Chain effect of Mn4+/ Mn3+ and OLattice on La1-xSrxMnO3 catalysts for lower thermally driven CO oxidation

被引:2
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.
引用
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页数:13
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