Title of Invention	A METHOD AND CONTROL SYSTEM FOR OPERATING A VARIABLE POWER OUTPUT SOLID OXIDE FUEL CELL STACK
Abstract	A method and apparatus for operating an intermediate-temperature solid-oxide fuel cell stack with a mixed ionic/electronic conducting electrolyte in order to increase its efficiency. The required power output of the solid-oxide fuel cell stack is determined and one or more operating conditions of the solid fuel cell stack are controlled dependent upon the determined required power output. The operating conditions that are controlled may be at least one or the temperature of the fuel cell stack and the dilution of fuel delivered to the fuel cell stack

Title of Invention

A METHOD AND CONTROL SYSTEM FOR OPERATING A VARIABLE POWER OUTPUT SOLID OXIDE FUEL CELL STACK

Abstract

A method and apparatus for operating an intermediate-temperature solid-oxide fuel cell stack with a mixed ionic/electronic conducting electrolyte in order to increase its efficiency. The required power output of the solid-oxide fuel cell stack is determined and one or more operating conditions of the solid fuel cell stack are controlled dependent upon the determined required power output. The operating conditions that are controlled may be at least one or the temperature of the fuel cell stack and the dilution of fuel delivered to the fuel cell stack

Full Text	FORM 2 THE PATENTS ACT, 1970 (39 of 1970) & THE PATENTS RULES, 2003 COMPLETE SPECIFICATION (See section 10, rule 13) "A METHOD AND PPARATUS FOR OPERATING AN INTERMEDIATE-TEMPERTURE SOLID-OXIDE FUEL CELL STACK WITH A MIXED IONIC/ELECTRONIC CONDUCTING ELECTROLYTE IN ORDER TO INCREASE ITS EFFICIENCY" CERES POWER LIMITED, aBritish company of Unit 18, Denvale Trade Park, Haslett Avenue East, Crawley, West Sussex RH10 1SS, UK. The following specification particularly describes the invention and the manner in which it is to be performed WO 2005/078843 PCT/GB2005/000355 2 A SOLID-OXIDE FUEL CELL STACK WITH A CTROLYTE A METHOD AND APPARATUS FOR OPERATING MIXED IONIC/ELECTRONIC CONDUCTING KUB a method and apparatus for operating a solid its efficiency, in particular by varying one or 10 15 20 25 The present invention relates to oxide fuel cell stack in order to increase more operating conditions of the fuel cell. Solid oxide fuel cells (SOFCs) are a promising means of generating electricity from either hydrogen or fossil fuels in a more efficient and environmentally acceptable manner than more traditional generating technologies. However traditional SOFCs operate at very high temperatures (greater than 900°C), and even more recent innovations have only been able to red ace this temperature to 700-800°C. This high temperature of operation leads to significant problems with the materials used in the construction of such fuel cell stacks and the related system components. Materials which can withstand prolonged oi expensive, fragile or both. Attempting stainless steels, at high operating at these temperatures tend to either be to use lower cost materials, such as ferritic temperatures causes problems with stack performance degradation due to oxidation of the metal and migration of volatile chromium species over prolonged periods at these high operating temperatures. In order to make a commercially attractive SOFC stack for mass-market applications, there is therefore a strong incentive to try and reduce the operating temperature of the stack and hence the cost of the materials required. At a temperature of below 650°C, low-cost materials of construction such as ferritic stainless steels are sufficiently stable as to allow long-term operation without significant stack performance degradation. Conventional SOFCs use an ytfcium-doped zirconium oxide (YSZ) electrolyte. This is a material which conducts oxide; ions at high temperatures, but not electrons. It is therefore well suited for use as a fuel cell electrolyte. Unfortunately YSZ is not a particularly good oxide ion conductor, and its ionic resistance becomes unpractically high below about 650°C, leading to very poor fuel cell performance. In order to WO 2005/078843 PCT/GB2005/000355 3 operate below this temperature, which as stated previously is highly desirable, a different electrolyte material is required Unlike, YSZ which does not conduct electrons, there are a number of mixed ionic/electronic conducting ceramic electrolyte materials which have a high ionic of conductivity below 650°C. In terms of its performance, stability and safety in handling, the most promising and widely used of these low-temperature mixed ionic/electronic conducting electrolyte materials is gadolinium-doped cerium oxide (CGO), although there are other materials such as other doped ceria oxides. CGO exhibits good ionic conductivity down to below 500°C. Unfortunately CGO is not as 15 10 stable as YSZ, and in a reducing atmosphere at temperature (such as mat normally found on the anode side of the fuel cell), Ce4+ ions can be reduced to Ce3+. This results in the electrolyte developing some electronic conductivity, resulting in a short-circuit current flowing within the fuel cell. This short-circuit is observed externally as a drop in the cell terrninal voltage at opencircuit, and results in a loss of efficiency in converting the energy in the fuel to electricity. This feature of CGO has led many people to reject it as an electrolyte material, as they consider the efficiency loss thrcaigh the internal short circuit is too severe for a practical device. 20 It is an object of the present invention to reduce at least some of the problems discussed above. According to a first aspect of ths present invention there is provided a method of operating a solid oxide fuel cell stack with a mixed ionic/electronic conducting electrolyte, the method comprising determining the required power output of the solid oxide fuel cell stack and 25 controlling one or more operating conditions of the solid oxide fuel cell stack dependent upon the determined power output. The operating conditions of the solid oxide fuel cell stack that are varied are preferably at least one of the temperature of the fuel cell stack and the dilution of fuel delivered to the fuel cell stack. 30 The electronic conductivity of CGO is strongly temperature dependent, and at a sufficiently low temperature the electronic leakage current can be reduced to an acceptable level. As the operating temperature of the CGO electrolyte material WO 2005/078843 PCT7GB2005/000355 4 reduces, so does the magnitude of the short-circuit effect. The effect reduces to such a degree that when the operating temperature reduces to 500°C the effect is negligible. Therefore CGO is a suitable electrolyte material when the fuel cell operating temperature is below a temperature of 650°C or more preferably 600°C. This is particularly the case under a high external load, where the flux of oxide ions through the electrolyte tends to reoxidise the Ce5+ ions to Ce4+, thus eliminating the electronic conductivity. The efficiency of a fuel cell stack with an electrolyte including cerium rises rapidly at above about 50% of its rated power, as the short-circuit current becomes small relative to the external circuit curr ;nt It can be demonstrated, for example that at near full power operation and at a temperature of less than 600°C, the efficiency of a CGO-based fuel cell is comparable with a YSZ-based fuel cell operating at temperatures in excess of 700°C and there is no significant penalty resulting from the use of CGO. 15 According to a second aspect of the present invention there is provided a control system for a solid-oxide fuel cell stack with a mixed ionic/electronic conducting electrolyte, the control system comprising means for determining a required power output of the stack and a controller for controlling one: or more operating conditions of the stack dependent upon the required power output The controller may be arranged to control at least one of the temperature of the stack and the dilution of fuel delivered to the stack. A fuel cell stack with a mixed ionic/electronic conducting electrolyte may be provided with a control system according to the second aspect of the present invention. 