Journal Article FZJ-2024-02656

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Dual-Protective Artificial Layer on Lithium Metal Anodes for Improved Electrochemical Performance – an in-Depth Morphological and Electrochemical Characterization

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2023
Soc. Pennington, NJ

Meeting abstracts MA2023-01(1), 400 - 400 () [10.1149/MA2023-011400mtgabs]

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Abstract: The energy density of traditional lithium ion batteries (LIB) based on graphite intercalation compounds as negative active material is approaching the theoretical limit and are restricting the increasing demand of high energy battery systems for various mobile and stationary applications.[1] Consequently, the implementation of active materials with high specific energies became prerequisite for future battery technologies. Therein, lithium metal is one of the most promising anode active materials to replace state-of-the-art graphite active materials, due to its high theoretical capacity and low electrode potential.[2]However, poor cycling performance, low Coulombic efficiency, and the uncontrollable Li dendrite growth during lithium electrodeposition/dissolution processes remain as predominant challenges.[3]Several approaches were proposed to eliminate dendrite formation by implementing a mechanically and electrochemically stable artificial solid electrolyte interphase or artificial protective coatings (aPC) by in-situ or ex-situ surface modifications.[4] These designed aPCs should feature an increased and uniform Li-ion flux, mechanical robustness and/or protection against electrolyte decomposition, during substantial volume changes upon electrodeposition/dissolution. However, aPCs fail to support long term cycling stability in lithium metal batteries since they cannot cover all requirements.[5] Therefore, it is crucial to design and understand dual- and multilayer system that address multiple aforementioned requisites.[6]In this contribution, a dual-protective artificial layer is constructed on Li metal by physical vapor deposition consisting of an intermetallic LiZn-layer, providing a uniform Li-ion flux, and an inorganic Li3N-layer, which is electron-blocking, thus reveal surface protective properties. In addition to electrochemical characterization, the Li electrodeposition/dissolution behavior was investigated by cryo-FIB/SEM analysis to unravel the mechanism behind the enhanced cycling stability in symmetrical Li||Li cells and cells with a layered oxide-based positive electrode.[1] R. Schmuch, R. Wagner, G. Hörpel, T. Placke, M. Winter, Nature Energy2018, 3, 267.[2] J. Liu, Z. Bao, Y. Cui, E. J. Dufek, J. B. Goodenough, P. Khalifah, Q. Li, B. Y. Liaw, P. Liu, A. Manthiram, Y. S. Meng, V. R. Subramanian, M. F. Toney, V. V. Viswanathan, M. S. Whittingham, J. Xiao, W. Xu, J. Yang, X.-Q. Yang, J.-G. Zhang, Nature Energy2019, 4, 180.[3] T. Placke, R. Kloepsch, S. Dühnen, M. Winter, Journal of Solid State Electrochemistry2017, 21, 1939.[4] N. Delaporte, Y. Wang, K. Zaghib, Frontiers in Materials2019, 6.[5] D. Lin, Y. Liu, Y. Cui, Nature Nanotechnology2017, 12, 194.[6] S. Lee, K.-s. Lee, S. Kim, K. Yoon, S. Han, M. H. Lee, Y. Ko, J. H. Noh, W. Kim, K. Kang, Science Advances2022, 8, 1.

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Contributing Institute(s):
  1. Helmholtz-Institut Münster Ionenleiter für Energiespeicher (IEK-12)
Research Program(s):
  1. 1221 - Fundamentals and Materials (POF4-122) (POF4-122)

Appears in the scientific report 2024
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 Record created 2024-04-11, last modified 2025-02-03



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