JP6951383B2 - Electrochemical reaction cell stack - Google Patents

Description

The techniques disclosed herein relate to electrochemical reaction cell stacks.

A solid oxide fuel cell (hereinafter referred to as "SOFC") is known as one of the fuel cells that generate power by utilizing an electrochemical reaction between hydrogen and oxygen. SOFCs are generally used in the form of fuel cell stacks comprising a plurality of fuel cell single cells (hereinafter, simply referred to as "single cells") arranged side by side in a predetermined direction. Each single cell includes an air electrode, a fuel electrode, and an electrolyte layer disposed between the air electrode and the fuel electrode in a predetermined direction. In general, many fuel electrodes contain zirconia.

In such a fuel cell stack, for example, due to the influence of the flow of gas supplied to the fuel chamber facing the fuel electrode and the air chamber facing the air electrode, the temperatures of the single cells during the power generation reaction are different from each other. There are a plurality of cell portions, for example, a high temperature cell portion and a low temperature cell portion whose temperature at the time of power generation reaction is lower than that of the high temperature cell portion. In the high temperature cell portion of the single cell, the conductivity in the electrolyte layer is higher than that in the low temperature cell portion, so that current concentration is likely to occur, and as a result, for example, the power generation efficiency of the fuel cell stack is lowered. Stack performance may be degraded.

On the other hand, conventionally, for example, in order to stabilize zirconia, the _{amount of solid solution of Y 2} O ₃ contained in the electrolyte layer is adjusted according to the temperature distribution in the electrolyte layer, which is caused by the temperature difference of a single cell. It is known that the current density becomes non-uniform (see Patent Document 1).

Japanese Unexamined Patent Publication No. 9-92304

However, conventionally, as a means for suppressing the non-uniformity of the current density due to the temperature difference of a single cell, a means different from partially changing the component amount of the electrolyte layer has not been sufficiently studied, and improvement has been made. There was room.

In addition, such a problem is electrolysis including a plurality of electrolytic single cells which are constituent units of a solid oxide type electrolytic cell (hereinafter referred to as “SOEC”) that generates hydrogen by utilizing an electrolysis reaction of water. This is a common issue for cell stacks. In the present specification, the fuel cell single cell and the electrolytic single cell are collectively referred to as an electrochemical reaction single cell, and the fuel cell stack and the electrolytic cell stack are collectively referred to as an electrochemical reaction cell stack.

This specification discloses a technique capable of solving the above-mentioned problems.

The techniques disclosed herein can be realized in the following forms.

(1) The electrochemical reaction cell stack disclosed in the present specification has an air electrode, a fuel electrode, and an electrolyte layer arranged between the air electrode and the fuel electrode in the first direction, respectively. In an electrochemical reaction cell stack comprising a plurality of electrochemical reaction single cells, wherein the fuel electrode contains zirconia, at least one of the plurality of electrochemical reaction single cells is the first electrochemical reaction single cell. There are a high-temperature cell portion and a low-temperature cell portion in which the positions in the direction of the above are different from each other and the temperatures at the time of the electrochemical reaction are different from each other. high temperature, in the case of performing Raman analysis on the layer comprising zirconia, wavenumber 440 cm ^-1 or more, the integral value of the intensity in the range of 690 cm ^-1 or less as the first integrated value, the wave number is 185cm ^-1 When the integrated value of the intensity in the range of 380 cm ^-1 or less is taken as the second integrated value, the first of the fuel electrodes included in the at least one electrochemical reaction single cell, which is contained in the high temperature cell portion. The first ratio, which is the ratio of the second integrated value to the first integrated value in the fuel pole portion, is the first ratio to the first integrated value in the second fuel pole portion included in the low temperature cell portion. It is larger than the second ratio, which is the ratio of the integrated values of 2.

In case of performing Raman analysis on the layer comprising zirconia, wavenumber 440 cm ^-1 or more, the integral value of the intensity in the range of 690 cm ^-1 or less as the first integrated value, the wave number is 185cm ^-1 or more, 380 cm ^- The integrated value of the intensity in the range of ^{1 or less is defined as the second integrated value.} At this time, in the present electrochemical reaction cell stack, at least one electrochemical reaction single cell among the plurality of electrochemical reaction single cells is positioned in the first direction (direction in which the air electrode and the fuel electrode are aligned). There are high-temperature cell portions and low-temperature cell portions that are different from each other and have different temperatures during the electrochemical reaction. Further, among the fuel poles included in the at least one electrochemical reaction single cell, the first ratio, which is the ratio of the second integrated value to the first integrated value in the first fuel pole portion included in the high temperature cell portion. Is higher than the second ratio, which is the ratio of the second integrated value to the first integrated value in the second fuel electrode portion included in the low temperature cell portion. That is, the first fuel electrode portion in the fuel electrode is included in the high temperature cell portion in which the temperature during the electrochemical reaction is relatively high and current concentration is likely to occur in the electrochemical reaction single cell as compared with the second fuel electrode portion. Is done. However, in the first fuel electrode portion, the ratio of the second integrated value to the first integrated value is higher than that in the second fuel electrode portion, so that the reaction resistance of the electrochemical reaction is high. Therefore, according to the present electrochemical reaction cell stack, it is caused by the temperature difference in the electrochemical reaction single cell as compared with the configuration in which the ratio of the second integrated value to the first integrated value is uniform over the entire fuel electrode. Therefore, it is possible to prevent the current density from becoming non-uniform.

(2) In the electrochemical reaction cell stack, the electrolyte layer contains zirconia, and the difference between the second ratio and the first ratio in the electrolyte layer is the second in the fuel electrode. The configuration may be smaller than the difference between the ratio and the first ratio. In general, the ratio of the second integral to the first integral in the electrolyte layer is that of the electrochemical reaction in a single cell, compared to the ratio of the second integral to the first integral in the fuel electrode. It greatly affects the reaction resistance. On the other hand, in the present electrochemical reaction cell stack, the difference between the second ratio and the first ratio in the electrolyte layer is smaller than the difference between the second ratio and the first ratio in the fuel electrode. Therefore, according to this electrochemical reaction cell stack, the current density becomes non-uniform due to the temperature difference in the electrochemical reaction single cell while suppressing the increase in the reaction resistance of the electrochemical reaction in the electrochemical reaction single cell. It can be suppressed.

