催化作用
X射线光电子能谱
氧化钴
钴
氧化物
过渡金属
相(物质)
化学
大气温度范围
相变
无机化学
材料科学
物理化学
化学工程
有机化学
热力学
物理
工程类
作者
Yu Tang,Lingjuan Ma,Henri Dou,Christopher M. Andolina,Yuting Li,Hongbin Ma,Stephen D. House,Xiaoyan Zhang,Judith C. Yang,Franklin Tao
摘要
In situ/operando studies of a heterogeneous catalyst are particularly valuable for achieving a fundamental understanding of catalytic mechanisms at a molecular level by establishing a correlation between the observed catalytic performance and the corresponding surface chemistry during catalysis. Herein, CO oxidation on cobalt oxides was studied via ambient pressure X-ray photoelectron spectroscopy (AP-XPS). During CO oxidation on CoO in the temperature range of 140-180 °C, the active surface phase of CoO progressively transforms to Co3O4. Kinetic studies of CO oxidation on the surface phase CoO at 80-120 °C and on the formed Co3O4 at 160-220 °C show that CoO and Co3O4 exhibit different activation barriers: 49.3 kJ mol-1 for CoO and 36.9 kJ mol-1 for Co3O4. This study demonstrates the transition of the active surface phase of a transition metal oxide-based catalyst under catalytic conditions with no change in the bulk phase of the catalyst.
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