25 Embodiments of the present invention will now be described by way of example with reference to the accompanying drawings, in which: Figure 1 shows the energy conversion efficiency of a fuel cell with a CGO- based electrolyte plotted against electrical power density at a range of temperatures from 500°C to 600°C; 30 Figure 2 shows the energy conversion efficiency of a fuel cell with a CGO- based electrolyte plotted against electrical power density at a range of fuel dilutions; WO 2005/078843 PCT/GB2005/000355 5 Figure 3 schematically shows as fuel cell stack with a control system for controlling one or more operating conditions of the fuel cell stack dependent upon a required power output; Figure 4 schematically shows a Solid Oxide Fuel Cell system operating on LPG fuel Figure 5 shows the stack (DC) and system (AC) power outputs during simulations of the system shown in Figure 4; Figure 6 shows the stack temperature during the simulations; Figure 7 shows the stoichiometric air ratio during the simulations; Figure 8 shows the resulting stack and system efficiencies during the simulations; Figure 9 shows the ionic and external currents within the stack during the simulations; Figure 10 shows the predicted voltage of a single fuel cell; Figure 11 shows the steam/ciabon ration in the reformer for a further simulation and Figure 12 shows the stack efficiency for the further simulation. Two strategies are presented below for the niinimisation of the short-circuit current under part-load conditions, thus maximising the efficiency of the fuel cell across its full operating range. METHOD 1 Figure 1 illustrates the results of a computer simulation of a CGO-based fuel cell with a nominal maximum specific power output of 0.2 wcm-2. Energy conversion efficiency is plotted against electrical power density at a range of operating temperatures from 500°C to 600°C. The energy conversion efficiency is defined as the electrical power output divided by the chemical energy in the hydrogen fuel consumed assuming 100% fuel conversion. These values are therefore the maximum theroretical efficiencies for this cell, and not the actual efficiencies, since in reality 100% fuel conversion is not possible. However the real trend would follow the same pattern. WO 2005/078843 PCT/GB2005/000355 6 It can be seen from Figure 1 that the maximum efficiency at any given power density is temperature dependent, and tliat the higher the power density, the higher the temperature at which maximum efficiency occurs. The reason for this is as follows. A lower temperature of operation reduces both the absolute magnitude of the electronic leakage current density, and the external circuit current density at which the electronic leakage current becomes negligible. This means that at low external current densities, a higher efficiency can be achieved at a low operating temperature. However, the low temperature also increases the various cell resistances, particularly the cathode over-potential. Thus for any given current density the voltage loss as a result of internal cell resistance will be higher, resulting in a lower efficiency at higher currents. However, at these higher current densities the electronic leakage current is negligible, even at a higher temperature, but the cell resistance is lower. This leads to a lower voltage loss in the internal cell resistance, and thus a higher cell terminal voltage and hence efficiency. 15 A clear strategy for optimising the efficiency of a stack with these characteristics is therefore to allow the stack temperature to vary in the range 500- 600°C, or possibly up to 650°C depending upon the required power output. This is relatively simple to achieve since higher electrical power output from the stack also results in a higher heat output, and by under-cooling the stack, the temperature can easily be allowed to rise with an increased power outpur, and vice-versa. However, in the event of a rapid increase in power demand, the stack may not be at a high enough temperature to enable that demand to be met Depending upon how rapidly the stack can be heated, it may be possible, if required, to cover this demand temporarily using some form of energy storage. As an alternative or in addition to the method described above, a second method of increasing the stack efficiency is presented below. Method 2 Figure 2 illustrates the results of anther computer simulation of a CG)-based cell, this time with a nominal maximilim power density of 0.4 Wcm-2. In this case the temperature was kept constant at 5700C,and the dilution of the hydrogen fuel with steam was varied. WO 2005/078843 PCT/GB2005/000355 7 10 15 20 25 30 It can be seen that diluting the fuel with increasing percentages of steam has much the same effect as reducing the temperature. This is largely because the addition of higher percentages of steam to the hydrogen fuel makes the fuel less reducing. This has the effect of lessening the tendency of Ce4+ ions in the electrolyte to reduce to Ce3+, and thus reduces the electronic conductivity of the electrolyte. However, diluting the fuel also increases the anode resistance and reduces the cell open-circuit voltage, thus reducing the maximum power output achievable. Another possible strategy to optimise the stack efficiency at part-load is to dilute the fuel with an increasing percentage of steam as the load falls. This method is with carbon dioxide, nitrogen, or a mixture of or if the fuel gas is carbon monoxide, or a mixture of hydrogen and carbon monoxide. A method of achieving this fuel dilution would be to mix the incoming fuel gas with a variable proportion of recycled eidiaust gas from the anode side of the stack. However, any method of diluting the anode fuel gas, for example by supplying steam, nitrogen and/or carbon dioxide from a separate source would fall within the scope of the present invention. Figure 3 schematically shows; a solid oxide fuel cell stack with mixed ionic/electronic conducting electrolyte!! with a control system for controlling at least one of the temperatures of the fuel cell stack and/or the dilution of the fuel delivered to the stack. Fuel cell stack 10 has an anode compartment 11 through which a hydrogen-containing fuel gas is passed, and a cathode compartment 12 through which air is passed. The fuel cell stack is made up of single or multiple arrangements of anode, electrolyte and cathode arranged in layers to achieve a functioning fuel cell stack. The stack has a fuel inlet 30, through which either hydrogen or a hydrocarbon fuel such as methane is passed, and an outlet conduit 70 through which anode compartment exhaust gases leave the stack. These exhaust gases are typically a mixture of steam and unreacted hydrogen. If the original fuel was a hydrocarbon, the exhaust gases will also contain carbon oxides. A recycle conduit 40 is provided which enables exhaust gases to be mixed with the incoming fuel, by means of a variable compressor 50. This WO 2005/078843 PCT/GB2005/000355 8 Compressor could either be an electrically driven blower or some form of ejector or jet pump. Optionally, the mixture of incoming fuel and recycled exhaust gases may be fed to reformer unit 31, which converts a hydrocarbon fuel to a mixture of hydrogen and carbon oxides by reaction with steam. The stack is also provided with an air inlet conduit 20, by which preheated air is fed to the stack, both as an oxidant an coolant. The pre-heating can occur by means that include using excess heat from the fuel cell stack, or recovering heat from the stack exhaust conduits, or using a separate heat source such as induction heating burning or recovering heat from another external process. The cathode compartment also has an outlet conduit 71 allow the exhaust gases to be removed from the stack. A microprocessor 60 is provided which may be part of a computer or printed