Hokkaido University · Materials Science
Toshifumi Satoh 교수의 연구실은 유기 전자소자 및 나노복합소재 분야에서 활발한 연구를 수행하고 있습니다. 주요 연구 방향은 유기 반도체 기반의 비휘발성 광기록 트랜지스터 메모리, 스트레처블 페로브스카이트 발광 소자, 그리고 나노소재 기반의 고성능 전도성 전극과 약물 캡슐화 시스템 개발입니다. 특히, 고분자 구조 설계를 통한 기능성 소재의 창출과 응용이 두드러지며, 나노구조의 정밀 제어와 응용 기술 개발에 중점을 두고 있습니다.
Figures are computed from collected data and may differ slightly.
A novel approach for using conjugated rod-coil materials as a floating gate in the fabrication of nonvolatile photonic transistor memory devices, consisting of n-type Sol-PDI and p-type C10-DNTT, is presented. Sol-PDI and C10-DNTT are used as dual functions of charge-trapping (conjugated rod) and tunneling (insulating coil), while n-type BPE-PDI and p-type DNTT are employed as the corresponding transporting layers. By using the same conjugated rod in the memory layer and transporting channel wit
A high enantiomer-selectivity for the polymerization of rac-lactide was achieved using chiral binaphthol-derived monophosphoric acids as organocatalysts. During the polymerization, d-lactide (DLA) preferentially polymerized via kinetic resolution with the maximum selectivity factor (kD/kL) of 28.3. The selective polymerization of DLA was derived from a dual activation, i.e., monomer activation and chain-end activation.
This Review article details the preparation and encapsulation–release properties of novel amphiphilic hyperbranched polymers with a micellar characteristic as a single molecule, which are referred to as “unimolecular micelles” or “unimolecular nanocapsules”. Amphiphilic hyperbranched polymers consisting of a hydrophilic hyperbranched polycarbohydrate core and hydrophobic shell possess an ability to encapsulate hydrophilic guest molecules and control the release of the encapsulated guest molecule
Perovskite light-emitting diode (PeLED) has been vigorously developed in recent years. As it has demonstrated good performance on the rigid substrates, the next important direction of PeLED is its integration with stretchable components to realize stretchable, responsive device. Here, we describe a facile fabrication of stretchable perovskite light-emissive touch-responsive devices (PeLETDs) by utilizing highly transparent and conductive polyurethane/silver nanowires (PU/AgNWs) as the electrode.
Novel transparent conductive electrodes (TCEs) with copper (Cu)/silver (Ag) core/shell nanofibers (NFs) containing random, aligned, and crossed structures were prepared using a combination of electrospinning (ES) and chemical reduction. The ES process was used to prepare continuous copper nanofibers (Cu-NFs), which were used as core materials and were then immersed in silver ink (Ag ink) to form a protective layer of Ag to protect the Cu-NFs from oxidation. The Ag shell layer protected the Cu-NF
To expand the potential of an organophosphate catalyst, ring-opening polymerization of cyclic esters, cyclic ester-ether, and cyclic carbonate was demonstrated under bulk conditions.
The ring-opening multibranching polymerizations of 1,6-anhydro-β-d-glucopyranose (1) and 1,6-anhydro-β-d-galactopyranose (2) have been studied in order to synthesize hyperbranched polysaccharides. The solution polymerization in propylene carbonate and the bulk polymerization of 1 and 2 using a thermally induced cationic initiator proceeded through a ring-opening reaction and a proton transfer reaction to afford highly water-soluble polysaccharides, i.e., poly-1 and poly-2, respectively. For the
Open papers in the app to read, cite, and organize with AI.