ArticleNano-micro letters2024
Branch-Chain-Rich Diisopropyl Ether with Steric Hindrance Facilitates Stable Cycling of Lithium Batteries at - 20 °C.
Article in Nano-micro letters, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- A Fluoroether Co-Solvent Engineering Interfacial and Solvation Dynamics for Durable Lithium-Oxygen Batteries.Angewandte Chemie (International ed. in English) · 2026Article
- Tailoring Weakly Coordinating Electrolytes via Orbital-Overlap-Enhanced Dipole-dipole Interactions for Low-Temperature Lithium-Ion Batteries.Advanced materials (Deerfield Beach, Fla.) · 2026Article
- Advanced Design of Three-Dimensional Lithiophilic Carbon-Based Hosts for Anode-Free Lithium Metal Batteries.Nano-micro letters · 2026Review
- Integrating Molecular Dynamics and Machine Learning for Solvation-Guided Electrolyte Optimization in Lithium Metal Batteries.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025Article
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Authors and funding
9 authors.
Funding
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Abstract
Li metal batteries (LMBs) offer significant potential as high energy density alternatives; nevertheless, their performance is hindered by the slow desolvation process of electrolytes, particularly at low temperatures (LT), leading to low coulombic efficiency and limited cycle stability. Thus, it is essential to optimize the solvation structure thereby achieving a rapid desolvation process in LMBs at LT. Herein, we introduce branch chain-rich diisopropyl ether (DIPE) into a 2.5 M Li bis(fluorosulfonyl)imide dipropyl ether (DPE) electrolyte as a co-solvent for high-performance LMBs at - 20 °C. The incorporation of DIPE not only enhances the disorder within the electrolyte, but also induces a steric hindrance effect form DIPE's branch chain, excluding other solvent molecules from Li
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