Monodisperse Ni-clusters anchored on carbon nitride for efficient photocatalytic hydrogen evolution
The active sites of monodisperse transition metal Ni-clusters were anchored on carbon nitride (CN) by an in situ photoreduction deposition method to promote the efficient separation of photogenerated charges and achieve high-efficiency photocatalytic activity for hydrogen evolution. The Ni-cluster/C...
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Published in | Chinese journal of catalysis Vol. 43; no. 2; pp. 536 - 545 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.02.2022
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Subjects | |
Online Access | Get full text |
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Summary: | The active sites of monodisperse transition metal Ni-clusters were anchored on carbon nitride (CN) by an in situ photoreduction deposition method to promote the efficient separation of photogenerated charges and achieve high-efficiency photocatalytic activity for hydrogen evolution. The Ni-cluster/CN exhibited a photocatalytic hydrogen production rate of 16.5 mmol·h–1·g–1 and a total turnover frequency (TOF (H2)) value of 461.14 h–1. X-ray absorption spectroscopy based on synchrotron radiation indicated that CN had two reaction centers to form stable interface interactions with monodispersed Ni-clusters, in which carbon can act as an electron acceptor, while nitrogen can act as an electron donor. Meanwhile, the hybrid electronic structure of the Ni-cluster/CN system was constructed, which was favorable for photocatalytic activity for hydrogen production. An in-depth understanding of the interfacial interaction between CN and Ni-clusters will have important reference significance on the mechanistic study of development based on the cocatalyst.
Monodisperse Ni-clusters were anchored on the CN surface for efficient photocatalytic hydrogen evolution. It has been proven that there is a stable interface interaction between monodisperse Ni-clusters and CN to construct the hybrid electronic structure of the Ni-cluster/CN system. |
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ISSN: | 1872-2067 1872-2067 |
DOI: | 10.1016/S1872-2067(21)63865-2 |