1. |
- Khodorkovskii, M. A., et al.
(author)
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Electronic spectra of ArXe molecules in the region of Xe* (5d, 7s, 7p, 6p '), 80 300-89 500 cm(-1), using resonantly enhanced multiphoton ionization
- 2010
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In: Journal of Physics B. - : IOP Publishing. - 0953-4075 .- 1361-6455. ; 43:23, s. 235101-
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Journal article (peer-reviewed)abstract
- The electronic spectra of ArXe molecules in the 80 300-89 500 cm(-1) region were recorded by (2 + n) and (3 + n) REMPI methods. The vibrational progressions attributed to transitions of molecules from the ground state to the bounded excited state and wide unstructured bands related to transitions to the continuous upper state were obtained. The molecular constants of ArXe* were calculated for all the observed progressions in the 80 300-87 000 cm(-1) region as an approximation of an anharmonic oscillator and the Morse potential. For different excited states the energy of harmonic oscillator and the dissociation energy are changed from 10 to 100 cm(-1) and from 70 to 750 cm(-1), respectively.
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2. |
- Khodorkovskii, M. A., et al.
(author)
-
Electronic spectra of ArXe molecules in the region of Xe* (6s ', 6p, 5d), 77 000-80 200 cm(-1), using resonantly enhanced multiphoton ionization
- 2010
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In: Journal of Physics B. - : IOP Publishing. - 0953-4075 .- 1361-6455. ; 43:15, s. 155101-
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Journal article (peer-reviewed)abstract
- The excited electronic states of ArXe molecules in the region 77 000-80 200 cm(-1) were studied using the (2+1) and (3+1) resonance-enhanced multiphoton ionization methods. The use of different methods of multi-photon excitation and Ar+ ion registration allowed us to obtain some new data. Molecular constants were obtained for previously unknown excited states of molecules with the following dissociation limits: ArXe* -> (ArS0)-S-1+Xe*6p[5/2](3) with Omega = 2, 3 symmetry; (ArS0)-S-1+Xe*6p[3/2](2) with Omega = 1, 2 symmetry; (XeS1)-S-0 -> Xe*6s'[1/2](1)(0) with Omega = 0(+) symmetry.
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3. |
- Khodorkovskii, M. A., et al.
(author)
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Electronic spectra of XeNe molecules in the range 77100-90100 cm(-1) near Xe* (6p, 5d, 6p', 7s, 7p, 6d) obtained by the (3+1) REMPI and (2+1) REMPI methods
- 2010
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In: Optics and Spectroscopy. - 0030-400X .- 1562-6911. ; 108:6, s. 899-914
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Journal article (peer-reviewed)abstract
- The electronic spectra of XeNe molecules in the range of 77100-90100 cm(-1) are measured by the method of laser resonance multiphoton ionization in a supersonic jet. The photoionization spectra are obtained upon two- and three-photon excitations of molecules and their ionization by the next photon. In the range of 80300-90100 cm(-1) near Xe*(5d, 6p', 6d, 7s, and 7p), the spectra are obtained for the first time. A whole number of vibrational systems are measured in this range. The majority of vibrational systems near Xe* (5d, 6d, 7p, and 7s) are located in the red range with respect to their dissociation limits. In the blue range with respect to the dissociation limits, continua corresponding to transitions of molecules from the ground state to repulsive potential curves of excited states are detected. For a number of excited states of XeNe molecules, the vibrational analysis is performed and molecular constants are estimated.
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4. |
- Khodorkovskii, M. A., et al.
(author)
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Multiphoton mass spectra of XeKr molecules in the range of excited Xe*6p[5/2](2,3) atoms
- 2007
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In: Optics and Spectroscopy. - 0030-400X .- 1562-6911. ; 102:6, s. 834-841
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Journal article (peer-reviewed)abstract
- Data on excited states of XeKr molecules in the energy range 78280-77600 cm(-1) are obtained. Using the method of multiphoton laser photoionization of molecules in a supersonic jet, five vibrational progressions of XeKr molecules are obtained, which are attributed to five electronic-vibrational transitions from the ground state of the XeKr molecule of the symmetry 0(+) to excited states of the symmetry Omega = 0(+), 1, 2 with the dissociation limit (KrS0)-S-1 + Xe*6p[5/2](2) and of the symmetry Omega = 1, 2 with the dissociation limit Kr + Xe*6p[5/2](3). The molecular constants of the corresponding excited states of the XeKr molecule are estimated.
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