None.
This invention relates to a method for producing solid oxide fuel cells with thickness graded electrolyte.
A solid oxide fuel cell (SOFC) system can be subjected to various interruptions that can prevent electricity from being generated from the SOFC system. One known problem is the unevenness of temperature across a SOFC when in operation.
SOFCs typically consist of three ceramic components, a dense electrolyte and two porous electrodes. Oxygen is reduced to oxygen ions in the cathode and the oxygen ions are transported through the thin electrolyte and react with fuel in the anode to generate water vapor and/or carbon dioxide. Electrons released at the anode flow through the external circuit and produce electricity. Performance of SOFC's is governed by ohmic resistance of the electrolyte and the polarization resistance of electrodes.
The operation of these SOFC's causes significant temperature gradients to exist due to various causes such as cooling effect from feeding gases, fuel utilization variation in different cell regions, the endothermic internal reforming of hydrocarbon fuels, and convection cooling around cell outer perimeters. In some SOFCs the temperature gradient can be as much as 150° C. Excessive temperature gradients will affect fuel cell efficiency since each fuel cell material is best suited for a particular temperature range. In addition, large temperature gradients can result in high levels of thermal stress which can impair durability and reliability of the cells and stacks.
There exists a need for a SOFC that can maintain an even temperature across the electrolyte surface during operation.
A solid oxide fuel cell comprising a variable thickness electrolyte layer in contact between an anode and a cathode. The solid oxide fuel cell also comprises a fuel inlet and a fuel outlet. In the solid oxide fuel cell, the variable thickness electrolyte layer is thinner n areas closer to the fuel inlet and thicker closer to the fuel outlet. A planar solid oxide fuel cell comprising an yttria-stabilized zirconia variable thickness electrolyte layer in contact between an anode, comprising nickel oxide and yttria-stabilized zirconia, and a cathode comprising lanthanum strontium cobalt ferrite and gadolinium doped ceria. The solid oxide fuel cell also comprises a fuel inlet and a fuel outlet. In this embodiment, the yttria-stabilized zirconia variable thickness electrolyte layer in areas closer to the fuel inlet of natural gas is thinner than in areas closer to the fuel outlet of natural gas. Additionally, the difference between the thickest area of the yttria-stabilized zirconia variable thickness electrolyte layer and the thinnest area of the yttria-stabilized zirconia variable thickness electrolyte layer is greater than about 2.0 μm.
A more complete understanding of the present invention and benefits thereof may be acquired by referring to the follow description taken in conjunction with the accompanying drawings in which:
Turning now to the detailed description of the preferred arrangement or arrangements of the present invention, it should be understood that the inventive features and concepts may be manifested in other arrangements and that the scope of the invention is not limited to the embodiments described or illustrated. The scope of the invention is intended only to be limited by the scope of the claims that follow.
The following examples of certain embodiments of the invention are given. Each example is provided by way of explanation of the invention, one of many embodiments of the invention, and the following examples should not be read to limit, or define, the scope of the invention.
During the operation of a SOFC fuel enters from one side (fuel inlet) and exits from the other side (fuel outlet). In different embodiments of the novel SOFC it is envisioned that the electrolyte layer will be thinner closer to the fuel inlet of fuel flow and thicker closer to the fuel outlet of fuel flow. In an alternate embodiment it is envisioned that the electrolyte layer will be thicker closer to the fuel inlet of fuel flow and thinner closer to the fuel outlet of fuel flow.
In one embodiment, the difference between the thickest area of the variable thickness electrolyte layer and the thinnest area of the variable thickness electrolyte layer is greater than about 50 μm, in other embodiments it is greater than 2 μm, 10 μm even 30 μm. In another embodiment, the difference between the thickest area of the variable thickness electrolyte layer and the thinnest area of the variable thickness electrolyte layer is from about 1 μm to about 50 μm. In yet another embodiment, wherein the difference between the thickest area of the variable thickness electrolyte layer and the thinnest area of the variable thickness electrolyte layer is from about 5 μm to about 10 μm.
In one embodiment, variable thickness electrolyte materials for the SOFC can be any conventionally known electrolyte materials. One example of electrolyte materials can include doped zirconia electrolyte materials, doped ceria materials or doped lanthanum gallate materials. Examples of dopants for the doped zirconia electrolyte materials can include: CaO, MgO, Y2O3, Sc2O3, Sm2O3 and Yb2O3. In one embodiment the variable thickness electrolyte material is a yttria-stabilized zirconia, (ZrO2)0.92(Y2O3)0.08.
