We present the full diagrammatic description of non-resonant impulsive femtosecond stimulated Raman spectroscopy in a multimode model system. In this technique the pump-probe scheme is exploited to study the vibrational structure of the sample via stimulated Raman scattering. We apply closed-time-path-loop diagrams to calculate the complete response of the system at the relevant perturbation order. We show that, in presence of low-frequency modes, coherences created by the impulsive pump modify the resulting Raman signal, which oscillates from gain to loss features, depending on the time delay between the pump and probe pulses. This leads to a redistribution of photons among the fields involved in the process and, consequently, the energy ...
Femtosecond stimulated Raman scattering is a time-resolved vibrational spectroscopic technique able ...
Stimulated Raman scattering (SRS) is analyzed with a three-state model. Using a diagrammatic density...
Photophysical and photochemical processes are often dominated by molecular vibrations in various ele...
Femtosecond stimulated Raman scattering (FSRS) spectroscopy is a powerful pump-probe technique that ...
We introduce a general theoretical description of non resonant impulsive femtosecond stimulated Rama...
We introduce a general theoretical description of non resonant impulsive femtosecond stimulated Rama...
Femtosecond broadband stimulated Raman spectroscopy (FSRS) is a new technique that produces high-res...
Photophysical and photochemical processes are ruled by the interplay between transient vibrational a...
© XXXX American Chemical Society A complete understanding of a photochemical reaction dynamics begin...
In impulsive stimulated Raman scattering, vibrational oscillations, coherently stimulated by a femto...
Femtosecond stimulated Raman scattering is a time-resolved vibrational spectroscopic technique able ...
Excited-state vibrational dynamics in molecules can be studied by an electronically off-resonant Ram...
The quantum theory for stimulated Raman spectroscopy from a moving wave packet using the third-order...
Stimulated Raman scattering has recently been used in label‐free vibrational imaging studies of live...
Impulsive stimulated Raman scattering (ISRS) observed by pump-probe experiments was considered. The ...
Femtosecond stimulated Raman scattering is a time-resolved vibrational spectroscopic technique able ...
Stimulated Raman scattering (SRS) is analyzed with a three-state model. Using a diagrammatic density...
Photophysical and photochemical processes are often dominated by molecular vibrations in various ele...
Femtosecond stimulated Raman scattering (FSRS) spectroscopy is a powerful pump-probe technique that ...
We introduce a general theoretical description of non resonant impulsive femtosecond stimulated Rama...
We introduce a general theoretical description of non resonant impulsive femtosecond stimulated Rama...
Femtosecond broadband stimulated Raman spectroscopy (FSRS) is a new technique that produces high-res...
Photophysical and photochemical processes are ruled by the interplay between transient vibrational a...
© XXXX American Chemical Society A complete understanding of a photochemical reaction dynamics begin...
In impulsive stimulated Raman scattering, vibrational oscillations, coherently stimulated by a femto...
Femtosecond stimulated Raman scattering is a time-resolved vibrational spectroscopic technique able ...
Excited-state vibrational dynamics in molecules can be studied by an electronically off-resonant Ram...
The quantum theory for stimulated Raman spectroscopy from a moving wave packet using the third-order...
Stimulated Raman scattering has recently been used in label‐free vibrational imaging studies of live...
Impulsive stimulated Raman scattering (ISRS) observed by pump-probe experiments was considered. The ...
Femtosecond stimulated Raman scattering is a time-resolved vibrational spectroscopic technique able ...
Stimulated Raman scattering (SRS) is analyzed with a three-state model. Using a diagrammatic density...
Photophysical and photochemical processes are often dominated by molecular vibrations in various ele...