Alloy/Interface-Induced activation of Metal-Phosphorus bonds in Ni5Cu3/CoP for efficient water splitting

IF 6.3 2区 材料科学 Q2 CHEMISTRY, PHYSICAL Applied Surface Science Pub Date : 2025-03-20 DOI:10.1016/j.apsusc.2025.163025
Wei Luo, Ning Long, Jing Peng, Wenbin Wang, Yimin Jiang, Wei Shen, Rongxing He, Wei Su, Ming Li
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Abstract

Designing and fabricating heterostructure electrocatalysts composed of alloys and transition metal compounds might be a promising strategy for high-efficiency electrocatalysis. Herein, by anchoring a layer of Ni5Cu3 alloy on CoP nanorods with the help of an electrodeposition strategy, an efficient alloy-compound heterointerface catalyst for water splitting, Ni5Cu3/CoP, was designed and fabricated successfully. As shown from the experiments, the alloying effect of the Ni5Cu3/CoP catalyst induced a super-strong interfacial coupling due to the significant electron outflow from the Ni5Cu3 alloy, and it was the synergy of this alloying effect and super-strong interfacial coupling that resulted in the significant activation of cobalt-phosphorus bonds on the catalyst surface to generate rich active sites, which remarkably activated the intrinsic activity of Ni5Cu3/CoP. Therefore, in alkaline condition, Ni5Cu3/CoP exhibited low hydrogen evolution reaction (HER) overpotential of 66 mV and oxygen evolution reaction (OER) overpotential of 190 mV at 10 mA·cm−2, respectively, as well as only needed a small cell voltage of 1.51 V to achieve 10 mA·cm−2 for overall water splitting. Density functional theory (DFT) results revealed that alloy-induced strong interfacial coupling considerably optimized the adsorption of OER and HER intermediates, improving the catalytic activity. These findings provided a valuable insight for the subsequent development of heterogeneous catalysts containing alloy components.

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设计和制造由合金和过渡金属化合物组成的异质结构电催化剂可能是实现高效电催化的一种有前途的策略。本文通过电沉积策略在 CoP 纳米棒上锚定一层 Ni5Cu3 合金,设计并成功制备了一种高效的合金-化合物异质界面催化剂 Ni5Cu3/CoP,用于水分离。实验结果表明,Ni5Cu3/CoP 催化剂的合金化效应使 Ni5Cu3 合金中的电子大量外流,从而产生了超强的界面耦合,正是这种合金化效应和超强界面耦合的协同作用,使催化剂表面的钴磷键被大量活化,产生了丰富的活性位点,显著激活了 Ni5Cu3/CoP 的内在活性。因此,在碱性条件下,Ni5Cu3/CoP 在 10 mA-cm-2 的条件下分别表现出较低的氢进化反应(HER)过电位(66 mV)和氧进化反应(OER)过电位(190 mV),并且只需较小的电池电压(1.51 V)即可实现 10 mA-cm-2 的整体水分离。密度泛函理论(DFT)结果表明,合金诱导的强界面耦合大大优化了 OER 和 HER 中间产物的吸附,提高了催化活性。这些发现为后续开发含有合金成分的异质催化剂提供了宝贵的启示。
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来源期刊
Applied Surface Science
Applied Surface Science 工程技术-材料科学:膜
CiteScore
12.50
自引率
7.50%
发文量
3393
审稿时长
67 days
期刊介绍: Applied Surface Science covers topics contributing to a better understanding of surfaces, interfaces, nanostructures and their applications. The journal is concerned with scientific research on the atomic and molecular level of material properties determined with specific surface analytical techniques and/or computational methods, as well as the processing of such structures.
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