(3) In the electrochemical reaction cell stack, the difference between the second ratio and the first ratio in the electrolyte layer may be 0.02 or less. According to the present electrochemical reaction cell stack, the reaction resistance of the electrochemical reaction in the electrochemical reaction single cell is higher than that in the configuration in which the difference between the second ratio and the first ratio in the electrolyte layer is higher than 0.02. The increase can be effectively suppressed.

The technique disclosed in the present specification can be realized in various forms, for example, an electrochemical reaction cell stack (fuel cell stack or electrolytic cell stack), an electrochemical reaction cell stack including an electrochemical reaction cell stack. It can be realized in the form of a reaction system (fuel cell system or electrolytic cell system), a method for producing them, and the like.

It is a perspective view which shows the appearance structure of the fuel cell stack 100 in embodiment. It is explanatory drawing which shows the XZ cross-sectional structure of the fuel cell stack 100 at the position of II-II of FIG. It is explanatory drawing which shows the YZ cross-sectional structure of the fuel cell stack 100 at the position of III-III of FIG. It is explanatory drawing which shows the XZ cross section configuration of two power generation units 102 adjacent to each other at the same position as the cross section shown in FIG. It is explanatory drawing which shows the YZ cross section configuration of two power generation units 102 adjacent to each other at the same position as the cross section shown in FIG. It is explanatory drawing which enlarges and shows the YZ cross-sectional structure of a part (X1 part of FIG. 5) of a single cell 110. It is explanatory drawing which shows the XY cross-sectional structure of the power generation unit 102 at the position of VII-VII of FIG. It is explanatory drawing which shows the result of the 1st performance evaluation. It is explanatory drawing which shows the result of the 2nd performance evaluation.

A. Embodiment:
A-1. composition:
(Structure of fuel cell stack 100)
FIG. 1 is a perspective view showing an external configuration of the fuel cell stack 100 according to the present embodiment, and FIG. 2 is an explanatory view showing an XZ cross-sectional configuration of the fuel cell stack 100 at the position II-II of FIG. FIG. 3 is an explanatory view showing a YZ cross-sectional configuration of the fuel cell stack 100 at the positions III-III of FIG. Each figure shows XYZ axes that are orthogonal to each other to identify the direction. In the present specification, for convenience, the Z-axis positive direction is referred to as "upward" and the Z-axis negative direction is referred to as "downward", but the fuel cell stack 100 actually has such an orientation. It may be installed in a different orientation. The same applies to FIGS. 4 and later. The fuel cell stack corresponds to an electrochemical reaction cell stack within the scope of claims.

The fuel cell stack 100 includes a plurality of power generation units 102 (seven in this embodiment) and a pair of end plates 104 and 106. The seven power generation units 102 are arranged side by side in a predetermined arrangement direction (vertical direction in the present embodiment). The pair of end plates 104 and 106 are arranged so as to sandwich an aggregate composed of seven power generation units 102 from above and below.

A plurality of holes (eight in this embodiment) penetrating in the vertical direction are formed on the peripheral edge of each layer (power generation unit 102, end plates 104, 106) constituting the fuel cell stack 100 in the Z direction. , The holes formed in each layer and corresponding to each other communicate with each other in the vertical direction to form a communication hole 108 extending in the vertical direction from one end plate 104 to the other end plate 106. In the following description, the holes formed in each layer of the fuel cell stack 100 to form the communication holes 108 are also referred to as “communication holes 108”.

A bolt 22 extending in the vertical direction is inserted into each communication hole 108, and the fuel cell stack 100 is fastened by the bolt 22 and the nuts 24 fitted on both sides of the bolt 22. As shown in FIGS. 2 and 3, between the nut 24 fitted on one side (upper side) of the bolt 22 and the upper surface of the end plate 104 forming the upper end of the fuel cell stack 100, and the bolt. An insulating sheet 26 is interposed between the nut 24 fitted on the other side (lower side) of the 22 and the lower surface of the end plate 106 forming the lower end of the fuel cell stack 100. However, in the place where the gas passage member 27 described later is provided, the insulating sheets arranged on the upper side and the lower side of the gas passage member 27 and the gas passage member 27 between the nut 24 and the surface of the end plate 106, respectively. 26 is intervening. The insulating sheet 26 is made of, for example, a mica sheet, a ceramic fiber sheet, a ceramic dust sheet, a glass sheet, a glass-ceramic composite agent, or the like.

The outer diameter of the shaft portion of each bolt 22 is smaller than the inner diameter of each communication hole 108. Therefore, a space is secured between the outer peripheral surface of the shaft portion of each bolt 22 and the inner peripheral surface of each communication hole 108. As shown in FIGS. 1 and 2, the position is near the midpoint of one side (the side on the positive side of the X axis among the two sides parallel to the Y axis) on the outer circumference of the fuel cell stack 100 in the Z direction. In the space formed by the bolt 22 (bolt 22A) and the communication hole 108 into which the bolt 22A is inserted, the oxidant gas OG is introduced from the outside of the fuel cell stack 100, and the oxidant gas OG is generated for each power generation. It functions as an oxidizer gas introduction manifold 161 that is a gas flow path supplied to the unit 102, and is the midpoint of the opposite side (the side on the negative direction of the X axis of the two sides parallel to the Y axis). The space formed by the bolt 22 (bolt 22B) located in the vicinity and the communication hole 108 into which the bolt 22B is inserted provides the oxidizer off-gas OOG, which is the gas discharged from the air chamber 166 of each power generation unit 102. It functions as an oxidizer gas discharge manifold 162 that discharges to the outside of the fuel cell stack 100. In this embodiment, for example, air is used as the oxidant gas OG.

