Dynamic structure of highly disordered manganese oxide catalysts for low-temperature CO oxidation

被引:43
|
作者
Tian, Fei-Xiang [1 ]
Zhu, Minghui [1 ]
Liu, Xianglin [1 ]
Tu, Weifeng [2 ]
Han, Yi-Fan [1 ,2 ]
机构
[1] East China Univ Sci & Technol, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
[2] Zhengzhou Univ, Minist Educ, Engn Res Ctr Adv Funct Mat Mfg, Zhengzhou 450001, Peoples R China
关键词
Low-temperature CO oxidation; Disordered manganese oxide; Oxygen vacancies; Mechanism; Kinetics; CARBON-MONOXIDE OXIDATION; BIRNESSITE-TYPE MNO2; NANOSTRUCTURED MNCEOX CATALYSTS; HIGH-EFFICIENCY; METAL-OXIDES; OXYGEN; FORMALDEHYDE; MECHANISM; REDUCTION; NANOPARTICLES;
D O I
10.1016/j.jcat.2021.07.016
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 dynamic structures of a highly disordered manganese oxide catalyst (HDMO) and intermediates were thoroughly studied from precursor to working catalyst. Excellent CO oxidation activity at low temperatures (T-50 = 83 degrees C) was performed over a HDMO in the presence of H2O and CO2 . The specific reaction rate of 4.56 mu mol(CO).g(cat)(1).s(-1) at 90 degrees C was approximately 25 times and 15 times higher than those of bixbyitetype alpha-Mn2O3 and cryptomelane-type alpha-MnO2, respectively. With X-ray photon electron spectroscopy (XPS), we reveal that more surface oxygen vacancies (O-v) and adsorbed oxygen species from the highly disordered structure could promote the redox property and oxygen release capability. In situ Raman and DRIFTS spectroscopy were used to identify a dynamic surface phase transformation during CO adsorption and oxidation. In combination with kinetic studies of CO oxidation, we conclude that there are two mixed mechanisms for CO oxidation over HDMO: the Langmuir-Hinshelwood (L-H) mechanism and the Mars-van Krevelen (MvK) mechanism. (C) 2021 Elsevier Inc. All rights reserved.
引用
收藏
页码:115 / 128
页数:14
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