X(1)Σ(+)(g)(O(+)(g)) emission in the vacuum ultraviolet (∼172 nm), induced by laser excitation of Ω(g) ← a(3)Σ(+)(u)(1(u), O(-)(u)) [Rydberg←Rydberg] transitions of the molecule, has confirmed the existence of structure between 720 and 770 nm (reported by Killeen and Eden [J. Chem. Phys. 84, 6048 (1986)]) but also reveals red-degraded vibrational bands extending to wavelengths beyond 800 nm. Spectral simulations based on calculations of Franck-Condon factors for assumed Ω(g) ← a(3)Σ(+)(u) transitions involving Ω = 0(±),1 gerade Rydberg states suggest that the upper level primarily responsible for the observed spectrum is an Ω = 1 state correlated, in the separated atom limit, with Xe(5p(6) (1)S0) + Xe(5p(5) 6p) and built on a predominantly A(2)Π3/2g molecular ion core. Specifically, the spectroscopic constants for the upper state of the 1(g) ← 1(u), O(±)(u) absorptive transitions are determined to be Te = 13,000 ± 150 cm(-1), ω'(e) = 120 ± 10 cm(-1), ω'(e)x'(e) = 1.1 ± 0.4 cm(-1), De = 3300 ± 300 cm(-1), and ΔR(e) = R'(e) = R''(e) = 0.3 ± 0.1 Å which are in general agreement with the theoretical predictions of the pseudopotential hole-particle formalism, developed by Jonin and Spiegelmann [J. Chem. Phys. 117, 3059 (2002)], for both the (5)1g and (3)O(+)(g) states of Xe2. These spectra exhibit the most extensive vibrational development, and provide evidence for the first molecular core-switching transition, observed to date for any of the rare gas dimers at small R (<4 Ǻ). Experiments in the green (545-555 nm) also provide improved absorption spectra, relative to data reported in 1986 and 1999, associated with Xe2 Rydberg states derived from the Xe(7p) orbital.
| Entry Date(s): |
Date Created: 20140703 Date Completed: 20150511 Latest Revision: 20140702 |
| Update Code: |
20221213 |
| DOI: |
10.1063/1.4884606 |
| PMID: |
24985643 |
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| Autor: |
Wagner CJ; Laboratory for Optical Physics and Engineering, Department of Electrical and Computer Engineering, University of Illinois, Urbana, Illinois 61801, USA., Galvin TC; Laboratory for Optical Physics and Engineering, Department of Electrical and Computer Engineering, University of Illinois, Urbana, Illinois 61801, USA., Eden JG; Laboratory for Optical Physics and Engineering, Department of Electrical and Computer Engineering, University of Illinois, Urbana, Illinois 61801, USA. |
| Jazyk: |
angličtina |
| Zdroj: |
The Journal of chemical physics [J Chem Phys] 2014 Jun 28; Vol. 140 (24), pp. 244312. |
| DOI: |
10.1063/1.4884606 |
| Abstrakt: |
Bound←bound transitions of the Xe dimer at small internuclear separation (R < 4.0 Å) have been observed in the 545-555 nm and 675-800 nm spectral regions by laser spectroscopy in the afterglow of a pulsed Xe microplasma with a volume of ∼160 nl. Transient suppression of Xe2 A(1)Σ(+)(u)(O(+)(u)) --> X(1)Σ(+)(g)(O(+)(g)) emission in the vacuum ultraviolet (∼172 nm), induced by laser excitation of Ω(g) ← a(3)Σ(+)(u)(1(u), O(-)(u)) [Rydberg←Rydberg] transitions of the molecule, has confirmed the existence of structure between 720 and 770 nm (reported by Killeen and Eden [J. Chem. Phys. 84, 6048 (1986)]) but also reveals red-degraded vibrational bands extending to wavelengths beyond 800 nm. Spectral simulations based on calculations of Franck-Condon factors for assumed Ω(g) ← a(3)Σ(+)(u) transitions involving Ω = 0(±),1 gerade Rydberg states suggest that the upper level primarily responsible for the observed spectrum is an Ω = 1 state correlated, in the separated atom limit, with Xe(5p(6) (1)S0) + Xe(5p(5) 6p) and built on a predominantly A(2)Π3/2g molecular ion core. Specifically, the spectroscopic constants for the upper state of the 1(g) ← 1(u), O(±)(u) absorptive transitions are determined to be Te = 13,000 ± 150 cm(-1), ω'(e) = 120 ± 10 cm(-1), ω'(e)x'(e) = 1.1 ± 0.4 cm(-1), De = 3300 ± 300 cm(-1), and ΔR(e) = R'(e) = R''(e) = 0.3 ± 0.1 Å which are in general agreement with the theoretical predictions of the pseudopotential hole-particle formalism, developed by Jonin and Spiegelmann [J. Chem. Phys. 117, 3059 (2002)], for both the (5)1g and (3)O(+)(g) states of Xe2. These spectra exhibit the most extensive vibrational development, and provide evidence for the first molecular core-switching transition, observed to date for any of the rare gas dimers at small R (<4 Ǻ). Experiments in the green (545-555 nm) also provide improved absorption spectra, relative to data reported in 1986 and 1999, associated with Xe2 Rydberg states derived from the Xe(7p) orbital. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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