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General Synthesis of Transition-Metal-Based Carbon-Group Intermetallic Catalysts for Efficient Electrocatalytic Hydrogen Evolution in Wide pH Range

机译:过渡金属基碳族金属间化合物催化剂的通用合成及其在宽pH值范围内高效电催化析氢

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摘要

Alloying is a well-accepted strategy for modulating the electronic structures of catalyst materials. Compared to disordered solid-solution alloys, intermetallic compounds feature ordered atomic arrangements and provide a unique platform with a rich and diverse resource to study the relationships among chemical composition, atomic structure, electronic structure, and properties. Unfortunately, it is still challenging to synthesize the nanostructures of intermetallic compounds for catalysis research. In this study, a series of intermetallic silicides (PtSi, RhSi, Ru2Si3, IrSi), germanide (Ru2Ge3), and stannides (Ru3Sn7, IrSn2, PdSn3, PdSn2) are rationally designed and constructed through a facile molten-salt-assisted route. As an example, the PtSi not only shows highly desirable electrocatalytic properties for the hydrogen evolution reaction (HER) with low overpotentials of 22, 38, and 66 mV at a current density of 10 mA cm(-2) in acidic, alkaline, and neutral media, respectively, but exhibits superior durability, as well as 97 faradic efficiency. The theoretical calculations suggest that the introduction of Si to Pt could weaken the binding energy between Pt and H atoms, which further facilitates the hydrogen generation during the HER process. Further, the findings inspired the authors to develop other kinds of metal-based carbon-group intermetallic phases with excellent activity in the HER and beyond.
机译:合金化是调控催化剂材料电子结构的一种公认的策略。与无序固溶合金相比,金属间化合物具有有序的原子排列特征,为研究化学成分、原子结构、电子结构和性能之间的关系提供了一个独特的平台和丰富多样的资源。不幸的是,合成金属间化合物的纳米结构用于催化研究仍然具有挑战性。本研究通过简单的熔盐辅助途径,合理设计和构建了一系列金属间硅化物(PtSi、RhSi、Ru2Si3、IrSi)、锗化物(Ru2Ge3)和锡化物(Ru3Sn7、IrSn2、PdSn3、PdSn2)。例如,在酸性、碱性和中性介质中,PtSi不仅在10 mA cm(-2)的电流密度下分别表现出22、38和66 mV的低过电位,而且表现出优异的耐久性,以及>97%的法拉迪效率。理论计算表明,在Pt中引入Si会削弱Pt和H原子之间的结合能,从而进一步促进HER过程中的氢气生成。此外,这些发现激发了作者开发其他种类的金属基碳基金属间相,这些相在HER及其他领域具有出色的活性。

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