摘要
Quasi-solid electrolytes can mitigate polyiodide shuttling and suppress parasitic reactions at zinc negative electrode in zinc-iodine batteries by reducing free water, but their limited liquid content often results in sluggish interfacial charge transfer. Here we show liquid-electrolyte-wetted quasi-solid electrolytes by combining single-atom-modified zeolites (single-atom = iron, cobalt, nickel, and copper) with zinc sulfate aqueous solution for high-rate zinc-iodine batteries. Theoretical calculations, in situ spectroscopy, and laser confocal microscopy reveal that the single-atom metal sites enhance iodine conversion kinetics and suppress polyiodide shuttling through a synergistic catalytic-adsorption effect, with iron-doped zeolite exhibiting the strongest performance. Iron-doped zeolite further stabilizes water molecules, suppresses side reactions, and promotes uniform zinc deposition. The iron-doped zeolite-assembled zinc-iodine batteries maintain a discharge capacity of 81.2 mAh g −1 (based on iodine mass) after 6,800 cycles at 4 A g −1 , while proof-of-concept pouch cells exhibit a capacity of 147.6 mAh g −1 (based on iodine mass) or 52 mAh g −1 (based on total positive electrode mass) after 200 cycles at 0.5 A g −1 . Lastly, iron-doped zeolite also demonstrates compatibility with other positive electrode materials for rechargeable zinc batteries.
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