SOFC interconnect barriers and methods of making same using masks
10541429 ยท 2020-01-21
Assignee
Inventors
Cpc classification
Y02E60/50
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
International classification
G03F1/00
PHYSICS
Abstract
A novel method to produce thin films spatially disposed on desired areas of workpieces is disclosed. Examples of include the formation of a yttria stabilized zirconia (YSZ) film formed on a desired portion of a stainless steel interconnect for solid oxide fuel cells by Atomic Layer Deposition (ALD). A number of methods to produce the spatially disposed YSZ film structures are described including polymeric and silicone rubber masks. The thin film structures have utility for preventing the reaction of glasses with metals, in particular alkali-earth containing glasses with ferritic stainless steels, allowing high temperature bonding of these materials.
Claims
1. A masking apparatus, comprising a mask material which is both flexible and thermally stable in the temperature range of 50-300 degrees Celsius, the mask material being removably attached to a substrate, wherein multiple masks and multiple substrates are removably stacked as a group, in order to prevent atomic layer deposition of a thin film on the substrates on the regions of the substrates covered by the masks.
2. The masking apparatus of claim 1, wherein the mask material is a polymer.
3. The masking apparatus of claim 1, wherein the mask material is silicone rubber.
4. The masking apparatus of claim 1, wherein the mask material is polyimide.
5. The masking apparatus of claim 1, wherein the mask material is held in place by clamping.
6. The masking apparatus of claim 1, wherein the clamping is accomplished by applying a differential pressure above and below the mask material.
7. A masking method, comprising choosing a mask material which is both flexible and thermally stable in the temperature range of 50-300 degrees Celsius, shaping the mask material into a shape which can conformally cover and thereby mask out a region of a substrate whereupon it is desirable not to deposit a thin film, removably attaching the shaped mask material to the substrate, removably stacking multiple masks and multiple substrates into a group, placing the stacked group into a deposition chamber, and depositing the thin film by atomic layer deposition, thereby covering at least part of the unmasked substrates with the thin film.
8. The masking method of claim 7, wherein attaching the shaped mask material to the substrate is accomplished by applying a differential pressure above and below the mask material.
9. The masking method of claim 7, wherein after depositing the thin film by atomic layer deposition, further removing the shaped mask material and incorporating a portion of the substrate into the structure of a solid oxide fuel cell.
10. The masking method of claim 7, wherein after depositing the thin film by atomic layer deposition, further removing the shaped mask material and bringing a portion of the substrate which has been covered by the thin film into contact with a vitreous reactive solid.
11. The masking method of claim 7, wherein attaching the shaped mask material to the substrate is accomplished by applying pressure above the mask material.
12. The masking method of claim 7, wherein attaching the shaped mask material to each of the substrates in the stacked group is accomplished by stacking alternating masks and substrates to form the stacked group, then applying pressure above and below the stacked group.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION OF THE INVENTION
(6) The present invention relates to the fabrication of zirconium oxide based ceramic barrier films on stainless steel by ALD with a complimentary method of limiting deposition of the film to desired areas.
(7)
(8) In one aspect, the invention relates to the use of ALD to deposit zirconium oxide based films. Alloying additions to the zirconia films include fluorite phase stabilizing elements such as yttrium (Y) and scandium (Sc). These stabilizing elements may be added in ranges from 4 mole percent to 8 mole percent for Y.sub.2O.sub.3, for example, to the zirconia in order to stabilize the zirconia over a wider temperature range. Grading of the YSZ through the thickness of the film may take place, with some regions having lower concentrations of the stabilizing element and other regions having higher concentrations of the stabilizing element.
(9) Using ALD, interlayers may also be added to the zirconium oxide based films, for example, aluminum oxide (Al.sub.2O.sub.3), forming a nanolaminate structure of alternating sublayers of aluminum oxide and zirconia, either or both materials of which may be doped with additional stabilizing elements. The nanolaminate may be a bilayer, having just two layers of different materials, or may have many alternating sublayers to form the overall thin film barrier structure. Grading of any sublayer within the nanolaminate may take place, with some regions of the sublayer having lower concentrations of the stabilizing element and other regions having higher concentrations of the stabilizing element. Use of one or more aluminum oxide sublayers in the nanolaminate may have benefits including, but not limited to, adhesion, nanolaminate stabilization, and diffusion prevention.
