Bimodal porous carbon as a negative electrode material for lithium-ion capacitors

被引:23
作者
Woo, Sang-Wook
Dokko, Kaoru
Nakano, Hiroyuki
Kanamura, Kiyoshi
机构
[1] Tokyo Metropolitan Univ, Grad Sch Urban Environm Sci, Dept Appl Chem, Hachioji, Tokyo 1920397, Japan
[2] Japan Sci & Technol Agcy, CREST, Kawaguchi, Saitama 3320012, Japan
关键词
lithium-ion capacitors; lithium-ion batteries; colloidal crystal; macroporous carbon;
D O I
10.5796/electrochemistry.75.635
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Bimodal porous carbons consisting of interconnected macropores and spherical mesopores, were prepared by colloidal crystal templating method. The template was prepared by evaporation process of suspensions containing monodisperse poly[styrene-(co-2-hydroxyethyl methacrylate)] (PSHEMA) latex and colloidal silica in water. The carbonization of PSHEMA at 1000 degrees C under inert atmosphere provided very thin carbon layer on the colloidal silica in the template, and the macropore corresponding to the PSHEMA particle size were formed simultaneously. After this procedure, bimodal porous carbons were obtained by removing the silica particles with hydrofluoric acid. Three kinds of bimodal porous carbons were prepared using PSHEMA latex of 450 nm and colloidal silica with three different average diameters of 10 similar to 20 nm, 40 similar to 50 nm, and 70 similar to 100 nm, respectively. Bimodal porous structure was observed with a field emission-scanning electron microscope. Nitrogen adsorption/desorption measurements revealed that the prepared samples involved macropore and mesopore with small amount of micropore. The bimodal porous carbons were electrochemically evaluated as a negative electrode of lithium-ion capacitor in ethylene carbonate and diethyl carbonate containing 1 mol dm(-3) LiClO4. The bimodal porous carbon prepared using silica of 10 similar to 20 nm showed a large capacitance of 360 F g(-1) at a high current density of 7.4 A g(-1).
引用
收藏
页码:635 / 640
页数:6
相关论文
共 31 条
[1]   An advanced hybrid electrochemical capacitor that uses a wide potential range at the positive electrode [J].
Aida, Taira ;
Yamada, Koji ;
Morita, Masayuki .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2006, 9 (12) :A534-A536
[2]   An asymmetric hybrid nonaqueous energy storage cell [J].
Amatucci, GG ;
Badway, F ;
Du Pasquier, A ;
Zheng, T .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2001, 148 (08) :A930-A939
[3]  
ANDO N, 2005, 46 BATT S JAP ABSTR
[4]   THE DETERMINATION OF PORE VOLUME AND AREA DISTRIBUTIONS IN POROUS SUBSTANCES .1. COMPUTATIONS FROM NITROGEN ISOTHERMS [J].
BARRETT, EP ;
JOYNER, LG ;
HALENDA, PP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (01) :373-380
[5]   DEPENDENCE OF THE ELECTROCHEMICAL INTERCALATION OF LITHIUM IN CARBONS ON THE CRYSTAL-STRUCTURE OF THE CARBON [J].
DAHN, JR ;
SLEIGH, AK ;
SHI, H ;
REIMERS, JN ;
ZHONG, Q ;
WAY, BM .
ELECTROCHIMICA ACTA, 1993, 38 (09) :1179-1191
[6]   Power-ion battery: bridging the gap between Li-ion and supercapacitor chemistries [J].
Du Pasquier, A ;
Plitz, I ;
Gural, J ;
Badway, F ;
Amatucci, GG .
JOURNAL OF POWER SOURCES, 2004, 136 (01) :160-170
[7]   A comparative study of Li-ion battery, supercapacitor and nonaqueous asymmetric hybrid devices for automotive applications [J].
Du Pasquier, A ;
Plitz, I ;
Menocal, S ;
Amatucci, G .
JOURNAL OF POWER SOURCES, 2003, 115 (01) :171-178
[8]   Influence of pore structure on electric double-layer capacitance of template mesoporous carbons [J].
Fuertes, AB ;
Pico, F ;
Rojo, JM .
JOURNAL OF POWER SOURCES, 2004, 133 (02) :329-336
[9]  
Gates B, 2000, ADV MATER, V12, P653, DOI 10.1002/(SICI)1521-4095(200005)12:9<653::AID-ADMA653>3.0.CO
[10]  
2-3