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Although the meticulous design of functional diversity within the polymer interfacial layer holds paramount significance in mitigating the challenges associated with hydrogen evolution reactions and dendrite growth in zinc anodes, this pursuit remains a formidable task. Here, a large-scale producible zinc-enriched/water-lean polymer interfacial layer, derived from carboxymethyl chitosan (CCS), is constructed on zinc anodes by integration of electrodeposition and a targeted complexation strategy for highly reversible Zn plating/stripping chemistry. Zinc ions-induced crowding effect between CCS skeleton creates a strong hydrogen bonding environment and squeezes the moving space for water/anion counterparts, therefore greatly reducing the number of active water molecules and alleviating cathodic I 3 – attack. Moreover, the as-constructed Zn 2+ -enriched layer substantially facilitate rapid Zn 2+ migration through the NH 2 –Zn 2+ -NH 2 binding/dissociation mode of CCS molecule chain. Consequently, the large-format Zn symmetry cell (9 cm 2 ) with a Zn-CCS electrode demonstrates excellent cycling stability over 1100 h without bulging. When coupled with an I 2 cathode, the assembled Zn–I 2 multilayer pouch cell displays an exceptionally high capacity of 140 mAh and superior long-term cycle performance of 400 cycles. This work provides a universal strategy to prepare large-scale production and high-performance polymer crowding layer for metal anode-based battery, analogous outcomes were veritably observed on other metals (Al, Cu, Sn).
Hu et al. (Tue,) studied this question.