Further, as shown in FIGS. 1 and 3, the vicinity of the midpoint of one side (the side on the positive direction of the Y axis among the two sides parallel to the X axis) on the outer circumference of the fuel cell stack 100 around the Z direction. In the space formed by the bolt 22 (bolt 22D) located in the above and the communication hole 108 into which the bolt 22D is inserted, the fuel gas FG is introduced from the outside of the fuel cell stack 100, and the fuel gas FG is generated by each power generation. A bolt 22 that functions as a fuel gas introduction manifold 171 to be supplied to the unit 102 and is located near the midpoint of the opposite side (the side on the negative side of the Y axis of the two sides parallel to the X axis). The space formed by (bolt 22E) and the communication hole 108 into which the bolt 22E is inserted sends the fuel off-gas FOG, which is the gas discharged from the fuel chamber 176 of each power generation unit 102, to the outside of the fuel cell stack 100. It functions as a fuel gas discharge manifold 172 to be discharged. In the present embodiment, for example, a hydrogen-rich gas obtained by reforming city gas is used as the fuel gas FG.

The fuel cell stack 100 is provided with four gas passage members 27. Each gas passage member 27 has a hollow cylindrical main body 28 and a hollow cylindrical branch 29 branched from the side surface of the main body 28. The hole of the branch portion 29 communicates with the hole of the main body portion 28. A gas pipe (not shown) is connected to the branch portion 29 of each gas passage member 27. Further, as shown in FIG. 2, the hole of the main body 28 of the gas passage member 27 arranged at the position of the bolt 22A forming the oxidant gas introduction manifold 161 communicates with the oxidant gas introduction manifold 161. The hole of the main body 28 of the gas passage member 27 arranged at the position of the bolt 22B forming the oxidant gas discharge manifold 162 communicates with the oxidant gas discharge manifold 162. Further, as shown in FIG. 3, the hole of the main body 28 of the gas passage member 27 arranged at the position of the bolt 22D forming the fuel gas introduction manifold 171 communicates with the fuel gas introduction manifold 171 and fuel gas. The hole of the main body 28 of the gas passage member 27 arranged at the position of the bolt 22E forming the discharge manifold 172 communicates with the fuel gas discharge manifold 172.

(Structure of end plates 104 and 106)
The pair of end plates 104 and 106 are substantially rectangular flat plate-shaped conductive members, and are made of, for example, stainless steel. One end plate 104 is located above the power generation unit 102 located at the top, and the other end plate 106 is located below the power generation unit 102 located at the bottom. A plurality of power generation units 102 are sandwiched by a pair of end plates 104 and 106 in a pressed state. The upper end plate 104 functions as a positive output terminal of the fuel cell stack 100, and the lower end plate 106 functions as a negative output terminal of the fuel cell stack 100.

(Structure of power generation unit 102)
FIG. 4 is an explanatory view showing an XZ cross-sectional configuration of two power generation units 102 adjacent to each other at the same position as the cross section shown in FIG. 2, and FIG. 5 is an explanatory view showing the XZ cross-sectional configuration of the two power generation units 102 adjacent to each other at the same position as the cross section shown in FIG. It is explanatory drawing which shows the YZ cross-sectional structure of two power generation units 102.

As shown in FIGS. 4 and 5, the power generation unit 102, which is the minimum unit of power generation, includes a single cell 110, a separator 120, an air pole side frame 130, an air pole side current collector 134, and a fuel pole side frame. It includes 140, a fuel electrode side current collector 144, and a pair of interconnectors 150 that form the uppermost layer and the lowermost layer of the power generation unit 102. Holes corresponding to the communication holes 108 into which the bolts 22 described above are inserted are formed in the peripheral edges of the separator 120, the air pole side frame 130, the fuel pole side frame 140, and the interconnector 150 in the Z direction. The single cell 110 corresponds to an electrochemical reaction single cell in the claims.

The interconnector 150 is a substantially rectangular flat plate-shaped conductive member, and is made of, for example, ferritic stainless steel. The interconnector 150 ensures electrical continuity between the power generation units 102 and prevents mixing of reaction gases between the power generation units 102. In the present embodiment, when two power generation units 102 are arranged adjacent to each other, one interconnector 150 is shared by two adjacent power generation units 102. That is, the upper interconnector 150 in a certain power generation unit 102 is the same member as the lower interconnector 150 in another power generation unit 102 adjacent to the upper side of the power generation unit 102. Further, since the fuel cell stack 100 includes a pair of end plates 104 and 106, the power generation unit 102 located at the top of the fuel cell stack 100 does not have the upper interconnector 150 and is located at the bottom. The power generation unit 102 does not include the lower interconnector 150 (see FIGS. 2 and 3).

The single cell 110 includes an air electrode (cathode) 114, a fuel electrode (anode) 116, and an electrolyte layer 112 arranged between the air electrode 114 and the fuel electrode 116. In the present embodiment, the thickness of the fuel pole 116 (size in the vertical direction) is thicker than the thickness of the air pole 114 and the electrolyte layer 112, and the fuel pole 116 supports another layer constituting the single cell 110. That is, the single cell 110 of the present embodiment is a fuel electrode support type single cell.

The electrolyte layer 112 is a flat plate-shaped member that is substantially rectangular in the Z direction, and is a dense layer (with a low porosity). The electrolyte layer 112 contains at least zirconia and is formed of, for example, solid oxides such as YSZ (yttria-stabilized zirconia), ScSZ (scandia-stabilized zirconia), and CaSZ (calcia-stabilized zirconia). As described above, the single cell 110 (power generation unit 102) of the present embodiment is a solid oxide fuel cell (SOFC) that uses a solid oxide as an electrolyte. In this embodiment, the thickness of the electrolyte layer 112 is 10 μm or less.

The air electrode 114 is a flat plate-shaped member that is substantially rectangular in the Z direction, and is, for example, a perovskite-type oxide (for example, LSCF (lanternstrontium cobalt iron oxide), LSM (lanternstrontium manganese oxide), LNF (lantern nickel iron). )).

