Activation of coal tar derived needle coke with K2CO3 into an active carbon of low surface area and its performance as unique electrode of electric double-layer capacitor

被引:103
作者
Mitani, S
Lee, SL
Saito, K
Yoon, SH
Korai, Y
Mochida, I [1 ]
机构
[1] Kyushu Univ, Inst Mat Chem & Engn, Fukuoka 8168570, Japan
[2] GS Caltex Corp, Taejon 305380, South Korea
[3] Nippon Steel Corp Ltd, Adv Technol Res Labs, Futtsu, Chiba 2938511, Japan
关键词
needle coke; activation; X-ray diffraction; electrochemical properties;
D O I
10.1016/j.carbon.2005.05.047
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
Raw needle coke from coal tar pitch was activated with K2CO3 at a coke:carbonate weight ratio of 1:4, to prepare all electrode for all electric double-layer capacitor (EDLC). Although the surface area of the coke activated at 900 degrees C for 3 h was as small as 20 m(2)/g with it very high yield, the coke achieved capacitances per weight and volume of 20 F/g and 20 F/ml, respectively, in the two-electrode system, by charging at 2.7 V. The surface area of KOH-activated coke with a similar ratio (coke:hydroxide = 1:4. wt:wt) was over 2300 m(2)/g, and it exhibited capacitance per weight and volume values of 42 F/g and 17 F/ml, respectively. The coke activated by K2CO3 was found to be further activated by the charging. This electrochemical activation, which has been reported as activation in all electric field, was investigated by cyclic voltammetry in order to clarify it. The graphitic and pore structures of the coke after the electrochemical activation were analyzed by XRD to confirm retention of the graphene structure. Xe-NMR showed that the formation of small new pores was induced in the cathode material, increasing the surface area from 6 m(2)/g to 18 m(2)/g before use, although the pore volume was around 0.015-0.017 m(3)/g both before and after the charging. This activation with K2CO3 and a deeper understanding of the activation on charging suggest future directions for the preparation of electrode carbon for EDLCs. (C) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2960 / 2967
页数:8
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