LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

Macropore-assisted electrolyte transfer inside binder-free templated carbon xerogels as carbon electrode for electric double layer capacitors

Photo from wikipedia

Abstract Capacitive performance of electric double layer capacitors is influenced by specific surface area, while pore structure also promotes electrolyte transfer inside a carbon electrode. Organic electrolytes require macropores, whereas… Click to show full abstract

Abstract Capacitive performance of electric double layer capacitors is influenced by specific surface area, while pore structure also promotes electrolyte transfer inside a carbon electrode. Organic electrolytes require macropores, whereas aqueous electrolytes operate best using mesopores for electrolyte transfer. Templated carbon xerogels (TCXs) were prepared from resorcinol and formaldehyde with cotton fibers as a hard template containing macropores, mesopores and micropores as the carbon electrode. Results suggested that macropores (>50 nm) were contiguously created and connected with mesopore diameters (2–50 nm), leading to convenient ion transport inside the TCXs. Vacuum drying formed sponge-like carbon xerogels that permitted electrolyte transfer. Despite the insignificant change of porous properties, TCXs possessing sponge-like carbon xerogels showed increased capacitance values from 137 F/g to 317 F/g at 200 mA/g in a three-electrode system as a result of macropore-assisted electrolyte transfer in aqueous electrolytes.

Keywords: carbon xerogels; carbon; carbon electrode; electrolyte transfer

Journal Title: European Polymer Journal
Year Published: 2020

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.