Designing Surface-Defect Engineering to Enhance the Solar-Driven Conversion of CO2 to C2 Products over Zn3In2S6/ZnS.

ABSTRACT

The manipulation of electronic structure and prevention of photogenerated carriers from being quenched in bulk defects during the photocatalytic CO2 reduction reaction (CRR) have been effectively demonstrated through surface vacancy and defect engineering. In this work, the electronic structure on the surface of Zn3In2S6/ZnS (ZIS/ZnS) is significantly modified by the introduction and control of the surface S vacancies (SV) through Ar-plasma treatment. EPR and XPS analyses confirmed that SV was exclusively present on the ZIS/ZnS surface. The resulting ZIS/ZnS heterojunction photocatalysts demonstrate an impressive 46.6% selectivity toward C2 products even in the absence of cocatalysts. The mechanism of photocatalytic CRR is further elucidated through in situ analysis. Theoretical calculations demonstrate that the presence of In and Zn atoms adjacent to SV significantly enhances the adsorption of CO2 and facilitates C-C coupling.