氧化铈
胶体金
催化作用
透射电子显微镜
纳米颗粒
材料科学
氧气
铈
氧化物
纳米技术
化学工程
活化能
化学
无机化学
物理化学
冶金
有机化学
工程类
生物化学
作者
Yasufumi Kuwauchi,Seiji Takeda,Hideto Yoshida,Keju Sun,Masatake Haruta,Hideo Kohno
出处
期刊:Nano Letters
[American Chemical Society]
日期:2013-06-20
卷期号:13 (7): 3073-3077
被引量:65
摘要
Aberration-corrected environmental transmission electron microscopy (ETEM) proved that catalytically active gold nanoparticles (AuNPs) move reversibly and stepwise by approximately 0.09 nm on a cerium oxide (CeO2) support surface at room temperature and in a reaction environment. The lateral displacements and rotations occur back and forth between equivalent sites, indicating that AuNPs are loosely bound to oxygen-terminated CeO2 and may migrate on the surface with low activation energy. The AuNPs are likely anchored to oxygen-deficient sites. Observations indicate that the most probable activation sites in gold nanoparticulate catalysts, which are the perimeter interfaces between an AuNP and a support, are not structurally rigid.
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