Publication:
Enhanced photocatalytic NOx oxidation and storage under visible-light irradiation by anchoring Fe3O4 nanoparticles on mesoporous graphitic carbon nitride (mpg-C3N4)

dc.contributor.coauthorIrfan, Muhammad
dc.contributor.coauthorSevim, Melike
dc.contributor.coauthorKocak, Yusuf
dc.contributor.coauthorBalci, Merve
dc.contributor.coauthorOzensoy, Emrah
dc.contributor.departmentDepartment of Chemistry
dc.contributor.kuauthorMetin, Önder
dc.contributor.schoolcollegeinstituteCollege of Sciences
dc.date.accessioned2024-11-09T22:50:43Z
dc.date.issued2019
dc.description.abstractSeveral mesoporous graphitic carbon nitride (mpg-C3N4) photocatalysts were synthesized by using a hard-tern plating method comprising thermal polycondensation of guanidine hydrochloride over silica spheres at three different temperatures (450, 500 and 550 degrees C). After structural characterization of these mpg-C3N4 photocatalysts, they were tested in NO(g) photo-oxidation under visible (VIS) light. The effects of polycondensation temperature on the structure and photocatalytic performance of mpg-C3N4 in NO photo-oxidation were studied. The results revealed that polycondensation temperature has a dramatic effect on the photocatalytic activity of mpg-C3N4 in NO photo-oxidation, where mpg-C3N4 synthesized at 500 degrees C (mpg-CN500) showed the best performance in NOx abatement as well as a high selectivity towards solid state NOx storage under VIS light illumination. Photocatalytic performance of the mpg-CN500 was further enhanced by the anchoring of 8.0 +/- 0.5 wt.% Fe3O4 nanoparticles (NPs) on it. Fe3O4/mpg-CN500 photocatalyst showed both high activity and high selectivity along with extended reusability without a need for a regeneration step. Enhanced photocatalytic NOx oxidation and storage efficiency of Fe3O4/mpg-CN500 photocatalyst was attributed to their mesoporous structure, high surface area and slow electron-hole recombination kinetics, efficient electron-hole separation and facile electron transfer from mpg-CN500 to Fe3O4 domains enhancing photocatalytic O-2 reduction, while simultaneously suppressing nitrate photo-reduction and decomposition to NO2(g).
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipScientific and Technological Research Council of Turkey (TUBITAK) [116M435]
dc.description.sponsorshipMinistry of Development of Turkey [DPT2006K - 120,470]
dc.description.sponsorshipTurkish Academy of Sciences EO, MI, MB, YK acknowledge the financial support from the Scientific and Technological Research Council of Turkey (TUBITAK) (Project Code: 116M435). EO acknowledges the scientific collaboration with TARLA project founded by the Ministry of Development of Turkey (project code: DPT2006K - 120,470). OM thanks to the Turkish Academy of Sciences for the financial support.
dc.description.volume249
dc.identifier.doi10.1016/j.apcatb.2019.02.067
dc.identifier.eissn1873-3883
dc.identifier.issn0926-3373
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85062167826
dc.identifier.urihttps://doi.org/10.1016/j.apcatb.2019.02.067
dc.identifier.urihttps://hdl.handle.net/20.500.14288/6720
dc.identifier.wos464487500014
dc.keywordsGraphitic carbon nitride
dc.keywordsIron oxide
dc.keywordsPhotocatalytic oxidation
dc.keywordsNox abatement
dc.keywordsDenox high-yield synthesis
dc.keywordsTio2
dc.keywordsAbatement
dc.keywordsPerformance
dc.keywordsRemoval
dc.keywordsSurface
dc.keywordsAir
dc.keywordsEfficient
dc.keywordsOxide
dc.keywordsNanocomposites
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofApplied Catalysis B-Environmental
dc.subjectChemistry, physical
dc.subjectEngineering, environmental
dc.subjectEngineering, chemical
dc.titleEnhanced photocatalytic NOx oxidation and storage under visible-light irradiation by anchoring Fe3O4 nanoparticles on mesoporous graphitic carbon nitride (mpg-C3N4)
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorMetin, Önder
local.publication.orgunit1College of Sciences
local.publication.orgunit2Department of Chemistry
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relation.isOrgUnitOfPublication.latestForDiscovery035d8150-86c9-4107-af16-a6f0a4d538eb
relation.isParentOrgUnitOfPublicationaf0395b0-7219-4165-a909-7016fa30932d
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