Gan Huihui, Cui Mingyu, Li Liang, Qiu Pengyuan, Xia Ye, Sun Jiajun, Zhu Wen
State Key Laboratory of Materials Processing and Die & Mould Technology, School of Materials Science and Engineering, Huazhong University of Science and Technology, Wuhan, Hubei 430074, People's Republic of China.
Langmuir. 2024 Oct 1;40(39):20745-20754. doi: 10.1021/acs.langmuir.4c02845. Epub 2024 Sep 20.
All-solid-state lithium metal batteries (ASSLMBs) have been regarded as promising candidates to settle the safety issues of liquid electrolytes for rechargeable lithium batteries. However, the currently reported gel polymer electrolytes still have flammable liquid solvents, thus leading to the potential safety hazard. Here, solvent-free deep eutectic solid polymer electrolytes (SPEs) are designed and fabricated via an polymerization, which are composed of a poly(vinylidene fluoride-hexafluoropropylene) (PVDF-HFP) electrospun membrane, succinonitrile (SN), poly(ethylene glycol) diacrylate (PEGDA200, = 200 g mol), lithium bis(trifluoromethanesulfonyl)imide (LiTFSI), and lithium difluoro(oxalato)borate (LiDFOB). The deep eutectic solvent (DES) with SN/LiTFSI provides a superior room-temperature ionic conductivity, while the PEGDA200 precursor acts as cross-linking network to form SPEs under thermal initiation for free radical polymerization, and LiDFOB can form a stable solid electrolyte interface (SEI) layer. The PVDF-HFP electrospun membrane with a three-dimensional nanofibrous network structure for SN/PEGDA200/LiTFSI/LiDFOB SPEs exhibits a wide electrochemical stability window, high lithium-ion transference number, and good compatibility with the lithium metal anode. Furthermore, the obtained SPEs assembled with Li//LiMnFePO, Li//LiFePO, and Li//LiNiCoMnO asymmetric cells show excellent cycling performance and rate capability at a wide temperature. This strategy provides a promising path in designing high-energy-density ASSLMBs for practical application.
全固态锂金属电池(ASSLMBs)被视为解决可充电锂电池液体电解质安全问题的有前途的候选者。然而,目前报道的凝胶聚合物电解质仍然含有易燃液体溶剂,因此存在潜在的安全隐患。在此,通过自由基聚合设计并制备了无溶剂的深共晶固态聚合物电解质(SPEs),其由聚(偏二氟乙烯-六氟丙烯)(PVDF-HFP)电纺膜、丁二腈(SN)、聚乙二醇二丙烯酸酯(PEGDA200, = 200 g mol)、双(三氟甲烷磺酰)亚胺锂(LiTFSI)和二氟草酸硼酸锂(LiDFOB)组成。含有SN/LiTFSI的深共晶溶剂(DES)具有优异的室温离子电导率,而PEGDA200前体作为交联网络在热引发下形成自由基聚合的SPEs,并且LiDFOB可以形成稳定的固体电解质界面(SEI)层。具有三维纳米纤维网络结构的用于SN/PEGDA200/LiTFSI/LiDFOB SPEs的PVDF-HFP电纺膜表现出宽的电化学稳定窗口、高的锂离子迁移数以及与锂金属负极良好的兼容性。此外,所制备的与Li//LiMnFePO、Li//LiFePO和Li//LiNiCoMnO不对称电池组装的SPEs在宽温度范围内表现出优异的循环性能和倍率性能。该策略为设计用于实际应用的高能量密度ASSLMBs提供了一条有前途的途径。