Issue 29, 2024

Internal electric field promoted charge separation via bismuth-based ternary heterojunctions with near-infrared light harvesting properties for efficient photoredox reactions

Abstract

1D-based heterostructured photocatalysts have attracted great attention in the field of solar-to-fuel conversion reactions owing to their distinctive electronic band structure and rich active sites. However, the rational design and interfacial charge carriers' regulation of 1D double S-scheme heterojunctions are still puzzling. In this work, a quaternary photocatalytic system of CdS/Bi/Bi2WO6/Bi2S3 (CBWO) with full spectrum utilization was developed. Photocatalytic tests revealed that the optimized CBWO heterostructured catalyst had the highest photocatalytic H2 evolution rate under UV-vis-NIR light irradiation were 4.2 and 29 times that of pure CdS and BWO photocatalysts, respectively. Detailed experiments together with structural characterization and charge transfer properties reveal that the double S-scheme heterojunction and Schottky junction with metallic Bi could significantly promote electron enrichment, which offers highly efficient reaction networks to facilitate the conversion of 2H+ towards H2 formation. These results provide a piece of important knowledge for the specific design and synthesis of excellent photocatalysts with full spectrum response in solar to H2 conversion reactions.

Graphical abstract: Internal electric field promoted charge separation via bismuth-based ternary heterojunctions with near-infrared light harvesting properties for efficient photoredox reactions

Supplementary files

Article information

Article type
Paper
Submitted
12 Apr 2024
Accepted
12 Jun 2024
First published
12 Jun 2024

J. Mater. Chem. A, 2024,12, 18498-18511

Internal electric field promoted charge separation via bismuth-based ternary heterojunctions with near-infrared light harvesting properties for efficient photoredox reactions

R. K. Chava, Y. Im and M. Kang, J. Mater. Chem. A, 2024, 12, 18498 DOI: 10.1039/D4TA02523G

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