Patent Application
20070207373
The present invention relates to solid oxide fuel cell (SOFC) cathode material compositions, and more particularly to SOFC cathode material compositions that contain Ca and Fe.
Devices commonly known as fuel cells comprise plates or tubes that directly convert to electricity the energy released by oxidation of hydrogen. Fuel cells offer the potential for a clean, quiet, and efficient power source for portable electric generation. Solid oxide fuel cells (SOFC), particularly tubular solid oxide fuel cells (TSOFC), are particularly attractive candidates for applications in distributed or centralized power applications.
SOFC technology has the potential for providing high power densities, long, stable performance lifetimes, the ability to utilize a broad source of fuels without expensive reforming or gas cleanup, and provide high system efficiencies for a wide range of power generation for transportation.
Initially, solid oxide fuel cells (SOFC) used lanthanum manganite (LSM) as the cathode—a good electron conductor, but a poor oxygen ion conductor. These electrodes are porous, up to 40% by volume and are placed adjacent to an yttria stabilized zirconia (YSZ) electrolyte. As the cathode is essentially only an electron conductor the reaction point where the oxygen molecule is ionized forming oxygen ions occurs at the point (triple point) where the air (pore), cathode (LSM) and electrolyte come together. In theory, the more points (higher surface area) the lower the interfacial polarization and the more efficient the ionization and exchange of oxygen. However, higher surface area cathodes tend to lead to increased in-plane resistance, higher polarization, and lower efficiency.
One route to improve upon the aforementioned problem is to alter the materials properties, introducing oxygen ion conductivity while maintaining electronic conduction, thus making the reaction point a reaction surface. In this case, oxygen is ionized and transported anywhere on the cathode surface-greatly reducing interfacial losses. This has been demonstrated with lanthanum ferrite and cobalt doped lanthanum ferrite.
At least one negative issue known to be associated with the use of the above-described materials is that they react with the zirconia electrolyte, forming unwanted insulating phases. Several other issues are the cost of La and that the oxygen ion conductivity is limited to less than 10% of the total conductivity. This is a constraint of the structure that has not been overcome by modifying the La-ferrite or La-magnetite compositions. Therefore, a new and different compositional approach is warranted.
U.S. Pat. No. 6,471,921 issued on Oct. 29, 2002 to Van Calcar, et al. entitled “Mixed Ionic and Electronic Conducting Ceramic Membranes for Hydrocarbon Processing” and U.S. Pat. No. 6,641,626 issued on Nov. 4, 2003 to Van Calcar, et al. entitled “Mixed Ionic and Electronic Conducting Ceramic Membranes for Hydrocarbon Processing” are referenced as relevant background information, the entire disclosures of which are incorporated herein by reference.
Accordingly, objects of the present invention include provision of SOFC cathode material compositions at a potentially lower cost (because inexpensive, readily available materials are used in the composition), higher oxygen ion conductivity, and lower interfacial resistance under operating conditions. Further and other objects of the present invention will become apparent from the description contained herein.
In accordance with one aspect of the present invention, the foregoing and other objects are achieved by a solid oxide fuel cell that includes a porous anode, a dense electrolyte in contact with the porous anode, and a porous cathode in contact with the dense electrolyte.
The porous cathode is characterized by a single-phase structure of Brownmillerite or Srebrodolskite, the composition thereof having the formula
(Ca2-xAx)(Fe2-yBy)O5±z
wherein:
A is at least one element selected from the group: rare earth elements, Bi, and alkaline elements;
B is at least one element selected from the group: Al, Ga, In, Mg, Si, and transition metal elements; 0≦x<2; 0≦y<2; and
z is a variable, the value of which is such that the overall composition has a generally neutral charge state.
For a better understanding of the present invention, together with other and further objects, advantages and capabilities thereof, reference is made to the following disclosure and appended claims in connection with the above-described drawings.
Referring to
In accordance with the present invention, the cathode 14 comprises at least one composition such as Ca2Fe2O5 and related compositions having the general formula
(Ca2-xAx)(Fe2-yBy)O5±z
Wherein:
A (A-site dopant) is at least one element selected from the group: rare earth elements (La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu), Bi, and alkaline elements such as Ba, Sr, Y, Na, Li, or K, for example;
B (B-site dopant) is at least one element selected from the group: Al, Ga, In, Mg, Si, and transition metal elements (Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Y, Zr, Nb, Mo, Tc, Ru, Rh, Pd, Ag, Cd, Hf, Ta, W, Re, Os, Ir, Pt, Au, and Hg);
0≦x<2 and 0≦y<2. Doping of at least one of the A site and the B site is optional. The value of z depends upon the values of x and y and the oxidation states of the Ca, A, Fe, and B elements. The value of z is such that the composition has a neutral charge state. In preferred materials, 0<z<1.
The morphology of new cathode material of the present invention is characterized by a single-phase structure that is an oxygen-deficient derivative of the perovskite structure, specifically either the Brownmillerite or the closely related Srebrodolskite structure.
The new cathode material of the present invention demonstrates high oxygen ion conductivity and when used as a cathode for a solid oxide fuel cell distributes the oxygen exchange from a single point to a three dimensional surface reducing interfacial polarization losses and improving fuel cell performance.
It will be apparent to the skilled artisan that, in view of Examples I and II, other A- and B-site dopants that have been contemplated, as listed hereinabove, will produce operable embodiments of the present invention.
While there has been shown and described what are at present considered the preferred embodiments of the invention, it will be obvious to those skilled in the art that various changes and modifications can be prepared therein without departing from the scope of the inventions defined by the appended claims.
The United States Government has rights in this invention pursuant to contract no. DE-AC05-00OR22725 between the United States Department of Energy and UT-Battelle, LLC.