circuit board for example. The microprocessor receives inputs from the stack temperature 13, the stack voltage 14 and the stack current 15. The microprocessor is arranged to control the stack temperature via control line 21, and the ratio of fresh fuel to recycled exhaust gas via control line 51,which controls the variable compressor 50. Alternatively the dilution of the incoming fuel may be controlled by the addition of a controlled amount of steam, carbon dioxide or an inert gas from another source. The control of the stack temperature via line 21 may be effected by a number of methods, or combinations of methods, including but not limited to: 1) Varying the volume of air fed to the stack 2) Varying the temperature of the air fed to the stack 3) Varying the concentration of unreformed hydrocarbon fuel entering the stack, assuming internal reforming occurs 4) Varying the temperature of the fuel entering the stack The microprocessor receives an input of the power output of the stack by multiplying the stack voltage and current signals 14 and 15. The microprocessor will contain a look-up table or similar which will contain the optimum stack temperature and/or fuel dilution for a given power output. The microprocessor will manipulate WO 2005/078843 PCT/GB2005/000355 9 10 15 control variables 21 and 51 to attempt) to achieve this optimum for a given power output. Figure 4 schematically illustrates a complete Solid Oxide Fuel Cell system operating on liquid petroleum gas (LPG) fuel. This system illustrates how a method of controlling an intermediate-temperature solid oxide fuel cell (IT-SOFC) stack described in method 1 could be implemented in practice. This system is illustrated as an example only, and many other configurations could be adopted which would achieve the same result LPG fuel is supplied through some form of mass flow control and desulphurising system 10. The fuel is mixed with steam from pipe 62 in mixer 21, at a for every mole of carbon in the fuel. The steam/LPG mixture is then preheated to around 430°C in the fuel heat exchanger 22, and then fed to the reformer 23. In the reformer the mixture is heated to around 700°C by means of heat exchange with tie exhaust gas stream, which is illustrated schematically by connection 51 from hoat exchanger 50. At this elevated temperature the hydrocarbons in the fuel (predominantly propane with a small fraction of butane, propylene and trace components such as pentane) react with the steam to form a hydrogen-rich reformate mixture. This reformate mixture would typically be 60-70% hydrogen by volume, with a lower percentage of steam, carbon monoxide, carbon dioxide and methane. This gas mixture is suitable for fuelling an SOFC stack without further treatment. The reformate mixture is cooled to a temperature suitable for feeding to the stack by means of the fuel heat exchanger 22, heating the incoming reactants in the process. The reformate mixture is then fed to the anode compartment 31 of the fuel cell stack 30 by means of the fuel inlet conduit 24. The fuel gas is partially consumed within the stack, and exhaust gas leaver the anode compartment of the stack by means of the exhaust conduit 41. The exhaust gas leaves at close to the temperature of the hottest part of the stack, typically 550-620°C depending on the operating condition. The exhaust gas is predominantly stearti and carbon dioxide, with smaller amounts of unburned hydrogen and carbon monoxide. Atmospheric air is drawn into tie system through air filter 90, by air blower 91. The blower 91 has a variable speed motor controlled by motor controller 93, and by WO 2005/078843 PCT/GB2005/000355 10 this means the mass-flow of air drawn toto the system can be varied. The mass flow of air being drawn into the system is measured by mass flow sensor 94. The air is provided both as an oxidant and as a means of cooling the SOFC stack, as it is normal for considerably more air to be fed than that required as an oxidant, the remainder carrying excess heat out of the stack. The air is fed from the mass flow sensor 94 to the air preheater 70, where it is preheated to a temperature suitable to he fed into the stack (typically 450-500°C). The incoming air is preheated by cooling tie hot exhaust gas stream 63. The preheated air is then fed to the cathode compartment 32 of the fuel cell stack 30 by means of air 10 conduit 72. As with the fuel, the oxygen in the air is partially consumed by the fuel cell reaction. The residual air, somewhat depleted of oxygen, leaves the stack by means of air exhaust conduit 42. As with the fuel gas, the air will typically be at close to the maximum stack temperature, typically 550-620°C depending on the operating condition. 15 Both the air and fuel exhaust conduits 41 and 42 feed into the system afterburner 40, in which the air and fuel exhaust streams are mixed together, and the unreacted hydrogen and carbon monoxide from the stack exhaust are burned conventionally to generate heat The resulting hot (typically 700-900°C) exhaust gas stream 43 is first fed through heat exchanger 50 to provide heat for the reformer 23. 20 The cooler gas stream 52 from heat exchanger 50 is then fed to steam generator 60, in which it is used to evaporate water supplied by feed pump 61. The resulting steam is then fed to the reformer via pipe 62. The exhaust gas, now cooled to around 600°C, is then fed to the air preheater 70 to preheat the incoming air. Finally the exhaust gas, still at around 250°C, is fed to heat exchanger 80 which can be used to recover waste 25 heat for a combined heat and power application. The stack is provided with an external power demand 110, which draws current off the stack via cable 111. The nature of the power demand could be one of a range of different applications. The system is provided with a microprocessor based control unit 100. This 30 measures the stack current via input L01, and the stack temperature via input 102. It also measures the mass flow of air entering the system via the mass-flow sensor 94 and input 104. The control unit controls the air blower 91 by means of the motor controller WO 2005/078843 PCT/GB2005/000355 11 93 and output 103. In this way the controller can control the air flow to the stack. The control unit 100 also controls the water feed pump 61 by output 105. In this way the ratio of steam to fuel in the reformer can also be changed. The performance of the system illustrated in figure 4 has been simulated on a 5 computer. The system simulated is based on a stack with a power output of 1 kW0, and a system supplying AC power. The AC power output of the system is always less than the stack power output because various parts of the system such as the air blower consume power. 10 In this simulation the system is operated for 10 minutes (600 seconds) at full AC power (800 W).The power is then ramped down to half AC power (400 W), and then the stack temperature is lowered fr r 2S°C by temporarily increasing the air flow to increase the rate of cooling within the stack. The clearly beneficial effect of lowering the stack temperature under part-load conditions can be seen. Figure 5 shows the stack(DC) and system (AC) power outputs during the 15 simulations, illustrating the ramping down of power from 800 to 400 We. Figure 6 shows the stack temperature during the simulation, and Figure 7 the stoichiometric air ratio. This represents the ratio of the actual air-flow to the theoretical air demand to supply enough oxygen for the fuel eel: reaction. It can be seen that at full power this ratio is around 10, representing the large amount of air required for stack cooling. The 20 air ratio then increases to a maximum of around 20 as the air flow is increased to cool the stack down. The increase in air flow at around 1100s is as a result of the stack temperature controller being reset to make it more sensitive as the stack temperature nears the new setpoint Figure 8 shows the resulting stack and system efficiencies. It can be seen that 25 with the stack temperature