Carbothermal synthesis of SnxSb anode material for secondary lithium-ion battery

被引:33
作者
Zhao, HL [1 ]
Ng, DHL
Lu, ZQ
Ma, NG
机构
[1] Univ Sci & Technol Beijing, Dept Inorgan Nonmet Mat, Beijing 100083, Peoples R China
[2] Chinese Univ Hong Kong, Dept Phys, Shatin, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
SnSb alloy; secondary lithium ion battery; carbothennal reduction; electrochemical capacity;
D O I
10.1016/j.jallcom.2004.10.060
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
SnxSb alloy powders were synthesized by carbothermal reduction from SnO2 and Sb2O3 in Ar atmosphere above 850 degrees C. The synthesis process of SnxSb powders was characterized by differential thermal analysis (DTA) and X-ray diffraction (XRD). The particle feature and electrochemical property of synthesized SnxSb powders were evaluated by scanning electron microscopy (SEM), transmission electron microscopy (TEM) and galvanostatical cycling tests. The results indicated that with the increase of SnO2 content in raw powders, the completely reduced temperature of SnO2 and Sb2O3 mixture increased. A certain amount of Sb was detected in 1000 degrees C-synthesized Sn,Sb powder with pre-designated SnO2/Sb2O3 molar ratio of 2:1, while only SnSb intermetallic peaks were shown in XRD pattern of 900 degrees C-heated Sn,Sb powders with pre-designated SnO2/Sb2O3 molar ratio of 4: 1. This is some inconsistent with Sn-Sb binary phase diagram. The evaporation of SnO2 during the heating process is considered to be responsible to this illogicality. The naturally cooled sample showed more fragile and easily to be crushed to submicrometer powders due to the polycrystalline microstructure characteristics of its particles, while quenched sample appeared to be much rigid attributable to its single-crystal particle feature. The synthesized SnxSb powders showed a higher charge and discharge capacity during the first several cycles compared with carbonaceous material. (c) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:192 / 200
页数:9
相关论文
共 28 条
[1]   A study of highly oriented pyrolytic graphite as a model for the graphite anode in Li-ion batteries [J].
Bar-Tow, D ;
Peled, E ;
Burstein, L .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1999, 146 (03) :824-832
[2]   Will advanced lithium-alloy anodes have a chance in lithium-ion batteries? [J].
Besenhard, JO ;
Yang, J ;
Winter, M .
JOURNAL OF POWER SOURCES, 1997, 68 (01) :87-90
[3]  
BOUKAMP BA, 1986, J ELECTROCHEM SOC, V133, P457
[4]   DOMINANT MOVING SPECIES IN THE FORMATION OF AMORPHOUS NIZR BY SOLID-STATE REACTION [J].
CHENG, YT ;
JOHNSON, WL ;
NICOLET, MA .
APPLIED PHYSICS LETTERS, 1985, 47 (08) :800-802
[5]   New anode systems for lithium ion cells [J].
Crosnier, O ;
Brousse, T ;
Devaux, X ;
Fragnaud, P ;
Schleich, DM .
JOURNAL OF POWER SOURCES, 2001, 94 (02) :169-174
[6]   Sol-gel TiO2 and W/TiO2 nanostructured thin films for control of drunken driving [J].
Garzella, C ;
Comini, E ;
Bontempi, E ;
Depero, LE ;
Frigeri, C ;
Sberveglieri, G .
SENSORS AND ACTUATORS B-CHEMICAL, 2002, 83 (1-3) :230-237
[7]   Lithium alloy negative electrodes formed from convertible oxides [J].
Huggins, RA .
SOLID STATE IONICS, 1998, 113 :57-67
[8]   Copper-tin anodes for rechargeable lithium batteries: an example of the matrix effect in an intermetallic system [J].
Kepler, KD ;
Vaughey, JT ;
Thackeray, MM .
JOURNAL OF POWER SOURCES, 1999, 81 :383-387
[9]   Nanosized Sn-Cu-B alloy anode prepared by chemical reduction for secondary lithium batteries [J].
Kim, DG ;
Kim, H ;
Sohn, HJ ;
Kang, T .
JOURNAL OF POWER SOURCES, 2002, 104 (02) :221-225
[10]   Sn-Zr-Ag alloy thin-film anodes [J].
Kim, YL ;
Lee, SJ ;
Baik, HK ;
Lee, SM .
JOURNAL OF POWER SOURCES, 2003, 119 :106-109