A Surface Defect-Promoted Ni Nanocatalyst with Simultaneously Enhanced Activity and Stability

被引:189
作者
He, Shan [1 ]
Li, Changming [1 ]
Chen, Hao [1 ]
Su, Dangsheng [2 ]
Zhang, Bingsen [2 ]
Cao, Xingzhong [3 ]
Wang, Baoyi [3 ]
Wei, Min [1 ]
Evans, David G. [1 ]
Duan, Xue [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[2] Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Peoples R China
[3] Chinese Acad Sci, Inst High Energy Phys, Beijing 100049, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Ni nanocatalyst; surface defect; low-temperature activation; CO2; methanation; layered double hydroxides; LAYERED DOUBLE HYDROXIDES; HIGH-TEMPERATURE; CARBON-DIOXIDE; VACANCY CLUSTERS; NANOPARTICLES; METHANATION; CATALYST; SHELL; HYDROGENATION; NANOCRYSTALS;
D O I
10.1021/cm303517z
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
How to achieve supported metal nanocatalysts with simultaneously enhanced activity and stability is of vital importance in heterogeneous catalysis and remains a challenging goal. In this work, a surface defect-promoted Ni nanocatalyst with a high dispersion and high particle density embedded on a hierarchical Al2O3 matrix was fabricated via a facile method involving an in situ reduction process, which exhibits excellent activity and stability simultaneously for the reaction of CO2 methanation. HRTEM, HAADF-STEM, EXAFS, and positron annihilation spectroscopy demonstrate the existence of abundant surface vacancy clusters that serve as active sites, accounting for the significantly enhanced low the temperature activity of the supported Ni nanoparticles. In addition, the anchoring effect from support gives rise to a high reaction stability, without sintering and/or aggregation of active species during long-term use.
引用
收藏
页码:1040 / 1046
页数:7
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