Lin Yuansheng, Zhang Xiangxin, Liu Yongchuan, Wang Qichao, Lin Changxin, Chen Sujing, Zhang Yining
College of Chemistry, Fuzhou University, Fuzhou 350108, PR China; Key Laboratory of Optoelectronic Materials Chemistry and Physics, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, 155 Yangqiao Road West, Fuzhou, Fujian 350002, PR China.
Key Laboratory of Optoelectronic Materials Chemistry and Physics, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, 155 Yangqiao Road West, Fuzhou, Fujian 350002, PR China.
J Colloid Interface Sci. 2022 Dec 15;628(Pt B):14-23. doi: 10.1016/j.jcis.2022.08.018. Epub 2022 Aug 6.
The High-Performance Li-LiFePO batteries (Li||LFP) realized by highly compatible electrolytes are considered to be the breakthrough point to achieve the stability and high energy density of lithium-ion battery (LIB) systems. However, the current prevailing commercial electrolytes can hardly be compatible with both LFP cathode and lithium anode simultaneously to an ideal extent. On this very note, we designed an advanced ether-based localized high concentration electrolyte (abbreviated as "ADE"), which exhibits extreme compatibility with LFP-based lithium metal batteries (Fb-LMBs). Equipped with ADE-electrolyte, the Li||LFP coin cell system can carry out more than 4000 fast-charging/discharging (3C for charge and 6C for discharge, respectively) rigorously cycles. Each cycle can not only sacrifice just 0.145‱ capacity on average compared with the original value, but also cycle at elevated temp (>200 fast charging/discharging cycles under 60 °C). This performance remains rare in liquid electrolyte systems in previous reports. The significantly enhanced electrochemical performance can be ascribed to the stabilization of both LFP-cathode/electrolyte and Li-metal-anode/electrolyte interphases. In addition, due to its specific solvated sheath structure, its wettability and flame-retarding properties are superior to those of the control group. This work expands the space for designing a stable fast-charge LFP-based system and sheds light on the possibility of replacing the most popular graphite||LFP system with Li ||LFP configuration with high energy density and stable cyclic performance.
通过高度兼容的电解质实现的高性能锂-磷酸铁锂电池(Li||LFP)被认为是实现锂离子电池(LIB)系统稳定性和高能量密度的突破点。然而,目前流行的商业电解质很难同时与LFP正极和锂负极在理想程度上兼容。基于此,我们设计了一种先进的基于醚的局部高浓度电解质(简称为“ADE”),它与基于LFP的锂金属电池(Fb-LMBs)表现出极高的兼容性。配备ADE电解质的Li||LFP硬币电池系统可以严格进行超过4000次快速充电/放电(充电为3C,放电为6C)循环。与原始值相比,每个循环平均仅损失0.145‱的容量,并且还可以在高温下循环(在60°C下进行>200次快速充电/放电循环)。这种性能在先前报道的液体电解质系统中仍然很少见。显著增强的电化学性能可归因于LFP正极/电解质和锂金属负极/电解质界面的稳定。此外,由于其特定的溶剂化鞘层结构,其润湿性和阻燃性能优于对照组。这项工作拓展了设计稳定的基于LFP的快速充电系统的空间,并为用具有高能量密度和稳定循环性能的Li||LFP配置取代最流行的石墨||LFP系统的可能性提供了线索。