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Intriguing interconnections among phase transition, magnetic moment, and valence disproportionation in 2H-perovskite
Qingbiao Zhao1, Jacques Darriet, Myung-Hwan Whangbo
1Department of Chemistry and Biochemistry, University of South Carolina, Columbia, South Carolina 29208, USA.
Abstract:
In this paper we report the crystal growth, structure determination, and magnetic properties of the 2H-perovskite related oxides, Sr(5)Co(4)O(12) and Sr(6)Co(5)O(15), as well as the charge disproportionation and associated phase transition of Sr(5)Co(4)O(12). Sr(5)Co(4)O(12) and Sr(6)Co(5)O(15) are the (m = 2, n = 3) and (m = 1, n = 1) members of the A(3m+3n)A'(n)B(3m+n)O(9m+6n) family, respectively. Sr(6)Co(5)O(15) crystallizes in the space group R32 with lattice parameters of a = 9.5020(10) Å and c = 12.379(8) Å. The structure solution shows that Sr(6)Co(5)O(15) is isostructural with Sr(6)Rh(5)O(15). Magnetic measurements do not indicate any long-range magnetic order, although the Weiss temperature of -248 K indicates the presence of dominant antiferromagnetic interactions. Sr(5)Co(4)O(12) crystallizes in the space group P-3c1 with lattice parameters of a = 9.4705(10) Å and c = 20.063(5) Å at room temperature. The single crystal structure solution revealed that the cobalt ions in the trigonal prismatic sites of Sr(5)Co(4)O(12) undergo a structural transition at ~170 K, where the cobalt atoms are in the center of the trigonal prisms below this temperature and move partially toward the faces above this temperature. This structure transition is accompanied by a change in the magnetic moment of the oxide and can be related to a valence disproportionation of the cobalt ions and a concomitant Jahn-Teller distortion. In addition, specific heat, Seebeck coefficient, electric conductivity, and magnetic measurements as well as bond valence sum calculations were carried out for Sr(5)Co(4)O(12). Sr(5)Co(4)O(12) exhibits strong magnetic anisotropy but no long-range magnetic order.
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