Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/22750
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dc.contributor.authorSkliri, Euaggelia-
dc.contributor.authorVamvasakis, Ioannis-
dc.contributor.authorPapadas, Ioannis T.-
dc.contributor.authorChoulis, Stelios A.-
dc.contributor.authorArmatas, Gerasimos S.-
dc.date.accessioned2021-06-22T08:16:03Z-
dc.date.available2021-06-22T08:16:03Z-
dc.date.issued2021-02-01-
dc.identifier.citationCatalysts, 2021, vol. 11, no. 2, articl. no. 199en_US
dc.identifier.issn20734344-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/22750-
dc.description.abstractSemiconductor photocatalysis has recently emerged as an effective and eco-friendly approach that could meet the stringent requirements for sustainable environmental remediation. To this end, the fabrication of novel photocatalysts with unique electrochemical properties and high catalytic efficiency is of utmost importance and requires adequate attention. In this work, dual component mesoporous frameworks of spinel ferrite ZnFe2O4 (ZFO) and MnFe2O4 (MFO) nanoparticles are reported as efficient photocatalysts for detoxification of hexavalent chromium (Cr(VI)) and organic pollutants. The as-prepared materials, which are synthesized via a polymer-templated aggregating self-assembly method, consist of a continuous network of linked nanoparticles (ca. 6–7 nm) and exhibit large surface area (up to 91 m2 g−1 ) arising from interstitial voids between the nanoparticles, according to electron microscopy and N2 physisorption measurements. By tuning the composition, MFO-ZFO composite catalyst containing 6 wt.% MFO attains excellent photocatalytic Cr(VI) reduction activity in the presence of phenol. In-depth studies with UV-visible absorption, electrochemical and photoelectrochemical measurements show that the performance enhancement of this catalyst predominantly arises from the suitable band edge positions of constituent nanoparticles that efficiently separates and transports the charge carriers through the interface of the ZFO/MFO junctions. Besides, the open pore structure and large surface area of these ensembled networks also boost the reaction kinetics. The remarkable activity and durability of the MFO-ZFO heterostructures implies the great possibility of implementing these new nanocomposite catalysts into a realistic Cr(VI) detoxification of contaminated wastewater.en_US
dc.formatpdfen_US
dc.language.isoenen_US
dc.relation.ispartofCatalystsen_US
dc.rightsThis article is an open access article distributed under the terms and conditions of the Creative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectZinc ferriteen_US
dc.subjectManganese ferriteen_US
dc.subjectMesoporous materialsen_US
dc.subjectNanoparticlesen_US
dc.subjectMetal oxidesen_US
dc.subjectElectronic band structureen_US
dc.subjectPhotocatalysisen_US
dc.subjectHexavalent chromiumen_US
dc.subjectOrganic pollutantsen_US
dc.subjectEnvironmental remediationen_US
dc.titleMesoporous Composite Networks of Linked MnFe2O4 and ZnFe2O4 Nanoparticles as Efficient Photocatalysts for the Reduction of Cr(VI)en_US
dc.typeArticleen_US
dc.collaborationUniversity of Creteen_US
dc.collaborationCyprus University of Technologyen_US
dc.subject.categoryChemical Sciencesen_US
dc.journalsOpen Accessen_US
dc.countryGreeceen_US
dc.countryCyprusen_US
dc.subject.fieldNatural Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.3390/catal11020199en_US
dc.identifier.scopus2-s2.0-85100561197-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85100561197-
dc.relation.issue2en_US
dc.relation.volume11en_US
cut.common.academicyear2020-2021en_US
item.fulltextWith Fulltext-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.openairetypearticle-
item.languageiso639-1en-
crisitem.journal.journalissn2073-4344-
crisitem.journal.publisherMDPI-
crisitem.author.deptDepartment of Mechanical Engineering and Materials Science and Engineering-
crisitem.author.facultyFaculty of Engineering and Technology-
crisitem.author.orcid0000-0002-7899-6296-
crisitem.author.parentorgFaculty of Engineering and Technology-
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