材料科学
过电位
电解质
制氢
可逆氢电极
分解水
催化作用
电解水
氢
化学物理
纳米技术
电解
化学工程
物理化学
电化学
工作电极
电极
有机化学
化学
工程类
光催化
生物化学
作者
Yemima Ehrnst,Peter Cameron Sherrell,Amgad R. Rezk,Leslie Y. Yeo
标识
DOI:10.1002/aenm.202203164
摘要
Abstract A novel strategy utilizing high‐frequency (10 MHz) hybrid sound waves to dramatically enhance hydrogen evolution reactions (HER) in notoriously difficult neutral electrolytes by modifying their network coordination state is presented. Herein, the practical limitations associated with existing electrolyzer technology is addressed, including the need for highly corrosive electrolytes and expensive electrocatalysts, by redefining conceptually‐poor hydrogen electrocatalysts in neutral electrolytes. The improvement in HER performance is attributed to the unique capability of the intense local electromechanical coupling arising from the acoustic‐forcing to ‘frustrate’ the tetrahedrally‐coordinated hydrogen bond network of water molecules at the electrode–electrolyte interface, resulting in the generation of a high concentration of “free” water molecules that are more readily able to access catalytic sites on the unmodified polycrystalline electrode. Together with the other synergistic effects that accompany the acoustic excitation (e.g., hydronium ion generation, convective relaxation of diffusion mass transfer limitations, and prevention of bubble build‐up and their removal from the electrode), the resultant overpotential reduction of 1.4 V at −100 mA cm −2 and corresponding 14‐fold increase in current density, together with a net‐positive energy saving of 27.3%, showcases the potential of the technology as a scalable platform for effectively enhancing the efficiency of green hydrogen production.
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