Band gap engineering in huge-gap semiconductor SrZrO3 for visible-light photocatalysis

被引:78
作者
Guo, Zhonglu [1 ,2 ]
Sa, Baisheng [1 ,3 ]
Pathak, Biswarup [4 ]
Zhou, Jian [1 ,2 ]
Ahuja, Rajeev [5 ,6 ]
Sun, Zhimei [1 ,2 ,3 ]
机构
[1] Xiamen Univ, Coll Mat, Dept Mat Sci & Engn, Xiamen 361005, Peoples R China
[2] Beihang Univ, Sch Mat Sci & Engn, Beijing 100191, Peoples R China
[3] Xiamen Univ, Collaborat Innovat Ctr Chem Energy Mat, Xiamen 361005, Peoples R China
[4] Indian Inst Technol Indore, Sch Basic Sci, Discipline Chem, Indore 452017, India
[5] Uppsala Univ, Dept Phys & Astron, Condensed Matter Theory Grp, S-75120 Uppsala, Sweden
[6] Royal Inst Technol, Dept Mat & Engn, S-10044 Stockholm, Sweden
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
Ab initio calculation; Visible-light photocatalysis; Huge band gap; Water splitting; WATER; HYDROGEN; SRTIO3; 1ST-PRINCIPLES; PHOTOLYSIS; SR2TA2O7; OXIDE; HOLE; WO3; SR;
D O I
10.1016/j.ijhydene.2013.11.055
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
Using SrZrO3 (SZO, the intrinsic band gap being 5.6 eV) as an example, we have investigated the design principles for huge-gap semiconductors with band gap larger than 5 eV for the application of efficient visible-light driven photocatalysts for splitting water into hydrogen. Based on the hybrid density function calculations, the electronic structures of mono-doped and co-doped SZO are investigated to obtain design principles for improving their photocatalytic activity in hydrogen generation. The cationic-anionic co-doping in SZO could reduce the band gap significantly and its electronic band position is excellent for the visible-light photocatalysis. This work reports a new type of candidate material for visible-light driven photocatalysis, i.e., huge-gap semiconductors with band gap larger than 5 eV. Furthermore, based on the present results we have proposed the design principles for band gap engineering that provides general guideline for other huge-gap semiconductors. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:2042 / 2048
页数:7
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