This invention relates to fuel cells.
Fuel cells are a type of electrochemical energy conversion device. In contrast to a battery, fuel cells do not store all of the chemicals that are to be converted; rather, at least one of the chemicals is supplied externally, usually from a fuel tank. Consequently, fuel cells do not run out of (internal) chemicals and so do not become “dead”, as batteries do. Fuel cells are known in a number of different varieties. Fuel cells based on hydrogen and oxygen are particularly common today. Fuel cells may be classified according to their electrolyte, for example alkaline fuel cells (AFCs), phosphoric-acid fuel cells (PAFCs), solid oxide fuel cells (SOFCs) and molten carbonate fuel cells (MCFCs).
Alkaline fuel cells are of particular interest because they operate at relatively low temperatures and pressures, are efficient and rugged. Acid fuel cells and fuel cells employing other aqueous electrolytes are also of interest. Such fuel cells typically comprise an electrolyte chamber separated from a fuel gas chamber (containing a fuel gas, typically hydrogen) and a further fuel gas chamber (containing an oxidant gas, usually air). The electrolyte chamber is separated from the gas chambers using electrodes. The standard electrodes for alkaline fuel cells comprise a conductive metal grid or mesh backbone, typically nickel, that provides a mechanical strength to the electrode. Onto the metal mesh or grid is deposited a slurry or dispersion of particulate poly tetra-fluoroethylene (PTFE), activated carbon and a catalyst metal, typically platinum.
Whilst use of alkaline fuel cells in the present invention is preferred, the invention is not limited to alkaline fuel cells but rather is suitable for other kinds of fuel cells, particularly those that operate at relatively low temperatures (say less than 100° C.).
Fuel cells typically comprise at least two electrodes fixed to plates or frames, which are typically plastic, and which are typically moulded together to form a stack. The stack has inlets and outlets for fuels and waste products, respectively. After a period of use the performance of the stack will deteriorate due to deterioration of the electrodes, which may become corroded. The stack is then thrown away and replaced with a new stack.
According to a first aspect of the invention there is provided a fuel-cell assembly comprising:
Fuel-cell electrodes are relatively low-cost, compared with other parts of the fuel cell stack. When the electrodes are moulded into a stack, the whole stack must be disposed of as a single unit when electrodes have deteriorated to the point at which they need replacing. By providing electrodes that are held loosely within the stack, the invention allows replacement of the electrodes, whilst allowing reuse of the other parts of the stack. The invention may therefore provide electrodes that are “loose”, in the sense that they can readily be removed from the stack and replaced. Since the stack may be disassembled, its constituent parts may be recycled or disposed of individually.
The electrodes may be of a shape complementary to the shape of the frame in which they are held, the shapes being such that the electrodes can be held only in one orientation. Allowing the electrodes to be installed in only one orientation eliminates the possibility of installing new electrodes in an incorrect orientation when old electrodes are replaced.
In a preferred embodiment the electrodes comprise: a substrate comprising a relatively hydrophilic plastics material, the substrate being permeable to aqueous fuel cell electrolytes; a conductive layer comprising a substantially uniform layer of conductive metal; and a catalyst layer. These layers may be discrete superimposed layers. Electrodes of that form are described in a PCT Patent Application by the same applicant PCT/GB2007/050104; the contents of that Application are hereby incorporated by reference. Such an electrode is relatively cheap compared with the cost of other components within the stack and so replacement of the electrodes and reuse of the rest of the stack is particularly cost efficient. However, the invention is not limited to use of such an electrode.
The stack may further comprise a monitor for monitoring the electrodes to determine when they need to be replaced. For a given power output, the current output from the stack is typically substantially fixed. Thus, the voltage may be monitored and, when the voltage falls below a predetermined value, a decision may be made to replace the electrode.
The clamp may comprise a resilient member. Use of a resilient member allows the stack to expand or contract with temperature changes without the clamping of the components being compromised. The clamp may comprise a strap strapped around the stack. The end plates of the stack which are in contact with the strap may be larger than the frames of the stack. The strap may be seated in a groove. The strap may be made from a material that expands and contracts with changes in temperature by an amount sufficient to prevent the clamping of the walls and electrodes from being compromised. There may be a plurality of straps.
The clamp may further comprise a cam and lever system arranged to apply a force to the straps and hence to retain the cell stack components together.
The invention will now be further described, by way of example only, with reference to the accompanying drawings in which:
Referring now to
In each of the examples the substrate 1 is a microporous sheet of polypropylene plastics material (SciMAT 700/70), which is hydrophilic and has an approximate thickness of between 100 to 400 μm, such as 125 μm, and a bubble point of between 8.0 to 15.0 kPa gauge. This material has a wicking rate of 90 mm per 600 seconds.
A 0.5 μm layer of silver is electro-less plated onto the substrate 1 to form a first layer 2 of conductive material. A second layer 3 of silver of thickness 3 μm is then electroplated onto the first layer 2 of conductive material. A protective 0.05 μm thick layer 4 of rhodium is then electroplated onto the second layer 3 of conductive material to complete the conductive layer structure.
