The theory for time-resolved, pump-probe, photoemission spectroscopy and other pump-probe experiments is developed. The formal development is completely general, incorporating all of the nonequilibrium effects of the pump pulse and the finite time width of the probe pulse, and including possibilities for taking into account band structure and matrix element effects, surface states, and the interaction of the photoexcited electrons with the system leading to corrections to the sudden approximation. We also illustrate the effects of windowing that arise from the finite width of the probe pulse in a simple model system by assuming the quasiequilibrium approximation
Femtosecond time-resolved photoelectron spectroscopy provides a unique tool to study the dynamics of...
Recent advances in laser technology allow us to follow electronic motion at its natural time-scale w...
Anticipating the experimental realization of attosecond pulses with photon energies of a few hundred...
The theory for time-resolved, pump-probe, photoemission spectroscopy and other pump-probe experiment...
The theory for time-resolved, pump-probe, photoemission spectroscopy and other pump-probe experiment...
Nonequilibrium calculations in the presence of an electric field are usually performed in a gauge, a...
We apply a time-frequency response theory of pump-probe spectroscopy, due to Yan, to the experiments...
Recent advances in light sources will allow probing of the fastest time scales relevant to chemistry...
We review recent work on the theory for pump/probe photoemission spectroscopy of electron‐phonon med...
The energy-time uncertainty is an intrinsic limit for time-resolved experiments imposing a tradeoff ...
215 p.Attosecond-transient absorption spectroscopy and attosecond time-resolved photoelectronspectro...
Molecular absorption and photoelectron spectra can be efficiently predicted with real-time time-depe...
We theoretically study how time- and angle-resolved photoemission spectroscopy can be applied for im...
In this work, we theoretically examine recent pump/probe photoemission experiments on the strongly c...
In this work we put forward a first-principles approach and propose an accurate diagrammatic approxi...
Femtosecond time-resolved photoelectron spectroscopy provides a unique tool to study the dynamics of...
Recent advances in laser technology allow us to follow electronic motion at its natural time-scale w...
Anticipating the experimental realization of attosecond pulses with photon energies of a few hundred...
The theory for time-resolved, pump-probe, photoemission spectroscopy and other pump-probe experiment...
The theory for time-resolved, pump-probe, photoemission spectroscopy and other pump-probe experiment...
Nonequilibrium calculations in the presence of an electric field are usually performed in a gauge, a...
We apply a time-frequency response theory of pump-probe spectroscopy, due to Yan, to the experiments...
Recent advances in light sources will allow probing of the fastest time scales relevant to chemistry...
We review recent work on the theory for pump/probe photoemission spectroscopy of electron‐phonon med...
The energy-time uncertainty is an intrinsic limit for time-resolved experiments imposing a tradeoff ...
215 p.Attosecond-transient absorption spectroscopy and attosecond time-resolved photoelectronspectro...
Molecular absorption and photoelectron spectra can be efficiently predicted with real-time time-depe...
We theoretically study how time- and angle-resolved photoemission spectroscopy can be applied for im...
In this work, we theoretically examine recent pump/probe photoemission experiments on the strongly c...
In this work we put forward a first-principles approach and propose an accurate diagrammatic approxi...
Femtosecond time-resolved photoelectron spectroscopy provides a unique tool to study the dynamics of...
Recent advances in laser technology allow us to follow electronic motion at its natural time-scale w...
Anticipating the experimental realization of attosecond pulses with photon energies of a few hundred...