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熔融锡溶剂扩展了液态金属催化作用。

Molten Sn solvent expands liquid metal catalysis.

作者信息

Tang Junma, Meftahi Nastaran, Christofferson Andrew J, Sun Jing, Yu Ruohan, Rahim Md Arifur, Tang Jianbo, Mao Guangzhao, Daeneke Torben, Kaner Richard B, Russo Salvy P, Kalantar-Zadeh Kourosh

机构信息

School of Chemical and Biomolecular Engineering, The University of Sydney, Sydney, Australia.

School of Chemical Engineering, University of New South Wales (UNSW), Sydney, Australia.

出版信息

Nat Commun. 2025 Jan 21;16(1):907. doi: 10.1038/s41467-025-56222-0.

Abstract

Regulating favorable assemblies of metallic atoms in the liquid state provides promise for catalyzing various chemical reactions. Expanding the selection of metallic solvents, especially those with unique properties and low cost, enables access to distinctive fluidic atomic structures on the surface of liquid alloys and offers economic feasibility. Here, Sn solvent, as a low-cost commodity, supports unique atomic assemblies at the interface of molten SnInCu, which are highly selective for H synthesis from hydrocarbons. Atomistic simulations reveal that distinctive adsorption patterns with hexadecane can be established with Cu transiently reaching the interfacial layer, ensuring an energy-favorable route for H generation. Experiments with a natural oil as feedstock underscore this approach's performance, producing 1.2 × 10mol/min of H with 5.0 g of catalyst at ~93.0% selectivity while offering reliable scalability and durability at 260 °C. This work presents an alternative avenue of tuning fluidic atomic structures, broadening the applications of liquid metals.

摘要

调控液态金属原子的有利组装为催化各种化学反应带来了希望。扩大金属溶剂的选择范围,尤其是那些具有独特性质且成本低廉的溶剂,能够在液态合金表面获得独特的流体原子结构,并具有经济可行性。在此,锡溶剂作为一种低成本的商品,在熔融的锡铟铜界面支持独特的原子组装,这种组装对烃类制氢具有高度选择性。原子模拟表明,随着铜瞬间到达界面层,可以与十六烷建立独特的吸附模式,确保生成氢的能量有利途径。以天然油为原料的实验强调了这种方法的性能,在约93.0%的选择性下,5.0克催化剂可产生1.2×10摩尔/分钟的氢气,同时在260°C下具有可靠的可扩展性和耐久性。这项工作提出了一种调整流体原子结构的替代途径,拓宽了液态金属的应用范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4361/11751482/e329a4b7afac/41467_2025_56222_Fig1_HTML.jpg

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