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    Fate of many-body localization in an Abelian lattice gauge theory

    Indrajit Sau1,*, Debasish Banerjee2,3,†, and Arnab Sen1,‡

    • *Contact author: tpis2@iacs.res.in
    • †Contact author: D.Banerjee@soton.ac.uk
    • ‡Contact author: tpars@iacs.res.in

    Phys. Rev. B 113, 024204 – Published 21 January, 2026

    DOI: https://doi.org/10.1103/p82k-5qnw

    Abstract

    We address the fate of many-body localization (MBL) of mid-spectrum eigenstates of a matter-free U(1) quantum-link gauge theory Hamiltonian with random couplings on ladder geometries. Apart from level spacing distribution indicators like disorder-averaged mean level spacing, we also consider an intensive estimator D∈[0,1/4], which acts as a measure of elementary plaquettes on the lattice that are active or inert in mid-spectrum eigenstates as well as the concentration of these eigenstates in Fock space, with D equal to its maximum value of 1/4 for Fock states in the electric flux basis. We calculate its distribution, p(D), for Lx×Ly lattices, with Ly=2 and 4, as a function of (a dimensionless) disorder strength α (α=0 implies zero disorder) using exact diagonalization in many disorder realizations. Although finite-size estimators based on level spacings do not give a reliable critical disorder strength, αc(Ly), beyond which MBL prevails as Lx→∞; a different estimator based on the skewness of p(D) gives αc(Ly=2)=31.04±0.54 using data for Lx≤14 due to faster convergence. p(D) for wider ladders with Ly=4 show a lower tendency to localize, suggesting a lack of MBL in two dimensions. A remarkable observation is the resolution of the (monotonic) infinite-temperature autocorrelation function of single plaquette diagonal operators in typical high-energy Fock states into a plethora of emergent timescales of increasing spatio-temporal heterogeneity as the disorder is increased. At intermediate α as well as for α slightly below αc(Ly), a fraction of randomly selected initial Fock states display striking oscillatory temporal behavior of such plaquette operators in spatial regions formed out of connected plaquettes.

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