SF6 Negative Ion Formation in Charge Transfer Experiments

Author:

Kumar Sarvesh12ORCID,Hoshino Masamitsu3ORCID,Kerkeni Boutheïna45ORCID,García Gustavo6ORCID,Ouerfelli Ghofrane7,Al-Mogren Muneerah Mogren8,Limão-Vieira Paulo1ORCID

Affiliation:

1. Atomic and Molecular Collisions Laboratory, CEFITEC-Centre of Physics and Technological Research, Department of Physics, Universidade NOVA de Lisboa, 2829-516 Caparica, Portugal

2. Chemical Sciences Division, Lawrence Berkeley National Laboratory, One Cyclotron Road, Berkeley, CA 94720, USA

3. Department of Materials and Life Sciences, Sophia University, Tokyo 102-8554, Japan

4. ISAMM, Université de la Manouba, La Manouba 2010, Tunisia

5. Département de Physique, LPMC, Faculté des Sciences de Tunis, Université de Tunis el Manar, Tunis 2092, Tunisia

6. Instituto de Física Fundamental, Consejo Superior de Investigaciones Científicas (CSIC), Serrano 113-bis, 28006 Madrid, Spain

7. Department of Physics, College of Khurma University, Taif University, P.O. Box 11099, Taif 21944, Saudi Arabia

8. Department of Chemistry, College of Sciences, King Saud University, P.O. Box 2455, Ryiadh 11451, Saudi Arabia

Abstract

In the present work, we report an update and extension of the previous ion-pair formation study of Hubers, M.M.; Los, J. Chem. Phys. 1975, 10, 235–259, noting new fragment anions from time-of-flight mass spectrometry. The branching ratios obtained from the negative ions formed in K + SF6 collisions, in a wide energy range from 10.7 up to 213.1 eV in the centre-of-mass frame, show that the main anion is assigned to SF5− and contributing to more than 70% of the total ion yield, followed by the non-dissociated parent anion SF6− and F−. Other less intense anions amounting to <20% are assigned to SF3− and F2−, while a trace contribution at 32u is tentatively assigned to S− formation, although the rather complex intramolecular energy redistribution within the temporary negative ion is formed during the collision. An energy loss spectrum of potassium cation post-collision is recorded showing features that have been assigned with the help of theoretical calculations. Quantum chemical calculations for the lowest-lying unoccupied molecular orbitals in the presence of a potassium atom are performed to support the experimental findings. Apart from the role of the different resonances participating in the formation of different anions, the role of higher-lying electronic-excited states of Rydberg character are noted.

Funder

Portuguese National Funding Agency

Radiation Biology and Biophysics Doctoral Training Programme RaBBiT

Spanish Ministerio de Ciencia e Innovación Project

Researchers Supporting Project

Publisher

MDPI AG

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