甲烷
烧结
氧化铈
催化作用
催化燃烧
化学工程
涂层
氧化物
铈
钯
燃烧
无机化学
材料科学
化学
纳米技术
冶金
有机化学
工程类
作者
Matteo Cargnello,Juan J. Delgado,Juan Carlos Hernández‐Garrido,Kevin Bakhmutsky,Tiziano Montini,José J. Calvino,Raymond J. Gorte,Paolo Fornasiero
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2012-08-09
卷期号:337 (6095): 713-717
被引量:906
标识
DOI:10.1126/science.1222887
摘要
There is a critical need for improved methane-oxidation catalysts to both reduce emissions of methane, a greenhouse gas, and improve the performance of gas turbines. However, materials that are currently available either have low activity below 400°C or are unstable at higher temperatures. Here, we describe a supramolecular approach in which single units composed of a palladium (Pd) core and a ceria (CeO(2)) shell are preorganized in solution and then homogeneously deposited onto a modified hydrophobic alumina. Electron microscopy and other structural methods revealed that the Pd cores remained isolated even after heating the catalyst to 850°C. Enhanced metal-support interactions led to exceptionally high methane oxidation, with complete conversion below 400°C and outstanding thermal stability under demanding conditions.
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