Title of article :
Oxidation of the hydrogenated diamond (100) surface
Author/Authors :
Pehrsson، نويسنده , , Pehr E and Mercer، نويسنده , , Thomas W، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2000
Abstract :
The surface composition and structure of natural diamond (100) surfaces subsequently oxidized with activated oxygen at Tsub≤35°C were investigated with high-resolution electron energy loss spectroscopy (HREELS), Auger electron spectroscopy, electron loss spectroscopy (ELS) and low-energy electron diffraction (LEED). Complete surface oxidation (oxygen coverage θ=1 ML) required doses of hundreds of kilolangmuirs of O2. HREELS vibrational spectra permitted identification of the specific surface oxygen species, and also provided information about the diamond surface states. Most surface sites lost their hydrogen at least once before becoming oxidized. The oxygen coverage θ increased quickly at first, and then more slowly as saturation was approached; different mechanisms or sites may have accounted for the decreased rate. The relative distribution of oxygen species varied with the oxidation conditions. Ether, carbonyl and hydroxyl groups appeared during the initial stages of oxidation, but the hydroxyl groups disappeared at higher coverages. Bridge-bonded ether groups dominated at saturation coverage, although smaller amounts of carbonyl and hydroxyl were still observed. The carbonyl and CH stretch frequencies increased with oxygen dose due to formation of higher oxidation states and/or hydrogen bonding between adjacent groups. ELS revealed only a low concentration of CC dimers on the oxidized surfaces, and no evidence of graphitization.
es generated by oxygen addition and then desorption were more reactive than surfaces generated by hydrogen desorption. Oxidized surfaces that were heated in vacuum and then rehydrogenated did not recover the sharp LEED patterns and HREELS spectra of the original plasma-smoothed surface. This effect was presumably due to surface roughening caused by oxygen desorption as CO and CO2, and creation of reactive high-energy sites that quickly bonded to available background gases and prevented large areas of organized surface reconstruction.
Keywords :
Electron energy loss spectroscopy (EELS) , Oxidation , diamond , Low energy electron diffraction (LEED) , Surface chemical reaction , Oxygen , Auger electron spectroscopy , Low index single crystal surfaces
Journal title :
Surface Science
Journal title :
Surface Science