光催化
空位缺陷
化学工程
材料科学
氢
纳米技术
曲面(拓扑)
催化作用
化学
工程类
结晶学
有机化学
几何学
数学
作者
Shuhua Lv,Hongmei Yuan,Miaomiao Xing,Kexin Li,Yen Leng Pak,Xing Gao,Deliang Zhang,Hongyu Mou,Jibin Song
标识
DOI:10.1016/j.cej.2024.152025
摘要
The cation exchange technology plays a significant role in designing high-performance photocatalysts at atomic scale. However, the chemical kinetic energy barrier greatly limits the application of cation exchange strategies. Herein, an effective surface vacancy engineering powered reverse cation exchange strategy was exploited to realize energy-unfavored cation exchange reactions. Cu vacancies are created on the surface of Cu2-xS nanoboxs (Cu2-xS NBs), which are subsequently occupied by Zn2+ ions. A hollow CuZnS nanoboxs (CuZnS NBs) were successfully prepared for photocatalytic hydrogen evolution. The prepared CuZnS NBs has abundant interfacial Zn-S bonds, which promote interfacial charge transfer (IFCT) as a rapidly electron bridge. In particular, the photocatalytic hydrogen evolution rate of CuZnS NBs under visible light is 2.06 mmol·g−1·h−1, which is 5.9 times higher than that of Cu2-xS. The synthetic mechanism and photocatalytic mechanism of the CuZnS was investigated from experiment and theoretical calculations. The surface vacancy powered reverse cation exchange strategy offers a new opportunity for the rational tailoring new-generation photocatalysts at the atomic scale.
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