Aqueous hybrid supercapacitors usually suffer from narrow voltage window and poor energy density limited by the thermodynamic decomposition of water. Based on necessary ion exchange membranes, the pH-decoupling strategy can be employed to extend the voltage windows of hybrid supercapacitors. We propose a novel low-impedance cation exchange membrane (CEM) with the interpenetrating network structure for the pH-decoupling strategy, which can be served as the separator for a AC//BiFeO3 supercapacitor to enhance its electrochemical performances. Two CEMs (CEM-1 and CEM-2) with different contents of the sulfonic acid (-SO3H) groups, are fabricated through the copolymerization of various monomers according to the predetermined stoichiometric ratios. FTIR, Raman and XPS spectra reflect that the CEM-2 has the higher content of the -SO3H groups than the CEM-1. The membrane parameter measurements confirm that the CEM-2 has the higher water content, lower membrane resistance and smaller membrane thickness than the CEM-1. The AC//BiFeO3 supercapacitor with the CEM-2 separator provides the higher gravimetric specific capacitance of 61 F g−1 at 1 A g−1, better coulombic efficiencies (97 % ∼ 103 %) and lower Rs value (39.74 Ω) than the AC//BiFeO3 supercapacitors with the CEM-1 separator. Moreover, the AC//BiFeO3 supercapacitor with the CEM-2 separator delivers the maximum energy density of 41.0 Wh kg−1 at the power density of 1.1 kW kg−1. The pH-decoupling strategy with this low-impedance CEM, opens up a new avenue for developing high-performance aqueous electrochemical energy storage devices.
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