Entropy-Driven Hybrid Gel Electrolyte Enables Practical High-Voltage Lithium Metal Batteries.

ACS Appl Mater Interfaces

State Key Laboratory of Powder Metallurgy, Central South University, Changsha, Hunan 410083, PR China.

Published: July 2024

AI Article Synopsis

  • Electrolyte engineering significantly improves lithium metal batteries (LMBs) by enhancing their performance with high-voltage cathodes and limited lithium anodes.
  • A new hybrid gel electrolyte, made by adding insoluble Li salts to standard electrolytes and using thermal polymerization, creates a more effective Li-ion solvation structure.
  • This innovative electrolyte promotes faster ionic transport and better Li morphology, leading to sustained performance in LMBs, demonstrated through extensive testing in both small and large battery configurations.

Article Abstract

Electrolyte engineering plays a crucial role in enhancing the performance of lithium metal batteries (LMBs) featuring high-voltage cathodes and limited lithium anodes, thereby unlocking their potential for high-energy electrochemical storage. Herein, an entropy-driven hybrid gel electrolyte with enhanced diversity in Li-ion solvation structures is designed by incorporating substantial amounts of insoluble LiPOF and LiNO salts into LiPF-based carbonate electrolytes, followed by thermal polymerization. Specifically, the Li solvation structures are modulated via ionophilic NO and POF to generate an anion-rich solvation sheath and thus promote anion reduction at the electrode-electrolyte interface. The interfaces enriched in anion-derived inorganic components facilitate rapid ionic transport, thus enabling smooth and dense Li morphology and ultimately enhancing the electrochemical performance of LMBs. As a result, this high-hybrid gel electrolyte confers LMBs employing high-voltage NCM cathodes, as demonstrated by sustained performance in both coin-cell (500 cycles at 4.5 V) and Ah-level pouch cell configurations under practical conditions (60 cycles, N/P: 1.92, and E/C: 2.0 g Ah ).

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http://dx.doi.org/10.1021/acsami.4c06826DOI Listing

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