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Dipolar interaction-mediated molecular anchoring electrolyte enables wide-temperature sodium-ion batteries with enhanced safety and durability
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  • Published: 15 April 2026

Dipolar interaction-mediated molecular anchoring electrolyte enables wide-temperature sodium-ion batteries with enhanced safety and durability

  • Yong-Li Heng1,
  • Zhen-Yi Gu1,
  • Yuan-Zheng Tang2,
  • Han-Hao Liu3,
  • Xiao-Tong Wang1,
  • Jie Wang3,
  • Shu-Yu Li3 &
  • …
  • Xing-Long Wu  ORCID: orcid.org/0000-0003-1069-91451 

Nature Communications , Article number:  (2026) Cite this article

We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Batteries

Abstract

Given intractable challenges faced by practical sodium-ion batteries in safety, lifespan and broad temperature adaptability with synergistic interfacial compatibility, persistent efforts in electrolyte engineering are imperative to expedite their commercialization. Here we design a molecular anchoring electrolyte with flame retardancy, oxidative/reductive reliability and electrochemical durability against various electrodes. Through multiple dipolar interactions (δ+H-δ-F and δ+H-δ-O), a dynamic hierarchical solvation network is constructed and its unique interface stabilization mechanism is revealed by multiscale characterizations and theoretical insights. The electrolyte endows high-voltage phosphate positive electrodes with high electrochemical durability (for instance, 87.6% of capacity retention after 5000 cycles at 2 C) through constructing robust interphases containing fluorine and nitrogen elements. Good compatibility with commercial layered oxide positive electrodes further indicates its versatility. Strikingly, the electrolyte also makes it feasible to operate under wide temperature range (−60 ~ 70 °C). Our proposed dipolar interaction regulation mechanism provides an effective approach for designing safe and durable electrolytes, stimulating practical application of wide-temperature sodium-ion batteries in pursuit of sustainable energy storage.

Data availability

The authors declare that all the relevant data within this paper and its Supplementary Information file are available from the corresponding author upon request. Source data are provided with this paper.

References

  1. Usiskin, R. et al. Fundamentals, status and promise of sodium-based batteries. Nat. Rev. Mater. 6, 1020–1035 (2021).

    Google Scholar 

  2. Yao, A., Benson, S. M. & Chueh, W. C. Critically assessing sodium-ion technology roadmaps and scenarios for techno-economic competitiveness against lithium-ion batteries. Nat. Energy 10, 404–416 (2025).

    Google Scholar 

  3. Park, S. et al. Obtaining V2(PO4)3 by sodium extraction from single-phase NaxV2(PO4)3 (1 < x < 3) positive electrode materials. Nat. Mater. 24, 234–242 (2024).

    Google Scholar 

  4. Guo, Y.-J. et al. Sodium layered oxide cathodes: properties, practicality and prospects. Chem. Soc. Rev. 53, 7828–7874 (2024).

    Google Scholar 

  5. Lu, X. et al. From lab to application: challenges and opportunities in achieving fast charging with polyanionic cathodes for sodium-ion batteries. Adv. Mater. 36, 2407359 (2024).

    Google Scholar 

  6. Tang, Y. et al. Sustainable layered cathode with suppressed phase transition for long-life sodium-ion batteries. Nat. Sustain. 7, 348–359 (2024).

    Google Scholar 

  7. Zhou, R. et al. Constructing anion solvation microenvironment toward durable high-voltage sodium-based batteries. Adv. Mater. 37, 2416748 (2025).

    Google Scholar 

  8. Xie, K., Ji, Y., Yang, L. & Pan, F. Electrolyte design strategies to construct stable cathode-electrolyte interphases for high-voltage sodium-ion batteries. Adv. Energy Mater. 15, 2405301 (2025).

    Google Scholar 

  9. Zhang, F. et al. Emerging chemistry for wide-temperature sodium-ion batteries. Chem. Rev. 124, 4778–4821 (2024).

    Google Scholar 

  10. Jiang, L. et al. Rational design of anti-freezing electrolytes for extremely low-temperature aqueous batteries. Nat. Energy 9, 839–848 (2024).

