Time and spectral resolution in resonance scattering and resonance fluorescence

E. Courtens and A. Szöke
Phys. Rev. A 15, 1588 – Published 1 April 1977; Erratum Phys. Rev. A 17, 2119 (1978)
PDFExport Citation

Abstract

The theory of resonance Raman effect, resonantly enhanced two-photon absorption, and resonance fluorescence—valid also for strong fields—is treated in a unified and simplified way. Dressed states, Bloch equations, and perturbation theory are used to calculate line positions, and integrated intensities both for steady state and transient excitation. The case of adiabatic following is solved explicitly; it occurs when an off-resonance incident pulse is turned on and off slowly. It leads to the identification of Raman scattering, two-photon absorption, and Rayleigh scattering with an adiabatic process while fluorescence and consecutive two-photon absorption with nonadiabaticity. Time-dependent spectra are defined in a rigorous way. Our formulas agree in the various limits with those that appear in the literature.

  • Received 19 August 1976

DOI:https://doi.org/10.1103/PhysRevA.15.1588

©1977 American Physical Society

Erratum

Authors & Affiliations

E. Courtens

  • IBM Zürich Research Laboratory, 8803 Rüschlikon, Switzerland

A. Szöke*

  • Joint Institute for Laboratory Astrophysics, University of Colorado and National Bureau of Standards, Boulder, Colorado 80309

  • *Visiting Fellow, 1975-76, on leave of absence from Tel Aviv University, Tel Aviv, Israel.

References (Subscription Required)

Click to Expand
Issue

Vol. 15, Iss. 4 — April 1977

Reuse & Permissions
Access Options
Author publication services for translation and copyediting assistance advertisement

Authorization Required


×
×

Images

×

Sign up to receive regular email alerts from Physical Review A

Log In

Cancel
×

Search


Article Lookup

Paste a citation or DOI

Enter a citation
×