IP Library › Granted Patent US 11,462,400
Granted Patent B1
US 11,462,400 · App. 17/651,713 · Granted Oct 4, 2022

Ultrawide bandgap semiconductor devices including magnesium germanium oxides

Inventor: Petar Atanackovic (Henley Beach South, AU)
Assignee: Silanna UV Technologies Pte Ltd
H01L21/02565H01L21/02576H01L21/02579H01L21/02631
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Quick Facts
Patent No.
US 11,462,400
App. No.
17/651,713
Granted
Oct 4, 2022
Kind
B1
Abstract

Various forms of Mg x Ge 1-x O 2-x are disclosed, where the MgxGe 1-x O 2-x are epitaxial layers formed on a substrate comprising a substantially single crystal substrate material. The epitaxial layer of Mg x Ge 1-x O 2-x has a crystal symmetry compatible with the substrate material. Semiconductor structures and devices comprising the epitaxial layer of Mg x Ge 1-x O 2-x are disclosed, along with methods of making the epitaxial layers and semiconductor structures and devices.

Claims (43)

1. A method of forming a semiconductor device, the method comprising:

providing a substrate comprising a substantially single crystal substrate material that has a crystal symmetry compatible with an epitaxial layer of Mg x Ge 1-x O 2-x ; and

co-depositing materials onto the substrate to form the epitaxial layer of Mg x Ge 1-x O 2-x , with x having a value of 0<x<1;

wherein the materials comprise at least two elements selected from Mg, Ge, and oxygen in accordance with the value of x, the Mg, Ge and oxygen being supplied by a Mg source, a Ge source, and an activated oxygen source, respectively; and

wherein the co-depositing comprises using a growth temperature of 400-500° C., and a flux ratio k of the Ge source to the Mg source (Φ Ge inc /Φ Mg inc ) of k=3 to 9.

2. The method of claim 1 , further comprising depositing a buffer layer between the substrate and the epitaxial layer of Mg x Ge 1-x O 2-x .

3. The method of claim 1 , wherein the co-depositing is performed using a molecular beam epitaxy process.

4. The method of claim 1 , wherein in the co-depositing, the epitaxial layer of Mg x Ge 1-x O 2-x self-assembles.

5. The method of claim 1 , wherein the Mg x Ge 1-x O 2-x is Mg 2 GeO 4 , wherein x=2/3.

6. The method of claim 1 , wherein the flux ratio k has a value from 3 to 7.5 and the Mg x Ge 1-x O 2-x is Mg 2 GeO 4 , wherein x=2/3.

7. The method of claim 1 , wherein the co-depositing comprises doping the epitaxial layer.

8. The method of claim 7 , wherein the doping comprises substituting a Ge site of a corresponding undoped Mg x Ge 1-x O 2-x crystal structure with Ga to result in a p-type conductivity.

9. The method of claim 7 , wherein the doping comprises substituting a Mg site of a corresponding undoped Mg x Ge 1-x O 2-x crystal structure with Ga to result in an n-type conductivity.

10. The method of claim 7 , wherein the doping comprises substituting a Ge site of a corresponding undoped Mg x Ge 1-x O 2-x crystal structure with Al to result in a p-type conductivity.

11. The method of claim 7 , wherein the doping comprises substituting a Mg site of a corresponding undoped Mg x Ge 1-x O 2-x crystal structure with Al to result in an n-type conductivity.

12. The method of claim 7 , wherein the doping comprises substituting a Ge site or a Mg site of a corresponding undoped Mg x Ge 1-x O 2-x crystal structure with Li + to result in an p-type conductivity.

13. The method of claim 7 , wherein the doping comprises substituting a Mg site of a corresponding undoped Mg x Ge 1-x O 2-x crystal structure with Ni + .

14. The method of claim 7 , wherein the doping comprises substituting an oxygen site of a corresponding undoped Mg x Ge 1-x O 2-x crystal structure with N 3+ .

15. The method of claim 7 , wherein the doping comprises:

placing a Ge atom in a first location that is occupied by Mg in a corresponding undoped Mg x Ge 1-x O 2-x unit cell structure; and

placing a Mg atom in a second location that is occupied by Ge in the corresponding undoped Mg x Ge 1-x O 2-x unit cell structure.

