In two-dimensional insulators with time-reversal (TR) symmetry, a nonzero local Berry curvature of low-energy massive Dirac fermions can give rise to nontrivial spin and charge responses, even though the integral of the Berry curvature over all occup
ied states is zero. In this work, we present a new effect induced by the electronic Berry curvature. By studying electron-phonon interactions in BaMnSb$_2$, a prototype two-dimensional Dirac material possessing two TR-related massive Dirac cones, we find that the nonzero local Berry curvature of electrons can induce a phonon angular momentum. The direction of this phonon angular momentum is locked to the phonon propagation direction, and thus we refer it as phonon helicity, in a way that is reminiscent of electron helicity in spin-orbit-coupled electronic systems. We discuss possible experimental probes of such phonon helicity.
Recent progress toward the fabrication of Majorana-based qubits has sparked the need for systematic approaches to optimize experimentally relevant parameters for the realization of robust Majorana bound states. Here, we introduce an efficient numeric
al method for the real-space optimization of tunable parameters, such as electrostatic potential profiles and magnetic field textures, in Majorana wires. Combining ideas from quantum control and quantum transport, our algorithm, applicable to any noninteracting tight-binding model, operates on a largely unexplored parameter space and opens new routes for Majorana bound states with enhanced robustness. Contrary to common belief, we find that spatial inhomogeneities of parameters can be a resource for the engineering of Majorana bound states.
Recent theoretical work has established the presence of hidden spin and orbital textures in non-magnetic materials with inversion symmetry. Here, we propose that these textures can be detected by nuclear magnetic resonance (NMR) measurements carried
out in the presence of an electric field. In crystals with hidden polarizations, a uniform electric field produces a staggered magnetic field that points to opposite directions at atomic sites related by spatial inversion. As a result, the NMR resonance peak corresponding to inversion partner nuclei is split into two peaks. The magnitude of the splitting is proportional to the electric field and depends on the orientation of the electric field with respect to the crystallographic axes and the external magnetic field. As a case study, we present a theory of electric-field-induced splitting of NMR peaks for $^{77}$Se, $^{125}$Te and $^{209}$Bi in Bi$_2$Se$_3$ and Bi$_2$Te$_3$. In conducting samples with current densities of $simeq 10^6, {rm A/cm}^2$, the splitting for Bi can reach $100, {rm kHz}$, which is comparable to or larger than the intrinsic width of the NMR lines. In order to observe the effect experimentally, the peak splitting must also exceed the linewidth produced by the Oersted field. In Bi$_2$Se$_3$, this requires narrow wires of radius $lesssim 1, mu{rm m}$. We also discuss other potentially more promising candidate materials, such as SrRuO$_3$ and BaIr$_2$Ge$_2$, whose crystal symmetry enables strategies to suppress the linewidth produced by the Oersted field.
Motivated by recent nuclear magnetic resonance (NMR) experiments, we present a microscopic sp3 tight-binding model calculation of the NMR shifts in bulk Bi2Se3, and Bi2Te3. We compute the contact, dipolar, orbital and core polarization contributions
to the carrier-density-dependent part of the NMR shifts in Bi209, Te125 and Se77. The spin-orbit coupling and the layered crystal structure result in a contact Knight shift with strong uniaxial anisotropy. Likewise, because of spin-orbit coupling, dipolar interactions make a significant contribution to the isotropic part of the NMR shift. The contact interaction dominates the isotropic Knight shift in Bi209 NMR, even though the electronic states at the Fermi level have a rather weak s-orbital character. In contrast, the contribution from the contact hyperfine interaction to the NMR shift of Se77 and Te125 is weak compared to the dipolar and orbital shifts therein. In all cases, the orbital shift is at least comparable to the contact and dipolar shifts, while the shift due to core polarization is subdominant (except for Te nuclei located at the inversion centers). By artificially varying the strength of spin-orbit coupling, we evaluate the evolution of the NMR shift across a band inversion but find no clear signature of the topological transition.
