高压全固态锂金属电池用互穿网络聚碳酸酯基复合电解质

Jiaxin Chen, Chao Wang, Guoxu Wang, D. Zhou, Li‐Zhen Fan
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引用次数: 5

摘要

探索具有良好的安全性、易加工性和高离子电导率的固体聚合物基复合电解质(SCPEs)对于发展先进的全固态锂金属电池(asslmb)具有重要意义。然而,电极与固体电解质之间的界面相容性差,导致界面阻抗大,削弱了电池的电化学性能。在对称聚碳酸酯单体的基础上,通过原位聚合丙烯酸丁酯、Li7La3Zr2O12 (LLZO)、锂二(三氟甲烷磺酸基)亚胺、丁二腈和2,2-偶氮二异丁腈,构建了互穿网络聚碳酸酯(INPC)基复合电解质。得益于各组分的协同作用和独特的结构特点,INPC&LLZO-SCPE可以有效地整合聚合物和无机电解质的优点,并提供卓越的离子电导率(25°C时为3.56 × 10-4S cm-1),令人印象深刻的Li+转移数[t(Li+) = 0.52]和高电化学稳定性窗口(高达5.0 V vs. Li+/Li)。在此基础上,制备了LiFePO4/INPC&LLZO-SCPE/Li和LiNi0.6Co0.2Mn0.2O2/INPC&LLZO-SCPE/Li充满电池,其初始容量分别为156.3和158.9 mAh g-1,在0.2℃和0.1℃下循环500次和100次后的容量保持率分别为86.8%和95.4%。本研究为构建新型高压asslmb用聚碳酸酯基复合电解质提供了一条新途径。
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An interpenetrating network polycarbonate-based composite electrolyte for high-voltage all-solid-state lithium-metal batteries
The exploration of solid polymer-based composite electrolytes (SCPEs) that possess good safety, easy processability, and high ionic conductivity is of great significance for the development of advanced all-solid-state lithium-metal batteries (ASSLMBs). However, the poor interfacial compatibility between the electrode and solid electrolyte leads to a large interfacial impedance that weakens the electrochemical performance of the battery. Herein, an interpenetrating network polycarbonate (INPC)-based composite electrolyte is constructed via the in-situ polymerization of butyl acrylate, Li7La3Zr2O12 (LLZO), Lithium bis(trifluoromethanesulphonyl)imide, succinonitrile and 2,2-azobisisobutyronitrile on the base of a symmetric polycarbonate monomer. Benefiting from the synergistic effect of each component and the unique structure features, the INPC&LLZO-SCPE can effectively integrate the merits of the polymer and inorganic electrolytes and deliver superior ionic conductivity (3.56 × 10-4S cm-1 at 25 °C), an impressive Li+ transference number [t(Li+) = 0.52] and a high electrochemical stability window (up to 5.0 V vs. Li+/Li). Based on this, full batteries of LiFePO4/INPC&LLZO-SCPE/Li and LiNi0.6Co0.2Mn0.2O2/INPC&LLZO-SCPE/Li are assembled, which exhibit large initial capacities of 156.3 and 158.9 mAh g-1 and high capacity retention of 86.8% and 95.4% over 500 and 100 cycles at 0.2 and 0.1 C, respectively. This work offers a new route for the construction of novel polycarbonate-based composite electrolytes for high-voltage ASSLMBs.
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