16. The method of claim 1 , further comprising forming the semiconductor device from the substrate and the epitaxial layer of Mg x Ge 1-x O 2-x .

17. A method of forming a semiconductor device, the method comprising:

providing a substrate comprising a substantially single crystal substrate material that has a crystal symmetry compatible with an epitaxial layer of Mg x Ge 1-x O 2-x ;

co-depositing materials onto the substrate to form the epitaxial layer of Mg x Ge 1-x O 2-x , with x having a value of 0≤x<1;

wherein the materials comprise at least two elements selected from Mg, Ge, and oxygen in accordance with the value of x, the Mg, Ge and oxygen being supplied by a Mg source, a Ge source, and an activated oxygen source, respectively; and

determining an elemental incident flux ratio of the Ge source to the Mg source (Φ Ge inc /Φ Mg inc ) according to a deposition surface temperature, to retain an adsorbed surface species ratio of the Ge to the Mg (Φ Ge ads /Φ Mg ads ).

18. The method of claim 17 , further comprising depositing a buffer layer between the substrate and the epitaxial layer of Mg x Ge 1-x O 2-x .

19. The method of claim 17 , wherein the co-depositing is performed using a molecular beam epitaxy process.

20. The method of claim 17 , wherein the Mg x Ge 1-x O 2-x is Mg 2 GeO 4 , wherein x=2/3.

21. The method of claim 17 , wherein the co-depositing comprises using a growth temperature of 400-500° C., and a flux ratio k of the Ge source to the Mg source (Φ Ge inc /Φ Mg inc ) of k=3 to 9.

22. The method of claim 17 , wherein the co-depositing comprises doping the epitaxial layer.

23. A method of forming a semiconductor device, the method comprising:

providing a substrate comprising a substantially single crystal substrate material that has a crystal symmetry compatible with an epitaxial layer of Mg x Ge 1-x O 2-x ;

co-depositing materials onto the substrate to form the epitaxial layer of Mg x Ge 1-x O 2-x , with x having a value of 0≤x<1;

wherein the materials comprise at least two elements selected from Mg, Ge, and oxygen in accordance with the value of x, the Mg, Ge and oxygen being supplied by a Mg source, a Ge source, and an activated oxygen source, respectively; and

forming a superlattice on the substrate, wherein the superlattice has a unit cell comprising a first layer and a second layer, wherein the first layer in the superlattice is the epitaxial layer of Mg x Ge 1-x O 2-x .

24. The method of claim 23 , wherein the second layer of the superlattice is a second epitaxial layer of Mg y Ge 1-y O 2-y , wherein y ranges from 0 to 1 and x≠y.

25. The method of claim 23 , further comprising depositing a buffer layer between the substrate and the epitaxial layer of Mg x Ge 1-x O 2-x .

26. The method of claim 23 , wherein the co-depositing is performed using a molecular beam epitaxy process.

27. The method of claim 23 , wherein the Mg x Ge 1-x O 2-x is Mg 2 GeO 4 , wherein x=2/3.

28. The method of claim 23 , wherein the co-depositing comprises using a growth temperature of 400-500° C., and a flux ratio k of the Ge source to the Mg source (Φ Ge inc /Φ Mg inc ) of k=3 to 9.

29. The method of claim 23 , wherein the co-depositing comprises doping the epitaxial layer.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 16, 2022
From: ATANACKOVIC, PETAR
To: SILANNA SEMICONDUCTOR PTY LTD
Reel/Frame 059279/0938 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 16, 2022
From: SILANNA SEMICONDUCTOR PTY LTD
To: SILANNA UV TECHNOLOGIES PTE LTD
Reel/Frame 059279/0977 →
Continuity (1)
Continuation PCTIB2021060414 · Nov 10, 2021
Cited By (13)
US 12,206,048 US 12,224,378 US 12,266,697 US 12,278,309 US 12,291,773 US 12,324,276 US 12,446,367 US 12,464,863 US 12,501,747 US 12,588,321 US 12,628,472 US 12,635,296 US 12,635,297