Wet-etchable, sacrificial liftoff layer compatible with high temperature processing

Abstract

A method for forming a wet-etchable, sacrificial lift-off layer or layers compatible with high temperature processing, a sacrificial layer, defined as consisting of a single film of one material or multiple films of multiple materials, that can tolerate high temperatures, is deposited on a substrate, called the original substrate, by sputtering or another suitable technique (e.g. evaporation, pulsed laser deposition, wet chemistry, etc.). Intermediate steps result in a lift-off layer attached to the lift-off substrate, that allow for separating the product from the original substrate.

Claims

1. A method of lift-off comprising: depositing a sacrificial layer on an original substrate, depositing a lift-off layer onto the sacrificial layer at a substrate temperature between 100 C. and 1000 C., bonding the lift-off layer to a lift-off substrate using an adhesive, and etching the sacrificial layer to obtain the lift-off layer attached to the lift-off substrate, wherein at least one of said depositing steps occurs under non-epitaxial conditions, and wherein the etching is sufficient to separate the lift-off layer and the lift-off substrate from the original substrate.

2. The method of claim 1, wherein one or both of said depositing steps occur by sputtering, evaporation, electrodeposition, pulsed laser deposition, or wet chemistry.

3. The method of claim 1, wherein the sacrificial layer is an acid soluble glass and wherein said etching is accomplished using acid.

4. The method of claim 3, wherein said glass is selected from the group consisting of fluoride glasses, phosphate glasses, chalcogenide glasses, and silicate glasses containing sodium silicate.

5. The method of claim 1, further comprising depositing a diffusion barrier between said sacrificial layer and said lift-off layer, wherein said etching also removes the diffusion barrier.

6. The method of claim 1, wherein the lift-off layer comprises copper indium gallium diselenide.

7. The method of claim 1, further comprising patterning the lift-off layer.

8. A method of lift-off comprising: depositing a sacrificial layer on an original substrate, depositing a lift-off layer onto the sacrificial layer at a substrate temperature between 100 C. and 1000 C., wherein the lift-off layer comprises copper indium gallium diselenide, Cu.sub.2ZnSn(S,Se).sub.4), cadmium telluride, iron disulfide, or a transparent conducting oxide, bonding the lift-off layer to a lift-off substrate using an adhesive, and etching the sacrificial layer to obtain the lift-off layer attached to the lift-off substrate, wherein at least one of said depositing steps occurs under non-epitaxial conditions, and wherein the etching is sufficient to separate the lift-off layer and the lift-off substrate from the original substrate.

9. The method of claim 8, wherein one or both of said depositing steps occur by sputtering, evaporation, electrodeposition, pulsed laser deposition, or wet chemistry.

10. The method of claim 8, wherein the sacrificial layer is an acid soluble glass and wherein said etching is accomplished using acid.

11. The method of claim 8, further comprising depositing a diffusion barrier between said sacrificial layer and said lift-off layer, wherein said etching also removes the diffusion barrier.

12. The method of claim 1, wherein the lift-off layer comprises said copper indium gallium diselenide.

13. The method of claim 8, further comprising patterning the lift-off layer.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is a flowchart of the method of the present embodiment;

(2) FIG. 2 is a photographic example of an SEM cross sectional image of a 3 m thick film of ASG on an SLG substrate;

(3) FIGS. 3(a)-3(d) are photographic images of the lift-off of a Mo film from a SLG substrate;

(4) FIG. 4 is a photographic image of a lift-off CIGS/Mo bilayer on a PI substrate; and

(5) FIG. 5 is a schematic diagram of an example of a lift-off process.

DETAILED DESCRIPTION

Definitions

(6) Before describing the present invention in detail, it is to be understood that the terminology used in the specification is for the purpose of describing particular embodiments, and is not necessarily intended to be limiting. Although many methods, structures and materials similar, modified, or equivalent to those described herein can be used in the practice of the present invention without undue experimentation, the preferred methods, structures and materials are described herein. In describing and claiming the present invention, the following terminology will be used in accordance with the definitions set out below.

(7) As used in this specification and the appended claims, the singular forms a, an, and the do not preclude plural referents, unless the content clearly dictates otherwise.

(8) As used herein, the term and/or includes any and all combinations of one or more of the associated listed items.

(9) As used herein, the term about when used in conjunction with a stated numerical value or range denotes somewhat more or somewhat less than the stated value or range, to within a range of 10% of that stated.

DESCRIPTION

(10) Referring now to FIG. 1, method 150 of the present embodiment for forming a wet-etchable, sacrificial lift-off layer or layers compatible with high temperature processing, can include depositing 151 a sacrificial layer on an original substrate by a suitable technique. If the sacrificial layer contains multiple films, method 150 can include etching the multiple films in etchants or solvents. Method 150 can further include depositing 155 a diffusion barrier layer to prevent the diffusion of ions or atoms, depositing 159 a lift-off layer onto the sacrificial layer, bonding 161 the lift-off layer to a lift-off substrate with an adhesive, etching 163 the sacrificial layer, resulting in a lift-off layer attached to the lift-off substrate, and separating 165 the product from the original substrate. In embodiments, the diffusion barrier is also etched in a suitable etchant.

(11) Optionally, the method can include processing the new substrate with the liftoff layer thermally up to a suitable temperature to complete the bonding, providing annealing and/or providing improved performance. The depositing of the sacrificial layer can be accomplished by sputtering or another suitable technique (e.g. evaporation, pulsed laser deposition, wet chemistry, etc.). The sacrificial layer may include an acid soluble glass (ASG)a glass composition tailored so that it has a high etch rate in HCl, HF, nitric, or another suitable acid. The diffusion layer can include, for example, but not limited to, silica (SiO.sub.x), other metal oxides, metal nitrides, or a metal. The diffusion barrier layer can become part of the sacrificial layer. The suitable etchant can include acid.

