Structural Evolution of Plasma-Sputtered Core-Shell Nanoparticles for Catalytic Combustion of Methane

被引:21
作者
Guo, Xiaoning [2 ,3 ]
Brault, Pascal [1 ]
Zhi, Guojuan [2 ,3 ]
Caillard, Amael [1 ]
Jin, Guoqiang [2 ]
Guo, Xiangyun [2 ]
机构
[1] Univ Orleans, CNRS, GREMI, UMR6606, F-45067 Orleans 2, France
[2] Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Peoples R China
[3] Chinese Acad Sci, Grad Univ, Beijing 100039, Peoples R China
关键词
PD-RH/CEO2-AL2O3 3-WAY CATALYST; MESOPOROUS SILICON-CARBIDE; LOW-TEMPERATURE; HYDROGEN-PEROXIDE; PD; OXIDATION; FE; DEPOSITION; SURFACE; CHEMISTRY;
D O I
10.1021/jp206606r
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
Fe@Pd, Fe@Pt, and Fe@Au core-shell nanoparticles supported by silicon carbide have been prepared by plasma sputtering deposition and employed as the catalyst for methane combustion. The core shell catalysts exhibit higher activities than single metallic catalysts due to surface alloying effects. With the surface alloying of the core shell nanopartides, Pd-O and Pt-O bonds become weak because the increase of the electron cloud density around Pd and Pt atoms due to the electron transfer from surface Fe to Pd or Pt atoms. Therefore, the activities of Fe@Pd/SiC and Fe@Pt/SiC increase with the reaction time. The activity of Fe@Au/SiC keeps invariant in the reaction because the Fe@Au core shell structure has high stability. Transmission electron microscopy and X-ray photoelectron spectroscopy results further confirm the structural evolution.
引用
收藏
页码:24164 / 24171
页数:8
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