Is it possible to prepare olivine-type LiFeSiO4?: A joint computational and experimental investigation

被引:41
作者
de Dompablo, M. E. Arroyo Y. [1 ]
Gallardo-Amores, J. M. [1 ]
Garcia-Martinez, J. [2 ]
Moran, E. [1 ]
Tarascon, J. -M. [3 ]
Armand, M. [3 ]
机构
[1] Univ Complutense Madrid, Fac Ciencias Quim, Dept Quim Inorgan, E-28040 Madrid, Spain
[2] Univ Alicante, Fac Ciencias, Dept Quim Inorgan, Alicante 03690, Spain
[3] Univ Picardie Jules Verne, LRCS, CNRS, UMR 6007, F-80039 Amiens, France
关键词
silicates; lithium batteries; first principles calculations; high pressure;
D O I
10.1016/j.ssi.2008.03.023
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
Silicates LiMSiO4 are potential positive electrode materials for lithium ion batteries. In this work we analyse from first principles calculations the relative stability of possible LiFeSiO4-Polymorphs within four structural types. Olivine-LiFeSiO4 is predicted to be more stable than the LiFeSiO4 prepared by delithiation of Li2FeSiO4; the latter being the only LiFeSiO4 compound reported so far. Attempts to prepare olivine-LiFeSiO4 from a mixture of reactants at ambient pressure (600-1100 degrees C) resulted in a mixture of quartz-SiO2, Li2SiO3, LiFe5O8 and LiFeSi2O6 phases. Conducting the reaction under HP conditions (40 kbar) leads to the formation of LiFeSi2O6 as a majority phase, regardless the nature of the reactants/precursors. First principles calculations indicate that the preparation of the olivine-LiFeSiO4 is then-nodynamically hindered due to the competition with the more stable LiFeSi2O6 pyroxene, in the range of pressure/temperature investigated. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1758 / 1762
页数:5
相关论文
共 16 条
[1]  
[Anonymous], 1944, Proceedings of the National Academy of Sciences of the United States of America
[2]  
[Anonymous], 1996, COMP MATER SCI, DOI DOI 10.1016/0927-0256(96)00008-0
[3]  
Armand M., 2002, World Patent, Patent No. 0227823
[4]   Novel olivine and spinel LiMAsO4 (M=3d-metal) as positive electrode materials in lithium cells [J].
Arroyo-de Dompablo, M. E. ;
Amador, U. ;
Alvarez, M. ;
Gallardo, J. M. ;
Garcia-Alvarado, F. .
SOLID STATE IONICS, 2006, 177 (26-32) :2625-2628
[5]   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
[6]   A computational investigation on the electrochemical properties of spinel-like LiCoAsO4 as positive electrode for lithium-ion batteries [J].
Arroyo-de Dompablo, M. Elena ;
Amador, Ulises .
SOLID STATE SCIENCES, 2006, 8 (08) :916-921
[7]  
CLARK JR, 2002, GOLDEN BOOK PHASE TR, V1, P1
[8]  
DEDOMPABLO MEA, 2005, ELECTROCHEM SOLID ST, V8, pA564
[9]   Structure and electrochemical performance of Li2MnSiO4 and Li2FeSiO4 as potential Li-battery cathode materials [J].
Dominko, R ;
Bele, M ;
Gaberscek, M ;
Meden, A ;
Remskar, M ;
Jamnik, J .
ELECTROCHEMISTRY COMMUNICATIONS, 2006, 8 (02) :217-222
[10]   Influence of the structure on the electrochemical performance of lithium transition metal phosphates as cathodic materials in rechargeable lithium batteries:: A new high-pressure form of LiMPO4 (M = Fe and Ni) [J].
García-Moreno, O ;
Alvarez-Vega, M ;
García-Alvarado, F ;
García-Jaca, J ;
Gallardo-Amores, JM ;
Sanjuán, ML ;
Amador, U .
CHEMISTRY OF MATERIALS, 2001, 13 (05) :1570-1576