Abstract
The use of solid electrolytes in lithium batteries promises to increase their power and energy density, but several challenges still need to be overcome. One critical issue is capacity-fading, commonly ascribed to various degradation reactions in the composite cathode. Chemical, electrochemical as well as chemo-mechanical effects are discussed to be the cause, yet no clear understanding of the mechanism of capacity fading is established. In this work, a model is proposed to interpret the low-frequency impedance of the cathode in terms of lithium diffusion within an ensemble of LiNi 1− x−y Co x Mn y O 2 (NCM) cathode active material particles with different particle sizes. Additionally, an electrochemical technique is developed to determine the electrochemically active mass in the cathode, based on the estimation of the state-of-charge via open circuit potential-relaxation. Tracking the length of lithium diffusion pathways and active mass over 40 charge-discharge cycles demonstrates that the chemo-mechanical evolution in the composite cathode is the major cause for cell capacity fading. Finally, it is shown that single-crystalline NCM is far more robust against chemo-mechanical degradation compared to polycrystalline NCM and can maintain a high cycling stability.
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CITATION STYLE
Conforto, G., Ruess, R., Schröder, D., Trevisanello, E., Fantin, R., Richter, F. H., & Janek, J. (2021). Editors’ Choice—Quantification of the Impact of Chemo-Mechanical Degradation on the Performance and Cycling Stability of NCM-Based Cathodes in Solid-State Li-Ion Batteries. Journal of The Electrochemical Society, 168(7), 070546. https://doi.org/10.1149/1945-7111/ac13d2
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