Positive Magneto-Resistance in Quasi-1D Conductors

We present here a simple qualitative model that interpolates between the high and low temperature properties of quasi-1D conductors. At high temperatures we argue that transport is governed by inelastic scattering whereas at low temperatures the conductance decays exponentially with the electron dephasing length. The crossover between these regimes occurs at the temperature at which the elastic and inelastic scattering times become equal. This model is shown to be in quantitative agreement with the organic conductor $TTT_2I_{3-\delta}$. Within this model, we also show that on the insulating side, the positive magnetoresistance of the form $(H/T)^2$ observed in $TTT_2I_{3-\delta}$ and other quasi-1D conductors can be explained by the role spin-flip scattering plays in the electron dephasing rate.Comment: 4 pages, Latex, no figure

Nanocrystalline lanthanide-doped Lu3Ga5O12 garnets: interesting materials for light-emitting devices

Nanocrystalline Lu3Ga5O12, with average particle sizes of 40 nm, doped with a wide variety of luminescent trivalent lanthanide ions have been prepared using a sol\u2013gel technique. The structural and morphological properties of the powders have been investigated by x-ray powder diffraction, high resolution transmission electron microscopy and Raman spectroscopy. Structural data have been refined and are presented for Pr3+, Eu3+, Gd3+, Ho3+, Er3+ and Tm3+ dopants, while room temperature excited luminescence spectra and emission decay curves of Eu3+-, Tm3+- and Ho3+-doped Lu3Ga5O12 nanocrystals have been measured and are discussed. The Eu3+ emission spectrum shows typical bands due to 5D0 \u21927FJ (J = 0, 1, 2, 3, 4) transitions and the broadening of these emission bands with the non-exponential behaviour of the decay curves indicates the presence of structural disorder around the lanthanide ions. Lanthanide-doped nanocrystalline Lu3Ga5O12 materials show better luminescence intensities compared to Y2O3, Gd3Ga5O12 and Y3Al5O12 nanocrystalline hosts. Moreover, the upconversion emission intensity in the blue-green region for the Tm3+- and Ho3+-doped samples shows a significant increase upon 647.5 nm excitation with respect to other common oxide hosts doped with the same lanthanide ions