| Literature DB >> 27893725 |
Eléonore Mourad1,2, Laura Coustan1,2, Pierre Lannelongue1,2, Dodzi Zigah3, Ahmad Mehdi1, André Vioux1, Stefan A Freunberger4, Frédéric Favier1,2, Olivier Fontaine1,2.
Abstract
Kinetics of electrochemical reactions are several orders of magnitude slower in solids than in liquids as a result of the much lower ion diffusivity. Yet, the solid state maximizes the density of redox species, which is at least two orders of magnitude lower in liquids because of solubility limitations. With regard to electrochemical energy storage devices, this leads to high-energy batteries with limited power and high-power supercapacitors with a well-known energy deficiency. For such devices the ideal system should endow the liquid state with a density of redox species close to the solid state. Here we report an approach based on biredox ionic liquids to achieve bulk-like redox density at liquid-like fast kinetics. The cation and anion of these biredox ionic liquids bear moieties that undergo very fast reversible redox reactions. As a first demonstration of their potential for high-capacity/high-rate charge storage, we used them in redox supercapacitors. These ionic liquids are able to decouple charge storage from an ion-accessible electrode surface, by storing significant charge in the pores of the electrodes, to minimize self-discharge and leakage current as a result of retaining the redox species in the pores, and to raise working voltage due to their wide electrochemical window.Entities:
Year: 2016 PMID: 27893725 DOI: 10.1038/nmat4808
Source DB: PubMed Journal: Nat Mater ISSN: 1476-1122 Impact factor: 43.841