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Springer theses

Two-Photon Photoassociation

Alexander Guttridge

Published Jan 1, 2019• 1 citation
Publisher
DOI
10.1007/978-3-030-21201-8_8

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Resonance-enhanced two-photon ionization (RETPI) is a powerful tool in ultracold molecular photoassociation spectroscopy measurement. Using the RETPI, the line shape of ultracold RbCs molecular photoassociation spectroscopy, which contains intensity and full width at half maximum, is measured and analyzed systematically with varied photoassociation laser intensity and ionization laser energy. The saturation of photoassociation spectroscopy at a high ionization laser energy is observed and the suppression phenomenon is observed at high photoassociation laser intensity. The saturation intensity of RbCs molecular photoassociation, the linewidths of excited state molecules in different rovibrational levels at zero photoassociation laser intensity, and two-photon ionization efficiency have been derived from the line shape of photoassociation spectroscopy. The line shape analysis of photoassociation spectroscopy is important for precision spectroscopic analysis.

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Abstract Using the quantum wave-packet method, we investigated the photoassociation (PA) processes of H + + He → HeH + in the ground electronic state (X 1 Σ g + ). Two cases are considered where the target vibrational state selected is v = 4 and 8, respectively. It is found (for the first time) that above-threshold dissociation (ATD) occurs alongside the PA process (PA-ATD). ATD dissociation can be the major loss mechanism for the PA process. Compared with the direct dissociation from a given vibrational state and continuum–continuum transitions to the same final energy, the overall PA-ATD process is enhanced in comparison to individual contributions due to correlations. The one-photon dissociation from the target vibrational state, the ATD signals from two-photon dissociation and the higher-order (three- and four-photon) dissociations are the results of different mechanisms.

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Two-photon photoassociative spectroscopy of ultracold Sr88

Y. N. Martinez de Escobar, Pascal G. Mickelson, Philippe Pellegrini +5 more

We present results from two-photon photoassociative spectroscopy of the least-bound vibrational level of the $X\phantom{\rule{0.2em}{0ex}}^{1}\ensuremath{\Sigma}_{g}^{+}$ state of the $^{88}\mathrm{Sr}_{2}$ dimer. Measurement of the binding energy allows us to determine the $s$-wave scattering length ${a}_{88}=\ensuremath{-}1.4(6){a}_{0}$. For the intermediate state, we use a bound level on the metastable $^{1}S_{0}\text{\ensuremath{-}}^{3}P_{1}$ potential, which provides large Franck-Condon transition factors and narrow one-photon photoassociative lines that are advantageous for observing quantum-optical effects such as Autler-Townes resonance splittings.

arXiv:0808.3434•Physical Review A•Dec 10, 2008•105 citations
Resonance-enhanced two-photon ionization (RETPI) is a powerful tool in ultracold molecular photoassociation spectroscopy measurement. Using the RETPI, the line shape of ultracold RbCs molecular photoassociation spectroscopy, which contains intensity and full width at half maximum, is measured and analyzed systematically with varied photoassociation laser intensity and ionization laser energy. The saturation of photoassociation spectroscopy at a high ionization laser energy is observed and the suppression phenomenon is observed at high photoassociation laser intensity. The saturation intensity of RbCs molecular photoassociation, the linewidths of excited state molecules in different rovibrational levels at zero photoassociation laser intensity, and two-photon ionization efficiency have been derived from the line shape of photoassociation spectroscopy. The line shape analysis of photoassociation spectroscopy is important for precision spectroscopic analysis.
Abstract Using the quantum wave-packet method, we investigated the photoassociation (PA) processes of H + + He → HeH + in the ground electronic state (X 1 Σ g + ). Two cases are considered where the target vibrational state selected is v = 4 and 8, respectively. It is found (for the first time) that above-threshold dissociation (ATD) occurs alongside the PA process (PA-ATD). ATD dissociation can be the major loss mechanism for the PA process. Compared with the direct dissociation from a given vibrational state and continuum–continuum transitions to the same final energy, the overall PA-ATD process is enhanced in comparison to individual contributions due to correlations. The one-photon dissociation from the target vibrational state, the ATD signals from two-photon dissociation and the higher-order (three- and four-photon) dissociations are the results of different mechanisms.
We present results from two-photon photoassociative spectroscopy of the least-bound vibrational level of the $X\phantom{\rule{0.2em}{0ex}}^{1}\ensuremath{\Sigma}_{g}^{+}$ state of the 88Sr2^{88}\mathrm{Sr}_{2}88Sr2​ dimer. Measurement of the binding energy allows us to determine the sss-wave scattering length ${a}_{88}=\ensuremath{-}1.4(6){a}_{0}$. For the intermediate state, we use a bound level on the metastable $^{1}S_{0}\text{\ensuremath{-}}^{3}P_{1}$ potential, which provides large Franck-Condon transition factors and narrow one-photon photoassociative lines that are advantageous for observing quantum-optical effects such as Autler-Townes resonance splittings.