| Literature DB >> 35668212 |
Md Arifur Rahim1, Jianbo Tang2, Andrew J Christofferson3,4, Priyank V Kumar2, Nastaran Meftahi3,4, Franco Centurion2, Zhenbang Cao2, Junma Tang2, Mahroo Baharfar2, Mohannad Mayyas2, Francois-Marie Allioux2, Pramod Koshy5, Torben Daeneke6, Christopher F McConville3,7, Richard B Kaner8,9, Salvy P Russo3,4, Kourosh Kalantar-Zadeh10.
Abstract
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 [Formula: see text] 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.Entities:
Year: 2022 PMID: 35668212 DOI: 10.1038/s41557-022-00965-6
Source DB: PubMed Journal: Nat Chem ISSN: 1755-4330 Impact factor: 24.274