Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/112161
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dc.contributorDepartment of Applied Physicsen_US
dc.creatorZhang, WXen_US
dc.creatorLi, ZHen_US
dc.creatorXiao, RSen_US
dc.creatorWang, XGen_US
dc.creatorDai, HLen_US
dc.creatorTang, Sen_US
dc.creatorZheng, JZen_US
dc.creatorYang, Men_US
dc.creatorYuan, SSen_US
dc.date.accessioned2025-04-01T03:11:13Z-
dc.date.available2025-04-01T03:11:13Z-
dc.identifier.issn1001-0521en_US
dc.identifier.urihttp://hdl.handle.net/10397/112161-
dc.language.isoenen_US
dc.publisherGeneral Research Institute for Nonferrous Metalsen_US
dc.rights© Youke Publishing Co., Ltd. 2024en_US
dc.rightsThis version of the article has been accepted for publication, after peer review (when applicable) and is subject to Springer Nature’s AM terms of use (https://www.springernature.com/gp/open-research/policies/accepted-manuscript-terms), but is not the Version of Record and does not reflect post-acceptance improvements, or any corrections. The Version of Record is available online at: https://doi.org/10.1007/s12598-024-03050-8.en_US
dc.subjectCatalytic progressen_US
dc.subjectDegradationen_US
dc.subjectGalvanic cellen_US
dc.subjectReal-time monitoringen_US
dc.titleReal-time electrochemical monitoring sensor for pollutant degradation through galvanic cell systemen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1800en_US
dc.identifier.epage1812en_US
dc.identifier.volume44en_US
dc.identifier.issue3en_US
dc.identifier.doi10.1007/s12598-024-03050-8en_US
dcterms.abstractHere, a novel real-time monitoring sensor that integrates the oxidation of peroxymonosulfate (PMS) and the in situ monitoring of the pollutant degradation process is proposed. Briefly, FeCo@carbon fiber (FeCo@CF) was utilized as the anode electrode, while graphite rods served as the cathode electrode in assembling the galvanic cell. The FeCo@CF electrode exhibited rapid reactivity with PMS, generating reactive oxygen species that efficiently degrade organic pollutants. The degradation experiments indicate that complete bisphenol A (BPA) degradation was achieved within 10 min under optimal conditions. The real-time electrochemical signal was measured in time during the catalytic reaction, and a linear relationship between BPA concentration and the real-time charge (Q) was confirmed by the equation ln(C0/C) = 4.393Q (correlation coefficients, R2 = 0.998). Furthermore, experiments conducted with aureomycin and tetracycline further validated the effectiveness of the monitoring sensor. First-principles investigation confirmed the superior adsorption energy and improved electron transfer in FeCo@CF. The integration of pollutant degradation with in situ monitoring of catalytic reactions offers promising prospects for expanding the scope of the monitoring of catalytic processes and making significant contributions to environmental purification.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationRare metals, Mar. 2025, v. 44, no. 3, p. 1800-1812en_US
dcterms.isPartOfRare metalsen_US
dcterms.issued2025-03-
dc.identifier.scopus2-s2.0-85208816026-
dc.identifier.eissn1867-7185en_US
dc.description.validate202504 bcchen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumbera3484a-
dc.identifier.SubFormID50227-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China; Natural Science Foundation of Jiangsu Province; Natural Science Foundation of Jiangsu Higher Education Institutions of Chinaen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryGreen (AAM)en_US
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