共 42 条
Chain effect of Mn4+/ Mn3+ and OLattice on La1-xSrxMnO3 catalysts for lower thermally driven CO oxidation
被引:0
|作者:
Duan, Xu
[1
]
Yang, Jian
[1
]
Zhu, Jiaqing
[1
]
Li, Hongbin
[1
]
Li, Huan
[1
]
Liu, Runxue
[1
]
Fang, Yujie
[1
]
Liu, Qingcai
[1
]
Liu, Weizao
[1
]
Ding, Chunlian
[1
]
Li, Jiangling
[1
]
Ren, Shan
[2
]
机构:
[1] Chongqing Univ, Coll Mat Sci & Engn, Chongqing 400044, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Energy & Power Engn, State Key Lab Multiphase Flow Power Engn, Xian 710049, Peoples R China
来源:
JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING
|
2024年
/
12卷
/
06期
基金:
中国国家自然科学基金;
关键词:
CO oxidation;
Thermal catalysis;
Oxygen vacancy;
Mv-K mechanism;
Lattice oxygen;
La1-xSrxMnO3;
PEROVSKITE OXIDE CATALYSTS;
CARBON-MONOXIDE;
CALCINATION TEMPERATURE;
PERFORMANCE;
NO;
SR;
SUBSTITUTION;
COMBUSTION;
SURFACE;
LAMNO3;
D O I:
10.1016/j.jece.2024.114938
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
In this work, a series of La1-xSrxMnO3 catalysts for CO oxidation were successfully fabricated via a facile sol-gel method with multistage calcination. By modifying the Sr doping quantity at A-site, the surface Mn4+/ Mn3+ ratio was manipulated, and thus lattice oxygen and oxygen vacancy concentrations of were further regulated by the system electron migration. This domino effect produced a radically different catalytic response, of which the optimal La0.4Sr0.6MnO3 samples performed the most excellent CO oxidation at lower temperature window. In-situ DRFITS spectra revealed catalytic intermediates and demonstrated the concurrence of dominant Mv-K mechanism and secondary E-R reaction pathway in CO oxidation over La0.4Sr0.6MnO3 under three types of thermodynamic states. The study is poised to enhance the propagation and practical employment of Sr-doped LaMnO3 perovskite catalysts, while supplying theoretical perspectives for the investigation towards underlying CO reaction mechanisms.
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