All‐Climate Energy‐Dense Cascade Aqueous Zn‐I <sub>2</sub> Batteries Enabled by a Polycationic Hydrogel Electrolyte

Y Yangyang Liu (State Key Laboratory for Mechanical Behavior of Materials, School of Instrument Science and Technology) L Longhai Zhang L Ling Liu Q Quanwei Ma (Institutes of Physical Science and Information Technology, School of Materials Science and Engineering, Leibniz International Joint Research Centre of Materials Sciences of Anhui Province) R Rui Wang P Peng Xiong H Hongbao Li (Institutes of Physical Science and Information Technology School of Materials Science and Engineering Leibniz International Joint Research Centre of Materials Sciences of Anhui Province Anhui University Hefei 230601 China) S Shilin Zhang (School of Chemical Engineering, Faculty of Sciences, Engineering and Technology) J Junnan Hao (School of Chemical Engineering) C Chaofeng Zhang (Institutes of Physical Science and Information Technology, School of Materials Science and Engineering, Leibniz International Joint Research Centre of Materials Sciences of Anhui Province)

Abstract

Abstract The practical development of aqueous zinc‐iodine (Zn‐I 2 ) batteries is greatly hindered by the low energy density resulting from conventional I 0 /I − conversion and the limited temperature tolerance. Here, a temperature‐insensitive polycationic hydrogel electrolyte borax‐bacterial cellulose / p (AM‐ co ‐VBIMBr) (denoted as BAVBr) for achieving an energy‐dense cascade aqueous Zn‐I 2 battery over a wide temperature range from −50 to 50 °C is designed. A comprehensive investigation, combining advanced spectroscopic investigation and DFT calculations, has revealed that the presence of Br species in the gel electrolyte facilitates the conversion reaction of Br 0 /Br − . Simultaneously, it activates the high voltage I + /I 0 redox reaction through interhalogen formation. Consequently, sequential and highly reversible redox reactions involving I 0 /I − , I + /I 0 , and Br 0 /Br − are achieved with the assistance of −NR 3 + units in BAVBr, effectively suppressing interhalogen hydrolysis in aqueous electrolyte. The cascade reactions lead to a high area capacity of 0.76 mAh cm −2 at a low I 2 loading of 1 mg cm −2 or 760 mAh g −1 based on the mass of iodine, demonstrating exceptional long‐term cycling stability over a wide temperature range from −50 to 50 °C. This study offers valuable insights into the rational design of electrolytes for high‐energy aqueous batteries, specifically tailored for wide‐temperature operation.

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 (10)

Y

Yangyang Liu

State Key Laboratory for Mechanical Behavior of Materials, School of Instrument Science and Technology

L

Longhai Zhang

L

Ling Liu

Q

Quanwei Ma

Institutes of Physical Science and Information Technology, School of Materials Science and Engineering, Leibniz International Joint Research Centre of Materials Sciences of Anhui Province

R

Rui Wang

P

Peng Xiong

H

Hongbao Li

Institutes of Physical Science and Information Technology School of Materials Science and Engineering Leibniz International Joint Research Centre of Materials Sciences of Anhui Province Anhui University Hefei 230601 China

S

Shilin Zhang

School of Chemical Engineering, Faculty of Sciences, Engineering and Technology

J

Junnan Hao

School of Chemical Engineering

C

Chaofeng Zhang

Institutes of Physical Science and Information Technology, School of Materials Science and Engineering, Leibniz International Joint Research Centre of Materials Sciences of Anhui Province