C. Muryn, D. Purdie, P. J. Hardman, Allen L. Johnson, N. S. Prakash, G. N. Raiker, G. Thornton, D. Law
{"title":"Sulphur-induced structural chemistry of oxide surfaces","authors":"C. Muryn, D. Purdie, P. J. Hardman, Allen L. Johnson, N. S. Prakash, G. N. Raiker, G. Thornton, D. Law","doi":"10.1039/DC9908900077","DOIUrl":null,"url":null,"abstract":"Surface EXAFS, NEXAFS and photoemission have been used to study the structure of surface phases resulting from reaction of H2S with NiO(100) and SO2 with TiO2(110). S K-edge SEXAFS data, in conjunction with the LEED pattern symmetry, suggest that the NiO(100)/H2S reaction at 570 K results in reduction of the substrate to form an azimuthally aligned Ni(100)c(2 × 2)S raft, with S occupying the fourfold Ni(100) hollow site. S K-edge NEXAFS results for SO2 adsorption on low-temperature TiO2(110) identify two surface SOx species: chemisorbed SO2 and SO2–4. The polarisation dependence of the NEXAFS suggests that the SO2 molecular plane lies close to parallel to the surface. Photoemission data also evidence chemisorption at 110 K and show that this precursor phase reacts further in a thermally activated process to form a stable surface sulphate-like species. A mechanism is suggested which involves SO2 bonding to a terrace Ti site, with an activated hop to an adjacent site in which sulphur bonds to two oxygen atoms on the raised row.","PeriodicalId":12210,"journal":{"name":"Faraday Discussions of The Chemical Society","volume":"31 1","pages":"77-89"},"PeriodicalIF":0.0000,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"29","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Faraday Discussions of The Chemical Society","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/DC9908900077","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 29
Abstract
Surface EXAFS, NEXAFS and photoemission have been used to study the structure of surface phases resulting from reaction of H2S with NiO(100) and SO2 with TiO2(110). S K-edge SEXAFS data, in conjunction with the LEED pattern symmetry, suggest that the NiO(100)/H2S reaction at 570 K results in reduction of the substrate to form an azimuthally aligned Ni(100)c(2 × 2)S raft, with S occupying the fourfold Ni(100) hollow site. S K-edge NEXAFS results for SO2 adsorption on low-temperature TiO2(110) identify two surface SOx species: chemisorbed SO2 and SO2–4. The polarisation dependence of the NEXAFS suggests that the SO2 molecular plane lies close to parallel to the surface. Photoemission data also evidence chemisorption at 110 K and show that this precursor phase reacts further in a thermally activated process to form a stable surface sulphate-like species. A mechanism is suggested which involves SO2 bonding to a terrace Ti site, with an activated hop to an adjacent site in which sulphur bonds to two oxygen atoms on the raised row.