普鲁士蓝
材料科学
电解质
聚偏氟乙烯
结晶度
复合数
离子电导率
快离子导体
化学工程
电化学
电化学窗口
无定形固体
电导率
锂(药物)
离子键合
纳米技术
多孔性
离子
无机化学
价(化学)
电极
作者
Shaochen Wei,Gaohui Du,Jingyi Jing,Huayu Li,Jingwei Dong,Ji Yang,Di Han,Shixian Chen,Wenqi Zhao,Qingmei Su
标识
DOI:10.1021/acsaem.5c03168
摘要
Composite solid electrolytes represent a promising approach in solid-state batteries, yet achieving both high ionic conductivity and interfacial stability remains challenging. In this work, we design high-performance composite electrolytes by incorporating lithium-embedded manganese Prussian blue analogues (Li-MnPBA) as functional fillers into a polyvinylidene fluoride (PVDF) matrix. The Li-MnPBA features an open framework, adjustable coordination environment, an expanded lattice (10.4684 Å), and tailored transition metal valence states. Its inherent lithium content and structural vacancies facilitate rapid Li+ diffusion and enhance interfacial stability. The incorporation of Li-MnPBA not only reduces the crystallinity of PVDF to promote amorphous region formation but also establishes continuous ion transport channels through its porous framework and transferable lithium ions. This dual effect significantly improves the ionic conductivity (1.63 × 10–4 S cm–1) and ion transference number (0.73) of the composite electrolyte. Additionally, it offers a wide electrochemical window (4.5 V) and robust mechanical strength, effectively suppressing lithium dendrite growth and enabling stable long-term cycling. When integrated into solid-state batteries, LiFePO4//Li cells deliver 131.4 mAh g–1 at 1C with 97.8% capacity retention after 150 cycles. Meanwhile, NCM811//graphite full cells demonstrate stable operation at a high rate. This research highlights the potential application of Li-MnPBA in composite electrolytes and presents a direction for the design of high-performance solid-state batteries.
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