Abstract:High-resolution synchrotron x-ray diffraction measurements were performed on single crystalline and powder samples of BiMn 2 O 5 . A linear temperature dependence of the unit cell volume was found between T N = 38 and 100 K, suggesting that a low-energy lattice excitation may be responsible for the lattice expansion in this temperature range. Between T* ϳ 65 K and T N , all lattice parameters showed incipient magnetoelastic effects, due to short-range spin correlations. An anisotropic strain along the a direct… Show more
“…well as in magnetically ordered nonpolar and polar models of these compounds were calculated with using the program "MagInter". The structural data for TbMn 2 O 5 at room temperature [35] and BiMn 2 O 5 at room temperature [36] and T = 100K [11] were taken for calculations and models development. Besides, in the above calculations we used the ionic radii determined by Shannon Tables 1 and 2.…”
Section: Critical Positions Of Intermediate Ionsmentioning
confidence: 99%
“…The compounds TbMn 2 O 5 [35] and BiMn 2 O 5 [11,36] respectively. Higher values of these AF-contributions result from the fact that the O2 and O3 ions are located in the central one-third part of the space between magnetic ions (l'/l) = 1.…”
Section: Characterization Of Magnetic Interactions and Their Competitmentioning
The origin of magnetic frustration was stated and the ions whose shift is accompanied by emerging magnetic ordering and ferroelectricity in TbMn 2 O 5 and BiMn 2 O 5 were determined on the basis of calculation of magnetic coupling parameters by using the structural data. The displacements accompanying the magnetic ordering are not polar, they just induce changes of bond valence (charge disordering) of Mn1 and Mn2, thus creating instability of the crystal structure. To approximate again the bond valence to the initial value (charge ordering) under magnetic ordering conditions is possible only due to polar displacement of Mn2 (or O1) and O4 ions along the b axis that is the cause of ferroelectric transition.
“…well as in magnetically ordered nonpolar and polar models of these compounds were calculated with using the program "MagInter". The structural data for TbMn 2 O 5 at room temperature [35] and BiMn 2 O 5 at room temperature [36] and T = 100K [11] were taken for calculations and models development. Besides, in the above calculations we used the ionic radii determined by Shannon Tables 1 and 2.…”
Section: Critical Positions Of Intermediate Ionsmentioning
confidence: 99%
“…The compounds TbMn 2 O 5 [35] and BiMn 2 O 5 [11,36] respectively. Higher values of these AF-contributions result from the fact that the O2 and O3 ions are located in the central one-third part of the space between magnetic ions (l'/l) = 1.…”
Section: Characterization Of Magnetic Interactions and Their Competitmentioning
The origin of magnetic frustration was stated and the ions whose shift is accompanied by emerging magnetic ordering and ferroelectricity in TbMn 2 O 5 and BiMn 2 O 5 were determined on the basis of calculation of magnetic coupling parameters by using the structural data. The displacements accompanying the magnetic ordering are not polar, they just induce changes of bond valence (charge disordering) of Mn1 and Mn2, thus creating instability of the crystal structure. To approximate again the bond valence to the initial value (charge ordering) under magnetic ordering conditions is possible only due to polar displacement of Mn2 (or O1) and O4 ions along the b axis that is the cause of ferroelectric transition.
“…In multiferroics, an impressive example is the RMn 2 O 5 (R¼ La, rare earth, Y and Bi) family of oxides, which are isostructural and contain infinite chains of Mn 4 + O 6 and octahedral sharing edges, linked together by Mn 3 + O 5 and RO 8 units [14][15][16]. These compounds undergo a ferroelectric transition just slightly below the antiferromagnetic (AFM) transition temperature, T N ¼39-45 K [17][18][19][20].…”
“…The Eu 3+ substitution at the Bi 3+ site leads to a slight contraction of the unit cell (Table 2) ions that form chains along the c axis [23][24][25] . Two experimental facts are worth to be noticed in Figure 4: firstly, the large difference in magnetization values between both samples, in the ordered state; secondly, the quite constant evolution of the FC magnetization below 20-30 K for the Eu-doped sample.…”
Section: X-ray Powder Diffraction and Rietveld Refinementmentioning
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