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Quantum critical magneto-transport at a continuous metal-insulator transition

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 Added by Prosenjit Haldar
 Publication date 2016
  fields Physics
and research's language is English




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In contrast to the seminal weak localization prediction of a non-critical Hall constant ($R_{H}$) at the Anderson metal-insulator transition (MIT), $R_{H}$ in quite a few real disordered systems exhibits both, a strong $T$-dependence and critical scaling near their MIT. Here, we investigate these issues in detail within a non-perturbative strong localization regime using cluster-dynamical mean field theory (CDMFT). We uncover $(i)$ clear and unconventional quantum-critical scaling of the $gamma$-function, finding that $gamma(g_{xy})simeq$ log$(g_{xy})$ over a wide range spanning the continuous MIT, very similar to that seen for the longitudinal conductivity, $(ii)$ strongly $T$-dependent and clear quantum critical scaling in both transverse conductivity and $R_{H}$ at the MIT. We find that these surprising results are in comprehensive and very good accord with signatures of a novel kind of localization in disordered NbN near the MIT, providing substantial support for our strong localization view.



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The celebrated Wiedemann-Franz (WF) law is believed to be robust in metals as long as interactions between electrons preserve their fermion-quasiparticle character. We study thermal transport and the fate of the WF law close to a continuous metal-insulator transition (MIT) in the Falicov-Kimball model (FKM) using cluster-dynamical mean-field theory (CDMFT). Surprisingly, as for electrical transport, we find robust and novel quantum critical scaling in thermal transport across the MIT. We unearth the deeper reasons for these novel findings in terms of (i) the specific structure of energy-current correlations for the FKM and (ii) the microscopic electronic processes which facil- itate energy transport while simultaneously blocking charge transport close to the MIT. However, within (C)DMFT, we also find that the WF law survives at T=0 in the incoherent metal right up to the MIT, even in absence of Landau quasiparticles.
203 - S. Kettemann , E. R. Mucciolo , 2009
It is well-known that magnetic impurities can change the symmetry class of disordered metallic systems by breaking spin and time-reversal symmetry. At low temperature these symmetries can be restored by Kondo screening. It is also known that at the Anderson metal-insulator transition, wave functions develop multifractal fluctuations with power law correlations. Here, we consider the interplay of these two effects. We show that multifractal correlations open local pseudogaps at the Fermi energy at some random positions in space. When dilute magnetic impurities are at these locations, Kondo screening is strongly suppressed. We find that when the exchange coupling J is smaller than a certain value J*, the metal-insulator transition point extends to a critical region in the disorder strength parameter and to a band of critical states. The width of this critical region increases with a power of the concentration of magnetic impurities.
A wide range of disordered materials, including disordered correlated systems, show Universal Dielectric Response (UDR), followed by a superlinear power-law increase in their optical responses over exceptionally broad frequency regimes. While extensively used in various contexts over the years, the microscopics underpinning UDR remains controversial. Here, we investigate the optical response of the simplest model of correlated fermions, Falicov-Kimball model (FKM), across the continuous metal-insulator transition (MIT) and analyze the associated quantum criticality in detail using cluster extension of dynamical mean field theory (CDMFT). Surprisingly, we find that UDR naturally emerges in the quantum critical region associated with the continuous MIT. We tie the emergence of these novel features to a many-body orthogonality catastrophe accompanying the onset of strongly correlated electronic glassy dynamics close to the MIT, providing a microscopic realization of Jonschers time-honored proposal as well as a rationale for similarities in optical responses between correlated electronic matter and canonical glass formers.
Metal-insulator transitions involve a mix of charge, spin, and structural degrees of freedom, and when strongly-correlated, can underlay the emergence of exotic quantum states. Mott insulators induced by the opening of a Coulomb gap are an important and well-recognized class of transitions, but insulators purely driven by spin correlations are much less common, as the reduced energy scale often invites competition from other degrees of freedom. Here we demonstrate a clean example of a spin-correlation-driven metal-insulator transition in the all-in-all-out pyrochlore antiferromagnet Cd2Os2O7, where the lattice symmetry is fully preserved by the antiferromagnetism. After the antisymmetric linear magnetoresistance from conductive, ferromagnetic domain walls is carefully removed experimentally, the Hall coefficient of the bulk reveals four Fermi surfaces, two of electron type and two of hole type, sequentially departing the Fermi level with decreasing temperature below the Neel temperature, T_N. Contrary to the common belief of concurrent magnetic and metal-insulator transitions in Cd2Os2O7, the charge gap of a continuous metal-insulator transition opens only at T~10K, well below T_N=227K. The insulating mechanism resolved by the Hall coefficient parallels the Slater picture, but without a folded Brillouin zone, and contrasts sharply with the behavior of Mott insulators and spin density waves, where the electronic gap opens above and at T_N, respectively.
365 - B. Hosseinkhani , J. Zaanen 2004
Using recent insights obtained in heavy fermion physics on the thermodynamic singularity structure associated with quantum phase transitions, we present here an experimental strategy to establish if the zero-temperature transition in the disordered two dimensional gas is a real quantum phase transition. We derive a overcomplete set of scaling laws relating the density and temperature dependence of the chemical potential and the effective mass, which are in principle verifyable by experiment.
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