The Oxidation Behavior of the √3×√3 Ag and Au/Si(111) Surfaces at Room Temperature Studied by Photoemission

1985 ◽  
Vol 54 ◽  
Author(s):  
J. J. Yeh ◽  
D. J. Friedman ◽  
R. Cao ◽  
J. Hwang ◽  
J. Nogami ◽  
...  

ABSTRACTThe differences of the room temperature oxidation behavior of ordered Ag/Si(111) and Au/Si(111) surfaces were studied by surface sensitive soft x-ray photoemission spectroscopy obtained with synchrotron radiation. Si surfaces covered with a monolayer of Ag or Au, once annealed to display a √3×√3 LEED pattern, were believed to be passivated against oxidation according to earlier reports. This work shows that these two surfaces oxidize but in a different way. Up to 104 L O2 exposures, the observed valence band of the Au/Si surface's valence band electron energy distribution curve is almost identical to that of the surface before oxygen exposure. But the corresponding Si 2p core level spectrum shows a small chemically shifted component indicating an initial stage of the formation of Si oxide. Thi3 chemically shifted signal becomes a strong peak at -3.7 eV below the clean Si position, characteristic of SiO2, after subsequent O2 exposures up to 1010 L. The Ag/Si system behaves in a similar fashion, but oxide growth saturates at 108 L, and the final oxides formed include a distribution of suboxides in addition to SiO2. Clearly, oxide formation is not prohibited by the presence of the ordered Au or Ag metal overlayer but delayed. Although the onset of oxidation is delayed compared to that for the clean Si surface, due to the metal-silicon bonding, the oxide formation is much faster once the surface starts to oxidize.

1982 ◽  
Vol 18 ◽  
Author(s):  
A. Cros ◽  
R. A. Pollak ◽  
K. N. Tu

The room temperature oxidation of PdSi, Pd2Si and Pd4Si has been studied using X-ray photoelectron spectroscopy (X-ray photoemission spectroscopy or electron spectroscopy for chemical analysis). We find that only silicon atoms in these silicides are oxidized and the oxidation of Pd4Si surfaces is enhanced compared with that of Pd2Si and PdSi, as is evidenced by both a higher silicon oxidation state and thicker oxide films. This behavior is discussed in terms of silicide stability and a spillover effect where palladium atoms catalyze molecular oxygen dissociation.


2014 ◽  
Vol 1019 ◽  
pp. 294-301
Author(s):  
H.C. Mantyi ◽  
L.A. Cornish ◽  
Lesley H. Chown ◽  
I. Alain Mwamba

Pure powders of titanium, aluminium, nickel and ruthenium were mechanically alloyed and melted in a button arc furnace under an argon atmosphere to produce two alloys of composition Ti-52.5Al-10.0Ni (at.%) and Ti-52.5Al-10.0Ni-0.2Ru (at.%). The alloys were then cut and metallographically prepared. Scanning electron microscopy (SEM) with energy dispersive X-ray spectroscopy (EDX) and X-ray diffraction (XRD) were used to characterize the samples. Thermogravimetric analysis (TGA) was used to analyze the oxidation behavior from room temperature up to 1050°C. The alloys were also oxidized in air at 1050°C for 120 hours. The Ti-52.5Al-10.0Ni (at.%) alloy formed dendrites of γ-TiAl (55.6 at.% Al) surrounded by a eutectic of γ-TiAl + Al3NiTi2 (τ3) phases. The Ti-52.5Al-10.0Ni-0.2Ru (at.%) alloy formed dendrites of γ-TiAl (53.6 at.% Al) surrounded by a eutectic of γ-TiAl + Al3NiTi2 (τ3). The ruthenium was mostly in solid solution (0.3 at.%) in the Al3NiTi2 (τ3) phase, although traces of it were present in the dendrites (0.1 at.% Ru). When oxidized in air from room temperature to 1050°C, the as-cast Ti-52.5Al-10.0Ni-0.2Ru (at.%) had a mass gain of 0.60% and the as-cast Ti-52.5Al-10.0Ni (at.%) had a mass gain of 0.97%. Isothermal oxidation of both alloys at 1050°C for 120 hours formed mixed metal oxides of TiO2+Al2O3 on the surface.


1998 ◽  
Vol 05 (01) ◽  
pp. 393-396 ◽  
Author(s):  
V. Di Castro ◽  
S. Ciampi ◽  
L. Sestili

The oxidation of a 9-Å-thick iron layer on MnO at room temperature has been investigated by X-ray photoelectron spectroscopy. By exposure to O 2, iron is oxidized first to Fe(II) and then to Fe(III). During the oxide formation a fast oxygen adsorption and initial oxidation to Fe(II) is followed by a slower oxygen incorporation and Fe(III) formation. After exposure to 1500 L O 2 Fe 3 O 4 seems to be formed at the surface, while the iron layer is not completely oxidized.


2005 ◽  
Vol 140 (4) ◽  
pp. 332-345 ◽  
Author(s):  
Ting Shi ◽  
Xiaofang Wang ◽  
Jun Deng ◽  
Zhenyi Wen

2018 ◽  
Vol 921 ◽  
pp. 168-176
Author(s):  
Chang Hai Zhou ◽  
Rui Yun Pan ◽  
Hai Tao Ma

The oxidation behavior of Fe-20Ni alloy under compressive stress in air was studied at 800, 900 °C. The results examined by using scanning electron microscope (SEM) and X-ray diffraction (XRD) indicates that the oxide scales were consisted of an external scale and a subscale which has an intragranular scale (above 5 h at 800 °C and 900 °C) and an intergranular scale. Compared with the unstressed specimen, the growth kinetics of external scale was accelerated by an applied compressive stress. Besides, the compressive stress induced an increase in the growths of intragranular scale and intergranular scale formed on the specimens oxidized at 900 °C. However, the effect of compressive stress on the growth of intergranular scale and intragranular scale was not obvious in the case of 800°C. In addition, cracks developed in the subscale for the specimens oxidized under 2.5 MPa compressive stress when the oxidation time exceeded 20 h.


2014 ◽  
Vol 941-944 ◽  
pp. 212-215
Author(s):  
Tao Zheng ◽  
Jing Tao Han

The oxidation behavior of SUS310S austenitic stainless steels was studied in isothermal conditions at different temperatures between 800oC and 1100oC for 96h in air. The oxidation kinetics was analyzed, the surface and cross-section of the oxide scale grown by oxidation were characterized by using scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), X-ray diffusion (XRD) and X-ray photoelectron spectroscopy (XPS). The SUS310S steel has high oxidation resistance at 800oC and with the increase of the temperature, the parabolic rate constants is constantly increasing. Examination of the morphology and composition of oxide layers reveals a double-layer structure, The inner layer is mainly chromium oxide (Cr2O3) and is covered by an uneven thinness outer layer of manganese-chromium or iron-chromium spinel oxide.


2010 ◽  
Vol 150 (41-42) ◽  
pp. 1991-1994 ◽  
Author(s):  
H.P. Song ◽  
G.L. Zheng ◽  
A.L. Yang ◽  
Y. Guo ◽  
H.Y. Wei ◽  
...  

1996 ◽  
Vol 68 (18) ◽  
pp. 2541-2543 ◽  
Author(s):  
G. Martin ◽  
A. Botchkarev ◽  
A. Rockett ◽  
H. Morkoç

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