A724 N. NESHEV Insiitute Received
of Kinetics and Catalysis, Bulgarian Academy 16 July 1984; accepted
for publication
of Sciences, 1040 Sofia, Bulgaria
17 July 1985
Oxygen adsorption on a Mo(ll1) surface is investigated at low pressures (lo-’ to 10e5 Pa) and room temperature by Auger electron spectroscopy (AES), low-energy electron diffraction (LEED), X-ray photoelectron spectroscopy (XPS) and ultra-violet photoelectron spectroscopy (UPS). In agreement with previous studies it is established that the surface is not reconstructed during adsorption and the oxygen forms no ordered structures. On the basis of kinetic and spectroscopy data, the formation of two adsorption states on the surface within 1 monolayer is established. The valence band of a clean surface is studied in detail.. An attempt is made to ascribe the peaks obtained to definite d states. The interaction between 0, and Mo(ll1) is discussed in terms of the results obtained and a comparison with the O,/W(lll) system is made.
209
Surface Science 164 (1985) 209-219 North-Holland, Amsterdam
SSIMS AND TDS INVESTIGATION DURING CO AND O2 EXPOSURE V. MATOLIN
*, S. CHANNAKHONE
OF CO ADSORPTION and E. GILLET
Laboratoire de Microscopic et Diffractions Electroniques, Faculte des Sciences et Techniques de Saint-Jerome, F- 13397 Marseille Cedex 13, France Received
14 November
1984; accepted
ON Pd(ll1)
for publication
UA 797,
19 July 1985
The CO adsorption on Pd(ll1) under the conditions of CO catalytic oxidation (i.e. at various surface temperature) has been studied using the techniques of thermal desorption spectroscopy (TDS) and static secondary ion mass spectroscopy (SSIMS). The linear relationship between the sum of ion intensity ratios C,(Pd.CO+/PdT) and CO coverage was confirmed combining the TDS and SSIMS data. The possibility of the adsorbate structure investigation by SSIMS method during catalytic reaction was demonstrated. The TDS data, obtained under catalytic conditions (without stopping CO + 0, exposure) made it possible to determine the catalytic turnover rate as a function of CO coverage.
Surface
220
Science 164 (1985) 220-234 North-Holland, Amsterdam
ANGLE-RESOLVED PHOTOEMISSION OF THE c(2 X 2) AND c(3 X 1) OXYGEN OVERLAYERS ON Fe(ll0) Y. SAKISAKA, T. KOMEDA, T. MIYANO and M. ONCHI Department
of Chemistry,
Faculty of Science, Kyoto University, Kyoto 606, Japan
S. MASUDA and Y. HARADA Department Japan
of Chemistry,
College of Arts and Sciences,
University
of Tokyo, Komaba,
Tokyo 153,