Dynamic Zn <sup>2+</sup> ‐Conductive Protective Layer for Durable Zinc Anode in Aqueous Zinc‐Ion Batteries

M Manxia Ma (Department of Chemical Physics University of Science and Technology of China Hefei Anhui China) K Kaiyue Zhu (State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China) W Weikang Jiang (Department of Chemical Physics University of Science and Technology of China Hefei Anhui China) W Weili Xie (State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China) M Minjing Zhao (State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China) Z Zhigang Shao W Weishen Yang (State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023, P. R. China)

Abstract

ABSTRACT The Zn anode in aqueous zinc‐ion batteries (AZIBs) suffers from hydrogen evolution reaction (HER), by‐product accumulation, and dendrite growth, severely restricting practical viability. To address these challenges concurrently, we propose a dynamic Zn 2+ ‐conductive protective layer strategy, which involves constructing an in situ ZnOHF layer on the Zn anode and incorporating F − into the electrolyte. Zn 2+ ‐conductivity and reducibility of ZnOHF layer guide uniform Zn nucleation and deposition, thereby inhibiting dendrite formation. Crucially, the addition of F − to the electrolyte enables the dynamic regeneration of the ZnOHF layer during cycling and the conversion of detrimental by‐products into favorable ZnOHF. Additionally, HER is effectively suppressed by isolating the Zn anode from the aqueous electrolyte via ZnOHF interfacial layer, and decreasing water activity through F − ‐induced elevation of electrolyte pH from 4.1 to 5. As a result, the protected Zn anode enables the symmetrical cell to operate stably for 3100 h at 0.5 mA cm −2 , and a full cell to retain 85% capacity after 4000 cycles at 10 A g −1 . Moreover, a 90 cm 2 pouch cell delivers an initial capacity of 240 mAh and maintains 70% capacity after 200 cycles, highlighting its practical viability. This work presents an effective and scalable interface engineering approach to realize durable Zn anodes for practical AZIBs.

Article Details

Volume / Issue Vol. 38, Issue 36
Published June 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (7)

M

Manxia Ma

Department of Chemical Physics University of Science and Technology of China Hefei Anhui China

K

Kaiyue Zhu

State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China

W

Weikang Jiang

Department of Chemical Physics University of Science and Technology of China Hefei Anhui China

W

Weili Xie

State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China

M

Minjing Zhao

State Key Laboratory of Catalysis Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 China

Z

Zhigang Shao

W

Weishen Yang

State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian 116023, P. R. China