In one embodiment, anode materials for the SOFC can be any conventionally known anode materials. Examples of the anode materials can include mixtures of NiO, yttria-stabilized zirconia, CuO, CoO, and FeO. In one embodiment the anode material is a mixture of 50 wt % NiO and 50 wt % yttria-stabilized zirconia. In another embodiment the anode material is a mixture of a nickel oxide and a gadolinium doped ceria.
In one embodiment, cathode materials for the SOFC can be any conventionally known cathode materials. One example of cathode materials can be perovskite-type oxides with the general formula ABO3, wherein A cations can be La, Sr, Ca, Pb, etc. and B cations can be Ti, Cr, Ni, Fe, Co, Zr, etc. Other examples of cathode materials can be mixtures of electronic conductors such as lanthanum strontium cobalt ferrite, lanthanum strontium manganite and ionic conductors such as yttria-stabilized zirconia, gadolinium doped ceria. Examples of the cathode materials include: La0.6Sr0.4CoO3-δ; Pr0.5Sr0.5FeO3-δ; Sr0.9Ce0.1Fe0.8Ni0.2O3-δ; Sr0.8Ce0.1Fe0.7Co0.3O3-δ; LaNi0.6Fe0.4O3-δ; Pr0.8Sr0.2Co0.2Fe0.8O3-δ; Pr0.7Sr0.3Co0.2Mn0.8O3-δ; Pr0.8Sr0.2FeO3-δ; Pr0.6Sr0.4Co0.8Fe0.2O3-δ; Pr0.4Sr0.6Co0.8Fe0.2O3-δ; Pr0.7Sr0.3Co0.9Cu0.1O3-δ; Ba0.5Sr0.5Co0.8Fe0.2O3-δ; Sm0.5Sr0.5CoO3-δ; Pr2NiO4+δ; and LaNi0.6Fe0.4O3-δ. In one embodiment the cathode material is a mixture of gadolinium-doped ceria (Ce0.9Gd0.1O2) and lanthanum strontium cobalt ferrite (La0.6Sr0.4Co0.2Fe0.8O3) or a mixture of gadolinium-doped ceria (Ce0.9Gd0.1O2) and samarium strontium cobaltite, Sm0.5Sr0.5CoO3.
In one embodiment, the formation of the variable thickness electrolyte layer is formed on an anode support using a spray coating process. Formation of the electrolyte slurry can be made by mixing suitable materials for forming the electrolyte powder with solvents, dispersants, binders and plasticizers to form a stable slurry. The resulting slurry is then applied on top of an anode substrate to form a continuous electrolyte layer using a spray nozzle. Variation in electrolyte thickness can be achieved either by adjusting flow rate of electrolyte slurry or by changing the number of spray passes. The number of passes can range from about 2 to about 50. Other methods for varying electrolyte thickness may include tape casting and lamination, dry pressing with specially designed pressing heads, and thermal spraying such as plasma spraying and high velocity oxy-fuel spraying.
An SOFC with a variable thickness electrolyte was made. Four thermocouples were placed along the SOFC along the variable thickness electrolyte layer. Thermocouple 1 (T1) was placed in an area wherein the electrolyte layer was 3-4 μm thick, thermocouple 2 (T2) was placed in an area wherein the electrolyte layer was 4-5 μm thick, thermocouple 3 (T3) was placed in an area wherein the electrolyte layer was 5-6 μm thick, and thermocouple 4 (T4) was placed in an area wherein the electrolyte layer was 7-8 μm thick.
This variable thickness electrolyte was operated to generate a current density of 200 mA/cm2 and 400 mA/cm2. A baseline cell with uniform electrolyte thickness of 6 μm, and thermocouples placed in the same location, was operated to generate a current density of 200 mA/cm2 and 400 mA/cm2 as well.
In closing, it should be noted that the discussion of any reference is not an admission that it is prior art to the present invention, especially any reference that may have a publication date after the priority date of this application. At the same time, each and every claim below is hereby incorporated into this detailed description or specification as an additional embodiment of the present invention.
Although the systems and processes described herein have been described in detail, it should be understood that various changes, substitutions, and alterations can be made without departing from the spirit and scope of the invention as defined by the following claims. Those skilled in the art may be able to study the preferred embodiments and identify other ways to practice the invention that are not exactly as described herein. It is the intent of the inventors that variations and equivalents of the invention are within the scope of the claims while the description, abstract and drawings are not to be used to limit the scope of the invention. The invention is specifically intended to be as broad as the claims below and their equivalents.
This application is a non-provisional application which claims the benefit of and priority to U.S. Provisional Application Ser. No. 62/560,355 filed Sep. 19, 2017, entitled “Solid Oxide Fuel Cells with Thickness Graded Electrolyte”, which is hereby incorporated by reference in its entirety.
Number | Date | Country | |
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62560355 | Sep 2017 | US |