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Oxidation features

Figure 4 shows a sequence of cyclic voltammograms recorded in a CO saturated solution of 0.5 M H.SO, which contained 10-5 M SnCl,. These voltammograms were recorded by increasing the upper limit of the potential during successive cycles. The major feature is the CO oxidation peak at 0.6 V(SCE) that is observed in the later scans. For cycles with an upper limit below this potential, there is a second, smaller oxidation feature at about 0.4 V. Control experiments using an SnCl /H.SO solution without CO show that this feature can be assigned to the oxidation of adsorbed Sn atoms. We note that the Sn oxidation step does not produce a well-resolved current maximum in the curves in Figure 4. We interpret this to indicate that adsorbed CO molecules are rapidly oxidized by newly generated Sn cations, thus regenerating the Sn adatoms and allowing further oxidation current to flow. Figure 4 shows a sequence of cyclic voltammograms recorded in a CO saturated solution of 0.5 M H.SO, which contained 10-5 M SnCl,. These voltammograms were recorded by increasing the upper limit of the potential during successive cycles. The major feature is the CO oxidation peak at 0.6 V(SCE) that is observed in the later scans. For cycles with an upper limit below this potential, there is a second, smaller oxidation feature at about 0.4 V. Control experiments using an SnCl /H.SO solution without CO show that this feature can be assigned to the oxidation of adsorbed Sn atoms. We note that the Sn oxidation step does not produce a well-resolved current maximum in the curves in Figure 4. We interpret this to indicate that adsorbed CO molecules are rapidly oxidized by newly generated Sn cations, thus regenerating the Sn adatoms and allowing further oxidation current to flow.
As the upper limit of the cycles approaches 0.5 V, the size of the Sn oxidation feature gradually decays. Cycles with an upper limit above 0.6 V are virtually indistinguishable from those recorded in CO saturated H.SO. without added SnCl,. This indicates... [Pg.378]

From the result obtained here, it is not known whether the adsorbate is only CO or other specie are also included. The oxidation features of adsorbates, however, are virtually the same with COad- Therefore it is practical to treat them simply as COad when the detail mechanisms are not the issue. [Pg.142]

Electrochemical and spectroscopic studies confirmed that COad the mayor adsorbates. The oxidation features of adsorbates are virtually the same with COad-... [Pg.190]

When an equivalently prepared surface was first scanned in the positive direction, Eig. 70B was obtained. There appear to be two components to the oxidation feature a peak at about 0.15 V superimposed on a slowly increasing background. Auger spectra of the resulting surface showed a marked decrease in the signal for Cd, indicating that some had been removed. In addition, the (1 X 1) LEED pattern was no longer present—... [Pg.189]

In addition to controlling the standard process parameters such as down force and the relative velocity, it is also important to have random access capability to route wafers through a CMP tool to optimize both performance and throughput. Low-down-force processes and special CMP pads are likely to be necessary to reduce copper dishing just as they improve oxide planarization. Furthermore, a balance between high relative velocity to reduce copper dishing and moderate relative velocity to minimize the sheering of small oxide feature may be necessary. [Pg.38]

A number of other cubane complexes of V(IV) have been reported. [Cp V(N)]4 can be reduced reversibly at Ef = 0.16 V versus Cp2Fe/THF [71]. A similar cubane complex [TpV(03P0Ph)]4 where phosphate groups bridge three TpV units displays four oxidation features, of which two are reversible (0.68, 1.13 V versus Ag/AgCl/CH2Cl2) and two are irreversible. Although bulk electrolysis at a potential suitable to remove one electron from the complex resulted in decomposition [72]. [Pg.371]

A second additional pattern dependent effect needs to be accounted for. As illustrated in the right side of Fig. 14, the effective oxide removal rate (which is modified in the removal rate diagram by the effective density) may also have an oxide space width dependence. That is, the removal rate diagram already accounts for the effective density, but for small oxide space sizes one observes even faster removal of the oxide space than density alone explains. We conjecture a relationship as shown in Fig. 14 based on localized high pressures near the edges of raised features. From contact wear analysis, as the oxide space width becomes small these high pressure peaks extend over a larger portion of the entire oxide feature and accelerate the oxide removal. [Pg.207]

