IP Library Granted Patent US 12692437
Granted Patent B2
US 12692437 · App. 18/848,658 · Granted Jul 28, 2026

Heat treatment of nanodiamond particles with controlled powder layer depth

Inventor: Yahua Bao (Provo, UT)
Assignee: Schlumberger Technology Corporation
C09K11/65B01J3/062C01B32/28C03C17/22B01J2203/0655B01J2203/0695C01P2006/60C03C2217/42C03C2217/70C03C2218/111C03C2218/116C03C2218/32
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12692437
App. No.
18/848,658
Granted
Jul 28, 2026
Kind
B2
Abstract

Luminescent diamond is made by creating vacancies in diamond grains and heat treating the diamond grains by controlling a thickness of the diamond grains on a substrate. The heat treatment may occur in a temperature range that does not burn the diamond grains, and the controlled thickness produces an even color change and/or promotes oxygen terminations on the diamond particle surfaces.

Claims (37)

1 . A method of making luminescent diamond consisting of:

subjecting a volume of precursor diamond grains to high-pressure/high-temperature conditions in a pressure cell and thereby forming diamond grains with luminescent centers, wherein the high-pressure/high-temperature conditions are from about 1300° C. to about 2500° C. and from about 3.0 GPa to about 10 GPa;

forming a suspension by suspending the diamond grains in a liquid;

adhering the suspension to a substrate and controlling a thickness of the suspension on the substrate;

heat treating the suspension on the substrate at a temperature not exceeding 650° C., thereby changing oxygen terminations on diamond particles of the suspension and increasing a photoluminescence intensity of the diamond grains; and

removing the diamond particles from the substrate and separating the removed diamond particles by grain size.

2 . The method of claim 1 , wherein the luminescent centers include at least one of nitrogen or silicon vacancies.

3 . The method of claim 1 , wherein the liquid includes water.

4 . The method of claim 3 , wherein the liquid includes a surface tension suppressant.

5 . The method of claim 4 , wherein the surface tension suppressant includes alcohol.

6 . The method of claim 1 , wherein the liquid is 10% to 100% alcohol by weight.

7 . The method of claim 1 , wherein the substrate is glass.

8 . The method of claim 1 , wherein the thickness is controlled to be less than 30 μm.

9 . The method of claim 8 , wherein the thickness is controlled to be less than 25 μm.

10 . The method of claim 8 , wherein the thickness is controlled to be between 1 μm and 15 μm.

11 . The method of claim 1 , wherein controlling the thickness includes removing material that exceeds a threshold thickness.

12 . The method of claim 1 , wherein adhering the suspension to the substrate includes drying the suspension.

13 . The method of claim 12 , wherein drying the suspension is performed at a temperature below a boiling point of the liquid and before heat treating the suspension.

14 . The method of claim 1 , wherein adhering the suspension to the substrate includes coating the suspension on the substrate using one or more of dip coating, spin coating, dry coating, or slip casting.

15 . The method of claim 1 , wherein heat treating the suspension includes heat treating at a temperature not exceeding 600° C.

16 . The method of claim 1 , wherein heat treating the suspension includes heat treating at a temperature not exceeding 550° C.

17 . The method of claim 1 , wherein heat treating the suspension is performed for a duration of up to two hours.

18 . The method of claim 1 , wherein heat treating the suspension is performed for a duration of between 30 minutes and 90 minutes.

19 . The method of claim 1 , wherein the pressure cell is configured to impose a differential or asymmetric pressure on the precursor diamond grains.

20 . The method of claim 1 , wherein:

the volume of precursor diamond grains is formed by consolidating and compacting a volume of pre-existing diamond grains; and

the volume of precursor diamond grains comprises intercrystalline diamond bonding.

21 . The method of claim 1 , wherein:

the volume of precursor diamond grains is formed by consolidating and compacting a volume of pre-existing diamond grains; and

the volume of precursor diamond grains does not comprise intercrystalline diamond bonding.

22 . A method of making luminescent diamond consisting of:

subjecting a volume of natural precursor diamond grains with an average grain size of from 10 μm to 50 μm to high-pressure/high-temperature conditions in a pressure cell and thereby forming diamond grains with luminescent centers, wherein the high-pressure/high-temperature conditions are from about 1300° C. to about 2500° C. and from about 3.0 GPa to about 10 GPa;

forming a suspension by separating the diamond grains into a powder and suspending the diamond grains in water;

adhering the suspension to a glass substrate and controlling a thickness of the suspension on the substrate to be from 5 μm to 15 μm, wherein the diamond grains have a concentration of from 0.1% to 10% by weight in the suspension;

heat treating the suspension on the substrate at a temperature in a range between 450° C. and 550° C. for 60 minutes, thereby changing at least one of a color of the suspension or oxygen terminations on diamond particles of the suspension and increasing a photoluminescence intensity of the diamond grains; and

removing the diamond particles from the substrate and separating the removed diamond particles by grain size,

wherein the pressure cell is configured to impose a differential or asymmetric pressure on the precursor diamond grains in order to plastically deform the precursor diamond grains and produce the luminescent centers in the diamond grains.