| Home > Workflow collections > In process > On the Role of Reaction Current Distribution to Attain Competitive Solid‐State Batteries |
| Journal Article | FZJ-2026-02160 |
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2026
Wiley-VCH
Weinheim
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Please use a persistent id in citations: doi:10.1002/anie.2890151
Abstract: Competitive solid-state batteries must allow for high areal loadings ($> 5 mAh⋅cm^{−2}$) and fast charging rates (> 2 C). Nevertheless,current academic research mainly focuses on systems with smaller loadings and lower C-rates. For established cell chemistries afocus shift is required when aiming toward practical application. Increasing the areal active material content and C-rates is oftenaccompanied by charge transport limitations in the electrodes. In this work, the role of reaction current distribution in compositeelectrodes is highlighted as solid-state batteries advance toward higher areal loadings and charging rates. Using NCM-argyrodite composites as a case study, we revisit Newman’s porous electrode theory in the context of solid-state batteries to rationalizecomposite electrode cycling performance. Further, operando high-energy X-ray diffraction is employed to track lithiation statesof NCM across the electrode as a function of state of charge. The results reveal significant improvements in reaction currentdistribution, when employing faster conducting $Li _{5.5} PS_{4.5} Cl_{1.5}$ instead of conventional $Li_6 PS_5 Cl$, underscoring the need for fastlithium-ion conductors to enable competitive solid-state batteries. This work demonstrates the importance of precisely controlling electrode composition to balance ionic and electronic transport, ensuring homogeneous utilization of the active material andmitigating local strain and overcharging.
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