Nitrogen-infused wet oxidation at
different temperatures (400–1000 °C) was employed to transform
tantalum–hafnia to hafnium-doped tantalum oxide films. High-temperature
wet oxidation at 1000 °C marked an onset of crystallization occurring
in the film, accompanied with the formation of an interfacial oxide
due to a reaction between the inward-diffusing hydroxide ions, which
were dissociated from the water molecules during wet oxidation. The
existence of nitrogen has assisted in controlling the interfacial
oxide formation. However, high-temperature oxidation caused a tendency
for the nitrogen to desorb and form N–H complex after reacting
with the hydroxide ions. Besides, the presence of N–H complex
implied a decrease in the passivation at the oxide–Si interface
by hydrogen. As a consequence, defect formation would happen at the
interface and influence the metal–oxide–semiconductor
characteristics of the samples. In comparison, tantalum–hafnia
subjected to nitrogen-infused wet oxidation at 600 °C has obtained
the highest dielectric constant, the largest band gap, and the lowest
slow trap density.