Kyoto University · 화학
칸아모리 켄요시 교수의 연구실은 유기-무기 하이브리드 아에로겔 소재의 설계 및 응용에 중점을 두고 있으며, 특히 고유연성, 초절연성, 기계적 내구성을 동시에 확보한 신소재 개발을 핵심 과제로 삼고 있습니다. 단일 전구체를 이용한 용액-젤 공정과 라디칼 중합을 접목한 간편한 합성 전략을 통해 다양한 기능성을 지닌 아에로겔을 대량으로 제조하는 데 성공했으며, 스마트 센서, 열 insulation, 유연 전자소자 등 응용 분야로의 확장을 추진하고 있습니다. 특히, 고분자 네트워크와 실리카 구조를 이중으로 결합한 이중 교차구조 설계로 기존 아에로겔의 취약점을 극복한 혁신적 연구가 두드러집니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
Transparent organic–inorganic hybrid aerogels and xerogels are prepared by using a sol–gel synthesis from a single trifunctional precursor, methyltrimethoxysilane (see figure). Obtained aerogels show a reversible shrinkage–recovery response against uniaxial compression. Aerogel-like xerogels are successfully obtained by evaporation drying under ambient pressure because the gels recover from the temporal shrinkage caused by the capillary force of a drying solvent. Pore properties and nanotextures
A facile yet versatile approach to transparent, highly flexible, machinable, superinsulating organic–inorganic hybrid aerogels is presented. This method involves radical polymerization of a single alkenylalkoxysilane to obtain polyalkenylalkoxysilane, and subsequent hydrolytic polycondensation to afford a homogeneous, doubly cross-linked nanostructure consisting of polysiloxanes and hydrocarbon polymer units. Here we demonstrate that novel aerogels based on polyvinylpolysilsesquioxane (PVPSQ), p
Aerogels are porous materials but show poor mechanical properties and limited functionality, which significantly restrict their practical applications. Preparation of highly bendable and processable aerogels with multifunctionality remains a challenge. Herein we report unprecedented superflexible aerogels based on polyvinylpolydimethylsiloxane (PVPDMS) networks, PVPDMS/polyvinylpolymethylsiloxane (PVPMS) copolymer networks, and PVPDMS/PVPMS/graphene nanocomposites by a facile radical polymerizat
Rigid macroporous poly(divinylbenzene) monoliths with good mechanical and thermal stability and possessing a well-defined bicontinous structure (see figure) are synthesized using living radical polymerization and a polymeric phase separator. The macropore size and volume can be independently tuned by varying the starting compositions of the mixtures. Scale bars represent 20 μm, a–d show increasing polydimethylsiloxane concentration.
Aerogels are attracting increasing attention due to their high thermal insulation ability as well as unique properties such as high porosity, surface area, and transparency. However, low mechanical strengths, originating from their unique porous structure, impede handling, formability, mass production, and extended applications. This minireview focuses on the strengthening of aerogels by several organic-inorganic hybridization strategies. In particular, successful strengthening methodologies, wh
Recently, many efforts have been made to develop various smart sensors. However, achieving flexible multifunctional sensors combining excellent sensing of temperature, strain, and pressure with a single material is still challenging. Here, we report unprecedented superhydrophobic ultraflexible reduced graphene oxide (rGO)/polyorganosiloxane aerogels and high-performance multifunctional temperature/strain/pressure sensors based on these aerogels. GO nanosheets are first cross-linked and reduced w
In recent decades, aerogels have attracted tremendous attention in academia and industry as a class of lightweight and porous multifunctional nanomaterial. Despite their wide application range, the low mechanical durability hinders their processing and handling, particularly in applications requiring complex physical structures. "Mechanically strengthened aerogels" have emerged as a potential solution to address this drawback. Since the first report on aerogels in 1931, various modified synthesi
Structural deformation of phase-separated methylsiloxane gel under the influence of a surface has been studied. Competitive wetting of siloxane gel phase on a surface during phase formation is found to significantly affect the final morphology in a confined space. When the spinodal wavelength is sufficiently shorter than the size of the available space, a uniform bicontinuous structure forms in confined geometry. However, gel skeletons in the vicinity of a surface are elongated with decreasing s
Macroporous cross-linked organic polymer monoliths with well-defined bicontinuous structure have been synthesized from 1,3-glycerol dimethacrylate (GDMA) in a solvent utilizing atom transfer radical polymerization (ATRP). With the addition of an adequate polymeric agent, poly(ethylene oxide) (PEO), spinodal decomposition was induced in the course of polymerization of GDMA. A homogeneous gelation by ATRP solidified the temporal biphasic morphology of spinodal decomposition, resulting in well-defi
The synthesis of highly crystalline macro-meso-microporous monolithic Cu3(btc)2 (HKUST-1; btc(3-) = benzene-1,3,5-tricarboxylate) is demonstrated by direct conversion of Cu(OH)2-based monoliths while preserving the characteristic macroporous structure. The high mechanical strength of the monoliths is promising for possible applications to continuous flow reactors.
Aerogels have attracted great interest for their unique properties, but their mechanical brittleness and poor functionality highly limit their practical applications. Herein, we report unprecedented superelastic multifunctional aminosilane-crosslinked reduced graphene oxide (AC<b>-</b>rGO) aerogels that are prepared via a facile and scalable strategy involving simultaneous crosslinking and reducing of graphene oxide nanosheets with different kinds of aminosilanes via C-N coupling and hydrolytic