    Google Scholar 

  11. Ko, S. et al. Rapid safety screening realized by accelerating rate calorimetry with lab-scale small batteries. Nat Energy, https://doi.org/10.1038/s41560-025-01751-7 (2025).

  12. Zhang, J., Gai, J., Song, K. & Chen, W. Advances in electrode/electrolyte interphase for sodium-ion batteries from half cells to full cells. Cell Rep. Phys. Sci. 3, 100868 (2022).

    Google Scholar 

  13. Zhang, J. et al. Critical review on cathode electrolyte interphase towards stabilization for sodium-ion batteries. Nano Energy 128, 109814 (2024).

    Google Scholar 

  14. Zheng, X. et al. Critical effects of electrolyte recipes for Li and Na metal batteries. Chem 7, 2312–2346 (2021).

    Google Scholar 

  15. Vinay, B. et al. Fluorine-free electrolytes in batteries: principles, strategies, and advances. Energy Environ. Sci. https://doi.org/10.1038/s41560-025-01751-7 (2025).

  16. Meng, Y. S., Srinivasan, V. & Xu, K. Designing better electrolytes. Science 378, 1065 (2022).

    Google Scholar 

  17. Li, Y. et al. Ether-based electrolytes for sodium ion batteries. Chem. Soc. Rev. 51, 4484–4536 (2022).

    Google Scholar 

  18. Li, C. et al. Nonaqueous liquid electrolytes for sodium-ion batteries: fundamentals, progress and perspectives. Adv. Energy Mater. 13, 2301758 (2023).

    Google Scholar 

  19. Chen, J. et al. Design of localized high-concentration electrolytes via donor number. ACS Energy Lett. 8, 1723–1734 (2023).

    Google Scholar 

  20. Ren, X. et al. Localized high-concentration sulfone electrolytes for high-efficiency lithium-metal batteries. Chem 4, 1877–1892 (2018).

    Google Scholar 

  21. Zeng, Z. et al. Non-flammable electrolytes with high salt-to-solvent ratios for Li-ion and Li-metal batteries. Nat. Energy 3, 674–681 (2018).

    Google Scholar 

  22. Fang, H. et al. Regulating ion-dipole interactions in weakly solvating electrolyte towards ultra-low temperature sodium-ion batteries. Angew. Chem. Int. Ed. 63, e202400539 (2024).

    Google Scholar 

  23. Niu, M. et al. Approaching fast ion transport via anion–dipole interaction in weakly solvated electrolytes enables stable Li-plating chemistry. Natl. Sci. Rev. 12, nwaf065 (2025).

    Google Scholar 

  24. Wang, C. et al. A weakly coordinating-intervention strategy for modulating Na+ solvation sheathes and constructing robust interphase in sodium-metal batteries. Nat. Commun. 15, 6292 (2024).

    Google Scholar 

  25. Jin, Y. et al. Low-solvation electrolytes for high-voltage sodium-ion batteries. Nat. Energy 7, 718–725 (2022).

    Google Scholar 

  26. Wang, Y. et al. Fluorine chemistry in rechargeable batteries: challenges, progress, and perspectives. Chem. Rev. 124, 3494–3589 (2024).

    Google Scholar 

  27. Chen, W. et al. Hybrid solvating electrolytes for practical sodium-metal batteries. Joule 9, 101811 (2025).

    Google Scholar 

  28. Wang, M., Zheng, M., Lu, J. & You, Y. High-entropy electrolyte toward battery working under extreme conditions. Joule 8, 2467–2482 (2024).

    Google Scholar 

  29. Kim, S. C. et al. High-entropy electrolytes for practical lithium metal batteries. Nat. Energy 8, 814–826 (2023).

    Google Scholar 

  30. Zeng, Y. et al. High-entropy mechanism to boost ionic conductivity. Science 378, 1320–1324 (2022).

    Google Scholar 

  31. Yang, Z. et al. Modulating ion–dipole interactions in nonflammable phosphonate-based electrolyte for safe and stable sodium-ion pouch cells. Natl. Sci. Rev. 12, nwae466 (2025).

