Hydrogen-Promoted Chlorination of RuO2(110)
(2010) In Journal of Physical Chemistry C 114(24). p.10901-10909- Abstract
- High-resolution core-level photoemission spectroscopy and temperature-programmed reaction experiments together with density functional theory calculations were used to elucidate on the atomic scale the chlorination mechanism of ruthenium dioxide RuO2(110) by hydrogen chloride exposure. The surface-selective chlorination accounts for the extraordinary stability of the RuO2 catalyst in the Sumitomo process-the heterogeneously catalyzed oxidation of hydrogen chloride by oxygen. The selective replacement of bridging oxygen atoms by chlorine atoms depends on the formation of water molecules serving as leaving groups. Water is produced by the chlorine-assisted recombination of two neighboring surface hydroxyl groups at around 450 K, a... (More)
- High-resolution core-level photoemission spectroscopy and temperature-programmed reaction experiments together with density functional theory calculations were used to elucidate on the atomic scale the chlorination mechanism of ruthenium dioxide RuO2(110) by hydrogen chloride exposure. The surface-selective chlorination accounts for the extraordinary stability of the RuO2 catalyst in the Sumitomo process-the heterogeneously catalyzed oxidation of hydrogen chloride by oxygen. The selective replacement of bridging oxygen atoms by chlorine atoms depends on the formation of water molecules serving as leaving groups. Water is produced by the chlorine-assisted recombination of two neighboring surface hydroxyl groups at around 450 K, a temperature where water instantaneously leaves the surface. Finally, the bridging vacancy is rapidly filled in by chlorine atoms, thereby forming bridging chlorine atoms. Preadsorbed hydrogen has shown to facilitate the chlorination process for stoichiometry reasons. The general strategy of transforming bridging O atoms into a good leaving group has been corroborated by the chlorination of RuO2(110) via CO pretreatment with CO2 as the leaving group and subsequent Cl-2 exposure. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1630394
- author
- Hofmann, Jan Philipp ; Zweidinger, Stefan ; Knapp, Marcus ; Seitsonen, Ari Paavo ; Schulte, Karina LU ; Andersen, Jesper N LU ; Lundgren, Edvin LU and Over, Herbert
- organization
- publishing date
- 2010
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Journal of Physical Chemistry C
- volume
- 114
- issue
- 24
- pages
- 10901 - 10909
- publisher
- The American Chemical Society (ACS)
- external identifiers
-
- wos:000278845300032
- scopus:77953790577
- ISSN
- 1932-7447
- DOI
- 10.1021/jp103199x
- language
- English
- LU publication?
- yes
- id
- 6f35036a-125c-43b0-863d-85e8715ef389 (old id 1630394)
- date added to LUP
- 2016-04-01 11:06:13
- date last changed
- 2022-01-26 05:22:05
@article{6f35036a-125c-43b0-863d-85e8715ef389, abstract = {{High-resolution core-level photoemission spectroscopy and temperature-programmed reaction experiments together with density functional theory calculations were used to elucidate on the atomic scale the chlorination mechanism of ruthenium dioxide RuO2(110) by hydrogen chloride exposure. The surface-selective chlorination accounts for the extraordinary stability of the RuO2 catalyst in the Sumitomo process-the heterogeneously catalyzed oxidation of hydrogen chloride by oxygen. The selective replacement of bridging oxygen atoms by chlorine atoms depends on the formation of water molecules serving as leaving groups. Water is produced by the chlorine-assisted recombination of two neighboring surface hydroxyl groups at around 450 K, a temperature where water instantaneously leaves the surface. Finally, the bridging vacancy is rapidly filled in by chlorine atoms, thereby forming bridging chlorine atoms. Preadsorbed hydrogen has shown to facilitate the chlorination process for stoichiometry reasons. The general strategy of transforming bridging O atoms into a good leaving group has been corroborated by the chlorination of RuO2(110) via CO pretreatment with CO2 as the leaving group and subsequent Cl-2 exposure.}}, author = {{Hofmann, Jan Philipp and Zweidinger, Stefan and Knapp, Marcus and Seitsonen, Ari Paavo and Schulte, Karina and Andersen, Jesper N and Lundgren, Edvin and Over, Herbert}}, issn = {{1932-7447}}, language = {{eng}}, number = {{24}}, pages = {{10901--10909}}, publisher = {{The American Chemical Society (ACS)}}, series = {{Journal of Physical Chemistry C}}, title = {{Hydrogen-Promoted Chlorination of RuO2(110)}}, url = {{http://dx.doi.org/10.1021/jp103199x}}, doi = {{10.1021/jp103199x}}, volume = {{114}}, year = {{2010}}, }