Strong coupling theory of heavy fermion criticality II.

We present a theory of the scaling behavior of the thermodynamic, transport and dynamical properties of a three-dimensional metal governed by d-dimensional fluctuations at a quantum critical point, where the electron quasiparticle effective mass diverges. We determine how the critical bosonic order parameter fluctuations are affected by the effective mass divergence. The coupled system of fermions and bosons is found to be governed by two stable fixed points: the conventional weak-coupling fixed point and a new strong-coupling fixed point, provided the boson-boson interaction is irrelevant. The latter fixed point supports hyperscaling, characterized by fractional exponents. The theory is applied to the antiferromagnetic critical point in certain heavy fermion compounds, in which the strong-coupling regime is reached.

Thermal and electrical transport across a magnetic quantum critical point.

A quantum critical point (QCP) arises when a continuous transition between competing phases occurs at zero temperature. Collective excitations at magnetic QCPs give rise to metallic properties that strongly deviate from the expectations of Landau's Fermi-liquid description, which is the standard theory of electron correlations in metals. Central to this theory is the notion of quasiparticles, electronic excitations that possess the quantum numbers of the non-interacting electrons. Here we report measurements of thermal and electrical transport across the field-induced magnetic QCP in the heavy-fermion compound YbRh(2)Si(2) (refs 2, 3). We show that the ratio of the thermal to electrical conductivities at the zero-temperature limit obeys the Wiedemann-Franz law for magnetic fields above the critical field at which the QCP is attained. This is also expected for magnetic fields below the critical field, where weak antiferromagnetic order and a Fermi-liquid phase form below 0.07 K (at zero field). At the critical field, however, the low-temperature electrical conductivity exceeds the thermal conductivity by about 10 per cent, suggestive of a non-Fermi-liquid ground state. This apparent violation of the Wiedemann-Franz law provides evidence for an unconventional type of QCP at which the fundamental concept of Landau quasiparticles no longer holds. These results imply that Landau quasiparticles break up, and that the origin of this disintegration is inelastic scattering associated with electronic quantum critical fluctuations--these insights could be relevant to understanding other deviations from Fermi-liquid behaviour frequently observed in various classes of correlated materials.

Critical quasiparticle theory applied to heavy fermion metals near an antiferromagnetic quantum phase transition.

We use the recently developed critical quasiparticle theory to derive the scaling behavior associated with a quantum critical point in a correlated metal. This is applied to the magnetic-field induced quantum critical point observed in YbRh(2)Si(2), for which we also derive the critical behavior of the specific heat, resistivity, thermopower, magnetization and susceptibility, the Grüneisen coefficient, and the thermal expansion coefficient. The theory accounts very well for the available experimental results.

Anisotropic in-plane resistivity in the nematic phase of the iron pnictides.

We show that the interference between scattering by impurities and by critical spin fluctuations gives rise to anisotropic transport in the Ising-nematic state of the iron pnictides. The effect is closely related to the non-Fermi-liquid behavior of the resistivity near an antiferromagnetic quantum critical point. Our theory not only explains the observed sign of the resistivity anisotropy Δρ in electron-doped systems but also predicts a sign change of Δρ upon sufficient hole doping. Furthermore, our model naturally addresses the changes in Δρ upon sample annealing and alkaline-earth substitution.

Quantum criticality in the iron pnictides and chalcogenides.

Superconductivity in the iron pnictides and chalcogenides arises at the border of antiferromagnetism, which raises the question of the role of quantum criticality. In this topical review, we describe the theoretical work that led to the prediction of a magnetic quantum critical point arising out of a competition between electronic localization and itinerancy, and the proposal for accessing it by using isoelectronic P substitution for As in the undoped iron pnictides. We go on to compile the emerging experimental evidence in support of the existence of such a quantum critical point in isoelectronically tuned iron pnictides. We close by discussing the implications of these results for the physics of the iron pnictides and chalcogenides.

Band narrowing and Mott localization in iron oxychalcogenides La2O2Fe2O(Se,S)2.

Bad metal properties have motivated a description of the parent iron pnictides as correlated metals on the verge of Mott localization. What has been unclear is whether interactions can push these and related compounds to the Mott-insulating side of the phase diagram. Here we consider the iron oxychalcogenides La2O2Fe2O(Se,S)2, which contain an Fe square lattice with an expanded unit cell. We show theoretically that they contain enhanced correlation effects through band narrowing compared to LaOFeAs, and we provide experimental evidence that they are Mott insulators with moderate charge gaps. We also discuss the magnetic properties in terms of a Heisenberg model with frustrating J1-J2-J2' exchange interactions on a "doubled" checkerboard lattice.

Iron pnictides as a new setting for quantum criticality.

Two major themes in the physics of condensed matter are quantum critical phenomena and unconventional superconductivity. These usually occur in the context of competing interactions in systems of strongly correlated electrons. All this interesting physics comes together in the behavior of the recently discovered iron pnictide compounds that have generated enormous interest because of their moderately high-temperature superconductivity. The ubiquity of antiferromagnetic ordering in their phase diagrams naturally raises the question of the relevance of magnetic quantum criticality, but the answer remains uncertain both theoretically and experimentally. Here, we show that the undoped iron pnictides feature a unique type of magnetic quantum critical point, which results from a competition between electronic localization and itinerancy. Our theory provides a mechanism to understand the experimentally observed variation of the ordered moment among the undoped iron pnictides. We suggest P substitution for As in the undoped iron pnictides as a means to access this example of magnetic quantum criticality in an unmasked fashion. Our findings point to the iron pnictides as a much-needed setting for quantum criticality, one that offers a unique set of control parameters.

Strong correlations and magnetic frustration in the high Tc iron pnictides.

We consider the iron pnictides in terms of a proximity to a Mott insulator. The superexchange interactions contain competing nearest-neighbor and next-nearest-neighbor components. In the undoped parent compound, these frustrated interactions lead to a two-sublattice collinear antiferromagnet (each sublattice forming a Néel ordering), with a reduced magnitude for the ordered moment. Electron or hole doping, together with the frustration effect, suppresses the magnetic ordering and allows a superconducting state. The exchange interactions favor a d-wave superconducting order parameter; in the notation appropriate for the Fe square lattice, its orbital symmetry is dxy. A number of existing and future experiments are discussed in light of the theoretical considerations.

Nonexponential relaxation and hierarchically constrained dynamics in a protein.

A scaling analysis within a model of hierarchically constrained dynamics is shown to reproduce the main features of nonexponential relaxation observed in kinetic studies of carbonmonoxymyoglobin.