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Imaging state-to-state reactive scattering in the Ar+ + H2 charge transfer reaction
The charge transfer reaction of Ar+ with H2 and D2 has been investigated in an experiment combining crossed beams with three-dimensional velocity map imaging. Angle-differential cross sections for two collision energies have been obtained for both neutral species. We find that the product ions are h...
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Published in: | The Journal of chemical physics 2017-07, Vol.147 (1), p.013940-013940 |
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container_title | The Journal of chemical physics |
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creator | Michaelsen, Tim Bastian, Björn Carrascosa, Eduardo Meyer, Jennifer Parker, David H. Wester, Roland |
description | The charge transfer reaction of Ar+ with H2 and D2 has been investigated in an experiment combining crossed beams with three-dimensional velocity map imaging. Angle-differential cross sections for two collision energies have been obtained for both neutral species. We find that the product ions are highly internally excited. In the reaction with H2, the spin-orbit excited Ar+ state’s coupling to the “resonant” vibrationally excited product
H
2
+
(
υ
= 2) dominates for both investigated energies, in line with previous investigations. The observed angular distributions, however, show significantly less back-scattering than was found previously. Furthermore, we discovered that the product ions are highly rotationally excited. In the case of Ar+ reacting with D2, the energetically closest lying vibrational levels are not strictly preferred and higher-lying vibrational levels are also populated. For both species, the backward-scattered products show higher internal excitation. |
doi_str_mv | 10.1063/1.4983305 |
format | article |
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H
2
+
(
υ
= 2) dominates for both investigated energies, in line with previous investigations. The observed angular distributions, however, show significantly less back-scattering than was found previously. Furthermore, we discovered that the product ions are highly rotationally excited. In the case of Ar+ reacting with D2, the energetically closest lying vibrational levels are not strictly preferred and higher-lying vibrational levels are also populated. For both species, the backward-scattered products show higher internal excitation.</description><identifier>ISSN: 0021-9606</identifier><identifier>EISSN: 1089-7690</identifier><identifier>DOI: 10.1063/1.4983305</identifier><identifier>CODEN: JCPSA6</identifier><language>eng</language><publisher>Melville: American Institute of Physics</publisher><subject>Charge transfer ; Investigations ; Scattering</subject><ispartof>The Journal of chemical physics, 2017-07, Vol.147 (1), p.013940-013940</ispartof><rights>Author(s)</rights><rights>2017 Author(s). Published by AIP Publishing.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2755-89434c1e3783c12e14f64ab7962c8a5cebf9555c0d19faa71fce92e4107efd53</citedby><cites>FETCH-LOGICAL-c2755-89434c1e3783c12e14f64ab7962c8a5cebf9555c0d19faa71fce92e4107efd53</cites><orcidid>0000-0002-5937-7393 ; 0000-0003-4338-8669 ; 0000-0003-0297-168X ; 0000-0001-7935-6066 ; 0000-0003-1303-2370</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://pubs.aip.org/jcp/article-lookup/doi/10.1063/1.4983305$$EHTML$$P50$$Gscitation$$H</linktohtml><link.rule.ids>314,777,779,781,792,27905,27906,76132</link.rule.ids></links><search><creatorcontrib>Michaelsen, Tim</creatorcontrib><creatorcontrib>Bastian, Björn</creatorcontrib><creatorcontrib>Carrascosa, Eduardo</creatorcontrib><creatorcontrib>Meyer, Jennifer</creatorcontrib><creatorcontrib>Parker, David H.</creatorcontrib><creatorcontrib>Wester, Roland</creatorcontrib><title>Imaging state-to-state reactive scattering in the Ar+ + H2 charge transfer reaction</title><title>The Journal of chemical physics</title><description>The charge transfer reaction of Ar+ with H2 and D2 has been investigated in an experiment combining crossed beams with three-dimensional velocity map imaging. Angle-differential cross sections for two collision energies have been obtained for both neutral species. We find that the product ions are highly internally excited. In the reaction with H2, the spin-orbit excited Ar+ state’s coupling to the “resonant” vibrationally excited product
H
2
+
(
υ
