材料科学
阳极
电解质
法拉第效率
电化学
硫化物
化学工程
降级(电信)
溶剂
表征(材料科学)
沉积(地质)
离子液体
干气
离子键合
离子电导率
阴极
作者
Maria Rosner,Şahin Cangaz,Felix Hippauf,Susanne Dörfler,Burak Aktekin,Thomas Meyer,Anja Henß,Thomas Abendroth,Holger Althues,Jürgen Janek,Stefan Kaskel
标识
DOI:10.1002/adfm.202518517
摘要
Abstract The solvent‐free processing of cell components is attracting growing interest, as it avoids energy‐intensive drying and solvent recovery procedures. In solid‐state batteries, the dry processing of solid electrolyte (SE) films results in improved ionic conductivities compared to wet processing and eliminates degradation due to residual solvent traces. For dry processing, the binder polytetrafluoroethylene (PTFE) is widely used due to its excellent fibrillation, but it shows poor electrochemical stability at low anode potentials. Here, the influence of processing parameters on the binder structure is evaluated, and the electrochemical degradation of the dry film separators is systematically investigated (e.g., CTTA measurements) at different anode potentials (Si and Li anode). A combination of electrochemical and surface characterization at the SE dry film/anode interface is conducted. The results confirm that processing has a large influence on the stability at the dry film/anode interface. By adapting the SE dry film processing, long‐term cycling in Si||NMC pouch cells is demonstrated over more than 1300 cycles. Additionally, a high initial coulombic efficiency of 92% and an average CE of 99.7% are obtained over 100 cycles, highlighting the potential of dry film separators for the application with Si anodes.
科研通智能强力驱动
Strongly Powered by AbleSci AI