2 research outputs found
Electronic correlation in the infrared optical properties of the quasi two dimensional -type BEDT-TTF dimer system
The polarized optical reflectance spectra of the quasi two dimensional
organic correlated electron system -(BEDT-TTF)Cu[N(CN)],
Br and Cl are measured in the infrared region. The former shows the
superconductivity at 11.6 K and the latter does the
antiferromagnetic insulator transition at 28 K. Both the
specific molecular vibration mode of the BEDT-TTF molecule and
the optical conductivity hump in the mid-infrared region change correlatively
at 38 K of -(BEDT-TTF)Cu[N(CN)]Br, although
no indication of but the insulating behaviour below 50-60 K are found in -(BEDT-TTF)Cu[N(CN)]Cl. The
results suggest that the electron-molecular vibration coupling on the
mode becomes weak due to the enhancement of the itinerant
nature of the carriers on the dimer of the BEDT-TTF molecules below ,
while it does strong below 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 and , respectively, which originates from the transitions between the upper
and lower Mott-Hubbard bands. The present observations demonstrate that two
different metallic states of -(BEDT-TTF)Cu[N(CN)]Br are
regarded as {\it a correlated good metal} below including the
superconducting state and {\it a half filling bad metal} above . In
contrast the insulating state of -(BEDT-TTF)Cu[N(CN)]Cl
below is the Mott insulator.Comment: 8 pages, 7 figure
Colossal magnetoresistance in Sr2-xNd1+xMn2O7 (x = 0.0, 0.1)
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