The present invention relates generally to solid oxide fuel cells, and, more particularly, to tubular solid-oxide fuel cells having an inner anode layer and multiple anodic current collection points to improve efficiency of the fuel cell.
Tubular solid oxide fuel cells (SOFCs). represent a significant advantage over planar-type SOFCs due to enhanced gas collection capability, ease of manufacture, and strength of the tubular design. Anode supported tubular SOFCs possess additional advantages over cathode or electrolyte supported cells due to lower cost, greater strength, and more intimate relationship with the critical gas component: the fuel. With this capture of the fuel, they also inherently have the ability to perform on-cell reformation of fuels rather than require external reforming equipment.
As shown in
One drawback of the current collection arrangement shown in
Siemens Westinghouse describes the use of a strip down the length of a cathode supported fuel cell, allowing current collection along the length, with only circumferential losses. With such a design, improved current collection is generally realized at the expense of a more complicated system design and greater variability in the packing of the tubular fuel cells.
In accordance with one aspect of the invention there is provided a solid-oxide fuel cell comprising a tubular inner anode having an inside and an outside; at least one tubular electrolyte segment formed on the outside of the anode; a tubular cathode segment formed on an outside of each electrolyte segment; and at least one discrete anodic current collector formed on the outside of the anode and accessible from outside of the fuel cell. The at least one discrete anodic current collector operates to reduce the effective operational length of the fuel cell.
In various alternative embodiments, each discrete anodic current collector may form a complete ring around the anode to maintain structural integrity. The anodic current collectors may be ceramic (e.g., LaCrO3 or other suitable dual atmosphere ceramic) or metallic (e.g., nickel or other suitable dual atmosphere metal).
In additional embodiments, the at least one discrete anodic current collector may include an anodic current collector positioned at a proximal end of the fuel cell and an anodic current collector positioned at a distal end of the fuel cell. A wire may be coupled to the anodic current collector positioned at the distal end of the fuel cell and run through the inside of the anode to the proximal end. The at least one. discrete anodic current collector may further include at least one additional anodic current collector positioned between the proximal and distal ends, for example, substantially at a mid-point of the fuel cell.
In further embodiments, the at least one discrete anodic current collector may include an anodic current collector positioned along the length of the anode away from the ends, for example, substantially at a mid-point of the fuel cell. The at least one discrete anodic current collector may additionally or alternatively include a plurality of anodic current collectors positioned along the length of the fuel cell, for example, an anodic current collector positioned substantially at a mid-point of the fuel cell and additional anodic current collectors positioned proportionally from each end of the fuel cell.
In still further embodiments, the fuel cell may include at least one cathodic current collector adjacent to each anodic current collector. For example, the fuel cell may include two electrolyte segments and corresponding cathode segments separated by an anodic current collector, in which case the at least one cathodic current collector may include a cathodic current collector associated with each of the cathode segments.
In still further embodiments, the fuel cell may include an end cap coupled to one end of the tubular inner anode and couplable to a tubular inner anode of another such fuel cell, wherein the end cap is operably as an anodic current collector for both fuel cells. Thus, a larger fuel cell may be constructed from multiple fuel cells interconnected via the end cap. Each fuel cell may have an end cap, in which case the end caps may be connected so as to form the larger fuel cell. The end cap(s) typically allow fuel to flow between the fuel cells.
The foregoing and advantages of the invention will be appreciated more fully from the following further description thereof with reference to the accompanying drawings wherein:
In embodiments of the present invention, current is collected from the inner anode layer of a tubular solid-oxide fuel cell (SOFC) at one or more discrete points along the length of the fuel cell rather than at a single end of the fuel cell or using a strip down the entire length of the fuel cell. For example, current can be collected from the anode layer at both ends of the fuel cell, once in the center of the fuel cell, or at any of a multitude of axial points along the length of the fuel cell. Such discrete current collection points generally reduce the effective operational length of each section, eliminate circumferential losses for cells of any diameter, and allow for a simplified current collection arrangement. The system can be easily arranged in multiple geometries, with exceptional thermal cycling robustness and ease of connection due to the use of the entire circumference in the tubular geometry (rather than a strip along one side, minimizing stress buildup by maximizing strength) and the discrete placement of the connections along the length. Generally speaking, the more current collection points per given length of fuel cell, the higher the peak power of that fuel cell under any given circumstance. This can result in substantial gains in overall system performance and significant reduction of fuel cell costs. Increasing the length of the fuel cell and adding additional current collection points along the length allow the fuel cell to be as long as desired without the penalty of increased resistances, equating to an increase in power directly proportional to the length of the fuel cell.
The anode current collectors can be manufactured in a variety of ways, including, but in no way limited to, use of multiple metallic joints at either end of the tubular cell, use of a ceramic connection at either end of the cell, use of metallic connections at some or multiple points along the cell length, and use of ceramic connection at some or multiple points along the cell length.
An exemplary ceramic current collector for an end of the SOFC can be made from an appropriately conductive material, such as LaCrO3, pressed into a form such that it forms a cap around the end of the tubular cell. It can then be simultaneously electrically connected and sealed by melting a metal (Au, Ag, Cu, Pt, Pd, Ni, Co, Zn are among the metals that could be used) brazing operation, or might be sintered together with one of these same metals, or a ceramic bond utilizing, among other materials, Fe, Si, Al, La, Cr, or Mn. This connection could also be formed by a ceramic-ceramic sinter bond. A ceramic or metallic lead (e.g., Ag) can be connected to the end cap, and current passed through it.
