The thermal desorption mass spectra of hydrogenated and water treated diamond powders were measured in the range from room temperature to 1250Β°C. After preliminary outgassing up to 1150Β°C. samples were either hydrogenated under 1 Pa hydrogen at 500-IOOOY or treated in water vapor at room temperature
Thermal desorption spectra of the oxidized surfaces of diamond powders
β Scribed by S Matsumoto; H Kanda; Y Sato; N Setaka
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- English
- Weight
- 425 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0008-6223
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β¦ Synopsis
Thermal desorption mass spectrometry was carried out in the range from room temperature to 960Β°C for the diamond powders oxidized in 10-2Torr 0, at temperatures from 25 to SSCC. The spectra show two desorption peaks (a., p) and the major peak (I seems to consist of at least four types of adsorption states (a, -a.,). The first state a, may arise from "labile" carbon atoms created during degassing, and disappears with high temperature oxidation changing into the more stable states (a? -q). IR absorption spectroscopy shows that (Ye -a4 states include carbonyl and ether structures. The minor peak /3 shows little change with oxidation temperature. The amount of oxygen chemisorbcd at 420Β°C (1.22 x 10'5atom/cm2) is in good agreement with the estimated value of full coverage.
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The thermal decomposition of surface oxides formed during the low pressure oxidation of Graphon was studied. Oxidation reactions were performed at 525", 575" and 625Β°C in a static reactor, using initial 0, pressures between 10 and 200 mtorr. The amount of surface oxide formed was found to increase w