82 research outputs found

    Structural, magnetic and vibrational characterization of the new organic-inorganic hybrid material, (C9H14N)2CoCl4

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    A new organic–inorganic hybrid material, bis (N, N-dimethylbenzylammonium) tetrachlorocobaltate (II), (C9H14N)2 CoCl4 was synthesized and analyzed by X-ray diffraction. Magnetization was used to investigate the magnetic properties. The structure was determined at room temperature in the triclinic space group P-1 with the following parameters: a = 10.491 (5)Å, b = 14.207 (2)Å, c = 16.187 (3)Å, α = 87.76 (3)°, β = 88.436 (8)°, γ = 89.897 (10)° and Z = 2. The structure can be described by the alternation of organic-inorganic layers parallel to (110) plan. The different components are connected by the Nsingle bondH⋯Cl hydrogen bonds between the cation and the anionic group [CoCl4]2-. Raman and infrared spectra were used to gain more information of the title compound. An assignment of the observed vibration modes is reported. This compound exhibits an antiferromagnetic (AFM) to paramagnetic (PM) phase transition at a temperature (TN) lower than 2 K. The values of paramagnetic Curie–Weiss temperature θCW, the nearest neighbor interaction Jnn, the classical nearest neighbor J cl and the dipolar Dnn interactions’ emphasize the existence of an antiferromagnetic interaction between the neighboring cobalt ions.publishe

    Magnetoelectric ordering of BiFeO3 from the perspective of crystal chemistry

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    In this paper we examine the role of crystal chemistry factors in creating conditions for formation of magnetoelectric ordering in BiFeO3. It is generally accepted that the main reason of the ferroelectric distortion in BiFeO3 is concerned with a stereochemical activity of the Bi lone pair. However, the lone pair is stereochemically active in the paraelectric orthorhombic beta-phase as well. We demonstrate that a crucial role in emerging of phase transitions of the metal-insulator, paraelectric-ferroelectric and magnetic disorder-order types belongs to the change of the degree of the lone pair stereochemical activity - its consecutive increase with the temperature decrease. Using the structural data, we calculated the sign and strength of magnetic couplings in BiFeO3 in the range from 945 C down to 25 C and found the couplings, which undergo the antiferromagnetic-ferromagnetic transition with the temperature decrease and give rise to the antiferromagnetic ordering and its delay in regard to temperature, as compared to the ferroelectric ordering. We discuss the reasons of emerging of the spatially modulated spin structure and its suppression by doping with La3+.Comment: 18 pages, 5 figures, 3 table
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