Publication:
Solar-light-driven photocatalytic hydrogen evolution activity of gCN/WS2 heterojunctions incorporated with the first-row transition metals

dc.contributor.coauthorAcar, Eminegul Genc
dc.contributor.coauthorAslan, Emre
dc.contributor.coauthorPatir, Imren Hatay
dc.contributor.departmentDepartment of Chemistry
dc.contributor.departmentDepartment of Chemistry
dc.contributor.kuauthorYılmaz, Seda
dc.contributor.kuauthorEroğlu, Zafer
dc.contributor.kuauthorMetin, Önder
dc.contributor.researchcenterKoç University Tüpraş Energy Center (KUTEM) / Koç Üniversitesi Tüpraş Enerji Merkezi (KÜTEM)
dc.contributor.researchcenterKoç University Surface Science and Technology Center (KUYTAM) / Koç Üniversitesi Yüzey Teknolojileri Araştırmaları Merkezi (KUYTAM)
dc.contributor.schoolcollegeinstituteGraduate School of Sciences and Engineering
dc.contributor.schoolcollegeinstituteCollege of Sciences
dc.date.accessioned2024-12-29T09:41:10Z
dc.date.issued2023
dc.description.abstractThe design of semiconductor-based heterojunctions is an effective strategy to build highly active photo-catalyst systems. In this study, tungsten disulfide (WS2) modified graphitic carbon nitride (gCN) hetero-junction (gCN/WS2) is incorporated with Co and Ni (gCN/WS2-Co and gCN/WS2-Ni) to enhance the photocatalytic hydrogen evolution reaction (HER) activity of gCN/WS2 via performing a chemical reduction method and characterized by advanced analytical techniques. The photocatalytic HER activities of gCN, gCN/ WS2, gCN/WS2-Ni and gCN/WS2-Co were measured as 0.126, 0.221, 0.237 and 0.249 mmol g-1h-1, respec-tively, under the visible light irradiation. The improvement of photocatalytic activity and stability of gCN/ WS2-Ni and gCN/WS2-Co nanocomposites could be attributed to the 2D/2D heterojunction structure, ex-tended light harvesting ability, increased electron-hole lifetime and decreased recombination rate of the charge carriers. Moreover, mechanistic studies revealed that a S-scheme heterojunction is attributed to the enhanced photocatalytic HER by the gCN/WS2-Ni and gCN/WS2-Co photocatalysts, which provides pro-moted efficiency by photocarrier transfer and separation.
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuTÜBİTAK
dc.description.sponsorsThe authors would like to thank The Scientific and Technological Research Council of Turkiye (TUBITAK, Project No: 119Z497), and Selcuk University Scientific Research Projects (20211014) for supporting this work. O.M. and I.H.P. also thank the Turkish Academy of Sciences (TUBA) for the partial financial support. This paper is part of Ph.D. thesis prepared by Eminegul GENC ACAR.
dc.description.volume950
dc.identifier.doi10.1016/j.jallcom.2023.169753
dc.identifier.eissn1873-4669
dc.identifier.issn0925-8388
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-85151820025
dc.identifier.urihttps://doi.org/10.1016/j.jallcom.2023.169753
dc.identifier.urihttps://hdl.handle.net/20.500.14288/23562
dc.identifier.wos982152300001
dc.keywordsGraphitic carbon nitride
dc.keywordsTungsten disulfide
dc.keywordsMetal doping effect
dc.keywordsHydrogen evolution reaction
dc.keywordsWater splitting
dc.keywordsSolar hydrogen
dc.languageen
dc.publisherElsevier Science Sa
dc.relation.grantnoScientific and Technological Research Council of Turkey (TUBITAK) [119Z497]
dc.relation.grantnoSelcuk University Scientific Research Projects [20211014]
dc.relation.grantnoTurkish Academy of Sciences (TUBA)
dc.sourceJournal of Alloys and Compounds
dc.subjectChemistry
dc.subjectPhysical
dc.subjectMaterials science
dc.subjectMultidisciplinary
dc.subjectMetallurgy
dc.subjectMetallurgical engineering
dc.titleSolar-light-driven photocatalytic hydrogen evolution activity of gCN/WS2 heterojunctions incorporated with the first-row transition metals
dc.typeJournal article
dspace.entity.typePublication
local.contributor.kuauthorYılmaz, Seda
local.contributor.kuauthorEroğlu, Zafer
local.contributor.kuauthorMetin, Önder
relation.isOrgUnitOfPublication035d8150-86c9-4107-af16-a6f0a4d538eb
relation.isOrgUnitOfPublication.latestForDiscovery035d8150-86c9-4107-af16-a6f0a4d538eb

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