Function‐Oriented Modular Molecular Design of a Chitin‐Derived Self‐Healable Binder for Promising Zinc Powder Anodes

X Xuanyu Zeng (Hubei Biomass‐Resource Chemistry and Environmental Biotechnology Key Laboratory, Hubei Provincial Engineering Research Center of Emerging Functional Coating Materials School of Resource and Environmental Sciences Wuhan University Wuhan P.R. China) Z Zhiqiang Wang L Le Yu (Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education, College of Chemistry & Materials Science) J Jing Huang S Sijun Wang (Hubei Biomass‐Resource Chemistry and Environmental Biotechnology Key Laboratory, Hubei Provincial Engineering Research Center of Emerging Functional Coating Materials School of Resource and Environmental Sciences Wuhan University Wuhan P.R. China) Z Zhaohui Wang (Key Laboratory of Organic Optoelectronics and Molecular Engineering, Department of Chemistry) C Chaoji Chen (Hubei Key Laboratory of Biomass Resource Chemistry and Environmental Biotechnology, Hubei International Scientific and Technological Cooperation Base of Sustainable Resource and Energy, Hubei Engineering Center of Natural Polymers-based Medical Materials, School of Resource and Environmental Science, Wuhan University)

Abstract

ABSTRACT Replacing zinc foil with Zn micropowders (ZnMPs) enhances manufacturing compatibility for Zn‐metal batteries but imposes challenges like uncontrolled Zn deposition and accelerated structural degradation, typically resulting in a short cycle life of < 50 cycles. Herein, we synthesize a multifunctional bottle‐brush polycationic binder based on naturally abundant and mechanically robust chitin, which enables exceptional long‐term Zn plating/stripping reversibility, averaging 99.5% Coulombic efficiency over 300 cycles. The design rationales are experimentally validated as follows: diverse functional groups integrated onto the chitin backbone provide multiple supramolecular interactions ensuring ZnMP electrodes’ spatial uniformity and structural robustness; Zn 2+ ‐carboxylate coordination simultaneously enhances the binder's mechanical strength (~1.2 MPa), toughness (~8.6 MJ m −3 ) and ionic conductivity (an 87% increase, reaching 1.72 × 10 −5 S cm − 1 ) upon swelling; while synergistic dynamic electrostatic interactions and hydrogen bonding permit rapid self‐recovery of the electrodes during cycling. This work underscores the promise of supramolecular engineering for binders targeting aggressive electrode chemistries.

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 (7)

X

Xuanyu Zeng

Hubei Biomass‐Resource Chemistry and Environmental Biotechnology Key Laboratory, Hubei Provincial Engineering Research Center of Emerging Functional Coating Materials School of Resource and Environmental Sciences Wuhan University Wuhan P.R. China

Z

Zhiqiang Wang

L

Le Yu

Key Laboratory of Synthetic and Natural Functional Molecule of the Ministry of Education, College of Chemistry & Materials Science

J

Jing Huang

S

Sijun Wang

Hubei Biomass‐Resource Chemistry and Environmental Biotechnology Key Laboratory, Hubei Provincial Engineering Research Center of Emerging Functional Coating Materials School of Resource and Environmental Sciences Wuhan University Wuhan P.R. China

Z

Zhaohui Wang

Key Laboratory of Organic Optoelectronics and Molecular Engineering, Department of Chemistry

C

Chaoji Chen

Hubei Key Laboratory of Biomass Resource Chemistry and Environmental Biotechnology, Hubei International Scientific and Technological Cooperation Base of Sustainable Resource and Energy, Hubei Engineering Center of Natural Polymers-based Medical Materials, School of Resource and Environmental Science, Wuhan University