Photoelectron Spectroscopic Study of Methanol Adsorbed Rutile TiO2(110) Surface

被引:3
作者
Hao, Qun-qing [1 ]
Wang, Zhi-qiang [1 ,2 ]
Dai, Dong-xu [1 ]
Zhou, Chuan-yao [1 ]
Yang, Xue-ming [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Mol React Dynam, Dalian 116023, Peoples R China
[2] Xidian Univ, Sch Phys & Optoelect Engn, Xian 710071, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Methanol; TiO2; Ultraviolet photoelectron spectroscopy; Level alignment; COUPLED ELECTRON-TRANSFER; LEVEL ALIGNMENT; TIO2; PHOTOCATALYSIS; BAND-GAP; PHOTOEMISSION; WATER; DISSOCIATION; PRINCIPLES; INTERFACES; SCIENCE;
D O I
10.1063/1674-0068/30/cjcp1711219
中图分类号
O64 [物理化学(理论化学)、化学物理学]; O56 [分子物理学、原子物理学];
学科分类号
070203 ; 070304 ; 081704 ; 1406 ;
摘要
Methanol/TiO2 (110) is a model system in the surface science study of photocatalysis where methanol is taken as a hole capture. However, the highest occupied molecular orbital of adsorbed methanol lies below the valence band maximum of TiO2, preventing the hole transfer. To study the level alignment of this system, electronic structure of methanol covered TiO2(110) surface has been measured by ultraviolet photoelectron spectroscopy and the molecular orbitals of adsorbed methanol have been clearly identified. The results indicate the weak interaction between methanol and TiO2 substrate. The static electronic structure also suggests the mismatch of the energy levels. These static experiments have been performed without band gap excitation which is the prerequisite of a photocatalytic process. Future study of the transient electronic structure using time-resolved UPS has also been discussed.
引用
收藏
页码:626 / 630
页数:5
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