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Highly Reversible Dendrite-Free Zinc Anode Enabled by a Bilayered Inorganic-Metal Interface Layer
Xiaoqi Liu1, Yu Zhang2, Liying Wang1
1State Key Laboratory of Heavy Oil Processing, School of Chemistry and Chemical Engineering, China University of Petroleum, Qingdao, Shandong 266580, China.
ACS Nano
|December 17, 2024
Summary
A novel bilayered zinc fluoride-indium interface (ZnF2-In@Zn) effectively suppresses dendrite growth and side reactions in zinc anodes. This breakthrough enhances cycling stability for aqueous zinc-ion batteries, paving the way for practical applications.
Area of Science:
- Materials Science
- Electrochemistry
- Energy Storage
Background:
- Dendrite growth and side reactions limit the stability of zinc metal anodes in aqueous zinc-ion batteries.
- These issues lead to premature battery failure and hinder practical application.
Purpose of the Study:
- To address dendrite growth and side reactions in zinc anodes.
- To improve the cycling stability of aqueous zinc-ion batteries.
Main Methods:
- In situ construction of a bilayered zinc fluoride-indium interface (ZnF2-In@Zn) on the zinc anode.
- Utilizing a simple solution-dipping strategy.
- Investigating the synergistic effects of the ZnF2 and In layers on Zn2+ desolvation and nucleation.
Main Results:
- The ZnF2-In@Zn anode achieved dendrite-free and side reaction-free zinc deposition.
- Demonstrated outstanding cycling stability exceeding 4200 hours at 1 mA cm-2.
- Achieved a cumulative capacity over 5250 mAh cm-2 even at a high current density of 5 mA cm-2.
Conclusions:
- The bilayered ZnF2-In interface effectively regulates Zn2+ behavior, enhancing anode performance.
- This interface engineering approach offers a promising strategy for developing stable and high-performance zinc anodes for batteries.
- The findings provide insights into overcoming key challenges in metal anode technology.
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