4.8 Article

How does lithium oxalyldifluoroborate enable the compatibility of ionic liquids and carbon-based capacitors?

期刊

JOURNAL OF POWER SOURCES
卷 276, 期 -, 页码 299-308

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jpowsour.2014.11.096

关键词

Ionic liquid; EDLC; LiODFB; Activated carbon; Acetamide; OZO

资金

  1. National Science Foundation of China [21373028, 21073233]
  2. National Key Basic Research and Development Program [2009CB220100]
  3. National 863 Program [2011AA11A256]
  4. New Century Educational Talents Plan of Chinese Education Ministry [NCET-12-0050]
  5. Beijing Novel Program [Z121103002512029]

向作者/读者索取更多资源

Lithium oxalyldifluoroborate (LiODFB) has several unique characteristics, such as high ionic conductivity over a wide temperature range and the ability to form and stabilize solid electrolyte interface films on graphite surfaces. A series of binary, room-temperature, molten electrolytes composed of LiODFB and organic compounds with acylamino groups (acetamide, oxazolidinone or OZO) have been synthesized. Fourier-transform infrared (FT-IR) spectroscopy indicates that C=O and N-H functional groups undergo blue or red shifts upon addition of LiODFB. The electrolytes have excellent thermal stabilities and electrochemical characteristics that allow them to be promising electrolytes for electrochemical double layer capacitors (EDLCs). Here, we examine 1:5 molar ratio LiODFB and acetamide/OZO ionic liquid (IL) electrolytes in EDLCs. IL compatibility with two types of carbon-based electrodes is investigated theoretically and experimentally. We simulate possible structures and ion diameters for the ILs, which must be compatible with pore sizes of the carbon electrodes. Mesoporous activated carbon AC2, with a pore size similar to the ionic diameter of LiODFB acetamide, has a specific capacitance of 154.2 Fg(-1) at 20 m Ag-1. Additionally, typical capacitive and reversibility behaviors can be seen in the charge discharge curves over 0-2 V. Finally, the EDLCs exhibit good charging/discharging performances. (C) 2014 Elsevier B.V. All rights reserved.

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