Maximization of thermal entanglement of arbitrarily interacting two qubits

We investigate the thermal entanglement of interacting two qubits. We maximize it by tuning a local Hamiltonian under a given interaction Hamiltonian. We prove that the optimizing local Hamiltonian takes a simple form which dose not depend on the temperature and that the corresponding optimized thermal entanglement decays as $1/(T log T)$ at high temperatures. We also find that at low temperatures the thermal entanglement is maximum without any local Hamiltonians and that the second derivative of the maximized thermal entanglement changes discontinuously at the boundary between the high- and low-temperature phases.Comment: 23 pages, 4 figure

Multiferroic properties of an \aa kermanite Sr2_2CoSi2_2O7_7 single crystal in high magnetic fields

The magnetic and dielectric properties of \aa kermanite Sr$_2$CoSi$_2$O$_7$ single crystals in high magnetic fields were investigated. We have observed finite induced electric polarization along the c axis in high fields, wherein all Co spins were forcibly aligned to the magnetic field direction. Existence of the induced polarization in the spin-polarized state accompanied with the finite slope in the magnetization curve suggests the possible role of the orbital angular momenta in the excited states as its microscopic origin. The emergence of the field-induced polarization without particular magnetic order can be regarded as the magnetoelectric effects of the second order from the symmetry point of view. A low magnetic field-driven electric polarization flip induced by a rotating field, even at room temperature, has been successfully demonstrated.Comment: 12 pages, 4 figure

Microwave properties of Nd_0.5Sr_0.5MnO_3: a key role of the (x^2-y^2)-orbital effects

Transmittance of the colossal magnetoresistive compound Nd_0.5Sr_0.5MnO_3 showing metal-insulator phase transition has been studied by means of the submm- and mm-wavelength band spectroscopy. An unusually high transparency of the material provided direct evidence for the significant suppression of the coherent Drude weight in the ferromagnetic metallic state. Melting of the A-type antiferromagnetic states has been found to be responsible for a considerable increase in the microwave transmission, which was observed at the transition from the insulating to the metallic phase induced by magnetic field or temperature. This investigation confirmed a dominant role of the (x^2-y^2)-orbital degree of freedom in the low-energy optical properties of Nd_0.5Sr_0.5MnO_3 and other doped manganites with planar (x^2-y^2)-orbital order, as predicted theoretically. The results are discussed in terms of the orbital-liquid concept.Comment: 8 pages, 3 figure

Chemical potential shift induced by double-exchange and polaronic effects in Nd_{1-x}Sr_xMnO_3

We have studied the chemical potential shift as a function of temperature in Nd$_{1-x}$Sr$_x$MnO$_3$ (NSMO) by measurements of core-level photoemission spectra. For ferromagnetic samples ($x=0.4$ and 0.45), we observed an unusually large upward chemical potential shift with decreasing temperature in the low-temperature region of the ferromagnetic metallic (FM) phase. This can be explained by the double-exchange (DE) mechanism if the $e_g$ band is split by dynamical/local Jahn-Teller effect. The shift was suppressed near the Curie temperature ($T_C$), which we attribute to the crossover from the DE to lattice-polaron regimes.Comment: 5 pages, 6 figure

Competition between ferromagnetic and charge-orbital ordered phases in Pr1−x_{1-x}Cax_{x}MnO3_3 for xx=1/4, 3/8, and 1/2

Spin, charge, and orbital structures in models for doped manganites are studied by a combination of analytic mean-field and numerical relaxation techniques. At realistic values for the electron-phonon and antiferromagnetic $t_{2g}$ spin couplings, a competition between a ferromagnetic (FM) phase and a charge-orbital ordered (COO) insulating state is found for $x$=1/4, 3/8, and 1/2, as experimentally observed in Pr$_{1-x}$Ca$_{x}$MnO$_3$ for $x$=0.3$\sim$0.5. The theoretical predictions for the spin-charge-orbital ordering pattern are compared with experiments. The FM-COO energy difference is surprisingly small for the densities studied, result compatible with the presence of a robust colossal-magnetoresistive effect in Pr$_{1-x}$Ca$_{x}$MnO$_3$ in a large density interval.Comment: 4 pages, Revtex, with 2 figures embedded in the text. Submitted to Phys. Rev.

Collapse of the charge ordering gap of Nd_{0.5}Sr_{0.5}MnO_{3} in an applied magnetic field

We report results of tunneling studies on the charge ordering compound Nd_{0.5}Sr_{0.5}MnO_{3} in a magnetic field up to 6T and for temperature down to 25K.We show that a gap (2\Delta_{CO} \approx 0.5eV opens up in the density of state (DOS) at the Fermilevel (E_F) on charge ordering (T_{CO}=150K) which collapses in an applied magnetic field when the charge ordered state melts. There is a clear correspondence between the behavior of the resistivity and the gap formation and its collapse in an applied magnetic field. We conclude that a gap in the DOS at E_F is necessary for the stability of the charge ordered state.Comment: 4 pages REVTeX, 5 postscript figures included, submitted to Phys. Rev. Let

Transport and structural study of pressure-induced magnetic states in Nd0.55Sr0.45MnO3 and Nd0.5Sr0.5MnO3

Pressure effects on the electron transport and structure of Nd1-xSrxMnO3 (x = 0.45, 0.5) were investigated in the range from ambient to ~6 GPa. In Nd0.55Sr0.45MnO3, the low-temperature ferromagnetic metallic state is suppressed and a low temperature insulating state is induced by pressure. In Nd0.5Sr0.5MnO3, the CE-type antiferromagnetic charge-ordering state is suppressed by pressure. Under pressure, both samples have a similar electron transport behavior although their ambient ground states are much different. It is surmised that pressure induces an A-type antiferromagnetic state at low temperature in both compounds

First Principles Study of Structural, Electronic and Magnetic Interplay in Ferroelectromagnetic Yttrium Manganite

We present results of local spin density approximation pseudopotential calculations for the ferroelectromagnet, yttrium manganite (YMnO3). The origin of the differences between ferroelectric and non-ferroelectric perovskite manganites is determined by comparing the calculated properties of yttrium manganite in its ferroelectric hexagonal and non-ferroelectric orthorhombic phases. In addition, orthorhombic YMnO3 is compared with the prototypical non-ferroelectric manganite, lanthanum manganite. We show that, while the octahedral crystal field splitting of the cubic perovskite structure causes a centro-symmetric Jahn-Teller distortion around the Mn3+ ion, the markedly different splitting in hexagonal perovskites creates an electronic configuration consistent with ferroelectric distortion. We explain the nature of the distortion, and show that a local magnetic moment on the Mn3+ ion is a requirement for it to occur.Comment: Replacement of earlier version with error in pseudopotentia