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Jung-Hyun Kim

Publications and source records attributed to Jung-Hyun Kim.

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Effect of Stress and Surface Roughness on Electrodeposition in All-Solid-State Batteries: A Computational Investigation

All-solid-state batteries (ASSBs) promise high energy density and enhanced safety, but their development is hindered by instability and incompatibility at solid-solid interfaces. In Li-metal ASSBs, lithium penetration occurs despite stiff ceramic electrolytes via grain boundaries, often initiated by minor Li/SE interfacial irregularities. Here we introduce a two-dimensional continuum model with electro-chemo-mechanical coupling to investigate interfacial current distribution in Li ASSBs with surface-roughened argyrodite electrolyte under stack pressures and applied current density. Our theoretical analysis and simulation studies highlight the critical role of mechanical stress in interfacial current distribution. We find that prominent stress variations around elongated surface protrusions are the key to nonuniform Li deposition, without which Li deposition becomes uniform even on a rough surface. Moreover, our parametric study elucidates that stress effects dominate the overpotential and current distribution under low interfacial current density to exchange current density ratios, otherwise the high interfacial resistance due to surface-roughness-induced interfacial area becomes dominant. With these insights, we also discuss the potential of engineering artificial interlayers to modulate interfacial current distributions, offering guidance for improving the long-term performance and reliability of ASSBs.

cond-mat.mtrl-sci

Phase-Field Simulation of Dendrite Evolution in All-Solid-State Sodium Batteries during Cycling

Dendrite growth during cycling remains a critical challenge for all-solid-state batteries (SSBs), limiting the full realization of their inherent safety and high energy density. In particular, the mechanisms of continuous dendrite penetration during charge-discharge cycling remain poorly understood and are difficult to characterize experimentally. This study applies a phase-field model, informed by density functional theory calculations, to rationalize and visualize the dendrite penetration behaviors during cycling in sodium (Na) SSBs with pure Na or Na-Sb alloy anodes and polycrystalline Na$_3$SbS$_4$ electrolyte. We show that dendrite stripping is intrinsically asymmetric with respect to plating due to grain boundary geometry, leading to the formation of isolated Na metal that persists between cycles. This residual Na metal becomes kinetically stabilized at grain-boundary junctions and is readily reactivated during subsequent plating, thereby accelerating and amplifying dendrite penetration. We further investigate the effects of applied voltage, solid-electrolyte microstructure, and anode chemistry on this phenomenon. These findings establish isolated Na metal as a key contributor for continued dendrite propagation in Na SSBs and provide design principles for stabilizing anode/electrolyte interfaces in Na SSBs.

cond-mat.mtrl-sci