Transient Polarized Cavities Mediate an Ultrafast and Stable Graphite Anode for Potassium‐Ion Batteries

ABSTRACT Conventional ester‐based electrolytes exhibit intrinsic limitations for potassium‐ion batteries (PIBs): ethylene carbonate is solid at room temperature, while propylene carbonate induces graphite exfoliation via solvent co‐intercalation and suffers from poor rate capability. To address these challenges, we design a dipole‐engineered electrolyte that enables the formation of transient polarized cavities upon K + desolvation. These cavities generate localized negative electrostatic potentials that attract incoming K + ions, effectively lowering the ion transport barrier. This mechanism not only enhances K + kinetics but also promotes the formation of a stable, ion‐conductive solid electrolyte interphase, enabling highly reversible K + (de)intercalation in graphite. As a result, the K||graphite half‐cell delivers a high capacity of 290 mAh g −1 at 50 mA g −1 with negligible decay over 16 months (> 1000 cycles), and retains 226 mAh g −1 even at 500 mA g −1 . This work reveals a cavity‐mediated ion transport mechanism that offers new insights for designing high‐rate, long‐life graphite anodes in PIBs.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2026-05-29
DOI
https://doi.org/10.1002/anie.6110810
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
0.00

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article

Transient Polarized Cavities Mediate an Ultrafast and Stable Graphite Anode for Potassium‐Ion Batteries

Mengkang Shen, Rongyao Yuan, Hongwei Fu, J Zhou et al.
Angewandte Chemie International Edition
Advancements in Battery Materials
article

Transient Polarized Cavities Mediate an Ultrafast and Stable Graphite Anode for Potassium‐Ion Batteries

Mengkang Shen, Rongyao Yuan, Hongwei Fu, J Zhou, Ling Fan, Bingan Lu
article en

Abstract

ABSTRACT Conventional ester‐based electrolytes exhibit intrinsic limitations for potassium‐ion batteries (PIBs): ethylene carbonate is solid at room temperature, while propylene carbonate induces graphite exfoliation via solvent co‐intercalation and suffers from poor rate capability. To address these challenges, we design a dipole‐engineered electrolyte that enables the formation of transient polarized cavities upon K + desolvation. These cavities generate localized negative electrostatic potentials that attract incoming K + ions, effectively lowering the ion transport barrier. This mechanism not only enhances K + kinetics but also promotes the formation of a stable, ion‐conductive solid electrolyte interphase, enabling highly reversible K + (de)intercalation in graphite. As a result, the K||graphite half‐cell delivers a high capacity of 290 mAh g −1 at 50 mA g −1 with negligible decay over 16 months (> 1000 cycles), and retains 226 mAh g −1 even at 500 mA g −1 . This work reveals a cavity‐mediated ion transport mechanism that offers new insights for designing high‐rate, long‐life graphite anodes in PIBs.

Angewandte Chemie International Edition
Central South University (CN), Hunan University (CN), Changsha University (CN)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, National Key Research and Development Program of China
Openalex Percentile: Top 9%
Advancements in Battery Materials
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