Fabrication of correlated electron material devices

1. A method comprising:

exposing a substrate, in a chamber, to a first precursor in a gaseous state, the first precursor comprising a transition metal oxide, a transition metal or a transition metal compound, or any combination thereof, and a first ligand;

exposing the substrate to a second precursor in a gaseous state, the second precursor comprising an oxide so as to form a first layer of a film of correlated electron material; and

repeating the exposing of the substrate to the first and second precursors a sufficient number of times so as to form additional layers of the film of correlated electron material, the film of correlated electron material exhibiting a first impedance state and a second impedance state, the first impedance state and the second impedance state to be substantially dissimilar from one another, at least 90% of the atomic concentration of the film of correlated electron material comprising the transition metal, the transition metal oxide the transition metal compound, or any combination thereof.

2. The method of claim 1 , wherein the film of correlated electron material comprises an electron back-donating material in an atomic concentration of between 0.1% and 10.0%.

3. The method of claim 2 , wherein the electron back-donating material comprises carbonyl.

4. The method of claim 1 , further comprising purging the chamber of the first precursor for between 0.5 seconds and 180.0 seconds.

5. The method of claim 1 , wherein the exposing of the substrate to the first precursor occurs over a duration of between 0.5 seconds and 180.0 seconds.

6. The method of claim 1 , further comprising repeating the exposing of the substrate between 50 and 900 times.

7. The method of claim 1 , further comprising repeating the exposing of the substrate until a thickness of the film of correlated electron material reaches between 1.5 nm and 150.0 nm.

8. The method of claim 1 , the first precursor comprising nickel amidinate (Ni(AMD)), nickel dicyclopentadienyl (Ni(Cp) 2 ), nickel diethylcyclopentadienyl (Ni(EtCp) 2 ), Bis(2,2,6,6-tetramethylheptane-3,5-dionato)Ni(II) (Ni(thd) 2 ), nickel acetylacetonate (Ni(acac) 2 ), bis(methylcyclopentadienyl)nickel (Ni(CH 3 C 5 H 4 ) 2 ), nickel dimethylglyoximate (Ni(dmg) 2 ), nickel 2-amino-pent-2-en-4-onato (Ni(apo) 2 ), Ni(dmamb) 2 (in which dmamb=1-dimethylamino-2-methyl-2-butanolate), Ni(dmamp) 2 (in which dmamp=1-dimethylamino-2-methyl-2-propanolate), Bis(pentamethylcyclopentadienyl)nickel (Ni(C 5 (CH 3 ) 5 ) 2 ) or nickel carbonyl (Ni(CO) 4 ), or any combination thereof.

9. The method of claim 1 , wherein the second precursor comprises oxygen (O 2 ), ozone (O 3 ), water (H 2 O), nitric oxide (NO), nitrous oxide (N 2 O) or hydrogen peroxide (H 2 O 2 ), or any combination thereof.

10. The method of claim 1 , wherein the exposing of the substrate to the first precursor, the exposing of the substrate to a second precursor, or any combination thereof, occurs at a temperature of between 20.0° and 1000.0° C.

11. The method of claim 1 , additionally comprising annealing the exposed substrate in the chamber.

12. The method of claim 11 , further comprising raising the temperature of the chamber to between 20.0° C. and 900.0° C. prior to initiating the annealing.

13. The method of claim 11 , wherein the exposed substrate is annealed in an environment comprising gaseous nitrogen (N 2 ), hydrogen (H 2 ), oxygen (O 2 ), water or steam (H 2 O), nitric oxide (NO), nitrous oxide (N 2 O), nitrogen dioxide (NO 2 ), ozone (O 3 ), argon (Ar), helium (He), ammonia (NH 3 ), carbon monoxide (CO), methane (CH 4 ), acetylene (C 2 H 2 ), ethane (C 2 H 6 ), propane (C 3 H 8 ), ethylene (C 2 H 4 ) or butane (C 4 H 10 ), or any combination thereof.

14. The method of claim 1 , wherein the transition metal comprises aluminum, cadmium, chromium, cobalt, copper, gold, iron, manganese, mercury, molybdenum, nickel, palladium, rhenium, ruthenium, silver, tin, titanium, vanadium, or zinc.