Tuning the strength of built-in electric field in 2D/2D g-C3N4/SnS2 and g-C3N4/ZrS2 S-scheme heterojunctions by nonmetal doping

Single photocatalysts usually exhibit unsatisfactory performance due to the serious recombination of photogenerated electron-hole pairs. Combining two photocatalysts to construct S-scheme heterojunction could solve this problem. In S-scheme mechanism, the interfacial built-in electric field (IEF) provides a vital driving force for efficient charge separation. Modifying the IEF is a feasible strategy to further improve the photocatalytic activity. Herein, a novel idea of tuning the strength of IEF in 2D/2D graphitic carbon nitride (g-C3N4)/MS2 (M = Sn, Zr) S-scheme heterojunctions by nonmetal doping was developed by employing density functional theory calculation. Three nonmetal elements (O, P, and S) were severally introduced into g-C3N4/MS2 composites. Charge density difference suggested that O and S doping led to increased interfacial electron transfer, while P doping had minimal influence. As expected, the calculated field strength of O- and S-doped g-C3N4/MS2 composites was significantly larger than that of pristine and P-doped g-C3N4/MS2 composites. Therefore, O and S doping endowed g-C3N4/MS2 S-scheme heterojunctions with enhanced IEF and more thorough charge transfer. Correspondingly, the experimentally synthesized O-C3N4/SnS2 composite exhibited better photocatalytic H-2-production activity than g-C3N4/SnS2 composite. This work proposed an original idea of employing proper nonmetal doping to magnify the advantage of S-scheme heterojunction in accelerating charge separation. (C) 2021 The Chinese Ceramic Society. Production and hosting by Elsevier B.V.

Automated summary

Tuning the strength of interfacial built-in electric field (IEF) in 2D/2D graphitic carbon nitride (g-C3N4)/MS2 (M = Sn, Zr) S-scheme heterojunctions through nonmetal doping significantly enhances photocatalytic activity. Oxygen and sulfur doping leads to increased interfacial electron transfer, resulting in better hydrogen production activity in photocatalysts.