The fuel electrode 116 is a substantially rectangular flat plate-shaped member having substantially the same size as the electrolyte layer 112 in the Z direction, and is a porous layer (having a higher porosity than the electrolyte layer 112). FIG. 6 is an enlarged explanatory view showing a YZ cross-sectional configuration of a part of the single cell 110 (X1 portion in FIG. 5). As shown in FIG. 6, the fuel pole 116 includes a substrate layer 310 constituting the lower surface of the fuel pole 116, and an active layer 320 arranged between the substrate layer 310 and the electrolyte layer 112. In this embodiment, the active layer 320 is adjacent to the electrolyte layer 112, and the substrate layer 310 is adjacent to the active layer 320.

The active layer 320 mainly exerts a function of reacting oxygen ions supplied from the electrolyte layer 112 with hydrogen or the like contained in the fuel gas FG to generate electrons and water vapor. The active layer 320 contains an oxygen ion conductive substance (YSZ, which is a ceramic in this embodiment) and an electron conductive substance (Ni, which is a transition metal in this embodiment). The thickness of the active layer 320 is, for example, 5 μm to 40 μm. The average particle size of Ni contained in the active layer 320 is, for example, 0.1 μm to 2 μm, and the average particle size of the oxide ion conductive ceramics (YSZ) contained in the active layer 320 is, for example, 0.1 μm to 2 μm. It is 2 μm. The average porosity of the active layer 320 is, for example, 5 vol% to 30 vol%. The substrate layer 310 mainly exerts a function of supporting the active layer 320, the electrolyte layer 112, and the air electrode 114. The substrate layer 310 also contains an oxygen ion conductive substance (YSZ) and an electron conductive substance (Ni). The thickness of the substrate layer 310 is, for example, 200 μm to 1000 μm. The average particle size of Ni contained in the substrate layer 310 is, for example, 0.1 μm to 2 μm, and the average particle size of the oxide ion conductive ceramics (YSZ) contained in the substrate layer 310 is, for example, 0.1 μm to 2 μm. It is 2 μm. The average porosity of the substrate layer 310 is, for example, 25 to 60 vol%, and the average porosity is, for example, 0.5 μm to 4 μm.

As shown in FIGS. 4 and 5, the separator 120 is a frame-shaped member in which a substantially rectangular hole 121 penetrating in the vertical direction is formed near the center, and is formed of, for example, metal. The peripheral portion of the hole 121 in the separator 120 faces the peripheral edge of the surface of the electrolyte layer 112 on the side of the air electrode 114. The separator 120 is bonded to the electrolyte layer 112 (single cell 110) by a bonding portion 124 formed of a brazing material (for example, Ag wax) arranged at the opposite portion thereof. The separator 120 partitions the air chamber 166 facing the air electrode 114 and the fuel chamber 176 facing the fuel electrode 116, and a gas leak from one electrode side to the other electrode side at the peripheral edge of the single cell 110. It is suppressed.

The air electrode side frame 130 is a frame-shaped member in which a substantially rectangular hole 131 penetrating in the vertical direction is formed near the center, and is formed of, for example, an insulator such as mica. The hole 131 of the air electrode side frame 130 constitutes an air chamber 166 facing the air electrode 114. The air electrode side frame 130 is in contact with the peripheral edge of the surface of the separator 120 opposite to the side facing the electrolyte layer 112 and the peripheral edge of the surface of the interconnector 150 facing the air electrode 114. .. Further, the air electrode side frame 130 electrically insulates between the pair of interconnectors 150 included in the power generation unit 102. Further, in the air electrode side frame 130, the oxidant gas supply communication hole 132 that communicates the oxidant gas introduction manifold 161 and the air chamber 166, and the oxidant gas that communicates the air chamber 166 and the oxidant gas discharge manifold 162. A discharge communication hole 133 is formed.

The fuel electrode side frame 140 is a frame-shaped member in which a substantially rectangular hole 141 penetrating in the vertical direction is formed near the center, and is formed of, for example, metal. Hole 141 of the fuel electrode side frame 140 constitutes a fuel chamber 176 facing the fuel electrode 116. The fuel electrode side frame 140 is in contact with the peripheral edge of the surface of the separator 120 facing the electrolyte layer 112 and the peripheral edge of the surface of the interconnector 150 facing the fuel electrode 116. Further, in the fuel electrode side frame 140, a fuel gas supply communication hole 142 that communicates the fuel gas introduction manifold 171 and the fuel chamber 176, and a fuel gas discharge communication hole 143 that communicates the fuel chamber 176 and the fuel gas discharge manifold 172. And are formed.

The fuel electrode side current collector 144 is arranged in the fuel chamber 176. The fuel electrode side current collector 144 includes an interconnector facing portion 146, an electrode facing portion 145, and a connecting portion 147 connecting the electrode facing portion 145 and the interconnector facing portion 146. For example, nickel or nickel alloy. , Stainless steel, etc. The electrode facing portion 145 is in contact with the surface of the fuel pole 116 opposite to the side facing the electrolyte layer 112, and the interconnector facing portion 146 is on the surface of the interconnector 150 facing the fuel pole 116. Are in contact. However, as described above, since the power generation unit 102 located at the bottom of the fuel cell stack 100 does not have the lower interconnector 150, the interconnector facing portion 146 in the power generation unit 102 is the lower end plate. It is in contact with 106. Since the fuel pole side current collector 144 has such a configuration, the fuel pole 116 and the interconnector 150 (or the end plate 106) are electrically connected to each other. A spacer 149 formed of, for example, mica is arranged between the electrode facing portion 145 and the interconnector facing portion 146. Therefore, the fuel pole side current collector 144 follows the deformation of the power generation unit 102 due to the temperature cycle and the reaction gas pressure fluctuation, and the fuel pole 116 and the interconnector 150 (or the end plate 106) via the fuel pole side current collector 144 follow. Good electrical connection with is maintained.

