Electronic phase separation in the rare earth manganates, (La1-xLnx)0.7Ca0.3MnO3 (Ln = Nd, Gd and Y)

All the three series of manganates showsaturation magnetization characteristic of ferromagnetism, with the ferromagnetic Tc decreasing with increasing in x up to a critical value of x, xc (xc = 0.6, 0.3, 0.2 respectively for Nd, Gd, Y). For x > xc, the magnetic moments are considerably smaller showing a small increase around TM, the value of TM decreasing slightly with increase in x or decrease in . The ferromagnetic compositions (x xc) show insulator-metal (IM) transitions, while the compositions with x > xc are insulating. The magnetic and electrical resistivity behavior of these manganates is consistent with the occurrence of phase separation in the compositions around xc, corresponding to a critical average radius of the A-site cation, , of 1.18 A. Both Tc and TIM increase linearly when < rA > > or x xc as expected of a homogenous ferromagnetic phase. Both Tc and TM decrease linearly with the A-site cation size disorder at the A-site as measured by the variance s2. Thus, an increase in s2 favors the insulating AFM state. Percolative conduction is observed in the compositions with > < rAc >. Electron transport properties in the insulating regime for x > xc conforms to the variable range hopping mechanism. More interestingly, when x > xc, the real part of dielectric constant (e') reaches a high value (104-106) at ordinary temperatures dropping to a very small (~500) value below a certain temperature, the value of which decreases with decreasing frequency.Comment: 27 pages; 11 figures, Submitted to J.Phys:Condens Matte

Spin Decoherence from Hamiltonian dynamics in Quantum Dots

The dynamics of a spin-1/2 particle coupled to a nuclear spin bath through an isotropic Heisenberg interaction is studied, as a model for the spin decoherence in quantum dots. The time-dependent polarization of the central spin is calculated as a function of the bath-spin distribution and the polarizations of the initial bath state. For short times, the polarization of the central spin shows a gaussian decay, and at later times it revives displaying nonmonotonic time dependence. The decoherence time scale dep ends on moments of the bath-spin distribuition, and also on the polarization strengths in various bath-spin channels. The bath polarizations have a tendency to increase the decoherence time scale. The effective dynamics of the central spin polarization is shown to be describ ed by a master equation with non-markovian features.Comment: 11 pages, 6 figures Accepted for publication in Phys.Rev

Understanding of the phase transformation from fullerite to amorphous carbon at the microscopic level

We have studied the shock-induced phase transition from fullerite to a dense amorphous carbon phase by tight-binding molecular dynamics. For increasing hydrostatic pressures P, the C60-cages are found to polymerise at P<10 GPa, to break at P~40 GPa and to slowly collapse further at P>60 GPa. By contrast, in the presence of additional shear stresses, the cages are destroyed at much lower pressures (P<30 GPa). We explain this fact in terms of a continuum model, the snap-through instability of a spherical shell. Surprisingly, the relaxed high-density structures display no intermediate-range order.Comment: 5 pages, 3 figure

Azoto

1. Introduzione p. 282 2. Determinazione dell\u2019azoto totale con analizzatore elementare p. 284 3. Determinazione dell\u2019azoto totale con metodo semi-micro-Kjeldahl p. 284 4. Determinazione dell\u2019azoto totale con metodo semi-micro-Kjeldahl modificato p. 287 5. Determinazione dell\u2019azoto totale estraibile con soluzione salina con metodo micro-Kjeldahl p. 291 6. Determinazione dell\u2019azoto totale estraibile con soluzione salina con metodo micro-Kjeldahl modificato p.294 7. Determinazione colorimetrica degli ioni ammonio estraibili p. 296 8. Determinazione colorimetrica degli ioni nitrato estraibili p. 298 9. Estrazione dell\u2019azoto totale idrolizzabile con acido cloridrico p. 300 10.Determinazione dell\u2019azoto totale idrolizzabile con acido cloridrico secondo il metodo micro-Kjeldahl p. 30

Droplet Fluctuations in the Morphology and Kinetics of Martensites

We derive a coarse grained, free-energy functional which describes droplet configurations arising on nucleation of a product crystal within a parent. This involves a new `slow' vacancy mode that lives at the parent-product interface. A mode-coupling theory suggests that a {\it slow} quench from the parent phase produces an equilibrium product, while a {\it fast} quench produces a metastable martensite. In two dimensions, the martensite nuclei grow as `lens-shaped' strips having alternating twin domains, with well-defined front velocities. Several empirically known structural and kinetic relations drop out naturally from our theory.Comment: 4 pages, REVTEX, and 3 .eps figures, compressed and uuencoded, Submitted to Phys. Rev. Let

