Ji‐Hun Seo
고려대학교 Materials Science · 재료과학
이 교수의 연구실은 주로 고분자 상호작용과 나노구조 재료를 기반으로 한 신소재 개발에 초점을 맞추고 있습니다. 특히, 폴리로타엑산 기반의 초분자 구조를 활용해 세포 반응 조절, 생체재료의 기계적·전기적 성능 향상, 그리고 고분자 전도체 및 유연 전도성 엘라스토머의 내구성 향상에 기여하고 있습니다. 연구는 생체적응성 재료, 스마트 재료, 그리고 에너지 저장 및 전도성 소재의 혁신적 설계를 목표로 하고 있습니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
The rapid response of integrin β1 molecules to an RGD peptide on a dynamic polyrotaxane surface was successfully induced. As a result, RGD peptides introduced on a highly dynamic cyclodextrin molecule enhanced the frequency of contact with specific integrin molecules on the cell membrane at the early stage of material-cell interactions.
Polymer surfaces with a wide range of hydrated surface mobility are developed by a simple deposition method with supramolecular block copolymers. The morphologies of adhering stem cells are greatly dependent on the surface mobility of polymers, and this induces significant changes in the cytoskeletal signaling pathway to direct the downstream stem cell differentiation.
Abstract Polymer plastic crystal electrolytes (PPCEs) have garnered significant attention for addressing the challenges associated with succinonitrile (SN), including its inadequate mechanical properties and side reactions with electrodes. However, a comprehensive investigation of the influence of the molecular structure of the polymer network on the states of SN within the network and its subsequent impact on ionic conductivities remains largely unexplored. To shed light on this critical aspect
A UV-cleavable supramolecular cross-linker was designed to effectively control the mechanical strength of photocurable resin plastics. The resin monomer-soluble polyrotaxane (PRX) cross-linker was synthesized by introducing a hydrophobic <i>n</i>-butyl group and a cross-linkable methacrylate group in α-cyclodextrin threading to a polyethylene glycol containing UV-cleavable end groups. The UV-cleavable PRX cross-linker was completely dissolved in 2-hydroxyethytl methacrylate (HEMA) and camphorqui
A conductive elastomer is stretchable and can exhibit ionic or electrical conductivity. However, its resistivity increases exponentially when a small number of strain changes are provided owing to irreversible internal deformation. Therefore, securing a wide range of linearity in the resistance–strain relationship is an important topic in the preparation of highly reliable conductive elastomers. Herein, an ionic conductive elastomer is prepared using 2-methoxyethyl acrylate (MA) and a molecular
The network structures of liquid crystal elastomers (LCEs) are crucial to impart rubbery behavior to LCEs and enable reversible actuation. Most LCEs developed to date are covalently linked, implying that the cross-links are fixed at a particular position. Herein, we report a new class of LCEs integrating polyrotaxanes (PRs) as slidable cross-links (PR-LCEs). Interestingly, the incorporation of a low loading (0.3-2.0 wt %) of the PR cross-linkers to the LCE causes a significant impact on various
Increasing molecular mobility of hydrated polyrotaxane (PRX)-coated surfaces was effective to promote the differentiation of mouse induced pluripotent stem cells (iPS cells) into cardiomyocytes.