Saini Sonakshi, Wright Salem C, Parvin Sahanaz, Baltrusaitis Jonas, McDowell Matthew T
School of Materials Science & Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.
Department of Chemical & Biomolecular Engineering, Lehigh University, Bethlehem, Pennsylvania 18015, United States.
ACS Appl Energy Mater. 2025 Jan 14;8(2):1143-1153. doi: 10.1021/acsaem.4c02697. eCollection 2025 Jan 27.
Electrolysis of impure water (such as seawater) has recently garnered research interest as it may enable hydrogen production at reduced costs. However, the tendency of impurity ions and other species to degrade electrocatalysts and membranes within an electrolyzer is a serious challenge. Here, we investigate the effects of copper impurities of varying concentrations on the hydrogen evolution reaction (HER) using platinum electrocatalysts. A decrease of current density is observed with an increasing copper concentration. By comparing the effect of ionic impurities on current density at different concentrations, we gain insight into how impurities can interfere with the HER at different potentials. Surface characterization of the electrodes reveals differences in the morphology and extent of copper deposition on HER-active platinum vs inactive gold electrodes. This enables an improved understanding of how copper nucleates and grows on the two types of electrodes under different electrochemical conditions while also confirming deposition in low-concentration cases, as present in seawater. The results indicate that copper electrodeposition competes with the HER, and the nature of copper electrodeposition varies depending on the electrocatalytic activity of the electrode. This study provides insight toward catalyst design that can withstand the effects of impurity-induced degradation over extended use.
对不纯的水(如海水)进行电解最近引起了研究兴趣,因为这可能以降低成本的方式制氢。然而,杂质离子和其他物质使电解槽内的电催化剂和膜降解的趋势是一个严峻挑战。在此,我们使用铂电催化剂研究了不同浓度的铜杂质对析氢反应(HER)的影响。随着铜浓度的增加,观察到电流密度降低。通过比较不同浓度下离子杂质对电流密度的影响,我们深入了解了杂质如何在不同电位下干扰析氢反应。电极的表面表征揭示了在析氢活性铂电极与非活性金电极上铜沉积的形态和程度差异。这有助于更好地理解在不同电化学条件下铜在两种类型电极上如何成核和生长,同时也证实了在海水等低浓度情况下的沉积。结果表明,铜电沉积与析氢反应相互竞争,并且铜电沉积的性质因电极的电催化活性而异。这项研究为催化剂设计提供了思路,使其能够在长期使用中抵御杂质诱导的降解影响。