Journal
ACS APPLIED MATERIALS & INTERFACES
Volume 15, Issue 19, Pages 23051-23057Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsami.3c00462
Keywords
all-solid-state battery; sulfide-based solid electrolyte; degradation mechanism; interfacial analysis; electron diffraction; X-ray absorption spectroscopy
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Interfacial engineering of sulfide-based solid electrolyte/lithium transition-metal oxide active materials in all-solid-state battery cathodes is essential for optimizing cell performance. Surface coating with a buffer layer, such as LiNbO3, is a typical method, but it may not be sufficient for harsh environments. This study investigates the interfacial degradation mechanism in half cells using Li6PS5Cl/LiNbO3-coated LiNi0.5Co0.2Mn0.3O2 cathode mixture. The results suggest that the degradation of the interfacial solid electrolyte region strongly impacts cell performance.
Interfacial engineering of sulfide-based solid electrolyte/lithiumtransition-metal oxide active materials in all-solid-state battery cathodes is vital for cell performance parameters, such as high-rate charge/discharge, long lifetime, and wide temperature range. A typical interfacial engineering method is the surface coating of the cathode active material with a buffer layer, such as LiNbO3. However, cell performance reportedly degrades under harsh environments even with a LiNbO3 coating, such as high temperatures and high cathode potentials. Therefore, we investigated the interfacial degradation mechanism focusing on the solid electrolyte side for half cells employing the cathode mixture of argyrodite-type Li6PS5Cl/LiNbO3-coated LiNi0.5Co0.2Mn0.3O2 exposed at 60 degrees C and 4.25 and 4.55 V vs Li/Li+ using transmission electron microscopy/electron diffraction (TEM/ ED) and X-ray absorption spectroscopy (XAS). The TEM/ED results indicated that the ED pattern of the argyrodite structure disappeared and changed to an amorphous phase as the cells degraded. Moreover, the crystal phases of LiCl and Li2S appeared simultaneously. Finally, XAS analysis confirmed the decrease in the PS4 units of the argyrodite structure and the increase in local P-S-P domains with delithiation from the interfacial solid electrolyte, corresponding to the TEM/ED results. In addition, the formation of P-O bonds was confirmed during degradation at higher cathode potentials, such as 4.55 V vs Li/Li+. These results indicate that the degradation of this interfacial region determines the cell performance.
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