Mesoscale and Nanoscale Physics (cond-mat.mes-hall)

Abstract: Stationary coherence in small conducting arrays has been shown to influence the transport efficiency of electronic nanodevices. Model schemes that capture the interplay between electron delocalization and system-reservoir interactions on the device performance are therefore important for designing next-generation nanojunctions powered by quantum coherence. We use a Lindblad open quantum system approach to obtain the current-voltage characteristics of small-size networks of interacting conducting sites subject to radiative and non-radiative interactions with the environment, for experimentally-relevant case studies. Lindblad theory is shown to reproduce recent measurements of negative conductance in single-molecule junctions using a biased two-site model driven by thermal fluctuations. For array sites with conducting ground and excited orbitals in the presence of radiative incoherent pumping, we show that Coulomb interactions that otherwise suppress charge transport can be overcome to produce light-induced currents. We also show that in nanojunctions having asymmetric transfer rates between the array and electrical contacts, an incoherent driving field can induce photocurrents at zero bias voltage whose direction depend on the type or orbital delocalization established between sites. Possible extensions of the theory are discussed.

Abstract: We report a topological phase transition in quantum-confined cadmium arsenide (Cd3As2) thin films under an in-plane Zeeman field when the Fermi level is tuned into the topological gap via an electric field. Symmetry considerations in this case predict the appearance of a two-dimensional Weyl semimetal (2D WSM), with a pair of Weyl nodes of opposite chirality at charge neutrality that are protected by space-time inversion (C2T) symmetry. We show that the 2D WSM phase displays unique transport signatures, including saturated resistivities on the order of h/e^2 that persist over a range of in-plane magnetic fields. Moreover, applying a small out-of-plane magnetic field, while keeping the in-plane field within the stability range of the 2D WSM phase, gives rise to a well-developed odd integer quantum Hall effect, characteristic of degenerate, massive Weyl fermions. A minimal four-band k.p model of Cd3As2, which incorporates first-principles effective g factors, qualitatively explains our findings.

Abstract: In this Reply we respond to the comment by Das Sarma and Pan [1] on Hess et al., Phys. Rev. Lett. 130, 207001, "Trivial Andreev Band Mimicking Topological Bulk Gap Reopening in the Nonlocal Conductance of Long Rashba Nanowires" [2]. First, we note that Das Sarma and Pan reproduce the key results of Hess et al., substantiating that our findings are entirely valid. Next, we clarify the incorrect statement by Das Sarma and Pan that the main result of Hess et al. requires a "contrived periodic pristine system", pointing out the extensive discussion of positional disorder in the Hess et al. We also demonstrate that nonlocal conductance features are generically reduced by disorder. This applies to both an Andreev band and to a genuine topological bulk gap reopening signature (BRS). In fact, the suppression of nonlocal conductance of a genuine BRS by disorder was discussed in, e.g., Pan, Sau, Das Sarma, PRB 103, 014513 (2021) [3]. We conclude that, contrary to the claims of Das Sarma and Pan, the minimal model of Hess et al. is relevant to current realistic nanowire devices where only a few overlapping ABSs would be required to mimic a BRS.

Abstract: The low-temperature phase diagram of a Bosonic system is predicted to contain an exotic quantum phase, called a supersolid, that is defined by broken translational symmetry and off-diagonal long-range order. This unique combination of properties enables a seemingly paradoxical scenario where a bosonic solid exhibits dissipationless mass flow. However, despite decades of extensive efforts, experimental realization of such a supersolid phase remains elusive. In this work we report experimental observation of a superfluid-to-insulating transition in the bosonic system of spatially indirect excitons in double layer graphene. Utilizing a variety of transport methods to characterize the superfluid-insulator phase boundary as a function of both density and temperature suggests the insulator to be a solid phase driven by repulsive dipole-dipole interactions in the dilute limit. The exciton solid exhibits a unique melting transition, with the high-temperature phase recovering a hallmark transport signature of off-diagonal long-range order, perfect Coulomb drag. The reentrant superfluid-like behaviour could indicate the low temperature solid also corresponds to a quantum coherent phase.

Abstract: In chiral crystals crystalline symmetries can protect multifold fermions, pseudo-relativistic masless quasiparticles that have no high-energy counterparts. Their realization in transition metal mono-silicides has exemplified their intriguing physical properties, such as long Fermi arc surface states and unusual optical responses. Recent experimental studies on amorphous transition metal mono-silicides suggest that topological properties may survive beyond crystals, even though theoretical evidence is lacking. Motivated by these findings, we theoretically study a tight-binding model of amorphous transition metal mono-silicides. We find that topological properties of multifold fermions survive in the presence of structural disorder that converts the semimetal into a diffusive metal. We characterize this topological diffusive metal phase with the spectral localizer, a real-space topological indicator that we show can signal multifold fermions. Our findings showcase how topological properties can survive in disordered metals, and how they can be uncovered using the spectral localizer.

Abstract: We provide a comprehensive theory of magnetic phases in two-dimensional triangulene crystals, using both Hubbard model and density functional theory (DFT) calculations. We consider centrosymmetric and non-centrosymmetric triangulene crystals. In all cases, DFT and mean-field Hubbard model predict the emergence of broken-symmetry antiferromagnetic (ferrimagnetic) phases for the centrosymmetric (non-centrosymmetric) crystals. This includes the special case of the [4,4]triangulene crystal, whose non-interacting energy bands feature a gap with flat valence and conduction bands. We show how the lack of contrast between the local density of states of these bands, recently measured via scanning tunneling spectroscopy, is a natural consequence of a broken-symmetry N\'eel state that blocks intermolecular hybridization. Using random phase approximation, we also compute the spin wave spectrum of these crystals, including the recently synthesized [4,4]triangulene crystal. The results are in excellent agreement with the predictions of a Heisenberg spin model derived from multi-configuration calculations for the unit cell. We conclude that experimental results are compatible with an antiferromagnetically ordered phase where each triangulene retains the spin predicted for the isolated species.

Abstract: Triangulenes are open-shell triangular graphene flakes with total spin increasing with their size. In the last years, on-surface-synthesis strategies have permitted fabricating and engineering triangulenes of various sizes and structures with atomic precision. However, direct proof of the increasing total spin with their size remains elusive. In this work, we report the combined in-solution and on-surface synthesis of a large nitrogen-doped triangulene (aza-[5]-triangulene) and the detection of its high spin ground state on a Au(111) surface. Bond-resolved scanning tunneling microscopy images uncovered radical states distributed along the zigzag edges, which were detected as weak zero-bias resonances in scanning tunneling spectra. These spectral features reveal the partial Kondo screening of a high spin state. Through a combination of several simulation tools, we find that the observed distribution of radical states is explained by a quintet ground state (S = 2), instead of the expected quartet state (S = 3/2), confirming the positively charged state of the molecule on the surface. We further provide a qualitative description of the change of (anti)aromaticity introduced by N-substitution, and its role in the charge stabilization on a surface, resulting in a S = 2 aza-[5]-triangulene on Au(111).