Long-range charge order in the low-temperature insulating phase of PrNiO3

被引:61
作者
Medarde, M. [1 ]
Fernandez-Diaz, M. T. [2 ]
Lacorre, Ph. [3 ]
机构
[1] Paul Scherrer Inst, Lab Dev & Methods, CH-5232 Villigen, Switzerland
[2] Inst Max Von Laue Paul Langevin, F-38042 Grenoble 9, France
[3] Univ Maine, Fac Sci & Tech, Lab Oxydes & Fluorures, F-72085 Le Mans 9, France
关键词
charge exchange; charge-ordered states; crystal structure; crystal symmetry; long-range order; metal-insulator transition; neutron diffraction; praseodymium compounds;
D O I
10.1103/PhysRevB.78.212101
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
We report the observation of a static long-range 2Ni(3+)-> Ni3+delta+Ni3-delta charge redistribution in PrNiO3 below T-MI=130 K by means of high-resolution powder neutron diffraction. In contrast to previous structural studies, these present data show that the symmetry of the low-temperature insulating phase is not orthorhombic but monoclinic P2(1)/n. The two available Ni sites host contracted and expanded NiO6 octahedra which alternate along the three pseudocubic perovskite axes, suggesting the existence of a Ni3+delta/Ni3-delta charge order similar to that reported for the nickelates with heavier lanthanide ions. The difference between the average Ni-O distances in the two Ni sites at T/T-MI=0.08 is 0.052(2) A, which is almost two times smaller than the value reported for LuNiO3 at T/T-MI=0.50 [0.084(4) A]. This result suggests a progressive decrease in delta by approaching the itinerant limit and gives further support to the charge disproportionation mechanism as an origin of the metal-insulator transition in the whole RNiO3 family.
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页数:4
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共 26 条
  • [1] Local lattice structure change in PrNiO3 across the metal-insulator transition:: X-ray absorption near-edge structure spectroscopy and ab initio calculations
    Acosta-Alejandro, M.
    de Leon, J. Mustre
    Medarde, M.
    Lacorre, Ph.
    Konder, K.
    Montano, P. A.
    [J]. PHYSICAL REVIEW B, 2008, 77 (08)
  • [2] Room-temperature monoclinic distortion due to charge disproportionation in RNiO3 perovskites with small rare-earth cations (R = Ho, Y, Er, Tm, Yb, and Lu):: A neutron diffraction study
    Alonso, JA
    Martínez-Lope, MJ
    Casais, MT
    García-Muñoz, JL
    Fernández-Díaz, MT
    [J]. PHYSICAL REVIEW B, 2000, 61 (03): : 1756 - 1763
  • [3] High-temperature structural evolution of RNiO3 (R = Ho, Y, Er, Lu) perovskites:: Charge disproportionation and electronic localization -: art. no. 094102
    Alonso, JA
    Martínez-Lope, MJ
    Casais, MT
    García-Muñoz, JL
    Fernández-Díaz, MT
    Aranda, MAG
    [J]. PHYSICAL REVIEW B, 2001, 64 (09)
  • [4] Alonso JA, 2006, Z NATURFORSCH B, V61, P346
  • [5] Charge disproportionation in YNiO3: ESR and susceptibility study -: art. no. 024429
    Causa, MT
    Sánchez, RD
    Tovar, M
    Alonso, JA
    Martínez-Lope, MJ
    [J]. PHYSICAL REVIEW B, 2003, 68 (02)
  • [6] REINVESTIGATION OF THE MIXED-METAL PERIODATES M'MIO6 (M' = ALKALI-METAL, M = GE, SN, PB)
    CURRIE, DB
    LEVASON, W
    OLDROYD, RD
    WELLER, MT
    [J]. JOURNAL OF MATERIALS CHEMISTRY, 1993, 3 (05) : 447 - 451
  • [7] Possible common ground for the metal-insulator phase transition in the rare-earth nickelates RNiO3 (R=Eu, Ho, Y) -: art. no. 153104
    de la Cruz, FP
    Piamonteze, C
    Massa, NE
    Salva, H
    Alonso, JA
    Martínez-Lope, MJ
    Casais, MT
    [J]. PHYSICAL REVIEW B, 2002, 66 (15) : 1 - 4
  • [8] FERNANDEZDIAZ M, 1991, THESIS U AUTONOMA MA
  • [9] STRUCTURAL CHARACTERIZATION AND POLYMORPHISM OF R2BANIO5 (R = ND, GD, DY, Y, HO, ER, TM, YB) STUDIED BY NEUTRON-DIFFRACTION
    GARCIAMATRES, E
    MARTINEZ, JL
    RODRIGUEZCARVAJAL, J
    ALONSO, JA
    SALINASSAHCNEZ, A
    SAEZPUCHE, R
    [J]. JOURNAL OF SOLID STATE CHEMISTRY, 1993, 103 (02) : 322 - 333
  • [10] SYNTHESIS, CRYSTAL-STRUCTURE, AND PROPERTIES OF METALLIC PRNIO3 - COMPARISON WITH METALLIC NDNIO3 AND SEMICONDUCTING SMNIO3
    LACORRE, P
    TORRANCE, JB
    PANNETIER, J
    NAZZAL, AI
    WANG, PW
    HUANG, TC
    [J]. JOURNAL OF SOLID STATE CHEMISTRY, 1991, 91 (02) : 225 - 237