    Google Scholar 

  32. Xu, Z. et al. High-voltage and intrinsically safe electrolytes for Li metal batteries. Nat. Commun. 15, 9856 (2024).

    Google Scholar 

  33. Liao, Y. et al. Pentafluoro(phenoxy)cyclotriphosphazene stabilizes electrode/electrolyte interfaces for sodium-ion pouch cells of 145 Wh Kg−1. Adv. Mater. 36, 2312287 (2024).

    Google Scholar 

  34. Zhang, H. et al. High-safety and high-voltage lithium metal batteries enabled by nonflammable diluted highly concentrated electrolyte. Nano Res. 17, 2638–2645 (2023).

    Google Scholar 

  35. Chen, J. et al. Nonflammable succinonitrile-based deep eutectic electrolyte for intrinsically safe high-voltage sodium-ion batteries. Adv. Mater. 36, 2400169 (2024).

    Google Scholar 

  36. Kelchtermans, A.-S. et al. Superconcentration strategy allows sodium metal compatibility in deep eutectic solvents for sodium-ion batteries. ACS Omega 9, 42343–42352 (2024).

    Google Scholar 

  37. Huang, Y. et al. Electrolytes and electrolyte/electrode interfaces in sodium-ion batteries: from scientific research to practical application. Adv. Mater. 31, 1808393 (2019).

    Google Scholar 

  38. Xiao, P. et al. Insights into the solvation chemistry in liquid electrolytes for lithium-based rechargeable batteries. Chem. Soc. Rev. 52, 5255–5316 (2023).

    Google Scholar 

  39. Zhang, Y. et al. Electrolyte design for lithium-ion batteries for extreme temperature applications. Adv. Mater. 36, 2308484 (2023).

    Google Scholar 

  40. Qin, M. et al. Rejuvenating propylene carbonate-based electrolyte through nonsolvating interactions for wide-temperature Li-ions batteries. Adv. Energy Mater. 12, 2201801 (2022).

    Google Scholar 

  41. Li, E. et al. Hierarchical doping electrolyte solvation engineering to achieve high-performance sodium-ion batteries in wide temperature. Energy Storage Mater. 73, 103805 (2024).

    Google Scholar 

  42. Chen, Y. et al. Trace ethylene carbonate-mediated low-concentration ether-based electrolytes for high-voltage lithium metal batteries. Energy Environ. Sci. 17, 5613–5626 (2024).

    Google Scholar 

  43. Cui, X. et al. 4.2 V O3-layered cathodes in sodium-ion pouch cells enabled by an intermolecular-reinforced ether electrolyte. Adv. Mater. 37, 2415611 (2025).

    Google Scholar 

  44. Wang, X. et al. Anion-mediated approach to overcome oxidation in ether electrolytes for high-voltage sodium-ion batteries. Nat. Commun. 16, 2536 (2025).

    Google Scholar 

  45. Wu, Y. et al. Electrostatic potential as solvent descriptor to enable rational electrolyte design for lithium batteries. Adv. Energy Mater. 13, 2300259 (2023).

    Google Scholar 

  46. Yu, Z. et al. Molecular design for electrolyte solvents enabling energy-dense and long-cycling lithium metal batteries. Nat. Energy 5, 526–533 (2020).

    Google Scholar 

  47. Li, N. et al. Insight into the probability of ethoxy(pentafluoro)cyclotriphosphazene (PFPN) as the functional electrolyte additive in lithium–sulfur batteries. RSC Adv. 14, 12754–12761 (2024).

    Google Scholar 

  48. Yu, J. et al. Regulated Li+ solvation via competitive coordination mechanism of organic cations for high voltage and fast charging lithium metal batteries. Angew. Chem. Int. Ed. 64, e202416092 (2024).

    Google Scholar 

  49. Wang, M. et al. Temperature-responsive solvation enabled by dipole-dipole interactions towards wide-temperature sodium-ion batteries. Nat. Commun. 15, 8866 (2024).

    Google Scholar 

  50. Chen, X. et al. Supramolecular “flame-retardant” electrolyte enables safe and stable cycling of lithium-ion batteries. Energy Storage Mater. 45, 182–190 (2022).

