Fast‐Charging Phosphorus Anodes Enabled by Fluorinated Weakly Solvated Electrolytes for Stable and High‐Rate Lithium Storage

H Huixian Xie (Joint Key Laboratory of the Ministry of Education Institute of Applied Physics and Materials Engineering University of Macau Avenida da Universidade Taipa Macau SAR 999078 P. R. China) L Lingwen Liu H Hongyi Chen (College of Chemistry and Chemical Engineering) K Kwan San Hui Z Zhuoheng Kuang (Joint Key Laboratory of the Ministry of Education Institute of Applied Physics and Materials Engineering University of Macau Avenida da Universidade Taipa Macau SAR 999078 P. R. China) G Guangmin Zhou Y Yuanmiao Sun (Institute of Technology for Carbon Neutrality) H Hui‐Ming Cheng (Faculty of Materials Science and Energy Engineering Shenzhen University of Advanced Technology Shenzhen China) K Kwun Nam Hui (Joint Key Laboratory of the Ministry of Education, Institute of Applied Physics and Materials Engineering, University of Macau, Avenida da Universidade, Taipa, Macau, SAR 999078, P. R. China)

Abstract

AbstractPhosphorus‐based anodes hold promise for energy storage due to their high theoretical capacity and favorable lithiation potential. However, their practical application is hindered by sluggish reaction kinetics and irreversible capacity loss, primarily attributed to multiphase lithiation/delithiation reactions and the dissolution of lithium polyphosphide intermediates. Herein, a universal design principle of weakly solvated electrolytes (WSEs) tailored for phosphorus‐based anodes is proposed. Combined with a high dielectric constant, and significant dipole moment, a fluorinated cosolvent is incorporated into a WSE to effectively suppress the dissolutions of lithium polyphosphides, enhance interfacial stability, and accelerate reaction kinetics. With this electrolyte, a phosphorus‐based anode achieves a remarkable capacity of 2615.2 mAh g⁻¹ at 1C, maintaining 91.7% capacity retention over 1000 cycles. Even at a high rate of 4 C, it delivers 2210.7 mAh g⁻¹ with an exceptional retention of 96.7% after 1500 cycles. Furthermore, at 0 °C, the anode sustains a capacity of 2016.7 mAh g⁻¹, with 97% retention after 300 cycles at 1C. This study provides a novel electrolyte design strategy to regulate the solvation sheath, paving the way for high‐rate, long‐cycle phosphorus‐based anodes suitable for fast‐charging applications.

Article Details

Volume / Issue Vol. 37, Issue 29
Published July 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (9)

H

Huixian Xie

Joint Key Laboratory of the Ministry of Education Institute of Applied Physics and Materials Engineering University of Macau Avenida da Universidade Taipa Macau SAR 999078 P. R. China

L

Lingwen Liu

H

Hongyi Chen

College of Chemistry and Chemical Engineering

K

Kwan San Hui

Z

Zhuoheng Kuang

Joint Key Laboratory of the Ministry of Education Institute of Applied Physics and Materials Engineering University of Macau Avenida da Universidade Taipa Macau SAR 999078 P. R. China

G

Guangmin Zhou

Y

Yuanmiao Sun

Institute of Technology for Carbon Neutrality

H

Hui‐Ming Cheng

Faculty of Materials Science and Energy Engineering Shenzhen University of Advanced Technology Shenzhen China

K

Kwun Nam Hui

Joint Key Laboratory of the Ministry of Education, Institute of Applied Physics and Materials Engineering, University of Macau, Avenida da Universidade, Taipa, Macau, SAR 999078, P. R. China