Tuning the π–π overlap and charge transport in single crystals of an organic semiconductor via solvation and polymorphism†
Abstract
Polymorphism is a central phenomenon in materials science that often results in important differences of the electronic properties of organic crystals due to slight variations in intermolecular distances and positions. Although a large number of π-conjugated organic compounds can grow as polymorphs, it is necessary to have at disposal a series of several polymorphs of the same molecule to establish clear and predictive structure–property relationships. We report here on the occurrence of two solvates and three polymorphs in single crystalline form of the organic p-type semiconductor 2,2′,6,6′-tetraphenyldipyranylidene (DIPO). When grown from chlorobenzene or toluene, the DIPO crystals spontaneously capture solvent molecules to form two pseudopolymorphic 1 : 1 binary solvates. Independently, three solvent-free DIPO polymorphs are obtained either from the vapor phase or from acetonitrile and benzene. Surprisingly, single crystal field-effect transistors (SC-FETs) reveal that the DIPO 1 : 1 binary solvate grown from chlorobenzene possesses a higher hole mobility (1.1 cm2 V−1 s−1) than the three solvent-free polymorphs (0.02–0.64 cm2 V−1 s−1). A refined crystallographic analysis combined with a theoretical transport model clearly shows that the higher mobility of the solvate results from an improved π–π overlap. Our observations demonstrate that solvation allows to tune the π–π overlap and transport properties of organic semiconductors by selecting appropriate solvents.
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