电解质
材料科学
阳极
堆栈(抽象数据类型)
电池(电)
电极
硫化物
硫化铜
自放电
锂(药物)
短路
集电器
阴极
计算机科学
电压
电气工程
铜
化学
冶金
内分泌学
物理化学
功率(物理)
工程类
程序设计语言
物理
医学
量子力学
作者
Gerrit Homann,Paul Meister,Lukas Stolz,Jan Paul Brinkmann,Jörn Kulisch,Torben Adermann,Martin Winter,Johannes Kasnatscheew
标识
DOI:10.1021/acsaem.0c00041
摘要
Solid electrolytes can be the key for the desired goal of increased safety and specific energies of batteries. On a cell and battery pack level, the all-solid nature and the absence of liquid electrolyte leakage are considered to enable safe and effective performance realization of the rechargeable Li metal electrode and bipolar cell stacking, respectively. Well performing Li metal cells with high-energy/voltage positive electrodes such as LiNi0.6Mn0.2Co0.2O2 (NMC622) can already be cycled when using a blend of the sulfidic solid electrolyte such as β-Li3PS4 (LPS) and Li salt in poly(ethylene)oxide (PEO). However, operation of a bipolar stack using these cell materials utilizing the common Al/Cu clad as bipolar plate results in an immediate short circuit, because of an ionic intercell connection via molten LiTFSI/PEO. Oversizing the area of the bipolar plates can prevent such a short circuit and indeed enables a partial charge of the stack, but after a certain time, the next cell failure is observed, consisting of severe, sulfur caused, corrosion of copper which was used as metal substrate for the lithium anode. The exchange of the sulfide incompatible Cu collector by (also area-oversized) stainless steel can finally enable a failure-free performance of the bipolar cell stack, which performs similar to a single cell with regard to cycling stability.
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