Boron-doped nitrogen-deficient carbon nitride-based Z-scheme heterostructures for photocatalytic overall water splitting

Photocatalytic overall water splitting can be achieved using Z-scheme systems that mimic natural photosynthesis by combining dissimilar semiconductors in series. However, coupling well-suited H 2 - and O 2 -evolving components remains challenging. Here, we fabricate a Z-scheme system for photocataly...

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Veröffentlicht in:Nature energy 2021-04, Vol.6 (4), p.388-397
Hauptverfasser: Zhao, Daming, Wang, Yiqing, Dong, Chung-Li, Huang, Yu-Cheng, Chen, Jie, Xue, Fei, Shen, Shaohua, Guo, Liejin
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Sprache:eng
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Zusammenfassung:Photocatalytic overall water splitting can be achieved using Z-scheme systems that mimic natural photosynthesis by combining dissimilar semiconductors in series. However, coupling well-suited H 2 - and O 2 -evolving components remains challenging. Here, we fabricate a Z-scheme system for photocatalytic overall water splitting based on boron-doped, nitrogen-deficient carbon nitride two-dimensional (2D) nanosheets. We prepare ultrathin carbon nitride nanosheets with varying levels of boron dopants and nitrogen defects, which leads to nanosheets that can act as either H 2 - or O 2 -evolving photocatalysts. Using an electrostatic self-assembly strategy, the nanosheets are coupled to obtain a 2D/2D polymeric heterostructure. Owing to their ultrathin nanostructures, strong interfacial interaction and staggered band alignment, a Z-scheme route for efficient charge-carrier separation and transfer is realized. The obtained heterostructure achieves stoichiometric H 2 and O 2 evolution in the presence of Pt and Co(OH) 2 co-catalysts, and the solar-to-hydrogen efficiency reaches 1.16% under one-sun illumination. Splitting water using suspensions of particulate carbon nitride-based photocatalysts may be a cheap way to produce hydrogen, but efficiencies have remained low. Now, Shen and colleagues use doped carbon nitride-based Z-scheme heterostructures to split water with a solar-to-hydrogen efficiency of 1.1% in the presence of metal-based co-catalysts.
ISSN:2058-7546
2058-7546
DOI:10.1038/s41560-021-00795-9