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Chinese Physics B

Photoexcitation of the one-dimensional extended Peierls–Hubbard model at quarter-filling

Yupeng Li, Yu-Chang 羽畅 Liu 刘, Yu-Zhuo 玉卓 Zhao 赵, Hantao Lu, Can Shao

Published Dec 4, 2025• 0 citations
Publisher

Abstract

Abstract Utilizing the time-dependent Lanczos method, we investigate the photoexcitation dynamics of the one-dimensional (1D) extended Peierls–Hubbard model at quarter filling. In equilibrium, it is well established that introducing the nearest-neighbour interaction V into the 1D Peierls–Hubbard model can lead to the formation of Mott–Hubbard excitons, which exhibit a characteristic frequency in the optical conductivity that is lower than the Mott gap. Ultrafast photoexcitation of this model gives rise to a transient metallic state for V < 2, characterized by several features, including a zero-frequency Drude peak in the post-pump optical conductivity, an increase in the density of charge carriers, and enhanced electron hopping between dimers. In contrast, when V ≥ 2, this metallic state is no longer observed, as photoinduced carriers bind to form excitons, thereby inhibiting metallic behavior. These results highlight a parallel between the optical excitation of the 1D extended Peierls–Hubbard model at quarter filling and that of the 1D extended Hubbard model at half filling, suggesting a universal mechanism governing their photoinduced responses.

DOI
10.1088/1674-1056/ae27af

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Physical review. B./Physical review. B•Aug 6, 2025•1 citation
Abstract Utilizing the time-dependent Lanczos method, we investigate the photoexcitation dynamics of the one-dimensional (1D) extended Peierls–Hubbard model at quarter filling. In equilibrium, it is well established that introducing the nearest-neighbour interaction V into the 1D Peierls–Hubbard model can lead to the formation of Mott–Hubbard excitons, which exhibit a characteristic frequency in the optical conductivity that is lower than the Mott gap. Ultrafast photoexcitation of this model gives rise to a transient metallic state for V < 2, characterized by several features, including a zero-frequency Drude peak in the post-pump optical conductivity, an increase in the density of charge carriers, and enhanced electron hopping between dimers. In contrast, when V ≥ 2, this metallic state is no longer observed, as photoinduced carriers bind to form excitons, thereby inhibiting metallic behavior. These results highlight a parallel between the optical excitation of the 1D extended Peierls–Hubbard model at quarter filling and that of the 1D extended Hubbard model at half filling, suggesting a universal mechanism governing their photoinduced responses.
Utilizing the exact diagonalization method, we investigate the one-dimensional Peierls-Hubbard model at quarter filling, where it manifests as an antiferromagnetic Mott insulator in units of dimers. By increasing the on-site Coulomb repulsion UUU, we observe a significant suppression of the Drude peak, based on a nonequilibrium linear-response theory capable of capturing the zero-frequency (Drude) weight of the optical conductivity under periodic boundary conditions. However, after the ultrafast photoirradiation of this model with large UUU, we detect a distinct enhancement of the Drude peak, signifying the onset of a photoinduced insulator-metal transition. Comparing these dynamics with the half-filled Hubbard model and a noninteracting spinless half-filled Su-Schrieffer-Heeger model (corresponding to the quarter-filled Peierls-Hubbard model with infinite UUU), we propose a mechanism for the photoinduced metallic state: The empty-occupied and double-occupied dimers serve as the photoinduced charge carriers, akin to the holons and doublons in the Hubbard model.
We investigate the time evolution of optical conductivity in the half-filled one-dimensional extended Hubbard model driven by a transient laser pulse, by using the time-dependent Lanczos method. Photoinduced in-gap excitations exhibit a qualitatively different structure in the spin-density wave (SDW) in comparison to the charge-density-wave (CDW) phase. In the SDW, the origin of a low-energy in-gap excitation is attributed to the even-odd parity of the photoexcited states, while in the CDW an in-gap state is due to confined photogenerated carriers. The signature of the in-gap excitations can be identified as a characteristic oscillation in the time evolution of physical quantities.
We study photoinduced optical responses of one-dimensional strongly correlated electron systems. The optical conductivity spectra are calculated for the ground state and a photoexcited state in the one-dimensional Hubbard model at half filling by using the exact diagonalization method. It is found that, in the Mott insulator phase, the photoexcited state has large spectral weights including the Drude weight below the optical gap. As a consequence, the spectral weight above the optical gap is largely reduced. These results imply that a metallic state is induced by photoexcitation. Comparison between the photoexcited and hole-doped states shows that the photoexcitation is similar to chemical doping.
We theoretically investigate pump-probe optical responses in the two-dimensional extended Hubbard model describing cuprates by using a time-dependent Lanczos method. At half filling, pumping generates photoinduced absorptions inside the Mott gap. A part of low-energy absorptions is attributed to the independent propagation of photoinduced holons and doublons. The spectral weight just below the Mott gap increases with decreasing the on-site Coulomb interaction UUU. We find that the next-nearest-neighbor Coulomb interaction V1{V}_{1}V1​ enhances this UUU dependence, indicating the presence of biexcitonic contributions formed by two holon-doublon pairs. Photopumping in hole-doped systems also induces spectral weights below remnant Mott-gap excitations, being consistent with recent experiments. The induced weights are less sensitive to V1{V}_{1}V1​ and may be related to the formation of a biexcitonic state in the presence of hole carriers.
We investigate the real-time dynamics of the half-filled one-dimensional extended Hubbard model in the strong-coupling regime, when driven by a transient laser pulse. Starting from a wide regime displaying a charge-density wave in equilibrium, a robust photoinduced in-gap state appears in the optical conductivity, depending on the parameters of the pulse. Here, by tuning its conditions, we maximize the overlap of the time-evolving wave function with excited states displaying the elusive bond-ordered wave of this model. Finally, we make a clear connection between the emergence of this order and the formation of the aforementioned in-gap state, suggesting the potential observation of purely electronic (i.e., not associated with a Peierls instability) bond-ordered waves in experiments involving molecular crystals.
By utilizing the twisted boundary conditions in the exact diagonalization method, we investigate the single-particle spectral function of the extended Peierls-Hubbard model at both half-filling and quarter-filling. In one-dimensional (1D) interacting systems, the spin-charge separation can typically be identified in the single-particle spectral function by observing the distinct spinon and holon bands. At half-filling, starting from the pure 1D Hubbard model with the on-site interaction U=10U=10U=10, we observe that the band structure indicative of the spin-charge separation gradually transitions to four individual bands as the Peierls instability $\ensuremath{\delta}$ increases. At U=10U=10U=10 and $\ensuremath{\delta}=0.2$ where the spin-charge separation is still observable, increasing the nearest-neighbor interaction VVV can drive the system to a charge-density-wave state when $V\ensuremath{\gtrsim}U/2$. At quarter-filling, on the other hand, the ground state of Peierls-Hubbard model manifests an antiferromagnetic Mott insulator in units of dimers. Increasing UUU results in only a very small gap in the single-particle spectrum because even for $U=+\ensuremath{\infty}$, with the model transforming into a noninteracting half-filled dimerized tight-binding model, its gap determined by the Peierls instability $\ensuremath{\delta}$ remains small. Conversely, increasing VVV can effectively open the single-particle gap and make the spinon and holon bands more prominent.