Yusuke Tsutsui

The structural and electronic properties of four isomers of didodecyl[1]-benzothieno[3,2-b][1]benzothiophene (C12-BTBT) have been investigated. Results show the strong impact of the molecular packing on charge carrier transport and electronic polarization properties. Field-induced time-resolved microwave conductivity measurements unravel an unprecedented high average interfacial mobility of 170 cm(2) V(-1) s(-1) for the 2,7-isomer, holding great promise for the field of organic electronics.

Abstract Use of organic molecules as lasing media has much potential to develop next‐generation optical devices as soft‐matter photonics with wideband tunability and large coherence area. Although mirrorless lasing was theoretically predicted and practically demonstrated in helical cholesteric liquid crystalline (LC) phases of organic compounds, recent studies on optical confinement have been much focused into hard‐crystalline phases of the molecules. Aggregation‐induced emission (AIE) and enhan

The intrinsic charge carrier transporting properties of two isomeric linear- and bent-shaped 7-ring benzo-fused thieno[3,2-b] thiophenes and their octyl-substituted analogues were newly investigated using flash-photolysis (FP-) and field-induced (FI-) time-resolved microwave conductivity (TRMC) techniques. FP-TRMC study in the solid state revealed that octyl-substitution potentially improved the photoconductivity due to the enhanced crystalline lamellar packing. After this screening process, loc

We report on a comprehensive measurement system for mobility and energy states of charge carriers in matter under dynamic chemical doping. The temporal evolution of the iodine doping process of poly(3-hexylthiophene) (P3HT) was monitored directly through electron paramagnetic resonance (EPR) and optical absorption spectroscopy, as well as differential electrical conductivity by the microwave conductivity measurement. The increase in conductivity was observed after the EPR intensity reached a max

Benzo-annulated aza[9]helicene ([9]AH) and thia[9]helicene ([9]TH) were prepared as novel π-extended heterohelicenes. [9]TH showed a quite short fluorescence lifetime of ∼0.3 ns and intense phosphorescence at low temperature that were attributed to its larger spin-orbit coupling and faster intersystem crossing between pseudo-degenerate S_1/2 and triplet states.

We developed circularly polarized light-time-resolved microwave conductivity (CPL-TRMC) for investigation of the CPL-dependent photoinduced charge carrier dynamics in chiral materials with chiroptical properties. Chiral <i>R</i>- or <i>S</i>-perylenediimide (PDI) molecular thin films were paired with handedness-sorted (6,5) and (11,-5) single-walled carbon nanotube (SWCNT) films to compose a donor (D)-acceptor (A) system for the spin-dependent charge separation process, and the D-A system was ex