Evolution of L-shell photoabsorption of the molecular-ion series SiHn+ (n=1,2,3): Experimental and theoretical studies

E. T. Kennedy, J.-P. Mosnier, P. van Kampen, J.-M. Bizau, D. Cubaynes, S. Guilbaud, S. Carniato, A. Puglisi, and N. Sisourat
Phys. Rev. A 97, 043410 – Published 10 April 2018

Abstract

We report on complementary laboratory and theoretical investigations of the 2p photoexcitation cross sections for the molecular-ion series SiHn+ (n=1,2,3) near the L-shell threshold. The experiments used an electron cyclotron resonance (ECR) plasma molecular-ion source coupled with monochromatized synchrotron radiation in a merged-beam configuration. For all three molecular ions, the Si2+ decay channel appeared dominant, suggesting similar electronic and nuclear relaxation patterns involving resonant Auger and dissociation processes, respectively. The total yields of the Si2+ products were recorded and put on absolute cross-section scales by comparison with the spectrum of the Si+ parent atomic ion. Interpretation of the experimental spectra ensued from a comparison with total photoabsorption cross-sectional profiles calculated using ab initio configuration interaction theoretical methods inclusive of vibrational dynamics and contributions from inner-shell excitations in both ground and valence-excited electronic states. The spectra, while broadly similar for all three molecular ions, moved towards lower energies as the number of screening hydrogen atoms increased from one to three. They featured a wide and shallow region below 107eV due to 2pσ* transitions to dissociative states, and intense and broadened peaks in the 107113eV region merging into sharp Rydberg series due to 2pnδ,nπ transitions converging on the LII,III limits above 113eV. This overall spectral shape is broadly replicated by theory in each case, but the level of agreement does not extend to individual resonance structures. In addition to the fundamental interest, the work should also prove useful for the understanding and modeling of astronomical and laboratory plasma sources where silicon hydride molecular species play significant roles.

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  • Received 5 July 2017
  • Revised 16 February 2018

DOI:https://doi.org/10.1103/PhysRevA.97.043410

©2018 American Physical Society

Physics Subject Headings (PhySH)

Atomic, Molecular & Optical

Authors & Affiliations

E. T. Kennedy1, J.-P. Mosnier1,*, P. van Kampen1, J.-M. Bizau2,3, D. Cubaynes2,3, S. Guilbaud2, S. Carniato4, A. Puglisi4, and N. Sisourat4

  • 1School of Physical Sciences and NCPST, Dublin City University, Dublin 9, Ireland
  • 2Institut des Sciences Moléculaires d’Orsay, CNRS, Université Paris–Sud, and Université Paris–Saclay, F-91405 Orsay, France
  • 3Synchrotron SOLEIL, L’Orme des Merisiers, Saint-Aubin, Boîte Postale 48, F-91192 Gif-sur-Yvette Cedex, France
  • 4Sorbonne Universités, UPMC Univ Paris 06, CNRS, UMR 7614, Laboratoire de Chimie Physique-Matière et Rayonnement, F-75005 Paris, France

  • *Jean-Paul.Mosnier@dcu.ie

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Issue

Vol. 97, Iss. 4 — April 2018

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