C-containing LiFePO4 materials - Part I: Mechano-chemical synthesis and structural characterization

被引:70
作者
Maccario, M. [1 ]
Croguennec, L. [1 ]
Wattiaux, A. [1 ]
Suard, E. [2 ]
Le Cras, F. [3 ]
Delmas, C. [1 ]
机构
[1] Univ Bordeaux 1, CNRS, ICMCB, F-33608 Pessac, France
[2] Inst Laue Langevin, F-38000 Grenoble, France
[3] Lab Composants Energie DRT LITEN DTNM LCE, Commissariat Energie Atom, Grenoble 9, France
关键词
LiFePO4; Lithium-ion batteries; Olivine; Phosphates; Mechano-chemical synthesis; X-ray and neutron diffraction; Mossbauer spectroscopy; Magnetic measurements;
D O I
10.1016/j.ssi.2008.07.004
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
C-LiFePO4 composites were synthesized by mechano-chemical activation using iron and lithium phosphates, and also cellulose as carbon precursor; this mixture was treated with 2 thermal treatments ("slow" or "fast" treatment) and 2 temperatures (575 degrees C or 800 degrees C). The four synthesized samples were pure olivine-type materials (XRD), but chemical analyses and Mossbauer spectroscopy show Li/Fe and P/Fe ratios larger than 1 and the presence of 5-6 at.% of Fe3+. Three hypotheses were considered to explain the presence of Fe3+ ions: (i) a chemical formula Li1-xFe1-xPO4 for the olivine-type phase, (ii) a mixture of olivine-type LiFePO4 and Fe3+ containing impuritie(s) or (iii) LiFePO4 with Fe3+ surface defects. These hypotheses were checked using different characterization methods such as X-ray diffraction, neutron diffraction and magnetic measurements, hypothesis (i) was shown not to be valid but none of hypotheses (ii) and (iii) was definitely confirmed. One can assume either the presence of a Fe3+ -rich phase (amorphous or nanocrystalline) or the occurrence of surface defects which can play a significant role as far as nanomaterials are concerned. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:2020 / 2026
页数:7
相关论文
共 55 条
[1]   Magnetic studies of the carbothermal effect on LiFePO4 [J].
Ait-Salah, A ;
Zaghib, K ;
Mauger, A ;
Gendron, F ;
Julien, CM .
PHYSICA STATUS SOLIDI A-APPLICATIONS AND MATERIALS SCIENCE, 2006, 203 (01) :R1-R3
[2]   High-temperature storage and cycling of C-LiFePO4/graphite Li-ion cells [J].
Amine, K ;
Liu, J ;
Belharouak, I .
ELECTROCHEMISTRY COMMUNICATIONS, 2005, 7 (07) :669-673
[3]   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
[4]   A comparative study of magnetic properties of LiFePO4 and LiMnPO4 [J].
Arcon, D ;
Zorko, A ;
Dominko, R ;
Jaglicic, Z .
JOURNAL OF PHYSICS-CONDENSED MATTER, 2004, 16 (30) :5531-5548
[5]   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
[6]   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
[7]   Crystal chemistry of the olivine-type LixFePO4 system (0 ≤ x ≤ 1) between 25 and 370°C [J].
Delacourt, C ;
Rodríguez-Carvajal, J ;
Schmitt, B ;
Tarascon, JM ;
Masquelier, C .
SOLID STATE SCIENCES, 2005, 7 (12) :1506-1516
[8]   The existence of a temperature-driven solid solution in LixFePO4 for 0 ≤ x ≤ 1 [J].
Delacourt, C ;
Poizot, P ;
Tarascon, JM ;
Masquelier, C .
NATURE MATERIALS, 2005, 4 (03) :254-260
[9]   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
[10]  
Delacourt C., 2005, THESIS U PICARDIE JU