Over the past decade, SnO has been considered a promising
p-type
oxide semiconductor. However, achieving high mobility in the fabrication
of p-type SnO films is still highly dependent on the post-annealing
procedure, which is often used to make SnO, due to its metastable
nature, readily convertible to SnO2 and/or intermediate
phases. This paper demonstrates a fully room-temperature fabrication
of p-type SnO
x
thin films using ion-beam-assisted
deposition. This technique offers independent control between ion
density, via the ion-gun anode current and oxygen flow rate, and ion
energy, via the ion-gun anode voltage, thus being able to optimize
the optical band gap and the hole mobility of the SnO films to reach
2.70 eV and 7.89 cm2 V–1 s–1, respectively, without the need for annealing. Remarkably, this
is the highest mobility reported for p-type SnO films whose fabrication
was carried out entirely at room temperature. Using first-principles
calculations, we rationalize that the high mobility is associated
with the fine-tuning of the Sn-rich-related defects and lattice densification,
obtained by controlling the density and energy of the oxygen ions,
both of which optimize the spatial overlap of the valence bands to
form a continuous conduction path for the holes. Moreover, due to
the absence of the annealing process, the Raman spectra reveal no
significant signatures of microcrystal formation in the films. This
behavior contrasts with the case involving the air-annealing procedure,
where a complex interaction occurs between the formation of SnO microcrystals
and the formation of SnO
x
intermediate
phases. This interplay results in variations in grain texture within
the film, leading to a lower optimum Hall mobility of only 5.17 cm2 V–1 s–1. Finally, we
demonstrate the rectification characteristics of all-fabricated-at-room-temperature
SnO
x
-based p–n devices to confirm
the viability of the p-type SnO
x
films.