金属锂
相关性(法律)
锂(药物)
固态
材料科学
纳米技术
工程物理
工程类
物理
热力学
政治学
电池(电)
心理学
精神科
法学
功率(物理)
作者
Lukas Stolz,Gerrit Homann,Martin Winter,Johannes Kasnatscheew
标识
DOI:10.1016/j.mattod.2020.11.025
摘要
In this work, different Li salt concentrations and ionic conductivities of poly(ethylene oxide)-based solid polymer electrolytes (PEO-based SPEs) are correlated with the performance of LiNi0.6Mn0.2Co0.2O2 (NMC622)||Li full cells. While the SPEs with different salt concentrations behave similarly in NMC622||Li cells at 60 °C, their influence on the specific capacities is significant at 40 °C. Below a distinct salt concentration, i.e. > 20:1 (EO:Li), a sudden blocking-type polarization appears, indicatable by an almost vertical voltage profile, both in full and in Li||Li symmetric cells. The corresponding time and current density for this polarization-type is shown to mathematically fit with the Sand equation, which subsequently allows calculation of DLi+. According this relation, lack of Li+ in the electrolyte close to the electrode surface can be concluded to be the origin of this polarization, but is shown to appear only for "kinetically limiting" conditions e.g. above a threshold current density, above a threshold SPE thickness and/or below a threshold salt concentration (ionic conductivity), i.e. at mass transfer limiting conditions. With the support of this relation, maximal applicable current densities and/or SPE thicknesses can be calculated and predicted for SPEs.
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