Well-ordered AI2O3 films have been prepared using an A1 deposition rate of 0.5 MLE.min (equivalent monolayer, calibrated on an Mo(llO) substrate using AES and TPD), at a background O2 pressure of 7 x 10 Torr, and an Mo(llO) substrate temperature at 300 K [58]. Following deposition, the films were annealed to 1200 K in O2 to improve the film order. Figure 1 shows representative AES spectra of alumina films at two different thicknesses [58]. An AES spectrum of a 2.0-nm film has a predominant Al (LVV) transition at 45 eV and an O (KLL) transition at 500 eV. The absence of a peak at 68 eV, characteristic of Al°, indicates that the film is fully oxidized. Features attributable to the Mo(llO) substrate can be seen in the 100-250-eV region. The thickness of the oxide films was calculated from the attenuation of the AES intensity ratio of the Al (LVV) feature relative to the Mo(MNN) feature. [Pg.307]

The solid line in Fig. 24 shows the CO stripping reaction from this surface. Subsequently, the experiment was restarted, and a new Pt(lll) surface was exposed to the Ru-containing solution, rinsed, and transferred to the electrochemical cell. Such a freshly prepared Ru/Au(lll) electrode was exposed to CO without electrochemical stabilization of the deposit. The dashed line in Fig. 24 shows the CO oxidation features obtained from this procedure. The data clearly indicate that most of the freshly prepared Ru precursor was... [Pg.108]

Beside the very low nitric oxide emissions that can be obtained even with high air preheating, the flameless oxidation features other interesting aspects such as ... [Pg.485]

Relationship between structures and unit cells of tet-PbO and pseudo-cubic oxides, (a) structure of tet-PbO (b) Structure of pseudo-cubic oxide featuring intercalated oxygen layer and changed co-ordination around Pb and O (c) Stacking sequence and principal dimensional changes [36]. [Pg.62]

Tetrafluoroethylene oxide features, with perfluoropropene oxide, in recent Russian work on fluoride-initiated reactions of perfluorodicarboxylic acid fluorides (perfluoromalonyl and perfluoroadipoyl difluoride) with peifluoro-oxirans,... [Pg.278]

Uses Antiskinning agent for air-drying alkyds, air-drying oils, oil-modified PU resins, paints/coatings that dry by oxidation Features Prevents formation of top film/skin on storage minimal effect on drying and film props. [Pg.348]

In the work of Yue-feng et al. (2007) were measured three galvanostatic curves for three positive electrodes containing various amounts of Ru. Capacitance of PsCs grows at an increase in the content of ruthenium. Besides, these curves are close to straight lines and this confirms that electrodes with ruthenium oxides feature capacitive behavior described by Conway (1999) (see above). [Pg.318]

This study deals with the preparation, properties and reactivity of high-surface-area Ni/Mg/Al mixed oxides featuring different Ni g ratios obtained from HT anionic clays. In HT precipitates all cations are present inside the brucite- pe layers, therefore the specific properties of each element may be evidenced without any interfraence due to phase segregation and/or physical dishomogeneity. [Pg.894]

The effect of temperature on CO oxidation is illustrated in Figure 2.6. It can be seen that increasing temperature shifts the electro-oxidation features... [Pg.60]


See other pages where Oxidation features is mentioned: [Pg.472]    [Pg.139]    [Pg.113]    [Pg.365]    [Pg.245]    [Pg.156]    [Pg.431]    [Pg.329]    [Pg.198]    [Pg.36]    [Pg.57]    [Pg.394]    [Pg.396]    [Pg.36]    [Pg.57]    [Pg.3858]    [Pg.197]    [Pg.365]    [Pg.198]    [Pg.65]    [Pg.103]    [Pg.383]    [Pg.665]    [Pg.207]    [Pg.245]    [Pg.410]    [Pg.267]    [Pg.432]    [Pg.380]    [Pg.1439]    [Pg.3907]    [Pg.119]   


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