Ultrafast X-Ray Absorption Spectroscopy of Strongly Correlated Systems: Core Hole Effect
Recently, ultrafast pump-probe spectroscopy has provided insightful information about the nonequilibrium dynamics of excitations in materials. In a typical experiment of time-resolved x-ray absorption spectroscopy, the systems are excited by a femtosecond laser pulse (pump pulse) followed by an x-ray probe pulse after a time delay to measure the absorption spectra of the photoexcited systems. We present a theory for nonequilibrium x-ray absorption spectroscopy in one-dimensional strongly correlated systems. The core hole created by the x ray is modeled as an additional effective potential of the core hole site, which changes the spectrum qualitatively. In equilibrium, the spectrum reveals the charge gap at half-filling and the metal-insulator transition in the presence of the core hole effect. Moreover, a pump-probe scheme is introduced to drive the system out of equilibrium before the x-ray probe. The effects of the pump pulse with varying frequencies, shapes, and fluences are discussed for the dynamics of strongly correlated systems in and out of resonance. The spectrum suggests that the driven insulating state has a metallic droplet around the core hole. The rich structures of the nonequilibrium x-ray absorption spectrum give more insight into the dynamics of electronic structures.