Synthesis and Electrochemical Performance of Graphene-Li2MnSiO4 Composite

被引:5
作者
Dai Liqin [1 ]
Wu Feng [1 ,3 ]
Guan Yibiao [2 ]
Fu Kai [2 ]
Jin Yi [2 ]
Gao Wei [1 ]
Wang Zhao [1 ]
Su Yuefeng [1 ,3 ]
机构
[1] Beijing Inst Technol, Beijing Key Lab Environm Sci & Engn, Sch Chem Engn & Environm, Beijing 100081, Peoples R China
[2] China Elect Power Res Inst, Beijing 100192, Peoples R China
[3] Natl Dev Ctr High Technol Green Mat, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
lithium ion batteries; cathode material; Li2MnSiO4; graphene; composite; LI2MNSIO4/C CATHODE MATERIAL; LI2MSIO4; M; LI2FESIO4; MN; ELECTRODES; LIFEPO4; FE;
D O I
10.6023/A13121291
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Graphene-Li2MnSiO4 composite cathodes for lithium ion batteries were successfully synthesized by hydrothermal assisted sol-gel method. XRD (X-ray diffraction), SEM (scanning electron microscope) and EIS (electrochemical impedance spectroscopy) were used to characterize the component, structure and morphology of the obtained composite materials. Electrochemical performance of the as-prepared materials was tested when composited with different amount of graphene oxide (2%, 4%, 6%, 8%, 10% and without graphene oxide). The experiment results indicated that composite materials belong to the orthorhombic Pmn2(1) space group and the addition of graphene oxide did not change the structure of the materials. Graphene and Li2MnSiO4 material were homogeneously composited with each other and it could be clearly observed the relatively transparent and thin layer graphene in the edges of the materials. The micro-scale particle of all the samples was agglomeration of nano-crystallites. When composited with appropriate amount of the graphene oxide, the particles became loose and some micropore structure was formed. The conductive network graphene could greatly promote the liquid electrolyte to pass through particles, facilitate the electron transport and restrain particles agglomeration. The sample with 6% graphene oxide yielded the best electrochemical performance in all the samples (the carbon content is 8.25%). Without calculating the carbon mass, this material delivered an initial discharging capacity of 166 mAh/g, and retained 101 mAh/g after 20 cycles at 1.5 similar to 4.8 V with a current density of 10 mA/g. Besides, compared with the pristine, the graphene-Li2MnSiO4 composite materials delivered an excellent rate performance. The improvement of specific capacity and rate performance was due to that the interconnected network structure of graphene oxide acted a key role in stabilizing the structure of composite materials and inhibiting structural damage in the charge-discharge process. Moreover, the surface charge transfer resistance of the Li2MnSiO4 was significantly decreased when composited with graphene oxide. It means that the enhancement of electronic conduction ability is one of the main reasons that contribute to improvement of the electrochemical performance of composite materials. Thus, the graphene is considered to be of significance in improving material electronic conductivity and enhancing the reversible lithium intercalation/deintercalation capacity of Li2MnSiO4 cathode materials.
引用
收藏
页码:583 / 589
页数:7
相关论文
共 36 条
[1]   Superior Lithium Storage Properties of Carbon Coated Li2MnSiO4 Cathodes [J].
Aravindan, V. ;
Karthikeyan, K. ;
Amaresh, S. ;
Lee, Y. S. .
ELECTROCHEMICAL AND SOLID STATE LETTERS, 2011, 14 (04) :A33-A35
[2]   Influence of carbon towards improved lithium storage properties of Li2MnSiO4 cathodes [J].
Aravindan, V. ;
Karthikeyan, K. ;
Kang, K. S. ;
Yoon, W. S. ;
Kim, W. S. ;
Lee, Y. S. .
JOURNAL OF MATERIALS CHEMISTRY, 2011, 21 (08) :2470-2475
[3]   Size controlled synthesis of Li2MnSiO4 nanoparticles: Effect of calcination temperature and carbon content for high performance lithium batteries [J].
Aravindan, V. ;
Ravi, S. ;
Kim, W. S. ;
Lee, S. Y. ;
Lee, Y. S. .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2011, 355 (02) :472-477
[4]   Comparative computational investigation of N and F substituted polyoxoanionic compounds The case of Li2FeSiO4 electrode material [J].
Armand, M. ;
Tarascon, J. -M. ;
Arroyo-de Dompablo, M. E. .
ELECTROCHEMISTRY COMMUNICATIONS, 2011, 13 (10) :1047-1050
[5]   Structural Polymorphism in Li2CoSiO4 Intercalation Electrodes: A Combined Diffraction and NMR Study [J].
Armstrong, A. Robert ;
Lyness, Christopher ;
Menetrier, Michel ;
Bruce, Peter G. .
CHEMISTRY OF MATERIALS, 2010, 22 (05) :1892-1900
[6]   On-demand design of polyoxianionic cathode materials based on electronegativity correlations:: An exploration of the Li2MSiO4 system (M = Fe, Mn, Co, Ni) [J].
Arroyo-de Dompablo, M. E. ;
Armand, M. ;
Tarascon, J. M. ;
Amador, U. .
ELECTROCHEMISTRY COMMUNICATIONS, 2006, 8 (08) :1292-1298
[7]   On the energetic stability and electrochemistry of Li2MnSiO4 polymorphs [J].
Arroyo-deDompablo, M. E. ;
Dominko, R. ;
Gallardo-Amores, J. M. ;
Dupont, L. ;
Mali, G. ;
Ehrenberg, H. ;
Jamnik, J. ;
Moran, E. .
CHEMISTRY OF MATERIALS, 2008, 20 (17) :5574-5584
[8]   Conductivity improvements to spray-produced LiFePO4 by addition of a carbon source [J].
Bewlay, SL ;
Konstantinov, K ;
Wang, GX ;
Dou, SX ;
Liu, HK .
MATERIALS LETTERS, 2004, 58 (11) :1788-1791
[9]   Graphene-based materials in electrochemistry [J].
Chen, Da ;
Tang, Longhua ;
Li, Jinghong .
CHEMICAL SOCIETY REVIEWS, 2010, 39 (08) :3157-3180
[10]  
[程琥 Cheng Hu], 2010, [电化学, Electrochemistry], V16, P296