflectance spectra (DRS) of S-N-WO3 exhibited a significant redshift of the absorption edge with new shoulders appearing at 470–650 nm, which became more intense as the nW:n(NH4)2S ratio increased from 1:5 and then decreased up to 1:25, with the maximum at 1:15. The values of nW:n(NH4)2S ratio dependence is consistent with the cases of the S and N contents. This suggests that S and N co-doped into the WO3 lattice are responsible for the considerable redshift in the absorption edge, with a new shoulder appearing at 470–650 nm owing to the intrabandgap formation above the valence band (VB) edge and a dopant energy level below the conduction band (CB) of WO3. Therefore, benefiting from the S and N co-doping, the S-N-WO3 photoanode generated a photoanodic current under visible light irradiation below 580 nm due to the photoelectrochemical (PEC) water oxidation, compared with pure WO3 doing so below 470 nm.

Keywords

• N, S co-doped
• water oxidation
• tungsten trioxide
• photoanode
• photoelectrochemical
• water splitting