摘要
Developing and employing photocatalysts with extended visible-light-absorption has emerged as a fundamental issue for the enhanced capability of photocatalytic H2 evolution from water splitting. Herein, a wide-spectrum light-responsive phenyl-grafted carbon nitride photocatalyst was synthesized. It was found that benzonquanmine-derived g-C3N4 (BCN) exhibits significantly extended light absorption (∼670 nm) compared with conventional melamine-derived g-C3N4 (MCN). Correspondingly, the photocatalytic H2-evolution rate of BCN (2846 μmol h−1 g−1) is five times as that of MCN under visible-light irradiation. Particularly, an impressive H2-evolution rate of 58 μmol h−1 g−1 could be achieved on BCN even under light irradiation beyond 620 nm. The outstanding photocatalytic H2-evolution performance could be not only attributed to the enriched photons generated from the enhanced solar energy harvesting, but also to the distinctly inhibited rapid recombination of photogenerated electron-hole pairs resulting from the incorporation of phenyl groups. This work furnishes a new train of thought for the designing of carbon-nitride-based photocatalysts with enhanced capability of visible-light-utilization.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 494-502 |
| 页数 | 9 |
| 期刊 | Journal of Colloid and Interface Science |
| 卷 | 622 |
| DOI | |
| 出版状态 | 已出版 - 15 9月 2022 |
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