Magnetic structures of the triphylite LiFePO4 and of its delithiated form FePO4

被引:305
作者
Rousse, G
Rodriguez-Carvajal, J
Patoux, S
Masquelier, C
机构
[1] Inst Max Von Laue Paul Langevin, F-38042 Grenoble 9, France
[2] Univ Paris 06, F-75252 Paris 05, France
[3] CEA Saclay, Lab Leon Brillouin CEA CNRS, F-91191 Gif Sur Yvette, France
[4] CEA Grenoble, Serv Phys Statist, F-38054 Grenoble 9, France
[5] Univ Picardie, Lab Reactiv & Chim Solides, F-80039 Amiens 9, France
关键词
D O I
10.1021/cm0300462
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
The magnetic structures of LiFePO4 and of its delithiated form FePO4 (triphylite, olivine group, space group Pnma) have been solved using neutron diffraction on polycrystalline samples. Both compounds show antiferromagnetic behavior below 52 K for LiFePO4 (Fe2+) and below 125 K for FePO4 (Fe3+), characterized by the appearance of extra peaks in the neutron diffraction patterns below the Neel temperature. These magnetic reflections are indexed with a propagation vector k = (0,0,0). The magnetic moments of the four iron atoms present in the unit cell are oriented along [010] for LiFePO4 and mostly along [100] (with a small component along [010]) for FePO4. The magnetic structures and the differences in the Neel temperatures are discussed in terms of super and super-super exchange intractions and of anisotropy of Fe2+. A comparison is made with other olivine compounds with similar cation distribution.
引用
收藏
页码:4082 / 4090
页数:9
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