<p>Perovskite nickelates ReNiO<sub>3</sub>,
where Re stands for rare earth elements like La, Nd, Sm … etc, display
metal-insulator transition (MIT) due to temperature variation and/or electron
doping. In this work, perovskite nickelate thin films were deposited by physical
vapor deposition (PVD) and chemical solution deposition (CSD) on LaAlO<sub>3</sub>
(LAO) substrate for epitaxial single-crystalline phase or on other substrates
such as Si / SiO<sub>2</sub> and fluorine doped tin oxide coated glass (FTO
glass) for the polycrystalline phase. Detailed deposition parameters will be
discussed and the thin film characteristics by the two deposition methods will
be compared.</p>
<p>Redox reactions between pristine
conducting phase (Ni<sup>3+</sup>) and correlated insulating phase (Ni<sup>2+</sup>),
controlling the band gap as well as the optical transparency of nickelates,
lead to the electrochromic activities of NdNiO<sub>3</sub> (NNO) thin films in
smart window applications. Both CSD-NNO and PVD-NNO thin films on LAO
substrates were systematically studied by electrochemical testing, including
cyclic voltammetry scans and bleaching/coloration treatments in an electrolyte.
A three-electrode set up was utilized with NNO thin film as the working
electrode and pH 12 KOH aqueous solution as the electrolyte. It was confirmed
that both CSD-NNO and PVD-NNO are electrochemically stable in the chosen
solution and the optical transmittance of the NNO films is highly tunable. One
significant advantage for CSD-NNO over PVD-NNO is the stronger electrochromic
activity due to the porous nature of the films prepared by CSD method.</p>
<p>The electron-doping induced
conductivity modulation of 10<sup>8 </sup>orders of magnitude motivates the
design of electronic devices with nickelates. During the process of platinum
(Pt) or palladium (Pd) assisted hydrogenation of nickelate thin films, the
nickel ions in the pristine state will be reduced due to the electron doping
while the protons will remain in perovskite lattice as interstitial defects.
The electron doping not only opens the energy band gap of the material, but
also creates a Schottky barrier at the metal-semiconductor interface
simultaneously. We will present an asymmetrical memory device with two
terminals, one side Pd and the other side Au, fabricated on SmNiO<sub>3</sub>
or NdNiO<sub>3</sub> thin films by e-beam lithography and photo lithography.
The charge carrier transport mechanisms of the devices will be discussed with
the current-voltage (I-V) characteristic analysis and resistance-temperature
(R-T) dependence study. In addition, collaborative work based on such
micro-nano devices including X-ray absorption (XAS) mapping affirming the
proton drift under external electrical fields and more device performances with
potential applications in neuromorphic computing and artificial intelligence,
will be discussed.</p>
LaNiO<sub>3</sub> (LNO),
as the only member of rare earth nickelates which does not display thermally
driven MIT, has been constructed in literature with structural modifications
such as LNO/LAO superlattice or ultrathin LNO with only a few unit-cell
thickness, to obtain MIT depending on temperature. Here we have successfully
deposited epitaxial LNO thin films on LAO substrates by CSD method with two
different solution concentrations (0.1M and 0.2M) resulting two sets of films,
namely 0.1M-LNO and 0.2M-LNO, with different thicknesses. Like other nickelates
such as SNO or NNO, the conductivity of LNO can also be suppressed by Pt
assisted electron doping which turns the pristine metallic LNO into insulating
H-LNO. LNO is so sensitive to hydrogen that its conductivity even shows
response at room temperature in H<sub>2</sub> rich gas. A series of devices
with “+” shaped LNO thin films were designed and fabricated by photo
lithography, with Pd electrodes at the film center and Au electrodes at four
corners. Devices fabricated on both 0.1M-LNO and 0.2M-LNO thin films showed
resistive switching and synaptic behavior across Pd-LNO-Au connection,
triggered by voltage pulses with a duration of hundreds of nanoseconds. The
detailed resistive switching mechanisms is proposed based on the electrical testing
results and thin film characterization. <br>