SciPost Phys. 20, 023 (2026) ·
published 27 January 2026
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We investigate the many-body localization (MBL) transition in the quantum Ising model with long-range interactions. Unlike spin chains with short-range interactions, where the MBL transition point remains elusive due to strong finite-size effects and local fluctuations, long-range interactions suppress such fluctuations and enable clearer signatures of critical behavior. Using exact results from a related Bethe lattice localization problem, we estimate the MBL threshold within logarithmic accuracy and find consistency with exact diagonalization. Although the critical disorder diverges in the thermodynamic limit, our results demonstrate that the critical regime can still be probed and highlight the relevance of this model to systems with dipole-dipole, elastic, or indirect exchange interactions.
Xiaolong Deng, Alexander L. Burin, Ivan M. Khaymovich
SciPost Phys. 13, 116 (2022) ·
published 24 November 2022
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We consider a 2d dipolar system, $d=2$, with the generalized dipole-dipole interaction $\sim r^{-a}$, and the power $a$ controlled experimentally in trapped-ion or Rydberg-atom systems via their interaction with cavity modes. We focus on the dilute dipolar excitation case when the problem can be effectively considered as single-particle with the interaction providing long-range dipolar-like hopping. We show that the spatially homogeneous tilt $\beta$ of the dipoles giving rise to the anisotropic dipole exchange leads to the non-trivial reentrant localization beyond the locator expansion, $a<d$, unlike the models with random dipole orientation. The Anderson transitions are found to occur at the finite values of the tilt parameter $\beta = a$, $0<a<d$, and $\beta = a/(a-d/2)$, $d/2<a<d$, showing the robustness of the localization at small and large anisotropy values. Both exact analytical methods and extensive numerical calculations show power-law localized eigenstates in the bulk of the spectrum, obeying recently discovered duality $a\leftrightarrow 2d-a$ of their spatial decay rate, on the localized side of the transition, $a>a_{AT}$. This localization emerges due to the presence of the ergodic extended states at either spectral edge, which constitute a zero fraction of states in the thermodynamic limit, decaying though extremely slowly with the system size.
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