Anodic performances of anisotropic carbon derived from isotropic quinoline pitch

被引:20
作者
Mochida, I [1 ]
Ku, CH [1 ]
Yoon, SH [1 ]
Korai, Y [1 ]
机构
[1] Kyushu Univ, Inst Adv Mat Study, Fukuoka 8168580, Japan
关键词
coke; calcination; carbonization; electrochemical properties;
D O I
10.1016/S0008-6223(98)00199-7
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 anodic performances of anisotropic carbon derived from quinoline pitch (CQP) to be used in the lithium ion battery were studied to clarify the influence of nitrogen in the carbon hexagonal sheet. The quinoline pitch was synthesized by using HF/BF3 as a catalyst. Nitrogen in the carbon existed as pyridinic, pyrrolic and quaternary types to be converted in this sequence, depending upon HTT. Above 1000 degrees C. nitrogen started to evolve, leaving vacancies in the sheer which were filled by graphitization at higher HTT. CQP prepared below 700 degrees C showed much lower discharge capacity than that derived from naphthalene pitch (CNP) at the same temperature. Higher temperature treatment reduced the capacity as observed commonly in the anisotropic carbon, however, the extent of reduction was smaller. Hence, the capacity became the same at 800 degrees C and larger at 1000 and 1200 degrees C than those of CNP. The capacity of CQP after the heat-treatment at 1000 degrees C, where the cycle stability was acceptable was 320 mAh g(-1). The nitrogen in the ring disturbs the growth and stacking of hexagonal sheets by the carbonization below 700 degrees C to reduce the capacity of CQP, whereas the vacancies due to nitrogen evolution by the heat-treatment at 1000 degrees C appeared to provide new type sites for lithium charge. Such sites gave potentials of charge and discharge at 0.5-1.0 V reversibly and capacity of 468 mAh g(-1). Higher temperature may remove such sites by graphitization. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:323 / 327
页数:5
相关论文
共 22 条
[11]   Lithium doping undoping in disordered coke carbons [J].
Mori, Y ;
Iriyama, T ;
Hashimoto, T ;
Yamazaki, S ;
Kawakami, F ;
Shiroki, H .
JOURNAL OF POWER SOURCES, 1995, 56 (02) :205-208
[12]   LAYERED-STRUCTURE BC2N AS A NEGATIVE ELECTRODE MATRIX FOR RECHARGEABLE LITHIUM BATTERIES [J].
MORITA, M ;
HANADA, T ;
TSUTSUMI, H ;
MATSUDA, Y ;
KAWAGUCHI, M .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1992, 139 (05) :1227-1230
[13]   A MECHANISM OF LITHIUM STORAGE IN DISORDERED CARBONS [J].
SATO, K ;
NOGUCHI, M ;
DEMACHI, A ;
OKI, N ;
ENDO, M .
SCIENCE, 1994, 264 (5158) :556-558
[14]  
TATSUMI K, 1923, J ELECTROCHEM SOC, P143
[15]   Electrochemical insertion of lithium into carbon synthesized from condensed aromatics [J].
Tokumitsu, K ;
Mabuchi, A ;
Fujimoto, H ;
Kasuh, T .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1996, 143 (07) :2235-2239
[16]   PREPARATION AND CHARACTERIZATION OF BXC1-X THIN-FILMS WITH THE GRAPHITE STRUCTURE [J].
WAY, BM ;
DAHN, JR ;
TIEDJE, T ;
MYRTLE, K ;
KASRAI, M .
PHYSICAL REVIEW B, 1992, 46 (03) :1697-1702
[17]   THE EFFECT OF BORON SUBSTITUTION IN CARBON ON THE INTERCALATION OF LITHIUM IN LIX(BZC1-Z)6 [J].
WAY, BM ;
DAHN, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1994, 141 (04) :907-912
[18]   LITHIUM INSERTION IN CARBONS CONTAINING NANODISPERSED SILICON [J].
WILSON, AM ;
DAHN, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1995, 142 (02) :326-332
[19]   Correlation between lithium intercalation capacity and microstructure in hard carbons [J].
Xing, WB ;
Xue, JS ;
Zheng, T ;
Gibaud, A ;
Dahn, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1996, 143 (11) :3482-3491
[20]   STRUCTURE AND PROPERTIES OF DEEPLY LI-DOPED POLYACENIC SEMICONDUCTOR-MATERIALS BEYOND C6LI STAGE [J].
YATA, S ;
KINOSHITA, H ;
KOMORI, M ;
ANDO, N ;
KASHIWAMURA, T ;
HARADA, T ;
TANAKA, K ;
YAMABE, T .
SYNTHETIC METALS, 1994, 62 (02) :153-158