Iodine‐Doped Sodium Vanadate Cathode for Improved Zn Ion Diffusion Kinetics

X Xinyue Hu (Division of Life Science, The Hong Kong University of Science and Technology) S Shengyong Gao T Tongen Lin (Australian Institute for Bioengineering and Nanotechnology and School of Chemical Engineering The University of Queensland St Lucia Queensland 4072 Australia) X Xiyue Peng (School of Chemical Engineering) Y Yongxin Huang Y Yiming Zhang X Xingchen Yang L Lina Wang (Department of Chemistry, Advanced Institute of Future Energy, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, State Key Laboratory of Porous Materials for Separation and Conversion) G Guangfu Luo (Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen China) Z Zhenhai Wen (State Key Laboratory of Structural Chemistry, and Fujian Provincial Key Laboratory of Materials and Techniques Toward Hydrogen Energy) B Bernt Johannessen (Australian Synchrotron, ANSTO) S Songcan Wang L Lianzhou Wang (Nanomaterials Centre, School of Chemical Engineering and Australian Institute for Bioengineering and Nanotechnology) B Bin Luo (Australian Institute for Bioengineering and Nanotechnology)

Abstract

Abstract The electrostatic interaction between zinc ions and the host structure significantly limits the practicality of vanadium‐based cathodes in aqueous zinc‐ion batteries (AZIBs). Herein, an anion doping strategy is demonstrated to mitigate electrostatic resistance and steric hindrance during zinc ion insertion by incorporating iodine atoms into the lattice of the cathode material, Na 2 V 6 O 16 ·3H 2 O. Iodine doping reduces the adsorption energy at the most stable site, thereby weakening the Zn 2+ ‐host interaction and lowering the Zn 2+ diffusion energy barrier, resulting in a one‐order‐of‐magnitude increase in the diffusion coefficient. Moreover, the large atomic size of iodine expands the host lattice, creating ample space for increased zinc ion storage capacity, further supported by the introduced oxygen vacancies. As a result, the iodine‐doped Na 2 V 6 O 16 ·3H 2 O cathode achieves an impressive specific capacity of 528.8 mAh g −1 at a current density of 0.5 A g −1 , and retains 262 mAh g −1 after 12,000 cycles at a high current rate of 10 A g −1 . This work provides new insights into the design of high‐performance cathode materials for AZIBs.

Article Details

Volume / Issue Vol. 37, Issue 46
Published November 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (14)

X

Xinyue Hu

Division of Life Science, The Hong Kong University of Science and Technology

S

Shengyong Gao

T

Tongen Lin

Australian Institute for Bioengineering and Nanotechnology and School of Chemical Engineering The University of Queensland St Lucia Queensland 4072 Australia

X

Xiyue Peng

School of Chemical Engineering

Y

Yongxin Huang

Y

Yiming Zhang

X

Xingchen Yang

L

Lina Wang

Department of Chemistry, Advanced Institute of Future Energy, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, State Key Laboratory of Porous Materials for Separation and Conversion

G

Guangfu Luo

Department of Materials Science and Engineering Southern University of Science and Technology Shenzhen China

Z

Zhenhai Wen

State Key Laboratory of Structural Chemistry, and Fujian Provincial Key Laboratory of Materials and Techniques Toward Hydrogen Energy

B

Bernt Johannessen

Australian Synchrotron, ANSTO

S

Songcan Wang

L

Lianzhou Wang

Nanomaterials Centre, School of Chemical Engineering and Australian Institute for Bioengineering and Nanotechnology

B

Bin Luo

Australian Institute for Bioengineering and Nanotechnology