氧烷
扩展X射线吸收精细结构
X射线吸收光谱法
催化作用
铜
离子键合
分解
无机化学
氧化物
化学
氧化态
材料科学
分析化学(期刊)
吸收光谱法
离子
谱线
生物化学
物理
有机化学
色谱法
量子力学
天文
作者
Maxim Zabilskiy,Iztok Arčon,Petar Djinović,Elena Tchernychova,Albin Pintar
出处
期刊:Chemcatchem
[Wiley]
日期:2021-01-15
卷期号:13 (7): 1814-1823
被引量:18
标识
DOI:10.1002/cctc.202001829
摘要
Abstract We performed in‐situ XAS study of N 2 O decomposition over CuO/CeO 2 catalysts. The Cu K‐edge and Ce L 3 ‐edge XANES and EXAFS analyses revealed the dynamic and crucial role of Cu 2+ /Cu + and Ce 4+ /Ce 3+ ionic pairs during the catalytic reaction. We observed the initial formation of reduced Cu + and Ce 3+ species during activation in helium atmosphere at 400 °C, while concentration of these species decreased significantly during steady‐state nitrous oxide degradation reaction (2500 ppm N 2 O in He at 400 °C). In‐situ EXAFS analysis further revealed a crucial role of copper−ceria interface in this catalytic reaction. We observed dynamic changes in average number of Cu−Ce scatters under reaction conditions, indicating an enlarging of the interface between both copper and ceria phases, where electron and oxygen transfer occurs.
科研通智能强力驱动
Strongly Powered by AbleSci AI