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Diagnosis of Diamond Film Growth

In the past years there have been an increasing number of studies identifying the primary gas-phase diamond growth precursor [65, 67, 80-87] in CVD techniques, which have been the subject of controversy. The growth rate and film quahty of materials synthesized by CVD processes depend critically on the composition of the species generated. [Pg.145]

Maity techniques exist for examining the composition of the species (including radical species) generated in CVD reactors optical emission spectroscopy (OES) [80], FT-IR spectroscopy [81] laser induced fluorescence (LIE) spectroscopy [82], diode laser IR absorption spectroscopy [83], and MS [84-87]. Each has its own strengths and shortcomings. A major advantage of MS over other techniques is its [Pg.145]

A detailed chemical kinetic mechanism was composed to describe the evolution of reaction species [88-92] in the pyrolysis of a hydrogen-diluted CH mixture, simulating the gas-phase conditions of diamond CVD in the MW reactor. Somewhat surprisingly atomic C is predicted [88] to have a large concentration at the surface. C atoms could conceivably play a role in diamond growth [90], [Pg.146]

The lAMS technique is applied in a simulation study of a diamond CVD reactor [93], It is most advantageous when the experimenter does not know a priori what species to expect. A second advantage is its adaptability to a wide variety of process environments. To simulate the reacting plasma environment, a sampling aperture, followed by the skimmer, is fixed at the center of the growth substrate (Fig. 5.8). Mass spectra were obtained (Fig. 5.9) with plasma activation in two modes (i) [Pg.146]


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