Magnetic circular dichroism and Faraday rotation spectra of Y3Fe5O12

Abstract
The magnetic circular dichroism (MCD), Faraday rotation (FR), and absorption spectra of Y3 Fe5 O12 at 77 K are presented between 10 000 and 25 000 cm1. Comparison of MCD and FR line shapes with absorption-band energies indicates that the Fe3+ crystal-field transitions are predominantly paramagnetic in nature. It is shown that spin-orbit mixing of the T1g4(G) excited crystal-field states into the ground state is sufficient to explain the observed MCD of the A1g6(S)T1g4(G) band without producing an unacceptable change in the ground-state g factor and is consistent with the observation of paramagnetic line shapes for the other Fe3+ crystalfield transitions. It is pointed out that previous analyses of the magneto-optic spectra of iron garnets above 20 000 cm1 are probably in error.