Sequential infiltration synthesis of group 13 oxide electronic materials

Patent metadata

Field	Value
Publication number	US-12104249-B2
Application number	US-201916515718-A
Country	US
Kind code	B2
Filing date	Jul 18, 2019
Priority date	Jul 18, 2019
Publication date	Oct 1, 2024
Grant date	Oct 1, 2024

Abstract

The sequential infiltration synthesis (SIS) of group 13 indium and gallium oxides (In2O3 and Ga2O3) into polymethyl methacrylate (PMMA) thin films is demonstrated. Examples highlight the an SIS process using trimethylindium (TMIn) and trimethylgallium (TMGa), respectively, with water. In situ Fourier transform infrared (FTIR) spectroscopy reveals that these metal alkyl precursors reversibly associate with the carbonyl groups of PMMA in analogy to trimethylaluminum (TMAl), however with significantly lower affinity. SIS with TMIn and water enables the growth of In2O3 at 80° C., well below the onset temperature of atomic layer deposition (ALD) using these precursors.

First claim

What is claimed is:

1. A method of depositing a group 13 oxide comprising:
providing a base material comprising a PMMA film in a reactor; and
depositing an oxide of indium or gallium using a sequential infiltration synthesis (SIS) process including at least one cycle of:
pulsing a first metal precursor comprising trimethylindium or trimethylgallium into the reactor for a first metal precursor pulse time;
exposing, at a temperature of 70-90° C., the base material to the first metal precursor for a first metal precursor exposure time and at a first partial pressure, the first metal precursor infiltrating at least a portion of the base material and binding therein with the base material to form a trimethyl-X-PMMA adduct with an ester group of the PMMA, where X is indium or gallium;
purging the reactor of the first metal precursor;
pulsing a co-reactant precursor into the reactor for a first co-reactant pulse time;
exposing the base material to the co-reactant precursor for a co-reactant precursor exposure time and at a second partial pressure, the co-reactant precursor infiltrating at least a portion of the base material and reacting with the trimethyl-X-PMMA adduct therein to form the oxide and release the ester group of the PMMA; and
purging the reactor of the co-reactant precursor,
wherein the co-reactant precursor is selected from the group consisting of water, ozone, and hydrogen peroxide.

2. The method of claim 1 , wherein the first metal precursor pulse time is greater than 0 seconds to 30 seconds.

3. The method of claim 1 , wherein the first metal precursor exposure time is greater than 0 seconds to 500 seconds.

4. The method of claim 1 , wherein purging the reactor proceeds for a first metal precursor purge time of greater than 0 seconds to 30 seconds and-comprises reducing the pressure within the reactor to substantially a vacuum.

5. The method of claim 4 , wherein the first metal precursor purge time is 2 seconds to 5 seconds.

6. The method of claim 1 , wherein the co-reactant precursor pulse time is greater than 0 seconds to 120 seconds.

7. The method of claim 1 , wherein the co-reactant precursor exposure time is greater than 0 seconds to 500 seconds.

8. The method of claim 1 , wherein purging the reactor of the co-reactant precursor proceeds for greater than 0 seconds to 500 seconds and comprises reducing the pressure within the reactor to substantially a vacuum.

9. The method of claim 1 , wherein the first metal precursor comprises gallium and the oxide is gallium oxide.

10. The method of claim 1 , further comprising depositing a dopant using the sequential infiltration synthesis (SIS) process, the dopant comprising zinc, tin, or a combination thereof.

11. The method of claim 1 wherein the first partial pressure is at least 50 Torr.

12. A method of depositing a group 13 oxide comprising:
providing a base material comprising a PMMA film in a reactor; and
depositing an oxide of indium or gallium using a sequential infiltration synthesis (SIS) process including at least one cycle of:
pulsing a metal precursor comprising trimethylindium or trimethylgallium into the reactor for a metal precursor pulse time;
exposing the base material to the metal precursor to form a trimethyl-X-PMMA adduct with an ester group of the PMMA, where X is indium or gallium, within the base material;
purging the reactor of the metal precursor for a metal precursor purge time that is less than the lifespan of the metal adduct;
pulsing a co-reactant precursor into the reactor for a first co-reactant pulse time;
exposing the base material to the co-reactant precursor for a co-reactant precursor exposure time and at a second co-reactant partial pressure, the co-reactant precursor infiltrating at least a portion of the base material and reacting with the trimethyl-X-PMMA adduct within the base material to form the oxide and release the ester group of the PMMA; and
purging the reactor of the co-reactant precursor,
wherein the co-reactant precursor comprises.

13. The method of claim 12 , wherein the at least once cycle comprises at least 10 cycles.

14. The method of claim 12 , wherein the SIS is at a reaction temperature of 70-90° C.

15. The method of claim 12 , wherein 70% of the trimethyl-X-PMMA adducts are reacted with the co-reactant.

Assignees

• Uchicago Argonne Llc
• Univ Chicago

Inventors

• Martinson Alex B
• Darling Seth B
• Waldman Ruben

Classifications

• C08L33/12

  Homopolymers or copolymers of methyl methacrylate · CPC title

• C08L39/06

  Homopolymers or copolymers of N-vinyl-pyrrolidones · CPC title

• C08L33/08

  Homopolymers or copolymers of acrylic acid esters · CPC title

• C23C16/407 Primary

  of zinc, germanium, cadmium, indium, tin, thallium or bismuth · CPC title

• C23C16/45527

  characterized by the ALD cycle, e.g. different flows or temperatures during half-reactions, unusual pulsing sequence, use of precursor mixtures or auxiliary reactants or activations · CPC title