Room-temperature atomic layer deposition of iron oxide using plasma excited humidified argon

Room-temperature atomic layer deposition (RT-ALD) of iron oxide is developed with a precursor of bis(N, N & PRIME;-diisopropyl-propionamidinate)iron [(DIPPA)(2)Fe] and plasma excited humidified Ar. Saturated conditions of (DIPPA)(2)Fe and plasma excited humidified Ar exposures at room temperature (23-25 & DEG;C) are investigated by in situ IR absorption spectroscopy for finding the RT-ALD process condition. Using the designated process, the growth per cycle of the iron oxide RT-ALD is confirmed as 0.15 nm/cycle based on the film thicknesses measured by the spectroscopic ellipsometer. The x-ray photoelectron spectroscopy suggests that the stoichiometry of the deposited iron oxide is closed to that of Fe2O3. The grown film is composed of partly crystallized iron oxides, confirmed by cross-sectional TEM and AFM. The RT deposited iron oxide exhibits a magnetic volume susceptibility of 1.52, which implies the applicability of the present coating for magnetic drug delivery. We discuss the surface reaction with the IR absorption spectroscopy and the quartz crystal microbalance. The (DIPPA)(2)Fe molecule is suggested to adsorb on the Fe2O3 surface with mixed first- and second-order reactions at RT. It is also suggested that amidinate ligands in (DIPPA)(2)Fe are released in the course of the adsorption and the remaining ligands are oxidized by the plasma excited humidified Ar. The RT iron oxide deposition is demonstrated, and the reaction mechanism of room-temperature ALD is discussed in this paper.& nbsp;