4.8 Article

Visualizing Lithium Distribution and Degradation of Composite Electrodes in Sulfide-based All-Solid-State Batteries Using Operando Time-of-Flight Secondary Ion Mass Spectrometry

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 1, Pages 580-586

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.0c18505

Keywords

all-solid-state battery; composite electrode; degradation; TOP-SIMS; operando

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This study utilizes operando time-of-flight secondary ion mass spectrometry to observe Li distribution and degradation in composite cathodes during cell operation. The nonuniform reaction of NCA particles during charge and discharge cycles was successfully visualized, while degradation at the NCA/LPS interface was also investigated. The technique provides insights into the optimized structures of composite electrodes and mechanisms of interfacial degradation.
Understanding the electrochemical reactions taking place in composite electrodes during cell cycling is essential for improving the performance of all-solid-state batteries. However, comprehensive in situ monitoring of Li distribution, along with measurement of the evolution of degradation, is challenging because of the limitations of the characterization techniques commonly used. This study demonstrates the observation of Li distribution and degradation in composite cathodes consisting of LiNi0.8Co0.15Al00.5O2 (NCA) and 75Li(2)S center dot 25P(2)S(5) (LPS) during cell operation using operando time-of-flight secondary ion mass spectrometry. The evolution of the nonuniform reaction of NCA particles during charge and discharge cycles was successfully visualized by mapping fragments containing Li. Furthermore, degradation of the NCA/LPS interface was investigated by mapping POx- and SO(x)(- )fragments, which are related to the solid electrolyte interphase. We found that during the charge-discharge cycle and application of a high-voltage stress to the composite electrodes, the PO3- and PO3- fragments increased monotonically, whereas the SO3- fragment exhibited a reversible increase-decrease behavior, implying the existence of a redox-active component at the NCA/LPS interface. The demonstrated technique provides insights into both the optimized structures of composite electrodes and the underlying mechanisms of interfacial degradation at active material/solid electrolyte interfaces.

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