Stabilizing Iodine Redox Mediator Enables High‐Performance Aqueous Zinc–Sulfur Batteries

J Jiahao Zhu L Lutong Shan (Department of Chemistry) W Wen Chen (Department of Immunology, St. Jude Children’s Research Hospital) M Min Chen Z Zhixiang Chen (Future Technology School, Shenzhen Technology University) H Haoran Tu S Siyuan Liu (Sydney Dental School, Faculty of Medicine and Health, Charles Perkins Centre) J Jingyi Liu X Xiaoxiao Liang (State Key Laboratory of Tropic Ocean Engineering Materials and Materials Evaluation School of Marine Technology and Equipment School of Materials Science and Engineering Hainan University Haikou China) Z Zhenyue Xing (State Key Laboratory of Tropic Ocean Engineering Materials and Materials Evaluation Hainan Provincial Key Lab of Fine Chem School of Marine Technology and Equipment Hainan University Haikou 570228 P.R. China) P Peng Rao (State Key Laboratory of Tropic Ocean Engineering Materials and Materials Evaluation Hainan University Haikou China) Z Zhenye Kang Z Zaowen Zhao X Xiaodong Shi X Xinlong Tian (School of Marine Technology and Equipment, State Key Laboratory of Tropic Ocean Engineering Materials and Materials Evaluation, School of Chemistry and Chemical Engineering)

Abstract

ABSTRACT Aqueous zinc–sulfur batteries (AZSBs) are regarded as promising candidates for high‐energy‐density and low‐cost energy storage devices. However, sluggish conversion reaction of sulfur‐loading cathode and notorious polyiodide shuttle of iodine redox mediator in aqueous electrolytes severely hinder the development of AZSBs. Herein, ammonia‐oxidized lignin (AOL) is introduced as electrolyte additive to stabilize the redox mediator function of ZnI 2 , which effectively facilitates the reversible sulfur conversion reaction (S 8 ↔ZnS). As demonstrated, AOL monomer is rich in active hydroxyl/amide moieties, and exhibits strong chemisorption capability for polyiodides as well as remarkable thermodynamic condition for iodine conversion reaction (I 3 − ↔I − ), which significantly blocks the ZnI 2 mediator loss and I 3 − /I 5 − shuttle behavior during cycling, thereby maximizing the catalytic effect of ZnI 2 for S 8 ↔ZnS reaction and high‐performance AZSBs. Consequently, the optimized AZSBs deliver high specific capacity of 1532 mAh g −1 at 0.5 A g −1 , and high reversible capacity of 326.2 mAh g −1 after 320 cycles at 2 A g −1 . Even if assembled into pouch batteries with high sulfur loading of 10 mg cm −2 , high capacity of 514.5 mAh g −1 is still maintained after 134 cycles at 0.5 A g −1 . This work provides novel insights to accelerate sulfur conversion reaction kinetics through stabilizing the redox mediators of AZSBs.

Article Details

Volume / Issue Vol. 38, Issue 14
Published March 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (15)

J

Jiahao Zhu

L

Lutong Shan

Department of Chemistry

W

Wen Chen

Department of Immunology, St. Jude Children’s Research Hospital

M

Min Chen

Z

Zhixiang Chen

Future Technology School, Shenzhen Technology University

H

Haoran Tu

S

Siyuan Liu

Sydney Dental School, Faculty of Medicine and Health, Charles Perkins Centre

J

Jingyi Liu

X

Xiaoxiao Liang

State Key Laboratory of Tropic Ocean Engineering Materials and Materials Evaluation School of Marine Technology and Equipment School of Materials Science and Engineering Hainan University Haikou China

Z

Zhenyue Xing

State Key Laboratory of Tropic Ocean Engineering Materials and Materials Evaluation Hainan Provincial Key Lab of Fine Chem School of Marine Technology and Equipment Hainan University Haikou 570228 P.R. China

P

Peng Rao

State Key Laboratory of Tropic Ocean Engineering Materials and Materials Evaluation Hainan University Haikou China

Z

Zhenye Kang

Z

Zaowen Zhao

X

Xiaodong Shi

X

Xinlong Tian

School of Marine Technology and Equipment, State Key Laboratory of Tropic Ocean Engineering Materials and Materials Evaluation, School of Chemistry and Chemical Engineering