{"title":"Dissecting the role of anions in surface reconstruction in urea oxidation to maximize assisted hydrogen production","authors":"Weiwei Bao, Mameng Yang, Taotao Ai, Jie Han, Zhifeng Deng, Xiangyu Zou, Peng Jiang, Junjun Zhang","doi":"10.1039/d4qi02333a","DOIUrl":null,"url":null,"abstract":"Transition metal chalcogenides (TMCs) are a category of electrocatalysts with favorable catalytic activity, however, the impact of oxidation and the leaching of chalcogens on the urea oxidation reaction (UOR) is not clear. Herein, 3D nanostructures of Mo-Ni<small><sub>3</sub></small>S<small><sub>2</sub></small> nanowire arrays densely grown on nickel foam (NF) were conceived and produced using a hydrothermal treatment. During the UOR process, S and Mo are electrooxidized to generate sulfite (SO<small><sub>3</sub></small><small><sup>2−</sup></small>) and molybdate (MoO<small><sub>4</sub></small><small><sup>2−</sup></small>), with SO<small><sub>3</sub></small><small><sup>2−</sup></small> further oxidized to sulfate (SO<small><sub>4</sub></small><small><sup>2−</sup></small>). Experiments proved that adding molybdate and sulfate actively improves the oxidation activity of Ni(OH)<small><sub>2</sub></small> and optimizes the adsorption/desorption of the UOR intermediates. The well-conceived Mo-Ni<small><sub>3</sub></small>S<small><sub>2</sub></small> bifunctional catalyst performs well in urea-aided hydrolysis at up to 82 mA cm<small><sup>−2</sup></small> at a voltage of 1.57 V with little performance degradation over 50 h. A promising avenue for new insights into the mechanisms underlying anionic surface reconstruction in the UOR process is offered in this work.","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":"29 1","pages":""},"PeriodicalIF":6.1000,"publicationDate":"2024-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d4qi02333a","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
Transition metal chalcogenides (TMCs) are a category of electrocatalysts with favorable catalytic activity, however, the impact of oxidation and the leaching of chalcogens on the urea oxidation reaction (UOR) is not clear. Herein, 3D nanostructures of Mo-Ni3S2 nanowire arrays densely grown on nickel foam (NF) were conceived and produced using a hydrothermal treatment. During the UOR process, S and Mo are electrooxidized to generate sulfite (SO32−) and molybdate (MoO42−), with SO32− further oxidized to sulfate (SO42−). Experiments proved that adding molybdate and sulfate actively improves the oxidation activity of Ni(OH)2 and optimizes the adsorption/desorption of the UOR intermediates. The well-conceived Mo-Ni3S2 bifunctional catalyst performs well in urea-aided hydrolysis at up to 82 mA cm−2 at a voltage of 1.57 V with little performance degradation over 50 h. A promising avenue for new insights into the mechanisms underlying anionic surface reconstruction in the UOR process is offered in this work.