{"title":"Copper Nanoparticles on Electrospun Carbon Nanofibers as Catalyst for Ullmann Coupling of Iodobenzene","authors":"Leiyong Zhang, Yunfei Wu, Shaohua Jiang, Haoqing Hou","doi":"10.1002/slct.202506710","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>In this study, polyacrylonitrile (PAN) nanofiber membranes were fabricated via electrospinning and subsequently carbonized at 2200°C to produce freestanding carbon nanofiber (CNF) substrates. The CNF membrane served as the working electrode in a three-electrode electrochemical system, with a copper sheet counter electrode and Ag/AgCl reference electrode. Copper nanoparticles supported on CNFs (Cu-NPs/CNFs) were synthesized through cyclic voltammetry (CV), where anodic dissolution of the Cu counter electrode generated Cu<sup>2+</sup> ions, followed by electrochemical reduction and deposition onto CNFs. Crucially, the number of CV scanning cycles (10-15 cycles) was optimized to achieve highly active catalysts. The Cu-NPs/CNFs demonstrated superior catalytic performance in the Ullmann coupling of iodobenzene compared to commercial Cu nanopowder, yielding biphenyl at 85%–89% versus 76.12% for the nanopowder. Material characterization revealed that increasing scan cycles enlarged both the particle density and size of Cu nanoparticles; catalysts prepared with 10-15 cycles exhibited uniform particles with diameters of 30–80 nm. Furthermore, the Cu-NPs/CNFs catalyst maintained structural integrity after 5 reaction cycles, retaining 78% biphenyl yield and demonstrating excellent reusability. This work establishes a controllable electrochemical route for fabricating efficient, separable, and durable carbon-supported metal catalysts.</p>\n </div>","PeriodicalId":146,"journal":{"name":"ChemistrySelect","volume":"11 13","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2026-03-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemistrySelect","FirstCategoryId":"92","ListUrlMain":"https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/slct.202506710","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
In this study, polyacrylonitrile (PAN) nanofiber membranes were fabricated via electrospinning and subsequently carbonized at 2200°C to produce freestanding carbon nanofiber (CNF) substrates. The CNF membrane served as the working electrode in a three-electrode electrochemical system, with a copper sheet counter electrode and Ag/AgCl reference electrode. Copper nanoparticles supported on CNFs (Cu-NPs/CNFs) were synthesized through cyclic voltammetry (CV), where anodic dissolution of the Cu counter electrode generated Cu2+ ions, followed by electrochemical reduction and deposition onto CNFs. Crucially, the number of CV scanning cycles (10-15 cycles) was optimized to achieve highly active catalysts. The Cu-NPs/CNFs demonstrated superior catalytic performance in the Ullmann coupling of iodobenzene compared to commercial Cu nanopowder, yielding biphenyl at 85%–89% versus 76.12% for the nanopowder. Material characterization revealed that increasing scan cycles enlarged both the particle density and size of Cu nanoparticles; catalysts prepared with 10-15 cycles exhibited uniform particles with diameters of 30–80 nm. Furthermore, the Cu-NPs/CNFs catalyst maintained structural integrity after 5 reaction cycles, retaining 78% biphenyl yield and demonstrating excellent reusability. This work establishes a controllable electrochemical route for fabricating efficient, separable, and durable carbon-supported metal catalysts.
期刊介绍:
ChemistrySelect is the latest journal from ChemPubSoc Europe and Wiley-VCH. It offers researchers a quality society-owned journal in which to publish their work in all areas of chemistry. Manuscripts are evaluated by active researchers to ensure they add meaningfully to the scientific literature, and those accepted are processed quickly to ensure rapid online publication.