An exemplary metallic current collector for an end of the SOFC can be made by the brazing of a Ni cap to the end of the cell, and the insertion of an Ag pin, which allows an electrical connection from the external (air) side of the cell to the internal (fuel) side. Current can then be passed through the connection. On the other side of the cell, a Ni cup can be brazed to the cell. This cup acts as both a current collection device and a fuel distribution device.
For a metallic current collector, two caps can be brazed onto two separate cells. The two cells can then be joined by a metallic connector into which both cells are screwed. This connector allows gas to flow between cells, while providing a connection between the two cells. An Ag pin can be attached to the connector to allow for anodic current collection. Pins could also be formed of any appropriate ceramic, metal, or otherwise conductive materials that would survive in oxidizing or reducing atmospheres.
For a ceramic current collector, an appropriate dual-atmosphere ceramic, such as LaCrO3, can be formed into a ring around the cell at the mid-length point. An Ag connection can be made to the ceramic as the anodic current collection point.
As shown in
In accordance with embodiments of the present invention, a SOFC could be made to whatever length is desired, with any diameter desired, and the effective cell length could be maintained constant. This significant result allows the formation of cells of any size dictated by other parameters (e.g., cost, packing density, ease of manufacture) without impact on the power that the cell can produce while minimizing the necessary fuel “manifolding.” When lengthening the cell or increasing the cell diameter, one or more connections generally need to be made as appropriate for the design.
Thus, the present invention may be embodied as a tubular SOFC having an inner anode and at least one anode current collector positioned so as to reduce the effective operational length of the fuel cell. Embodiments preferably minimize circumferential and axial losses while providing significant power improvement and potentially cost savings.
Embodiments may include a single anode current collector located away from the ends of the fuel cell (e.g., substantially at a midpoint of the fuel cell), anode current collectors at both ends of the fuel cell, anode current collectors at multiple points along the length of the fuel cell, or a combination of these. Current collectors may be ceramic or metallic. Ceramic current collectors may be formed from LaCrO3 or other suitable dual atmosphere ceramic and may be formed by plasma spray methods, vacuum infiltration, or sintering. Metal current collectors may be formed from Ni or other suitable dual atmosphere metal.
A single fuel cell may be fabricated from multiple fuel cell segments coupled together by an anode current collector. For example, two caps can be brazed onto two separate cells. The two cells can then be joined by a metallic connector into which both cells are screwed. This connector allows gas to flow between cells, while providing a connection between the two cells. An Ag pin can be attached to the connector to allow for anodic current collection. Pins could also be formed of any appropriate ceramic, metal, or otherwise conductive materials that would survive in oxidizing or reducing atmospheres.
The present invention may also be embodied as a tubular SOFC having an inner anode layer, an electrolyte layer, a cathode layer, and anode current collectors positioned at both ends of the fuel cell, for example, as shown in
The present invention may also be embodied as a tubular SOFC having an inner anode layer, an electrolyte layer, a cathode layer, at least one anode current collector formed around the anode at a point along the length of the anode away from the ends, for example, as shown in
The present invention may also be embodied as a method for fabricating a tubular SOFC involving forming or attaching anode current collectors at both ends of a fuel cell having an inner anode. The anode current collectors may be ceramic or metallic.
The present invention may also be embodied as a method for fabricating a tubular SOFC involving forming at least one anode current collector around an inner fuel cell anode. Multiple anode current collectors can be placed at different points along the length of the fuel cell. One or more cathode current collectors may be positioned adjacent to each anode current collector. The anode current collector(s) may be ceramic or metallic.
Prototype fuel cells were tested with some of the variations described above. All cells were tested at 800 degrees Celsius, 75% fuel utilization on a 3%H20/H2 gas mixture with six times the required air. Cells were maintained at these conditions as power was peaked, and that value recorded. It was found that the prototypes generally had significantly improved performance over current SOFCs that use a current collector at one end only. It was also found that the use of the ceramic or metallic connection components had no significant effect on performance. The following table summarizes the relative performance of the experimental cells:
In order to collect current from an anode current collector, an external connector (e.g., silver) may be attached to the current collector. For example, in an SOFC having anode current collectors at both ends of the SOFC as shown in
Thus, in one alternative embodiment, a wire is run from the far end cap through the inside of the tube to the near end of the tube, for example, for coupling with a near end cap or manifold.
Thus, the present invention may be embodied as a tubular SOFC having an inner anode with an anode current collector positioned at one end of the fuel cell and a wire electrically coupled to the anode current collector and passing through the interior of the fuel cell to the other end of the fuel cell. The wire may be coupled to an end cap that is attached to the anode current collector.
The present invention is not limited to the embodiments described herein or by the performance information disclosed herein. For example, one or more discrete anodic current collectors can be used in solid-oxide fuel cells having an inner anode generally in order to reduce the effective operational length of the fuel cell.
The present invention may be embodied in other specific forms without departing from the true scope of the invention. The described embodiments are to be considered in all respects only as illustrative and not restrictive.
This patent application claims priority from U.S. Provisional Patent Application No. 60/671,595 entitled CURRENT COLLECTION IN ANODE SUPPORTED TUBULAR FUEL CELLS, which was filed on Apr. 15, 2005 in the names of Jolyon Rawson, Michael Brown, Neil Fernandes, Norman F. Bessette, and Douglas S. Schmidt, and is hereby incorporated herein by reference in its entirety.
This invention was made with Government support under DE-FC26-03NT 41838 awarded by the U.S. Department of Energy. The Government has certain rights in this invention.
Number | Date | Country | |
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60671595 | Apr 2005 | US |