Precise fabrication of surface-reconstructed LaMnO3 perovskite with enhanced catalytic performance in CH4 oxidation

被引:46
作者
Chen, Huawei [1 ]
Li, Jinpeng [1 ]
Cui, Wei [1 ]
Fei, Zhaoyang [1 ]
Tian, Qingqing [1 ]
Liu, Qing [1 ]
Chen, Xian [1 ]
Cui, Mifen [1 ]
Zhang, Zhuxiu [1 ]
Tang, Jihai [1 ]
Qiao, Xu [1 ]
机构
[1] Nanjing Tech Univ, Coll Chem Engn, State Key Lab Mat Oriented Chem Engn, Nanjing 211816, Peoples R China
基金
中国国家自然科学基金;
关键词
Catalytic combustion; A-site dissolution; MnOx/LaMnO3; catalyst; Methane; METHANE COMBUSTION; VINYL-CHLORIDE; A-SITE; CO; OXIDE; NO; CE; TOLUENE; SUBSTITUTION; REDUCTION;
D O I
10.1016/j.apsusc.2019.144112
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
In this study, MnOx/LaMnO3 catalyst (LMO) was successfully synthesized through a selectively etched method, wherein MnOx was in-situ formed on the surface of LaMnO3. The modified LMO catalysts possessed the large specific surface area, high molar ratios of Mn4+ /(Mn-4 + Mn3+), and outstanding low-temperature reducibility. Moreover, the more efficient electron transfer from Mn3+/Mn4+ redox cycles and O-2 double left right arrow O-L due to the generation of oxygen defects contributed to the strong interaction between MnOx and LaMnO3. Among all LMO catalysts, the LMO-4 (etched 40 min) catalyst exhibited the excellent activity (T-90 at 448 degrees C), stability and optimum endurability in methane catalytic combustion (5 vol% water) during the steady state of 100 h, which could be greatly assigned to its larger specific surface area, superior low temperature reducibility, the highest molar ratio Mn4+ and better oxygen mobility. The lowest apparent activation energy (E-a) of LMO-4 catalyst (61.8 kJ/mol) was in good accordance with its optimum catalytic activity for methane combustion.
引用
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页数:9
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