用于工业条件下碱性水电解的两种闭环镍基催化剂

IF 2.6 4区 化学 Q3 ELECTROCHEMISTRY
Li Zhu, Qing-Yun Fang, Si-Tong Liu, Bing Li, Fang Li, Zhen-Guo Guo, Ning Deng, Jian-Bo He
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引用次数: 0

摘要

本文介绍了两种闭环镍基催化剂的制备和性能评估。镍-钼和镍-铁的(氢)氧化物涂层被电沉积到工业镍网上,随后在碱性水电解中用作阴极和阳极(NiMo@NM 和 NiFe@NM)。两种催化剂都形成了完全闭环的结构,将镍网上的每根镍丝包围起来,从而增强了与基体的结合强度。NiMo@NM||NiFe@NM 组件在电池电压仅为 1.91 V 和室温条件下的电流密度达到了 200 mA cm-2,并在超过 280 小时的时间内保持了这一性能水平。在接近工业化的条件下(70 °C、6 M KOH、400 mA cm-2),制氢的比能耗可降至 4.1 kWh Nm-3 (H2)。我们希望这项研究能帮助缩小催化剂研究与实际工业应用之间的差距。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Two closed-loop nickel-based catalysts for use in alkaline water electrolysis under industrial conditions

Two closed-loop nickel-based catalysts for use in alkaline water electrolysis under industrial conditions

This paper presents the preparation and performance evaluation of two closed-loop nickel-based catalysts. The (hydro)oxide coatings of nickel-molybdenum and nickel-iron were electrodeposited onto industrial nickel meshes, which were subsequently used as the cathode and anode (NiMo@NM and NiFe@NM) in alkaline water electrolysis. Both catalysts formed a fully closed-loop configuration, surrounding each nickel wire on the nickel mesh, thereby enhancing the bonding strength with the substrate. The NiMo@NM||NiFe@NM assembly achieved a current density of 200 mA cm−2 at a cell voltage of only 1.91 V and room temperature, maintaining this level of performance for over 280 h. A single-stack flow cell was used to examine the changes in cell voltage in relation to temperature, current density, and electrolyte flow rate and concentration. The specific energy consumption for hydrogen production can be reduced to 4.1 kWh Nm−3 (H2) under near-industrial conditions (70 °C, 6 M KOH, 400 mA cm−2). We hope that this study can help bridge the gap between catalyst studies and practical industrial applications.

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来源期刊
CiteScore
4.80
自引率
4.00%
发文量
227
审稿时长
4.1 months
期刊介绍: The Journal of Solid State Electrochemistry is devoted to all aspects of solid-state chemistry and solid-state physics in electrochemistry. The Journal of Solid State Electrochemistry publishes papers on all aspects of electrochemistry of solid compounds, including experimental and theoretical, basic and applied work. It equally publishes papers on the thermodynamics and kinetics of electrochemical reactions if at least one actively participating phase is solid. Also of interest are articles on the transport of ions and electrons in solids whenever these processes are relevant to electrochemical reactions and on the use of solid-state electrochemical reactions in the analysis of solids and their surfaces. The journal covers solid-state electrochemistry and focusses on the following fields: mechanisms of solid-state electrochemical reactions, semiconductor electrochemistry, electrochemical batteries, accumulators and fuel cells, electrochemical mineral leaching, galvanic metal plating, electrochemical potential memory devices, solid-state electrochemical sensors, ion and electron transport in solid materials and polymers, electrocatalysis, photoelectrochemistry, corrosion of solid materials, solid-state electroanalysis, electrochemical machining of materials, electrochromism and electrochromic devices, new electrochemical solid-state synthesis. The Journal of Solid State Electrochemistry makes the professional in research and industry aware of this swift progress and its importance for future developments and success in the above-mentioned fields.
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