Micro‐Terraced Surface Induced Directional Two‐Dimensional Diffusion Enables Dendrite‐Free Zinc Anodes

P Pengfei Zhang C Chao Geng C Canhuang Li (Catalonia Institute for Energy Research-IREC, Sant Adrià de Besòs, Barcelona 08930, Spain) J Jin‐Ming Wu (State Key Laboratory of Silicon and Advanced Semiconductor Materials School of Materials Science and Engineering Zhejiang University Hangzhou China) M Minhua Cao (Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, Wisconsin 53705, United States) T Tulai Sun W Wei Wen (Key Laboratory of Applied Chemistry of Chongqing Municipality and Chongqing Key Laboratory of Soft-Matter Material Chemistry and Function Manufacturing, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China)

Abstract

ABSTRACT Aqueous zinc batteries have garnered significant attention owing to their low cost, high intrinsic safety, and environmental friendliness. However, their practical application is still hindered by poor cycling stability, primarily caused by uncontrolled Zn dendrite growth. Conventional strategies to suppress dendrites generally aim to convert undesired 2D diffusion, which favors dendrite formation, into 3D diffusion to promote uniform Zn deposition. In contrast, this study reports a dendrite‐free Zn plating behavior achieved through directional 2D diffusion enabled by a micro‐terraced surface, which is achieved by a Ti 4+ ‐etching strategy. Unlike conventional 2D diffusion, where Zn atoms aggregate and form dendrites, on the micro‐terraced surface Zn atoms rapidly and orderly migrate along the terraces toward their intersection boundaries, resulting in uniform, dendrite‐free plating. The micro‐terraced Zn anodes deliver exceptional cycling stability over 6250 cycles at 5 mA cm −2 /1 mAh cm −2 . When paired with I 2 cathode, the full cells achieve above 83.4% capacity retention and average Coulombic efficiencies of 99.89% over 5000 cycles at 1.5 A g −1 . This work provides mechanistic insights into Zn deposition and offers a new design paradigm for developing high‐stability energy storage systems.

Article Details

Volume / Issue Vol. 38, Issue 16
Published March 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (7)

P

Pengfei Zhang

C

Chao Geng

C

Canhuang Li

Catalonia Institute for Energy Research-IREC, Sant Adrià de Besòs, Barcelona 08930, Spain

J

Jin‐Ming Wu

State Key Laboratory of Silicon and Advanced Semiconductor Materials School of Materials Science and Engineering Zhejiang University Hangzhou China

M

Minhua Cao

Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, Wisconsin 53705, United States

T

Tulai Sun

W

Wei Wen

Key Laboratory of Applied Chemistry of Chongqing Municipality and Chongqing Key Laboratory of Soft-Matter Material Chemistry and Function Manufacturing, School of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China