Innovative hydrogel electrolyte enhances energy density and reduces self-discharge in zinc-iodine batteries, suggesting improved storage solutions.
Aqueous zinc-iodine batteries (AZIBs) leveraging four-electron I⁻/I⁰/I⁺ redox chemistry show great promise in safe energy storage systems. However, realizing Ah-level AZIBs with industrial-grade parameters (≥10 mg cm⁻² mass loading) remains fundamentally challenging. Here, we prepare the hydrogel electrolyte with mesoporous nanoparticles SBA-15 (MNPHE) by a nanoconfined polymerization strategy. The framework confinement effect, anion confinement effect, and free water confinement effect are achieved through Lewis acid-base interactions and hydrogen bond networks. The multiconfinement effects yield simultaneous ultrahigh mechanical strength (501 kPa tensile strength) and a record-high Zn²⁺ transference number (tZn²⁺ = 0.95), which collectively suppressed polyiodide generation and I⁺ species hydrolysis. This results in markedly enhanced reversibility and kinetics for four-electron I⁻/I⁰/I⁺ redox chemistry under a high-I₂-mass-loading cathode. Based on MNPHE, the Zn||I₂ full cells display a record-low self-discharge rate with only 20% capacity loss after three months and a prolonged lifetime of 100,000 cycles at 25 C. Furthermore, Ah-level four-electron Zn||I₂ pouch cells achieve excellent cyclability of 800 cycles and an ultrahigh cathode-mass-specific energy density of 466.7 Wh kg⁻¹, surpassing all aqueous Zn-based systems in the Ah-level regime.
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Liu et al. (2026) studied this question.
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