Abstract

The construction of S-scheme heterojunction photocatalysts has been regarded as an effective avenue to facilitate the conversion of solar energy to fuel. However, there are still considerable challenges with regard to efficient charge transfer, the abundance of catalytic sites, and extended light absorption. Herein, an S-scheme heterojunction of 2D/2D zinc porphyrin-based metal-organic frameworks/BiVO 4 nanosheets (Zn-MOF/BVON) was fabricated for efficient photocatalytic CO 2 conversion. The optimal one shows a 22-fold photoactivity enhancement when compared to the previously reported BiVO 4 nanoflake (ca. 15 nm), and even exhibits ~2-time improvement than the traditional g-C 3 N 4 /BiVO 4 heterojunction. The excellent photoactivities are ascribed to the strengthened S-scheme charge transfer and separation, promoted CO 2 activation by the well-dispersed metal nodes Zn 2 (COO) 4 in the Zn-MOF, and extended visible light response range based on the results of the electrochemical reduction, electron paramagnetic resonance, and in-situ diffuse reflectance infrared Fourier transform spectroscopy. The dimension-matched Zn-MOF/BVON S-scheme heterojunction endowed with highly efficient charge separation and abundant catalytic active sites contributed to the superior CO 2 conversion. This study offers a facile strategy for constructing S-scheme heterojunctions involving porphyrin-based MOFs for solar fuel production. 2D/2D zinc porphyrin-based metal-organic framework (ZnMOF)/BiVO 4 nanosheet S-scheme composites have been successfully constructed with exceptional photoactivity depending on the efficient S-scheme charge transfer and separation, extended visible light response range, and good CO 2 activation by Zn 2 (COO) 4 nodes.

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