Multi-hierarchical CuS/SnIn4S8 S-scheme heterojunction for superior photothermal-assisted photocatalytic hydrogen production
[Display omitted] •Multi-hierarchical CuS/SnIn4S8 S-scheme heterojunction is reported for the first time.•The S-scheme heterostructure greatly facilitates the charge separation and transfer.•The outstanding photothermal property substantially improves the catalytic reactions.•The catalyst exhibits i...
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Veröffentlicht in: | Separation and purification technology 2024-10, Vol.345, p.127253, Article 127253 |
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Format: | Artikel |
Sprache: | eng |
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•Multi-hierarchical CuS/SnIn4S8 S-scheme heterojunction is reported for the first time.•The S-scheme heterostructure greatly facilitates the charge separation and transfer.•The outstanding photothermal property substantially improves the catalytic reactions.•The catalyst exhibits impressive full-spectrum photocatalytic hydrogen production.
Various methods aimed at enhancing light trapping and charge separation efficiencies have emerged as a central research focus in the field of photocatalysis. This study marks the successful construction of CuS/SnIn4S8 composite photocatalysts for the first time. Firstly, the interesting multi-hierarchical architecture enables efficient light harvesting and abundant active sites. Secondly, the excellent photothermal effect of the composite makes its surface temperature reach up to 173 °C after 300 s exposure to simulated sunlight. Thirdly, the S-scheme heterojunction establishes a unique channel guaranteeing improved charge separation and transfer as well as boosted charge reactivity. Thanks to these synergistic effects, the developed CuS/SnIn4S8 heterostructure demonstrates superior solar-driven photocatalytic water splitting for hydrogen production, with an average hydrogen evolution rate of as high as 6235.72 μmol g−1 h−1, which is 20 times and 4 times higher than that of single-phase CuS and SnIn4S8, respectively. This work proposes a novel concept for the design of photothermal-assisted composite photocatalysts. |
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ISSN: | 1383-5866 1873-3794 |
DOI: | 10.1016/j.seppur.2024.127253 |