Monolithic Carbide-derived Carbon Films with Superior Volumetric Capacitance

Abstract not Available.</jats:p

Porous Carbon Films for Maximizing Supercapacitor Performance

Abstract not Available.</jats:p

Monolithic Carbide-Derived Carbon Films for Micro-Supercapacitors

Microcapacitors for Manufacture Capacitors can store small amounts of charge, and as they can charge and discharge quickly, they work well with batteries for recovering power, such as in regenerative braking in hybrid cars. For very small power requirements, capacitors have not been competitive with microbatteries, but using monolithic carbon films to store the charge, Chmiola et al. (p. 480 ) demonstrate the feasibility of such applications. The small pores in the carbon films are sufficiently large to allow electrolyte transport and can be made using a processing technique compatible with current chip manufacturing. Such microcapacitors can thus be integrated with electronics to make autonomous sensors or implantable devices. </jats:p

Ionic Liquids as model electrolytes for Electrical Double Layer Capacitors

Abstract not Available.</jats:p

Charge Storage Mechanism in Sub-Nanometer Pores and its Consequence for Electrical Double Layer Capacitors

Abstract not Available.</jats:p

Relation between the Ion Size and Pore Size for an Electric Double-Layer Capacitor

The research on electrochemical double layer capacitors (EDLC), also known as supercapacitors or ultracapacitors, is quickly expanding because their power delivery performance fills the gap between dielectric capacitors and traditional batteries. However, many fundamental questions, such as the relations between the pore size of carbon electrodes, ion size of the electrolyte, and the capacitance have not yet been fully answered. We show that the pore size leading to the maximum double-layer capacitance of a TiC-derived carbon electrode in a solvent-free ethyl-methylimmidazolium-bis(trifluoro-methane-sulfonyl)imide (EMI-TFSI) ionic liquid is roughly equal to the ion size (∼0.7 nm). The capacitance values of TiC−CDC produced at 500 °C are more than 160 F/g and 85 F/cm3 at 60 °C, while standard activated carbons with larger pores and a broader pore size distribution present capacitance values lower than 100 F/g and 50 F/cm3 in ionic liquids. A significant drop in capacitance has been observed in pores that were larger or smaller than the ion size by just an angstrom, suggesting that the pore size must be tuned with sub-angstrom accuracy when selecting a carbon/ion couple. This work suggests a general approach to EDLC design leading to the maximum energy density, which has been now proved for both solvated organic salts and solvent-free liquid electrolytes