Rotational aspects of short-pulse population transfer in diatomic molecules

Y. B. Band*, S. Kallush, Roi Baer

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

Abstract

A fully-selective population transfer scheme for diatomic molecules using short-duration (<ns) laser pulses is developed via the concept of light-induced potentials. It explicitly takes rotational degrees of freedom into account. We apply it to a specific Na2 transition from the lowest ro-vibrationic state to a single ro-vibrational state of a doubly excited electronic state via an intermediate electronic state. The process insures total selective population transfer with pulses short compared to the molecule rotation time. However, an estimate of the multiphoton ionization rate using time-dependent density functional theory suggests that ionization may significantly adversely affect the transfer.

Original languageAmerican English
Pages (from-to)23-27
Number of pages5
JournalChemical Physics Letters
Volume392
Issue number1-3
DOIs
StatePublished - 1 Jul 2004

Bibliographical note

Funding Information:
Useful conversations with Carl J. Williams are gratefully acknowledged. This work was supported in part by grants from the Israel Science Foundation for a Center of Excellence (Grant No. 8006/03), by the Binational (US–Israel) Science Foundation under Grant No. 2002147, and by the GIF under Grant No. 699.

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