材料科学
电解质
相位反转
聚烯烃
化学工程
热稳定性
多孔性
电极
陶瓷
分离器(采油)
电化学
润湿
复合数
复合材料
膜
化学
图层(电子)
物理化学
工程类
物理
热力学
生物
遗传学
作者
Aaron J. Blake,Ryan R. Kohlmeyer,James O. Hardin,Eric A. Carmona,Benji Maruyama,John D. Berrigan,Hong Huang,Michael F. Durstock
标识
DOI:10.1002/aenm.201602920
摘要
This study establishes an approach to 3D print Li‐ion battery electrolytes with controlled porosity using a dry phase inversion method. This ink formulation utilizes poly(vinyldene fluoride) in a mixture of N ‐methyl‐2‐pyrrolidone (good solvent) and glycerol (weak nonsolvent) to generate porosity during a simple drying step. When a nanosized Al 2 O 3 filler is included in the ink, uniform sub‐micrometer pore formation is attained. In other words, no additional processing steps such as coagulation baths, stretching, or etching are required for full functionality of the electrolyte, which makes it a viable candidate to enable completely additively manufactured Li‐ion batteries. Compared to commercial polyolefin separators, these electrolytes demonstrate comparable high rate electrochemical performance (e.g., 5 C), but possess better wetting characteristics and enhanced thermal stability. Additionally, this dry phase inversion method can be extended to printable composite electrodes, yielding enhanced flexibility and electrochemical performance over electrodes prepared with only good solvent. Finally, sequentially printing this electrolyte ink over a composite electrode via a direct write extrusion technique has been demonstrated while maintaining expected functionality in both layers. These ink formulations are an enabling step toward completely printed batteries and can allow direct integration of a flexible power source in restricted device areas or on nonplanar surfaces.
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