IP Library › Granted Patent US 12,209,023
Granted Patent B2
US 12,209,023 · App. 17/470,621 · Granted Jan 28, 2025

Low temperature, high yield synthesis of hydrogen terminated highly porous amorphous silicon, and nanomaterials and composites from Zintl phases

Inventors: Michael J. Wagner (Rockville, MD); Nathan A. Banek (Rockville, MD)
Assignee: The George Washington University
C01B33/021C06B43/00H01M4/58H01M10/0525C01P2002/72C01P2002/82C01P2004/04C01P2006/12C01P2006/16C01P2006/40
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Quick Facts
Patent No.
US 12,209,023
App. No.
17/470,621
Granted
Jan 28, 2025
Kind
B2
Abstract

The present disclosure relates to an improved process for the synthesis of hydrogen terminated silicon from Zintl phases. The hydrogen terminated silicon is useful, for example, as explosives, chemical and biochemical sensors, optoelectronic materials and Li-ion battery anode ion storage materials. The present disclosure also relates to an improved process for the synthesis of nanomaterials and composites from Zintl phases. The nanomaterials and composites are useful, for example, as ion storage materials.

Claims (48)

1. A process for preparing hydrogen terminated silicon, the process comprising:

a) reacting a silicon containing Zintl compound with an aluminum compound, optionally in the presence of a support material

b) optionally isolating the resulting product;

c) adding a hydroxyl containing compound to produce the hydrogen terminated silicon; and

d) optionally isolating the hydrogen terminated silicon,

wherein step a) is conducted:

i) by mechanical milling;

ii) in a solvent; or

iii) in a molten salt comprising the aluminum compound in combination with one or more alkali metal halides, alkali earth metal halides, or any combination thereof.

2. The process according to any one of claim 1 , wherein the hydrogen terminated silicon is substantially amorphous.

3. The process according to claim 1 , wherein the hydrogen terminated silicon has a surface area of about 100 to about 1500 m 2 /g.

4. The process according to claim 1 , wherein the hydrogen terminated silicon has a porosity of about 40 to about 90%.

5. The process according to claim 1 , wherein the hydrogen terminated silicon has a Barret-Joyner-Halenda (BJH) desorption cumulative pore volume of about 0.4 to about 1.1 cm 3 /g.

6. The process according to claim 1 , wherein the hydrogen terminated silicon has an average Barret-Joyner-Halenda (BJH) desorption pore width of about 1 to about 40 nm.

7. The process according to claim 1 , wherein the hydroxyl containing compound is an alcohol, a hydroxyl containing polymer, a carboxylic acid, or any combination thereof.

8. The process according to claim 1 , wherein the hydroxyl containing compound is an alcohol.

9. The process according to claim 1 , wherein the hydroxyl containing compound is methanol, ethanol, propanol, isopropanol, pentanol, hexanol, or any combination thereof.

10. The process according to claim 1 , wherein step c) further comprises adding an inorganic acid.

11. The process according to claim 1 , wherein step c) further comprises adding hydrochloric acid.

12. The process according to claim 1 , wherein the Zintl compound is a compound comprising a) a Group 1 metal, a Group 2 metal, or any combination thereof, and b) silicon.

13. The process according to claim 1 , wherein the Group 1 and/or Group 2 metal is selected from Li, Na, K, Rb, Cs, Be, Mg, Cn, Sr, Ba, and any combination thereof.

14. The process according to claim 1 , wherein the Group 1 and/or Group 2 metal is Mg.

15. The process according to claim 1 , wherein the Zintl compound is Mg 2 Si.

16. The process according to claim 1 , wherein the aluminum compound is selected from halides, oxides, alkoxides, hydroxides, sulfates, sulfites, nitrates, nitrites, phosphates, and phosphites of aluminum, hydrates of any of the foregoing, and any combination thereof.

17. The process according to claim 1 , wherein the aluminum compound is an aluminum halide.

18. The process according to claim 1 , wherein the aluminum compound is AlCl 3 , AlBr 3 , AlI 3 , or any combination thereof.

19. The process according to claim 1 , wherein the support material, if present, is selected from carbonaceous materials, metals, glasses, oxides, nitrides, borides, and any combination thereof.

20. The process according to claim 1 , wherein the support material, if present, is a carbonaceous material selected from carbon spheres, graphite, carbon nanotubes, carbon nanofibers, carbon fibers, hard and soft carbons, activated carbons, carbon blacks, amorphous carbons, soots, graphene, fullerenes, coal, coke, fossil fuel derived materials, biomass, biochar, charcoal, chars, and any combination thereof.

21. The process according to claim 1 , wherein the support material, if present, is selected from a multiwall graphene nanoshell (MGNS), graphite, and any combination thereof.

22. The process according to claim 1 , wherein step a) is conducted in a solvent, in the solid state, by molten salt or by solid/solid reaction.

23. The process according to claim 1 , wherein step a) is conducted in a molten salt comprising an aluminum compound, optionally in combination with one or more alkali metal halides, alkali earth metal halides, or any combination thereof.

24. The process according to claim 1 , wherein step a) is conducted in a solvent selected from aromatic hydrocarbons, nonaromatic hydrocarbons, amines, aprotic solvents, and any combination thereof.

25. The process according to claim 1 , wherein step a) is conducted in a solvent selected from cyclohexane, toluene, and any combination thereof.

26. The process according to claim 1 , wherein step a) is conducted at a temperature ranging between about 50° C. and about 600° C.

27. The process according to claim 1 , wherein the hydrogen terminated silicon comprises between 0 and about 20 wt. % Al.

28. The process according to claim 1 , wherein step a) is conducted at a temperature ranging between about 50° C. and about 200° C.

29. The process according to claim 1 , wherein step a) is conducted at a temperature ranging between about 100° C. and about 200° C.

30. The process according to claim 1 , wherein step a) is conducted at a temperature ranging between about 120° C. and about 180° C.

31. The process according to claim 1 , wherein step a) is conducted at a temperature of about 125° C.

32. The process according to claim 1 , wherein step a) is conducted at a temperature of about 180° C.

33. The process according to claim 1 , wherein the hydrogen terminated silicon comprises between 0 and about 15 wt. % Al.

34. The process according to claim 1 , wherein the hydrogen terminated silicon comprises between 0 and about 10 wt. % Al.

35. The process according to claim 1 , wherein the hydrogen terminated silicon comprises between 0 and about 5 wt. % Al.

36. The process according to claim 1 , wherein the hydrogen terminated silicon comprises between 0 and about 4 wt. % Al.

37. The process according to claim 1 , wherein the hydrogen terminated silicon comprises between 0 and about 3 wt. % Al.

38. The process according to claim 1 , wherein the hydrogen terminated silicon comprises between 0 and about 2 wt. % Al.

39. The process according to claim 1 , wherein the hydrogen terminated silicon comprises between 0 and about 1 wt. % Al.

40. The process according to claim 1 , wherein the hydrogen terminated silicon comprises between about 1 and about 3 wt. % Al.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 11, 2024
From: WAGNER, MICHAEL J.; BANEK, NATHAN A.
To: THE GEORGE WASHINGTON UNIVERSITY
Reel/Frame 069204/0085 →
Continuity (4)
Continuation In Part 16478327
Provisional Application 63166618 · Mar 26, 2021
Provisional Application 62450392 · Jan 25, 2017
Related Publication 20220073356A1 · Mar 10, 2022
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