A new design strategy for polyimides/carbon nanotube networks is reported, aiming to passivate the hydrogen-evolution mechanism on the molecular structures of electrodes, thus substantially boosting their aqueous energy-storage capabilities. The intrinsic sluggish hydrogen-evolution activity of polyimides is further passivated via Li(+) association during battery charging, leading to a much wider voltage window and exceptional energy-storage capability.
Keywords: aqueous batteries; passivated HER activity; polyimides; power density; voltage window.
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