Show simple item record

Files in this item

Thumbnail

Item metadata

dc.contributor.authordos Santos, John Marques
dc.contributor.authorJagadamma, Lethy Krishnan
dc.contributor.authorCameron, Joseph
dc.contributor.authorWiles, Alan A.
dc.contributor.authorWilson, Claire
dc.contributor.authorSkabara, Peter J.
dc.contributor.authorSamuel, Ifor D. W.
dc.contributor.authorCooke, Graeme
dc.date.accessioned2021-07-29T14:30:10Z
dc.date.available2021-07-29T14:30:10Z
dc.date.issued2021-07-15
dc.identifier.citationdos Santos , J M , Jagadamma , L K , Cameron , J , Wiles , A A , Wilson , C , Skabara , P J , Samuel , I D W & Cooke , G 2021 , ' New thiophene-based conjugated macrocycles for optoelectronic applications ' , Journal of Materials Chemistry C , vol. Advance Article . https://doi.org/10.1039/D1TC02002Aen
dc.identifier.issn2050-7526
dc.identifier.otherPURE: 275227382
dc.identifier.otherPURE UUID: 634480db-92dd-462b-bad3-df9904575806
dc.identifier.otherRIS: urn:E2B3EABC9417DD848907AFF3786D3550
dc.identifier.otherORCID: /0000-0002-4339-2484/work/97885502
dc.identifier.otherWOS: 000673566500001
dc.identifier.urihttp://hdl.handle.net/10023/23680
dc.descriptionGC acknowledges the EPSRC for funding (EP/E036244/1). JMS acknowledges the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior – Brasil (CAPES) – Finance Code 001 for PhD funding. JMS also acknowledges Dr Nor Basid Adiwibawa Prasetya for helpful advice. Dr L. K. Jagadamma acknowledges support from a Marie Skłodowska-Curie Individual Fellowship (European Commission) (MCIF: No. 745776).en
dc.description.abstractThiophene-based semiconductors are amongst the most successful materials in organic electronics. In this contribution, we present the synthesis and characterisation of two thiophene-based macrocycles as well as their evaluation in organic-electronic devices. McT-1 is composed of ten thiophene moieties, whereas in McT-2, four additional electron-deficient benzothiadiazole moieties are incorporated to form a donor–acceptor (D–A) π-system. Red-shifted and broadened absorption spectra as well as more positive redox potentials are observed in McT-2, whereas McT-1 displays a sharper absorption band with a higher extinction coefficient. Macrocycle McT-1 shows emission in the yellow region whereas McT-2 displays emission in the red wavelength region. DFT calculations predict the macrocycles to comprise of mainly the E,E isomers with a near-planar structure, which is further supported by the single crystal X-ray structure for McT-1. Their charge transporting properties are determined by fabricating thin-film OFETs. The photovoltaic properties of McT-1 and McT-2 are also investigated by fabricating bulk heterojunction (BHJ) devices and their potential as photodetectors has been evaluated.
dc.format.extent15
dc.language.isoeng
dc.relation.ispartofJournal of Materials Chemistry Cen
dc.rightsCopyright © 2021 The Author(s). Open Access. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.en
dc.subjectQD Chemistryen
dc.subjectDASen
dc.subject.lccQDen
dc.titleNew thiophene-based conjugated macrocycles for optoelectronic applicationsen
dc.typeJournal articleen
dc.description.versionPublisher PDFen
dc.contributor.institutionUniversity of St Andrews.School of Chemistryen
dc.contributor.institutionUniversity of St Andrews.School of Physics and Astronomyen
dc.contributor.institutionUniversity of St Andrews.Centre for Energy Ethicsen
dc.contributor.institutionUniversity of St Andrews.Centre for Biophotonicsen
dc.contributor.institutionUniversity of St Andrews.Condensed Matter Physicsen
dc.identifier.doihttps://doi.org/10.1039/D1TC02002A
dc.description.statusPeer revieweden


This item appears in the following Collection(s)

Show simple item record