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Hafnium oxide films have been deposited on silicon substrates by metal organic chemical vapor deposition using the novel single precursor, hafnium 3-methyl-3-pentoxide {Hf[OC(CH 3 )(C 2 H 5 ) 2 ] 4, Hf(mp) 4 }, with no additional oxygen source, and the deposition mechanism was elucidated. Hf(mp) 4 is a liquid at room temperature and has a moderate vapor pressure comparable to that of hafnium tert -butoxide, Hf(O t Bu) 4, and a lower residual weight (<10%) in thermogravimetric analysis. The deposition rate was found to be ∼27 Å/min at 400 °C, and the activation energy was 68.1 kJ/mol, which is higher than those of other hafnium alkoxide and hafnium amide precursors. By gas chromatography/mass spectroscopy and nuclear magnetic resonance analyses of the thermally decomposed vapor phase products collected during the deposition of HfO 2 films, it was clearly found that they are grown via β-hydrogen elimination processes of the Hf(mp) 4 single precursor. Negligible carbon incorporation of the HfO 2 films, examined by X-ray photoelectron spectroscopy and depth-profiling Auger electron spectroscopy, indicates that, except for the β-hydrogen elimination processes, no additional decomposition and/or recombination processes contributed to the HfO 2 film growth. The morphology, crystallinity, and electrical properties of the HfO 2 films were characterized by scanning electron microscopy, atomic force microscopy, X-ray diffraction, and capacitance−voltage and current−voltage measurements.
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Yang et al. (2005) studied this question.
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