김주형 교수
Joohyung Kim
KAIST 김재철AI대학원 · 공학
연구실 소개
김주형 교수의 연구실은 리튬이on과 나트륨이온 배터리, 리튬-황 배터리 등 차세대 고성능 에너지 저장 소재를 중심으로 연구를 진행하고 있습니다. 특히, 나노구조적 복합재료(예: GeS₂/rGO, Sn-S/그래핀 등)를 설계하여 고용량·고안정성 양극 소재의 개발에 주력하고 있으며, 전기화학적 안정성과 사이클 수명 향상을 위한 나노구조 제어 및 도핑 기법에 초점을 맞추고 있습니다. 또한, 고가의 플라티넘을 대체할 수 있는 내구성 있는 3차원 나노포orous 박막 전기촉매 개발도 함께 진행하고 있습니다.
연구 현황
연구 성과 추이
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
주요 논문
15Abstract Sodium ion batteries (NIBs) have become attractive promising alternatives to lithium ion batteries in a broad field of future energy storage applications. The development of high‐performance anode materials has become an essential factor and a great challenge toward satisfying the requirements for NIBs, advancement. This work is the first report on GeS 2 nanocomposites uniformly distributed on reduced graphene oxide (rGO) as promising anode materials for NIBs prepared via a facile hydro
Abstract To date, the possible depletion of lithium resources has become relevant, giving rise to the interest in Na‐ion batteries (NIBs) as promising alternatives to Li‐ion batteries. While extensive investigations have examined various transition metal oxides and chalcogenides as anode materials for NIBs, few of these have been able to utilize their high specific capacity in sodium‐based systems because of their irreversibility in a charge/discharge process. Here, the mixed Sn–S nanocomposites
Rechargeable lithium-ion batteries (LIBs) have been rapidly expanding from IT based applications to uses in electric vehicles (EVs), smart grids, and energy storage systems (ESSs), all of which require low cost, high energy density and high power density.The increasing demand for LIBs has resulted in increasing price of the lithium source, which is a major obstacle to wider application.To date, the possible depletion of lithium resources has become relevant, giving rise to the interest in Na-ion
Abstract The exploitation of state‐of‐the‐art Pt/C electrocatalysts for polymer electrolyte membrane fuel cells (PEMFCs) is mostly limited, due to high Pt loading and durability issues caused by electrochemical instability of the carbon support in high potential regimes. In this study, the authors report that high‐compressive 3D Pt nanostructured thin films can considerably increase the catalytic activity and electrochemical durability of electrocatalysts under PEMFC device operating conditions.
The layered δ‐MnO 2 (dMO) is an excellent cathode material for rechargeable aqueous zinc‐ion batteries owing to its large interlayer distance (~0.7 nm), high capacity, and low cost; however, such cathodes suffer from structural degradation during the long‐term cycling process, leading to capacity fading. In this study, a Co‐doped dMO composite with reduced graphene oxide (GC‐dMO) is developed using a simple cost‐effective hydrothermal method. The degree of disorderness increases owing to the het
Lithium-sulfur (Li−S) batteries are attracting significant research attention because of their high theoretical energy density (2500 Wh kg−1) and excellent economic feasibility. However, commercialization has proven difficult owing to their low electronic conductivity and the dissolution of lithium polysulfide (Li2Sx; x=1–8). In particular, lithium polysulfide dissolution is known to be caused by high-order polysulfide generated at the start of the discharge process. Thus, the control of this fa
High Resolution Image Download MS PowerPoint Slide Li–S batteries have received significant attention owing to their high energy density, nontoxicity, low cost, and eco-friendliness. However, the dissolution of lithium polysulfide during the charge/discharge process and its extremely low electron conductivity hinder practical applications of Li–S batteries. Herein, we report a sulfur-infiltrated carbon cathode material with a spherical morphology and conductive polymer coating. The material was
Abstract Aqueous Zn‐ion batteries (AZIBs) are promising energy‐storage devices owing to their exceptional safety, long cycle life, simple production, and high storage capacity. Manganese oxides are considered potential cathode materials for AZIBs, primarily because of their safety, low cost, simple synthesis, and high storage capacity. However, MnO 2 ‐based cathodes tend to deteriorate structurally during long‐term cycling, which reduces their reversible capacity. In this study, an advanced α‐Mn
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