Abstract

Heterojunction photocatalysts possess high efficiency in photogenerated electron-hole separation, which give significant advantages in the field of solar hydrogen production. Herein, a novel ZnIn2S4@S doped g-C3N4 (ZIS@SCN) heterojunction with mesoporous structure was prepared for photocatalytic water splitting under visible light. Characterization showed that the element of S was successfully introduced into g-C3N4 (CN) by replacing N to form C–S–C bonds and significantly enhanced the visible light absorption ability. The constructed heterojunction exhibited excellent photocatalytic hydrogen evolution under visible light. The best performance belonged to the sample of ZIS@100SCN. The corresponding H2 production rate reached 9.3 mmol h−1 g−1, which was 1.87-fold higher than that of the undoped one. More importantly, the heterojunction realized overall water splitting of H2 and O2 evolution simultaneously with good stability. The mechanism analysis indicted that introducing the element of S could regulate the band structure of CN and induce the charge transfer switching of a ZnIn2S4@g-C3N4 (ZIS@CN) photocatalyst from Ⅰ-type to S-scheme, which promoted the efficient spatial charge separation and maintained the high redox ability of the ZIS and SCN. This work provides an insight in construction high performance S-scheme heterojunction for water splitting with a doping method.

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