Revisiting NO2 on Ag(111):: a detailed TPD and RAIRS study

被引:32
|
作者
Huang, WX [1 ]
White, JM [1 ]
机构
[1] Univ Texas, Ctr Mat Chem, Dept Chem & Biochem, Austin, TX 78712 USA
关键词
infrared absorption spectroscopy; thermal desorption; surface chemical reaction; silver; nitrogen oxides; single crystal surfaces;
D O I
10.1016/S0039-6028(03)00332-7
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The interactions of NO2 with Ag(1 1 1) at various temperatures were investigated by means of temperature programmed desorption and reflection-adsorption infrared spectroscopy and found to be sensitively coverage- and temperature-dependent. During dosing at 508 K, NO2 decomposes into NO(g) and O(a). NO2 decomposes at 215 K also, however, NO and 0 remain adsorbed. The NO(a) occupy threefold-bridged sites and atop sites in sequence. Orientations of the NO(a) axes are affected by neighboring O(a). A sharp and narrow desorption peak (gamma-NO) arises for high NO2 doses. During dosing at 90 K, decomposition occurs initially and is followed sequentially by accumulation of NO2(a), NO3(a), N2O4 monolayer and N2O4 multilayer. NO2(a) chemisorbs to form a Ag(1 1 1) mu-N, O-nitrito surface chelate with C, symmetry. Upon heating, the N2O4 multilayer and monolayer desorb molecularly while most NO2(a) disproportionates into NO(g) or NO(a) and NO3(a) at 165 K. Surface NO3(a) decomposes below 320 K. All surface species except O(a) desorb below 500 K. (C) 2003 Published by Elsevier Science B.V.
引用
收藏
页码:455 / 470
页数:16
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