催化作用
沸石
烧结
材料科学
纳米颗粒
化学工程
钯
铑
焦炭
金属
贵金属
铂金
无机化学
纳米技术
冶金
化学
有机化学
工程类
作者
Jian Zhang,Liang Wang,Bingsen Zhang,Haishuang Zhao,Ute Kolb,Yihan Zhu,Lingmei Liu,Yu Han,Guoxiong Wang,Chengtao Wang,Dang Sheng Su,Bruce C. Gates,Feng‐Shou Xiao
出处
期刊:Nature Catalysis
[Springer Nature]
日期:2018-07-06
卷期号:1 (7): 540-546
被引量:335
标识
DOI:10.1038/s41929-018-0098-1
摘要
Supported metal nanoparticle catalysts are widely used in industry but suffer from deactivation resulting from metal sintering and coke deposition at high reaction temperatures. Here, we show an efficient and general strategy for the preparation of supported metal nanoparticle catalysts with very high resistance to sintering by fixing the metal nanoparticles (platinum, palladium, rhodium and silver) with diameters in the range of industrial catalysts (0.8–3.6 nm) within zeolite crystals (metal@zeolite) by means of a controllable seed-directed growth technique. The resulting materials are sinter resistant at 600–700 °C, and the uniform zeolite micropores allow for the diffusion of reactants enabling contact with the metal nanoparticles. The metal@zeolite catalysts exhibit long reaction lifetimes, outperforming conventional supported metal catalysts and commercial catalysts consisting of metal nanoparticles on the surfaces of solid supports during the catalytic conversion of C1 molecules, including the water-gas shift reaction, CO oxidation, oxidative reforming of methane and CO2 hydrogenation. Supported metal nanoparticles are indispensable catalysts in industry, yet they are often subjected to severe sintering. Now, a general method based on metal immobilization within zeolite is reported for the preparation of highly sinter-resistant catalysts for a broad range of industrially relevant processes.
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