钒酸铋
单斜晶系
电子
光催化
表面状态
光致发光
人口
电子转移
化学
Crystal(编程语言)
材料科学
电荷(物理)
光化学
化学物理
结晶学
晶体结构
曲面(拓扑)
光电子学
物理
催化作用
几何学
社会学
计算机科学
人口学
量子力学
程序设计语言
数学
生物化学
作者
Hui Ling Tan,Xiaoming Wen,Rose Amal,Yun Hau Ng
标识
DOI:10.1021/acs.jpclett.6b00428
摘要
The {010} and {110} crystal facets of monoclinic bismuth vanadate (m-BiVO4) has been demonstrated to be the active reduction and oxidation sites, respectively. Here, we show using dual-faceted m-BiVO4 with distinctly different dominant exposed facets, one which is {010}-dominant and the other {110}-dominant, contrary to prediction, the former m-BiVO4 exhibits superior photooxidation activities. The population of photogenerated electrons and holes on the surface are revealed to be proportional to the respective surface areas of {010} and {110} exposed on m-BiVO4, as evidenced by steady-state photoluminescence (PL) measurements in the presence of charge scavengers. The better photoactivity of {010}-dominant m-BiVO4 is attributed to prompt electron transfer facilitated by the presence of more photogenerated electrons on the larger {010} surface. Additionally, the greater extent of electron trapping in {110}-dominant m-BiVO4 also deteriorates its photoactivity by inducing electron-hole pair recombination.
科研通智能强力驱动
Strongly Powered by AbleSci AI