Interface regulation of Zr-MOF/Ni2P@nickel foam as high-efficient electrocatalyst for pH-universal hydrogen evolution reaction

磷化物 过电位 电催化剂 材料科学 电解质 金属有机骨架 催化作用 化学工程 纳米技术 化学 电极 电化学 吸附 物理化学 冶金 生物化学 工程类
作者
Yue Li,Nannan He,Xiaohong Chen,Bo Fang,Xinjuan Liu,Haibo Li,Zhiwei Gong,Ting Lu,Likun Pan
出处
期刊:Journal of Colloid and Interface Science [Elsevier BV]
卷期号:656: 289-296 被引量:36
标识
DOI:10.1016/j.jcis.2023.11.113
摘要

Currently, the development of economical and effective non-noble metal electrocatalysts is vital for advancing hydrogen evolution reaction (HER) and enabling its widespread applications. The customizable pore structure and enormous surface area of metal–organic frameworks (MOFs) have made them to become promising non-noble metal electrocatalysts for HER. However, MOFs have some challenges, including low conductivity and instability, which can result in them having high overpotentials and slow reaction kinetics in electrocatalytic processes. In this work, we present an innovative approach for synthesizing cost-effective and high-efficient Zr-MOF-derived pH-universal electrocatalysts for HER. It entails creating the interfaces of the electrocatalysts with suitable proportions of phosphide nanostructures. Zr-MOF/Ni2P@nickel foam (NF) electrodes with interface regulated by Ni2P nanostructures were successfully developed for high-efficient pH-universal HER electrocatalysts. The presence of Ni2P nanostructures with abundant active sites at the Zr-MOFs@NF interfaces boosted the electronic conductivity and local charge density of the hybrid electrocatalysts. This helped to improve their reaction kinetics and electrocatalytic activity. By optimizing the Ni2P amount, Zr-MOF/Ni2P@NF demonstrated impressive stability and superior HER activities, with a low overpotential of 149 mV (acidic electrolytes) and 143 mV (alkaline electrolytes) at 10 mA cm−2. The proven strategy in this work can be expanded to many types of MOF-based materials for wider practical applications.
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