The Influence of Alkaline Earth Metal Cations on the Performance of Platinum Electrodes during Brine Electrolysis

被引:0
|
作者
Alvarez, Daniela V. Fraga [1 ,2 ,3 ]
Bushiri, Daniela A. [1 ,2 ,3 ]
Schuchert, Maya [1 ]
Burga, Bernardo [1 ]
Price, Abbey Piatt [1 ,2 ,3 ]
Baxter, Amanda F. [1 ]
Esposito, Daniel V. [1 ,2 ,3 ]
Carneiro, Juliana S. A. [1 ,2 ,3 ]
机构
[1] Columbia Univ, Dept Chem Engn, 500 W 120th St, New York, NY 10027 USA
[2] Columbia Univ, Columbia Electrochem Energy Ctr, New York, NY USA
[3] Columbia Univ, Lenfest Ctr Sustainable Energy, New York, NY USA
基金
新加坡国家研究基金会;
关键词
Cation; Hydrogen evolution reaction; Hydrolysis; Bifunctional; Interfacial water networks; EVOLUTION ACTIVITY; HYDROXIDE; SEAWATER; PH; DESIGN; ENERGY;
D O I
10.1002/cssc.202402780
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The performance of platinum electrodes towards the hydrogen evolution reaction (HER) during pH-neutral brine electrolysis was investigated in the presence of alkaline earth metal cations, with a focus on Mg2+ ions. This study aimed to understand the impact of these cations and/or their hydroxide deposits on electrode performance. Electrochemical measurements, including chronoamperometry and polarization curves, were conducted in pH-neutral electrolytes with varying Mg2+ concentrations (0 mM to 55 mM) in 1 M Na2SO4 solution. Contrary to concerns that Mg(OH)2 deposits might impair performance, Pt electrodes exhibited improved HER activity across all Mg2+ concentrations compared to Mg-free electrolytes. To distinguish the effects of hydroxide deposits from solvated cation interactions with the electrocatalyst, other divalent cations (Ca2+, Sr2+, Mn2+) with varying solubility product constants were also tested. All cations enhanced HER performance, including those unlikely to form deposits under the tested conditions. Our results point to cation acidity and Gibbs free energy of hydration as effective descriptors for predicting the role of divalent cations in HER kinetics. In situ image analysis revealed that Mg(OH)2 deposits are periodically removed by evolving hydrogen bubbles, preventing the blockage of active sites. In situ Raman spectroscopy further confirmed the formation of Mg(OH)2 deposits during HER.
引用
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页数:13
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