Field-induced reversible insulator-to-metal transition and the onset of ferroelectricity in molybdenum trioxide films

This paper presents the experimental evidence of reversible insulator-metal transition (IMT) in thin-film amorphous molybdenum trioxide (MoO3) induced by electric fields of just a few volts. The presence of oxygen vacancies in MoO3 is considered to play a significant role in the reported reversible IMT. The oxygen vacancies not only impact MoO3 stoichiometry but also the optical bandgap. The subthreshold slope for IMT in 10 nm-thick MoO3-based devices is 48.3 mV/decade, which represents a transition from an insulator to a metallic state, and the electric field threshold for such a transition was found to be equal to 0.034 V/A. Following the IMT in MoO3, there are six orders of magnitude differences between the resistivity of the insulator state (27.5M Omega O at -9 V) and the metallic state (80 Omega between +5 and +9 V). In addition, we reported stabilization of a nanocrystalline hexagonal MoO3 (h-MoO3) phase in thicker MoO3 (150 nm-thick) in the presence of oxygen vacancies that behave as a wide bandgap (3.1 eV) ferroelectric semiconductor with a coercive field of about 50 kV/cm, a saturation polarization of about 30 mu C/cm(2), and a remanent polarization of about 10 mu C/cm(2). This ferroelectricity in nanocrystalline h-MoO3 (150 nm-thick) remains stable even after 8 months of storage of the sample in ambient conditions, with remanent polarization increasing up to 20 mu C/cm(2). These are unexpected results from MoO3. Published under an exclusive license by AIP Publishing.