Mg II Absorption Systems in SDSS QSO Spectra

We present the results of a MgII absorption-line survey using QSO spectra from the SDSS EDR. Over 1,300 doublets with rest equivalent widths greater than 0.3\AA and redshifts $0.366 \le z \le 2.269$ were identified and measured. We find that the $\lambda2796$ rest equivalent width ($W_0^{\lambda2796}$) distribution is described very well by an exponential function $\partial N/\partial W_0^{\lambda2796} = \frac{N^*}{W^*} e^{-\frac{W_0}{W^*}}$, with $N^*=1.187\pm0.052$ and $W^*=0.702\pm0.017$\AA. Previously reported power law fits drastically over-predict the number of strong lines. Extrapolating our exponential fit under-predicts the number of $W_0 \le 0.3$\AA systems, indicating a transition in $dN/dW_0$ near $W_0 \simeq 0.3$\AA. A combination of two exponentials reproduces the observed distribution well, suggesting that MgII absorbers are the superposition of at least two physically distinct populations of absorbing clouds. We also derive a new redshift parameterization for the number density of $W_0^{\lambda2796} \ge 0.3$\AA lines: $N^*=1.001\pm0.132(1+z)^{0.226\pm0.170}$ and $W^*=0.443\pm0.032(1+z)^{0.634\pm 0.097}$\AA. We find that the distribution steepens with decreasing redshift, with $W^*$ decreasing from $0.80\pm0.04$\AA at $z=1.6$ to $0.59\pm0.02$\AA at $z=0.7$. The incidence of moderately strong MgII $\lambda2796$ lines does not show evidence for evolution with redshift. However, lines stronger than $\approx 2$\AA show a decrease relative to the no-evolution prediction with decreasing redshift for $z \lesssim 1$. The evolution is stronger for increasingly stronger lines. Since $W_0$ in saturated absorption lines is an indicator of the velocity spread of the absorbing clouds, we interpret this as an evolution in the kinematic properties of galaxies from moderate to low z.Comment: 50 pages, 26 figures, accepted for publication in Ap

Decomposition of time-covariant operations on quantum systems with continuous and/or discrete energy spectrum

Every completely positive map G that commutes which the Hamiltonian time evolution is an integral or sum over (densely defined) CP-maps G_\sigma where \sigma is the energy that is transferred to or taken from the environment. If the spectrum is non-degenerated each G_\sigma is a dephasing channel followed by an energy shift. The dephasing is given by the Hadamard product of the density operator with a (formally defined) positive operator. The Kraus operator of the energy shift is a partial isometry which defines a translation on R with respect to a non-translation-invariant measure. As an example, I calculate this decomposition explicitly for the rotation invariant gaussian channel on a single mode. I address the question under what conditions a covariant channel destroys superpositions between mutually orthogonal states on the same orbit. For channels which allow mutually orthogonal output states on the same orbit, a lower bound on the quantum capacity is derived using the Fourier transform of the CP-map-valued measure (G_\sigma).Comment: latex, 33 pages, domains of unbounded operators are now explicitly specified. Presentation more detailed. Implementing the shift after the dephasing is sometimes more convenien

Equivariant map superalgebras

Suppose a group $\Gamma$ acts on a scheme $X$ and a Lie superalgebra $\mathfrak{g}$. The corresponding equivariant map superalgebra is the Lie superalgebra of equivariant regular maps from $X$ to $\mathfrak{g}$. We classify the irreducible finite dimensional modules for these superalgebras under the assumptions that the coordinate ring of $X$ is finitely generated, $\Gamma$ is finite abelian and acts freely on the rational points of $X$, and $\mathfrak{g}$ is a basic classical Lie superalgebra (or $\mathfrak{sl}(n,n)$, $n > 0$, if $\Gamma$ is trivial). We show that they are all (tensor products of) generalized evaluation modules and are parameterized by a certain set of equivariant finitely supported maps defined on $X$. Furthermore, in the case that the even part of $\mathfrak{g}$ is semisimple, we show that all such modules are in fact (tensor products of) evaluation modules. On the other hand, if the even part of $\mathfrak{g}$ is not semisimple (more generally, if $\mathfrak{g}$ is of type I), we introduce a natural generalization of Kac modules and show that all irreducible finite dimensional modules are quotients of these. As a special case, our results give the first classification of the irreducible finite dimensional modules for twisted loop superalgebras.Comment: 27 pages. v2: Section numbering changed to match published version. Other minor corrections. v3: Minor corrections (see change log at end of introduction