Synergistic Anion‐Reinforced Solvation Chemistry and Cationic Electrostatic Shielding for Fast‐Charging Sodium‐Ion Full Batteries Over a Wide Temperature Range

X Xinhui Zeng (Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering) J Jian Chen X Xu Xu (Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering) W Wenxi Kuang (Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering) X Xiaoyan Shi (Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering) X Xiaosa Zhang (Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering) Y Yun Wan (Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering) Z Zhiming Zhou (Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering) X Xunzhu Zhou (Zhejiang Provincial Key Laboratory of Advanced Battery Materials and Technology) A Amit Kumar S Shu‐Lei Chou (Institute For Carbon Neutralization Technology College of Chemistry and Materials Engineering Wenzhou University Wenzhou Zhejiang China) L Lin Li

Abstract

ABSTRACT Sodium‐ion batteries (SIBs) capable of stable operation under fast‐charging conditions across a wide temperature range are of great significance for the efficient utilization of intermittent renewable clean energy. Herein, a multifunctional electrolyte additive containing tetrabutylammonium (TBA + ) cation and perchlorate (ClO 4 − ) anion is employed to construct an environmentally friendly fluorine‐free electrolyte system, significantly enhancing the temperature tolerance and fast‐charging performance of SIBs. Specifically, the TBA + cations, due to their low reduction potential, induce an electrostatic shielding effect that guides the uniform distribution of Na + flux on the electrode surface. Meanwhile, the introduced ClO 4 − anions facilitate the formation of the anion‐reinforced solvation structure. This structure effectively reduces the desolvation energy barrier of Na + and promotes the formation of a stable electrode‐electrolyte interface with high ionic conductivity. This synergistic mechanism effectively suppresses Na plating during fast charging and mitigates continuous electrolyte decomposition and transition metal dissolution. Consequently, the assembled Prussian blue||hard carbon (PB||HC) full cell demonstrates excellent fast‐charging performance across a wide temperature range (10–100°C). More importantly, the PB||HC 18650 cylindrical cell exhibits a superior cycling stability and outstanding rate performance at an elevated temperature of 55°C, demonstrating the great potential of this electrolyte system for practical applications.

Article Details

Volume / Issue Vol. 1, Issue 1
Published June 24, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (12)

X

Xinhui Zeng

Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering

J

Jian Chen

X

Xu Xu

Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering

W

Wenxi Kuang

Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering

X

Xiaoyan Shi

Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering

X

Xiaosa Zhang

Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering

Y

Yun Wan

Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering

Z

Zhiming Zhou

Institute for Carbon Neutralization Technology, College of Chemistry and Materials Engineering

X

Xunzhu Zhou

Zhejiang Provincial Key Laboratory of Advanced Battery Materials and Technology

A

Amit Kumar

S

Shu‐Lei Chou

Institute For Carbon Neutralization Technology College of Chemistry and Materials Engineering Wenzhou University Wenzhou Zhejiang China

L

Lin Li