Hua Zhang , Nianpeng Li , Sanshuang Gao , Anran Chen , Qihang Qian , Qingquan Kong , Bao Yu Xia , Guangzhi Hu
{"title":"Quenching-induced atom-stepped bimetallic sulfide heterointerface catalysts for industrial hydrogen generation","authors":"Hua Zhang , Nianpeng Li , Sanshuang Gao , Anran Chen , Qihang Qian , Qingquan Kong , Bao Yu Xia , Guangzhi Hu","doi":"10.1016/j.esci.2024.100311","DOIUrl":null,"url":null,"abstract":"<div><div>Developing non-noble metal hydrogen evolution reaction (HER) electrocatalysts with high activity and durability at ampere-level current densities is vital for emerging anion exchange membrane (AEM) water electrolysis, but it remains challenging. Here we present an atom-stepped nickel–cobalt bimetallic sulfide (AS-Ni<sub>3</sub>S<sub>2</sub>/Co<sub>3</sub>S<sub>4</sub>) heterostructure that exhibits superior HER performance, with ultra-low overpotentials of 28 and 195 mV at current densities of 10 and 2000 mA cm<sup>−2</sup>, respectively. Experimental analyses and theoretical calculations revealed that the work-function-induced interfacial built-in electric field drives electron transfer from Ni<sub>3</sub>S<sub>2</sub> to Co<sub>3</sub>S<sub>4</sub> via Ni–S–Co interfacial bridging, which effectively accelerates water activation and optimizes hydrogen adsorption and desorption. An AEM electrolyzer using an AS-Ni<sub>3</sub>S<sub>2</sub>/Co<sub>3</sub>S<sub>4</sub> heterostructure as the cathode required cell voltages of only 1.71 and 1.79 V to reach 1.0 and 2.0 A cm<sup>−2</sup>, respectively, and operated stably for 1200 h without activity degradation.</div></div>","PeriodicalId":100489,"journal":{"name":"eScience","volume":"5 2","pages":"Article 100311"},"PeriodicalIF":42.9000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"eScience","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667141724001046","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
Developing non-noble metal hydrogen evolution reaction (HER) electrocatalysts with high activity and durability at ampere-level current densities is vital for emerging anion exchange membrane (AEM) water electrolysis, but it remains challenging. Here we present an atom-stepped nickel–cobalt bimetallic sulfide (AS-Ni3S2/Co3S4) heterostructure that exhibits superior HER performance, with ultra-low overpotentials of 28 and 195 mV at current densities of 10 and 2000 mA cm−2, respectively. Experimental analyses and theoretical calculations revealed that the work-function-induced interfacial built-in electric field drives electron transfer from Ni3S2 to Co3S4 via Ni–S–Co interfacial bridging, which effectively accelerates water activation and optimizes hydrogen adsorption and desorption. An AEM electrolyzer using an AS-Ni3S2/Co3S4 heterostructure as the cathode required cell voltages of only 1.71 and 1.79 V to reach 1.0 and 2.0 A cm−2, respectively, and operated stably for 1200 h without activity degradation.