为金属锂电池制造超薄、柔性和高电压卤化物基复合固态电解质的可扩展浆状铸造技术

Junjie Chen , Yu Wang , Yanke Lin , Jianbo Xu , Yiju Li , Tianshou Zhao
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摘要

具有高离子电导率、高电压和小厚度的柔性复合聚合物电解质对于实现高能量密度固态锂金属电池(SSLMB)的规模化制造至关重要。由于卤化物的密度(2.5-3.0 g cm-3)比氧化物的密度(4.0 g cm-3)低、离子电导率高(10-3 S cm-1)、模量高、电压高,因此卤化物可作为有效的功能性锂离子导电填料,用于构建薄型、轻质、高性能的复合聚合物电解质,同时实现 SSLMB 的高能量密度。然而,由于卤化物固体电解质材料易受普通极性溶剂的化学影响,因此限制了用于实用 SSLMB 的卤化物基复合聚合物电解质的规模化浆料浇铸制造。为此,我们筛选出一种双功能低极性溶剂--碳酸二甲酯,使通常与浆料不相容的卤化物也能用于可扩展的浆料制造。结果,一种超薄(10 微米)、柔韧的卤化物掺杂复合电解质被开发出来,这种电解质具有高达 4.8 V 的电化学窗口(相对于 Li+/Li)、高热稳定性和理想的自熄灭能力。得益于填料、盐和聚合物之间相互作用所产生的多种锂离子传输机制,所获得的复合聚合物电解质在 25 °C 时的离子电导率高达 0.325 mS cm-1。基于卤化物基复合电解质组装的固态锂|锂铁PO4电池在0.2 C条件下实现了153 mAh g-1的高容量,循环175次后容量保持率达98%;锂|镍0.6钴0.2锰0.2O2电池可在4.3 V截止电压下稳定循环,在0.2 C条件下实现了160 mAh g-1的高容量,循环170次后容量保持率达89%。这项工作为大规模制造用于高性能 SSLMB 的超薄、柔性卤化物基复合电解质提供了有效策略。
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Scalable Slurry-Casting Fabrication of Ultrathin, Flexible, and High-Voltage Halide-based Composite Solid-State Electrolytes for Lithium Metal Batteries

Flexible composite polymer electrolytes with high ionic conductivity, high voltage, and small thickness are critical for achieving scalable fabrication of high-energy-density solid-state lithium metal batteries (SSLMBs). Owing to the intrinsically lower density (2.5–3.0 g cm−3) than that of oxides (>4.0 g cm−3), high ionic conductivity (∼10−3 S cm−1), high modulus, and high voltage, halides can be used as effective functional Li-ion-conductive fillers to construct thin, lightweight, and high-performance composite polymer electrolytes while achieving high-energy-density of SSLMBs. Nevertheless, the chemical vulnerability of halide solid electrolyte materials to common polar solvents restricts the scalable slurry-casting fabrication of halide-based composite polymer electrolytes for practical SSLMBs. To this end, a bi-functional low-polarity solvent, dimethyl carbonate, is screened to render halides, which are usually slurry-incompatible, amenable to scalable slurry fabrication. As a result, an ultrathin (10 µm) and flexible halide-incorporated composite electrolyte with a high electrochemical window up to 4.8 V vs. Li+/Li, high thermal stability, and desirable self-extinguishing ability is developed. Benefiting from the multiple Li-ion transport mechanisms enabled by the interaction between fillers, salts, and polymers, the obtained composite polymer electrolyte can achieve a high ionic conductivity of 0.325 mS cm–1 at 25 °C. The assembled solid-state Li|LiFePO4 cell based on the halide-based composite electrolyte achieves a high capacity of 153 mAh g−1 at 0.2 C with a capacity retention of 98% after 175 cycles, and the Li|LiNi0.6Co0.2Mn0.2O2 cell can stably cycle at a cut-off voltage of 4.3 V and achieve a high capacity of 160 mAh g−1 at 0.2 C with a capacity retention of 89% after 170 cycles. This work provides an effective strategy for large-scale manufacturing of ultrathin and flexible halide-based composite electrolytes for high-performance SSLMBs.

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