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Bifunctional iron molybdate as highly effective heterogeneous electro-Fenton catalyst and Li-ion battery anode

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dc.contributor.authorSanthoshkumar, P.-
dc.contributor.authorHussain, Sajjad-
dc.contributor.authorVikraman, Dhanasekaran-
dc.contributor.authorKaruppasamy, K.-
dc.contributor.authorHussain, Tassawar-
dc.contributor.authorRamesh, Sivalingam-
dc.contributor.authorKim, Heung Soo-
dc.contributor.authorKim, Hyun-Seok-
dc.date.accessioned2023-04-27T13:40:57Z-
dc.date.available2023-04-27T13:40:57Z-
dc.date.issued2022-01-
dc.identifier.issn0045-6535-
dc.identifier.issn1879-1298-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/3758-
dc.description.abstractThree-dimensional materials have attracted considerable interest in energy and environmental remediation fields. Iron molybdate (FMO) materials have prepared via a facile hydrothermal technique with glycerol assistance, and their structural and chemical composition confirmed using various physico-chemical techniques. The prepared bi-functional material is a strong candidate for energy storage and electrocatalytic degradation of Methylene blue and Congo red. Experimental results confirmed the synthesized FMO-10 catalyst was extremely efficient for methylene blue and Congo red breakdown, achieving 91 % and 96 % degradation in 36 h, respectively. This high catalytic activity was attributed to FMO significant visible light absorption, and reactive OH formation from H2O2 synergistically triggered by both Fe3+ and MoO42-. Prepared FMO samples demonstrated excellent potential as negative electrode material for lithium ion batteries. Electrode specific capacity initially dropped then rebounded to 1265 mAh g(-1) after 100 cycles at 100 mA g(-1) change rate between 0.01 and 3.0 V.-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier Ltd.-
dc.titleBifunctional iron molybdate as highly effective heterogeneous electro-Fenton catalyst and Li-ion battery anode-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.chemosphere.2021.131846-
dc.identifier.scopusid2-s2.0-85111983244-
dc.identifier.wosid000704801600004-
dc.identifier.bibliographicCitationChemosphere, v.286, pp 1 - 11-
dc.citation.titleChemosphere-
dc.citation.volume286-
dc.citation.startPage1-
dc.citation.endPage11-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaEnvironmental Sciences & Ecology-
dc.relation.journalWebOfScienceCategoryEnvironmental Sciences-
dc.subject.keywordPlusMETHANOL OXIDATION-
dc.subject.keywordPlusRAMAN-SPECTROSCOPY-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusDEGRADATION-
dc.subject.keywordPlusOXIDE-
dc.subject.keywordPlusNANOSTRUCTURES-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusREMOVAL-
dc.subject.keywordPlusWASTE-
dc.subject.keywordPlusUV-
dc.subject.keywordAuthor3D architecture-
dc.subject.keywordAuthorTemplate-free-
dc.subject.keywordAuthorNegative electrode-
dc.subject.keywordAuthorOrganic pollutant-
dc.subject.keywordAuthorCatalysts-
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College of Engineering > Department of Electronics and Electrical Engineering > 1. Journal Articles
College of Engineering > Department of Energy and Materials Engineering > 1. Journal Articles
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