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Register a new userMany-Body Effective Energy Theory: photoemission at strong correlation
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In this work we explore the performance of a recently derived many-body effective energy theory for the calculation of photoemission spectra in the regime of strong electron correlation. We apply the theory to paramagnetic MnO, FeO, CoO, and NiO, which are typical examples of strongly correlated materials and, therefore, a challenge for standard theories. We show that our methods open a correlation gap in all the oxides studied without breaking the symmetry. Although the materials seem similar, we show that an analysis of the occupation numbers reveals that the nature of the gap is not the same for these materials. Overall the results are very promising, although improvements are clearly required, since the band gap is overestimated for all the systems studied. We indicate some possible strategies to further develop the theory.
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Using a separable many-body variational wavefunction, we formulate a self-consistent effective Hamiltonian theory for fermionic many-body system. The theory is applied to the two-dimensional Hubbard model as an example to demonstrate its capability and computational effectiveness. Most remarkably for the Hubbard model in 2-d, a highly unconventional quadruple-fermion non-Cooper-pair order parameter is discovered.
We construct an analytic theory of many-body localization (MBL) in random spin chains. The approach is based on a first quantized perspective in which MBL is understood as a localization phenomenon on the high dimensional lattice defined by the discrete Hilbert space of the clean system. We construct a field theory on that lattice and apply it to discuss the stability of a weak disorder (`Wigner-Dyson) and a strong disorder (`Poisson) phase.
We carry out an analytical study of quantum spin ice, a U$(1)$ quantum spin liquid close to the classical spin ice solution for an effective spin $1/2$ model with anisotropic exchange couplings $J_{zz}$, $J_{pm}$ and $J_{zpm}$ on the pyrochlore lattice. Starting from the quantum rotor model introduced by Savary and Balents in Phys. Rev. Lett. 108, 037202 (2012), we retain the dynamics of both the spinons and gauge field sectors in our treatment. The spinons are described by a bosonic representation of quantum XY rotors while the dynamics of the gauge field is captured by a phenomenological Hamiltonian. By calculating the one-loop spinon self-energy, which is proportional to $J_{zpm}^2$, we determine the stability region of the U$(1)$ quantum spin liquid phase in the $J_{pm}/J_{zz}$ vs $J_{zpm}/J_{zz}$ zero temperature phase diagram. From these results, we estimate the location of the boundaries between the spin liquid phase and classical long-range ordered phases.
The description of dynamics of strongly correlated quantum matter is a challenge, particularly in physical situations where a quasiparticle description is absent. In such situations, however, the many-body Kubo formula from linear response theory, involving matrix elements of the current operator computed with many-body wavefunctions, remains valid. Working directly in the many-body Hilbert space and not making any reference to quasiparticles (or lack thereof), we address the puzzle of linear in temperature ($T$-linear) resistivity seen in non-Fermi liquid phases that occur in several strongly correlated condensed matter systems. We derive a simple criterion for the occurrence of $T$-linear resistivity based on an analysis of the contributions to the many-body Kubo formula, determined by an energy invariant $f$-function involving current matrix elements and energy eigenvalues that describes the DC conductivity of the system in the microcanonical ensemble. Using full diagonalization, we test this criterion for the $f$-function in the spinless nearest neighbor Hubbard model, and in a system of Sachdev-Ye-Kitaev dots coupled by weak single particle hopping. We also study the $f$-function for the spin conductivity in the 2D Heisenberg model with similar conclusions. Our work suggests that a general principle, formulated in terms of many-body Hilbert space concepts, is at the core of the occurrence of $T$-linear resistivity in a wide range of systems, and precisely translates $T$-linear resistivity into a notion of energy scale invariance far beyond what is typically associated with quantum critical points.
Many of the fascinating and unconventional properties of several transition-metal compounds with partially filled d-shells are due to strong electronic correlations. While local correlations are in principle treated exactly within the frame of the dynamical mean-field theory, there are two major and interlinked routes for important further methodical advances: On the one hand, there is a strong need for methods being able to describe material-specific aspects, i.e., methods combining the DMFT with modern band-structure theory, and, on the other hand, nonlocal correlations beyond the mean-field paradigm must be accounted for. Referring to several concrete example systems, we argue why these two routes are worth pursuing and how they can be combined, we describe several related methodical developments and present respective results, and we discuss possible ways to overcome remaining obstacles.
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