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CHEMICAL VAPOR DEPOSITION OF THIN FILM MATERIALS FOR ...

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However, there is sizeable run-to-run growth rate variation for films grown at a specific<br />

temperature, particularly at higher deposition temperatures (up to 8%). The growth rate is<br />

sensitive to the position of the substrate in the reaction zone. This is likely related to the<br />

temperature and precursor concentration distribution in our hot wall tube reactor, which can be<br />

approximated by a plug flow reactor (PFR). From the vaporizer gas outlet to the substrate surface,<br />

the tube temperature gradually increases to the reaction zone temperature due to thermal<br />

conductance while the precursor concentration decreases because of thermal decomposition and<br />

deposition on the surrounding tube wall. The highest growth rate can be achieved over a<br />

particular region of the reactor because of a favorable combination of temperature and precursor<br />

concentration. By inspecting the color of the tube walls after each experiment, we found that<br />

most of the deposition occurs in a small volume (tube length of ~2 inch) close to the entrance of<br />

the reaction zone.<br />

To better understand the effect of precursor concentration in the solvent on the film<br />

growth rate, both half and double of the original concentration of the precursor solution (listed in<br />

Table 4) were employed for growth at a substrate temperature of 600˚C, with all the other<br />

process conditions held constant. The film growth increases almost linearly with increasing<br />

concentration (0.39, 0.75, and 1.42 μm hr respectively). The film deposited with lower<br />

concentration of precursors does not show any obvious change in surface roughness and<br />

chemical composition. However, the enhanced growth rate obtained for deposition with the<br />

higher concentration is compromised by increased surface roughness and an Fe rich<br />

stoichiometry. From a mass-transfer limited assumption, it is possible that the increased<br />

concentrations of Ni and Fe species in the hydrodynamic boundary layer affect their relative<br />

diffusion rates,[85] however, mass transfer limitations are not easily determined in this set-up<br />

81

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