We calculate spectra of magnetic excitations in the spin-spiral state of perovskite manganates. The spectra consist of several branches corresponding to different polarizations and different ways of diffraction from the static magnetic order. Goldsto
ne modes and opening of gaps at zero and non-zero energies due to the crystal field and the Dzyaloshinski-Moriya anisotropies are discussed. Comparing results of the calculation with available experimental data we determine values of effective exchange parameters and anisotropies. To simplify the spin-wave calculation and to get a more clear physical insight in the structure of excitations we use the {sigma}-model-like effective field theory to analyze the Heisenberg Hamiltonian and to derive the spectra.
The distribution of electrons and holes in the CuO$_2$ plane of the high-temperature superconducting cuprates is determined with nuclear magnetic resonance through the quadrupole splittings of $^{17}$O and $^{63}$Cu. Based on new data for single crys
tals of electron-doped Pr$_{2-x}$Ce$_x$CuO$_4$(x=0, 0.05, 0.10, 0.15) as well as Nd$_{2-x}$Ce$_x$CuO$_4$ (x=0, 0.13) the changes in hole contents $n_d$ of Cu 3d$(x^2-y^2)$ and $n_p$ of O 2$p_sigma$ orbitals are determined and they account for the stoichiometrically doped charges, similar to hole-doped lsco. It emerges that while $n_d+2n_p=1$ in all parent materials as expected, $n_d$ and $n_p$ vary substantially between different groups of materials. Doping holes increases predominantly $n_p$, but also $n_d$. To the contrary, doping electrons predominantly decreases $n_d$ and only slightly $n_p$. However, $n_p$ for the electron doped systems is higher than that in hole doped La$_{1.85}$Sr$_{0.15}$CuO$_4$. Cuprates with the highest maximum $T_{rm c}$s appear to have a comparably low $n_d$ while, at the same time, $n_p$ is very high. The rather high oxygen hole content of the Pr$_2$CuO$_4$ and Nd$_2$CuO$_4$ with the low $n_d$ seems to make them ideal candidates for hole doping to obtain the highest $T_{rm c}$.
We argue that the magnetic susceptibility data, Refs. 1-3, for the low-density two-dimensional (2D) silicon-based electron gas indicate that magnetically active electrons are localised in spin-droplets. The droplets exist in both the insulating and m
etallic phases, and interact ferromagnetically, forming an effective 2D Heisenberg ferromagnet. Comparing the data with known analytical and numerical results for a 2D Heisenberg ferromagnet, we determine that JS^2 approx 0.6K, where S is the spin of the droplet and J is the ferromagnetic exchange constant between droplets. We further argue that most likely S=1 with four electrons occupying each droplet on average. We discuss the dependence of the magnetic susceptibility and the specific heat on the external magnetic field, which follows from the model, and hence we suggest further experimental tests of the model.
At doping below 6% the bilayer cuprate YBa2Cu3O{6+y} is a collinear antiferromagnet. Independent of doping the value of the staggered magnetization at zero temperature is about 0.6mu_B. This is the maximum value of the magnetization allowed by quantu
m fluctuations of localized spins. In this low doping regime the compound is a normal conductor with a finite resistivity at zero temperature. These experimental observations create a unique opportunity for theory to perform a controlled calculation of the electron spectral function. In the present work we perform this calculation within the framework of the extended t-J model. As one expects the Fermi surface consists of small hole pockets centered at (pi/2,pi/2). The electron spectral function is very strongly anisotropic with maximum of intensity located at the inner parts of the pockets and with very small intensity at the outer parts. We also found that the antiferromagnetic correlations act against the bilayer bonding-antibonding splitting destroying it. The bilayer Fermi surface splitting is practically zero.
A possibility to describe magnetism in the iron pnictide parent compounds in terms of the two-dimensional frustrated Heisenberg $J_1$-$J_2$ model has been actively discussed recently. However, recent neutron scattering data has shown that the pnictid
es have a relatively large spin wave dispersion in the direction perpendicular to the planes. This indicates that the third dimension is very important. Motivated by this observation we study the $J_1$-$J_2$-$J_c$ model that is the three dimensional generalization of the $J_1$-$J_2$ Heisenberg model for $S = 1/2$ and S = 1. Using self-consistent spin wave theory we present a detailed description of the staggered magnetization and magnetic excitations in the collinear state. We find that the introduction of the interlayer coupling $J_c$ suppresses the quantum fluctuations and strengthens the long range ordering. In the $J_1$-$J_2$-$J_c$ model, we find two qualitatively distinct scenarios for how the collinear phase becomes unstable upon increasing $J_1$. Either the magnetization or one of the spin wave velocities vanishes. For $S = 1/2$ renormalization due to quantum fluctuations is significantly stronger than for S=1, in particular close to the quantum phase transition. Our findings for the $J_1$-$J_2$-$J_c$ model are of general theoretical interest, however, the results show that it is unlikely that the model is relevant to undoped pnictides.
The role of Coulomb disorder, either of extrinsic origin or introduced by dopant ions in undoped and lightly-doped cuprates, is studied. We demonstrate that charged surface defects in an insulator lead to a Gaussian broadening of the Angle-Resolved P
hotoemisson Spectroscopy (ARPES) lines. The effect is due to the long-range nature of the Coulomb interaction. A tiny surface concentration of defects about a fraction of one per cent is sufficient to explain the line broadening observed in Sr$_2$CuO$_2$Cl$_2$, La$_2$CuO$_{4}$, and Ca$_{2}$CuO$_{2}$Cl$_{2}$. Due to the Coulomb screening, the ARPES spectra evolve dramatically with doping, changing their shape from a broad Gaussian form to narrow Lorentzian ones. To understand the screening mechanism and the lineshape evolution in detail, we perform Hartree-Fock simulations with random positions of surface defects and dopant ions. To check validity of the model we calculate the Nuclear Quadrupole Resonance (NQR) lineshapes as a function of doping and reproduce the experimentally observed NQR spectra. Our study also indicates opening of a substantial Coulomb gap at the chemical potential. For a surface CuO$_2$ layer the value of the gap is of the order of 10 meV while in the bulk it is reduced to the value about a few meV.
