Phonon Raman scattering in A2Mn2O7 (A=Tl,In,Y)
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Abstract
Raman scattering of optical phonons in polycrystalline A2Mn2O7 (A=Y, In, and Tl) are reported as a function of temperature. For A=In and Tl a hardening of the two lowest energy modes is observed below Tc that we associate to a phonon modulation of the exchange interaction. These data suggest superexchange as the mechanism responsible for magnetic ordering in these systems. All but one of the Raman modes in the In- and Tl-based compounds appear at lower frequencies when compared with those in the Y-based one. This frequency shift may be due to the strong hybridization of the Tl(In) 6s(5s) orbital with O 2p and Mn 3d, claimed by recent band-structure calculations on these materials.
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Mn<sub>2</sub>
O<sub>7</sub>
(A=Tl,In,Y)</title>
<author><name sortKey="Granado, E" uniqKey="Granado E">E. Granado</name>
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<front><div type="abstract" xml:lang="en">Raman scattering of optical phonons in polycrystalline A<sub>2</sub>
Mn<sub>2</sub>
O<sub>7</sub>
(A=Y, In, and Tl) are reported as a function of temperature. For A=In and Tl a hardening of the two lowest energy modes is observed below T<sub>c</sub>
that we associate to a phonon modulation of the exchange interaction. These data suggest superexchange as the mechanism responsible for magnetic ordering in these systems. All but one of the Raman modes in the In- and Tl-based compounds appear at lower frequencies when compared with those in the Y-based one. This frequency shift may be due to the strong hybridization of the Tl(In) 6s(5s) orbital with O 2p and Mn 3d, claimed by recent band-structure calculations on these materials.</div>
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Mn<sub>2</sub>
O<sub>7</sub>
(A=Tl,In,Y)</s1>
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(A=Y, In, and Tl) are reported as a function of temperature. For A=In and Tl a hardening of the two lowest energy modes is observed below T<sub>c</sub>
that we associate to a phonon modulation of the exchange interaction. These data suggest superexchange as the mechanism responsible for magnetic ordering in these systems. All but one of the Raman modes in the In- and Tl-based compounds appear at lower frequencies when compared with those in the Y-based one. This frequency shift may be due to the strong hybridization of the Tl(In) 6s(5s) orbital with O 2p and Mn 3d, claimed by recent band-structure calculations on these materials.</s0>
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