BiVO4 {010} and {110} Relative Exposure Extent: Governing Factor of Surface Charge Population and Photocatalytic Activity

被引:260
作者
Tan, Hui Ling [1 ]
Wen, Xiaoming [2 ]
Amal, Rose [1 ]
Ng, Yun Hau [1 ]
机构
[1] Univ New S Wales, Sch Chem Engn, Particles & Catalysis Res Grp, Sydney, NSW 2052, Australia
[2] Univ New S Wales, Sch Photovolta & Renewable Energy Engn, Australian Ctr Adv Photovolta, Sydney, NSW 2052, Australia
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2016年 / 7卷 / 07期
基金
澳大利亚研究理事会;
关键词
ULTRAFAST CARRIER DYNAMICS; FERMI-LEVEL EQUILIBRATION; VISIBLE-LIGHT; TIO2; NANOPARTICLES; REACTIVITY; PARTICLES; MECHANISM; WATER; SIZE; PHOTOOXIDATION;
D O I
10.1021/acs.jpclett.6b00428
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
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.
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页码:1400 / 1405
页数:6
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