The air electrode side current collector 134 is arranged in the air chamber 166. The air electrode side current collector 134 is composed of a plurality of substantially square columnar current collector elements 135, and is formed of, for example, ferritic stainless steel. The air electrode side current collector 134 is in contact with the surface of the air electrode 114 opposite to the side facing the electrolyte layer 112 and the surface of the interconnector 150 on the side facing the air electrode 114. However, as described above, since the power generation unit 102 located at the top of the fuel cell stack 100 does not have the upper interconnector 150, the air electrode side current collector 134 in the power generation unit 102 has an upper end plate. It is in contact with 104. Since the air electrode side current collector 134 has such a configuration, the air electrode 114 and the interconnector 150 (or the end plate 104) are electrically connected to each other. The air electrode side current collector 134 and the interconnector 150 may be configured as an integral member. Further, the air electrode side current collector 134 may be covered with a conductive coat, and a conductive bonding layer for bonding the air electrode 114 and the air electrode side current collector 134 is interposed between the air electrode side current collector 134 and the air electrode side current collector 134. You may be doing it.

A-2. Operation of fuel cell stack 100:
As shown in FIGS. 2 and 4, the oxidant gas OG is supplied via a gas pipe (not shown) connected to the branch portion 29 of the gas passage member 27 provided at the position of the oxidant gas introduction manifold 161. Then, the oxidant gas OG is supplied to the oxidant gas introduction manifold 161 through the holes of the branch portion 29 and the main body portion 28 of the gas passage member 27, and the oxidant gas introduction manifold 161 oxidizes each power generation unit 102. It is supplied to the air chamber 166 through the agent gas supply communication hole 132. Further, as shown in FIGS. 3 and 5, the fuel gas FG is supplied via a gas pipe (not shown) connected to the branch portion 29 of the gas passage member 27 provided at the position of the fuel gas introduction manifold 171. Then, the fuel gas FG is supplied to the fuel gas introduction manifold 171 through the holes of the branch portion 29 and the main body portion 28 of the gas passage member 27, and the fuel gas supply communication of each power generation unit 102 is performed from the fuel gas introduction manifold 171. It is supplied to the fuel chamber 176 through the hole 142.

When the oxidant gas OG is supplied to the air chamber 166 of each power generation unit 102 and the fuel gas FG is supplied to the fuel chamber 176, power is generated by the electrochemical reaction of the oxidant gas OG and the fuel gas FG in the single cell 110. Will be. This power generation reaction is an exothermic reaction. In each power generation unit 102, the air pole 114 of the single cell 110 is electrically connected to one of the interconnectors 150 via the air pole side current collector 134, and the fuel pole 116 is via the fuel pole side current collector 144. It is electrically connected to the other interconnector 150. Further, the plurality of power generation units 102 included in the fuel cell stack 100 are electrically connected in series. Therefore, the electric energy generated in each power generation unit 102 is taken out from the end plates 104 and 106 that function as the output terminals of the fuel cell stack 100. Since the SOFC generates electricity at a relatively high temperature (for example, 700 ° C. to 1000 ° C.), the fuel cell stack 100 is a heater (for example, until the high temperature can be maintained by the heat generated by the power generation after the start-up. It may be heated by (not shown).

As shown in FIGS. 2 and 4, the oxidant off-gas OOG discharged from the air chamber 166 of each power generation unit 102 is discharged to the oxidant gas discharge manifold 162 through the oxidant gas discharge communication hole 133, and further oxidized. The fuel cell stack 100 is passed through the holes of the main body 28 and the branch 29 of the gas passage member 27 provided at the position of the agent gas discharge manifold 162, and the gas pipe (not shown) connected to the branch 29. It is discharged to the outside of. Further, as shown in FIGS. 3 and 5, the fuel off-gas FOG discharged from the fuel chamber 176 of each power generation unit 102 is discharged to the fuel gas discharge manifold 172 through the fuel gas discharge communication hole 143, and further, the fuel gas. Through the holes of the main body 28 and the branch 29 of the gas passage member 27 provided at the position of the discharge manifold 172, and through a gas pipe (not shown) connected to the branch 29, to the outside of the fuel cell stack 100. It is discharged.

A-3. Detailed configuration of fuel pole 116:
As a premise, each term is defined as follows.
"First integrated value": in the case of performing a Raman analysis on the layer comprising zirconia, wavenumber 440 cm ^-1 or more, the integral value of the intensity peak in the range of 690 cm ^-1 or less.
Raman analysis is shown, for example, in "Taro Shimonosono, 5 outsiders, Solid State lonics, (Netherlands), Elsevier BV, 2012, volume225, p.69-72". It is an analysis according to the Raman spectroscopy.
Further, wave number 440 cm ^-1 or more, 690 cm ^-1 or less in the range indicates the range of the intensity peaks crystal system zirconia belongs to the cubic and tetragonal. The first integral value is the integral value (area) of the intensity peak after the background (impure peak) is removed by the background treatment in the range of the intensity peaks in which the zirconia crystal system belongs to cubic and tetragonal crystals. Value). In this embodiment, a known linear method is used as the background treatment. The straight line method is a method in which both ends of the intensity peak in the target range of the intensity peak are connected by a straight line and the area on the straight line is used as the integral value of the intensity peak.

"Second integral value": in the case of performing a Raman analysis on the layer comprising zirconia, wavenumber 185cm ^-1 or more, the integral value of the intensity peak in the range of 380 cm ^-1 or less.
Wavenumber 185cm ^-1 or more, 380 cm ^-1 The following range indicates the crystal system of zirconia ranges of intensity peaks belonging to tetragonal. The second integral value is the integral value (area value) of the intensity peak after the background is removed by the above-mentioned background treatment in the range of the intensity peak in which the zirconia crystal system belongs to the tetragonal crystal system.

