电解质
电化学
离子液体
阴极
锂(药物)
化学工程
材料科学
碳酸丙烯酯
碳酸盐
石墨
氧气
无机化学
离子键合
离子
电极
化学
催化作用
冶金
有机化学
物理化学
内分泌学
工程类
医学
作者
Lennart Wichmann,Jan‐Paul Brinkmann,Mingzeng Luo,Yong Yang,Martin Winter,Richard Schmuch,Tobias Placke,Aurora Gómez-Martín
标识
DOI:10.1002/batt.202200075
摘要
Abstract Lithium‐rich disordered rocksalts (DRX) are a promising class of cathode materials for high‐energy lithium ion batteries (LIBs) and lithium metal batteries (LMBs) due to the high initial specific capacities (>200 mAh g −1 ) as well as flexible chemical composition. However, challenges concerning severe capacity fade and voltage decay upon cycling at high cut‐off voltages are still to be overcome. Moreover, state‐of‐the‐art carbonate‐based electrolytes can be decomposed by reactive oxygen species released by DRX materials during cycling. In this work, the electrochemical performance of Li 1.25 Fe 0.5 Nb 0.25 O 2 (LFNO) || Li LMB and LFNO || graphite LIB cells is compared for a conventional, carbonate‐based electrolyte and the solvate ionic liquid (SIL) [Li(G3)][TFSI] (G3: triethyleneglycoldimethylether). Cycle life is notably improved by the chemically more stable ionic liquid electrolyte, as the anionic redox activity of LFNO is prolonged compared to the carbonate‐based cells. This work represents an important step toward an improved cycle life of DRX cathodes.
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