RESUMEN
An asymmetric polymer capacitor was prepared from pyrene (PY), aniline (ANI), and commercially available activated carbon (AC) through a solvent-free preparation. PY and ANI were adsorbed into the AC host material in the gas phase and electrochemically polymerized exclusively inside the AC pores in an aqueous H2SO4 electrolyte (1 M). No volumetric expansion of the AC particles occurred upon the adsorption of monomers and their subsequent polymerizations; thus, the volumetric capacitance was enhanced by the inclusion of pseudocapacitive polypyrene (PPY) and polyaniline (PANI). The PPY and PANI structures formed inside the AC pores are very thin and have a large contact area with the conductive carbon surfaces. Therefore, the charge transfer distance between the polymers and the carbon surfaces was drastically shortened, significantly reducing the charge transfer resistance; i.e., high power density. The maximum volumetric capacitances for the PPY- and PANI-hybridized AC reached 314 and 299 F cm-3, respectively. Moreover, the strong adhesion derived from their large contact areas and adsorption capability of AC endow these materials with long cycle lifetimes. The PPY- and PANI-hybridized AC have different redox potentials and can be assembled into an asymmetric capacitor. The volumetric capacitance obtained for the asymmetric capacitor further surpassed that of the symmetric capacitor consisting of pristine AC, with high power density and long cycle lifetimes.
RESUMEN
Polyaniline (PANI) was synthesized exclusively inside the micropores of activated carbon (AC). This nanosized PANI was smaller than 2 nm in diameter and allowed for fast redox reactions, exhibiting superior pseudocapacitance in terms of power and energy densities over the electric double layer capacitance generated inside the micropores.