The ratio of the second integrated value to the first integrated value is the strength with which the zirconia crystal system contained in the target layer containing zirconia (fuel electrode 116, electrolyte layer 112, etc.) belongs to cubic crystals and tetragonal crystals. peak (440 cm ^-1 or more, 690 cm ^-1 or less) for the integral value of the intensity peaks crystal system zirconia belongs to tetragonal (185cm ^-1 or more, 380 cm ^-1 or less) ratio of the integral value of. Therefore, the larger the ratio of the second integrated value to the first integrated value, the larger the ratio of zirconia belonging to the tetragonal crystal system. Further, the oxygen ion conductivity of the zirconia tetragonal crystal is lower than the oxygen ion conductivity of the zirconia cubic crystal. Further, the mechanical strength of the zirconia tetragonal crystal is higher than the mechanical strength of the zirconia cubic crystal. Therefore, the larger the ratio of the second integrated value to the first integrated value, the lower the oxygen ion conductivity in the layer containing zirconia (larger reaction resistance) and the higher the mechanical strength of the layer containing zirconia. ..

"High temperature side ratio R1": The ratio of the second integrated value to the first integrated value in the high temperature corresponding portion of the target layer (fuel electrode 116, electrolyte layer 112, etc.) containing zirconia. The high temperature side ratio R1 corresponds to the first ratio in the claims.
"Low temperature side ratio R2": The ratio of the second integrated value to the first integrated value in the low temperature corresponding portion of the target layer (fuel electrode 116, electrolyte layer 112, etc.) containing zirconia. The low temperature side ratio R2 corresponds to the second ratio in the claims.
The high temperature compatible portion of the target layer is a portion of the single cell 110 included in the cell portion (high temperature cell portion) where the temperature during the power generation reaction is relatively high in the vertical direction (Z direction). The low temperature compatible part of the target layer is located in the single cell 110 at a position different from the high temperature compatible part in the vertical direction, and the temperature during the power generation reaction is relatively lower than that of the high temperature compatible part. It is a part included in the part (low temperature cell part). When the target layer is the fuel pole 116, the high temperature compatible portion corresponds to the first fuel pole portion in the claims, and the low temperature compatible portion corresponds to the second fuel pole portion in the claims. Equivalent to.

FIG. 7 is an explanatory view showing an XY cross-sectional configuration of the power generation unit 102 at the position of VII-VII of FIG. In FIG. 7, in the Z direction, the single cell 110 extends in the direction of the gas flow path of the fuel gas FG (Y-axis direction) and the direction orthogonal to the direction of the gas flow path (X-axis). It is divided into nine even cell portions by two virtual straight lines extending in the direction). In the present embodiment, of the nine cell portions in the single cell 110, three cell portions located on the upstream side of the gas flow path of the fuel gas FG are designated as the upstream cell portion H1 and downstream of the gas flow path of the fuel gas FG. The three cell portions located on the side are referred to as a downstream cell portion H3, and the three cell portions located between the upstream cell portion H1 and the downstream cell portion H3 are referred to as an intermediate cell portion H2.

In the fuel cell stack 100 of the present embodiment, of the nine cell portions in the single cell 110, the middle of the three cell portions arranged in the direction orthogonal to the gas flow path direction (X-axis direction) in the vertical direction. The cell portion located in is higher in temperature during the power generation reaction than the cell portions located at both ends. That is, the cell portion located in the center becomes a high temperature cell portion, and the cell portions located at both ends become a low temperature cell portion. For example, with respect to the three intermediate cell portions H2, the central cell portion H21 located in the center becomes the high temperature cell portion, and the two intermediate cell portions H22 located at both ends become the low temperature cell portion. Further, in the present embodiment, among the nine cell portions in the single cell 110, the cell portion having the highest temperature during the power generation reaction is the cell portion (three intermediate cell portions) located at the center of the single cell 110 in the vertical direction. Of H2, it was an intermediate cell portion H2 (hereinafter, also referred to as “center cell portion H21”) located in the center. That is, the central cell portion H21 becomes a high temperature cell portion, and the other eight cell portions become low temperature cell portions. The same applies to other layers of interest (electrolyte layer 112, etc.) containing zirconia.

The fuel cell stack 100 of the present embodiment satisfies the first condition regarding the fuel electrode 116.
<First condition>
For each of the plurality of single cells 110 provided in the fuel cell stack 100, the high temperature side ratio R1 (R11) in the fuel pole 116 provided in the single cell 110 is set to the low temperature side ratio R2 (R21) in the fuel pole 116. Larger than that.
The difference (= R21-R11) of the low temperature side ratio R2 (R21) with respect to the high temperature side ratio R1 (R11) in the fuel electrode 116 is preferably larger than 0.02.

Further, the fuel cell stack 100 of the present embodiment satisfies the second condition regarding the fuel electrode 116 and the electrolyte layer 112.
<Second condition>
The difference (absolute value) between the low temperature side ratio R2 (R22) and the high temperature side ratio R1 (R12) in the electrolyte layer 112 is the difference between the low temperature side ratio R2 (R21) and the high temperature side ratio R1 (R11) in the fuel electrode 116. Smaller than (absolute value).

Further, the fuel cell stack 100 of the present embodiment satisfies the third condition regarding the electrolyte layer 112.
<Third condition>
The difference between the low temperature side ratio R2 (R22) and the high temperature side ratio R1 (R12) in the electrolyte layer 112 is 0.02 or less.

A-4. Manufacturing method of fuel cell stack 100:
First, a single cell 110 is produced. Specifically, it is as follows.
(Preparation of green sheet for fuel electrode substrate layer)
With respect to the mixed powder (100 parts by weight) of NiO powder (50 parts by weight) and YSZ powder (50 parts by weight), organic beads (15% by weight with respect to the mixed powder) which are pore-forming materials, and butyral resin , DOP, which is a plasticizer, a dispersant, and a mixed solvent of toluene + ethanol are added and mixed with a ball mill to prepare a slurry. Organic beads are, for example, spherical particles formed of a polymer such as polymethyl methacrylate or polystyrene. The obtained slurry is thinned by the doctor blade method to prepare a green sheet for a fuel electrode substrate layer having a thickness of 200 μm to 250 μm. The ratio of NiO powder and YSZ powder in the green sheet for the fuel electrode substrate layer can be appropriately changed as long as the performance is satisfied. For example, even if the NiO powder: YSZ powder is 60:40 or 40:60. I do not care. That is, the NiO powder can be appropriately changed between 40 and 60 parts by weight so that the mixed powder of the NiO powder and the YSZ powder is 100 parts by weight, and the rest can be the YSZ powder. Further, the YSZ powder is produced by mixing 10YSZ (about 18 wt% Y ₂ O ₃ ) (cubic crystal) and 3YSZ (about 6 wt% Y ₂ O ₃ ) (tetragonal crystal). At this time, by changing the mixing ratio of the 10YSZ and 3YSZ, the content of _Y 2 _{O 3} in the YSZ (wt%) (hereinafter referred to as "YSZ amount") is to prepare different types of YSZ powder together, By using these a plurality of types of YSZ powders, it is possible to produce a plurality of types of green sheets for a fuel electrode substrate layer in which the ratio of the second integrated value to the first integrated value is different from each other. The same applies to the green sheet for the fuel electrode active layer and the green sheet for the electrolyte layer, which will be described later.

