钴
催化作用
X射线光电子能谱
氧气
吸附
氧化态
金属
过渡金属
无机化学
钙钛矿(结构)
化学状态
材料科学
化学
化学工程
物理化学
结晶学
冶金
有机化学
工程类
作者
Elizaveta M. Borodina,Liliya V. Yafarova,T. A. Kryuchkova,T. F. Sheshko,А. Г. Чередниченко,Irina A. Zvereva
出处
期刊:Catalysts
[MDPI AG]
日期:2022-12-22
卷期号:13 (1): 8-8
被引量:4
标识
DOI:10.3390/catal13010008
摘要
The effect of the substitution of cobalt into the GdFeO3 perovskite structure on the selective hydrogenation of CO was investigated. A series of GdCoxFe1−xO3 (x = 0; 0.2; 0.5; 0.8; 1) samples were synthesized by sol-gel technology and characterized by XRD, BET specific area, DSC, TG, EDX and XPS. The experimental data made it possible to reveal a correlation between the state of iron and cobalt atoms, the fractions of surface and lattice oxygen, and catalytic characteristics. It has been found that varying the composition of GdCoxFe1−xO3 complex oxides leads to a change in the oxygen-metal binding energy in Gd-O-Me, the ratio of metals in various oxidation states, and the amount of surface and lattice oxygen, which affects the adsorption and catalytic characteristics of complex oxides.
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