Oxidation behavior of cobalt nanoparticles studied by in situ environmental transmission electron microscopy

被引:15
作者
Zhang, Dejiong [1 ]
Jin, Chuanhong [1 ]
Li, Z. Y. [2 ]
Zhang, Ze [1 ]
Li, Jixue [1 ]
机构
[1] Zhejiang Univ, Sch Mat Sci & Engn, State Key Lab Silicon Mat, Hangzhou 310027, Zhejiang, Peoples R China
[2] Univ Birmingham, Sch Phys & Astron, Nanoscale Phys Res Lab, Birmingham B15 2TT, W Midlands, England
基金
中国国家自然科学基金;
关键词
Cobalt; Nanoparticle; Oxidation dynamics; Parabolic rate; Environmental transmission electron microscopy (ETEM); Electron irradiation; OXYGEN; TEM; NANOCRYSTALS; TEMPERATURE; REDUCTION; SURFACE; CO3O4;
D O I
10.1016/j.scib.2017.05.003
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The dynamics of oxidation of cobalt nanoparticles were directly revealed by in situ environmental transmission electron microscopy. Firstly, cobalt nanoparticles were oxidized to polycrystalline cobalt monoxide, then to polycrystalline tricobalt tetroxide, in the presence of oxygen with a low partial pressure. Numerous cavities (or voids) were formed during the oxidation, owing to the Kirkendall effect. Analysis of the oxides growth suggested that the oxidation of cobalt nanoparticles followed a parabolic rate law, which was consistent with diffusion-limited kinetics. In situ transmission electron microscopy allowed potential atomic oxidation pathways to be considered. The outward diffusion of cobalt atoms inside the oxide layer controlled the oxidation, and formed the hollow structure. Irradiation by the electron beam, which destroyed the sealing effect of graphite layer coated on the cobalt surface and resulted in fast oxidation rate, played an important role in activating and promoting the oxidations. These findings further our understanding on the microscopic kinetics of metal nanocrystal oxidation and knowledge of energetic electrons promoting oxidation reaction. (C) 2017 Science China Press. Published by Elsevier B.V. and Science China Press. All rights reserved.
引用
收藏
页码:775 / 778
页数:4
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