maintained at around 590°C, mere is a significant fall in efficiency as the load is reduced. This is as a result of increasing electronic conductivity in the electrolyte as the current-density is reduced.However, as the stack temperature falls the efficiency recovers until it is comparable with the full-load efficiency. In fact the stack efficiency is better than the full load efficiency as a result 30 of the higher cell voltage. However the system efficiency is a little worse as a result of fixed parasitic power demands such as that required to run the control system. WO 2005/078843 PCT/GB2005/000355 12 Figure 9 shows the ionic and external currents within the stack. The external current is the current flowing in the external circuit, and the ionic current is the sum of the external current and the electronic leakage current It can be seen that the gap between these two lines, representing ths magnitude of the electronic leak, increases as the external current falls. However, it am also be seen mat the gap closes as the stack temperature falls under part-load conditions. Finally figure 10 shows the predicted voltage of a single fuel cell. It can be seen that the cell voltage increases as the load is reduced, as would be expected. It can also be seen that the cell voltage actually falls a little as the stack cools, which would normally represent a loss of efficiency as the cell resistance increases. However, the benefits of reducing the leakage current outweighs the increase in resistance provided the temperature fall is not too large. A second simulation was performed to demonstrate the effect of diluting the fuel on the system efficiency at part load (method 2). A similar simulation was 15 performed where the stack was run at full power for 10 minutes, and then dropped to half power. However this time the stack was maintained at a constant temperature but the mass flow of water to the steam venerator from pump 61 was increased in two stages. This has the effect of increasing the steam/carbon ratio in the reformer from 2.0 to 3.5, and thus increasing the dilution of the fuel in the stack, as is illustrated in figure 20 11. The effect on the stack efficiency can be seen in figure 12. The benefit of this approach is less marked than changing the stack temperature (method 1), but a small improvement in efficiency is clearly apparent. Many variations may be madi; to the examples described above whilst still falling within the scope of mis invention. For example the microprocessor may just 25 control the stack temperature but not the fuel dilution, or vice-versa. WO 2005/078843 PCT/GB2005/000355 13 CLAIMS 1. A method of operating a solid oxide fuel cell stack with mixed ionic/electronic conducting electrolytes, the method comprising determining the required power output of the solid oxide fuel cell stack and controlling one or more operating conditions of the solid oxide fuel cell stack dependent upon the determined power output. 2. A method according to claim 1, oxide fuel cell stack that are controlled cell stack and the dilution of fuel wherein the operating conditions of the solid are at least one of the temperature of the fuel delivered to the fuel cell stack. temperature fuel 15 3. A method according to claim 2 oxide fuel cell stack is reduced, the the power output of the solid oxide cell stack is increased. wherein as the power output of the solid of the fuel cell stack is reduced and as cell is increased, the temperature of the fuel 4. A method according to claim 2 or claim 3, wherein the temperature of the fuel cell stack is maintained at 650°C or below. 20 5. A method according to claim 4, maintained at 600°C or below. wherein the temperature of the fuel cell stack is 6. A method according to any of claims 2 to 5, wherein the fuel delivered to the fuel cell stack is diluted with a predetermined amount of steam, carbon dioxide, nitrogen or a mixture including steam, carbon dioxide and/or nitrogen. 7. A method according to any of fuel cell stack is diluted with a anode side of the fuel cell. claims 2 to 5, wherein the fuel delivered to the variable proportion of recycled exhaust gas from an WO 2005/078843 PCT/GB2005/000355 14 8. A method according to any of claims 2 to 7, wherein as the power output of the solid oxide fuel cell stack is reduced, the dilution of the fuel delivered to the fuel cell stack is increased and as the power output of the solid oxide fuel cell is increased, the dilution of the fuel delivered to the fuel cell stack is reduced. 9. A method according to any of the preceding claims applied to a solid oxide fuel cell with an electrolyte including gadolinium-doped cerium oxide. 10. A method substantially as hereinbefore described with reference to the 10 accompanying drawings. 15 11. A control system for a solid oxide fuel cell stack with a mixed ionic/electronic conducting electrolyte, the control system comprising means for determining a required power output of the stack and a controller for controlling one or more operating conditions of the stack dependent upon the required power output. 20 12. A control system according to control at least one of the temperature the stack. claim 11, wherein the controller is arranged to of the stack and the dilution of fuel delivered to 25 13. A control system according to claim 12, wherein the controller reduces the temperature of the stack as a result of the determining means determining that the required power output is reducing and the controller increases the temperature of the stack as a result of the determining means determining that the required power output is increasing. 14. A control system according determining means monitors an electric to any one of claim 11 to 13, wherein the al power output from the stack. 30 15. A control system according to any of claims 11 to 14, wherein the controller maintains the temperature of the stack at 650° or below. WO 2005/078843 PCT/GB2005/000355 15 16. A control system according to claim 15, wherein the controller maintains the temperature of the stack at 600°C or below. 17. A control system according to any one of claims 11 to 16, wherein the controller arranges the fuel delivered to the fuel cell stack to be diluted with a predetermined amount of steam, carbon dioxide, nitrogen or a mixture including steam, carbon dioxide and/or nitrogen. 10 18. A control system according to controller arranges the fuel delivered to proportion of recycled exhaust gas from any one of claims 11 to 17, wherein the the fuel cell stack to be diluted with a variable anode sides of the fuel cell stack. 15 19. A control system according to any one of claims 11 to 18, wherein the controller increases the dilution of the fuel delivered to the fuel cell stack as a result of the determining means determining that the required power output is reducing and the controller reducing the dilution of the fuel delivered to the fuel cell stack as a result of the determining means determining that the required power output is increasing. 20. A control system substantially as hereinbefore described with reference to the 20 accompanying drawings. 21. A fuel cell stack with mixed ionic/electronic conducting electrolytes including a control system according to any one of claims 11 to 20. 25 22. A fuel cell stack substantially accompanying drawings. as hereinbefore described with reference to the Dated this 30th day of August, 2006 s. AFSSAR OF K & S PARTNERS AGENT FOR THE APPLICANT(S) 16 ABSTRACT A method and apparatus for operating an intermediate-temperature solid-oxide fuel cell stack with a mixed ionic/electronic conducting electrolyte in order to increase its efficiency. The required power output of the solid-oxide fuel cell stack is determined and one or more operating conditions of the solid fuel cell stack are controlled dependent upon the determined required power output. The operating conditions that are controlled may be at least one or the temperature of the fuel cell stack and the dilution of fuel delivered to the fuel cell stack

