Cobalt phosphide nanoarrays on a borate-modified nickel foam substrate as an efficient dual-electrocatalyst for overall water splitting

IF 9.7 1区 化学 Q1 CHEMISTRY, PHYSICAL Journal of Colloid and Interface Science Pub Date : 2024-12-09 DOI:10.1016/j.jcis.2024.12.046
Ruijuan Zhou, Jinghao Zhang, Junxi Long, Lingfeng Li, Qinglan Ye, Xuetang Xu, Fan Wang
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Abstract

Developing efficient non-noble metal dual-functional electrocatalysts for overall water splitting is essential for the production of green hydrogen. Given the significant advantages of self-supporting electrodes, regulating the growth of self-supporting nanoarrays on a conductive substrate is conducive to improving the electrocatalytic activity. In this work, aligned cobalt phosphide (CoP) nanowire arrays grown on borate-modified Ni foam substrate (CoP/R-NF) were utilized as a bifunctional electrocatalyst for both hydrogen evolution reactions (HER) and oxygen evolution reactions (OER) in alkaline solution. The borate interfacial layer regulated the growth behavior of CoP nanowires, promoting a tip-enhanced electric field effect, facilitating an enhanced bimetallic synergistic effect. The CoP/R-NF electrode showed substantial catalytic activity for HER (η10 = 35 mV, 70 mV dec-1) and OER (241 mV, 32 mV dec-1). Moreover, a low cell voltage of 1.50 V to drive 10 mA cm−2 current density for overall water-splitting was achieved in an alkaline water electrolyzer, with long-term durability of 200 h at 100 mA cm−2, indicating the potential application of CoP/R-NF as a bifunctional catalyst for clean and renewable energy utilization. Such a synthetic strategy could pave the way for the development of non-noble bifunctional electrocatalysts for comprehensive water splitting.

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硼酸盐改性泡沫镍衬底上磷化钴纳米阵列作为一种高效的双电催化剂用于整体水分解。
开发高效的非贵金属双功能全水分解电催化剂是实现绿色制氢的关键。考虑到自支撑电极的显著优势,调节自支撑纳米阵列在导电衬底上的生长有利于提高电催化活性。在这项工作中,在硼酸修饰的Ni泡沫衬底(CoP/R-NF)上生长的排列磷化钴(CoP)纳米线阵列被用作碱性溶液中析氢反应(HER)和析氧反应(OER)的双功能电催化剂。硼酸盐界面层调节了CoP纳米线的生长行为,促进了尖端增强的电场效应,促进了双金属协同效应的增强。CoP/R-NF电极对HER (η10 = 35 mV, 70 mV dec1)和OER (241 mV, 32 mV dec1)具有较强的催化活性。此外,在碱性水电解槽中实现了1.50 V的低电池电压驱动10 mA cm-2的整体水分解电流密度,在100 mA cm-2下的长期耐久性为200 h,表明CoP/R-NF作为清洁和可再生能源利用的双功能催化剂的潜在应用前景。该合成策略可为非贵金属双功能电催化剂的开发铺平道路。
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来源期刊
CiteScore
16.10
自引率
7.10%
发文量
2568
审稿时长
2 months
期刊介绍: The Journal of Colloid and Interface Science publishes original research findings on the fundamental principles of colloid and interface science, as well as innovative applications in various fields. The criteria for publication include impact, quality, novelty, and originality. Emphasis: The journal emphasizes fundamental scientific innovation within the following categories: A.Colloidal Materials and Nanomaterials B.Soft Colloidal and Self-Assembly Systems C.Adsorption, Catalysis, and Electrochemistry D.Interfacial Processes, Capillarity, and Wetting E.Biomaterials and Nanomedicine F.Energy Conversion and Storage, and Environmental Technologies
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