Yu-Ting Liu, Quan-Jiang Lv, Hang Cong, Wen-Feng Zhao, Qing-Mei Ge, Nan Jiang and Qi-Long Zhu
{"title":"Ultrafine cucurbit[n]uril (n = 5–8)–Ni nanocomposites as highly efficient catalysts for the electrocatalytic oxygen evolution reaction†","authors":"Yu-Ting Liu, Quan-Jiang Lv, Hang Cong, Wen-Feng Zhao, Qing-Mei Ge, Nan Jiang and Qi-Long Zhu","doi":"10.1039/D5QI00013K","DOIUrl":null,"url":null,"abstract":"<p >Nickel-based oxygen evolution reaction (OER) electrocatalysts have garnered significant attention due to their high catalytic activity and abundant reserves. In this study, we report a series of cucurbit[<em>n</em>]uril (CB[<em>n</em>], <em>n</em> = 5–8) functionalized Ni nanocomposites (CB[<em>n</em>]–Ni, <em>n</em> = 5–8) to synergistically enhance the OER catalytic activity in alkaline media. The sizes and electronic structures of CB[<em>n</em>]–Ni can be precisely controlled using CB[<em>n</em>] with varying cavity sizes. Among these CB[<em>n</em>]–Ni nanocomposites, CB[7]–Ni presented superior OER performance compared to other CB[<em>n</em>]–Ni (<em>n</em> = 5, 6, and 8) and CB-free Ni nanocomposites. <em>Operando</em> electrochemical impedance spectroscopy (EIS) studies demonstrated that CB[7]–Ni initiated the OER at a relatively low applied potential of 1.5 V <em>vs.</em> RHE, achieving a superior turnover frequency of 0.24 s<small><sup>−1</sup></small> at 1.55 V <em>vs.</em> RHE. Additionally, spectroscopic measurements and theoretical calculations revealed that the incorporation of CB[7] regulates the electronic structure of the active Ni nanocomposite and lowers the activation energy for the formation of the *OOH intermediate, thereby facilitating the OER process. This work not only broadens the application of supramolecular macrocycles in electrocatalysis but also provides a novel strategy for the design of electrocatalysts.</p>","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":" 12","pages":" 4115-4123"},"PeriodicalIF":6.4000,"publicationDate":"2025-03-21","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/2025/qi/d5qi00013k","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
Nickel-based oxygen evolution reaction (OER) electrocatalysts have garnered significant attention due to their high catalytic activity and abundant reserves. In this study, we report a series of cucurbit[n]uril (CB[n], n = 5–8) functionalized Ni nanocomposites (CB[n]–Ni, n = 5–8) to synergistically enhance the OER catalytic activity in alkaline media. The sizes and electronic structures of CB[n]–Ni can be precisely controlled using CB[n] with varying cavity sizes. Among these CB[n]–Ni nanocomposites, CB[7]–Ni presented superior OER performance compared to other CB[n]–Ni (n = 5, 6, and 8) and CB-free Ni nanocomposites. Operando electrochemical impedance spectroscopy (EIS) studies demonstrated that CB[7]–Ni initiated the OER at a relatively low applied potential of 1.5 V vs. RHE, achieving a superior turnover frequency of 0.24 s−1 at 1.55 V vs. RHE. Additionally, spectroscopic measurements and theoretical calculations revealed that the incorporation of CB[7] regulates the electronic structure of the active Ni nanocomposite and lowers the activation energy for the formation of the *OOH intermediate, thereby facilitating the OER process. This work not only broadens the application of supramolecular macrocycles in electrocatalysis but also provides a novel strategy for the design of electrocatalysts.