Electrolyte design improves ionic conductivity in zinc–iodine batteries, suggesting enhanced battery performance.
Rechargeable aqueous zinc–iodine (Zn–I 2 ) batteries are promising due to their eco‐friendliness and low cost. However, challenges such as Zn dendrite growth, anode corrosion, and polyiodide shuttling in electrolytes persist. Here, chitosan and agar hydrogel has been prepared as electrolyte, in which the hydrophilic groups in polymers form solvation structure of Zn 2+ . Due to the minimal water content in the system, ClO 4 − also participates in the Zn 2+ solvation structure, further reducing the number of solvated water molecules. Notably, the resulting hydrogel exhibits low water content yet achieves higher ionic conductivity (26.62 mS cm −1 ) than typical water‐poor gels. The reduced activity of H 2 O suppresses Zn dendrite growth and corrosion, significantly extending the electrochemical window to 3.02 V. The assembled Zn||Zn symmetric cells demonstrate exceptional electrochemical stability, operating for over 4000 h at 1 mA cm −2 . For the iodine cathode, elemental iodine is fully adsorbed onto the carbon host. The layered porous structure of the electrode considerably increases its surface area, providing more active sites to facilitate electron transfer and ion diffusion. This, along with uniform iodine dispersion, enhances the practical iodine reaction ratio, yielding a high specific capacity of 186.5 mAh g −1 at 5 A g −1 .
No takes yet. Share an insight, caveat, or question.
Bai et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: