極寒環境向けリチウム電池を実現する新電解液戦略を開発 (Winter-Ready Lithium Batteries: Scientists Use “Polarity-Contrast” Electrolyte Strategy to Outsmart Extreme Cold)

2026-05-26 中国科学院(CAS)

中国科学院大連化学物理研究所の陳忠偉教授、羅丹教授、王東東教授らの研究チームは、極低温環境でも高性能を維持できるリチウム金属電池向けの新しい電解液設計戦略「極性コントラスト(polarity-contrast)」を開発した。低温下ではイオン輸送の低下やリチウムイオンの脱溶媒和反応の遅延、電極界面での副反応増加により電池性能が大きく低下する。研究チームは、ジメトキシメタン(DMM)とフルオロエチレンカーボネート(FEC)を組み合わせた電解液により、陰イオン主導型の安定した溶媒和構造を形成し、リチウムイオンの移動と反応速度を向上させた。さらに、LiFを多く含む安定な固体電解質界面(SEI)を形成することで、低温でも均一なリチウム析出と高い可逆性を実現した。その結果、Li||SPANフルセルは−40℃で150サイクル後も初期容量の80%を維持し、Ah級パウチセルも−20℃で50サイクルの安定動作を示した。本成果は、電気自動車や宇宙開発、寒冷地向けエネルギー貯蔵技術の発展に貢献する新たな低温対応電解液設計指針を提供する。

極寒環境向けリチウム電池を実現する新電解液戦略を開発 (Winter-Ready Lithium Batteries: Scientists Use “Polarity-Contrast” Electrolyte Strategy to Outsmart Extreme Cold)
Polarity-contrast electrolyte for low-temperature lithium metal batteries (Image by REN Jingxuan, WANG Dongdong)

<関連情報>

Anion Coordination Transition Enabled by Ion–Dipole Interactions At Low Temperatures

Jingxuan Ren,Dongdong Wang,Yufeng Chen,Renming Liu,Xinli Guo,Dan Luo,and Zhongwei Chen
Journal of the American Chemical Society  Published: April 30, 2026
DOI:https://doi.org/10.1021/jacs.6c03001

Abstract

While constructing anion-involved solvation structures is key to improving electrolyte performance at low temperatures (LTs), conventional strategies that primarily manipulate Li+–solvent interactions present significant challenges. These include weakened anion coordination, impeded ion transport, and aggravated interfacial side reactions, making the realization of effective LT operation elusive. Here, we propose a “polarity-contrast” electrolyte design strategy, which enables the construction of a LT-stable, anion-rich solvation structure through deliberate regulation of anion–solvent interactions. The solvent pairs, dimethoxymethane (DMM) and fluoroethylene carbonate (FEC), which exhibits the lowest and highest maximum electrostatic potential, respectively, were selected for electrolyte engineering. At LTs, the weakened interactions between primary solvent DMM and FSI promote the coordination of solvation of anions. Meanwhile, the coordinated FEC cosolvent enhances ion–dipole interactions with FSI, further anchoring these anions within the solvation sheath. This FSI-dominated solvation environment facilitates the formation of a fluorine-rich solid electrolyte interphase, which in turn enables uniform Li deposition under LT conditions. Therefore, Li||SPAN full cells demonstrate excellent LT performance, including a high areal capacity of 4.5 mAh cm–2 and 150 cycles with 80% retention at −40 °C. Notably, Ah-level Li||SPAN pouch cells demonstrate 50 cycles at −20 °C with exceptional capacity–temperature–lifespan balance, surpassing the most reported LT LMBs.

0402電気応用
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