High-pressure phase transition and properties of spinel ZnMn2O4

被引:117
作者
Åsbrink, S [1 ]
Waskowska, A
Gerward, L
Olsen, JS
Talik, E
机构
[1] Univ Stockholm, Arrhenius Lab, Dept Inorgan Chem, S-10691 Stockholm, Sweden
[2] Polish Acad Sci, Inst Low Temp & Struct Res, PL-50950 Wroclaw, Poland
[3] Tech Univ Denmark, Dept Phys, Lyngby 2800, Denmark
[4] Univ Copenhagen, Niels Bohr Inst, Orsted Lab, Copenhagen 2100, Denmark
[5] Silesian Univ, Inst Phys, PL-40007 Katowice, Poland
来源
PHYSICAL REVIEW B | 1999年 / 60卷 / 18期
关键词
D O I
10.1103/PhysRevB.60.12651
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
X-ray photoelectron spectroscopy, magnetic measurements, and a single-crystal x-ray structure determination at normal pressure have shown that Jahn-Teller active manganese ions in ZnMn2O4 are present in one valence state (III) on the octahedral sites of the spinel structure. The high-pressure behavior of ZnMn2O4 was investigated up to 52 GPa using the energy-dispersive x-ray diffraction technique and synchrotron radiation. The structural first-order phase transition from the body-centered to primitive-tetragonal cell takes place at P-c = 23 GPa. The high-pressure phase is metastable down to normal pressure. The c/a ratio reduces from 1.62 to 1.10 above P-c and remains nearly pressure independent in the high-pressure phase. The transition is attributed to the changes in electron configuration of the Mn3+ ions. According to the crystal field theory, the e(g) electron of octahedrally coordinated Mn3+ is either in the d(z)(2) orbital or in the d(x2-y2). In the first configuration the MnO6 octahedron will be elongated and this is the case at normal pressure, while the second configuration gives the flattened octahedron. In the high-pressure phase some proportion of the e(g) electrons of the Mn3+ ions is moved to the d(x2-y2) level, which is revealed as an abrupt fall of observed magnitude of the distortion of the bulk crystal above P-c. [S0163-1829(99)08341-1].
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页码:12651 / 12656
页数:6
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