High-Mobility Organic Mixed Conductors with a low Synthetic Complexity Index via Direct Arylation Polymerization

UDC.coleccionInvestigación
UDC.departamentoFísica e Ciencias da Terra
UDC.endPage7688
UDC.grupoInvGrupo de Polímeros
UDC.institutoCentroCITENI - Centro de Investigación en Tecnoloxías Navais e Industriais
UDC.issue20
UDC.journalTitleChemical Science
UDC.startPage7679
UDC.volume15
dc.contributor.authorKimpel, Joost
dc.contributor.authorKim, Youngseok
dc.contributor.authorAsatryan, Jesika
dc.contributor.authorMartín, Jaime
dc.contributor.authorKroon, Renee
dc.contributor.authorMüller, Christian
dc.date.accessioned2025-12-04T15:44:37Z
dc.date.available2025-12-04T15:44:37Z
dc.date.issued2024-04-19
dc.description.abstract[Abstract]: Through direct arylation polymerization, a series of mixed ion-electron conducting polymers with a low synthetic complexity index is synthesized. A thieno[3,2-b]thiophene monomer with oligoether side chains is used in direct arylation polymerization together with a wide range of aryl bromides with varying electronic character from electron-donating thiophene to electron-accepting benzothiadiazole. The obtained polymers are less synthetically complex than other mixed ion–electron conducting polymers due to higher yield, fewer synthetic steps and less toxic reagents. Organic electrochemical transistors (OECTs) based on a newly synthesized copolymer comprising thieno[3,2-b]thiophene with oligoether side chains and bithiophene exhibit excellent device performance. A high charge-carrier mobility of up to μ = 1.8 cm2 V−1 s−1 was observed, obtained by dividing the figure of merit [μC*] from OECT measurements by the volumetric capacitance C* from electrochemical impedance spectroscopy, which reached a value of more than 215 F cm−3.
dc.description.sponsorshipWe acknowledge funding from the European Union's Horizon 2020 research and innovation programme through the Marie Skłodowska-Curie grant agreement no. 955837 (HORATES) and the Knut and Alice Wallenberg Foundation through a Wallenberg Scholar grant. J. M. thanks MICINN/FEDER for grant Ref. PID2021-126243NB-I00. We thank Lars ¨Ohrström for providing access to single X-ray crystallography, Ergang Wang for providing several commercially available monomers, Diego Ropero Hinojosa and Michael Sommer for providing access to high temperature NMR, as well as Rukiya Matsidik and Michael Sommer for performing MALDI-ToF measurements. DFT calculations were enabled by resources provided by Chalmers e- Commons. The project was in part performed at the Chalmers Materials Analysis Laboratory (CMAL).
dc.identifier.citationChem. Sci., 2024, 15, 7679
dc.identifier.doihttps://doi.org/10.1039/D4SC01430H
dc.identifier.issn2041-6539
dc.identifier.urihttps://hdl.handle.net/2183/46604
dc.language.isoeng
dc.publisherRoyal Society of Chemistry
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/955837
dc.relation.projectIDinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2021-2023/PID2021-126243NB-I00/ES/LA SEMI-PARACRISTALINIDAD: UN NUEVO MODELO ESTRUCTURAL PARA POLIMEROS SEMICONDUCTORES
dc.relation.urihttps://doi.org/10.1039/D4SC01430H
dc.rightsAttribution 4.0 Internationalen
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleHigh-Mobility Organic Mixed Conductors with a low Synthetic Complexity Index via Direct Arylation Polymerization
dc.typejournal article
dc.type.hasVersionVoR
dspace.entity.typePublication
relation.isAuthorOfPublication6a835bf1-9470-4a16-b175-495bc20a12e2
relation.isAuthorOfPublication256e7a30-b3dd-4d95-81fc-c6a0996914eb
relation.isAuthorOfPublication.latestForDiscovery6a835bf1-9470-4a16-b175-495bc20a12e2

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