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Luttinger Liquid Physics and Spin-Flip Scattering on Helical Edges

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 Added by Martin Hohenadler
 Publication date 2011
  fields Physics
and research's language is English




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We investigate electronic correlation effects on edge states of quantum spin-Hall insulators within the Kane-Mele-Hubbard model by means of quantum Monte Carlo simulations. Given the U(1) spin symmetry and time-reversal invariance, the low-energy theory is the helical Tomanaga-Luttinger model, with forward scattering only. For weak to intermediate interactions, this model correctly describes equal-time spin and charge correlations, including their doping dependence. As apparent from the Drude weight, bulk states become relevant in the presence of electron-electron interactions, rendering the forward-scattering model incomplete. Strong correlations give rise to slowly decaying transverse spin fluctuations, and inelastic spin-flip scattering strongly modifies the single-particle spectrum, leading to graphene-like edge state signatures. The helical Tomanaga-Luttinger model is completely valid only asymptotically in the weak-coupling limit.



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We show that the paradigmatic Ruderman-Kittel-Kasuya-Yosida (RKKY) description of two local magnetic moments coupled to propagating electrons breaks down in helical Luttinger Liquids when the electron interaction is stronger than some critical value. In this novel regime, the Kondo effect overwhelms the RKKY interaction over all macroscopic inter-impurity distances. This phenomenon is a direct consequence of the helicity (realized, for instance, at edges of a time-reversal invariant topological insulator) and does not take place in usual (non-helical) Luttinger Liquids.
Gapless Luttinger liquid is conventionally viewed as topologically trivial, unless it hosts degenerate ground states and or entanglement spectrum, which necessitates partial bulk degree of freedom to be gapped out. Here we predict an emergent gapless topological Luttinger liquid which is beyond the conventional scenarios and is characterized by the nontrivial many-body bulk spin texture, and propose feasible scheme for experimental observation. We consider a one-dimensional spin-orbit coupled Fermi-Hubbard model with fractional filling, whose low-energy physics is effectively described by a spinless Luttinger liquid and is trivial in the conventional characterization. We show that, as being tuned by the filling factor and interaction strength, the many-body ground state may exhibit nontrivial winding in its bulk spin texture in the projected momentum space, manifesting an emergent topological phase. A topological transition occurs when the projected spin-state at a high symmetry momentum becomes fully mixed one, resulting from competing processes of particle scattering to the lower and higher subbands, for which the spin texture at such momentum point is ill-defined, but the Luttinger liquid keeps gapless through the transition. Surprisingly, at relatively small filling the Luttinger liquid remains topologically nontrivial even at infinitely strong interaction. The results can be generalized to finite temperature which facilitates the real experimental detection. This work shows a novel gapless topological Luttinger liquid whose characterization is beyond the low-energy effective theory, and can be verified based on current experiments.
We present a 14N nuclear magnetic resonance study of a single crystal of CuBr4(C5H12N)2 (BPCB) consisting of weakly coupled spin-1/2 Heisenberg antiferromagnetic ladders. Treating ladders in the gapless phase as Luttinger liquids, we are able to fully account for (i) the magnetic field dependence of the nuclear spin-lattice relaxation rate 1/T_1 at 250 mK and for (ii) the phase transition to a 3D ordered phase occuring below 110 mK due to weak interladder exchange coupling. BPCB is thus an excellent model system where the possibility to control Luttinger liquid parameters in a continuous manner is demonstrated and Luttinger liquid model tested in detail over the whole fermion band.
We develop a theory for manipulating the effective band structure of interacting helical edge states realized on the boundary of two-dimensional time-reversal symmetric topological insulators. For sufficiently strong interaction, an interacting edge band gap develops, spontaneously breaking time-reversal symmetry on the edge. The resulting spin texture, as well as the energy of the the time-reversal breaking gaps, can be tuned by an external moire potential (i.e., a superlattice potential). Remarkably, we establish that by tuning the strength and period of the potential, the interacting gaps can be fully suppressed and interacting Dirac points re-emerge. In addition, nearly flat bands can be created by the moire potential with a sufficiently long period. Our theory provides a novel way to enhance the coherence length of interacting helical edges by suppressing the interacting gap. The implications of this finding for ongoing experiments on helical edge states is discussed.
We study one-dimensional Kondo Lattices (KL) which consist of itinerant electrons interacting with Kondo impurities (KI) - localized quantum magnetic moments. We focus on KL with isotropic exchange interaction between electrons and KI and with a high KI density. The latter determines the principal role of the indirect interaction between KI for the low energy physics. Namely, the Kondo physics becomes suppressed and all properties are governed by spin ordering. We present a first-ever comprehensive analytical theory of such KL at an arbitrary doping and predict a variety of regimes with different electronic phases. They range from commensurate insulators (at filling factors 1/2, 1/4 and 3/4) to metals with strongly interacting conduction electrons (close to these three special cases) to an exotic phase of a helical metal. The helical metals can provide a unique platform for realization of an emergent protection of ballistic transport in quantum wires. We compare out theory with previously obtained numerical results and discuss possible experiments where the theory could be tested.
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