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Zn metal anode suffers from dendrite issues and passive byproducts, which severely plagues the practical application of aqueous Zn metal batteries. Herein, a polyzwitterionic cross-linked double network hydrogel electrolyte composed of physical crosslinking (hyaluronic acid) and chemical crosslinking (synthetic zwitterionic monomer copolymerized with acrylamide) is introduced to overcome these obstacles. On the one hand, highly hydrophilic physical network provides an energy dissipation channel to buffer stress and builds a H2O-poor interface to avoid side reactions. On the other hand, the charged groups (sulfonic and imidazolyl) in chemical crosslinking structure build anion/cation transport channels to boost ions’ kinetics migration and regulate the typical solvent structure [Zn(H2O)6]2+ to R-SO3 [Zn(H2O)4]2+, with uniform electric field distribution and significant resistance to dendrites and parasitic reactions. Based on the above functions, the symmetric zinc cell exhibits superior cycle stability for more than 420 h at a high current density of 5 mA·cm−2, and Zn||MnO2 full cell has a reversible specific capacity of 150 mAh·g−1 after 1000 cycles at 2 C with this hydrogel electrolyte. Furthermore, the pouch cell delivers impressive flexibility and cyclability for energy-storage applications.

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Publication history
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Acknowledgements

Publication history

Received: 09 January 2024
Revised: 27 January 2024
Accepted: 28 January 2024
Published: 03 April 2024
Issue date: June 2024

Copyright

© Tsinghua University Press 2024

Acknowledgements

Acknowledgements

This work was supported by the Science Technology and Innovation Team in University of Henan Province (No. 24IRTSTHN002), the National Natural Science Foundation of China (No. 22279121), and China Postdoctoral Science Foundation (No. 2022M712863), and DFT calculations were supported by the National Supercomputing Centre in Zhengzhou and the funding of Zhengzhou University.

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