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
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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.
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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。
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