L. Schnieder, K. Seekamp-Rahn, F. Liedeker, H. Steuwe, K. Welge
{"title":"Hydrogen exchange reaction H + D2 in crossed beams","authors":"L. Schnieder, K. Seekamp-Rahn, F. Liedeker, H. Steuwe, K. Welge","doi":"10.1039/DC9919100259","DOIUrl":null,"url":null,"abstract":"Despite its fundamental importance as the prototypical bimolecular reaction, the hydrogen exchange reaction still remains a challenging and open problem, both experimentally and theoretically. Theory has now developed to a stage much superior to that of experiment. Nowhere is this more true than, for example, in the determination of differential scattering cross-sections, state-to-state specific with respect to the vibrational and rotational degrees of freedom of the molecular products. In this paper we describe a new experimental approach to such measurements, and present first results from crossed-beam studies of the H + D2 reaction (at relative translational energies of 1.29 and 0.54 eV) using the novel technique of hydrogen Rydberg atom time-of-flight spectroscopy to monitor the velocity and angular distributions of the D atom product.","PeriodicalId":12210,"journal":{"name":"Faraday Discussions of The Chemical Society","volume":"39 1","pages":"259-269"},"PeriodicalIF":0.0000,"publicationDate":"1991-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"79","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Faraday Discussions of The Chemical Society","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/DC9919100259","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 79
Abstract
Despite its fundamental importance as the prototypical bimolecular reaction, the hydrogen exchange reaction still remains a challenging and open problem, both experimentally and theoretically. Theory has now developed to a stage much superior to that of experiment. Nowhere is this more true than, for example, in the determination of differential scattering cross-sections, state-to-state specific with respect to the vibrational and rotational degrees of freedom of the molecular products. In this paper we describe a new experimental approach to such measurements, and present first results from crossed-beam studies of the H + D2 reaction (at relative translational energies of 1.29 and 0.54 eV) using the novel technique of hydrogen Rydberg atom time-of-flight spectroscopy to monitor the velocity and angular distributions of the D atom product.