김한성 교수
Han‐Sung Kim
연세대학교 화공생명공학과 · 공학
연구실 소개
김한성 교수의 연구실은 에너지 저장 소재 및 전기화학 장치의 핵심 성능 향상을 목표로 하며, 주로 슈퍼커퍼시터와 연료전지 등에서 활용 가능한 고성능 산화물-탄소 복합 소재의 설계 및 합성에 중점을 두고 있습니다. 특히 망가니즈 산화물, 백금 촉매, 질소 doping된 그래프트 펠트, 그리고 다공성 그래핀 등의 나노소재를 활용해 전기화학적 안정성과 고출력 특성을 확보하는 데 기여하고 있습니다. 또한, 탄소 부식 방지 및 촉매 분포 최적화를 위한 신소재 및 표면 기능화 기법 개발에도 주력하고 있습니다.
연구 현황
연구 성과 추이
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
주요 논문
15Mn/Pb and Mn/Ni mixed oxide were prepared at ambient temperature by reduction of KMnO4 with Mn, Pb, and Ni salts. This low-temperature approach provides amorphous structure of the active material. The specific capacitance of pure MnO2 was estimated to be 166 F/g and increased to 210 and 185 F/g for Mn/Ni and Mn/Pb oxides, respectively. The carbon loading was optimized at 20 wt %. Based on a single electrode, the Mn/Ni mixed oxide showed a high rate capability of 3.12 Wh/kg at constant power disc
A new approach to preventing electrochemical carbon corrosion in the cathode of polymer electrolyte membrane fuel cells (PEMFCs) was developed. The addition of 2 wt % IrO(2) (0.016 mg cm(-2)) to the catalyst layer of the cathode was demonstrated to reduce the electrochemical corrosion of carbon by 76% at 1.6 V(NHE) and 70 °C compared with a commercial Pt/C catalyst of the same Pt loading of 0.4 mg cm(-2) and under the same test conditions. The IrO(2) was shown to behave as a catalyst for water e
A novel method for preparing nitrogen-doped graphite felts as positive electrodes in vanadium redox flow batteries was developed and studied. These materials were synthesized by directly coating a thin polypyrrole layer on the graphite felt surface followed by subsequent carbonization in the presence of Co (NGF-Co).
Abstract Herein, we introduce a simple method to prepare hierarchical graphene with a tunable pore structure by activating graphene oxide (GO) with a two-step thermal annealing process. First, GO was treated at 600 °C by rapid thermal annealing in air, followed by subsequent thermal annealing in N 2 . The prepared graphene powder comprised abundant slit nanopores and micropores, showing a large specific surface area of 653.2 m 2 /g with a microporous surface area of 367.2 m 2 /g under optimized
Abstract As an alternative to the oxidative acid treatment, a noncovalent π – π interaction method is employed to deposit Pt electrocatalysts on highly hydrophobic carbon nanofibers (CNFs) for the application of polymer electrolyte membrane (PEM) fuel cells. Three different functionalization agents, namely benzyl mercaptan (BM), 1‐aminopyrene (AP), and 1‐pyrenecarboxylic acid (PCA), are used to functionalize CNFs and the effect of these groups on the electrochemical properties is examined. While
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