東京大学 · Materials Science
Vincent Tung 교수의 연구실은 나노구조 탄소 소재와 2차원 물질을 중심으로 한 혁신적 소재 개발에 주력하고 있습니다. 그래핀, 탄소나노튜브, MXene, MoS₂ 등 다양한 나노소재를 복합화하여 전도성, 기계적 강도, 유연성 및 기능성을 동시에 확보한 나노복합재료를 설계하고 있으며, 특히 수용액 기반의 친환경적 공정을 통해 전자소자 및 에너지 장치에 응용 가능한 스케일러블 소재 기술을 개발하고 있습니다. 이는 태양전지, 생체통합 전자기기, 에너지 저장 장치 등 다양한 분야에서의 실용화를 견인하고 있습니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
We report the formation of a nanocomposite comprised of chemically converted graphene and carbon nanotubes. Our solution-based method does not require surfactants, thus preserving the intrinsic electronic and mechanical properties of both components, delivering 240 ohms/square at 86% transmittance. This low-temperature process is completely compatible with flexible substrates and does not require a sophisticated transfer process. We believe that this technology is inexpensive, is massively scala
Skin-mountable microelectronics are garnering substantial interest for various promising applications including human-machine interfaces, biointegrated devices, and personalized medicine. However, it remains a critical challenge to develop e-skins to mimic the human somatosensory system in full working range. Here, we present a multifunctional e-skin system with a heterostructured configuration that couples vinyl-hybrid-silica nanoparticle (VSNP)-modified polyacrylamide (PAM) hydrogel with two-d
Heterojunctions between different graphitic nanostructures, including fullerenes, carbon nanotubes and graphene-based sheets, have attracted significant interest for light to electrical energy conversion. Because of their poor solubility, fabrication of such all-carbon nanocomposites typically involves covalently linking the individual constituents or the extensive surface functionalization to improve their solvent processability for mixing. However, such strategies often deteriorate or contamin
Graphene oxide (GO) can be viewed as a two-dimensional, random diblock copolymer with distributed nanosize graphitic patches and highly oxidized domains, thus capable of guiding the assembly of other materials through both π-π stacking and hydrogen bonding. Upon mixing GO and conducting polymer poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) in water, a dispersion with dramatically increased viscosity is obtained, which turns into sticky thin films upon casting. Surprisingly,
Metallic molybdenum disulfide (MoS<sub>2</sub>), <i>e</i>.<i>g</i>., 1T phase, is touted as a highly promising material for energy storage that already displays a great capacitive performance. However, due to its tendency to aggregate and restack, it remains a formidable challenge to assemble a high-performance electrode without scrambling the intrinsic structure. Here, we report an electrohydrodynamic-assisted fabrication of 3D crumpled MoS<sub>2</sub> (c-MoS<sub>2</sub>) and its formation of a
Abstract The emerging molybdenum disulfide (MoS 2 ) offers intriguing possibilities for realizing a transformative new catalyst for driving the hydrogen evolution reaction (HER). However, the trade‐off between catalytic activity and long‐term stability represents a formidable challenge and has not been extensively addressed. This study reports that metastable and temperature‐sensitive chemically exfoliated MoS 2 (ce‐MoS 2 ) can be made into electrochemically stable (5000 cycles), and thermally r
Design and development of an efficient, nonprecious catalyst with structural features and functionality necessary for driving the hydrogen evolution reaction (HER) in an alkaline medium remain a formidable challenge. At the root of the functional limitation is the inability to tune the active catalytic sites while overcoming the poor reaction kinetics observed under basic conditions. Herein, we report a facile approach to enable the selective design of an electrochemically efficient cobalt phosp
In this perspective, we describe a new type of photovoltaic all-carbon composites, in which single walled carbon nanotubes (SWCNTs) and fullerenes are directly co-assembled and processed in water using graphene oxide (GO) as a surfactant. Solar cells made with C60/SWCNTs/reduced GO as the active layer and an additional evaporated C60 blocking layer yield a power conversion efficiency of 0.21%, which can be significantly increased to 0.85% by replacing C60 with the better absorber C70. These resu
Atomically thin 2D films and their van der Waals heterostructures have demonstrated immense potential for breakthroughs and innovations in science and technology. Integrating 2D films into electronics and optoelectronics devices and their applications in electronics and optoelectronics can lead to improve device efficiencies and tunability. Consequently, there has been steady progress in large-area 2D films for both front- and back-end technologies, with a keen interest in optimizing different g
Water-processed GO:SWCNT thin films have been used as interfacial layers to serially connect two P3HT:PCBM bulk heterojunction solar cells in both regular and inverted structures. The resulting tandem architecture produces a higher VOC, reaching by average 84% of the ideal value (i.e., the sum of VOC of both subcells) for the regular structure, and by average 80% for the inverted structure, respectively.
Conjugated polyaniline can impact the field of water filtration membranes due to its hydrophilic and antibacterial nature, facile and inexpensive synthesis procedure, heat and acid tolerance, and unique doping/dedoping chemistry. However, the gelation effect, its rigid backbone, and the limited hydrophilicity of polyaniline severely restrict the adaptability to membranes and their antifouling performance. This Mini Review summarizes important works of polyaniline-related ultrafiltration membrane
Abstract Tin (II) selenide (SnSe) is an emerging 2D material with many intriguing properties, such as record‐high thermoelectric figure of merit (ZT), purely in‐plane ferroelectricity, and excellent nonlinear optical properties. To explore these functional properties and related applications, a crucial step is to develop controllable routes to synthesize large‐area, ultrathin, and high‐quality SnSe crystals. Physical vapor deposition (PVD) constitutes a reliable method to synthesize 2D SnSe, how
2D transition metal dichalcogenide (TMD) layered materials are promising for future electronic and optoelectronic applications. The realization of large-area electronics and circuits strongly relies on wafer-scale, selective growth of quality 2D TMDs. Here, a scalable method, namely, metal-guided selective growth (MGSG), is reported. The success of control over the transition-metal-precursor vapor pressure, the first concurrent growth of two dissimilar monolayer TMDs, is demonstrated in conjunct