IP Library Granted Patent US 7,192,483
Granted Patent B2
US 7,192,483 · App. 10/491,858 · Granted Mar 20, 2007

Method for diamond coating substrates

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Quick Facts
Patent No.
US 7,192,483
App. No.
10/491,858
Granted
Mar 20, 2007
Kind
B2
Abstract

The present invention relates to a method for diamond coating of substrates in which the substrate is exposed in a vacuum atmosphere to a reactive gas mixture excited by means of a plasma discharge, the plasma discharge comprising a plasma beam ( 14 ) in an evacuated receiver ( 16 ) that is formed between a cathode chamber ( 1 ) and an anode ( 2 ), and the reactive gas mixture comprising a reactive gas and a working gas, the reactive gas in ( 9 ) and the working gas in ( 8 ) and/or ( 9 ) introduced into the receiver, and the receiver ( 16 ) is evacuated by a pump arrangement ( 15 ), and the hydrogen concentration of the reactive gas mixture being 0–45 vol. %.

Claims (39)

1. Method for diamond coating of substrates in which the substrate is exposed in a vacuum atmosphere to a reactive gas mixture excited by means of a plasma discharge, the plasma discharge comprising a plasma beam ( 14 ) in an evacuated receiver ( 16 ) that is formed between a cathode chamber ( 1 ) and an anode ( 2 ), and the reactive gas mixture comprising a reactive gas and a working gas, the reactive gas in ( 9 ) and the working gas in ( 8 ) and/or ( 9 ) introduced into the receiver, and the receiver ( 16 ) is evacuated by a pump arrangement ( 15 ), and the hydrogen concentration of the reactive gas mixture being 0–20 vol. % and the H 2 concentration of the reactive gas mixture is chosen such that the diamond coating has an average crystallite size of less than 50 nm.

2. Method as defined by claim 1 , wherein the H 2 concentration of the reactive gas mixture is chosen such that the diamond coating has an average crystallite size between 1 and 30 nm.

3. Method as defined by any of claims 1 – 2 , with the H 2 concentration of the reactive gas mixture chosen such that the substrate temperature established without external additional heating or cooling is between 300° C. and 750° C.

4. Method as defined by claim 1 , with the concentration of the reactive gas in the reactive gas mixture lying between 0.1 and 85 vol. %.

5. Method as defined by claim 4 , wherein the reactive gas contains one or more gases, which is chosen from the group of gaseous compounds consisting of H 2 , C-containing gases and N-containing gases, especially N 2 .

6. Method as defined by claim 1 , wherein the working gas comprises at least one noble gas.

7. Method as defined by claim 1 , wherein the plasma beam ( 14 ) is formed as a low voltage arc discharge, preferably as high current arc discharge.

8. Method as defined by claim 7 , wherein the arc current is between 50 and 750 A.

9. Method as defined by claim 1 , wherein the substrate, as far as the region of highest plasma density is concerned, is arranged radially offset along the axis of the plasma beam.

10. Method as defined by claim 9 , wherein the distance of the substrate from the axis of the plasma beam is between 3 and 20 cm.

11. Method as defined by any of claims 9 – 10 , wherein the distance of the substrate from the axis of the plasma beam ( 14 ) is chosen such that the plasma density in the region of the substrate is at most 20% of the maximum of the plasma density along the axis of the plasma beam ( 14 ).

12. Method as defined by claims 1 , 2 and 4 – 10 , whereby the plasma density distribution is influenced by a magnetic field that runs essentially parallel to the axis of the plasma beam and is generated by the arrangement of magnetic coils ( 10 , 11 ).

13. Method as defined by claim 12 , wherein the magnetic field on the axis of the plasma beam has a strength of 0–200 Gauss.

14. Method as defined by any of claims 1 - 2 and 4 - 10 , whereby the substrate temperature lies between 300 and 900° C.

15. Method as defined by any of claims 1 – 2 and 4 – 10 , characterized by the fact that the overall pressure in the receiver ( 1 ) is between 10 and 10 3 Pa.

16. Method as defined by any of claims 1 – 2 and 4 – 10 , wherein the flow of the reactive gas mixture runs essentially parallel to the axis of the plasma beam and is between 200 and 10,000 sccm.

17. Method as defined by claims 1 – 2 and 4 – 10 , wherein the values for the arc current, the magnetic field, the overall pressure, the reactive gas composition, the concentration of the working gas and the distance from the arc axis are chosen from the following ranges:

Arc current:

50–750 A, especially 50–400 A

Magnetic field in the centre

0–200 Gauss, especially 0–100 Gauss

of the plasma beam:

Overall pressure of the

10–10 5 , especially 10–10 3 Pa

gas mixture:

Reactive gas mixture:

H 2

0–20% and preferred 0–15%

Other reactive gases

0.1–40%, especially 0–25%

and especially preferred 0–15%

Working gas

Remainder up to 100%

Distance from arc axis

3–30, especially 3–20 cm.

18. Method for producing a coated substrate, wherein on the substrate at least a first and a second layer are deposited, the first layer being closer to the substrate surface than the second layer and containing aluminium, silicon, or an element of groups IVB, VB, VIB or VIIB of the periodic table in an elemental form or as a compound, and the second layer located on the first layer and consisting of a diamond coating which is deposited by a method defined in claim 1 .

19. Coated substrate as obtainable by the method defined in claim 18 .

20. Method for producing a coated substrate, wherein on the substrate at least a first and a second layer are deposited, the first layer being closer to the substrate surface than the second layer and containing aluminium, silicon, or an element of groups IVB, VB, VIB or VIIB of the periodic table in an elemental form or as a compound, and the second layer located on the first layer and consisting of a diamond coating which is deposited by a method defined in claim 17 .

21. Coated substrate as obtainable by the method defined in claim 20 .

Assignments (4)
CHANGE OF NAME Recorded May 5, 2022
From: OERLIKON SURFACE SOLUTIONS AG, TRUBBACH
To: OERLIKON SURFACE SOLUTIONS AG, PFÄFFIKON
Reel/Frame 059912/0979 →
CHANGE OF NAME Recorded May 3, 2022
From: OERLIKON TRADING AG, TRUBBACH
To: OERLIKON SURFACE SOLUTIONS AG, TRUBBACH
Reel/Frame 059795/0243 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 27, 2010
From: OC OERLIKON BALZERS AG; BALZERS AKTIENGESELLSCHAFT; UNAXIS BALZERS AG
To: OERLIKON TRADING AG, TRUBBACH
Reel/Frame 023848/0306 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 16, 2004
From: FRANZ, DAVID; KARNER, JOHANN
To: UNAXIS BALZERS AKTIENGESELLSCHAFT
Reel/Frame 015835/0909 →