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Hydrophobic liquid electrolyte interphases for efficient aqueous zinc batteries

  • Guanjie Li
  • , Shilin Zhang*
  • , Jodie Yuwono
  • , Xinyu Li
  • , Javen Qinfeng Shi
  • , Chunsheng Wang*
  • , Zaiping Guo*
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

Expanding the electrochemical stability window of aqueous electrolyte solutions is a viable strategy to improve battery performance. Using water-in-salt aqueous electrolyte solutions, the solid electrolyte interphase formed on the negative electrode enables an electrochemical stability window up to 3.0 V, but this often reduces ionic conductivity and increases costs. Here, to circumvent these issues, we report the use of hydrophobic and electrode-philic ether-based additives in 3-molal aqueous zinc trifluoromethanesulfonate electrolyte solutions. These additives, characterized by a weak Zn-ion solvation capability, are soluble in the aqueous electrolyte solution at low concentrations (below 2 mol%). They can be adsorbed on both positive and negative electrode surfaces, inhibiting Zn dendrite growth, forming a liquid electrolyte interphase that extends the electrochemical stability window to 3.08 V, enabling high bulk ionic conductivity (about 54 mS cm−1 at 25 °C) and ensuring the non-flammability of the aqueous electrolyte solution. This nanoengineered electrolyte approach enables a Zn||NaV3O8 single-layer pouch cell to operate 500 stable cycles (average Coulombic efficiency of 99.95%) with a specific discharge capacity retention of 80% at 500 mA g−1 and 25 °C with a calculated initial specific energy of 132 Wh kg−1 (based on the mass of the negative and positive electrode active materials).
© The Author(s) 2026
Original languageEnglish
JournalNature Nanotechnology
Online published1 Jun 2026
DOIs
Publication statusPublished - 2026
Externally publishedYes

Funding

This work was supported by the Australian Research Council (DP250102252 to S.Z. and FL210100050 to Z.G.). C.W. acknowledges support from the Aqueous Battery Consortium, an energy innovation hub under the US Department of Energy, Office of Basic Energy Sciences, Division of Materials Science and Engineering. S.Z. acknowledges financial support from the Australian Research Council (DE240100159). J.A.Y. acknowledges the high-performance computing facilities provided by the National Computational Infrastructure (NCI) Australia. X.L. and J.Q.S. acknowledge financial support from the Responsible AI Research Centre, an initiative of Adelaide University, CSIRO Data61 and the Government of South Australia. Components of this research were undertaken on the PD and SAXS/wide-angle X-ray scattering beamlines at the Australian Synchrotron, part of ANSTO, through the merit-based beamtime proposals (M21781 to S.Z. and M21924 to G.L.). We acknowledge R.-S. Liu for help in the NAP-XPS experiments. Open access funding provided by Adelaide University

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 7 - Affordable and Clean Energy
    SDG 7 Affordable and Clean Energy

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