2 research outputs found

    Electronic correlation in the infrared optical properties of the quasi two dimensional κ\kappa-type BEDT-TTF dimer system

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    The polarized optical reflectance spectra of the quasi two dimensional organic correlated electron system κ\kappa-(BEDT-TTF)2_{2}Cu[N(CN)2_{2}]YY, Y=Y = Br and Cl are measured in the infrared region. The former shows the superconductivity at TcT_{\rm c} \simeq 11.6 K and the latter does the antiferromagnetic insulator transition at TNT_{\rm N} \simeq 28 K. Both the specific molecular vibration mode ν3(ag)\nu_{3}(a_{g}) of the BEDT-TTF molecule and the optical conductivity hump in the mid-infrared region change correlatively at TT^{*} \simeq 38 K of κ\kappa-(BEDT-TTF)2_{2}Cu[N(CN)2_{2}]Br, although no indication of TT^{*} but the insulating behaviour below TinsT_{\rm ins} \simeq 50-60 K are found in κ\kappa-(BEDT-TTF)2_{2}Cu[N(CN)2_{2}]Cl. The results suggest that the electron-molecular vibration coupling on the ν3(ag)\nu_{3}(a_{g}) mode becomes weak due to the enhancement of the itinerant nature of the carriers on the dimer of the BEDT-TTF molecules below TT^{*}, while it does strong below TinsT_{\rm ins} because of the localized carriers on the dimer. These changes are in agreement with the reduction and the enhancement of the mid-infrared conductivity hump below TT^{*} and TinsT_{\rm ins}, respectively, which originates from the transitions between the upper and lower Mott-Hubbard bands. The present observations demonstrate that two different metallic states of κ\kappa-(BEDT-TTF)2_{2}Cu[N(CN)2_{2}]Br are regarded as {\it a correlated good metal} below TT^{*} including the superconducting state and {\it a half filling bad metal} above TT^{*}. In contrast the insulating state of κ\kappa-(BEDT-TTF)2_{2}Cu[N(CN)2_{2}]Cl below TinsT_{\rm ins} is the Mott insulator.Comment: 8 pages, 7 figure

    Colossal magnetoresistance in Sr2-xNd1+xMn2O7 (x = 0.0, 0.1)

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    Magnetization and magnetotransport measurements have been used to study the composition dependence of the electronic properties of the Ruddlesden-Popper phases Sr2NdMn2O7 and Sr1.9Nd1.1Mn2O7. Although their behaviour differs in detail, both compounds show a colossal magnetoresistance (CMR) effect (>10 000% in 14 T) in the temperature range 4.2 ? T/K ? 100. However, neither material shows a transition to a ferromagnetic state above 4.2 K, and both materials have higher resistivities (>103 ? cm for 4.2 ? T/K ? 100) than the metallic oxides previously found to show CMR. In view of the low conductivity and the absence of ferromagnetism, the CMR of these phases is not readily explained by a doubleexchange mechanism
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