阐明 25 平方厘米纯水非贵金属阴离子交换膜电解槽的性能限制

IF 3.5 4区 化学 Q2 ELECTROCHEMISTRY ChemElectroChem Pub Date : 2024-10-21 DOI:10.1002/celc.202400334
Michelle Sophie Lemcke, Dr. Stefan Loos, Dr. Nadine Menzel, Prof. Dr. Michael Bron
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引用次数: 0

摘要

阴离子交换膜(AEM)电解水技术已成为在碳中和经济中生产氢气的一项前景广阔的技术。为推动其工业应用,我们对电极面积为 25 cm2 的非贵金属 AEM 电解槽进行了性能评估。重点是纯水操作,在 2.2 V 电压下实现 0.26 A cm-2 的电流密度。为了获得更好的理解,AEM 电解槽还在 KOH 水溶液中运行,在 2.2 V 电压下产生 1.2 A cm-2。通过添加液体电解质和改变电池组件,找出了出现性能限制的原因和改进 AEM 电解槽的方法。电化学阻抗分析表明,在低电流密度条件下,阳极上由于迟缓的 OER 动力学造成的活化损失是限制因素。在较高的电流密度下,即工业应用所关注的操作范围内,膜的欧姆电阻是限制纯水操作高性能的主要因素。
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Elucidating the Performance Limitations of a 25 cm2 Pure-Water-Fed Non-Precious Metal Anion Exchange Membrane Electrolyzer Cell

Anion exchange membrane (AEM) water electrolysis has emerged as a promising technology for producing hydrogen in a carbon-neutral economy. To advance its industrial application, performance evaluations of non-precious metal AEM electrolyzers with electrode areas of 25 cm2 were conducted. The focus was on pure water operation, achieving a current density of 0.26 A cm−2 at a voltage of 2.2 V. To gain a better understanding, the AEM electrolyzer was also operated in aqueous KOH, yielding 1.2 A cm−2 at 2.2 V. By adding a liquid electrolyte and by varying cell components, causes of the occurring performance limitations and ways to improve the AEM electrolyzer were identified. Electrochemical impedance analysis showed that the activation loss at the anode due to sluggish OER kinetics was the limiting factor at low current densities. At higher current densities, which is the operating range of interest for industrial application, the ohmic resistance from the membrane was the dominant factor limiting high performance in pure water operation.

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来源期刊
ChemElectroChem
ChemElectroChem ELECTROCHEMISTRY-
CiteScore
7.90
自引率
2.50%
发文量
515
审稿时长
1.2 months
期刊介绍: ChemElectroChem is aimed to become a top-ranking electrochemistry journal for primary research papers and critical secondary information from authors across the world. The journal covers the entire scope of pure and applied electrochemistry, the latter encompassing (among others) energy applications, electrochemistry at interfaces (including surfaces), photoelectrochemistry and bioelectrochemistry.
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