Boride-mediated and carbon nanotube-scaffolded synthesis of cobalt-based electrocatalyst for efficient and stable alkaline hydrogen evolution at industrial-scale current density†

IF 6.4 1区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR Inorganic Chemistry Frontiers Pub Date : 2025-02-28 DOI:10.1039/D4QI03298E
Runze Wang, Yanmei Ren, He Wen, Zhengjun Chen and Ping Wang
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Abstract

Tailored synthesis of earth-abundant alkaline hydrogen evolution electrocatalysts, featuring optimized metal/oxide heterointerfacial structures and rapid charge-/mass-transfer characteristics, remains a significant challenge in advancing water electrolysis as a viable technology for sustainable hydrogen production. Herein, we report the boride-mediated and carbon nanotubes (CNT)-scaffolded synthesis of a cobalt-based electrocatalyst that can effectively address the key factors influencing alkaline HER performance. Specifically, a cobalt foam (CF) supported composite catalyst (Co/CoO/CNT) was prepared via a three-step procedure: (1) combustion synthesis of CNT networks on a CF surface, (2) electroless plating of the boride precursor onto the surface of CNT-decorated CF, and (3) annealing treatment to induce solid-phase reaction between the boride and adjacent CoO. The boride-mediated synthesis allows for the formation of abundant Co/CoO heterointerfacial boundaries, which serve as active sites for alkaline HER. The pre-growth of CNT networks enables the construction of a hierarchical mesoporous–macroporous architecture, rendering improved active site accessibility and enhanced water transport and gas release in the catalyst layer. In addition, the incorporation of conductive CNTs helps improve charge-transfer kinetics. Benefiting from these favorable attributes, the Co/CoO/CNT/CF catalyst showed excellent alkaline HER performance, requiring only 17 and 185 mV overpotentials to afford current densities of 10 and 500 mA cm−2, respectively, and maintaining long-term stability at high current densities up to 1000 mA cm−2. Furthermore, the catalyst exhibited fairly good performance in alkaline natural seawater electrolysis, enabling stable hydrogen production at 500 mA cm−2 for over 100 hours.

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硼化物介导和碳纳米管支架合成钴基电催化剂,用于工业规模电流密度下高效稳定的碱氢析氢
定制合成地球上丰富的碱性析氢电催化剂,具有优化的金属/氧化物异质界面结构和快速的电荷/传质特性,仍然是推动水电解作为可持续制氢的可行技术的重大挑战。在此,我们报道了硼化物介导和碳纳米管(CNT)支架合成的钴基电催化剂,可以有效地解决影响碱性HER性能的关键因素。具体来说,通过三个步骤制备了泡沫钴(CF)负载的复合催化剂(Co/CoO/CNT):(1)在CF表面燃烧合成碳纳米管网络,(2)化学镀硼化物前驱体到碳纳米管修饰的CF表面,(3)退火处理诱导硼化物与相邻CoO之间的固相反应。硼化物介导的合成允许形成丰富的Co/CoO异质界面边界,作为碱性HER的活性位点。碳纳米管网络的预生长能够构建分层介孔-大孔结构,改善活性位点的可达性,增强催化剂层中的水输送和气体释放。此外,导电碳纳米管的掺入有助于改善电荷转移动力学。得益于这些有利特性,Co/CoO/CNT/CF催化剂表现出优异的碱性HER性能,仅需要17和185 mV过电位即可分别提供10和500 mA cm - 2的电流密度,并在高达1000 mA cm - 2的高电流密度下保持长期稳定性。此外,该催化剂在碱性天然海水电解中表现出相当好的性能,在500 mA cm−2条件下稳定产氢100小时以上。
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来源期刊
Inorganic Chemistry Frontiers
Inorganic Chemistry Frontiers CHEMISTRY, INORGANIC & NUCLEAR-
CiteScore
10.40
自引率
7.10%
发文量
587
审稿时长
1.2 months
期刊介绍: The international, high quality journal for interdisciplinary research between inorganic chemistry and related subjects
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