Hyung Mo Jeong
성균관대학교 공과대학 기계공학부 · 공학
이 교수의 연구실은 고성능 에너지 저장 소재의 개발에 초점을 맞추고 있으며, 특히 그래핀, 실리콘, 구리 기반 촉매, 나노결정, 고체전해질 등 다양한 나노소재를 활용한 초용량 축전기 및 리튬이온 배터리 기술을 연구하고 있습니다. 주요 연구 방향은 에너지 밀도 향상과 사이클 수명 향상을 동시에 확보하는 고성능 전극 설계 및 나노구조 제어 기반의 물리화학적 메커니즘 규명입니다. 특히 유연성, 스케일업 가능성, 환경 친화성까지 고려한 실용적 응용 가능성을 추구합니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
Although various carbon nanomaterials including activated carbon, carbon nanotubes, and graphene have been successfully demonstrated for high-performance ultracapacitors, their capacitances need to be improved further for wider and more challenging applications. Herein, using nitrogen-doped graphene produced by a simple plasma process, we developed ultracapacitors whose capacitances (∼280 F/g(electrode)) are about 4 times larger than those of pristine graphene based counterparts without sacrific
Due to its excellent capacity, around 4000 mA h g−1, silicon has been recognized as one of the most promising lithium-ion battery anodes, especially for future large-scale applications including electrical vehicles and utility power grids. Nevertheless, Si suffers from a short cycle life as well as limitations for scalable electrode fabrication. Herein, we report a novel design for highly robust and scalable Si anodes: Si nanoparticles embedded in porous nitrogen-doped carbon spheres (NCSs). The
Abstract Copper (Cu) offers a means for producing value‐added fuels through the electrochemical reduction of carbon dioxide (CO 2 ), i.e., the CO 2 reduction reaction (CO 2 RR), but designing Cu catalysts with significant Faradaic efficiency to C 2+ products remains as a great challenge. This work demonstrates that the high activity and selectivity of Cu to C 2+ products can be achieved by atomic‐scale spacings between two facets of Cu particles. These spacings are created by lithiating CuO x pa
Nanocrystals are promising structures, but they are too large for achieving maximum energy storage performance. We show that rescaling 3-nm particles through lithiation followed by delithiation leads to high-performance energy storage by realizing high capacitance close to the theoretical capacitance available via ion-to-atom redox reactions. Reactive force-field (ReaxFF) molecular dynamics simulations support the conclusion that Li atoms react with nickel oxide nanocrystals (NiO-n) to form lith
Abstract All‐solid‐state battery (ASSB) technology is the focus of considerable interest owing to their safety and the fact that their high energy density meets the requirements of emerging battery applications, such as electric vehicles and energy storage systems (ESSs). In light of this, current research on high‐energy ASSBs harnesses the benefits of solid‐state battery systems by employing anode materials with high energy densities. Owing to the excellent physical safety of solid electrolytes
Abstract Aqueous electrochemical energy storages are of enormous attention due to their high safety and being environmentally friendly, but they must satisfy very challenging standards in energy and power densities over long repeated charging/discharging cycles. Herein, a strategy to realize high‐performance aqueous hybrid capacitors (AHCs) using pseudocapacitive negative and positive electrodes is reported. Polymer chains, which are synthesized by in situ polymerization of polyaniline on reduce
Abstract Realization of safe electrochemical energy storages with high energy density and long cycle life along with the high power density enabling fast charging is a major challenge. Here, a strategy to realize high‐performance aqueous energy storages using porous Mn 3 O 4 (p‐MG) positive and porous Fe 2 O 3 (p‐FG) negative electrodes, where granular nanoclusters composing nanoparticles are produced on graphene through lithiation‐induced conversion and the shortened ion diffusion lengths in p‐
We report that ammonia borane with a high uptake capacity for hydrogen can be encapsulated in a metal-organic framework (MOF) via capillary action, where the MOF functions as a chemical guide to control the hydrogen desorption pathways of ammonia borane by releasing only pure hydrogen, lowering its hydrogen desorption temperature, and suppressing its volumetric expansion during hydrogen desorption.
Zeolitic imidazolate framework-302 (ZIF-302)-embedded cellulose acetate (CA) membranes for osmotic driven membrane process (ODMPs) were fabricated using the phase inversion method. We investigated the effects of different fractions of ZIF-302 in the CA membrane to understand their influence on ODMPs performance. Osmotic water transport was evaluated using different draw solution concentrations to investigate the effects of ZIF-302 contents on the performance parameters. CA/ZIF-302 membranes show
Abstract Most advanced hydrogen evolution reaction (HER) catalysts show high activity under alkaline conditions. However, the performance deteriorates at a natural and acidic pH, which is often problematic in practical applications. Herein, a rhenium (Re) sulfide–transition‐metal dichalcogenide heterojunction catalyst with Re‐rich vacancies (NiS 2 ‐ReS 2 ‐V) has been constructed. The optimized catalyst shows extraordinary electrocatalytic HER performance over a wide range of pH, with ultralow ov
Lithium (Li) metal has attracted significant attention as next-generation anode material owing to its high theoretical specific capacity and low potential. For enabling the practical application of Li-metal as an anode according to energy demands, suppressing dendrite growth by controlling the Li-ion (Li<sup>+</sup>) is crucial. In this study, metal-organic frameworks comprising bipyridinic nitrogen linker (M-bpyN) are proposed as 3-dimensional (3D) Li guiding matrix. The proposed approach creat