Many chemists have attempted syntheses of extended π-electron network molecules because of the widespread interest in the chemistry, physics and materials science of such molecules and their potential applications. In particular, extended phenacene molecules, consisting of coplanar fused benzene rings in a repeating W-shaped pattern have attracted much attention because field-effect transistors (FETs) using phenacene molecules show promisingly high performance. Until now, the most extended phenacene molecule available for transistors was [8]phenacene, with eight benzene rings, which showed very high FET performance. Here, we report the synthesis of a more extended phenacene molecule, [9]phenacene, with nine benzene rings. Our synthesis produced enough [9]phenacene to allow the characterization of its crystal and electronic structures, as well as the fabrication of FETs using thin-film and single-crystal [9]phenacene. The latter showed a field-effect mobility as high as 18 cm2 V−1 s−1, which is the highest mobility realized so far in organic single-crystal FETs.
Field-effect transistors have been fabricated using [8]phenacene single-crystals, showing the maximumμvalue of 8.2 cm2V−1s−1. The CMOS inverter circuit has also been fabricated.
A new phenacene-type molecule with five fused aromatic rings was synthesized: 2,7-didodecylphenanthro[2,1-b:7,8-b′]dithiophene ((C12H25)2-i-PDT), with two terminal thiophene rings. Field-effect transistors (FETs) using thin films of this molecule were fabricated using various gate dielectrics, showing p-channel normally-off FET properties with field-effect mobilities (μ) greater than 1 cm2 V−1 s−1. The highest μ value in the thin-film FETs fabricated in this study was 5.4 cm2 V−1 s−1, when a 150 nm-thick ZrO2 gate dielectric was used. This implies that (C12H25)2-i-PDT is very suitable for use in a transistor. Its good FET performance is fully discussed, based on electronic/topological properties and theoretical calculations.
Surface structure relaxation of organic
semiconductors affects
the properties of organic devices, although such relaxation has not
been well explored. Only two examples have been experimentally reported;
tetracene shows a large surface relaxation, while rubrene exhibits
no relaxation. Therefore, a systematic investigation of the surface
relaxation is conducted on [n]phenacenes (n = 5, 7, and 9). Electron density analyses are performed
based on the synchrotron surface X-ray scattering with the aid of
first-principles calculations. The results show little surface relaxation
in [n]phenacenes.
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