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首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Decorating mesoporous silicon with amorphous metal-phosphorous-derived nanocatalysts towards enhanced photoelectrochemical water reduction
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Decorating mesoporous silicon with amorphous metal-phosphorous-derived nanocatalysts towards enhanced photoelectrochemical water reduction

机译:用非晶态金属-磷衍生的纳米催化剂修饰介孔硅,以提高光电化学减水率

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摘要

Developing earth-abundant catalysts as alternatives to noble metals and facile approaches that can integrate catalysts to photoelectrodes for the hydrogen evolution reaction (HER) are critical for the successful application of solar-driven water splitting devices. Herein, we presented a facile and universal synthetic route that can incorporate a series of amorphous metal-phosphorous-derived (denoted as M-P) HER catalysts with p-Si under ambient conditions. An onset potential of +0.3 V vs. reversible hydrogen electrode (RHE) and a photocurrent density of ca. 20 mA cm(-2) at 0 V vs. RHE were obtained under simulated AM 1.5G solar illumination (100 mW cm(-2)), and are among the best values ever reported for Si photocathodes decorated with noble-metal-free catalysts. This excellent performance is ascribed to the drastically reduced charge transfer resistance across the p-Si and electrolyte due to the combination of a high quality semiconductor/catalyst interface and highly active cocatalysts with an amorphous nature. Moreover, the M-Ps/p-Si photocathodes demonstrated excellent stability due to the protection afforded by the M-Ps catalysts that were intimately adhered to p-Si.
机译:开发出富含地球的催化剂作为贵金属的替代品,并且可以将催化剂整合到光电极中以进行析氢反应(HER)的简便方法对于成功应用太阳能驱动的水分解装置至关重要。本文中,我们提出了一种简便而通用的合成路线,该路线可以在环境条件下将一系列非晶态金属衍生的(称为M-P)HER催化剂与p-Si结合使用。相对于可逆氢电极(RHE)的起始电势为+0.3 V,光电流密度为ca。在模拟AM 1.5G太阳光照(100 mW cm(-2))下获得了0 V vs. RHE时的20 mA cm(-2),这是有史以来关于无贵金属装饰的Si光电阴极的最佳值之一催化剂。优异的性能归因于高质量半导体/催化剂界面和具有非晶态性质的高活性助催化剂的结合,大大降低了p-Si和电解质之间的电荷转移阻力。而且,由于紧密粘附于p-Si的M-Ps催化剂提供的保护,M-Ps / p-Si光电阴极表现出优异的稳定性。

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