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Register a new userDistinct Electronic Structure for the Extreme Magnetoresistance in YSb
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An extreme magnetoresistance (XMR) has recently been observed in several non-magnetic semimetals. Increasing experimental and theoretical evidence indicates that the XMR can be driven by either topological protection or electron-hole compensation. Here, by investigating the electronic structure of a XMR material, YSb, we present spectroscopic evidence for a special case which lacks topological protection and perfect electron-hole compensation. Further investigations reveal that a cooperative action of a substantial difference between electron and hole mobility and a moderate carrier compensation might contribute to the XMR in YSb.
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We report extremely large positive magnetoresistance of 1.72 million percent in single crystal TaSb$_{2}$ at moderate conditions of 1.5 K and 15 T. The quadratic growth of magnetoresistance (MR $propto,B^{1.96}$) is not saturating up to 15 T, a manifestation of nearly perfect compensation with $<0.1%$ mismatch between electron and hole pockets in this semimetal. The compensation mechanism is confirmed by temperature-dependent MR, Hall and thermoelectric coefficients of Nernst and Seebeck, revealing two pronounced Fermi surface reconstruction processes without spontaneous symmetry breaking, textit{i.e.} Lifshitz transitions, at around 20 K and 60 K, respectively. Using quantum oscillations of magnetoresistance and magnetic susceptibility, supported by density-functional theory calculations, we determined that the main hole Fermi surface of TaSb$_{2}$ forms a unique shoulder structure along the $F-L$ line. The flat band top of this shoulder pocket is just a few meV above the Fermi level, leading to the observed topological phase transition at 20 K when the shoulder pocket disappears. Further increase in temperature pushes the Fermi level to the band top of the main hole pocket, induced the second Lifshitz transition at 60 K when hole pocket vanishes completely.
The resistance of a metal in a magnetic field can be very illuminating about its ground state. Some famous examples include the integer and fractional quantum Hall effectscite{Klitzing-QHE,Tsui-FQHE}, Shubnikov-de Haas oscillationscite{SdH}, and weak localizationcite{Lee-WL} emph{et al}. In non-interacting metals the resistance typically increases upon the application of a magnetic fieldcite{Pippard-MR}. In contrast, in some special circumstances metals, with anisotropic Fermi surfacescite{Kikugawa-PdCoO2LMR} or a so-called Weyl semimetal for instancecite{Nielsen-ABJ,Son-ChirAnom}, may have negative magnetoresistance. Here we show that semimetallic TaAs$_2$ possesses a gigantic negative magnetoresistance ($-$98% in a field of 3 T at low temperatures), with an unknown mechanism. Density functional calculations illustrate that TaAs$_2$ is a new topological semimetal [$mathbb{Z}_2$ invariant (0;111)] without a Dirac dispersion. This demonstrates that the presence of negative magnetoresistance in non-magnetic semimetals cannot be uniquely attributed to the Adler-Bell-Jackiw anomaly of bulk Dirac/Weyl fermions. Our results also imply that the OsGe$_2$-type monoclinic dipnictides are likely a material basis where unconventional topological semimetals may be found.
We introduce a spectral density functional theory which can be used to compute energetics and spectra of real strongly--correlated materials using methods, algorithms and computer programs of the electronic structure theory of solids. The approach considers the total free energy of a system as a functional of a local electronic Green function which is probed in the region of interest. Since we have a variety of notions of locality in our formulation, our method is manifestly basis--set dependent. However, it produces the exact total energy and local excitational spectrum provided that the exact functional is extremized. The self--energy of the theory appears as an auxiliary mass operator similar to the introduction of the ground--state Kohn--Sham potential in density functional theory. It is automatically short--ranged in the same region of Hilbert space which defines the local Green function. We exploit this property to find good approximations to the functional. For example, if electronic self--energy is known to be local in some portion of Hilbert space, a good approximation to the functional is provided by the corresponding local dynamical mean--field theory. A simplified implementation of the theory is described based on the linear muffin--tin orbital method widely used in electronic strucure calculations. We demonstrate the power of the approach on the long--standing problem of the anomalous volume expansion of metallic plutonium.
While in strongly correlated materials one often focuses on local electronic correlations, the influence of non-local exchange and correlation effects beyond band-theory can be pertinent in systems with more extended orbitals. Thus in many compounds an adequate theoretical description requires the joint treatment of local and non-local self-energies. Here, I will argue that this is the case for the iron pnictide and chalcogenide superconductors. As an approach to tackle their electronic structure, I will detail the implementation of the recently proposed scheme that combines the quasi-particle self-consistent GW approach with dynamical mean-field theory: QSGW+DMFT. I will showcase the possibilities of QSGW+DMFT with an application on BaFe2As2. Further, I will discuss the empirical finding that in pnictides dynamical and non-local correlation effects separate within the quasi-particle band-width.
The LDA+DMFT method is a very powerful tool for gaining insight into the physics of strongly correlated materials. It combines traditional ab-initio density-functional techniques with the dynamical mean-field theory. The core aspects of the method are (i) building material-specific Hubbard-like many-body models and (ii) solving them in the dynamical mean-field approximation. Step (i) requires the construction of a localized one-electron basis, typically a set of Wannier functions. It also involves a number of approximations, such as the choice of the degrees of freedom for which many-body effects are explicitly taken into account, the scheme to account for screening effects, or the form of the double-counting correction. Step (ii) requires the dynamical mean-field solution of multi-orbital generalized Hubbard models. Here central is the quantum-impurity solver, which is also the computationally most demanding part of the full LDA+DMFT approach. In this chapter I will introduce the core aspects of the LDA+DMFT method and present a prototypical application.
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