Solvation engineering decouples bulk and interfacial chemistry for robust potassium-ion batteries
solvation structure that is regulated by anion-solvent interactions, while maintaining adequate anion participation in the solvation sheath. This configuration exhibits interface stabilization and low desolvation barriers, with a kinetic compensation mechanism yielding a higher K⁺ transference number. When assembled in potassium batteries, it achieves highly reversible K plating/stripping with a Coulombic efficiency of 98.9% in K||Cu cells, 85% capacity retention over 1600 cycles in a graphite electrode, and stable, fast-cycling performance in both K||Prussian blue analogue half-cells and graphite||Prussian blue analogue full-cells over a wide working temperature range of -20 to +45 °C. This work establishes a viable approach for tailoring specific electrolyte properties by precisely tuning microscopic solvation structures through anion-solvent interaction.
Authors
- X.C. Li (ORCID: https://orcid.org/0000-0002-5981-2762)
- Yihan Yang
- Dianwei Zhang
- Xuemei Ma
- J Zhou
- Hongwei Fu
- Apparao M. Rao (ORCID: https://orcid.org/0000-0002-1450-3499)
- Fuxiang Li (ORCID: https://orcid.org/0000-0003-0050-5853)
- Bingan Lu (ORCID: https://orcid.org/0000-0002-0075-5898)
Institutions
- Central South University of Forestry and Technology (CN)
- Central South University (CN)
- Hunan University (CN)
- Wuhan Textile University (CN)
- Clemson University (US)
Publication Details
- Journal
- Nature Communications
- Published
- 2026-04-21
- DOI
- https://doi.org/10.1038/s41467-026-71940-9
- Primary Topic
- Advancements in Battery Materials
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Clemson University
- National Natural Science Foundation of China
- Wuhan Textile University