Full Text

FORM 2

THE PATENTS ACT, 1970 (39 of 1970)

& THE PATENTS RULES, 2003
COMPLETE SPECIFICATION
(See section 10, rule 13)

"A METHOD AND PPARATUS FOR OPERATING AN INTERMEDIATE-TEMPERTURE SOLID-OXIDE FUEL
CELL STACK WITH A MIXED IONIC/ELECTRONIC
CONDUCTING ELECTROLYTE IN ORDER TO INCREASE ITS EFFICIENCY"

CERES POWER LIMITED, aBritish company of Unit 18, Denvale Trade Park, Haslett Avenue East, Crawley, West Sussex RH10 1SS, UK.

The following specification particularly describes the invention and the manner in which it is to be performed

WO 2005/078843

PCT/GB2005/000355

2

A SOLID-OXIDE FUEL CELL STACK WITH A CTROLYTE
A METHOD AND APPARATUS FOR OPERATING MIXED IONIC/ELECTRONIC CONDUCTING KUB

a method and apparatus for operating a solid its efficiency, in particular by varying one or
10
15
20
25

The present invention relates to oxide fuel cell stack in order to increase more operating conditions of the fuel cell.
Solid oxide fuel cells (SOFCs) are a promising means of generating electricity from either hydrogen or fossil fuels in a more efficient and environmentally acceptable manner than more traditional generating technologies. However traditional SOFCs operate at very high temperatures (greater than 900°C), and even more recent innovations have only been able to red ace this temperature to 700-800°C. This high temperature of operation leads to significant problems with the materials used in the construction of such fuel cell stacks and the related system components. Materials which can withstand prolonged oi expensive, fragile or both. Attempting stainless steels, at high operating at these temperatures tend to either be to use lower cost materials, such as ferritic temperatures causes problems with stack performance degradation due to oxidation of the metal and migration of volatile chromium species over prolonged periods at these high operating temperatures.
In order to make a commercially attractive SOFC stack for mass-market applications, there is therefore a strong incentive to try and reduce the operating temperature of the stack and hence the cost of the materials required. At a temperature of below 650°C, low-cost materials of construction such as ferritic stainless steels are sufficiently stable as to allow long-term operation without significant stack performance degradation.
Conventional SOFCs use an ytfcium-doped zirconium oxide (YSZ) electrolyte. This is a material which conducts oxide; ions at high temperatures, but not electrons. It is therefore well suited for use as a fuel cell electrolyte. Unfortunately YSZ is not a

particularly good oxide ion conductor,

and its ionic resistance becomes unpractically

high below about 650°C, leading to very poor fuel cell performance. In order to

WO 2005/078843

PCT/GB2005/000355

3

operate below this temperature, which as stated previously is highly desirable, a different electrolyte material is required
Unlike, YSZ which does not conduct electrons, there are a number of mixed ionic/electronic conducting ceramic electrolyte materials which have a high ionic of
conductivity below 650°C. In terms of its performance, stability and safety in handling, the most promising and widely used of these low-temperature mixed

ionic/electronic conducting electrolyte

materials is gadolinium-doped cerium oxide

(CGO), although there are other materials such as other doped ceria oxides. CGO

exhibits good ionic conductivity down
to below 500°C. Unfortunately CGO is not as
15
10 stable as YSZ, and in a reducing atmosphere at temperature (such as mat normally found on the anode side of the fuel cell), Ce4+ ions can be reduced to Ce3+. This results in the electrolyte developing some electronic conductivity, resulting in a short-circuit current flowing within the fuel cell. This short-circuit is observed externally as a drop in the cell terrninal voltage at opencircuit, and results in a loss of efficiency in converting the energy in the fuel to electricity.
This feature of CGO has led many people to reject it as an electrolyte material, as they consider the efficiency loss thrcaigh the internal short circuit is too severe for a practical device.
20
It is an object of the present invention to reduce at least some of the problems discussed above.
According to a first aspect of ths present invention there is provided a method of operating a solid oxide fuel cell stack with a mixed ionic/electronic conducting electrolyte, the method comprising
determining the required power output of the solid oxide fuel cell stack and
25
controlling one or more operating conditions of the solid oxide fuel cell stack dependent upon the determined power output.
The operating conditions of the solid oxide fuel cell stack that are varied are preferably at least one of the temperature of the fuel cell stack and the dilution of fuel delivered to the fuel cell stack.
30
The electronic conductivity of CGO is strongly temperature dependent, and at a sufficiently low temperature the electronic leakage current can be reduced to an acceptable level. As the operating temperature of the CGO electrolyte material

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PCT7GB2005/000355

4

reduces, so does the magnitude of the short-circuit effect. The effect reduces to such a degree that when the operating temperature reduces to 500°C the effect is negligible. Therefore CGO is a suitable electrolyte material when the fuel cell operating temperature is below a temperature of 650°C or more preferably 600°C. This is particularly the case under a high external load, where the flux of oxide ions through the electrolyte tends to reoxidise the Ce5+ ions to Ce4+, thus eliminating the electronic conductivity.
The efficiency of a fuel cell stack with an electrolyte including cerium rises rapidly at above about 50% of its rated power, as the short-circuit current becomes small relative to the external circuit curr ;nt
It can be demonstrated, for example that at near full power operation and at a temperature of less than 600°C, the efficiency of a CGO-based fuel cell is comparable with a YSZ-based fuel cell operating at temperatures in excess of 700°C and there is
no significant penalty resulting from the use of CGO.
15
According to a second aspect of the present invention there is provided a control system for a solid-oxide fuel cell stack with a mixed ionic/electronic conducting electrolyte, the control system comprising
means for determining a required power output of the stack and a controller for controlling one: or more operating conditions of the stack dependent upon the required power output
The controller may be arranged to control at least one of the temperature of the stack and the dilution of fuel delivered to the stack.
A fuel cell stack with a mixed ionic/electronic conducting electrolyte may be
provided with a control system according to the second aspect of the present invention.
25 Embodiments of the present invention will now be described by way of
example with reference to the accompanying drawings, in which:
Figure 1 shows the energy conversion efficiency of a fuel cell with a CGO-
based electrolyte plotted against electrical power density at a range of temperatures
from 500°C to 600°C;
30 Figure 2 shows the energy conversion efficiency of a fuel cell with a CGO-
based electrolyte plotted against electrical power density at a range of fuel dilutions;

