Capacitance‐Enhanced Battery: Integrating High‐Density Battery Capacity with Supercapacitive Swiftness in an Ultra‐Large MXene Architecture

Y Yilin Li L Lili Wang (Department of Chemistry) Z Ziqi Sun D Dongdong Li (Key Laboratory for Ultrafine Materials of Ministry of Education, Shanghai Engineering Research Center of Hierarchical Nanomaterials, School of Materials Science and Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China) Z Zeyu Yuan H Haoran Liu (Marine Biogeochemistry Division, GEOMAR Helmholtz Centre for Ocean Research) G Guangshe Li (State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry) J Junzhi Li (State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of Chemistry Jilin University Changchun 130012 P. R. China) W Wei Han

Abstract

Abstract The rapid advancement of electrochemical energy storage based on earth‐abundant sodium (Na) ions necessitates the seamless integration of high energy density and fast charge–discharge kinetics. A persistent challenge in this domain is the sluggish ion migration kinetics associated with the large ionic radii of Na + ions, which significantly impact high‐energy output applications, such as acceleration and climbing. Herein, a concept of Capacitance‐Enhanced Battery (CEB) is proposed that leverages an ultra‐large MXene framework interfaced with a Bi 2 S 3 @ZnS composite(hereafter abbreviated as BiZnS) to form a C@BiZnS@V 4 C 3 heterostructure for reaching a dynamic dual‐mechanism response. At low current densities, the system operates predominantly in a battery mode, wherein sodium‐ion alloying and conversion reactions within the BiZnS framework ensure high energy retention. At high current densities, the heterostructure facilitates a supercapacitive mode, where active sites at the MXene and BiZnS surfaces and interfaces engage in rapid ion adsorption–desorption, enabling instantaneous energy delivery. This dual functionality imparts exceptional electrochemical performance of the Na‐ion batteries, with a remarkable specific capacity of 270.4 mAh g −1 at an ultra‐high current density of 100 A g −1 and extraordinary durability, maintaining outstanding electrochemical stability over 10 000 cycles at 20 A g −1 . These findings underscore the transformative potential of CEBs and establish dual‐mechanism electrodes for next‐generation energy storage systems.

Article Details

Volume / Issue Vol. 37, Issue 42
Published October 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (9)

Y

Yilin Li

L

Lili Wang

Department of Chemistry

Z

Ziqi Sun

D

Dongdong Li

Key Laboratory for Ultrafine Materials of Ministry of Education, Shanghai Engineering Research Center of Hierarchical Nanomaterials, School of Materials Science and Engineering, East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China

Z

Zeyu Yuan

H

Haoran Liu

Marine Biogeochemistry Division, GEOMAR Helmholtz Centre for Ocean Research

G

Guangshe Li

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry

J

Junzhi Li

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry College of Chemistry Jilin University Changchun 130012 P. R. China

W

Wei Han