Article ID Journal Published Year Pages File Type
1535792 Optics Communications 2013 6 Pages PDF
Abstract

When atoms are excited by laser radiation the conventional wisdom dictates that the spectral excitation profile – the excited-state population vs the detuning – broadens as the radiation intensity increases. This common expectation has been shown to be incorrect in the fluorescence signal following two-photon excitation of xenon atoms by a Gaussian laser pulse, which showed almost no power broadening [T. Halfmann, T. Rickes, N.V. Vitanov, K. Bergmann, Optics Communications, 220 (2003) 353] Here we go a step further and show that for a class of pulse shapes, the falling edges of which vanish as inverse powers of time, ∝t−n∝t−n (with n>1n>1), the spectral excitation profile must exhibit power narrowing, i.e. the spectral linewidth scales as Ω0−1/(n−1), where Ω0Ω0 is the Rabi frequency of the transition. We provide a simple physical explanation based upon the notions of adiabatic evolution and coherent population return and discuss important experimental applications.

Related Topics
Physical Sciences and Engineering Materials Science Electronic, Optical and Magnetic Materials
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