    Google Scholar 

  51. Zhao, Z., Liu, C., Lai, T., Cui, Z. & Manthiram, A. Macromolecule-enriched solvation enabling high-voltage sodium-ion batteries. Angew. Chem. Int. Ed. 137, e202423625 (2025).

  52. Lai, P. et al. Revealing the evolution of solvation structure in low-temperature electrolytes for lithium batteries. Energy Storage Mater. 67, 103314 (2024).

    Google Scholar 

  53. Feng, Y. H. et al. Dual-anionic coordination manipulation induces phosphorus and boron-rich gradient interphase towards stable and safe sodium metal batteries. Angew. Chem. Int. Ed. 64, e202415644 (2024).

    Google Scholar 

  54. Li, Y. et al. Sole-solvent high-entropy electrolyte realizes wide-temperature and high-voltage practical anode-free sodium pouch cells. Adv. Mater. 37, 2419764 (2025).

    Google Scholar 

  55. Gao, Y. et al. Advanced interphases layers for dendrite-free sodium metal anodes. ACS Appl. Mater. Interfaces 17, 17881–17894 (2025).

    Google Scholar 

  56. Liu, P. et al. Inorganic–organic hybrid multifunctional solid electrolyte interphase layers for dendrite-free sodium metal anodes. Angew. Chem. Int. Ed. 62, e202312413 (2023).

    Google Scholar 

  57. Gu, Z.-Y. et al. Precisely controlled preparation of an advanced Na3V2(PO4)2O2F cathode material for sodium ion batteries: the optimization of electrochemical properties and electrode kinetics. Inorg. Chem. Front. 6, 988–995 (2019).

    Google Scholar 

  58. Liang, H.-J. et al. Electrolyte chemistry toward ultrawide-temperature (−25 to 75 °C) sodium-ion batteries achieved by phosphorus/silicon-synergistic interphase manipulation. J. Am. Chem. Soc. 146, 7295–7304 (2024).

    Google Scholar 

  59. Frisch, M. J. et al. Gaussian 16, Revision C.01 Gaussian, Inc., Wallingford CT http://gaussian.com/citation/ (2016).

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Acknowledgements

We acknowledge the financial support from the National Key Research and Development Program of China (2023YFE0202000), National Natural Science Foundation of China (No. 52502221 and 52472089), Natural Science Foundation of Jilin Province (No. 20250101013JJ), and National Postdoctoral Program for Innovative Talents (No. BX20240062), Fundamental Research Funds for the Central Universities (No. 2412025QG001).

Author information

Authors and Affiliations

  1. State Key Laboratory of Integrated Optoelectronics, and MOE Key Laboratory for UV Light-Emitting Materials and Technology, Department of Physics, Northeast Normal University, Changchun, China

    Yong-Li Heng, Zhen-Yi Gu, Xiao-Tong Wang & Xing-Long Wu

  2. Qingdao University of Science and Technology, Qingdao, China

    Yuan-Zheng Tang

  3. Department of Chemistry, Northeast Normal University, Changchun, China

    Han-Hao Liu, Jie Wang & Shu-Yu Li

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Contributions

Y.-L.H., Z.-Y.G., and X.-L.W. conceived the idea and designed the experiments. Y.-L.H. performed the material characterizations and electrochemical measurements with assistance from Z.-Y.G., H.-H.L., X.-T.W., and S.-Y.L. J.W. contributed to the NMR tests. Y.-Z.T. provided support in the field of theoretical calculations. Y.-L.H. analyzed the data and prepared the paper with contributions from all authors.

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Correspondence to Zhen-Yi Gu or Xing-Long Wu.

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Heng, YL., Gu, ZY., Tang, YZ. et al. Dipolar interaction-mediated molecular anchoring electrolyte enables wide-temperature sodium-ion batteries with enhanced safety and durability. Nat Commun (2026). https://doi.org/10.1038/s41467-026-71861-7

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  • Received: 28 May 2025

  • Accepted: 25 March 2026

  • Published: 15 April 2026

  • DOI: https://doi.org/10.1038/s41467-026-71861-7

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