(10) The oxide ALD process uses pulses of a metal cation containing precursor and an oxidizing agent. The pulses are separated by pulses of inert gas to prevent reaction in the gas phase. A series of pulses characterized by a precursor dose pulse, purge pulse, oxidizer pulse, and purge pulse is known as an ALD cycle. The process may be carried out under constant flow, or the gas flow may be stopped at intervals during dosing to allow diffusion of species.
(11) In the deposition process, each ALD metal cation layer may use a mixture of precursors to produce multielement films, such as in the case of the previously mentioned yttria stabilization of zirconia, or different ratios of pulses may be used to produce a final film which contains multiple elements. In this latter case, where different ratios of pulses are used, one might, for example, use 9 pulse cycles of a zirconium precursor and oxidizer followed by 1 pulse cycle of yttrium precursor and oxidizer to produce a film containing approximately 10% of yttria in zirconia. Partial saturation of metal cation layers, each cycle with or without full reaction with oxidizers, may also be used to allow this composition mixture with fewer overall cycles. A heat treatment or anneal may then be used to interdiffuse the layers and produce a desired overall mixture such as YSZ. Note that a barrier layer on a metallic substrate may be directly in contact with the metallic substrate material, or may be over other layers which may be present on the substrate for various reasons such as, but not limited to, adhesion, nucleation, thermal expansion coefficient matching or crystallization of the barrier layer.
(12) Metalorganic precursors for yttrium, scandium and zirconium include a number of metalorganic compounds, including ketonates, iminates, alkoxides, amides, amidinates, guanidinates, and cyclopentadienyls. In general, many of these compounds are useful for ALD. Specifically, amides of Zr show excellent reactivity with water as an oxidizing agent. Useful amide sources for Zr include tetrakisdimethylamido Zr (TDMAZ), tetrakisdiethylamido Zr (TDEAZ), and tetrakisethylmethylamido Zr (TEMAZ). Yttrium and scandium sources with good reactivity for water include triscyclopentadienyl Y (Y(Cp).sub.3), trismethylcyclopentadienyl Y (Y(Me-Cp).sub.3), trispropylcyclopentadienyl Y (Y(Pr-Cp).sub.3), triscyclopentadienyl Sc (Sc(Cp).sub.3), trismethylcyclopentadienyl Sc (Sc(Me-Cp).sub.2), and trisproylcyclopentadienyl Sc (Sc(Pr-Cp).sub.2). Other oxidants may include ozone or oxygen plasma.
(13) ALD may be carried out with solid or liquid sources held in bubblers through which a carrier gas is flowed to convey the source to the deposition chamber. The sources may also be dissolved in an organic solvent as individual sources or combined together. Key criteria of a solvent system are (1) high boiling point to reduce the chance of flash off of the solvent, (2) high solubility for the compound, (3) low cost. Useful hydrocarbon solvents may include, for example: octane, decane, isopropanol, cyclohexane, tetrahydrofuran, and butyl acetate or mixtures comprising these and other organic solvents. Lewis base adducts may also be incorporated as additions to the solvent(s) for beneficial effects on solubility and to prevent possible oligimerization of the precursor molecules. Examples of useful Lewis Bases include polyamines polyethers, crown ethers, and the like. Pentamethylenediamine is a one example of a polyamine. Examples of polyethers include various glymes such as mono-, di-, tri-, and tetraglyme.
(14) Turning to the deposition process, we note that most ALD processes exhibit what is known as an ALD window with respect to temperature. In this temperature range, growth of the film is surface mononlayer saturation limited. The practical result is that deposition (thickness) per ALD cycle is the same, as long as sufficient material is provided to the surface. After saturation, further supply of material in the gas phase does not increase growth per cycle. The primary objective in the present invention is the formation of a film of as conformal in nature as possible, i.e., with a uniform thickness over asperities. Crystallinity is also preferred. The upper end of the ALD window temperature range offers a good mix of conformality and the potential for good crystallinity. Post-deposition annealing in an oxygen containing atmosphere may also be used to promote crystallinity in the film.
(15) The deposition system may have an automated throttle valve that allows pressure to be controlled independently of flow. In this way, residence times can be manipulated more directly. The hot-wall type reactor is one type of reactor that may be used to deposit the subject films. Alternatives include batch hot-wall reactor or warm-wall showerhead type reactors.
