A facial strategy to synthesize Pd/Co3O4 nanosheets with enhanced performance for methane catalytic oxidation

被引:27
|
作者
Yang, Nating [1 ,2 ]
Ni, Shenglin [1 ]
Sun, Yuhan [1 ]
Zhu, Yan [1 ,3 ]
机构
[1] Chinese Acad Sci, Shanghai Adv Res Inst, CAS Key Lab Low Carbon Convers Sci & Engn, Shanghai 201210, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Nanjing Univ, Sch Chem & Chem Engneering, Nanjing 210093, Jiangsu, Peoples R China
来源
MOLECULAR CATALYSIS | 2018年 / 452卷
关键词
Thermal-stability; Palladium based catalyst; Metal-support interaction; Catalytic oxidation; LOW-TEMPERATURE; PD CATALYSTS; SURFACE-CHEMISTRY; COMBUSTION; CO3O4; WATER; PD/GAMMA-AL2O3; DEACTIVATION; SUPPORT; AL2O3;
D O I
10.1016/j.mcat.2018.03.016
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
Pd-based catalysts that prepared by traditional impregnation or co-precipitate method show remarkable activity for catalytic oxidation of hydrocarbon, unfortunately they tend to deactivate in the long-term reaction process or at high temperature by sintering and transformation of active species. We now report a facile strategy to synthesize Pd/Co3O4 with superior catalytic durability for the methane catalytic oxidation. In this method, Pd ions coordinate with -CoOCH2COOH that derived from Co precursor and form the Pd-Co precursor complex at first, this complex was further calcined into Pd/Co3O4 catalysts with strong interaction between Pd and cobalt oxide. Methane catalytic oxidation experiment demonstrated that such Pd-based catalyst possesses intrinsically enhanced catalytic activity and exhibits a high resistance toward deactivate in the harsh reaction condition, in sharp contrast to the conventional catalysts prepared via impregnation or deposition-precipitation routes. TEM, XPS, O-2-TPO, and isotopic experiments further indicate that the Pd/Co3O4 could form stronger interaction between PdO and Co3O4 and produce more actives species during long-term reaction.
引用
收藏
页码:28 / 35
页数:8
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