Impact of Gas Bubble Evolution Dynamics on Electrochemical Reaction Overpotentials in Water Electrolyser Systems

IF 3.3 3区 化学 Q2 CHEMISTRY, PHYSICAL The Journal of Physical Chemistry C Pub Date : 2025-02-25 DOI:10.1021/acs.jpcc.5c00220
Byron Ross, Sophia Haussener, Katharina Brinkert
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Abstract

This study establishes a theoretical framework to elucidate the impact of gas bubble evolution dynamics on the reaction overpotentials in electrolytic hydrogen and oxygen production. By distinguishing between ohmic, activation, and concentration overpotentials, we formulate governing equations to determine the influence of gas bubble growth and detachment on each overpotential component. Additionally, we employ SHapley Additive exPlanations (SHAP) analysis to interpret the patterns identified by a regression neural network trained on our analytical equations. Our findings indicate that gas bubble evolution dynamics impact reaction overpotentials to different degrees, leading to divergent escalation rates and requiring targeted improvement strategies. We therefore systematically investigate the impact of key parameters influencing the gas bubble evolution dynamics such as the electrode surface wettability, the electrolyte concentration and the temperature on mitigating reaction overpotentials. Measures, such as enhancing the electrode hydrophilicity from 90 to 160°, reduces the activation and concentration overpotentials by up to 54.0% and 79.3%, respectively. Moreover, by increasing the electrolyte molarity from 0.5 to 1 M, ohmic and concentration overpotentials can be reduced by 47.1% and 72.1%, respectively, with diminishing performance returns beyond 2 M. Higher temperatures result in mild to moderate decreases across all overpotential components by improving electrolyte conductivity and mass transfer. In summary, this analysis provides valuable insights not only for optimizing electrolytic hydrogen and oxygen production devices, but it also offers the opportunity to transfer gained insights into other gas-evolving electrochemical systems and supports their optimization toward higher energy conversion efficiencies.

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本研究建立了一个理论框架,以阐明气泡演化动力学对电解制氢制氧反应过电位的影响。通过区分欧姆过电势、活化过电势和浓度过电势,我们制定了控制方程,以确定气泡生长和脱离对每个过电势成分的影响。此外,我们还采用 SHapley Additive exPlanations(SHAP)分析法来解释根据我们的分析方程训练的回归神经网络所确定的模式。我们的研究结果表明,气泡演化动力学对反应过电位的影响程度不同,从而导致了不同的升级率,需要有针对性的改进策略。因此,我们系统地研究了电极表面润湿性、电解质浓度和温度等影响气泡演化动力学的关键参数对缓解反应过电位的影响。将电极亲水性从 90° 提高到 160° 等措施可将活化过电位和浓度过电位分别降低 54.0% 和 79.3%。此外,通过将电解质摩尔浓度从 0.5 M 提高到 1 M,欧姆过电位和浓度过电位可分别降低 47.1% 和 72.1%,超过 2 M 后性能回报会逐渐降低。总之,这项分析不仅为优化电解制氢和制氧设备提供了宝贵的见解,而且还为将所获得的见解应用于其他气体演变电化学系统提供了机会,并为优化这些系统以提高能量转换效率提供了支持。
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来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
期刊介绍: The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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