Tao Zhang, Xiao Li, Yuxuan Yu, Keith C Gordon, Guiyin Xu, Meifang Zhu
Current research on separators for lithium metal batteries lacks unified theoretical frameworks and essential quantitative parameters, limiting reversibility, interfacial stability, and lifespan. Herein, we reveal a pronounced nonlinear correlation between the separator dielectric constant and ion transport kinetics. Specifically, an organic-aqueous interfacial reaction is employed to drive polycondensation on the polypropylene separator, enabling wide-range tuning of the separator dielectric constant (2.7-9.1). The dielectric constant serves as an effective descriptor of separator polarization under the internal electric field of the cell. The separator with an intermediate dielectric constant (∼5.4) optimizes the trade-off among ion transport kinetics, SEI stability, and lithium deposition, whereas excessively low or high dielectric constants favor organic-rich SEI formation and restricted transport kinetics, respectively. This strategy enables a Li||LiFePO4 pouch cell (416.4 Wh kg-1, excluding packaging weight) to retain 76.88% of its initial capacity after 1000 cycles.