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Flexible paper electrodes for supercapacitors were prepared with partially-exfoliated graphite and polypyrrole as the active materials. Graphite was coated on paper with pencil drawing and then electrochemically exfoliated using the cyclic voltammetry (CV) technique to obtain the exfoliated graphite (EG)-coated paper (EG-paper). Polypyrrole (PPy) doped with β-naphthalene sulfonate anions was deposited on EG-paper through in-situ polymerization, leading to the formation of PPy-EG-paper. The as-prepared PPy-EG-paper showed a high electrical conductivity of 10.0 S·cm-1 and could be directly used as supercapacitor electrodes. The PPy-EG-paper electrodes gave a remarkably larger specific capacitance of 2148 F·g-1 at a current density of 0.8 mA.cm-2, compared to PPy-graphite-paper (848 F·g-1). The capacitance value of PPy-EG-paper could be preserved by 80.4% after 1000 charge/discharge cycles. In addition, the PPy-EG-paper electrodes demonstrated a good rate capability and a high energy density of 110.3 Wh·kg-1 at a power density of 121.9W·kg-1. This work will pave the way for the discovery of efficient paper-based electrode materials. [ABSTRACT FROM AUTHOR]

A simple, facile and low-cost method for recycling of supercapacitor materials is proposed. This process aims to recover some fundamental components of a used supercapacitor, namely the electrolyte salt tetraethyl ammonium tetrafluoroborate (TEABF4) dissolved in an aprotic organic solvent such as acetonitrile (ACN), the carbonaceous material (activated charcoal, carbon nanotubes) purified, the current collector (aluminium foil) and the separator (paper) for further utilization. The method includes mechanical shredding of the supercapacitor in order to reduce its size, and separation of aluminium foil and paper from the carbonaceous resources containing TEABF4 by sieving. The extraction of TEABF4 from the carbonaceous material was based on its solubility in water and subsequent separation through filtering and distillation. A cyclic voltammetry curve of the recycled carbonaceous material revealed supercapacitor behaviour allowing a potential reutilization. Furthermore, as BF4− stemming from TEABF4 can be slowly hydrolysed in an aqueous environment, thus releasing F− anions, which are hazardous, we went on to their gradual trapping with calcium acetate and conversion to non-hazardous CaF2. [ABSTRACT FROM AUTHOR]