Tuning of organic heterojunction conductivity by the substituents' electronic effects in phthalocyanines for ambipolar gas sensors

dc.contributor.authorSahin, Zeynel
dc.contributor.authorMeunier-Prest, Rita
dc.contributor.authorDumoulin, Fabienne
dc.contributor.authorKumar, Abhishek
dc.contributor.authorIsci, Umit
dc.contributor.authorBouvet, Marcel
dc.date.accessioned2025-10-29T11:22:55Z
dc.date.issued2021
dc.departmentFakülteler, Temel Bilimler Fakültesi, Kimya Bölümü
dc.description.abstractExploiting organic heterojunction effects in electrical devices are an important strategy to improve the electrical conductivity, which can be utilized into improving the conductometric gas sensors performances. In this endeavor, the present article reports fabrication of organic heterostructures in a bilayer device configuration incorporating octa-substituted nickel phthalocyanines (NiPc) and radical lutetium bis-phthalocyanine (LuPc2) and investigates their sensing properties towards NH3 vapor. NiPc having hexyl sulfanyl, hexyl sulfonyl and p-carboxyphenoxy moieties are synthesized, which electronic effects are electron donating, accepting and moderate accepting, respectively, also validated by cyclic voltammetry. The electronic effects of substituents in NiPc modulate the interfacial electrical conductivity and the type of the organic heterojunction formed. The electron acceptor and donor groups favor the formation of accumulation and accumulation/depletion heterojunctions, which are also correlated to negative and positive response towards NH3, respectively. Among the studied heterojunction devices, the one based on hexyl sulfanyl groups, revealed the highest and the most stable response in 10-90 ppm of NH3 and under variable relative humidity (rh) (10-70 %). Interestingly, the bilayer device having p-carboxyphenoxy substituted NiPc, exhibited ambipolar behavior such that its p-type semiconducting nature is changed into n-type at higher rh values, also demonstrated by change in its negative response into positive towards NH3.
dc.description.sponsorshipScientific and Technological Research Council of Turkey (TUBITAK) [117Z623/39745WG]
dc.description.sponsorshipFrench Embassy in Turkey [117Z623/39745WG]
dc.description.sponsorshipAgence Nationale de la Recherche [OUTSMART ANR-2015-CE39-0004-03]
dc.description.sponsorshipEuropean Union through the FABER program
dc.description.sponsorshipConseil Regional de Bourgogne through the FABER program
dc.description.sponsorshipEuropean Union through the PARI SMT 08 program
dc.description.sponsorshipConseil Regional de Bourgogne through the PARI SMT 08 program
dc.description.sponsorshipEuropean Union through the CDEA program
dc.description.sponsorshipConseil Regional de Bourgogne through the CDEA program
dc.description.sponsorshipPIAExcellence ISITE-BFC (CoMICS program 2019-2022: Chemistry of Molecular Interactions - Catalysis and Sensors)
dc.description.sponsorshipThe Scientific and Technological Research Council of Turkey (TUBITAK) and the French Embassy in Turkey are gratefully acknowledged for the bilateral Partenariat Hubert Curien between Turkey and France (project PHC-Bosphorus 117Z623/39745WG). The authors are thankful to Agence Nationale de la Recherche for a generous funding throughout the project (OUTSMART ANR-2015-CE39-0004-03). Authors would also like to thank European Union and Conseil Regional de Bourgogne for providing financial support through the FABER and the PARI SMT 08 and CDEA programs. Authors thank SATT SAYENS for supporting the analytical platform (PACSMUB) at ICMUB. Dr. Vaibhav Vibhu (Forschungszentrum Julich, Germany) is thanked for SEM and EDS analyses of LuPc2 thin films. This work was supported by the PIAExcellence ISITE-BFC (CoMICS program 2019-2022: Chemistry of Molecular Interactions - Catalysis and Sensors) (A. K.). The Ministere de la Cohesion des Territoires et des Relations avec les Collectivites Territoriales (France) and the Conseil Regional de Bourgogne are thanked for the CPER.
dc.identifier.doi10.1016/j.snb.2021.129505
dc.identifier.issn0925-4005
dc.identifier.orcid0000-0002-6285-0524
dc.identifier.orcid0000-0001-5597-3879
dc.identifier.orcid0000-0002-7719-7652
dc.identifier.orcid0000-0002-2272-6633
dc.identifier.orcid0000-0002-0388-8338
dc.identifier.orcid0000-0002-4306-9644
dc.identifier.scopus2-s2.0-85100055942
dc.identifier.scopusqualityN/A
dc.identifier.urihttps://doi.org/10.1016/j.snb.2021.129505
dc.identifier.urihttps://hdl.handle.net/20.500.14854/9174
dc.identifier.volume332
dc.identifier.wosWOS:000618774600007
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherElsevier Science Sa
dc.relation.ispartofSensors and Actuators B-Chemical
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20251020
dc.subjectMolecular materials
dc.subjectPhthalocyanine
dc.subjectConductometric Transducer
dc.subjectHeterojunction
dc.subjectGas sensor
dc.subjectAmmonia
dc.titleTuning of organic heterojunction conductivity by the substituents' electronic effects in phthalocyanines for ambipolar gas sensors
dc.typeArticle

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