Evidence of universal spectral collapse at a marginal dynamical regime
This study proposes that incoherent electronic states in strongly correlated materials arise not from disorder or material-specific mechanisms, but from self-generated dynamical disorder induced by competing fluctuations. In this marginal dynamical regime, electron dynamics naturally couple with time-dependent scattering, yielding the spectral function form ρ(z)=exp(-z²/4)D_ν(z), where z is the scaled energy, D_ν is the parabolic cylinder function, and ν=-1/2 is fixed. By independently scaling the angle-resolved photoemission spectroscopy (ARPES) energy distribution curves of the cuprates Nd₂₋ₓCeₓCuO₄ and Bi₂Sr₂CaCu₂O₈₊δ, the Kagome metal CsCr₃Sb₅, and the bilayer nickelate La₃Ni₂O₇, all datasets collapse onto a single universal curve, with only the amplitude and energy scale varying among materials. This spectral collapse indicates that microscopic details such as lattice geometry, band structure, and chemical composition become irrelevant in the low-energy regime, exhibiting fixed-point-like dynamical behavior. The result establishes a unified quantitative framework for the continuously dominant ARPES spectra across diverse strongly correlated materials.