FeO6 Octahedral Distortion Activates Lattice Oxygen in Perovskite Ferrite for Methane Partial Oxidation Coupled with CO2 Splitting

被引:295
作者
Zhang, Xianhua [1 ]
Pei, Chunlei [1 ]
Chang, Xin [1 ]
Chen, Sai [1 ]
Liu, Rui [1 ]
Zhao, Zhi-Jian [1 ]
Mu, Rentao [1 ]
Gong, Jinlong [1 ,2 ]
机构
[1] Tianjin Univ, Collaborat Innovat Ctr Chem Sci & Engn, Sch Chem Engn & Technol, Key Lab Green Chem Technol,Minist Educ, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Joint Sch Natl Univ Singapore & Tianjin Univ, Int Campus, Fuzhou 350207, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
FINDING SADDLE-POINTS; H BOND ACTIVATION; REDOX CATALYSTS; OXIDES; COMBUSTION; PERFORMANCE; REACTIVITY; EVOLUTION; ENERGY; LA;
D O I
10.1021/jacs.0c04643
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Modulating lattice oxygen in metal oxides that conducts partial oxidation of methane in balancing C-H activation and syngas selectivity remains challenging. This paper describes the discovery of distorting FeO6 octahedra in La1-xCexFeO3 (x = 0, 0.25 0.5, 0.75, 1) orthorhombic perovskites for the promotion of lattice oxygen activation. By combined electrical conductivity relaxation measurements and density functional theory calculations studies, this paper describes the enhancement of FeO6 octahedral distortion in La1-xCexFeO3 promoting their bulk oxygen mobility and surface oxygen exchange capability. Consequently, LaosCeasFeO(3) with the highest FeO6 distortion achieves exceptional syngas productivity of similar to 3 and 8 times higher than LaFeO(3)( )and CeFeO3, respectively, in CH4 partial oxidation step with simultaneous high CO2 conversion (92%) in the CO2-splitting step at 850 degrees C. The results exemplify the feasibility to tailor the active lattice oxygen of perovskite by modulating the distortion of BO6 in ABO(3), which ultimately influences their reaction performance in chemical looping processes.
引用
收藏
页码:11540 / 11549
页数:10
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