A 0.5 μm layer of silver is electro-less plated onto the substrate 1 to form a first layer 2 of conductive material, followed by electroplating copper to form a second layer 3 of thickness 5 μm of conductive material, followed by electroplating a protective layer 4 of nickel, 1 μm thick.
A 0.5 μm layer 2 of silver is electro-less plated onto the substrate 1 to form a first layer of conductive material, followed by electroplating 5 μm thickness of nickel to form a second layer 3 of conductive material.
The example catalyst mixtures for both cathode and anode electrodes use a combination of catalyst, binder and solvent which are spray-coated onto the conductor layers of Examples 1, 2 and 3 above. The binder may for example be polyethylene (such as PE1020 from Exxon-Mobil), and the solvent isododecane. Percentage weights refer to the total mass of the dry materials before the addition of a suitable solvent.
The cathode catalyst mixtures A to C below include an oxygen reduction catalyst.
The anode catalyst mixtures D and E below include a hydrogen oxidation catalyst.
Referring now to
Referring now to
Electrodes 11 and 12 locate in the shallow recesses 211 on opposite sides of each bipolar plate 206, with the catalyst-carrying face of the electrode 11 or 12 facing the respective blind recess 207 or 209 respectively. Before assembly of the stack components, the opposed surfaces of each frame 204 (including that of the raised portion 205) is covered with gasket sealant 215; this adheres to the frame 204 and dries to give a non-tacky outer surface, while remaining resilient. The components are then assembled as described, so that the raised portions 205 locate in the shallow recesses 211, securing the electrodes 11 and 12 in place. The sealant 215 ensures that electrolyte in the chambers 208 cannot leak out, and that gases cannot leak in, around the edges of the electrodes 11 and 12, and also ensures that gases cannot leak out between adjacent frames 204 and 210.
The surfaces of the frames 210 of the bipolar plates 206, including the outer edge surface, are provided with a nickel coating, for example by electro-less deposition. This coating of nickel provides an electrical connection between an anode 11 on one side and a cathode 12 on the other side, so that the fuel cells 10 are connected in series with each other in the cell stack. This coating may alternatively be of other conducting materials.
The flow of electrolyte to and from the electrolyte chambers (apertures 208), and the flows of the gases to and from the gas chambers (recesses 207 and 209), follow respective fluid flow ducts defined by aligned apertures through the plates 202 and 206; only one such set of apertures 216 and 218 are shown. This set of apertures 216 and 218 provides electrolyte to the electrolyte chambers 208 via narrower transverse ducts 220. The sealant 215 is placed so as not to block the apertures 216. At one end of the stack 200 is an end plate 230 which defines a blind recess 209 on one face but is blank on the outer face, and defines ports 232 communicating with the fluid flow ducts through which the gases and electrolyte flow to or from the stack 200, each port 232 comprising a cylindrical recess on the outer face of the end plate 230. At the other end is an end plate 234 (see
After assembly of the stack 200 the components are secured together for example using a strap 235 (shown partly broken away) around the entire stack 200.
Referring now to
If it is subsequently necessary to replace one of the electrodes 11 or 12, this can be achieved after removing the cap 250, withdrawing the stack 200, and undoing the strap 235 (not shown in
The electrodes 11 and 12 are not mechanically bonded to the plates 202 and 206, which has a number of implications. First, electrodes 11 and 12 are readily separated from the rest of stack 200. When the electrodes 11, 12 complete their service life, the stack 200 is removed as described above from the system in which it is installed and it may be replaced by a previously overhauled stack 200; the system thus has little down-time. The used stack 200 is dismantled to replace the old electrodes 11, 12 so that it is ready for re-use. Consequently, replacement of the stack costs only the cost of the new electrodes (and labour costs for their installation). It may subsequently be possible to refurbish the old electrodes 11, 12 offsite.
Second, the lack of mechanical bonding means that accurate assembly of stack 200 is particularly important, as there are more parts to be correctly located. In order to aid accurate assembly, parts are arranged to be joined together or assembled in one orientation only. This is ensured for example by the cut-out 222 and complementary projection described above (
Third, as the electrodes 11, 12 are not mechanically bonded to the plates 202 and 206, the stack 200 must be held together by some other means; but this should be readily releasable, so that the stack 200 may be dismantled easily. This is ensured by for example the strap 235 (
During operation the clamping force holding the stack together must be sufficient to prevent any fluid leakage, despite variations in the length of the stack as its temperature varies. The pressure applying plate 252 may therefore incorporate a spring system. The spring system can either be in the form of a mechanical spring (for example, a helical, or leaf spring) or in the form of a suitable resilient plastic material.
Whilst the present invention has been described and illustrated with reference to particular embodiments, it will be appreciated by those of ordinary skill in the art that the invention lends itself to many different variations not specifically illustrated herein. For that reason, reference should be made to the claims for determining the true scope of the present invention.
Number | Date | Country | Kind |
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0604598.3 | Mar 2006 | GB | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/GB2007/050106 | 3/7/2007 | WO | 00 | 10/20/2008 |