Tokyo Institute of Technology · 재료과학
Minoru Ashizawa 교수의 연구실은 주로 유기 반도체 소재의 설계 및 응용에 초점을 맞추고 있습니다. 특히, 딱지피릴로피롤(DDP), 티엔오프로이인디고(TII) 등의 π-공명 구조를 기반으로 한 고성능 고분자 및 소분자 유기 반도체를 개발하며, 분자 구조 조절을 통해 전자적 성능, 기계적 특성 및 막 구조를 정밀하게 제어하는 데 중점을 두고 있습니다. 이는 유기 전계효과 트랜지스터 및 태양전지 등 유연하고 저비용의 전자소자 응용을 목표로 합니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
Conjugation breakers (CBs) with different H-bonding chemistries and linker flexibilities are designed and incorporated into a diketopyrrolopyrrole (DPP)-based conjugated polymer backbone. The effects of H-bonding interactions on polymer semiconductor morphology, mechanical properties, and electrical performance are systematically investigated. We observe that CBs with an H-bonding self-association constant >0.7 or a denser packing tendency are able to induce higher polymer chain aggregation and
A series of pyrene derivatives containing thienyl groups, 1−3, has been prepared using the Suzuki coupling reaction. Recrystallization from solution and physical vapor transport (PVT) method afforded different types of crystals of 1. From the mixture of isomers of 2, the 1,8-isomer preferably crystallized from solution, whereas the 1,6-isomer crystal was obtained by the PVT method. Fabricating single-crystal-based field-effect transistors of the above compounds we directly compared the field-eff
Six conjugated polymers based on thienoisoindigo (TII) and thiophene-flanked diketopyrrolopyrrole (TDPP) units bearing either branched-alkyl or siloxane-terminated alkyl solubilizing groups have been synthesized.
A novel planar π-conjugated small molecule, benzothienoisoindigo (BTII), in which additional benzene rings are fused with the thieoisoindigo (TII) unit, has been designed and synthesized.
The influence of molecular planarity on field-effect-transistor and photovoltaic cell performance in thienoisoindigo derivatives has been studied.
<italic>N</italic>-Unsubstituted thienoisoindigo and the diphenyl derivative are prepared and these molecules exhibit ambipolar performance in organic thin film transistors.
Organic materials absorbing near-infrared (NIR) light are very attractive for the fabrication of optoelectronic devices. In this study, we developed an ultralow energy gap copolymer TzQI-TDPP composed of thiadiazoloquinoxalinimide (TzQI) and thiophene-flanked diketopyrrolopyrrole (TDPP) repeat units. TzQI-TDPP has a nearly identical narrow energy gap (0.60 eV) to that of the p-channel thienoisoindigo-based homopolymer PTII. Both polymers exhibit broad and intense optical absorption in the NIR-II
Abstract Selenium-substituted TTM-TTP (2,5-bis[4,5-bis(methylthio)-1,3-dithiol-2-ylidene]-1,3,4,6-tetrathiapentalene) derivatives (1a–1d), in which several 1,3-dithiole rings of the bis-fused TTF framework are replaced by 1,3-diselenole rings, have been prepared. In particular, we have accomplished the first selenium substitution of the inner TTP part (1a). The 1:1 composition iodine salt, (1a)I3, is an insulator constructed of the donor trimers. The 1:1 GaCl4 salt, (1a)GaCl4, has a uniform colu
Abstract Bis-fused TTF(tetrathiafulvalene) derivatives with a cyclohexane ring 1a-c have been synthesized. One of their radical-cation salts (1b)2Au(CN)2 exhibits high conductivity σrt=160 Scm−1 and is metallic down to 120 K. Its structure consists of weakly dimerized columns with relatively small intercolumnar interactions.