Lyddane-Sachs-Teller relationship in linear magnetoelectrics

In a linear magnetoelectric the lattice is coupled to electric and magnetic fields: both affect the longitudinal-transverse splitting of zone-center optical phonons on equal footing. A response matrix relates the macroscopic fields (D,B) to (E,H) at infrared frequencies. It is shown that the response matrices at frequencies 0 and \infty fulfill a generalized Lyddane-Sachs-Teller relationship. The rhs member of such relationship is expressed in terms of weighted averages over the longitudinal and transverse excitations of the medium, and assumes a simple form for an harmonic crystal.Comment: 4 pages, no figur

Electron Localization in the Insulating State

The insulating state of matter is characterized by the excitation spectrum, but also by qualitative features of the electronic ground state. The insulating ground wavefunction in fact: (i) sustains macroscopic polarization, and (ii) is localized. We give a sharp definition of the latter concept, and we show how the two basic features stem from essentially the same formalism. Our approach to localization is exemplified by means of a two--band Hubbard model in one dimension. In the noninteracting limit the wavefunction localization is measured by the spread of the Wannier orbitals.Comment: 5 pages including 3 figures, submitted to PR

DESIGN AND PERFORMANCE OF INTRA-TRAIN FEEDBACK SYSTEMS AT ATF2

The major goals of the final focus test beam line facility ATF2 are to provide electron beams with a few tens of nanometer beam sizes and beam stability control at the nanometer level. In order to achieve such a level of stability beam-based feedback systems are necessary at different timescales to correct static and dynamic effects. In particular, we present the design of intra-train feedback systems to correct the impact of fast jitter sources. We study a bunchto- bunch feedback system installed in the extraction line to combat the ring extraction transverse jitters. In addition, we design a bunch-to-bunch feedback system at the interaction point for correction of position jitter due to the fast vibration of the magnets in the final focus. Optimum feedback software algorithms are discussed and simulation results are presented

Electron localization : band-by-band decomposition, and application to oxides

Using a plane wave pseudopotential approach to density functional theory we investigate the electron localization length in various oxides. For this purpose, we first set up a theory of the band-by-band decomposition of this quantity, more complex than the decomposition of the spontaneous polarization (a related concept), because of the interband coupling. We show its interpretation in terms of Wannier functions and clarify the effect of the pseudopotential approximation. We treat the case of different oxides: BaO, $\alpha$-PbO, BaTiO$_3$ and PbTiO$_3$. We also investigate the variation of the localization tensor during the ferroelectric phase transitions of BaTiO$_3$ as well as its relationship with the Born effective charges

Zone-Center Dynamical Matrix in Magnetoelectrics

In ordinary dielectrics the dynamical matrix at the zone center in general is a nonanalytic function of degree zero in the wavevector q. Its expression (for a crystal of arbitrary symmetry) is well known and is routinely implemented in first principle calculations. The nonanalytic behavior occurs in polar crystals and owes to the coupling of the macroscopic electric field E to the lattice. In magnetoelectric crystals both electric and magnetic fields, E and H, are coupled to the lattice, formally on equal footing. We provide the general expression for the zone center dynamical matrix in a magnetoelectric, where the E and H couplings are accounted for in a symmetric way. As in the ordinary case, the dynamical matrix is a nonanalytic function of degree zero in q, and is exact in the harmonic approximation. For the sake of completeness, we address other issues, and in particular we solve a problem which might arise in first-principle implementations, where-differently than here-the basic fields are E and B (not H).Comment: 7 pages, no figure. One page added in v2, prompted by a Refere

Strong-correlation effects in Born effective charges

Large values of Born effective charges are generally considered as reliable indicators of the genuine tendency of an insulator towards ferroelectric instability. However, these quantities can be very much influenced by strong electron correlation and metallic behavior, which are not exclusive properties of ferroelectric materials. In this paper we compare the Born effective charges of some prototypical ferroelectrics with those of magnetic, non-ferroelectric compounds using a novel, self-interaction free methodology that improves on the local-density approximation description of the electronic properties. We show that the inclusion of strong-correlation effects systermatically reduces the size of the Born effective charges and the electron localization lengths. Furthermore we give an interpretation of the Born effective charges in terms of band energy structure and orbital occupations which can be used as a guideline to rationalize their values in the general case.Comment: 10 pages, 4 postscript figure

Quantum-Mechanical Position Operator and Localization in Extended Systems

We introduce a fundamental complex quantity, $z_{L}$, which allows us to discriminate between a conducting and non-conducting thermodynamic phase in extended quantum systems. Its phase can be related to the expectation value of the position operator, while its modulus provides an appropriate definition of a localization length. The expressions are valid for {\it any} fractional particle filling. As an illustration we use $z_{L}$ to characterize insulator to ``superconducting'' and Mott transitions in one-dimensional lattice models with infinite on-site Coulomb repulsion at quarter filling.Comment: 4 pages, REVTEX, 1 ps figure

From band insulator to Mott insulator in one dimension

We derive the phase diagram for the one-dimensional model of a ferroelectric perovskite recently introduced by Egami, Ishihara and Tachiki [Science, {\bf 261}, 1307 (1993)]. We show that the interplay between covalency, ionicity and strong correlations results in a spontaneously dimerized phase which separates the weak-coupling band insulator from the strong-coupling Mott insulator. The transition from the band insulator to the dimerized phase is identified as an Ising critical point. The charge gap vanishes at this single point with the optical conductivity diverging as $\sigma(\omega)\sim \omega^{-3/4}$. The spin excitations are gapless above the second transition to the Mott insulator phase.Comment: 4 pages LaTex (RevTex) and 1 postscript figure included by eps

Topological nature of polarization and charge pumping in ferroelectrics

Electric polarization or transferred charge due to an adiabatic change of external parameters $\vec{Q}$ is expressed in terms of a vector field defined in the $\vec{Q}$ space. This vector field is characterized by strings, i.e., trajectories of band-crossing points. In particular, the transverse component is given by the Biot-Savart law in a nonlocal way. For a cyclic change of $\vec{Q}$ along a loop C, the linking number between this string and C represents the amount of the pumped charge, which is quantized to be an integer as discussed by Thouless.Comment: 5 pages including 4 figure

Transition from band insulator to Mott insulator in one dimension: Critical behavior and phase diagram

We report a systematic study of the transition from a band insulator (BI) to a Mott insulator (MI) in a one-dimensional Hubbard model at half-filling with an on-site Coulomb interaction U and an alternating periodic site potential V. We employ both the zero-temperature density matrix renormalization group (DMRG) method to determine the gap and critical behavior of the system and the finite-temperature transfer matrix renormalization group method to evaluate the thermodynamic properties. We find two critical points at U = $U_c$ and U = $U_s$ that separate the BI and MI phases for a given V. A charge-neutral spin-singlet exciton band develops in the BI phase (U<$U_c$) and drops below the band gap when U exceeds a special point Ue. The exciton gap closes at the first critical point $U_c$ while the charge and spin gaps persist and coincide between $U_c$<U<$U_s$ where the system is dimerized. Both the charge and spin gaps collapse at U = $U_s$ when the transition to the MI phase occurs. In the MI phase (U>$U_s$) the charge gap increases almost linearly with U while the spin gap remains zero. These findings clarify earlier published results on the same model, and offer insights into several important issues regarding an appropriate scaling analysis of DMRG data and a full physical picture of the delicate nature of the phase transitions driven by electron correlation. The present work provides a comprehensive understanding for the critical behavior and phase diagram for the transition from BI to MI in one-dimensional correlated electron systems with a periodic alternating site potential.Comment: long version, 10 figure