Xinxin Guo, Mengmeng Zhou, Ziwu Liu, Shiheng Mu, Kaijia Wang, Huanqiang Shi, Fang Wang, Shijian Lu, Zhonghai Ni and Guiqing Liu
{"title":"A high-entropy FeCoMnCuNi diselenide self-standing electrode with outstanding water-electrolysis performance in alkaline medium†","authors":"Xinxin Guo, Mengmeng Zhou, Ziwu Liu, Shiheng Mu, Kaijia Wang, Huanqiang Shi, Fang Wang, Shijian Lu, Zhonghai Ni and Guiqing Liu","doi":"10.1039/D4QI01835D","DOIUrl":null,"url":null,"abstract":"<p >Developing non-noble metal efficient electrocatalysts with high activity and stability is extremely essential for hydrogen generation by water electrolysis with low cost. Herein, we report a novel binder-free high-entropy self-standing electrode with a unique three-dimensional structure and petunia-, needle- and fork-like morphology prepared by the hydrothermal and selenization methods. Due to high entropy, lattice distortion and high-curvature tip-enhancement effects, the prepared FeCoMnCuNiSe<small><sub>2</sub></small> with an ultralow overpotential of 71.6 mV at 100 mA cm<small><sup>−2</sup></small> exhibited superior activity for the hydrogen evolution reaction (HER) in 1.0 M KOH solution, far outperforming almost all reported advanced non-noble metal HER catalysts. More impressively, the assembled FeCoMnCuNiSe<small><sub>2</sub></small>||FeCoMnCuNiSe<small><sub>2</sub></small> overall-water splitting device with more than 45 h of continuous operational stability at 10, 20 and 50 mA cm<small><sup>−2</sup></small> in 1.0 M KOH required a remarkably low cell voltage of 1.30 V at 10 mA cm<small><sup>−2</sup></small> as well, demonstrating a promising practical application prospect in future water electrolysis.</p>","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":" 22","pages":" 7936-7946"},"PeriodicalIF":6.4000,"publicationDate":"2024-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/qi/d4qi01835d","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
Developing non-noble metal efficient electrocatalysts with high activity and stability is extremely essential for hydrogen generation by water electrolysis with low cost. Herein, we report a novel binder-free high-entropy self-standing electrode with a unique three-dimensional structure and petunia-, needle- and fork-like morphology prepared by the hydrothermal and selenization methods. Due to high entropy, lattice distortion and high-curvature tip-enhancement effects, the prepared FeCoMnCuNiSe2 with an ultralow overpotential of 71.6 mV at 100 mA cm−2 exhibited superior activity for the hydrogen evolution reaction (HER) in 1.0 M KOH solution, far outperforming almost all reported advanced non-noble metal HER catalysts. More impressively, the assembled FeCoMnCuNiSe2||FeCoMnCuNiSe2 overall-water splitting device with more than 45 h of continuous operational stability at 10, 20 and 50 mA cm−2 in 1.0 M KOH required a remarkably low cell voltage of 1.30 V at 10 mA cm−2 as well, demonstrating a promising practical application prospect in future water electrolysis.