Li Zhuo, Fu Jialong, Zheng Sheng, Li Dinggen, Guo Xin
State Key Laboratory of Material Processing and Die and Mould Technology, Laboratory of Solid State Ionics, School of Materials Science and Engineering, Huazhong University of Science and Technology, Wuhan, 430074, P. R. China.
School of Energy and Power Engineering, Huazhong University of Science and Technology, Wuhan, 430074, P. R. China.
Small. 2022 Apr;18(17):e2200891. doi: 10.1002/smll.202200891. Epub 2022 Mar 19.
Practical applications of polymer electrolytes in lithium (Li) metal batteries with high-voltage Ni-rich cathodes have been hindered by the dendrite growth and poor oxidative stability of electrolytes. Herein, a self-healing polymer electrolyte is developed by in situ copolymerization of 2-(3-(6-methyl4-oxo-1,4-dihydropyrimidin-2-yl)ureido)ethyl methacrylate (UPyMA) and ethylene glycol methyl ether acrylate (EGMEA) monomers. With the electrolyte, the dendrite growth is inhibited by spontaneously repairing dendrite-induced defects, cracks, and voids at the Li/electrolyte interface; the suppressed dendrite growth and associated electro-chemo behaviors are visualized by the kinetic Mont-Carlo simulation. Benefitting from the high ionic conductivity, wide electrochemical window and good interfacial stability, the self-healing polymer electrolyte enables stable cycling of the LiNi Mn Co O (NMC811) cathode under 4.7 V, achieving a high specific capacity of ≈228.8 mAh g and capacity retention of 80.4% over 500 cycles. The new electrolyte is very promising for developing highly safe and dendrite-free Li metal batteries with high energy density.
聚合物电解质在具有高压富镍阴极的锂金属电池中的实际应用受到电解质枝晶生长和氧化稳定性差的阻碍。在此,通过甲基丙烯酸2-(3-(6-甲基-4-氧代-1,4-二氢嘧啶-2-基)脲基)乙酯(UPyMA)和乙二醇甲基醚丙烯酸酯(EGMEA)单体的原位共聚制备了一种自修复聚合物电解质。使用该电解质时,枝晶生长通过自发修复锂/电解质界面处枝晶诱导的缺陷、裂纹和空隙而受到抑制;通过动力学蒙特卡洛模拟可以观察到枝晶生长的抑制以及相关的电化学行为。受益于高离子电导率、宽电化学窗口和良好的界面稳定性,自修复聚合物电解质能够使LiNiMnCoO(NMC811)阴极在4.7V下稳定循环,实现约228.8mAh g的高比容量和500次循环后80.4%的容量保持率。这种新型电解质对于开发具有高能量密度、高度安全且无枝晶的锂金属电池非常有前景。