The A 2 -X 2 + (0,0) band of ZrN between 5620 and 5890 A has been studied using laser polarization, laser-induced fluorescence, and wavelength-resolved fluorescence spectroscopy. All the 12 branches expected from a 2 -2 + transition have been observed and assigned. Both nondegenerate and degenerate
Laser spectroscopy of the B2Σ+–X2Σ+ (0,0) band of ZrN
✍ Scribed by Hongbing Chen; Yongfang Li; D.K.-W Mok; A.S.-C Cheung
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- English
- Weight
- 184 KB
- Volume
- 218
- Category
- Article
- ISSN
- 0022-2852
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✦ Synopsis
The (0,0) band of the B 2 R þ -X 2 R þ transition of ZrN between 404.1 and 407.1 nm was recorded and rotationally analyzed using laser induced fluorescence (LIF) spectroscopy. Small local rotational perturbations have been found for both spin components. For 90 ZrN, perturbations are found at J ¼ 23:5 of the F 1 component and J ¼ 17:5 and 43.5 of the F 2 component. The perturbation of the F 1 component at J ¼ 23:5 shifts to J ¼ 18:5 for 94 ZrN. Our analysis indicates that these perturbations are caused by more than one electronic state. A least-squares fit of the unperturbed line positions yielded approximated molecular constants for the v ¼ 0 level of the B 2 R þ state of three isotopic molecules. Ab initio calculations have been performed to obtain spectroscopic properties of the ground and low-lying doublet and quartet states. The agreement between calculated and observed spectroscopic properties of the low-lying doublet states is good.
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