Shilin Bo, Yang Xiang, Qiong Xiang, Li Li, Xun Huang, Zidong Wei
{"title":"促进还是抑制氢进化活性?钠离子和季铵盐离子在金属/水界面上的竞争","authors":"Shilin Bo, Yang Xiang, Qiong Xiang, Li Li, Xun Huang, Zidong Wei","doi":"10.1039/d5sc01034a","DOIUrl":null,"url":null,"abstract":"Quaternary ammonium salts (QAS) 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 QAS 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 QAS alone accelerates hydrogen evolution compared to NaOH solutions. Conversely, when 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, QAS enhances the hydrogen bond network, thereby facilitating the hydrogen evolution reaction. However, coexistence of Na+ and QAS leads to hydration competition, creating gaps in the hydrogen bond network near the surface and impeding hydrogen transport. These findings enhance our understanding of QAS in hydrogen evolution and guide future interface modulation strategies.","PeriodicalId":9909,"journal":{"name":"Chemical Science","volume":"218 1","pages":""},"PeriodicalIF":7.6000,"publicationDate":"2025-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Promotion or suppression on hydrogen evolution activity? The competition between sodium cation and quaternary ammonium ions at metal/water interface\",\"authors\":\"Shilin Bo, Yang Xiang, Qiong Xiang, Li Li, Xun Huang, Zidong Wei\",\"doi\":\"10.1039/d5sc01034a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Quaternary ammonium salts (QAS) 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 QAS 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 QAS alone accelerates hydrogen evolution compared to NaOH solutions. Conversely, when 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, QAS enhances the hydrogen bond network, thereby facilitating the hydrogen evolution reaction. However, coexistence of Na+ and QAS leads to hydration competition, creating gaps in the hydrogen bond network near the surface and impeding hydrogen transport. These findings enhance our understanding of QAS in hydrogen evolution and guide future interface modulation strategies.\",\"PeriodicalId\":9909,\"journal\":{\"name\":\"Chemical Science\",\"volume\":\"218 1\",\"pages\":\"\"},\"PeriodicalIF\":7.6000,\"publicationDate\":\"2025-04-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Science\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5sc01034a\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Science","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5sc01034a","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Promotion or suppression on hydrogen evolution activity? The competition between sodium cation and quaternary ammonium ions at metal/water interface
Quaternary ammonium salts (QAS) 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 QAS 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 QAS alone accelerates hydrogen evolution compared to NaOH solutions. Conversely, when 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, QAS enhances the hydrogen bond network, thereby facilitating the hydrogen evolution reaction. However, coexistence of Na+ and QAS leads to hydration competition, creating gaps in the hydrogen bond network near the surface and impeding hydrogen transport. These findings enhance our understanding of QAS in hydrogen evolution and guide future interface modulation strategies.
期刊介绍:
Chemical Science is a journal that encompasses various disciplines within the chemical sciences. Its scope includes publishing ground-breaking research with significant implications for its respective field, as well as appealing to a wider audience in related areas. To be considered for publication, articles must showcase innovative and original advances in their field of study and be presented in a manner that is understandable to scientists from diverse backgrounds. However, the journal generally does not publish highly specialized research.