Magnetoelastic coupling in [Ru2(O2CMe)4]3[Cr(CN)6] molecule-based magnet

被引:14
|
作者
Brinzari, T. V. [1 ]
Chen, P. [1 ]
Tung, L. -C. [2 ]
Kim, Y. [2 ]
Smirnov, D. [2 ]
Singleton, J. [3 ]
Miller, Joel. S. [4 ]
Musfeldt, J. L. [1 ]
机构
[1] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
[2] Natl High Magnet Field Lab, Tallahassee, FL 32310 USA
[3] Los Alamos Natl Lab, Natl High Magnet Field Lab, Los Alamos, NM 87545 USA
[4] Univ Utah, Dept Chem, Salt Lake City, UT 84112 USA
基金
美国国家科学基金会;
关键词
INFRARED-SPECTRA; ORDERING TEMPERATURE; BUILDING-BLOCKS; PHASE-DIAGRAM; RAMAN; ENHANCEMENT; COMPLEXES; 3-D; CR;
D O I
10.1103/PhysRevB.86.214411
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Infrared and Raman vibrational spectroscopies were employed to explore the lattice dynamics of [Ru-2(O2CMe)(4)](3)[Cr(CN)(6)] through the field- and temperature-driven magnetic transitions. The high field work reveals systematic changes in the C equivalent to N stretching mode and Cr-containing phonons as the system is driven away from the antiferromagnetic state. The magnetic intersublattice coalescence transition at B-c similar or equal to 0.08 T, on the contrary, is purely magnetic and takes place with no lattice involvement. The variable temperature spectroscopy affirms overall [Cr(CN)(6)](3-) flexibility along with stronger intermolecular interactions at low temperature. Based on a displacement pattern analysis, we discuss the local lattice distortions in terms of an adaptable chromium environment. These findings provide deeper understanding of spin-lattice coupling in [Ru-2(O2CMe)(4)](3)[Cr(CN)(6)] and may be useful in the development of technologically important molecule-based magnets. DOI: 10.1103/PhysRevB.86.214411
引用
收藏
页数:7
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