摘要
Molecular catalysts have attracted significant attention in photocatalytic CO 2 reduction (PCR) due to well-defined structure and exceptional catalytic selectivity. However, they are still limited by recycling challenges and inherent instability. Forming an organic-inorganic composite can address these issues and enhance PCR performance simultaneously. Herein, we developed a flower-like Z-scheme heterojunction of cobalt porphyrin ([meso-tetra(4-sulfonatophenyl)porphyrin], CoTPPS) and ZnIn 2 S 4 (ZIS). The optimized ZIS@CoTPPS exhibited a superior CO evolution rate of 388.26 μmol g −1 h −1 , which is 8.96 times of pristine ZIS (43.32 μmol g −1 h −1 ). The superior PCR activity is contributed by the enhanced light absorption, and photoinduced charge separation facilitated by the Z-scheme structure and the cobalt active sites. Moreover, theoretical calculations confirm the heterojunction relies on a substantial interfacial coupling between the Zn atoms of ZIS and the sulfonic acid groups of CoTPPS through coordination assembly. This investigation affords a useful inspiration for consciously constructing novel ZIS-incorporated atomistic Z-scheme photocatalysts.
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