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Figure 3 schematically shows as fuel cell stack with a control system for controlling one or more operating conditions of the fuel cell stack dependent upon a required power output;
Figure 4 schematically shows a Solid Oxide Fuel Cell system operating on LPG fuel
Figure 5 shows the stack (DC) and system (AC) power outputs during simulations of the system shown in Figure 4;
Figure 6 shows the stack temperature during the simulations;
Figure 7 shows the stoichiometric air ratio during the simulations;
Figure 8 shows the resulting stack and system efficiencies during the simulations;
Figure 9 shows the ionic and external currents within the stack during the simulations;
Figure 10 shows the predicted voltage of a single fuel cell;
Figure 11 shows the steam/ciabon ration in the reformer for a further simulation and
Figure 12 shows the stack efficiency for the further simulation.
Two strategies are presented below for the niinimisation of the short-circuit current under part-load conditions, thus maximising the efficiency of the fuel cell across its full operating range.

METHOD 1

Figure 1 illustrates the results of a computer simulation of a CGO-based fuel cell with a nominal maximum specific power output of 0.2 wcm-2. Energy conversion efficiency is plotted against electrical power density at a range of operating temperatures from 500°C to 600°C. The energy conversion efficiency is defined as the electrical power output divided by the chemical energy in the hydrogen fuel consumed assuming 100% fuel conversion. These values are therefore the maximum theroretical efficiencies for this cell, and not the actual efficiencies, since in reality 100% fuel conversion is not possible. However the real trend would follow the same pattern.

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It can be seen from Figure 1 that the maximum efficiency at any given power density is temperature dependent, and tliat the higher the power density, the higher the temperature at which maximum efficiency occurs. The reason for this is as follows. A lower temperature of operation reduces both the absolute magnitude of the electronic leakage current density, and the external circuit current density at which the electronic leakage current becomes negligible. This means that at low external current densities, a higher efficiency can be achieved at a low operating temperature. However, the low temperature also increases the various cell resistances, particularly the cathode over-potential. Thus for any given current density the voltage loss as a result of internal cell resistance will be higher, resulting in a lower efficiency at higher currents. However, at these higher current densities the electronic leakage current is negligible, even at a higher temperature, but the cell resistance is lower. This leads to a lower voltage loss in the internal cell resistance, and thus a higher cell terminal voltage and hence efficiency.
15 A clear strategy for optimising the efficiency of a stack with these
characteristics is therefore to allow the stack temperature to vary in the range 500-
600°C, or possibly up to 650°C depending upon the required power output. This is relatively simple to achieve since higher electrical power output from the stack also results in a higher heat output, and by under-cooling the stack, the temperature can easily be allowed to rise with an increased power outpur, and vice-versa.
However, in the event of a rapid increase in power demand, the stack may not
be at a high enough temperature to enable that demand to be met Depending upon
how rapidly the stack can be heated, it may be possible, if required, to cover this demand temporarily using some form of energy storage.
As an alternative or in addition to the method described above, a second
method of increasing the stack efficiency is presented below.

Method 2
Figure 2 illustrates the results of anther computer simulation of a CG)-based cell, this time with a nominal maximilim power density of 0.4 Wcm-2. In this case the temperature was kept constant at 5700C,and the dilution of the hydrogen fuel with steam was varied.

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10
15
20
25
30

It can be seen that diluting the fuel with increasing percentages of steam has much the same effect as reducing the temperature. This is largely because the addition of higher percentages of steam to the hydrogen fuel makes the fuel less reducing. This has the effect of lessening the tendency of Ce4+ ions in the electrolyte to reduce to Ce3+, and thus reduces the electronic conductivity of the electrolyte. However, diluting the fuel also increases the anode resistance and reduces the cell open-circuit voltage, thus reducing the maximum power output achievable.
Another possible strategy to optimise the stack efficiency at part-load is to dilute the fuel with an increasing percentage of steam as the load falls. This method is
with carbon dioxide, nitrogen, or a mixture of or if the fuel gas is carbon monoxide, or a mixture of hydrogen and carbon monoxide.
A method of achieving this fuel dilution would be to mix the incoming fuel gas with a variable proportion of recycled eidiaust gas from the anode side of the stack.
However, any method of diluting the anode fuel gas, for example by supplying steam, nitrogen and/or carbon dioxide from a separate source would fall within the scope of the present invention.
Figure 3 schematically shows; a solid oxide fuel cell stack with mixed ionic/electronic conducting electrolyte!! with a control system for controlling at least one of the temperatures of the fuel cell stack and/or the dilution of the fuel delivered to the stack.
Fuel cell stack 10 has an anode compartment 11 through which a hydrogen-containing fuel gas is passed, and a cathode compartment 12 through which air is passed. The fuel cell stack is made up of single or multiple arrangements of anode, electrolyte and cathode arranged in layers to achieve a functioning fuel cell stack. The stack has a fuel inlet 30, through which either hydrogen or a hydrocarbon fuel such as methane is passed, and an outlet conduit 70 through which anode compartment exhaust gases leave the stack. These exhaust gases are typically a mixture of steam and unreacted hydrogen. If the original fuel was a hydrocarbon, the exhaust gases will also contain carbon oxides. A recycle conduit 40 is provided which enables exhaust gases to be mixed with the incoming fuel, by means of a variable compressor 50. This

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Compressor could either be an electrically driven blower or some form of ejector or jet pump.
Optionally, the mixture of incoming fuel and recycled exhaust gases may be fed to reformer unit 31, which converts a hydrocarbon fuel to a mixture of hydrogen and carbon oxides by reaction with steam.
The stack is also provided with an air inlet conduit 20, by which preheated air is fed to the stack, both as an oxidant an coolant. The pre-heating can occur by means that include using excess heat from the fuel cell stack, or recovering heat from the stack exhaust conduits, or using a separate heat source such as induction heating burning or recovering heat from another external process. The cathode compartment also has an outlet conduit 71 allow the exhaust gases to be removed from the stack.
A microprocessor 60 is provided which may be part of a computer or printed circuit board for example. The microprocessor receives inputs from the stack temperature 13, the stack voltage 14 and the stack current 15. The microprocessor is arranged to control the stack temperature via control line 21, and the ratio of fresh fuel to recycled exhaust gas via control line 51,which controls the variable compressor 50. Alternatively the dilution of the incoming fuel may be controlled by the addition of a controlled amount of steam, carbon dioxide or an inert gas from another source.
The control of the stack temperature via line 21 may be effected by a number of methods, or combinations of methods, including but not limited to:
1) Varying the volume of air fed to the stack
2) Varying the temperature of the air fed to the stack
3) Varying the concentration of unreformed hydrocarbon fuel entering the stack, assuming internal reforming occurs
4) Varying the temperature of the fuel entering the stack

