A 20-core copper(I) nanocluster as electron-hole recombination inhibitor on TiO2 nanosheets for enhancing photocatalytic H2 evolution.
A 20-core copper(I) nanocluster as electron-hole recombination inhibitor on TiO2 nanosheets for enhancing photocatalytic H2 evolution.
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DOI:
10.1039/d1nr04683g
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发表时间:
2021-09
期刊:
影响因子:
6.7
通讯作者:
Yundong Cao;Hui-Ping Hao;Huaqiang Liu;Di Yin;Mingliang Wang;Guang-gang Gao;Lin-lin Fan;Hong Li
中科院分区:
文献类型:
--
作者:
Yundong Cao;Hui-Ping Hao;Huaqiang Liu;Di Yin;Mingliang Wang;Guang-gang Gao;Lin-lin Fan;Hong Li
For the design of atom-precise copper nanoclusters, besides the exploration of their aesthetic cage-like architectures, their structural modulation and potential applications are being extensively explored. Herein, an atom-precise 20-core copper(I)-alkynyl nanocluster (UJN-Cu20) protected by ethinyloestradiol ligands issynthesized. By virtue of outer-shell hydroxyl groups, UJN-Cu20 could be uniformly modified on the surface of TiO2 nanosheets via hydrogen bonding interactions, thus forming an efficient nanocomposite photocatalyst for hydrogen evolution. By constructing a Z-scheme heterojunction, the photocatalytic hydrogen evolution activity of the nanocomposite (13 mmol g-1 h-1) significantly improved as compared to that of TiO2 nanosheets (0.4 mmol g-1 h-1). As a narrow bandgap cocatalyst, UJN-Cu20 is confirmed to effectively inhibit the electron-hole recombination on the surface of the TiO2 nanosheet, which provides a new concept for the design of copper cluster-assisted effective photocatalysts.