Surface Reconstruction-Induced Site-Specific Charge Separation and Photocatalytic Reaction on Anatase TiO2(001) Surface

被引:38
作者
Xiong, Feng [1 ,2 ]
Yin, Li-Li [3 ,4 ]
Wang, Zhengming [1 ,2 ]
Jin, Yuekang [1 ,2 ]
Sun, Guanghui [1 ,2 ]
Gong, Xue-Qing [3 ,4 ]
Huang, Weixin [1 ,2 ]
机构
[1] Univ Sci & Technol China, CAS Key Lab Mat Energy Convers, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Peoples R China
[2] Univ Sci & Technol China, Dept Chem Phys, Hefei 230026, Peoples R China
[3] East China Univ Sci & Technol, Ctr Computat Chem, Key Lab Adv Mat, Meilong Rd 130, Shanghai 200237, Peoples R China
[4] East China Univ Sci & Technol, Res Inst Ind Catalysis, Meilong Rd 130, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
TOTAL-ENERGY CALCULATIONS; METHANOL PHOTOCHEMISTRY; METHYL FORMATE; TIO2; TIO2(110); FORMALDEHYDE; CHEMISTRY; OXYGEN; WATER; MECHANISM;
D O I
10.1021/acs.jpcc.7b02154
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
Photocatalytic reaction of methanol on an anataseTiO(2)(001)-(1 x 4) reconstructed' surface, a prototype reaction for photocatalysis, was studied by means of X-ray photoelectron spectroscopy, thermal desorption spectrum, and densityfunctional theory calculations, Photocatalytic oxidation reaction, was observed toexclusively occur at the Ti-4C sites of the (1 x 4) added row but not at the Ti-5C sites-of the (1 x 1) basal surface, The accompanying density functional theory calculation results demonstrate that the valence band maximum is localized at the-oxygen atoms of the (1 x 4) added row and the methoxy species bonded to the Ti-4C sites, respectively, for the clean and methanol-covered, anatase TiO2(001)-(1 x 4) surfaces. This leads to-a Ti-4C site-specific oxidation of the methoxy species by photogenerated holes. These results reveal a concept of surface reconstruction-induced site-specific charge separation and photocatalytic reaction on oxide ph-otocatalysts that will greatly deepen the understanding of the vital role of oxide surface structure in photocatalytic reactions.
引用
收藏
页码:9991 / 9999
页数:9
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