Mechanistic insights into pH-dependent hydrogen electrocatalysis by flipping interfacial water

13 September 2021, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

A grand challenge in electrochemistry is to understand and promote electrochemical processes by exploring and exploiting the interface. Herein, we promoted the hydrogen evolution and oxidation reactions (HER/HOR) of platinum in base by employing N-methylimidazoles to reorientate interfacial water against the interfacial electric field as evidenced by in situ spectroscopic characterization of the interface. We accordingly established a unified mechanism by which the HER/HOR in acid and base proceeds via diffusion of proton and hydroxide, respectively, through interface via interfacial water by the Grotthuss mechanism. This mechanism accounts for the pH-dependent HER/HOR kinetics of platinum, a long-standing puzzle. Furthermore, we demonstrated 40% performance improvement of an anion exchange membrane electrolyzer by adding 1,2-dimethylimidazole into the alkaline solution fed into its Pt cathode.

Keywords

electrochemistry
hydrogen evolution and oxidation reactions
N-methylimidazoles
electrolyzer
interfacial water

Supplementary materials

Title
Description
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Title
Mechanistic insights into pH-dependent hydrogen electrocatalysis by flipping interfacial water
Description
Materials and Methods Tables S1 - S3 Fig S1 - S9 References (50 - 57)
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