催化作用
纳米晶
金属
钯
一氧化碳
材料科学
分散性
铂金
镍
化学工程
过渡金属
无机化学
纳米技术
化学
冶金
有机化学
高分子化学
工程类
作者
Matteo Cargnello,Vicky Doan‐Nguyen,Thomas R. Gordon,Rosa E. Diaz,Eric A. Stach,Raymond J. Gorte,Paolo Fornasiero,Christopher B. Murray
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2013-07-19
卷期号:341 (6147): 771-773
被引量:1281
标识
DOI:10.1126/science.1240148
摘要
Interactions between ceria (CeO2) and supported metals greatly enhance rates for a number of important reactions. However, direct relationships between structure and function in these catalysts have been difficult to extract because the samples studied either were heterogeneous or were model systems dissimilar to working catalysts. We report rate measurements on samples in which the length of the ceria-metal interface was tailored by the use of monodisperse nickel, palladium, and platinum nanocrystals. We found that carbon monoxide oxidation in ceria-based catalysts is greatly enhanced at the ceria-metal interface sites for a range of group VIII metal catalysts, clarifying the pivotal role played by the support.
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