4.6 Article

Eutectic mixture of Protic Ionic Liquids as an Electrolyte for Activated Carbon-Based Supercapacitors

期刊

ELECTROCHIMICA ACTA
卷 155, 期 -, 页码 164-173

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2014.12.130

关键词

Eutectic; Protic ionic liquid; Supercapacitor; Activated carbon

资金

  1. Conseil de la Region Centre through the Sup'Caplipe project

向作者/读者索取更多资源

One of the drawbacks of ionic liquids is that some of them are solid or very viscous at room temperature; this prevents their use as electrolytes in energy storage systems. One solution consists of a binary mixture of pure, solid salts with the formation of a eutectic, allowing it to be used at room temperature. This work describes, for the first time, the formulation and use of a binary mixture of protic ionic liquids (PILs) based on the same H-bond donor, pyrrolidinium cation, with nitrate ([Pyrr][NO3]) and bis(trifluoromethanesulfonyl) imide ([Pyrr][TFSI]) anions as an electrolyte for carbon-based supercapacitors. The physicochemical and thermal properties of mixtures as a function of composition and temperature were fully investigated and related to their electrochemical behavior as an electrolyte. The electrochemical characterization of some selected optimal compositions (x([Pyrr][NO3]) = 0.64, 0.72, 0.80) shows, at first, good capacitive behavior (up to 148 F g (1)) at a potential voltage of 2.0 V. Moreover, above 2.0 V, anion intercalation was observed, increasing the specific capacitance up to 209 F g (1). At 2.5V during cycling, the characteristic peak of anion intercalation/deintercalation decreases, caused by saturation of the positive electrode by anions. Finally, accelerated aging tests showed good capacity retention (> 80%) at 2.0 V during 110 hours for x([Pyrr][NO3]) = 0.72, at 25 degrees C. According to these results, the use of eutectic PIL binary mixtures is a promising way to design adapted electrolytes according to the material electrode for energy devices at room temperature. (C) 2015 Published by Elsevier Ltd.

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