Monodisperse Ni-clusters anchored on carbon nitride for efficient photocatalytic hydrogen evolution

被引:0
作者
Jian, Liang [1 ]
Zhang, Huizhen [1 ]
Liu, Bing [1 ]
Pan, Chengsi [1 ]
Dong, Yuming [1 ]
Wang, Guangli [1 ]
Zhong, Jun [2 ]
Zheng, Yongjie [3 ]
Zhu, Yongfa [1 ,4 ]
机构
[1] International Joint Research Center for Photo-responsive Molecules and Materials, School of Chemical and Material Engineering, Jiangnan University, Jiangsu, Wuxi,214122, China
[2] Institute of Functional Nano and Soft Materials Laboratory (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University, Jiangsu, Suzhou,215123, China
[3] Qingdao Geological Exploration Institute of China Metallurgical Geology Bureau, Shandong, Qingdao,266109, China
[4] Department of Chemistry, Tsinghua University, Beijing,100084, China
来源
Chinese Journal of Catalysis | 2022年 / 43卷 / 02期
关键词
Carbon nitride;
D O I
暂无
中图分类号
学科分类号
摘要
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. © 2022 Dalian Institute of Chemical Physics, the Chinese Academy of Sciences
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页码:536 / 545
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