Preparation of Kevlar-derived carbon fibers and their anodic performances in Li secondary batteries

Citation
Ks. Ko et al., Preparation of Kevlar-derived carbon fibers and their anodic performances in Li secondary batteries, CARBON, 39(11), 2001, pp. 1619-1625
Citations number
22
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
CARBON
ISSN journal
00086223 → ACNP
Volume
39
Issue
11
Year of publication
2001
Pages
1619 - 1625
Database
ISI
SICI code
0008-6223(2001)39:11<1619:POKCFA>2.0.ZU;2-N
Abstract
We report here the preparation of Kevlar-derived carbon fibers and the prel iminary results on their anodic performances in Li secondary batteries. The single- or two-step carbonization process is employed for the preparation. In the single-step process, the Kevlar flocks are heat-treated under At at mosphere from 25 to 800 degreesC with a heating rate of 5 degreesC min(-1), but an additional intermediate heating at a fixed temperature between 330 and 510 degreesC for 2 h is applied in the two-step preparation. The two-st ep carbonization allows a higher carbon yield than that achieved in the sin gle-step one (ca. 36%). In particular, a maximum yield (ca. 50%) is observe d with an intermediate heating at 400-410 degreesC. The infrared study indi cates that the higher carbon yield achieved in the two-step process is inde bted to the formation of condensed/cross-linked polyaromatic molecules duri ng the intermediate heating period, which seemingly alleviates the volatile loss in the subsequent higher temperature heating. The Kevlar-derived carb on fibers exhibit the charge-dis charge behaviors that are commonly observe d in non-graphitizable carbons. Here, the carbon made by the two-step proce ss (intermediate heating at 410 degreesC) delivers a higher discharge capac ity than the single-step ones. In particular, a notably high capacity near zero volts is observed in the two-step carbon that is associated with the L i+ removal from the micropores. The higher population of micropores in the two-step carbons may be explained by the enriched formation of cross-linked polyaromatics during the intermediate heating. (C) 2001 Elsevier Science L td. All rights reserved.