Zinc-ion hybrid supercapacitors (ZHSs) are promising energy storage systems integrating high energy density and high-power density, whereas they are plagued by the poor electrochemical stability and inferior kinetics of zinc anodes. Herein, we report an electrolyte additive-assembled interconnecting molecules-zinc anode interface, realizing highly stable and fast-kinetics zinc anodes for ZHSs. The sulfobutyl groups-grafted β-cyclodextrin (SC) supramolecules as a trace additive in ZnSO₄ electrolytes not only adsorb on zinc anodes but also self-assemble into an interconnecting molecule interface benefiting from the mutual attraction between the electron-rich sulfobutyl group and the electron-poor cavity of the adjacent SC supramolecule. The interconnecting molecules-zinc anode interface provides abundant anion-trapping cavities and zincophilic groups to enhance Zn²⁺ transference number and homogenize Zn²⁺ deposition sites, and meanwhile, it accelerates the desolvation of hydrated Zn²⁺ to improve zinc deposition kinetics and inhibit active water molecules from inducing parasitic reactions at the zinc deposition interface, making zinc anodes present superior reversibility with 99.7% Coulombic efficiency, ~ 30 times increase in operation lifetime and an outstanding cumulative capacity at large current densities. ZHSs with 20,000-cycle life and optimized rate capability are thereby achieved. This work provides an inspiring strategy for designing zinc anode interfaces to promote the development of ZHSs.
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Li et al. (2025) studied this question.
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