= 2) dominates for both investigated energies, in line with previous investigations. The observed angular distributions, however, show significantly less back-scattering than was found previously. Furthermore, we discovered that the product ions are highly rotationally excited. In the case of Ar+ reacting with D2, the energetically closest lying vibrational levels are not strictly preferred and higher-lying vibrational levels are also populated. For both species, the backward-scattered products show higher internal excitation.</description><subject>Charge transfer</subject><subject>Investigations</subject><subject>Scattering</subject><issn>0021-9606</issn><issn>1089-7690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp90E1PAjEQBuDGaCKiB_9BEy8qWex0-7E9GqJCQuJB7k0pU1gCu9gWE_-9i3Dy4Gnm8Mxk5iXkFtgQmCqfYChMVZZMnpEesMoUWhl2TnqMcSiMYuqSXKW0ZoyB5qJHPiZbt6ybJU3ZZSxyW_w2NKLzuf5CmrzLGeOB1A3NK6TPcUAHdMypX7m4RJqja1LAeJppm2tyEdwm4c2p9sns9WU2GhfT97fJ6HlaeK6lLCojSuEBS12VHjiCCEq4uTaK-8pJj_NgpJSeLcAE5zQEj4ajAKYxLGTZJ_fHtbvYfu4xZbutk8fNxjXY7pMFA1opqZno6N0fum73semOsxy4EEaKLrw-eTgqH9uUIga7i_XWxW8LzB7StWBP6Xb28WiTr7vAuq__wT-AtHeG</recordid><startdate>20170707</startdate><enddate>20170707</enddate><creator>Michaelsen, Tim</creator><creator>Bastian, Björn</creator><creator>Carrascosa, Eduardo</creator><creator>Meyer, Jennifer</creator><creator>Parker, David H.</creator><creator>Wester, Roland</creator><general>American Institute of Physics</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8FD</scope><scope>H8D</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5937-7393</orcidid><orcidid>https://orcid.org/0000-0003-4338-8669</orcidid><orcidid>https://orcid.org/0000-0003-0297-168X</orcidid><orcidid>https://orcid.org/0000-0001-7935-6066</orcidid><orcidid>https://orcid.org/0000-0003-1303-2370</orcidid></search><sort><creationdate>20170707</creationdate><title>Imaging state-to-state reactive scattering in the Ar+ + H2 charge transfer reaction</title><author>Michaelsen, Tim ; Bastian, Björn ; Carrascosa, Eduardo ; Meyer, Jennifer ; Parker, David H. ; Wester, Roland</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2755-89434c1e3783c12e14f64ab7962c8a5cebf9555c0d19faa71fce92e4107efd53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Charge transfer</topic><topic>Investigations</topic><topic>Scattering</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Michaelsen, Tim</creatorcontrib><creatorcontrib>Bastian, Björn</creatorcontrib><creatorcontrib>Carrascosa, Eduardo</creatorcontrib><creatorcontrib>Meyer, Jennifer</creatorcontrib><creatorcontrib>Parker, David H.</creatorcontrib><creatorcontrib>Wester, Roland</creatorcontrib><collection>CrossRef</collection><collection>Technology Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of chemical physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Michaelsen, Tim</au><au>Bastian, Björn</au><au>Carrascosa, Eduardo</au><au>Meyer, Jennifer</au><au>Parker, David H.</au><au>Wester, Roland</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Imaging state-to-state reactive scattering in the Ar+ + H2 charge transfer reaction</atitle><jtitle>The Journal of chemical physics</jtitle><date>2017-07-07</date><risdate>2017</risdate><volume>147</volume><issue>1</issue><spage>013940</spage><epage>013940</epage><pages>013940-013940</pages><issn>0021-9606</issn><eissn>1089-7690</eissn><coden>JCPSA6</coden><abstract>The charge transfer reaction of Ar+ with H2 and D2 has been investigated in an experiment combining crossed beams with three-dimensional velocity map imaging. Angle-differential cross sections for two collision energies have been obtained for both neutral species. We find that the product ions are highly internally excited. In the reaction with H2, the spin-orbit excited Ar+ state’s coupling to the “resonant” vibrationally excited product
H
2
+
(
υ
= 2) dominates for both investigated energies, in line with previous investigations. The observed angular distributions, however, show significantly less back-scattering than was found previously. Furthermore, we discovered that the product ions are highly rotationally excited. In the case of Ar+ reacting with D2, the energetically closest lying vibrational levels are not strictly preferred and higher-lying vibrational levels are also populated. For both species, the backward-scattered products show higher internal excitation.</abstract><cop>Melville</cop><pub>American Institute of Physics</pub><doi>10.1063/1.4983305</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-5937-7393</orcidid><orcidid>https://orcid.org/0000-0003-4338-8669</orcidid><orcidid>https://orcid.org/0000-0003-0297-168X</orcidid><orcidid>https://orcid.org/0000-0001-7935-6066</orcidid><orcidid>https://orcid.org/0000-0003-1303-2370</orcidid><oa>free_for_read</oa></addata></record> |
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language | eng |
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source | American Institute of Physics:Jisc Collections:Transitional Journals Agreement 2021-23 (Reading list); AIP - American Institute of Physics |
subjects | Charge transfer Investigations Scattering |
title | Imaging state-to-state reactive scattering in the Ar+ + H2 charge transfer reaction |
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