CO2 as a probe for monitoring the surface defects on TiO2(110) -: Temperature-programmed Desorption

被引:135
作者
Thompson, TL [1 ]
Diwald, O [1 ]
Yates, JT [1 ]
机构
[1] Univ Pittsburgh, Ctr Surface Sci, Dept Chem, Pittsburgh, PA 15260 USA
关键词
D O I
10.1021/jp030430m
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 adsorption and thermal desorption of CO2 bound to both oxidized and reduced TiO2(110) surfaces has been studied using temperature-programmed desorption. For the stoichiometric and fully oxidized surface, a single thermal desorption feature (E-d = 48.5 kJ/mol) is measured and attributed to CO2 bound to regular fivefold coordinated Till atoms. For the fully reduced TiO2(110) surface, CO2 binds not only to regular sites, but also to oxygen vacancy sites (E-d = 54.0 kJ/mol), created by thermal annealing. The variation in the characteristic CO2 desorption kinetics was measured as a function of the surface reduction temperature, and the systematic production of increasing levels of surface defects is observed in the temperature range of 600-1100 K. This investigation was complimented by a comparison of the characteristic CO2 desorption features from a TiO2(110) surface which was prepared by sputtering and direct annealing, without annealing in O-2 flux. It was found that after annealing to temperatures above 900 K, the CO2 thermal desorption is very similar for surfaces prepared by the two methods, regardless of surface preparation.
引用
收藏
页码:11700 / 11704
页数:5
相关论文
共 24 条
[1]   The surface science of titanium dioxide [J].
Diebold, U .
SURFACE SCIENCE REPORTS, 2003, 48 (5-8) :53-229
[2]   Intrinsic defects on a TiO2(110)(1x1) surface and their reaction with oxygen:: a scanning tunneling microscopy study [J].
Diebold, U ;
Lehman, J ;
Mahmoud, T ;
Kuhn, M ;
Leonardelli, G ;
Hebenstreit, W ;
Schmid, M ;
Varga, P .
SURFACE SCIENCE, 1998, 411 (1-2) :137-153
[3]   Evidence for the tunneling site on transition-metal oxides: TiO2(110) [J].
Diebold, U ;
Anderson, JF ;
Ng, KO ;
Vanderbilt, D .
PHYSICAL REVIEW LETTERS, 1996, 77 (07) :1322-1325
[4]   INTRINSIC DEFECTS OF TIO2(110) - INTERACTION WITH CHEMISORBED O2, H-2, CO, AND CO2 [J].
GOPEL, W ;
ROCKER, G ;
FEIERABEND, R .
PHYSICAL REVIEW B, 1983, 28 (06) :3427-3438
[5]   PHOTOLYSIS OF CHEMISORBED DIOXYGEN ON PD(111) - DEPENDENCE ON PHOTON ENERGY [J].
HANLEY, L ;
GUO, XC ;
YATES, JT .
JOURNAL OF CHEMICAL PHYSICS, 1989, 91 (11) :7220-7227
[6]   Interaction of molecular oxygen with the vacuum-annealed TiO2(110) surface:: Molecular and dissociative channels [J].
Henderson, MA ;
Epling, WS ;
Perkins, CL ;
Peden, CHF ;
Diebold, U .
JOURNAL OF PHYSICAL CHEMISTRY B, 1999, 103 (25) :5328-5337
[7]   Surface perspective on self-diffusion in rutile TiO2 [J].
Henderson, MA .
SURFACE SCIENCE, 1999, 419 (2-3) :174-187
[8]   Evidence for bicarbonate formation on vacuum annealed TiO2(110) resulting from a precursor-mediated interaction between CO2 and H2O [J].
Henderson, MA .
SURFACE SCIENCE, 1998, 400 (1-3) :203-219
[9]   Oxygen-induced restructuring of the TiO2(110) surface:: a comprehensive study [J].
Li, M ;
Hebenstreit, W ;
Gross, L ;
Diebold, U ;
Henderson, MA ;
Jennison, DR ;
Schultz, PA ;
Sears, MP .
SURFACE SCIENCE, 1999, 437 (1-2) :173-190
[10]   FTIR study of adsorption and photoassisted oxygen isotopic exchange of carbon monoxide, carbon dioxide, carbonate, and formate on TiO2 [J].
Liao, LF ;
Lien, CF ;
Shieh, DL ;
Chen, MT ;
Lin, JL .
JOURNAL OF PHYSICAL CHEMISTRY B, 2002, 106 (43) :11240-11245