Magnetic structural studies of the two polymorphs of Li3Fe2(PO4)3:: Analysis of the magnetic ground state from super-super exchange interactions

被引:47
作者
Rousse, G
Rodríguez-Carvajal, J
Wurm, C
Masquelier, C
机构
[1] Inst Max Von Laue Paul Langevin, F-38042 Grenoble 9, France
[2] CEA Saclay, CNRS, Lab Leon Brillouin, F-91191 Gif Sur Yvette, France
[3] Univ Picardie, Lab React & Chim Solides, F-80039 Amiens 9, France
关键词
D O I
10.1021/cm011054q
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 nuclear and magnetic structures of the monoclinic (P2(1)/n, A-LFP) and rhombohedral (R (3) over bar B-LFP) forms of Li3Fe2(PO4)(3) have been solved by using powder neutron diffraction at room temperature and 1.5 K on polycrystalline samples. Both structures are built on [Fe-2(PO4)(3)] 'lantern units' that are connected in a different way for each form. Measurements by a superconducting quantum interference device reveal a global antiferromagnetic behavior with ordering temperatures of 25 and 23 K for the A and B forms, respectively. Both magnetic structures, determined from symmetry analysis and Rietveld refinements of neutron diffraction data recorded at 1.5 K are collinear. The magnetic moments are perpendicular to [001] in both structures. The obtained magnetic moments are 4.7 and 3.9 mu (B) per iron atom for the A form (ferrimagnetic ordering of the two iron sublattices) and 4.7,mu (B) for the NASICON (B-LFP) form. The Fe atoms are oriented antiparallel within the [Fe-2(PO4)(3)] lantern units, while parallel orientation takes place between Fe atoms that do not belong to the same [Fe-2(PO4)(3)] lantern unit. Using numerical calculations we have established a magnetic phase diagram and determined the necessary constraints to be satisfied by the values of the exchange interactions to obtain the observed magnetic structures as the ground state.
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页码:4527 / 4536
页数:10
相关论文
共 37 条
[11]   THERMAL VARIATION OF PITCH OF HELICAL SPIN CONFIGURATIONS [J].
FREISER, MJ .
PHYSICAL REVIEW, 1961, 123 (06) :2003-&
[12]   Rhombohedral form of Li3V2(PO4)3 as a cathode in Li-ion batteries [J].
Gaubicher, J ;
Wurm, C ;
Goward, G ;
Masquelier, C ;
Nazar, L .
CHEMISTRY OF MATERIALS, 2000, 12 (11) :3240-+
[13]   Spectroscopic and magnetic properties of α-Li3Fe2(PO4)3:: A two-sublattice ferrimagnet [J].
Goñi, A ;
Lezama, L ;
Moreno, NO ;
Fournès, L ;
Olazcuaga, R ;
Barberis, GE ;
Rojo, T .
CHEMISTRY OF MATERIALS, 2000, 12 (01) :62-66
[14]  
Goodenough J. B., 1963, MAGNETISM CHEM BOND
[15]  
GOODENOUGH JB, 1997, Patent No. 08840523
[16]   V2(PO4)3 - A NOVEL NASICON-TYPE VANADIUM PHOSPHATE SYNTHESIZED BY OXIDATIVE DEINTERCALATION OF SODIUM FROM NA3V2(PO4)3 [J].
GOPALAKRISHNAN, J ;
RANGAN, KK .
CHEMISTRY OF MATERIALS, 1992, 4 (04) :745-747
[17]   THE NATURE OF MAGNETIC-ORDERING AT 47K IN NA3FE2(PO4)3 [J].
GREAVES, C ;
SLATER, PR ;
SLASKI, M ;
MUIRHEAD, CM .
PHYSICA B, 1994, 194 :199-200
[18]   CRYSTAL-STRUCTURES AND CRYSTAL-CHEMISTRY IN SYSTEM NA1+XZR2SIXP3-XO12 [J].
HONG, HYP .
MATERIALS RESEARCH BULLETIN, 1976, 11 (02) :173-182
[20]   STUDY OF ANHYDROUS IRON(III) SULFATE BY MAGNETIC-SUSCEPTIBILITY, MOSSBAUER, AND NEUTRON-DIFFRACTION TECHNIQUES [J].
LONG, GJ ;
LONGWORTH, G ;
BATTLE, P ;
CHEETHAM, AK ;
THUNDATHIL, RV ;
BEVERIDGE, D .
INORGANIC CHEMISTRY, 1979, 18 (03) :624-632