摘要
The search for effective and highly selective photocatalysts for CO 2 transformation is exceptionally desirable yet challenging. Herein, a novel BiVO 4 @PCN-224(Cu) heterostructure was constructed by growing BiVO 4 nanosheets on the surface of PCN-224(Cu) rods for visible-light-driven CO 2 photoreduction. The obtained BiVO 4 @PCN-224(Cu) heterostructure could selectively reduce CO 2 into CO in the absence of sacrificial reagents. The CO yield over the optimized sample reached 70.5 μmol g −1 h −1 (corresponding to an apparent quantum yield of 0.42% at 450 nm), a 5.1-fold increase over pristine PCN-224(Cu). The boosted activity of the hybrid could be credited to the S-scheme heterojunction formed at the interface of PCN-224(Cu) and BiVO 4 , which facilitated the separation of photogenerated charges and ameliorated the redox capability. In-situ XPS and hydroxyl radical determination confirmed the S-scheme charge transfer mode. This study provides a new strategy for constructing S-scheme heterojunctions involving metalloporphyrin-based metal-organic frameworks for high-performance CO 2 conversion.
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