MICRO AND NANO STRUCTURING OF A DIAMOND SUBSTRATE
20220350249 · 2022-11-03
Inventors
- Mariusz RADTKE (Frankfurt am Main, DE)
- Elke Katja NEU-RUFFING (Bexbach, DE)
- Abdallah SLABLAB (La Courneuve, FR)
Cpc classification
G03F7/0757
PHYSICS
G03F7/0035
PHYSICS
G03F7/11
PHYSICS
G03F7/0752
PHYSICS
International classification
G03F7/11
PHYSICS
G03F7/00
PHYSICS
Abstract
A process of structuring a diamond substrate, comprising the steps of (a) depositing an adhesion layer on a face of the diamond substrate; (b) coating a resist layer on the adhesion layer; (c) removing parts of the resist layer so as to expose parts of the adhesion layer and form a corresponding structuring mask; (d) etching the adhesion layer and the diamond substrate (2) through the structuring mask so as to structure the diamond substrate; wherein the adhesion layer is a non-metallic compound comprising oxides.
Claims
1.-16. (canceled)
17. A process of structuring a diamond substrate, comprising the steps of: (a) depositing an adhesion layer on a face of the diamond substrate; (b) coating a resist layer on the adhesion layer; (c) removing parts of the resist layer so as to expose parts of the adhesion layer and form a corresponding structuring mask; and (d) etching the adhesion layer and the diamond substrate through the structuring mask so as to structure said diamond substrate, wherein at least one of the structures comprise one or more colour centres; and wherein the adhesion layer comprises substantially a non-metallic compound.
18. The process according to claim 17, wherein the non-metallic compound comprises at least one of the following list: silicon, silicon oxide, germanium and germanium oxide, and any combination thereof.
19. The process according to claim 17, wherein at step (a) the adhesion layer is deposited by electron beam physical vapour deposition, plasma activated chemical vapour deposition, thermal deposition or atomic layer deposition.
20. The process according to claim 17, wherein the adhesion layer extends homogeneously over the whole face of the diamond substrate.
21. The process according to claim 17, wherein the adhesion layer has a thickness of at least 1 nm and of not more than 200 nm.
22. The process according to claim 17, wherein step (d) comprises the following sub-steps: (d1) etching the adhesion layer through the structuring mask so as to expose parts of the diamond substrate; and (d2) etching the diamond substrate through the structuring mask so as to structure said diamond substrate.
23. The process according to claim 22, wherein sub-steps (d1) and (d2) are achieved by plasma with reactive gases.
24. The process according to claim 23, wherein the reactive gases in step (d1) is fluorine-based and the reactive gas in step (d2) is oxygen based.
25. The process according to claim 17, wherein the resist layer is an electron beam resist layer or a photo resist layer and step (c) is achieved by electron beam lithography or optical lithography, and subsequent development of the resist.
26. The process according to claim 17, wherein the resist layer comprises a silsesquioxane.
27. The process according to claim 26, wherein the silsesquioxane comprises Hydrogen silsesquioxane HSQ.
28. The process according to claim 17, comprising the further step of: (e1) removing the structuring mask and the adhesion layer that remains further to step (d).
29. The process according to claim 28, wherein step (e2) is achieved by wet etching.
30. The process according to claim 17, comprises the further steps of: (e2) removing the structuring mask so that the adhesion layer remains on the structures; (f) coating a further resist layer on the adhesion layer remaining on the structures; (g) removing parts of the further resist layer so as to expose parts of the adhesion layer on the structure and form a further structuring mask; (h) etching the adhesion layer and the diamond substrate through the further structuring mask so as to further structure the structures of said diamond substrate.
31. The process according to claim 30, wherein step (h) comprises the following sub-steps: (h1) etching the adhesion layer through the further structuring mask so as to expose parts of the structures of the diamond substrate; and (h2) etching the diamond substrate through the further structuring mask so as to further structure said diamond substrate.
32. The process according to claim 30, wherein step (e2) is achieved by wet etching.
33. The process according to claim 17, wherein the structures comprise structures with a height of at least 1 nm and of not more than 10 000 nm.
