Relativistic multichannel treatment of autoionization Rydberg series of 4s2nf(n= 4 − 23)Jπ= (7/2)° for scandium
Feng-Dong Jia, Jingyang Wang, Zhong Zhi-Ping
Abstract
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Feng-Dong Jia, Jingyang Wang, Zhong Zhi-Ping
Abstract
Open-access reader
Based on relativistic multichannel theory, this paper calculates the energy levels of autoionization Rydberg series 4s 2 n f( n = 4 − 23) J π = (7/2)° of scandium at different levels of approximation within the framework of multichannel quantum defect theory. The present results show that the dipole polarizations play an important role. Considering the dynamical dipole polarization effects, this paper finds that the difference between calculated and experimental quantum defects for the 4s 2 n f( n = 4 − 23) J π = (7/2)° series is generally about 0.01–0.03. Furthermore, the reason that 4s 2 16f is obscured in experimental spectra is suggested to be the interaction with the neighbouring resonance state converged to 3d 2 ( 1 G 4 )of Sc + .
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Based on relativistic multichannel theory, this paper calculates the energy levels of autoionization Rydberg series 4s 2 n f( n = 4 − 23) J π = (7/2)° of scandium at different levels of approximation within the framework of multichannel quantum defect theory. The present results show that the dipole polarizations play an important role. Considering the dynamical dipole polarization effects, this paper finds that the difference between calculated and experimental quantum defects for the 4s 2 n f( n = 4 − 23) J π = (7/2)° series is generally about 0.01–0.03. Furthermore, the reason that 4s 2 16f is obscured in experimental spectra is suggested to be the interaction with the neighbouring resonance state converged to 3d 2 ( 1 G 4 )of Sc + .
Key concepts: Autoionization, Scandium, Quantum defect, Rydberg formula, Physics, Atomic physics, Series (stratigraphy), Polarization (electrochemistry)