Title :
Electrochemical studies of V2O5-CNTs nanocomposite
Author :
Wu, Guangming ; Wang, Airong ; Zhang, Mingxia ; Yang, Huiyu ; Zhang, Zhihua ; Zhou, Bin ; Shen, Jun
Author_Institution :
Pohl Inst. of Solid State Phys., Tongji Univ., Shanghai
Abstract :
Carbon nanotubes (CNTs) doped vanadium pentoxide (V2O5) porous aerogels are a good kind of material as the cathode material in lithium batteries due to their layered structure, high energy density, good reversibility, high capacity for lithium ion insertion. V2O5-CNTs nanocomposites were synthesized by a sol-gel method, using the solvent exchange and ambient pressure drying technique. Electrochemical measurements of the nanocomposite were tested. The lithium ion capacity and cycle ability of the composites were investigated by galvanostatic discharge-charge cycling. The results showed that the nanocomposite had the higher capacity, about 384.0 mAh/g in the first discharge process and 256.3 mAh/g in the second discharge cycle. The charge-transfer reaction at the electrode/electrolyte interface and the kinetic mechanism were too studied by using electrochemical impedance spectroscopy.
Keywords :
aerogels; carbon nanotubes; electrochemical electrodes; electrochemical impedance spectroscopy; lithium; nanocomposites; secondary cells; sol-gel processing; vanadium compounds; V2O5; ambient pressure drying technique; carbon nanotubes; cathode material; charge-transfer reaction; electrochemical impedance spectroscopy; electrochemical measurements; electrode-electrolyte interface; galvanostatic discharge-charge cycling; kinetic mechanisms; lithium batteries; lithium ion capacity; lithium ion insertion; nanocomposites; sol-gel method; solvent exchange technique; vanadium pentoxide porous aerogels; Battery charge measurement; Carbon nanotubes; Cathodes; Electrodes; Kinetic theory; Lithium; Nanocomposites; Organic materials; Solvents; Testing;
Conference_Titel :
Nanoelectronics Conference, 2008. INEC 2008. 2nd IEEE International
Conference_Location :
Shanghai
Print_ISBN :
978-1-4244-1572-4
Electronic_ISBN :
978-1-4244-1573-1
DOI :
10.1109/INEC.2008.4585501