Surfactant based sol-gel approach to nanostructured LiFePO4 for high rate Li-ion batteries

被引:306
作者
Choi, Daiwon
Kumta, Prashant N.
机构
[1] Carnegie Mellon Univ, Dept Mat Sci & Engn, Pittsburgh, PA 15213 USA
[2] Carnegie Mellon Univ, Dept Biomed Engn, Pittsburgh, PA 15213 USA
基金
美国国家科学基金会;
关键词
lithium-ion battery; cathode; LiFePO4; surfactant; sol-gel approach;
D O I
10.1016/j.jpowsour.2006.09.082
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 [物理化学]; 081704 [应用化学];
摘要
Porous nanostructured LiFePO4 powder with a narrow particle size distribution (100-300 nm) for high rate lithium-ion battery cathode application was obtained using an ethanol based sol-gel route employing lauric acid as a surfactant. The synthesized LiFePO4 powders comprised of agglomerates of crystallites < 65 nm in diameter exhibiting a specific surface area ranging from 8 m(2) g(-1) to 36 m(2) g(-1) depending on the absence or presence of the surfactant. The LiFePO4 obtained using lauric acid resulted in a specific capacity of 123 mAh g(-1) and 157 mAh g(-1) at discharge rates of 10C and 1C with less than 0.08% fade per cycle, respectively. Structural and microstructural characterization were performed using X-ray diffraction (XRD), scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM) with energy dispersive X-ray (EDX) analysis while electronic conductivity and specific surface area were determined using four-point probe and N-2 adsorption techniques. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1064 / 1069
页数:6
相关论文
共 40 条
[1]
Lithium extraction/insertion in LiFePO4:: an X-ray diffraction and Mossbauer spectroscopy study [J].
Andersson, AS ;
Kalska, B ;
Häggström, L ;
Thomas, JO .
SOLID STATE IONICS, 2000, 130 (1-2) :41-52
[2]
Fine-particle lithium iron phosphate LiFePO4 synthesized by a new low-cost aqueous precipitation technique [J].
Arnold, G ;
Garche, J ;
Hemmer, R ;
Ströbele, S ;
Vogler, C ;
Wohlfahrt-Mehrens, A .
JOURNAL OF POWER SOURCES, 2003, 119 :247-251
[3]
Lithium iron(II) phospho-olivines prepared by a novel carbothermal reduction method [J].
Barker, J ;
Saidi, MY ;
Swoyer, JL .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2003, 6 (03) :A53-A55
[4]
Electron microscopy study of the LiFePO4 to FePO4 phase transition [J].
Chen, GY ;
Song, XY ;
Richardson, TJ .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2006, 9 (06) :A295-A298
[5]
Reducing carbon in LiFePO4/C composite electrodes to maximize specific energy, volumetric energy, and tap density [J].
Chen, ZH ;
Dahn, JR .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2002, 149 (09) :A1184-A1189
[6]
Microscale measurements of the electrical conductivity of doped LiFePO4 [J].
Chung, SY ;
Chiang, YM .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2003, 6 (12) :A278-A281
[7]
Electronically conductive phospho-olivines as lithium storage electrodes [J].
Chung, SY ;
Bloking, JT ;
Chiang, YM .
NATURE MATERIALS, 2002, 1 (02) :123-128
[8]
A novel concept for the synthesis of an improved LiFePO4 lithium battery cathode [J].
Croce, F ;
D'Epifanio, A ;
Hassoun, J ;
Deptula, A ;
Olczac, T ;
Scrosati, B .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2002, 5 (03) :A47-A50
[9]
Size effects on carbon-free LiFePO4 powders [J].
Delacourt, C. ;
Poizot, P. ;
Levasseur, S. ;
Masquelier, C. .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2006, 9 (07) :A352-A355
[10]
One-step low-temperature route for the preparation of electrochemically active LiMnPO4 powders [J].
Delacourt, C ;
Poizot, P ;
Morcrette, M ;
Tarascon, JM ;
Masquelier, C .
CHEMISTRY OF MATERIALS, 2004, 16 (01) :93-99