Hydrothermal Synthesis of Nanosized LiMnO2-Li2MnO3 Compounds and Their Electrochemical Performances

被引:38
作者
Huang, Xingkang [1 ,2 ,3 ]
Zhang, Qingshun [1 ]
Chang, Haitao [1 ]
Gan, Jianlong [1 ]
Yue, Hongjun [2 ,3 ]
Yang, Yong [2 ,3 ]
机构
[1] Fujian Nanping Nanfu Battery Co Ltd, Nanping 353000, Peoples R China
[2] Xiamen Univ, Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
[3] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金;
关键词
FE-SUBSTITUTED LI2MNO3; LITHIUM-MANGANESE OXIDE; POSITIVE ELECTRODE MATERIAL; ORTHORHOMBIC LIMNO2; CATHODE MATERIALS; ION BATTERIES; CHEMICAL-COMPOSITION; CATION DISTRIBUTION; BEHAVIOR; DIFFRACTION;
D O I
10.1149/1.3054397
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Nanosized LiMnO2-LiMnO3 compounds were synthesized by a hydrothermal method. The contents of Li2MnO3 and LiMnO2 in these compounds vary with the employed molar ratio of starting materials [i.e., (NH4)(2)S2O8/MnSO4]. The effects of the reaction time and temperature on the hydrothermal products were investigated. The hydrothermally prepared LiMnO2-Li2MnO3 compounds have higher electrochemical activities compared to those obtained from conventional solid-state reaction at high temperature [e.g., during the initial discharging process at 20 mA g(-1), o-LiMnO2 (sample LMO-1) and Li2MnO3 (sample LMO-4) delivered at 184 and 247 mAh respectively]. Meanwhile, such nanosized compounds exhibited good rate capabilities (e.g., at a current density of 200 mA g(-1), sample LMO-4 delivered a capacity of 208 mAh g(-1), 84% of that obtained at 20 mA g(-1)). Comparison of electrochemical performances among the four nanosized compounds obtained from our hydrothermal conditions indicates that the Li2MnO3 has the higher discharge capacity while the o-LiMnO2 shows the better cyclability. (C) 2009 The Electrochemical Society.
引用
收藏
页码:A162 / A168
页数:7
相关论文
共 44 条
[1]  
Ammundsen B, 2001, ADV MATER, V13, P943, DOI 10.1002/1521-4095(200107)13:12/13<943::AID-ADMA943>3.0.CO
[2]  
2-J
[3]   Overcharging manganese oxides:: Extracting lithium beyond Mn4+ [J].
Armstrong, AR ;
Robertson, AD ;
Bruce, PG .
JOURNAL OF POWER SOURCES, 2005, 146 (1-2) :275-280
[4]   Electrochemical cyclability of orthorhombic LiMnO2 - Characterization of cycled materials [J].
Croguennec, L ;
Deniard, P ;
Brec, R .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1997, 144 (10) :3323-3330
[5]   Electrochemical behavior of orthorhombic LiMnO2: Influence of the grain size and cationic disorder [J].
Croguennec, L ;
Deniard, P ;
Brec, R ;
Biensan, P ;
Broussely, M .
SOLID STATE IONICS, 1996, 89 (1-2) :127-137
[6]   LITHIUM-ION CELL-BASED ON ORTHORHOMBIC LIMNO2 [J].
DAVIDSON, IJ ;
MCMILLAN, RS ;
MURRAY, JJ ;
GREEDAN, JE .
JOURNAL OF POWER SOURCES, 1995, 54 (02) :232-235
[7]   AN INVESTIGATION OF SPINEL-RELATED AND ORTHORHOMBIC LIMNO2 CATHODES FOR RECHARGEABLE LITHIUM BATTERIES [J].
GUMMOW, RJ ;
THACKERAY, MM .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1994, 141 (05) :1178-1182
[8]   Controllable synthesis of α- and β-MnO2:: cationic effect on hydrothermal crystallization [J].
Huang, Xingkang ;
Lv, Dongping ;
Yue, Hongjun ;
Attia, Adel ;
Yang, Yong .
NANOTECHNOLOGY, 2008, 19 (22)
[9]   Preparation and properties of manganese oxide/carbon composites by reduction of potassium permanganate with acetylene black [J].
Huang, Xingkang ;
Yue, Hongjun ;
Attia, Adel ;
Yang, Yong .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2007, 154 (01) :A26-A33
[10]   Synthesis, electrochemistry, and structural studies of lithium intercalation of a nanocrystalline Li2MnO3-like compound [J].
Jain, GR ;
Yang, JS ;
Balasubramanian, M ;
Xu, JJ .
CHEMISTRY OF MATERIALS, 2005, 17 (15) :3850-3860