以ZIF为牺牲模板制备双功能电催化剂FeNi-LDH@L-NiCoP

IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Molecular Catalysis Pub Date : 2025-03-22 DOI:10.1016/j.mcat.2025.115052
Boxuan Zhang , Jinxing Cui , Zhifang Li , Changlong Yang , Weiwei Dong , Ke Li
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引用次数: 0

摘要

水电解制氢的关键是设计低成本、高催化活性的催化剂。本文以叶状沸石酰肼骨架(L-Co-ZIF)为前驱体,经磷化制备NiCoP (L-NCP),再通过水热结晶法生长FeNi层状双氢氧化物(FeNi- ldh),制备了FeNi层状双Hydroxide@L-NCP/泡沫镍(FeNi-LDH@L-NCP/NF)。FeNi-LDH@L-NCP/NF是一种特殊的析氢反应(HER)和析氧反应(OER)催化剂。结果表明,FeNi-LDH@L-NCP/NF的过电位较低,在10 mA·cm-2和1 M KOH条件下,HER和OER的过电位分别为106和220 mV。这是因为由于ZIF模板的作用,形成了更有序的L-NCP,有利于电解质和电极之间的快速电荷转移,从而提高了其催化性能。FeNi-LDH和L-NCP的协同作用也有助于活性。
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Fabrication of excellent bifunctional electrocatalyst FeNi-LDH@L-NiCoP using ZIF as a sacrifice template for alkaline electrolysis of water
The key to generating hydrogen by electrolysis of water is to design the low-cost and high-catalytic activity catalyst. In this paper, FeNi-Layered Double Hydroxide@L-NCP/nickel foam (FeNi-LDH@L-NCP/NF) is prepared using leaf-like zeolitic imidazolate framework (L-Co-ZIF) as the precursor, phosphating to produce NiCoP (denoted as L-NCP) and then growing FeNi layered double hydroxide (FeNi-LDH) through a hydrothermal crystallization method. FeNi-LDH@L-NCP/NF is an exceptional catalyst for hydrogen evolution reaction (HER) as well as oxygen evolution reaction (OER). It shows the low overpotential of FeNi-LDH@L-NCP/NF and the values are 106 and 220 mV at 10 mA·cm-2 in 1 M KOH for HER and OER, respectively. This is because the more ordered L-NCP is formed due to the role of the ZIF templates, which favors rapid charge transfer between the electrolyte and the electrode, thereby promoting its catalytic performance. The synergistic effect of FeNi-LDH and L-NCP also contributes to activity.
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来源期刊
Molecular Catalysis
Molecular Catalysis Chemical Engineering-Process Chemistry and Technology
CiteScore
6.90
自引率
10.90%
发文量
700
审稿时长
40 days
期刊介绍: Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are: Heterogeneous catalysis including immobilized molecular catalysts Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis Photo- and electrochemistry Theoretical aspects of catalysis analyzed by computational methods
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