Hikosaka Yasumasa, Mitsuke Koichiro
UVSOR Facility, Institute for Molecular Science, Myodaiji, Okazaki 444-8585, Japan.
J Chem Phys. 2004 Jul 8;121(2):792-9. doi: 10.1063/1.1758212.
Two-dimensional photoelectron spectroscopy of hydrogen iodide (HI) has been performed in the photon energy region of 11.10-14.85 eV, in order to investigate dynamical properties on autoionization and neutral dissociation of Rydberg states HI*(RA) converging to HI+(A 2Sigma1/2(+)). A two-dimensional photoelectron spectrum exhibits strong vibrational excitation of HI+(X 2Pi) over a photon energy region from approximately 12 to 13.7 eV, which is attributable to the autoionizing feature of the 5 dpi HI*(RA) state. A noticeable set of stripes in the photon energy region of 13.5-14.5 eV is assigned as resulting from autoionization of the atomic Rydberg states of I* converging to I+ (3P0 or 3P1). The formation of I* is understood in terms of predissociation of multiple HI*(RA) states by way of the repulsive Rydberg potential curves converging to HI+(4Pi1/2).
为了研究向HI⁺(A²Σ₁/₂⁺)收敛的里德堡态HI*(RA)的自电离和中性解离的动力学性质,在11.10 - 14.85 eV的光子能量区域对碘化氢(HI)进行了二维光电子能谱研究。二维光电子能谱在大约12至13.7 eV的光子能量区域表现出HI⁺(X²Π)的强烈振动激发,这归因于5dpi HI*(RA)态的自电离特征。在13.5 - 14.5 eV的光子能量区域中一组明显的条纹被认为是由向I⁺(³P₀或³P₁)收敛的I的原子里德堡态的自电离产生的。I的形成可通过多个HI*(RA)态通过收敛到HI⁺(4Π₁/₂)的排斥性里德堡势曲线的预解离来理解。