(12) Referring now to FIG. 2, a cross sectional scanning electron microscope (SEM) image of an ASG layer on an SLG substrate is shown. A billet of ASG (Pegasus Glassworks, Inc., glass composition PM11) is formed into a sputtering target that is 3 in diameter and thick. The target is then bonded to a thick copper backing plate. A 1 square by 1.6 mm thick piece of soda lime glass (SLG), used as the original substrate, is cleaned in subsequent solutions of surfactant, deionized water, acetone, and isopropanol. A layer of ASG, approximately 2-4 m thick, is sputtered onto the substrate to serve as the sacrificial layer. A layer of Mo, approximately 600 nm thick, is then sputtered onto the surface at room temperature to serve as the lift-off layer. The sample is then removed from the deposition system.

(13) Referring now to FIGS. 3(a)-3(d), images of the lift-off process are shown at various stages of the etch process. The ASG lift-off layer is etched in HCl. The images were taken at a) 0 min., b) 4 min., c) 30 min., and d) after completion of the 3.5 hour etch. A piece of wide, 1 mil thick Kapton polyimide tape serves as the lift-off substrate and is adhered to part of the Mo surface using the tape's adhesive. The sample is etched in an HCL:H.sub.2O, 1:10 solution for approximately 3.5 hours. This process dissolves the ASG and separates the lift-off layer and lift-off substrate from the SLG substrate. The Mo film begins to separate from the soda lime substrate as the ASG is etched. The sample, just after being placed in the HCl solution is shown in FIG. 3(a). The portion of the film that is not under the tape is visibly separating in FIG. 3(b), while the film under the tape is partially etched in FIG. 3(c). The lift-off layer on the lift-off substrate, separated from the SLG substrate is shown in FIG. 3(d).

(14) Referring now to FIGS. 4 and 5, a photograph of the product is shown (FIG. 4) and a schematic diagram of the process by which the product was formed is shown (FIG. 5). The SLG substrate is the original substrate, the ASG and SiO.sub.x together are the sacrificial layer, the CIGS and Mo are the lift-off layer, the epoxy is the adhesive, and the PI is the lift-off substrate. A billet of ASG (Pegasus Glassworks, Inc., glass composition PM11) is formed into a sputtering target that is 3 in diameter and thick. The target is then bonded to a thick copper backing plate. A 1 square by 1.6 mm thick piece of soda lime glass, used as the original substrate, is cleaned in subsequent solutions of surfactant, deionized water, acetone, and isopropanol. A layer of ASG, approximately 4 m thick, is sputtered onto the substrate. A layer of SiO.sub.x, approximately 100 nm thick, is deposited on the sample via E-beam evaporation. The ASG and SiO.sub.x together comprise the sacrificial layer. A 2 m thick CIGS film is then RF sputtered from a quaternary target onto the sample while maintaining a substrate temperature of 550 C. at a power of 150 W. A layer of Mo, approximately 600 nm thick, is then sputtered onto the surface at room temperature. The CIGS and Mo together comprise the lift-off layer. The sample is then removed from the deposition system. A 1 square of flexible polyimide (PI) is bonded to the lift-off layer (directly to the Mo layer) with EPO-TEK 353-ND epoxy, and the epoxy is cured on a hot plate at a temperature of approximately 150 C. for 30 minutes. The PI serves as the lift-off substrate, and the epoxy is the adhesive. The sample is etched in reagent strength hydrochloric acid (HCl) for approximately 20 hours. This process dissolves the ASG and separates the lift-off layer, lift-off substrate, and SiO.sub.x from the original substrate. The sample is then etched in an HF:H.sub.2O, 1:1 solution for 30 s to dissolve the SiO.sub.x layer. The resulting product is the lift-off layer (a CIGS/Mo bilayer) on the lift-off substrate (a flexible PI substrate). In this example, the CIGS was deposited at a substrate temperature of 550 C.a temperature that the PI lift-off substrate could not withstand.

(15) Any suitable glass composition that yields a wet-etchable film could be used for the lift-off layer. The lift-off layer could be base-soluble, water soluble, or organic soluble, rather than acid-soluble. The lift-off layer could consist solely of SiO.sub.x. The lift-off substrate could be bonded to the lift-off layer with any suitable method, such as those based on silicone, polyurethane, thermoplastics, or pressure sensitive adhesives, rather than epoxy. During etching, force may be applied to aid in separation of the lift-off layer and the original substrate. Lift-off could be performed on a lift-off layer that is not bonded to a lift-off substrate, and the free film could be attached to a new substrate via adhesive, van der Waals forces, or friction. Lift-off could be performed on a lift-off layer that is not bonded to a lift-off substrate, and the free film could be used in flake or suspension form. The lift-off layer could be patterned via shadow mask, lithography or any other suitable means prior to lift-off. For PV applications, CIGS could be deposited via any suitable technique, such as evaporation, electrodeposition, etc., rather than sputtering. For PV applications other photovoltaic materials including, but not limited to, CZTS (Cu.sub.2ZnSn(S,Se).sub.4), cadmium telluride, and iron disulfide can be used instead of CIGS. Non-photovoltaic films, such as transparent conducting oxides, can be used as the lift-off layer.

(16) All documents mentioned herein are hereby incorporated by reference for the purpose of disclosing and describing the particular materials and methodologies for which the document was cited.

(17) Although the present invention has been described in connection with preferred embodiments thereof, it will be appreciated by those skilled in the art that additions, deletions, modifications, and substitutions not specifically described may be made without departing from the spirit and scope of the invention. Terminology used herein should not be construed as being means-plus-function language unless the term means is expressly used in association therewith.