Optical study of 4f excitations in rare earth cuprates

Several recent examples are used to demonstrate that Raman and infrared spectroscopy can be successfully used as a novel experimental tool to study microscopic processes involving 4f electrons in rare earth (RE) cuprates. Raman-active crystal field (CF) excitations in Nd₂CuO₄ were measured under hyd...

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Збережено в:
Бібліографічні деталі
Дата:2002
Автор: Nekvasil, V.
Формат: Стаття
Мова:English
Опубліковано: Фізико-технічний інститут низьких температур ім. Б.І. Вєркіна НАН України 2002
Назва видання:Физика низких температур
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Онлайн доступ:http://dspace.nbuv.gov.ua/handle/123456789/130230
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Назва журналу:Digital Library of Periodicals of National Academy of Sciences of Ukraine
Цитувати:Optical study of 4f excitations in rare earth cuprates / V.Nekvasil // Физика низких температур. — 2002. — Т. 28, № 7. — С. 739-744. — Бібліогр.: 28 назв. — англ.

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Digital Library of Periodicals of National Academy of Sciences of Ukraine
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Резюме:Several recent examples are used to demonstrate that Raman and infrared spectroscopy can be successfully used as a novel experimental tool to study microscopic processes involving 4f electrons in rare earth (RE) cuprates. Raman-active crystal field (CF) excitations in Nd₂CuO₄ were measured under hydrostatic pressure up to ∼7 GPa. The observed pressure-induced shifts of the CF levels were interpreted using density-functional-theory-based ab initio calculations and the superposition model. An infrared transmission study of the ⁴Ij, J=9/2, 11/2, 13/2 multiplets of Nd³⁺ in Nd₂CuO₄ reveals a splitting of the Kramers doublets of the order of a few cm⁻¹ due to the Nd-Cu exchange interaction. This study shows that these splittings can be described by an effective anisotropic exchange Hamiltonian for the Nd³⁺ ion expressed in terms of spherical tensor operators up to the sixth order. The isotropic term in the exchange Hamiltonian vanishes for symmetry reasons in this case. An analysis of the infrared transmission spectra in RE₁₊xBa₂₋xCu3O₆₊δ (RE=Nd,Sm) up to ∼ 10 000 cm⁻¹ indicates that, besides the regular sites, the RE ions also occupy Ba sites, even in the samples with the cation stoichiometry 1–2–3.