최종현 교수

Abstract Ni‐rich layered LiNi x Co y Mn 1− x − y O 2 (LNCM) with Ni content over >90% is considered as a promising lithium ion battery (LIB) cathode, attributed by its low cost and high practical capacity. However, Ni‐rich LNCM inevitably suffers rapid capacity fading at a high state of charge due to the mechanochemical breakdown; in particular, the microcrack formation has been regarded as one of the main culprits for Ni‐rich layered cathode failure. To address these issues, Ni‐rich layered

Epidermal electronics are extensively explored as an important platform for future biomedical engineering. Epidermal devices are typically fabricated using high‐cost methods employing complex vacuum microfabrication processes, limiting their widespread potential in wearable electronics. Here, a low‐cost, solution‐based approach using electroconductive reduced graphene oxide (RGO) sheets on elastic and porous poly(dimethylsiloxane) (PDMS) thin films for multifunctional, high‐performance, graphene

The suppression of oxygen oxidation is proposed as the critical origin of Zr doping on LiNi 0.92 Co 0.04 Mn 0.04 O 2 layered oxide LIB cathode material.

Tin phosphide (Sn₄P₃) has emerged as an anode for sodium ion batteries (SIBs) due to its high reversible capacity and low redox potential.

Ni-rich layered LiNi_1-x-y Co_x Mn_y O₂ systems are the most promising cathode materials for high energy density Li-ion batteries (LIBs). However, Ni-rich cathode materials inevitably suffer from rapid capacity fading and poor rate capability owing to structural instability and unstable surface side reactions. Zr doping has proven to be an effective method to enhance the cycle and rate performances by stabilizing the structure and increasing the Li<sup>+<

Molybdenum disulfide (MoS₂), a well-known solid lubricant for low friction surface coatings, has recently drawn attention as an analogue two-dimensional (2D) material beyond graphene. When patterned to produce vertically grown, nanoflower-structures, MoS₂ shows promise as a functional material for hydrogen evolution catalysis systems, electrodes for alkali metal-ion batteries, and field-emission arrays. Whereas the wettability of graphene has been substantially investigated

The transfer of graphene from its growth substrate to a target substrate has been widely investigated for its decisive role in subsequent device integration and performance. Thus far, various reported methods of graphene transfer have been mostly limited to planar or curvilinear surfaces due to the challenges associated with fractures from local stress during transfer onto three-dimensional (3D) microstructured surfaces. Here, we report a robust approach to integrate graphene onto 3D microstruct

In this work, nitrogen-doped activated carbon was produced from waste coffee powder using a two-step chemical activation process. Nitrogen doping was achieved by treating the coffee powder with melamine, prior to chemical activation. The produced nitrogen-doped carbon resulted in a very high surface area of 1824 m2/g and maintained a high graphitic phase as confirmed by Raman spectroscopy. The elemental composition of the obtained coffee-derived carbon was analyzed using X-ray photoelectron spec

SnO₂-Fe₂O₃-C triple-shell hollow nano-spheres are fabricated by combining the template-based sol-gel coating technique and hydrothermal method, and their electrochemical performance as an anode for lithium ion batteries (LIBs) is investigated, particularly focusing on their structural stability and long term cyclability. To accomplish this, same-sized SnO₂ solid spheres, Fe₂O₃ solid spheres, SnO₂-Fe₂O<sub>3</

A new P2-type Na0.7(Ni0.6Co0.2Mn0.2)O2 was prepared via co-precipitation and its electrochemical properties as a cathode for sodium ion batteries were compared with those of O3-type Na(Ni0.6Co0.2Mn0.2)O2, focusing on phase stability and cycling performance. The P2-type delivered a high capacity of 108 mA h g-1 after 300 cycles at 2C.