Spectroscopic Studies on Astrophysically Interesting TaO TaS, ZrS and SiO⁺ Molecules

Abstract

The true experimental potential energy curves for the electronic ground states of astrophysically important TaO, TaS, ZrS and SiO⁺molecules are constructed by using the Rydberg–Klein–Rees method as modified by Vanderslice et al. The ground state dissociation energies are determined by curve fitting techniques using the five parameters Hulburt-Hirschfelder (H-H) function. The estimated dissociation energies are 8.19 ± 0.17, 6.9 ±0.14, 5.89 ± 0.12 and 5.75 ± 0.12 eVfor TaO, TaS, ZrS and SiO⁺ respectively. These values are in good agreement with the literature values. The r-centriods and Franck–Condon factors (FC Factors) for the bands of K ² φ _5/2 - X ² Δ _3/2 (K-X) system of TaO, A-X ² Δ (A-X) and B-X ² Δ (B-X)systems of TaS, B ¹ Π - X¹ Σ⁺ (B-X) system of ZrS and B ²Σ⁺ - X² Σ⁺ (B-X) and A ² Π - X² Σ⁺ (A-X)systems of SiO⁺ molecules have been calculated. The Franck–Condon factors (FC factors) are evaluated by the approximate analytical methods of Jarmain and Fraser. The absence of the bands of these systems is explained.