(Preparation of green sheet for fuel polar active layer)
A butyral resin, a plasticizer DOP, a dispersant, and a toluene + ethanol mixed solvent are added to a mixed powder (100 parts by weight) of NiO powder (60 parts by weight) and YSZ powder (40 parts by weight). In addition, the mixture is prepared by mixing with a ball mill. Further, organic beads (3.9% by weight with respect to the mixed powder) as a pore-forming material are further added to the mixed powder and mixed with a ball mill to adjust the slurry, whereby the porosity is fueled. It is possible to produce a green sheet for a fuel polar active layer, which is higher than the green sheet for a polar substrate layer. The obtained slurry is thinned by the doctor blade method to prepare a green sheet for a fuel polar active layer having a thickness of 6 μm to 36 μm (for example, 20 μm). The ratio of NiO powder and YSZ powder in the green sheet for the fuel polar active layer can be appropriately changed as long as the performance is satisfied. For example, even if the NiO powder: YSZ powder is 50:50 or 40:60. I do not care. That is, the NiO powder can be appropriately changed between 40 and 60 parts by weight so that the mixed powder of the NiO powder and the YSZ powder is 100 parts by weight, and the rest can be the YSZ powder.

(Preparation of green sheet for electrolyte layer)
Butyral resin, plasticizer DOP, dispersant, and toluene + ethanol mixed solvent are added to YSZ powder (100 parts by weight) and mixed with a ball mill to prepare a slurry. The obtained slurry is thinned by the doctor blade method to prepare a green sheet for an electrolyte layer having a thickness of 10 μm.

(Lamination of electrolyte layer 112 and fuel electrode 116)
The green sheet for the fuel electrode substrate layer, the green sheet for the fuel electrode active layer, and the green sheet for the electrolyte layer are attached and degreased at about 280 ° C., and further fired at about 1350 ° C. to obtain the electrolyte layer 112 and the fuel electrode. A laminate with 116 is obtained. Here, for example, when the green sheet for the fuel polar active layer is attached, the portion of the single cell 110 corresponding to the high temperature cell portion has a second portion with respect to the first integrated value as compared with the portion corresponding to the low temperature cell portion. Attach the green sheet for the fuel polar active layer, which has a high ratio of the integral values of.

(Formation of air pole 114)
A _{mixed solution of La 0.6} Sr _0.4 Co _0.2 Fe _0.8 O ₃ powder and isopropyl alcohol is prepared. A fired body can be obtained by spray-coating the prepared mixed liquid on the surface of the electrolyte layer 112 in the laminated body and firing at 1100 ° C. to form an air electrode 114.

After that, the remaining assembly steps (for example, joining the air electrode 114 and the air electrode side current collector 134 and fastening the fuel cell stack 100 with the bolt 22) are performed, and the assembly of the fuel cell stack 100 is completed.

A-5. Effect of this embodiment:
As described above, the fuel cell stack 100 in the present embodiment includes a plurality of single cells 110. Each single cell 110 includes an air pole 114, a fuel pole 116, and an electrolyte layer 112 disposed between the air pole 114 and the fuel pole 116. Each fuel pole 116 contains zirconia. Here, in such a fuel cell stack 100, for example, due to the influence of the flow of the fuel gas FG supplied to the fuel chamber 176, the single cell 110 has a plurality of cell portions having different temperatures during the power generation reaction. exist. In the high temperature cell portion of the single cell 110, the conductivity in the electrolyte is higher than that in the low temperature cell portion, so that current concentration is likely to occur. As a result, the current density in the plane direction in the single cell 110 becomes non-uniform, which causes, for example, a decrease in the performance of the fuel cell stack 100 (for example, a decrease in the initial voltage, a decrease in durability, etc.). Further, the high temperature cell portion of the single cell 110 is liable to be damaged (for example, cracked) due to the generation of thermal stress. On the other hand, according to the present embodiment, the high temperature cell portion of the single cell 110 has higher strength than the low temperature cell portion, so that damage to the single cell 110 due to the generation of thermal stress can be suppressed. can.

On the other hand, in the present embodiment, for each of the plurality of single cells 110 provided in the fuel cell stack 100, the high temperature side ratio R1 (R11) in the fuel pole 116 provided in the single cell 110 is the fuel pole. It is larger than the low temperature side ratio R2 (R21) in 116 (first condition). That is, the high temperature compatible portion (for example, the central cell portion H21 in FIG. 7) of the fuel electrode 116 has an electrochemical reaction (power generation reaction) in the single cell 110 as compared with the low temperature compatible portion (for example, the intermediate cell portions H22 located at both ends). It is included in the high temperature cell part where the temperature at the time is relatively high and current concentration is likely to occur. However, in the high temperature compatible portion of the fuel electrode 116, the ratio of the second integrated value to the first integrated value is higher than that in the low temperature compatible portion, so that the reaction resistance of the power generation reaction is high. Therefore, according to the present embodiment, the current density due to the temperature difference in the single cell 110 is compared with the configuration in which the ratio of the second integrated value to the first integrated value is uniform over the entire fuel electrode 116. Can be suppressed from becoming non-uniform.

