双功能
光催化
掺杂剂
兴奋剂
分解
电子转移
材料科学
肖特基势垒
费米能级
化学工程
光化学
纳米技术
电子
催化作用
光电子学
化学
有机化学
工程类
物理
生物化学
二极管
量子力学
作者
Li Yang,Zhiqiang Liu,Wenjing Qi,Haiyang Shi,Kaiyan Wang,Xuefei Wang,Ping Wang,Feng Chen,Huogen Yu
标识
DOI:10.1016/j.apsusc.2024.159664
摘要
Au/BiVO4 is considered as one of promising composite photocatalytic materials for H2O2 synthesis due to its suitable band structure and exceptional two-electron O2 reduction selectivity. However, the rapid decomposition of H2O2 caused by holes and the slow charge transfer resulting from high Schottky barrier between BiVO4 and Au limit its highly-efficient H2O2 production. In this work, a doping strategy is proposed to solve the above two limitations. Here, as the dopant, Gd is uniformly distributed in BiVO4 crystal, while Au is selectively modified on the electron-rich (010) facets of BiVO4. Consequently, 0.1wt% Gd-doped Au/BiVO4 photocatalyst is proved to present highest H2O2-production performance with 2.07 mmol L−1 (AQE = 7.44 %) within 2 h, which is 1.39 times higher than that of Au/BiVO4. The improvement of photocatalytic activity for Au/BiVO4:Gd photocatalyst is mainly attributed to substitution of Gd at Bi-site, which inhibits the decomposition of H2O2, and lowers the Fermi energy level of BiVO4 to match with that of Au, giving rise to fast charge transfer and enhanced two-electron reduction activity of O2. This work provides a new perspective for improving the performance of photocatalyst materials modified by metal cocatalyst.
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