(16) Process conditions favorable for ALD of zirconia based films are in the temperature range of 150250 C. with pressures in the range of 1-5 Torr. Surface preparation (termination) can be very important in ALD. Pre-treatments to promote uniform nucleation include aqueous acids/bases compatible with the substrate and that result in H or OH termination of the substrate surface.
(17) Embodiments for ALD of zirconia based films on ferritic stainless steel include the following examples.
Example 1
(18) A yttria stabilized zirconia film is deposited on ferritic stainless steel using TDEAZ and Y(Cp).sub.3 at 220 C. Reactor pressure is 2 Torr. Dose times for TDEAZ, Y(Cp).sub.3 and water vapor are 5 seconds. Purge times are 10 seconds. Nitrogen is used to transport the precursors to the deposition chamber and as the inert purge. A number of ALD cycles are used to deposit the film, with a ratio of 6 Zr cycles to 1 Y cycle. Interspersed in the ALD cycles are cycles of Al.sub.2O.sub.3 deposited using trimethylaluminum (TMA). The overall film thickness is between 5 and 500 nm.
Example 2
(19) A yttria stabilized zirconia film is deposited on ferritic stainless steel using TDEAZ and Y(Me-Cp).sub.3 at 230 C. Reactor pressure is 1 Torr. Dose times for TDEAZ, Y(Me-Cp).sub.3 and water vapor are 5 seconds. Purge times are 10 seconds. Nitrogen is used to transport the precursors to the deposition chamber and as the inert purge. A number of ALD cycles are used to deposit the film, with a ratio of 6 Zr cycles to 1 Y cycle. A hydroxide terminating treatment is used before ALD. The ferritic stainless steel has a Cr.sub.2O.sub.3 surface layer that is exposed to dilute nitric acid for 10 seconds at room temperature. The surface is rinsed in water and then exposed to a mixture of sulfuric acid and 30% hydrogen peroxide-water in a 3:1 ratio for 10 seconds. The surface is then rinsed and dried. The Y dose is applied first to the substrate, followed by Zr. The overall film thickness is between 5 and 500 nm.
Example 3
(20) A yttria stabilized zirconia film is deposited on ferritic stainless steel using TDMAZ and Y(Me-Cp).sub.3 at 230 C. Reactor pressure is 1 Torr. Dose times for TDMAZ, Y(Me-Cp).sub.3 and water vapor are 5 seconds. Purge times are 10 seconds. Nitrogen is used to transport the precursors to the deposition chamber and as the inert purge. A number of ALD cycles are used to deposit the film, with a ratio of 6 Zr cycles to 1 Y cycle. A dense, highly conformal YSZ film deposited on ferritic stainless steel using 798 ALD cycles is shown in the SEM micrographs of
(21) In another aspect, the invention relates to the use of zirconia based ceramic films fabricated in such a manner as a reaction blocking layer with alkali-earth containing glasses. In
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(23) In another aspect, the invention relates to the use of masking to restrict deposition of the barrier layer to desired areas on the workpiece. It is well known that ALD processes coat workpieces quite uniformly and typically over all exposed surfaces. It is therefore a great advantage to devise a scheme by which only a portion of the surface is coated, specifically in a desired area. For SOFC interconnects, the desired area is the perimeter of the interconnect where the glass seal is formed. It is desired not to coat the central area of the interconnect where electrical conductivity is needed. A thermally stable mask is used. The low thin film deposition temperature achievable via use of ALD in this invention is particularly advantageous in allowing use of inexpensive, easily shaped, flexible and reusable mask materials such as elastomers to carry out this masking process.
Example 4
(24) A self-adhesive polyimide film is applied to the substrate prior to deposition of YSZ by ALD. After deposition, the polyimide film is peeled off.
Example 5
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(26) Multiple substrates and masks may be stacked to allow many substrates to be coated simultaneously. The masks may be continuous sheets of silicone rubber or gasket like sheets where a perimeter seal protects and interior area. The masks may be clamped outside of the ALD process (ex-situ) or inside the ALD process chamber (in-situ) by suitable mechanisms such as a camshaft actuated via a rotary vacuum feed-through. Mask materials may also be applied or attached to the substrate as liquids or viscous liquids by dispensing or flowing the mask material onto the substrate, which case the shaping of the mask structure may be carried out by methods such as lithography, stencils, stamps, etc.
(27) The subject invention may be embodied in the forgoing examples that are by no means restrictive, but intended to illustrate the invention.