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Anchored Cu single atoms on porous g-C(3)N(4) for superior photocatalytic H(2) evolution from water splitting
One of the most promising strategies for producing hydrogen is photocatalytic water splitting, in which the photocatalyst is a key component. Among many semiconductor photocatalysts, g-C(3)N(4) has attracted great attention due to its narrow band gap, excellent stability and low cost. However, pract...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10020988/ https://www.ncbi.nlm.nih.gov/pubmed/36936854 http://dx.doi.org/10.1039/d3ra00775h |
Sumario: | One of the most promising strategies for producing hydrogen is photocatalytic water splitting, in which the photocatalyst is a key component. Among many semiconductor photocatalysts, g-C(3)N(4) has attracted great attention due to its narrow band gap, excellent stability and low cost. However, practical application is limited by its poor intrinsic activity. In this work, a high-performance porous g-C(3)N(4) (PCN) photocatalyst with anchored Cu single atoms (CuSAs) was synthesized by a one-step co-heating approach. The obtained Cu1.5–PCN displays an excellent hydrogen evolution rate (HER) of 2142.4 μmol h(−1) g(−1) under visible light (=420 nm), which is around 15 and 109 times higher than those of PCN and bulk g-C(3)N(4), respectively. In addition, it also shows good stability during H(2) evolution. The results of experimental research and DFT simulations indicate that the single Cu ions formed bonds with the N-ring and these remain stable. Meanwhile, the special electronic structure of the Cu–N charge bridge extends the light absorption band to the visible-light region (380–700 nm). This high-performance and low-cost photocatalyst has great potential in solar energy conversion. |
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