催化作用
化学
离子液体
镓
脱氢
多相催化
钯
X射线光电子能谱
金属
相(物质)
化学工程
无机化学
有机化学
工程类
作者
Nicola Taccardi,Mathias Grabau,Jonas Debuschewitz,Monica Distaso,Marco Brandl,Rainer Hock,Florian Maier,Christian Papp,Jannis Erhard,Christian Neiß,Wolfgang Peukert,Andreas Görling,Hans‐Peter Steinrück,Peter Wasserscheid
出处
期刊:Nature Chemistry
[Nature Portfolio]
日期:2017-07-24
卷期号:9 (9): 862-867
被引量:306
摘要
A strategy to develop improved catalysts is to create systems that merge the advantages of heterogeneous and molecular catalysis. One such system involves supported liquid-phase catalysts, which feature a molecularly defined, catalytically active liquid film/droplet layer adsorbed on a porous solid support. In the past decade, this concept has also been extended to supported ionic liquid-phase catalysts. Here we develop this idea further and describe supported catalytically active liquid metal solutions (SCALMS). We report a liquid mixture of gallium and palladium deposited on porous glass that forms an active catalyst for alkane dehydrogenation that is resistant to coke formation and is thus highly stable. X-ray diffraction and X-ray photoelectron spectroscopy, supported by theoretical calculations, confirm the liquid state of the catalytic phase under the reaction conditions. Unlike traditional heterogeneous catalysts, the supported liquid metal reported here is highly dynamic and catalysis does not proceed at the surface of the metal nanoparticles, but presumably at homogeneously distributed metal atoms at the surface of a liquid metallic phase.
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