\(\mathrm{P}_{2}\) molecules in the electronically excited \(C^{1} \Sigma_{\mathrm{u}}^{+}\)state were selectively formed in \(v^{\prime}=11\) by \(\mathrm{ArF}\) laser ( \(193.3 \mathrm{~nm}\) ) irradiation of phosphine/argon mixtures. The intensities of emissions to the vibrational levels \(v^{\pr
TheH1Σ+g(v= 0 and 1) andEF1Σ+g(v= 28 and 32) States of D2: Term Values and Fluorescence Lifetimes
✍ Scribed by H. Suzuki; M. Nakata; Y. Ogi; K. Tsukiyama
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 146 KB
- Volume
- 191
- Category
- Article
- ISSN
- 0022-2852
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✦ Synopsis
The extreme ultraviolet-visible double resonant excitation method was applied to the gerade Rydberg states of D 2 molecules. Tunable coherent extreme ultraviolet radiation near 103 nm prepared D 2 in the B 1 ⌺ u ϩ (v ϭ 7, J) state. Visible laser light subsequently brought them to the H 1 ⌺ g ϩ (v ϭ 0 and 1), EF 1 ⌺ g ϩ (v ϭ 28 and 32), and GK 1 ⌺ g ϩ (v ϭ 2 and 5) states. Our term values for the GK 1 ⌺ g ϩ state were in complete agreement with previous values, while deviations beyond the experimental error were found for the H 1 ⌺ g ϩ (v ϭ 1) and EF 1 ⌺ g ϩ (v ϭ 28 and 32) states. The fluorescence lifetimes, measured under a collision-free environment for the first time, were in reasonable agreement with ab initio calculations.
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