Abstract Recent advancements in Zn-halogen batteries have focused on enhancing the adsorptive or catalytic capability of host materials and stabilizing complex intermediates with electrolyte additives, while the halogen-ion electrolyte modifications exhibit strong potential for integrated interfacial regulation. Herein, we design an electrically insulating rigid electrolyte container to immobilize a liquid halogen-ion electrolyte for separator-free Zn-halogen batteries with customizable electron transfer. Robust hydrogen bonding of hydroxyl groups in SiO 2 with fluorinated moieties in PVDF- hfp regulates Zn 2+ solvation and suppresses H 2 O activity, while multi-channels formed by microcracks and interparticle gaps not only enhance mass transfer but also buffer interfacial electric field, jointly enabling a durable Zn plating/stripping. Effective confinement of intermediates also ensures the high reversibility across single-(I − /I 0 ), double-(I − /I 0 /I⁺), and triple-(I − /I 0 /I⁺, Cl − /Cl 0 ) electron transfer mechanisms at cathode, as evidenced by the double-electron transfer systems exhibiting a low capacity decay rate of 0.02‰ over 4500 cycles at 10 mA cm −2 and a high areal capacity of 11.9 mAh cm −2 at 2 mA cm −2 . This work presents a novel “container engineering” approach to halogen-ion electrolyte design and provides fundamental insights into the relationships between redox reversibility and reaction kinetics.
Zhou et al. (Mon,) studied this question.