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A wide range of materials, like d-wave superconductors, graphene, and topological insulators, share a fundamental similarity: their low-energy fermionic excitations behave as massless Dirac particles rather than fermions obeying the usual Schrodinger Hamiltonian. This emergent behavior of Dirac fermions in condensed matter systems defines the unifying framework for a class of materials we call Dirac materials. In order to establish this class of materials, we illustrate how Dirac fermions emerge in multiple entirely different condensed matter systems and we discuss how Dirac fermions have been identified experimentally using electron spectroscopy techniques (angle-resolved photoemission spectroscopy and scanning tunneling spectroscopy). As a consequence of their common low-energy excitations, this diverse set of materials shares a significant number of universal properties in the low-energy (infrared) limit. We review these common properties including nodal points in the excitation spectrum, density of states, specific heat, transport, thermodynamic properties, impurity resonances, and magnetic field responses, as well as discuss many-body interaction effects. We further review how the emergence of Dirac excitations is controlled by specific symmetries of the material, such as time-reversal, gauge, and spin-orbit symmetries, and how by breaking these symmetries a finite Dirac mass is generated. We give examples of how the interaction of Dirac fermions with their distinct real material background leads to rich novel physics with common fingerprints such as the suppression of back scattering and impurity-induced resonant states.
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We present a short pedagogical introduction to the physics of Dirac materials, restricted to graphene and two- dimensional topological insulators. We start with a brief reminder of the Dirac and Weyl equations in the particle physics context. Turning to condensed matter systems, semimetallic graphene and various Dirac insulators are introduced, including the Haldane and the Kane-Mele topological insulators. We also discuss briefly experimental realizations in materials with strong spin-orbit coupling.
Recently it was suggested that transient excitonic instability can be realized in optically-pumped two-dimensional (2D) Dirac materials (DMs), such as graphene and topological insulator surface states. Here we discuss the possibility of achieving a transient excitonic condensate in optically-pumped three-dimensional (3D) DMs, such as Dirac and Weyl semimetals, described by non-equilibrium chemical potentials for photoexcited electrons and holes. Similar to the equilibrium case with long-range interactions, we find that for pumped 3D DMs with screened Coulomb potential two possible excitonic phases exist, an excitonic insulator phase and the charge density wave phase originating from intranodal and internodal interactions, respectively. In the pumped case, the critical coupling for excitonic instability vanishes; therefore, the two phases coexist for arbitrarily weak coupling strengths. The excitonic gap in the charge density wave phase is always the largest one. The competition between screening effects and the increase of the density of states with optical pumping results in a reach phase diagram for the transient excitonic condensate. Based on the static theory of screening, we find that under certain conditions for the value of the dimensionless coupling constant screening in 3D DMs can be weaker than in 2D DMs. Furthermore, we identify the signatures of the transient excitonic condensate that could be probed by scanning tunneling spectroscopy, photoemission and optical conductivity measurements. Finally, we provide estimates of critical temperatures and excitonic gaps for existing and hypothetical 3D DMs.
Driven and non-equilibrium quantum states of matter have attracted growing interest in both theoretical and experimental studies in condensed matter physics. We review recent progress in realizing transient collective states in driven or pumped Dirac materials (DMs). In particular, we focus on optically-pumped DMs which have been theoretically proposed as a promising platform for observation of a transient excitonic instability. Optical pumping combined with the linear (Dirac) dispersion of the electronic spectrum offers a knob for tuning the effective interaction between the photoexcited electrons and holes, and thus provides a way of reducing the critical coupling for excitonic instability. As a result, a transient excitonic condensate could be achieved in a pumped DM while it is not feasible in equilibrium. We provide a unifying theoretical framework for describing transient collective states in two- and three-dimensional DMs. We describe experimental signatures of the transient excitonic state and summarize numerical estimates of the magnitude of the effect, namely the size of the dynamically-induced excitonic gaps and the values of the critical temperatures for several specific systems. We also discuss general guidelines for identifying promising material candidates.Finally, we comment recent experimental efforts in realizing transient excitonic condensate in pumped DMs and outline outstanding issues and possible future directions.
Dirac semimetal (DSM) hosts four-fold degenerate isolated band-crossing points with linear dispersion, around which the quasiparticles resemble the relativistic Dirac Fermions. It can be described by a 4 * 4 massless Dirac Hamiltonian which can be decomposed into a pair of Weyl points or gaped into an insulator. Thus, crystal symmetry is critical to guarantee the stable existence. On the contrary, by breaking crystal symmetry, a DSM may transform into a Weyl semimetal (WSM) or a topological insulator (TI). Here, by taking hexagonal LiAuSe as an example, we find that it is a starfruit shaped multiple nodal chain semimetal in the absence of spin-orbit coupling(SOC). In the presence of SOC, it is an ideal DSM naturally with the Dirac points locating at Fermi level exactly, and it would transform into WSM phase by introducing external Zeeman field or by magnetic doping with rare-earth atom Sm. It could also transform into TI state by breaking rotational symmetry. Our studies show that DSM is a critical point for topological phase transition, and the conclusion can apply to most of the DSM materials, not limited to the hexagonal material LiAuSe.
We study the occurrence of symmetry-enforced topological band crossings in tetragonal crystals with strong spin-orbit coupling. By computing the momentum dependence of the symmetry eigenvalues and the global band topology in the entire Brillouin zone, we determine all symmetry-enforced band crossings in tetragonal space groups. In particular, we classify all Dirac and Weyl degeneracies on points, lines, and planes, and find a rich variety of topological degeneracies. This includes, among others, double Weyl points, fourfold-double Weyl points, fourfold-quadruple Weyl points, Weyl and Dirac nodal lines, as well as topological nodal planes. For the space groups with symmetry-enforced Weyl points, we determine the minimal number of Weyl points for a given band pair and, remarkably, find that materials in space groups 119 and 120 can have band pairs with only two Weyl points in the entire Brillouin zone. This simplifies the topological responses, which would be useful for device applications. Using the classification of symmetry-enforced band crossings, we perform an extensive database search for candidate materials with tetragonal space groups. Notably, we find that Ba$_5$In$_4$Bi$_5$ and NaSn$_5$ exhibit twofold and fourfold Weyl nodal lines, respectively, which cross the Fermi energy. Hf$_3$Sb and Cs$_2$Tl$_3$ have band pairs with few number of Weyl points near the Fermi energy. Furthermore, we show that Ba$_3$Sn$_2$ has Weyl points with an accordion dispersion and topological nodal planes, while AuBr and Tl$_4$PbSe$_3$ possess Dirac points with hourglass dispersions. For each of these candidate materials we present the ab-initio band structures and discuss possible experimental signatures of the nontrivial band topology.
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