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ACTA PHOTONICA SINICA

Spectrum Resonance Energy Transfer and Energy Analysis of Resorption

葛立新 GE Li-xin, 高淑梅 Gao Shumei, 吕思斌 L Si-bin

Published Jan 1, 2011• 0 citations
Publisher
DOI
10.3788/gzxb20114010.1500

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We propose and demonstrate the velocity transfer spectroscopy of a V-type energy structure with Rb atoms at 420 nm transition. The weak oscillator strength of a lower excited state for V-type energy structure atoms limits the high signal-to-noise ratio of atomic laser spectroscopy, which can be usually realized by optical-optical double-resonance or double-resonance optical pumping for cascade-type energy structure atoms. For 87 Rb atoms, the weak 420 nm transition spectrum between the energy level of 5 2 S 1/2 and 6 2 P 3/2 is transferred to the spectrum on lower excited states at 780 nm with strong oscillator strength, which is recorded by a 780 nm probe laser. This method, which is similar to the electron-shelving detection method, at a certain degree can indirectly measure a higher excited state transition with weak oscillator strength for any V-type energy structure of atoms by transferring the transition spectrum information of the very weak oscillator strength to the strong oscillator strength in an optical-optical double-resonance configuration.
Bath-induced coherence transfer effects on a time- and frequency-resolved resonant light scattering spectrum is theoretically investigated using the Markoff master equation. According to Eberly and Wódkiewicz, a general expression for an experimentally observable spectrum in terms of a molecular response function is derived within the density matrix formalism. To generalize our previous results of the bath-induced coherence transfer which were derived based on a displaced harmonic oscillator model [Y. Ohtsuki and Y. Fujimura, J. Chem. Phys. 91, 3903 (1989)], an eigenstate basis is used to represent a relevant system for investigating characteristics of the transfer. By the present model, we clarify the dependence of the bath-induced coherence transfer on the energy-level structure of the intermediate states associated with the transfer, i.e., energy mismatch effects. It is shown that if the energy mismatch of these states is smaller than dephasing rates, the bath-induced coherence transfer occurs resonantly. In the other cases, the energy mismatch brings about a modulation in the time evolution of the superposition state created by the bath-induced coherence transfer, which strongly diminishes the efficiency of the transfer. The resonance condition is derived analytically and is confirmed by numerical calculations of quantum beats induced by the bath-induced coherence transfer. The possibility of very rapid dephasing of a quantum beat signal which cannot be explained in terms of dephasing rates is also shown, when the transition moments have such values that give π-phase-shifted quantum beats in bath-induced fluorescence.
Collisional transfer of excitation energy from cadmium to caesium was investigated using methods of sensitized fluorescence. A mixture of cadmium and caesium vapors at low pressure was irradiated with Cd 3263.0 Å resonance radiation producing a population of Cd (53P1) atoms whose inelastic collisions with ground-state Cs atoms resulted in a transfer of excitation energy to a close-lying S, P, D and F states in caesium. The subsequent decay of these states manifested itself in the emission of sensitized fluorescence spectrum. Intensity measurements on the components of the spectrum by means of energy calibrated detector yielded some 50 cross-section values whose magnitudes range from 0.2 Å2 to 30.0 Å2 and which exhibit a pronounced resonances with ΔE the energy defect between Cd (53P1) and the appropriate level in caesium.