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Colloidal synthetic methods of amorphous molybdenum phosphide nanoparticles for hydrogen evolution reaction catalysts

机译:无定形钼磷化物纳米粒子氢化反应催化剂的胶体合成方法

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摘要

Transition metal phosphides (TMPs) have recently emerged as promising hydrogen evolution reaction (HER) catalytic alternatives to platinum. Among them, molybdenum phosphide (MoP) has attracted extensive attention due to its high electrical conductivity, good stability, and Pt-like electronic structure; however, there is no systematic comparison of its different colloidal synthetic routes. This study systematically compares two colloidal synthetic methods, one-pot and two-step, for amorphous MoP and the associated morphological changes during their reaction time. The amorphous MoP nanoparticles synthesized via the two-step method within 4 h exhibited the highest HER performance with an overpotential of 177 mV in 0.50 M H(2)SO(4)for a current density of -10 mA cm(-2); this might be due to their highly developed Mo-P bondings revealed by X-ray photoelectron spectroscopy analysis. Thus, this work demonstrates that the HER catalytic performance of MoP can be significantly influenced by its synthetic method and reaction time.
机译:最近过渡金属磷化磷酸(TMP)作为有前途的氢进化反应(她)铂的催化替代品。其中,磷化钼(MOP)由于其高电导率,良好的稳定性和PT样电子结构而引起了广泛的关注;但是,其不同的胶体合成路线没有系统的比较。本研究系统地比较了两种胶体合成方法,单罐和两步,用于无定形拖把和反应时间期间的相关形态变化。通过在4小时内通过两步方法合成的无定形摩托型纳米颗粒,其性能最高,其在0.50 m H(2)所以(4)中的177mV的过电位,电流密度为-10 mA cm(-2);这可能是由于X射线光电子能谱分析显示的高度发达的MO-P键。因此,这项工作表明,她的冰布催化性能可能受到其合成方法和反应时间的显着影响。

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