Single Ti3+ Ion Catalyzes NO Reduction on Stoichiometric Titanium Oxide Cluster Anions (TiO2)n- (n=1-11)

被引:15
作者
Chen, Jiao-Jiao [1 ,2 ,3 ]
Liu, Yun-Zhu [1 ,2 ,3 ,4 ]
Liu, Qing-Yu [1 ,2 ,3 ]
Li, Xiao-Na [1 ,2 ,3 ]
He, Sheng-Gui [1 ,2 ,3 ,4 ]
机构
[1] Chinese Acad Sci, Inst Chem, State Key Lab Struct Chem Unstable & Stable Specie, Beijing 100190, Peoples R China
[2] Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
[3] Chinese Acad Sci, Res Educ Ctr Excellence Mol Sci, Beijing 100190, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
single Ti3+ ion; stoichiometric titanium oxide clusters (TiO2)(n)(-); catalytic NO reduction by CO; mass spectrometry; quantum chemical calculations; RUTILE TIO2(110); BAND-GAP; OXIDATION; NANOPARTICLES; TIO2; PHOTOCATALYSIS; ISOPRENE; SURFACES; SITES;
D O I
10.1021/acscatal.2c02006
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
Titanium dioxide (TiO2) is an important oxide material owing to its extraordinary catalytic reactivity in a wide range of applications. Different species on the surface of TiO2 have been proposed to contribute to its reactivity, while the intriguing catalytic role of a Ti3+ ion has not been substantiated to date. Herein, benefiting from state-of-the-art mass spectrometry and quantum chemical calculations, we demonstrated that an exposed single Ti3+ ion on stoichiometric titanium oxide clusters (TiO2)(n)(-) (n = 1-11) works independently to catalyze NO reduction by CO. The single-electron mechanism to reduce NO into N2O was discovered, and an atomic oxygen radical (O & BULL;-) on products (TiO2)(n)O- that is highly reactive (e.g., in CO oxidation) was created. This finding is pivotal for providing a fundamental strategy to utilize an isolated Ti3+ ion on the surface of TiO2 and points out that this catalytic behavior can be a potential pathway in the atmosphere for pollutant removal.
引用
收藏
页码:8768 / 8775
页数:8
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