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首页> 外文期刊>Frontiers in Chemistry >In situ Engineering of Hollow Porous Mo2C@C Nanoballs Derived From Giant Mo-Polydopamine Clusters as Highly Efficient Electrocatalysts for Hydrogen Evolution
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In situ Engineering of Hollow Porous Mo2C@C Nanoballs Derived From Giant Mo-Polydopamine Clusters as Highly Efficient Electrocatalysts for Hydrogen Evolution

机译:在衍生自巨型MO-多德莫胺簇的中空多孔MO2C @ C纳米纳瓦布的原位工程,作为高效电催化剂的氢进化

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摘要

Low-cost nd highly effective catalysts are crucial to the electrocatalytic hydrogen evolution reaction (HER) and molybdenum carbides are a promising candidate because of their high reserves, stability, low cost, and structural diversity. In this work, we report a simple method to fabricate hollow porous Mo2C@C nanoball through a hydrothermal preparation of molybdenum precursors at high temperature. Specifically, we combined interfacial polymerization and chelation effect to synthesize the Mo-polydopamine (Mo-PDA) precursor. Then, the result shows that the Mo2C@C-3 only requires an ultralow Tafel slopes (~55 mV dec-1) and low overpotential (~167 mV) at 50 mA cm-2 in 0.5 M H2SO4 electrolyte, with long-term cycling stability. Besides, the Mo2C@C-3 also exhibits outstanding activity and stability under extensive HER tests in alkaline media. This study opens a new perspective for the development of highly porous molybdenum carbide-based materials for electrochemical applications.
机译:低成本Nd高效催化剂对电催化氢进化反应(她)和钼是一种很有希望的候选者,因为它们的高储备,稳定性,低成本和结构多样性。在这项工作中,我们通过高温下钼前体的水热制剂报告了一种制造中空多孔MO2C @ C纳米的简单方法。具体地,我们组合界面聚合和螯合效果以合成Mo-多碳胺(Mo-PDA)前体。然后,结果表明,MO2C @ C-3只需要在0.5M H2SO4电解质中以50 mA CM-2的UltraLow Tafel斜率(〜55mV Dec-1)和低过电压(〜167mV),长期循环稳定性。此外,MO2C @ C-3还在碱性介质的广泛考试中表现出出色的活动和稳定性。本研究开辟了一种新的电化学应用碳化物基材料的开发的新视角。

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