arXiv subjects

Qirong Yao

Publications and source records attributed to Qirong Yao.

4 recordsLinked to original sources

arXiv2026

Local spectroscopy of loop current order with individual magnetic atoms

Hidden ordered states--characterized by order parameters that elude conventional probes--pose a fundamental challenge for their identification in quantum materials. Recent experiments report evidence for time-reversal symmetry breaking orbital magnetic order and anomalous transport signatures in the $2a\times2a$ charge density wave state of the kagome metal CsV$_3$Sb$_5$ at a temperature $T<30\,$K. Theoretical analyses propose that a time-reversal symmetry breaking loop-current order could exist as the ground state of this charge density wave. However, this microscopic interpretation remains debated and experimentally unverified. In this work, we employ individual magnetic atoms as local quantum sensors to examine the quasiparticle excitations of the charge density wave in CsV$_3$Sb$_5$ with the scanning tunneling microscope. Our spectroscopic measurements show that the magnetic moment of Co induces a spatially localized $dI/dV$ peak inside the spectral gap of the charge density wave near the Fermi energy. Conducting temperature-dependent spectroscopy, we find that this spectral feature emerges at $T<30\,$K. By comparing our experimental observations with results of quantum many-body simulations and realistic tight-binding model calculations, we show that this spectroscopic signature can be naturally interpreted as a local flux defect in a loop current ordered state, arising from the Kondo coupling of the magnetic moment of Co with the loop current electrons. The excellent agreement between our experimental and theoretical results suggests the presence of loop-current order in the $2a\times2a$ charge density wave of CsV$_3$Sb$_5$ at $T<30\,$K. Our results provide a microscopic picture to the observation of time-reversal symmetry breaking orbital magnetism and anomalous transport signatures detected in measurements of the macroscopic material properties.

cond-mat.str-el↗

arXiv2023

Kinkless electronic junction along one dimensional electronic channel

Here we report the formation of type-A and type-B electronic junctions without any structural discontinuity along a well-defined 1-nm-wide one-dimensional electronic channel within a van der Waals layer. We employ scanning tunneling microscopy and spectroscopy techniques to investigate the atomic and electronic structure along peculiar domain walls formed on the charge-density-wave phase of 1T-TaS2. We find distinct kinds of abrupt electronic junctions with discontinuities of the band gap along the domain walls, which do not have any structural kinks and defects. Our density-functional calculations reveal a novel mechanism of the electronic junction formation; they are formed by a kinked domain wall in the layer underneath through substantial electronic interlayer coupling. This work demonstrates that the interlayer electronic coupling can be an effective control knob over several-nanometer-scale electronic property of two-dimensional atomic monolayers.

cond-mat.str-el↗

arXiv2023

Robust Luttinger liquid state of 1D Dirac fermions in a van der Waals system Nb$_9$Si$_4$Te$_{18}$

We report on the Tomonaga-Luttinger liquid (TLL) behavior in fully degenerate 1D Dirac fermions. A ternary van der Waals material Nb$_9$Si$_4$Te$_{18}$ incorporates in-plane NbTe$_2$ chains, which produce a 1D Dirac band crossing Fermi energy. Tunneling conductance of electrons confined within NbTe2 chains is found to be substantially suppressed at Fermi energy, which follows a power law with a universal temperature scaling, hallmarking a TLL state. The obtained Luttinger parameter of ~0.15 indicates strong electron-electron interaction. The TLL behavior is found to be robust against atomic-scale defects, which might be related to the Dirac electron nature. These findings, as combined with the tunability of the compound and the merit of a van der Waals material, offer a robust, tunable, and integrable platform to exploit non-Fermi liquid physics.

cond-mat.str-el↗

arXiv2017

Spatially resolved electronic structure of twisted graphene

We have used scanning tunneling microscopy and spectroscopy to resolve the spatial variation of the density of states of twisted graphene layers on top of a highly oriented pyrolytic graphite substrate. Owing to the twist a moire pattern develops with a periodicity that is substantially larger than the periodicity of a single layer graphene. The twisted graphene layer has electronic properties that are distinctly different from that of a single layer graphene due to the nonzero interlayer coupling. For small twist angles (about 1-3.5 degree) the integrated differential conductivity spectrum exhibits two well-defined Van Hove singularities. Spatial maps of the differential conductivity that are recorded at energies near the Fermi level exhibit a honeycomb structure that is comprised of two inequivalent hexagonal sub-lattices. For energies |E-E_F|>0.3 eV the hexagonal structure in the differential conductivity maps vanishes. We have performed tight-binding calculations of the twisted graphene system using the propagation method, in which a third graphene layer is added to mimic the substrate. This third layer lowers the symmetry and explains the development of the two hexagonal sub-lattices in the moire pattern. Our experimental results are in excellent agreement with the tight-binding calculations.

cond-mat.mes-hall↗