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تسجيل مستخدم جديدNonlinear spectroscopy of collective modes in excitonic insulator
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The nonlinear optical response of an excitonic insulator coupled to lattice degrees of freedom is shown to depend in strong and characteristic ways on whether the insulating behavior originates primarily from electron-electron or electron-lattice interactions. Linear response optical signatures of the massive phase mode and the amplitude (Higgs) mode are identified. Upon nonlinear excitation resonant to the phase mode, a new in-gap mode at twice the phase mode frequency is induced, leading to a huge second harmonic response. Excitation of in-gap phonon modes leads to different and much smaller effects. A Landau-Ginzburg theory analysis explain these different behavior and reveals that a parametric resonance of the strongly excited phase mode is the origin of the photo-induced mode in the electron-dominant case. The difference in the nonlinear optical response serve as a measure of the dominant mechanism of the ordered phase.
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Excitonic insulators host a condensate of electron-hole pairs at equilibrium, giving rise to collective many-body effects. Although several materials have emerged as excitonic insulator candidates, evidence of long-range coherence is lacking and the
origin of the ordered phase in these systems remains controversial. Here, using ultrafast pump-probe microscopy, we investigate the possible excitonic insulator Ta$_2$NiSe$_5$. Below 328 K, we observe the anomalous micrometer-scale propagation of coherent modes at velocities of the order of $sim10^5$ m/s, which we attribute to the hybridization between phonon modes and the phase mode of the condensate. We develop a theoretical framework to support this explanation and propose that electronic interactions provide a significant contribution to the ordered phase in Ta$_2$NiSe$_5$. These results allow us to understand how the condensates collective modes transport energy and interact with other degrees of freedom. Our study provides a unique paradigm for the investigation and manipulation of these properties in strongly correlated materials.
An excitonic insulator (EI) is an unconventional quantum phase of matter in which excitons, bound pairs of electrons and holes, undergo Bose--Einstein condensation, forming a macroscopic coherent state. While its existence was first hypothesized half
a century ago, the EI has eluded experimental observation in bulk materials for decades. In the last few years, a resurgence of interest in the subject has been driven by the identification of several candidate materials suspected to support an excitonic condensate. However, one obstacle in verifying the nature of these systems has been to find signatures of the EI that distinguish it from a normal insulator. To address this, we focus on a clear qualitative difference between the two phases: the existence of Goldstone modes born by the spontaneous breaking of a $U(1)$ symmetry in the EI. Even if this mode is gapped, as occurs in the case of an approximate symmetry, this branch of collective modes remains a fundamental feature of the low-energy dynamics of the EI provided the symmetry-breaking is small. We study a simple model that realizes an excitonic condensate, and use mean field theory within the random-phase approximation to determine its collective modes. We subsequently develop a diagrammatic method to incorporate the effects of disorder perturbatively, and use it to determine the scattering rate of the collective modes. We interpret our results within an an effective field theory. The collective modes are found to be robust against symmetry-preserving disorder, implying an experimental fingerprint unique to the EI: the ballistic propagation of low-lying modes over mesoscopic distances, at electronic-scale velocities. We suggest this could affect thermal transport at low temperatures, and could be observed via spatially-resolved pump-probe spectroscopy through the coherent response of phonons that hybridize with the collective modes.
We consider a two-band spinless model describing an excitonic insulator (EI) on the two-dimensional square lattice with anisotropic hopping parameters and electron-phonon (el-ph) coupling, inspired by the EI candidate Ta$_2$NiSe$_5$. We systematicall
y study the nature of the collective excitations in the ordered phase which originates from the interband Coulomb interaction and the el-ph coupling. When the ordered phase is stabilized only by the Coulomb interaction (pure EI phase), its collective response exhibits a massless phase mode in addition to the amplitude mode. We show that in the BEC regime, the signal of the amplitude mode becomes less prominent and that the anisotropy in the phase mode velocities is relaxed compared to the model bandstructure. Through coupling to the lattice, the phase mode acquires a mass and the signal of the amplitude mode becomes less prominent. Importantly, character of the softening mode at the boundary between the normal semiconductor phase and the ordered phase depends on the parameter condition. In particular, we point out that even for el-ph coupling smaller than the Coulomb interaction the mode that softens to zero at the boundary can have a phonon character. We also discuss how the collective modes can be observed in the optical conductivity. Furthermore, we study the effects of nonlocal interactions on the collective modes and show the possibility of realizing a coexistence of an in-gap mode and an above-gap mode split off from the single amplitude mode in the system with the local interaction only.
The layered chalcogenide Ta$_{2}$NiSe$_{5}$ has been proposed to host an excitonic condensate in its ground state, a phase that could offer a unique platform to study and manipulate many-body states at room temperature. However, identifying the domin
ant microscopic contribution to the observed spontaneous symmetry breaking remains challenging, perpetuating the debate over the ground state properties. Here, using broadband ultrafast spectroscopy we investigate the out-of-equilibrium dynamics of Ta$_{2}$NiSe$_{5}$ and demonstrate that the transient reflectivity in the near-infrared range is connected to the systems low-energy physics. We track the status of the ordered phase using this optical signature, establishing that high-fluence photoexcitations can suppress this order. From the sub-50 fs quenching timescale and the behaviour of the photoinduced coherent phonon modes, we conclude that electronic correlations provide a decisive contribution to the excitonic order formation. Our results pave the way towards the ultrafast control of an exciton condensate at room temperature.
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the second-Born approximation (2BA) within the Kadanoff-Baym formalism, the generalized Kadanoff-Baym Ansatz (GKBA) implemented with the 2BA and the infinite time-evolving block decimation (iTEBD) method. It is found that the GKBA gives the best agreement with iTEBD and captures the relevant physics. We find that excitations to the particle-hole continuum and resonant excitations of the equilibrium exciton result in a qualitatively different dynamics. In the former case, the exciton binding energy remains positive and the frequency of the corresponding coherent oscillations is smaller than the band gap. On the other hand, resonant excitations trigger a collective mode whose frequency is larger than the band gap. We discuss the origin of these different behaviors by evaluating the nonequilibrium susceptibility using the nonthermal distribution and a random phase approximation. The peculiar mode with frequency larger than the band gap is associated with a partial population inversion with a sharp energy cutoff. We also discuss the effects of the cooling by a phonon bath. We demonstrate the real-time development of coherence in the polarization, which indicates excitonic condensation out of equilibrium.
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