催化作用
钯
纳米晶
氧化铈
铈
反应性(心理学)
一氧化碳
纳米
材料科学
过渡金属
氧气储存
氧化还原
化学工程
无机化学
金属
化学
纳米技术
有机化学
冶金
替代医学
复合材料
病理
工程类
医学
作者
Valery Muravev,Alexander Parastaev,Yannis van den Bosch,Bianca Ligt,Nathalie Claes,Sara Bals,Nikolay Kosinov,Emiel J. M. Hensen
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2023-06-15
卷期号:380 (6650): 1174-1179
被引量:100
标识
DOI:10.1126/science.adf9082
摘要
The catalytic performance of heterogeneous catalysts can be tuned by modulation of the size and structure of supported transition metals, which are typically regarded as the active sites. In single-atom metal catalysts, the support itself can strongly affect the catalytic properties. Here, we demonstrate that the size of cerium dioxide (CeO2) support governs the reactivity of atomically dispersed palladium (Pd) in carbon monoxide (CO) oxidation. Catalysts with small CeO2 nanocrystals (~4 nanometers) exhibit unusually high activity in a CO-rich reaction feed, whereas catalysts with medium-size CeO2 (~8 nanometers) are preferred for lean conditions. Detailed spectroscopic investigations reveal support size-dependent redox properties of the Pd-CeO2 interface.
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