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Updated: May 23, 2025

A Simple, Low-cost, and Robust System to Measure the Volume of Hydrogen Evolved by Chemical Reactions with Aqueous Solutions
Published on: August 17, 2016
Promotion or suppression of hydrogen evolution activity? The competition between sodium cations and quaternary
Shilin Bo1, Yang Xiang1, Qiong Xiang1
1Center of Advanced Electrochemical Energy, State Key Laboratory of Advanced Chemical Power Sources, School of Chemistry and Chemical Engineering, Chongqing University Chongqing 40004 P. R. China huangxun@cqu.edu.cn zdwei@cqu.edu.cn.
Abstract:
Quaternary ammonium salts (QASs) are frequently utilized to modulate the structure of the cathodic electric double layer in processes such as water electrolysis and hydrogenation reactions. However, literature reports have shown that QASs can both suppress and promote hydrogen evolution activity, yet the underlying mechanisms remain incompletely understood. In this study, we experimentally observed that the presence of QASs alone accelerates hydrogen evolution compared to NaOH solutions. Conversely, when the QAS is combined with Na+ or H+, it inhibits hydrogen evolution. Ab initio molecular dynamics simulation and surface-enhanced infrared absorption spectroscopy results indicate that Na+ ions disrupt the hydrogen bond network at the interface, leading to a disorder in the water chain arrangement. In contrast, QASs enhance the hydrogen bond network, thereby facilitating the hydrogen evolution reaction. However, coexistence of Na+ and QASs leads to hydration competition, creating gaps in the hydrogen bond network near the surface and impeding hydrogen transport. These findings enhance our understanding of QASs in hydrogen evolution and guide future interface modulation strategies.
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