Broken magnetic symmetry due to charge-order ferroelectricity discovered in (TMTTF) 2 X salts by multifrequency ESR
Broken magnetic symmetry due to charge-order ferroelectricity discovered in (TMTTF) 2 X salts by multifrequency ESR
复制标题
通过多频 ESR 在 (TMTTF) 2 X 盐中发现电荷级铁电性导致的磁对称性破坏
DOI:
10.1103/physrevb.85.144428
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发表时间:
2012
影响因子:
3.7
通讯作者:
M. Dressel
中科院分区:
文献类型:
--
作者:
S. Yasin;B. Salameh;E. Rose;M. Dumm;H.-A. Krug von Nidda;A. Loidl;M. Ozerov;G. Untereiner;L.K. Montgomery;M. Dressel
We have investigated the charge-ordered state of the quasi-one-dimensional organic charge-transfer salts (TMTTF)(where TMTTF stands for tetramethyltetrathiafulvalene andAsF, SbF, and SCN) by performing comprehensive electron-spin-resonance (ESR) experiments at several frequencies forK. At elevated temperatures all compounds show a linear increase of. Below the charge-ordering transitionimportant anomalies are observed in both the temperature dependence and the anisotropy of the ESR linewidth. In the case of the centrosymmetric anions PF, AsF, and SbF, the linewidth doubles its periodicity when rotated in a plane normal to the molecule axis; and it exhibits a significant frequency dependence. This enhanced linewidth is caused by anisotropic Zeeman interaction that we identify as a relaxation process in the charge-ordered state where magnetically inequivalent sites are present in adjacent stacks. Thus, charge order not only produces ferroelectricity but also breaks the symmetry of the magnetic degree of freedom in these organic quantum spin chains. For (TMTTF)SCN charge order coincides with the ordering of the non-centrosymmetric anions; the large contribution of dipolar interaction dominates the relaxation process.