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在水分解中,使分子金属氧化物氧化还原介体的催化析氢反应解耦。

Decoupled catalytic hydrogen evolution from a molecular metal oxide redox mediator in water splitting.

机构信息

WestCHEM, School of Chemistry, University of Glasgow, University Avenue, Glasgow G12 8QQ, UK.

出版信息

Science. 2014 Sep 12;345(6202):1326-30. doi: 10.1126/science.1257443.

Abstract

The electrolysis of water using renewable energy inputs is being actively pursued as a route to sustainable hydrogen production. Here we introduce a recyclable redox mediator (silicotungstic acid) that enables the coupling of low-pressure production of oxygen via water oxidation to a separate, catalytic hydrogen production step outside the electrolyzer that requires no post-electrolysis energy input. This approach sidesteps the production of high-pressure gases inside the electrolytic cell (a major cause of membrane degradation) and essentially eliminates the hazardous issue of product gas crossover at the low current densities that characterize renewables-driven water-splitting devices. We demonstrated that a platinum-catalyzed system can produce pure hydrogen over 30 times faster than state-of-the-art proton exchange membrane electrolyzers at equivalent platinum loading.

摘要

人们正在积极探索利用可再生能源输入进行水的电解,以此作为可持续制氢的途径。在这里,我们引入了一种可回收的氧化还原介体(硅钨酸),它能够将通过水氧化产生的低压氧气与外部的催化制氢步骤相耦合,而这个外部的制氢步骤不需要电解后的能量输入。这种方法避免了在电解槽内产生高压气体(这是导致膜降解的主要原因),并且基本上消除了在表征可再生能源驱动的水分解装置的低电流密度下产品气体交叉的危险问题。我们证明,在相同的铂负载量下,一种铂催化体系的制氢速度比最先进的质子交换膜电解槽快 30 多倍。

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