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A rhodium/silicon co-electrocatalyst design concept to surpass platinum hydrogen evolution activity at high overpotentials

机译:铑/硅共电催化剂设计概念在高超电势下超越了铂氢的析出活性

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摘要

Currently, platinum-based electrocatalysts show the best performance for hydrogen evolution. All hydrogen evolution reaction catalysts should however obey Sabatier's principle, that is, the adsorption energy of hydrogen to the catalyst surface should be neither too high nor too low to balance between hydrogen adsorption and desorption. To overcome the limitation of this principle, here we choose a composite (rhodium/silicon nanowire) catalyst, in which hydrogen adsorption occurs on rhodium with a large adsorption energy while hydrogen evolution occurs on silicon with a small adsorption energy. We show that the composite is stable with better hydrogen evolution activity than rhodium nanoparticles and even exceeding those of commercial platinum/carbon at high overpotentials. The results reveal that silicon plays a key role in the electrocatalysis. This work may thus open the door for the design and fabrication of electrocatalysts for high-efficiency electric energy to hydrogen energy conversion.
机译:当前,铂基电催化剂显示出最佳的析氢性能。但是,所有的析氢反应催化剂都应遵守Sabatier的原理,即氢气对催化剂表面的吸附能不应太高或太低而不能在氢的吸附和解吸之间达到平衡。为了克服该原理的局限性,在这里我们选择一种复合(铑/硅纳米线)催化剂,其中氢在吸附能大的铑上发生吸附,而氢在吸附能小的硅上发生析氢。我们表明,该复合材料具有比铑纳米粒子更好的析氢活性,并且在高超电势下甚至超过了商品铂/碳,具有很高的析氢活性。结果表明,硅在电催化中起关键作用。因此,这项工作可以为将高效电能转化为氢能的电催化剂的设计和制造打开大门。

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