Time-resolved photoemission spectroscopy on correlated electrons: Insights from dynamical mean-field theory

被引:4
|
作者
Eckstein, Martin [1 ]
机构
[1] Univ Erlangen Nurnberg, Dept Phys, D-91058 Erlangen, Germany
基金
欧洲研究理事会;
关键词
Nonequilibrium DMFT; Time-resolved ARPES; Photodoping;
D O I
10.1016/j.elspec.2021.147108
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Time- and angular-resolved photoemission spectroscopy (trARPES) can directly probe the electronic structure of quantum materials out of equilibrium. This can shed light on the interaction of the electrons with spin, lattice, and orbital degrees of freedom, and help to unravel pathways towards novel out-of-equilibrium phases. Dynamical mean-field theory (DMFT) and its extensions provide a versatile toolbox to interpret such experiments through a theoretical simulation of the underlying microscopic processes. The approach can be applied both to Mott insulators and correlated metals, and it is formulated in terms of non-equilibrium Green's functions, which directly relate to the photoemission spectrum. This article reviews the theoretical description of trARPES within DMFT and related diagrammatic non-equilibrium Green's function techniques. Several applications are discussed, including the photo-induced melting of excitonic order, femtosecond relaxation processes in Mott insulators, and the manipulation of the electronic structure of Mott and charge transfer insulators using photodoping and strong THz fields.
引用
收藏
页数:9
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