Cold ion chemistry within a Rydberg-electron orbit: test of the spectator role of the Rydberg electron in the He(n) + CO → C(n′) + O + He reaction
Recently, a new method has been introduced to study ion-molecule reactions at very low collision energies, down to below k _B ⋅ 1 K (Allmendinger et al 2016 ChemPhysChem 17 3596). To eliminate the acceleration of the ions by stray electric fields in the reaction volume, the reactions are observed wi...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
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IOP Publishing
2021-01-01
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| Series: | New Journal of Physics |
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| Online Access: | https://doi.org/10.1088/1367-2630/ac231d |
| _version_ | 1797750079066472448 |
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| author | Fernanda B V Martins Valentina Zhelyazkova Christian Seiler Frédéric Merkt |
| author_facet | Fernanda B V Martins Valentina Zhelyazkova Christian Seiler Frédéric Merkt |
| author_sort | Fernanda B V Martins |
| collection | DOAJ |
| description | Recently, a new method has been introduced to study ion-molecule reactions at very low collision energies, down to below k _B ⋅ 1 K (Allmendinger et al 2016 ChemPhysChem 17 3596). To eliminate the acceleration of the ions by stray electric fields in the reaction volume, the reactions are observed within the orbit of a Rydberg electron with large principal quantum number n > 20. This electron is assumed not to influence the reaction taking place between the ion core and the neutral molecules. This assumption is tested here with the example of the He( n ) + CO → C( n ′) + O + He reaction, which is expected to be equivalent to the He ^+ + CO → C ^+ + O + He reaction, using a merged-beam approach enabling measurements of relative reaction rates for collision energies E _coll in the range from 0 to about k _B ⋅ 25 K with a collision-energy resolution of ∼ k _B ⋅ 200 mK at E _coll = 0. In contrast to the other ion-molecule reactions studied so far with this method, the atomic ion product (C ^+ ) is in its electronic ground state and does not have rotational and vibrational degrees of freedom so that the corresponding Rydberg product [C( n ′)] cannot decay by autoionization. Consequently, one can investigate whether the principal quantum number is effectively conserved, as would be expected in the spectator Rydberg-electron model. We measure the distribution of principal quantum numbers of the reactant He( n ) and product C( n ′) Rydberg atoms by pulsed-field ionization following initial preparation of He( n ) in states with n values between 30 and 45 and observe that the principal quantum number of the Rydberg electron is conserved during the reaction. This observation indicates that the Rydberg electron is not affected by the reaction, from which we can conclude that it does not affect the reaction either. This conclusion is strengthened by measurements of the collision-energy-dependent reaction yields at n = 30, 35 and 40, which exhibit the same behavior, i.e. a marked decrease below E _coll ≈ k _B ⋅ 5 K. |
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| institution | Directory Open Access Journal |
| issn | 1367-2630 |
| language | English |
| last_indexed | 2024-03-12T16:27:32Z |
| publishDate | 2021-01-01 |
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| record_format | Article |
| series | New Journal of Physics |
| spelling | doaj.art-79f729aa11e34df58289579207a497702023-08-08T15:38:14ZengIOP PublishingNew Journal of Physics1367-26302021-01-0123909501110.1088/1367-2630/ac231dCold ion chemistry within a Rydberg-electron orbit: test of the spectator role of the Rydberg electron in the He(n) + CO → C(n′) + O + He reactionFernanda B V Martins0https://orcid.org/0000-0002-3338-8246Valentina Zhelyazkova1https://orcid.org/0000-0001-7211-6561Christian Seiler2Frédéric Merkt3https://orcid.org/0000-0002-4897-2234Laboratory of Physical Chemistry, ETH Zurich , CH-8093 Zurich, SwitzerlandLaboratory of Physical Chemistry, ETH Zurich , CH-8093 Zurich, SwitzerlandLaboratory of Physical Chemistry, ETH Zurich , CH-8093 Zurich, SwitzerlandLaboratory of Physical Chemistry, ETH Zurich , CH-8093 Zurich, SwitzerlandRecently, a new method has been introduced to study ion-molecule reactions at very low collision energies, down to below k _B ⋅ 1 K (Allmendinger et al 2016 ChemPhysChem 17 3596). To eliminate the acceleration of the ions by stray electric fields in the reaction volume, the reactions are observed within the orbit of a Rydberg electron with large principal quantum number n > 20. This electron is assumed not to influence the reaction taking place between the ion core and the neutral molecules. This assumption is tested here with the example of the He( n ) + CO → C( n ′) + O + He reaction, which is expected to be equivalent to the He ^+ + CO → C ^+ + O + He reaction, using a merged-beam approach enabling measurements of relative reaction rates for collision energies E _coll in the range from 0 to about k _B ⋅ 25 K with a collision-energy resolution of ∼ k _B ⋅ 200 mK at E _coll = 0. In contrast to the other ion-molecule reactions studied so far with this method, the atomic ion product (C ^+ ) is in its electronic ground state and does not have rotational and vibrational degrees of freedom so that the corresponding Rydberg product [C( n ′)] cannot decay by autoionization. Consequently, one can investigate whether the principal quantum number is effectively conserved, as would be expected in the spectator Rydberg-electron model. We measure the distribution of principal quantum numbers of the reactant He( n ) and product C( n ′) Rydberg atoms by pulsed-field ionization following initial preparation of He( n ) in states with n values between 30 and 45 and observe that the principal quantum number of the Rydberg electron is conserved during the reaction. This observation indicates that the Rydberg electron is not affected by the reaction, from which we can conclude that it does not affect the reaction either. This conclusion is strengthened by measurements of the collision-energy-dependent reaction yields at n = 30, 35 and 40, which exhibit the same behavior, i.e. a marked decrease below E _coll ≈ k _B ⋅ 5 K.https://doi.org/10.1088/1367-2630/ac231dion-molecule reactionsRydberg statescold chemistry |
| spellingShingle | Fernanda B V Martins Valentina Zhelyazkova Christian Seiler Frédéric Merkt Cold ion chemistry within a Rydberg-electron orbit: test of the spectator role of the Rydberg electron in the He(n) + CO → C(n′) + O + He reaction New Journal of Physics ion-molecule reactions Rydberg states cold chemistry |
| title | Cold ion chemistry within a Rydberg-electron orbit: test of the spectator role of the Rydberg electron in the He(n) + CO → C(n′) + O + He reaction |
| title_full | Cold ion chemistry within a Rydberg-electron orbit: test of the spectator role of the Rydberg electron in the He(n) + CO → C(n′) + O + He reaction |
| title_fullStr | Cold ion chemistry within a Rydberg-electron orbit: test of the spectator role of the Rydberg electron in the He(n) + CO → C(n′) + O + He reaction |
| title_full_unstemmed | Cold ion chemistry within a Rydberg-electron orbit: test of the spectator role of the Rydberg electron in the He(n) + CO → C(n′) + O + He reaction |
| title_short | Cold ion chemistry within a Rydberg-electron orbit: test of the spectator role of the Rydberg electron in the He(n) + CO → C(n′) + O + He reaction |
| title_sort | cold ion chemistry within a rydberg electron orbit test of the spectator role of the rydberg electron in the he n co c n o he reaction |
| topic | ion-molecule reactions Rydberg states cold chemistry |
| url | https://doi.org/10.1088/1367-2630/ac231d |
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