Jin Feng1, Yang Yang2, Zhang An-Min1, Ji Jian-Ting1, 2, Zhang Qing-Ming1, 2, 3, †
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(color online) (a) Magneto-Raman spectra of Co[N(CN)2]2 at T = 5.5 K under magnetic fields up to 34 T. The strong field-dependent feature, assigned as a Co2+ electronic excitation, is marked with an asterisk. (b) Raman shift versus applied fields, showing the hybridized electronic and phonon excitations in Co[N(CN)2]2. The red curves are fitting results using the theory of Ref. [36]. The inset shows a schematic energy level diagram for Co2+ electronic states. The red (solid) arrow shows a plausible candidate for the 114 ± 5 cm−1 excitation in Raman spectra. (c) Temperature dependence of magneto-Raman spectra at 18.6 ± 0.1 T. Black (dashed) lines are peak fits tracking the behavior of Co2+ electronic excitations, which displays no sensitivity to Curie temperature ∼ 9 K. Reprinted with permission from Ref. [34], copyright 2013 by the American Physical Society.
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