Theory of time-resolved optical spectroscopy on correlated electron systems
Martin Eckstein, Marcus Kollar

TL;DR
This paper develops a theoretical framework using dynamical mean-field theory to analyze time-resolved optical spectroscopy data, specifically relating reflectivity to nonequilibrium optical conductivity in correlated electron systems.
Contribution
It introduces a method to express nonequilibrium optical conductivity in terms of real-time Green functions within dynamical mean-field theory.
Findings
Demonstrates the approach on the Falicov-Kimball model
Analyzes ultrafast formation of the gapped phase
Provides insights into electron dynamics in correlated materials
Abstract
The real-time dynamics of interacting electrons out of equilibrium contains detailed microscopic information about electronically correlated materials, which can be read out with time-resolved optical spectroscopy. The reflectivity that is typically measured in pump-probe experiments is related to the nonequilibrium optical conductivity. We show how to express this quantity in terms of real-time Green functions using dynamical mean-field theory. As an application we study the electrical response of the Falicov-Kimball model during the ultrafast buildup of the gapped phase at large interaction.
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