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Fabrication of Fe2O3 nanostructure on CNT for oxygen evolution reaction

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dc.contributor.authorPalem, Ramasubba Reddy-
dc.contributor.authorMeena, Abhishek-
dc.contributor.authorSoni, Ritesh-
dc.contributor.authorMeena, Jagdeesh-
dc.contributor.authorLee, Soo-Hong-
dc.contributor.authorPatil, Supriya A.-
dc.contributor.authorAnsar, Sabah-
dc.contributor.authorKim, Hyun-Seok-
dc.contributor.authorIm, Hyunsik-
dc.contributor.authorBathula, Chinna-
dc.date.accessioned2023-04-27T08:41:07Z-
dc.date.available2023-04-27T08:41:07Z-
dc.date.issued2022-10-
dc.identifier.issn0272-8842-
dc.identifier.issn1873-3956-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/2358-
dc.description.abstractThe carbon-based composite materials prepared through green synthetic approach are attracting greater interest in electrochemical applications due to their sustainable nature. Herein, we developed Fe2O3 and Fe2O3@CNT composite materials via a green mechanochemical one-pot method. The as prepared composite materials were characterized by X-ray diffraction (XRD), energy dispersive X-Ray spectroscopy (EDS), field emission scanning microscopy (FE-SEM), high resolution transmission electron microscopy (HR-TEM), and X-ray photoelectron spectroscopy (XPS), respectively. Incorporating Fe2O3 nanoparticles on CNT surface tunes its electronic structure as well increases active sites and thus enhance the oxygen evolution reaction (OER) performance. As a result, the fabricated Fe2O3@CNT is a highly effective and balanced electrocatalyst that delivers superior current density (j = 10 mA cm(-2)) at low overpotential (eta = 270 mV) for OER compared with pristine Fe2O3 (eta = 290 mV) in 1 M KOH. Further, Fe2O3@CNT electrocatalyst shows high long-term durability in 1 M KOH for 100 h, fulfilling all the advantageous viable standards for OER.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier Ltd-
dc.titleFabrication of Fe2O3 nanostructure on CNT for oxygen evolution reaction-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.ceramint.2022.04.322-
dc.identifier.scopusid2-s2.0-85129728956-
dc.identifier.wosid000877350900004-
dc.identifier.bibliographicCitationCeramics International, v.48, no.19, pp 29081 - 29086-
dc.citation.titleCeramics International-
dc.citation.volume48-
dc.citation.number19-
dc.citation.startPage29081-
dc.citation.endPage29086-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryMaterials Science, Ceramics-
dc.subject.keywordPlusHYDROGEN EVOLUTION-
dc.subject.keywordPlusELECTROCATALYSTS-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusEFFICIENT-
dc.subject.keywordPlusCOMPOSITE-
dc.subject.keywordPlusOER-
dc.subject.keywordAuthorFe2O3@CNT-
dc.subject.keywordAuthorOxygen evolution reaction-
dc.subject.keywordAuthorElectrocatalyst-
dc.subject.keywordAuthorLong-term durablity-
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College of Advanced Convergence Engineering > ETC > 1. Journal Articles
College of Advanced Convergence Engineering > Division of System Semiconductor > 1. Journal Articles
College of Engineering > Department of Electronics and Electrical Engineering > 1. Journal Articles
College of Life Science and Biotechnology > Department of Biomedical Engineering > 1. Journal Articles

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