光催化
解吸
分子
电子转移
吸附
电子
基质(水族馆)
氢原子
氢键
材料科学
半导体
氢
化学
金属
光化学
催化作用
物理化学
光电子学
物理
有机化学
地质学
海洋学
量子力学
烷基
作者
Qingjie Luan,Xiangdong Xue,Hongtai Feng,Tao Lü,Dongxue Zhou,Tengfei Chen,Mengxi Tan,Wenjun Dong
标识
DOI:10.1016/j.apcatb.2023.122932
摘要
Molecular-type cocatalysts can achieve the maximum electron transfer and minimum light absorption loss by virtue of their size advantage. Herein, a novel hydrophilic molecule-semiconductor hybrid P4@Vs-ZnIn2S4-x photocatalyst was successfully developed by in-situ P4 molecular anchoring on S defect ZnIn2S4-x (VS-ZnIn2S4-x). The electron-rich P4 molecules are anchored on the Zn-S4 surface through S vacancies, forming Zn-P and S-P bonds that can promote electron injection from the electron-rich P4 molecular to Vs-ZnIn2S4-x substrate and reduce the adsorption/desorption barrier of H intermediate on S atom of Zn-S4 plane. Meanwhile, the electrostatic potential depression around P4 promoted the directional migration of in-plane photogenerated electrons, and pooled electrons to the highly active P sites and S sites, thereby accelerating the kinetics of hydrogen evolution. As a result, P4@Vs-ZnIn2S4-x achieves an optimal photocatalytic hydrogen evolution activity of 26.1 mmol g-1 h-1 under visible light, which is 6.2 times higher than 4.2 mmol g-1 h-1 for Vs-ZnIn2S4-x.
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