Skin B/N-doped anatase TiO2 {001} nanoflakes for visible-light photocatalytic water oxidation

被引:7
|
作者
Deng, Guoqiang [1 ,2 ]
Kang, Xiangdong [1 ]
Yang, Yongqiang [1 ,2 ]
Wang, Lianzhou [3 ]
Liu, Gang [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, 72 Wenhua Rd, Shenyang 110016, Peoples R China
[2] Univ Sci & Technol China, Sch Mat Sci & Engn, 72 Wenhua Rd, Shenyang 110016, Peoples R China
[3] Univ Queensland, Nanomat Ctr, Sch Chem Engn & AIBN, Brisbane, Qld 4072, Australia
基金
中国国家自然科学基金;
关键词
Visible light absorption; Nanoflakes; Transport distance; Photocatalytic water oxidation; Red TiO2; TITANIUM-DIOXIDE; OXYGEN VACANCY; NO; MICROSPHERES; ABSORPTION; HYDROGEN;
D O I
10.1016/j.jcis.2023.06.046
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 limited visible-light-responsive photoactivities of most doped wide-bandgap photocatalysts with widened absorption range have long been the obstacles for the efficient conversion of solar energy to chemical energy by photocatalysis. The weak transport ability of visible-light-induced low-energy charge carriers, and numerous recombination centers arising from the energy-band modifiers along the transport path are two major factors responsible for such a mismatch. A potential solution is to shorten the transport path of photo-induced charges in well-modulated light absorbers with low-dimensional structure and the spatially concentrated dopants underneath their surfaces. As a proof of concept, skin B/N-doped red anatase TiO2 {001} nanoflakes with the absorption edge up to 675 nm were synthesized in this study. Experimental results revealed that boron dopants in the TiO2 nanoflakes from the hydrolysis of nanosized TiB2 played a crucial role in controlling nitrogen doping in the surface layer of the nanoflakes. As visible light excitation occurs at the surface layer, the photons can be sufficiently absorbed by the formed energy levels at the surface layers, and the photogenerated charge carriers can effectively migrate to the surface, thus leading to efficient visible-light-responsive photocatalytic oxygen evolution activity from water oxidation.
引用
收藏
页码:140 / 147
页数:8
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