Taeho Yoon
경희대학교 공과대학 · 공학
Taeho Yoon 교수의 연구실은 리튬이온 배터리의 핵심 소재인 실리콘 음극과 고전압 정극의 안정성 향상을 목표로 하며, SEI(고체 전해질 상호면)의 열적 거동과 전기화학적 거동을 깊이 있게 분석하고 있습니다. 특히, 전해질 구성 성분, 전극 재료의 표면 화학, 전도성 나노소재와의 복합화를 통해 배터리 수명과 효율을 극대화하는 데 초점을 맞추고 있습니다. MOFs와 나노탄소 복합체를 활용한 고성능 전극 소재 개발도 활발히 진행되고 있습니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
Thermal behavior of the solid electrolyte interphase (SEI) on a silicon electrode for lithium ion batteries has been investigated by TGA. In order to provide a better understanding of the thermal decomposition of the SEI on silicon, the thermal decomposition behavior of independently synthesized lithium ethylene dicarbonate (LEDC) was investigated as a model SEI. The model SEI (LEDC) has three stages of thermal decomposition. Over the temperature range of 50–300 °C, LEDC decomposes to evolve CO2
A thorough analysis of the evolution of the voltage profiles of silicon nanoparticle electrodes upon cycling has been conducted. The largest changes to the voltage profiles occur at the earlier stages (> 0.16 V vs Li/Li+) of lithiation of the silicon nanoparticles. The changes in the voltage profiles suggest that the predominant failure mechanism of the silicon electrode is related to incomplete delithiation of the silicon electrode during cycling. The incomplete delithiation is attributed to re
Abstract Next‐generation Li‐ion batteries are being developed with high‐voltage cathodes to maximize their energy and power densities. However, the commercialization of high‐voltage cathodes has been delayed due to the degradations of active materials and electrolytes in long‐term cycling. Recent advances have made significant improvements in these issues; however, the corrosion of Al current collector and its effects on battery performances have not been studied in detail despite its importance
Silicon electrodes were cycled with electrolytes containing different salts to investigate the effect of salt on the electrochemical performance and SEI structure. Comparable capacity retention were observed for the 1.2 M LiPF6, LiTFSI and LiClO4 electrolytes in ethylene carbonate (EC):dimethyl carbonate (DEC), 1:1, but severe fading was observed for the 1.2 M LiBF4 electrolyte. The differential capacity plots and EIS analysis reveals that failure of the 1.2 M LiBF4 electrolyte is attributed to