催化作用
铂金
镓
化学
甲醇
金属
无机化学
基质(化学分析)
多相催化
化学物理
有机化学
色谱法
作者
Md. Arifur Rahim,Jianbo Tang,Andrew J. Christofferson,Priyank V. Kumar,Nastaran Meftahi,Franco Centurion,Zhenbang Cao,Junma Tang,Mahroo Baharfar,Mohannad Mayyas,Francois‐Marie Allioux,Pramod Koshy,Torben Daeneke,C. F. McConville,Richard B. Kaner,Salvy P. Russo,Kourosh Kalantar‐zadeh
出处
期刊:Nature Chemistry
[Springer Nature]
日期:2022-06-06
卷期号:14 (8): 935-941
被引量:89
标识
DOI:10.1038/s41557-022-00965-6
摘要
Insights into metal–matrix interactions in atomically dispersed catalytic systems are necessary to exploit the true catalytic activity of isolated metal atoms. Distinct from catalytic atoms spatially separated but immobile in a solid matrix, here we demonstrate that a trace amount of platinum naturally dissolved in liquid gallium can drive a range of catalytic reactions with enhanced kinetics at low temperature (318 to 343 K). Molecular simulations provide evidence that the platinum atoms remain in a liquid state in the gallium matrix without atomic segregation and activate the surrounding gallium atoms for catalysis. When used for electrochemical methanol oxidation, the surface platinum atoms in the gallium–platinum system exhibit an activity of \({\sim {2.8} \times {10^7}\,{{{\mathrm{mA}}}}\,{{{{\mathrm{mg}}}}_{{{{\mathrm{Pt}}}}}^{ - 1}}},\) three orders of magnitude higher than existing solid platinum catalysts. Such a liquid catalyst system, with a dynamic interface, sets a foundation for future exploration of high-throughput catalysis.
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