Measuring cycle efficiency and capacitance of chemically activated carbons in propylene carbonate

被引:39
作者
Cazorla-Amoros, D. [1 ]
Lozano-Castello, D. [1 ]
Morallon, E. [2 ,3 ]
Bleda-Martinez, M. J. [1 ]
Linares-Solano, A. [1 ]
Shiraishi, S. [4 ]
机构
[1] Univ Alicante, Dept Quim Inorgan, E-03080 Alicante, Spain
[2] Univ Alicante, Dept Quim Fis, E-03080 Alicante, Spain
[3] Univ Alicante, Inst Univ Mat, E-03080 Alicante, Spain
[4] Gunma Univ, Grad Sch Engn, Dept Chem & Chem Biol, Gunma 3768515, Japan
关键词
DOUBLE-LAYER CAPACITANCE; ELECTROCHEMICAL CHARACTERIZATION; SURFACE-CHEMISTRY; ELECTROLYTES; DECOMPOSITION; STABILITY; BEHAVIOR; FIBERS; LIQUID;
D O I
10.1016/j.carbon.2009.12.039
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The cycle efficiency and capacitance of two KOH-activated carbons have been tested in 0 5 M tetraethylammonium tetrafluoroborate in propylene carbonate (TEABF(4)/PC) under different conditions of temperature (room temperature and 70 degrees C) and voltage (0-3 V) The materials tested include a KOH-activated carbon before and after treatment with different acids and hydrogen at high temperature to remove most of the oxygen groups and inorganic impurities Porous texture and surface chemistry characterization have been carried out before and after cycling to understand the changes in the properties of activated carbons during the cycles it has been observed that the treatment with different acids and hydrogen at high temperature produces materials with higher cycling stability The results point out that the observed electrode degradation is mainly due to some pore blockage caused by reaction of the solvent with the functional groups on the carbon The blockage of porosity is higher for the sample with higher oxygen content, indicating that the treatment carried out to remove the oxygen groups has an important positive effect, giving electrodes with a much lower degradation under very aggressive conditions in a TEABF4/PC medium (C) 2009 Elsevier Ltd All rights reserved
引用
收藏
页码:1451 / 1456
页数:6
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