Using Spatial Confinement to Decipher Polymorphism in the Organic Semiconductor p-DTS(FBTTh2)2
| UDC.coleccion | Investigación | |
| UDC.departamento | Física e Ciencias da Terra | |
| UDC.endPage | 2415 | |
| UDC.grupoInv | Grupo de Polímeros | |
| UDC.institutoCentro | CITENI - Centro de Investigación en Tecnoloxías Navais e Industriais | |
| UDC.issue | 7 | |
| UDC.journalTitle | Journal of Materials Chemistry C | |
| UDC.startPage | 2410 | |
| UDC.volume | 12 | |
| dc.contributor.author | Marina, Sara | |
| dc.contributor.author | Martín, Jaime | |
| dc.date.accessioned | 2025-10-22T12:17:59Z | |
| dc.date.available | 2025-10-22T12:17:59Z | |
| dc.date.issued | 2024-01-08 | |
| dc.description.abstract | [Abstrac]: Many molecular semiconductors show a pronounced polymorphism; i.e. they can adopt different crystal arrangements depending, e.g., on temperature, pressure, and selected solidification pathways. This renders reliable fabrication of molecular semiconductor devices challenging, as minute changes in processing can lead to numerous structures and, hence, optoelectronic responses. Here, we demonstrate using the example of p-DTS(FBTTh₂)₂ that spatial confinement at the nanoscale can be exploited to detect specific polymorphs and the conditions under they form. A new polymorph exhibiting a higher charge-carrier mobility compared to previously reported p-DTS(FBTTh₂)₂ crystal forms is found at elevated temperatures and high degree of confinement, illustrating the benefit of our approach and promising that spatial confinement will find wide- spread application to understand and control polymorph formation in organic semiconductors. | |
| dc.description.sponsorship | This work is supported by MCINN/FEDER (under ref. PID2021- 126243NB-I00 and PGC2018-095411-B-I00) and Xunta de Galicia (Proyectos de Consolidacio´n ref. ED431F 2021/009). J. M. thanks MCINN for the Ramo´n y Cajal contract. N. S. in addition gratefully acknowledges support from the IdEx Bordeaux Excellence program (ANR-10-IDEX-03-02). The authors would like to acknowledge the financial support provided by the IONBIKE RISE project. This project has received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement no. 823989. All authors acknowledge the synchrotron radiation source ELETTRA (Trieste, Italy) for providing beam time and the staff from the SAXS beamline for support. This work was authored in part by the National Renewable Energy Laboratory, operated by Alliance for Sustainable Energy, LLC, for the U. S. Department of Energy (DOE) under Contract No. DE-AC36- 08GO28308. Funding for TRMC measurements was provided by the Solar Photochemistry Program, Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences, U. S. Department of Energy. The views expressed in the article do not necessarily represent the views of the DOE or the U. S. Government. The U. S. Government retains and the publisher, by accepting the article for publication, acknowledges that the U. S. Government retains a nonexclusive, paidup, irrevocable, worldwide license to publish or reproduce the published form of this work, or allow others to do so, for U. S. Government purposes. J. M. thanks MICINN/FEDER for the Grant PID2021-126243NB-I00. | |
| dc.description.sponsorship | Xunta de Galicia; ED431F 2021/009 | |
| dc.identifier.citation | S. Marina, M. Dyson, X. Rodríguez-Martínez, O. G. Reid, R. Li, G. Rumbles, D. Smilgies, A. Amassian, M. Campoy-Quiles, N. Stingelin and J. Martín, J. Mater. Chem. C, 2024, 12, 2410–2415. | |
| dc.identifier.doi | https://doi.org/10.1039/D3TC03640E | |
| dc.identifier.issn | 2050-7534 | |
| dc.identifier.uri | https://hdl.handle.net/2183/46061 | |
| dc.language.iso | eng | |
| dc.publisher | Royal Society of Chemistry | |
| dc.relation.projectID | info:eu-repo/grantAgreement/EC/H2020/823989 | |
| dc.relation.projectID | info: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.projectID | info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PGC2018-095411-B-I00/ES/CONVERSION EFICIENTE DE ENERGIA SOLAR VISIBLE E INFRARROJA MEDIANTE ARQUITECTURAS DE TIPO ARCOIRIS/ | |
| dc.relation.uri | https://doi.org/10.1039/D3TC03640E | |
| dc.rights | Attribution 4.0 International | en |
| dc.rights.accessRights | open access | |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
| dc.title | Using Spatial Confinement to Decipher Polymorphism in the Organic Semiconductor p-DTS(FBTTh2)2 | |
| dc.type | journal article | |
| dc.type.hasVersion | VoR | |
| dspace.entity.type | Publication | |
| relation.isAuthorOfPublication | 256e7a30-b3dd-4d95-81fc-c6a0996914eb | |
| relation.isAuthorOfPublication.latestForDiscovery | 256e7a30-b3dd-4d95-81fc-c6a0996914eb |
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