34. The process according to claim 17, wherein at least one of the structures comprise nitrogen-vacancy centres.
35. The process according to claim 17, wherein the adhesion layer is amorphous.
Description
DRAWINGS
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DETAILED DESCRIPTION
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[0049] The structuring process of the diamond substrate consists essentially in coating a resist layer on a face of the diamond substrate, removing parts of the resist layer for forming a structuring mask, and etching the diamond substrate through the structuring mask. To that end, the structuring mask made of the resist layer must properly adhere to the diamond structure. Etching of diamond requires however high-energy and/or oxygen plasmas which under certain circumstances require specific resits that might not properly adhere to the diamond substrate. The invention provides depositing an adhesion layer on the diamond substrate before coating the resist layer. The adhesion layer is made of a non-metallic compound and comprises oxides. Metallic compounds tend indeed to oxidize rapidly in contact with ambient air, showing thereby poor adhesion properties with the resist layer. Oxides of non-metallic compound are at the contrary formed during deposition and provide a good adhesion to the diamond substrate.
[0050] Before structuring the diamond substrate, the later can be cleaned, for instance mechanically and/or chemically. Mechanical cleaning can comprise rubbing with a wipe wetter with solvent, dipping in a solvent like acetone, ultrasound bath and drying. Chemical cleaning can comprise immersion in acid, in various instances a mixture of 3 acids HNO.sub.3, H.sub.2SO.sub.4 and HClO.sub.4. The acid mixture can be heated during immersion until it changes colour from transparent to yellow, corresponding to the production of chlorine dioxide radicals responsible for the cleaning. The ratio of these acids is advantageously 1.sub.v:1.sub.v:1.sub.v.
[0051] A stress relief etching can be performed after cleaning and before structuring. This etching can be made with a plasma, for instance an inductively coupled plasma, reactive ion etching ICP/RIE reactor, so as to remove a thin layer, e.g., between 3 and 5 μm, on the face that is to be structured.
[0052] The diamond substrate can be placed on a silicon chip and attached thereto by gluing. It can then be nitrogen ion implanted in an ion implanter and thereafter be annealed, e.g., at a temperatures of at least 400° C., in various instances 900° C., during at least 100 minutes.
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[0056] In
[0057] After the EBL writing of the resist layer, the diamond substrate is developed by immersion in a solvent. For instance, the diamond substrate (with the silicon chip) can be immersed in a solution comprising tetramethylammonium hydroxide (TMAH), e.g., at 25%, for a duration of at least 10 seconds. It can then be immersed into ultrapure water, and thereafter several times in acetone and afterwards in isopropyl alcohol until the non-exposed regions are totally removed.
[0058] In
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[0060] For instance, the etching step is achieved in two sub-steps, namely a first sub-step of removal of the adhesion layer 14 by reactive ions of SF.sub.6 etching through the structuring mask 24, followed by a second sub-step of etching through the structuring mask 24 the material of the diamond substrate by reactive ions of O.sub.2.
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[0066] In
[0067] After the lithography writing of the further resist layer, the diamond substrate is developed by immersion in a solvent. The diamond substrate (with the silicon chip) can be immersed in a solution comprising tetramethylammonium hydroxide (TMAH), e.g., at 25%, for a duration of at least 10 seconds. It can then be immersed into ultrapure water, and thereafter several times in acetone and afterwards in isopropyl alcohol until the non-exposed regions are totally removed.
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[0070] The further structuring process which has been described in relation with
[0071] The reliability of this plasma transfer and further cleaning process and its influence on shallowly (10-15 nm) implanted colour centres in diamond was evaluated by means of optically detected magnetic resonance (ODMR). Negatively charged nitrogen vacancies, NV(−) possess electronic spin and exhibit a resonance at 2.87 GHz, which can be perceived as a fingerprint of this colour centre. The experimentally obtained ODMR spectrum and photoluminescence map based on nano-pillars of 200 nm diameter etched into the diamond by the method presented here show that the adhesion layer is totally removed and also that there is no bleaching after longer irradiation times, indicating no surface damage and therefore no alternation in the electronic structure of shallowly underlying nitrogen vacancy. This conclusion can be directly related to the reliability of the presented method and perfect adhesion of the tone resist.