Quantitative DielectricConstant Engineering of theSeparator for Reversible Lithium Metal Batteries

Abstract 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.

Authors

Institutions

Publication Details

Journal
Journal of the American Chemical Society
Published
2026-08-13
DOI
https://doi.org/10.1021/jacs.6c06934
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Quantitative DielectricConstant Engineering of theSeparator for Reversible Lithium Metal Batteries

Guiyin Xu, Yuxuan Yu, Keith C. Gordon, Tao Zhang et al.
Journal of the American Chemical Society
Advanced Battery Materials and Technologies
article

Quantitative DielectricConstant Engineering of theSeparator for Reversible Lithium Metal Batteries

Guiyin Xu, Yuxuan Yu, Keith C. Gordon, Tao Zhang, Meifang Zhu, Li Xiao
article en

Abstract

Abstract 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.

Journal of the American Chemical Society
Donghua University (CN), University of Otago (NZ)
National Natural Science Foundation of China, Shanghai Rising-Star Program, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 18%
Advanced Battery Materials and Technologies
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Quantitative DielectricConstant Engineering of theSeparator for Reversible Lithium Metal Batteries — Guiyin Xu, Yuxuan Yu, et al. · Journal of the American Chemical Society (2026) | TGRS Research Map | TGRS