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Supramolecular Chalcogen‐Bonded Semiconducting Nanoribbons at Work in Lighting Devices

Deborah Romito, Elisa Fresta, Luca M. Cavinato, Hanspeter Kählig, Heinz Amenitsch, Laura Caputo, Yu‐Sheng Chen, Paolo Samorı́, Jean‐Christophe Charlier, Rubén D. Costa, Davide Bonifazi

2022Angewandte Chemie International Edition36 citationsDOIOpen Access PDF

Abstract

Abstract This work describes the design and synthesis of a π‐conjugated telluro[3,2‐ β ][1]‐tellurophene‐based synthon that, embodying pyridyl and haloaryl chalcogen‐bonding acceptors, self‐assembles into nanoribbons through chalcogen bonds. The ribbons π‐stack in a multi‐layered architecture both in single crystals and thin films. Theoretical studies of the electronic states of chalcogen‐bonded material showed the presence of a local charge density between Te and N atoms. OTFT‐based charge transport measurements showed hole‐transport properties for this material. Its integration as a p‐type semiconductor in multi‐layered Cu I ‐based light‐emitting electrochemical cells (LECs) led to a 10‐fold increase in stability (38 h vs . 3 h) compared to single‐layered devices. Finally, using the reference tellurotellurophene congener bearing a C−H group instead of the pyridyl N atom, a herringbone solid‐state assembly is formed without charge transport features, resulting in LECs with poor stabilities (<1 h).

Topics & Concepts

ChalcogenSupramolecular chemistrySynthonMaterials scienceCrystallographySemiconductorElectrochemistryConjugated systemChemistryNanotechnologyOptoelectronicsCrystal structureStereochemistryPolymerPhysical chemistryComposite materialElectrodeCrystallography and molecular interactionsOrganoselenium and organotellurium chemistryOrganic and Molecular Conductors Research
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