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Reconfiguring the Coordination Structure in Deep Eutectic Electrolytes for Enabling Stable Operation of Zinc-Ion Batteries. | LitMetric

Reconfiguring the Coordination Structure in Deep Eutectic Electrolytes for Enabling Stable Operation of Zinc-Ion Batteries.

Nano Lett

State Key Laboratory of Nonlinear Mechanics, Institute of Mechanics, Chinese Academy of Sciences, Beijing 100190, China.

Published: November 2024

AI Article Synopsis

  • Highly stable aqueous Zn-ion batteries are essential for commercial use but face challenges like side reactions and dendrite growth that can cause failures.
  • A new hydrated deep eutectic electrolyte was developed using 1,3-propanediol, which helps stabilize the battery by altering the water structure and reducing unwanted side reactions.
  • This innovative electrolyte enhances the longevity and performance of various Zn-ion battery configurations, paving the way for more efficient battery technology.

Article Abstract

Highly stable aqueous Zn-ion batteries are of great importance for commercial applications. The challenging issues of interfacial side reactions and rampant dendrite growth cause short circuit and premature failure of aqueous Zn-ion batteries. Herein, a hydrated deep eutectic electrolyte is formulated to tackle such problems, which adopts 1,3-propanediol as a cosolvent. 1,3-Propanediol molecules can enter into the Zn solvation structure to from a lean-water electrolyte and drastically diminish the activity of water molecules through reinforcing the hydrogen bond network. Meanwhile, PDO molecules exclude the neighboring water to modulate the electric double layer configuration, thus impeding water-mediated side reactions and inducing an inorganic-rich interphase. Consequently, this hydrated deep eutectic electrolyte ensures long-term stability of Zn-Zn, Zn-Cu, and Zn-I cells. The favorable influence exerted by PDO molecules provides the guidance for constructing high-performance aqueous Zn-ion batteries.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.nanolett.4c03480DOI Listing

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