Sulphur-induced structural chemistry of oxide surfaces

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.
硫诱导的氧化物表面结构化学
利用表面EXAFS、NEXAFS和光电发射技术研究了H2S与NiO(100)和SO2与TiO2(110)反应后的表面相结构。S K-edge SEXAFS数据,结合LEED模式对称性,表明在570 K下NiO(100)/H2S反应导致底物还原,形成一个方位排列的Ni(100)c(2 × 2)S raft,其中S占据了四倍Ni(100)空心位点。低温TiO2(110)表面SO2吸附的S K-edge NEXAFS结果鉴定出两种表面SO2:化学吸附的SO2和SO2 - 4。NEXAFS的偏振依赖性表明SO2分子平面接近于表面平行。光发射数据也证明了110 K下的化学吸附,并表明该前驱相在热活化过程中进一步反应,形成稳定的表面硫酸盐样物质。提出了一种机制,涉及到SO2键合到一个台阶Ti位点,与一个激活跳到相邻的位置,其中硫键合到两个氧原子在凸起的行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信