The microprocessor receives an input of the power output of the stack by multiplying the stack voltage and current signals 14 and 15. The microprocessor will contain a look-up table or similar which will contain the optimum stack temperature and/or fuel dilution for a given power output. The microprocessor will manipulate

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10
15

control variables 21 and 51 to attempt) to achieve this optimum for a given power output.
Figure 4 schematically illustrates a complete Solid Oxide Fuel Cell system operating on liquid petroleum gas (LPG) fuel. This system illustrates how a method of controlling an intermediate-temperature solid oxide fuel cell (IT-SOFC) stack described in method 1 could be implemented in practice. This system is illustrated as an example only, and many other configurations could be adopted which would achieve the same result
LPG fuel is supplied through some form of mass flow control and desulphurising system 10. The fuel is mixed with steam from pipe 62 in mixer 21, at a
for every mole of carbon in the fuel. The steam/LPG mixture is then preheated to around 430°C in the fuel heat exchanger 22, and then fed to the reformer 23. In the reformer the mixture is heated to around 700°C by means of heat exchange with tie exhaust gas stream, which is illustrated schematically by connection 51 from hoat exchanger 50. At this elevated temperature the hydrocarbons in the fuel (predominantly propane with a small fraction of butane, propylene and trace components such as pentane) react with the steam to form a hydrogen-rich reformate mixture. This reformate mixture would typically be 60-70% hydrogen by volume, with a lower percentage of steam, carbon monoxide, carbon dioxide and methane. This gas mixture is suitable for fuelling an SOFC stack without further treatment.
The reformate mixture is cooled to a temperature suitable for feeding to the stack by means of the fuel heat exchanger 22, heating the incoming reactants in the
process. The reformate mixture is then fed to the anode compartment 31 of the fuel cell stack 30 by means of the fuel inlet conduit 24. The fuel gas is partially consumed within the stack, and exhaust gas leaver the anode compartment of the stack by means
of the exhaust conduit 41. The exhaust gas leaves at close to the temperature of the hottest part of the stack, typically 550-620°C depending on the operating condition. The exhaust gas is predominantly stearti and carbon dioxide, with smaller amounts of unburned hydrogen and carbon monoxide.
Atmospheric air is drawn into tie system through air filter 90, by air blower 91. The blower 91 has a variable speed motor controlled by motor controller 93, and by

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this means the mass-flow of air drawn toto the system can be varied. The mass flow of air being drawn into the system is measured by mass flow sensor 94. The air is provided both as an oxidant and as a means of cooling the SOFC stack, as it is normal for considerably more air to be fed than that required as an oxidant, the remainder carrying excess heat out of the stack.
The air is fed from the mass flow sensor 94 to the air preheater 70, where it is preheated to a temperature suitable to he fed into the stack (typically 450-500°C). The incoming air is preheated by cooling tie hot exhaust gas stream 63. The preheated air is then fed to the cathode compartment 32 of the fuel cell stack 30 by means of air
10 conduit 72. As with the fuel, the oxygen in the air is partially consumed by the fuel cell reaction. The residual air, somewhat depleted of oxygen, leaves the stack by means of air exhaust conduit 42. As with the fuel gas, the air will typically be at close to the maximum stack temperature, typically 550-620°C depending on the operating condition.
15 Both the air and fuel exhaust conduits 41 and 42 feed into the system
afterburner 40, in which the air and fuel exhaust streams are mixed together, and the unreacted hydrogen and carbon monoxide from the stack exhaust are burned conventionally to generate heat The resulting hot (typically 700-900°C) exhaust gas stream 43 is first fed through heat exchanger 50 to provide heat for the reformer 23.
20 The cooler gas stream 52 from heat exchanger 50 is then fed to steam generator 60, in which it is used to evaporate water supplied by feed pump 61. The resulting steam is then fed to the reformer via pipe 62. The exhaust gas, now cooled to around 600°C, is then fed to the air preheater 70 to preheat the incoming air. Finally the exhaust gas, still at around 250°C, is fed to heat exchanger 80 which can be used to recover waste
25 heat for a combined heat and power application.
The stack is provided with an external power demand 110, which draws current off the stack via cable 111. The nature of the power demand could be one of a range of different applications.
The system is provided with a microprocessor based control unit 100. This
30 measures the stack current via input L01, and the stack temperature via input 102. It also measures the mass flow of air entering the system via the mass-flow sensor 94 and input 104. The control unit controls the air blower 91 by means of the motor controller

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93 and output 103. In this way the controller can control the air flow to the stack. The control unit 100 also controls the water feed pump 61 by output 105. In this way the ratio of steam to fuel in the reformer can also be changed.
The performance of the system illustrated in figure 4 has been simulated on a
5 computer. The system simulated is based on a stack with a power output of 1 kW0, and
a system supplying AC power. The AC power output of the system is always less than
the stack power output because various parts of the system such as the air blower
consume power.
10
In this simulation the system is operated for 10 minutes (600 seconds) at full AC power (800 W).The power is then ramped down to half AC power (400 W), and then the stack temperature is lowered fr r 2S°C by temporarily increasing the air flow to increase the rate of cooling within the stack. The clearly beneficial effect of lowering the stack temperature under part-load conditions can be seen.
Figure 5 shows the stack(DC) and system (AC) power outputs during the
15 simulations, illustrating the ramping down of power from 800 to 400 We. Figure 6 shows the stack temperature during the simulation, and Figure 7 the stoichiometric air ratio. This represents the ratio of the actual air-flow to the theoretical air demand to supply enough oxygen for the fuel eel: reaction. It can be seen that at full power this ratio is around 10, representing the large amount of air required for stack cooling. The
20 air ratio then increases to a maximum of around 20 as the air flow is increased to cool the stack down. The increase in air flow at around 1100s is as a result of the stack temperature controller being reset to make it more sensitive as the stack temperature nears the new setpoint
Figure 8 shows the resulting stack and system efficiencies. It can be seen that
25 with the stack temperature maintained at around 590°C, mere is a significant fall in efficiency as the load is reduced. This is as a result of increasing electronic conductivity in the electrolyte as the current-density is reduced.However, as the stack temperature falls the efficiency recovers until it is comparable with the full-load efficiency. In fact the stack efficiency is better than the full load efficiency as a result
30 of the higher cell voltage. However the system efficiency is a little worse as a result of

fixed parasitic power demands such as

that required to run the control system.

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Figure 9 shows the ionic and external currents within the stack. The external current is the current flowing in the external circuit, and the ionic current is the sum of the external current and the electronic leakage current It can be seen that the gap between these two lines, representing ths magnitude of the electronic leak, increases as the external current falls. However, it am also be seen mat the gap closes as the stack temperature falls under part-load conditions.
Finally figure 10 shows the predicted voltage of a single fuel cell. It can be seen that the cell voltage increases as the load is reduced, as would be expected. It can also be seen that the cell voltage actually falls a little as the stack cools, which would
normally represent a loss of efficiency as the cell resistance increases. However, the benefits of reducing the leakage current outweighs the increase in resistance provided the temperature fall is not too large.

A second simulation was performed to demonstrate the effect of diluting the fuel on the system efficiency at part load (method 2). A similar simulation was

15 performed where the stack was run at full power for 10 minutes, and then dropped to half power. However this time the stack was maintained at a constant temperature but the mass flow of water to the steam venerator from pump 61 was increased in two stages. This has the effect of increasing the steam/carbon ratio in the reformer from 2.0 to 3.5, and thus increasing the dilution of the fuel in the stack, as is illustrated in figure
20 11. The effect on the stack efficiency can be seen in figure 12. The benefit of this approach is less marked than changing the stack temperature (method 1), but a small improvement in efficiency is clearly apparent.
Many variations may be madi; to the examples described above whilst still falling within the scope of mis invention. For example the microprocessor may just
25 control the stack temperature but not the fuel dilution, or vice-versa.

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CLAIMS

1. A method of operating a solid oxide fuel cell stack with mixed ionic/electronic conducting electrolytes, the method comprising determining the required power output of the solid oxide fuel cell stack and controlling one or more operating conditions of the solid oxide fuel cell stack dependent upon the determined power output.

2. A method according to claim 1, oxide fuel cell stack that are controlled cell stack and the dilution of fuel

wherein the operating conditions of the solid are at least one of the temperature of the fuel delivered to the fuel cell stack.

temperature
fuel
15

3. A method according to claim 2 oxide fuel cell stack is reduced, the the power output of the solid oxide cell stack is increased.

wherein as the power output of the solid of the fuel cell stack is reduced and as cell is increased, the temperature of the fuel

4. A method according to claim 2 or claim 3, wherein the temperature of the fuel cell stack is maintained at 650°C or below.
20

5. A method according to claim 4, maintained at 600°C or below.

wherein the temperature of the fuel cell stack is

6. A method according to any of claims 2 to 5, wherein the fuel delivered to the fuel cell stack is diluted with a predetermined amount of steam, carbon dioxide, nitrogen or a mixture including steam, carbon dioxide and/or nitrogen.

7. A method according to any of fuel cell stack is diluted with a anode side of the fuel cell.

claims 2 to 5, wherein the fuel delivered to the variable proportion of recycled exhaust gas from an

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8. A method according to any of claims 2 to 7, wherein as the power output of the solid oxide fuel cell stack is reduced, the dilution of the fuel delivered to the fuel cell stack is increased and as the power output of the solid oxide fuel cell is increased, the dilution of the fuel delivered to the fuel cell stack is reduced.
9. A method according to any of the preceding claims applied to a solid oxide fuel cell with an electrolyte including gadolinium-doped cerium oxide.

10. A method substantially as hereinbefore described with reference to the
10 accompanying drawings.

15

11. A control system for a solid oxide fuel cell stack with a mixed ionic/electronic
conducting electrolyte, the control system comprising
means for determining a required power output of the stack and
a controller for controlling one or more operating conditions of the stack
dependent upon the required power output.

20

12. A control system according to control at least one of the temperature the stack.

claim 11, wherein the controller is arranged to of the stack and the dilution of fuel delivered to

25

13. A control system according to claim 12, wherein the controller reduces the temperature of the stack as a result of the determining means determining that the required power output is reducing and the controller increases the temperature of the stack as a result of the determining means determining that the required power output

is increasing.
14. A control system according determining means monitors an electric

to any one of claim 11 to 13, wherein the al power output from the stack.

30

15. A control system according to any of claims 11 to 14, wherein the controller maintains the temperature of the stack at 650° or below.

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16. A control system according to claim 15, wherein the controller maintains the temperature of the stack at 600°C or below.

17. A control system according to any one of claims 11 to 16, wherein the
controller arranges the fuel delivered to the fuel cell stack to be diluted with a predetermined amount of steam, carbon dioxide, nitrogen or a mixture including steam, carbon dioxide and/or nitrogen.

10

18. A control system according to controller arranges the fuel delivered to proportion of recycled exhaust gas from

any one of claims 11 to 17, wherein the the fuel cell stack to be diluted with a variable anode sides of the fuel cell stack.

15

19. A control system according to any one of claims 11 to 18, wherein the controller increases the dilution of the fuel delivered to the fuel cell stack as a result of the determining means determining that the required power output is reducing and the controller reducing the dilution of the fuel delivered to the fuel cell stack as a result of the determining means determining that the required power output is increasing.

20. A control system substantially as hereinbefore described with reference to the
20 accompanying drawings.
21. A fuel cell stack with mixed ionic/electronic conducting electrolytes including
a control system according to any one of claims 11 to 20.

25 22. A fuel cell stack substantially accompanying drawings.

as hereinbefore described with reference to the

Dated this 30th day of August, 2006

s. AFSSAR
OF K & S PARTNERS AGENT FOR THE APPLICANT(S)

16
ABSTRACT
A method and apparatus for operating an intermediate-temperature solid-oxide fuel cell stack with a mixed ionic/electronic conducting electrolyte in order to increase its efficiency. The required power output of the solid-oxide fuel cell stack is determined and one or more operating conditions of the solid fuel cell stack are controlled dependent upon the determined required power output. The operating conditions that are controlled may be at least one or the temperature of the fuel cell stack and the dilution of fuel delivered to the fuel cell stack

A METHOD AND CONTROL SYSTEM FOR OPERATING A VARIABLE POWER OUTPUT SOLID OXIDE FUEL CELL STACK

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