Also, in general, the ratio of the second integral to the first integral in the electrolyte layer 112 is the electrochemical ratio in the single cell 110 to the ratio of the second integral to the first integral in the fuel pole 116. It greatly affects the reaction resistance of the reaction (power generation reaction). On the other hand, in the present embodiment, the difference between the low temperature side ratio R2 (R22) and the high temperature side ratio R1 (R12) in the electrolyte layer 112 is the low temperature side ratio R2 (R21) and the high temperature side ratio R1 in the fuel electrode 116. It is smaller than the difference from (R11) (second condition). Therefore, according to the present embodiment, while suppressing an increase in the reaction resistance of the electrochemical reaction in the single cell 110, it is possible to suppress the non-uniformity of the current density due to the temperature difference in the plane direction in the single cell 110. can do.

In the present embodiment, as described above, the thickness of the electrolyte layer 112 is relatively thin (10 μm or less). Therefore, it is particularly difficult to partially change the thickness of the electrolyte layer 112 and to delicately control the thickness of the electrolyte layer 112 as in the conventional technique. Further, even if the thickness of the electrolyte layer 112 can be partially changed, as described above, the ratio of the second integral value to the first integral value in the electrolyte layer 112 is the second integral value in the fuel electrode. Compared with the ratio of the second integral value to the integral value of 1, it greatly affects the reaction resistance of the electrochemical reaction in the single cell 110. Therefore, the thickness of the electrolyte layer 112 is preferably substantially uniform over the entire length in the direction of the gas flow path of the fuel gas FG. That is, according to the present embodiment, it is possible to suppress the non-uniformity of the current density due to the temperature difference in the plane direction in the single cell 110 without requiring the control of the thickness of the electrolyte layer 112.

Further, in the present embodiment, the difference between the low temperature side ratio R2 (R22) and the high temperature side ratio R1 (R12) in the electrolyte layer 112 is 0.02 or less (third condition). As a result, according to the present embodiment, the difference between the low temperature side ratio R2 (R22) and the high temperature side ratio R1 (R12) in the electrolyte layer 112 is higher than 0.02, and the electrochemical in the single cell 110 is obtained. The increase in reaction resistance of the reaction can be effectively suppressed.

A-6. First performance evaluation:
FIG. 8 is an explanatory diagram showing the first performance evaluation result.

A-6-1. For each cell sample:
In the first performance evaluation, the YSZ compounding amount (wt%) and the tetragonal area ratio of zirconia in each layer containing zirconia (the substrate layer 310 and the active layer 320 of the fuel electrode 116, the electrolyte layer 112) and the tetragonal area ratio of zirconia (relative to the first integrated value). The relationship between the ratio of the second integrated value) and the performance of the single cell was evaluated. For the first performance evaluation, cell samples of 6 button cells (cell samples 1 to 6) were used. Each cell sample was prepared according to the method for manufacturing the fuel cell stack 100 (single cell 110) of the above-described embodiment. In the button cell of each cell sample, the vertical thickness of the substrate layer of the fuel electrode is 800 μm, the vertical thickness of the active layer is 20 μm, and the vertical thickness of the electrolyte layer is 10 μm. be.

As shown in FIG. 8, the six cell samples have different YSZ blending amounts (zirconia tetragonal area ratio) in at least one layer of the substrate layer of the fuel electrode, the active layer, and the electrolyte layer. In the cell sample 1, the YSZ content of the substrate layer and the active layer is 11% (zirconia tetragonal area ratio is 0.18), and the YSZ content of the electrolyte layer is 15% (zirconia tetragonal area ratio is 0). .12). The cell sample 2 differs from the cell sample 1 in that the YSZ compounding amount of the substrate layer is 15% (the tetragonal area ratio of zirconia is 0.12).

In the cell sample 3, the YSS content of the substrate layer and the active layer was 15% (the tetragonal area ratio of zirconia was 0.12), and the YSZ content of the electrolyte layer was 11% (zirconia) with respect to the cell sample 1. The tetragonal area ratio of is 0.18). The cell sample 4 differs from the cell sample 3 in that the amount of YSZ compounded in the electrolyte layer is 15% (the tetragonal area ratio of zirconia is 0.12). The cell sample 5 is different from the cell sample 4 in that the amount of YSS in the active layer is 18% (the tetragonal area ratio of zirconia is 0.10). The cell sample 6 is different from the cell sample 5 in that the YSZ compounding amount of the substrate layer is 18% (the tetragonal area ratio of zirconia is 0.10).

The method for specifying the tetragonal area ratio of zirconia in each layer containing zirconia is as follows.
Electrolyte layer: The electrolyte layer of the button cell was divided into three in the thickness direction, and microscopic Raman analysis was performed on a cross section close to the fuel electrode side.
Fuel electrode: After etching the cross section of the fuel electrode of the button cell with hydrochloric acid, micro-Raman analysis was performed on the zirconia in the center of the active layer in the thickness direction.
The LabRAM HR800 manufactured by HORIBA, Ltd. was used as the micro Raman spectroscope. Other measurement conditions and the calculation method of the tetragonal area ratio of zirconia are as follows: "Taro Shimonosono, 5 outsiders, Solid State lonics, (Netherlands), Elsevier BV, 2012, volume225, p. The procedure was the same as for .69-72 ".

A-6-2. Evaluation items and evaluation methods:
^{In the first performance evaluation, two items, the current density (A / cm 2} ) and the strength (MPa) of the button cell of each cell sample, were evaluated. As an evaluation of the current density, at 700 ° C., an oxidizing agent gas (air) was supplied to the air electrode side of the button cell at 250 ml / min, and the fuel gas (4% H ₂ O and 96% H) was supplied to the fuel electrode side. _{While supplying (mixed gas with 2} ) at 330 ml / min, ^{a voltage of up to 0.75 A / cm 2} was acquired, and from its current-voltage characteristics, the current density of the button cell when a voltage of 0.95 V was applied. Was measured. As an evaluation of strength, a three-point bending test was performed. In the three-point bending test, the button cell is processed to a predetermined size and placed on a three-point bending tester equipped with a pair of fulcrums and an indenter. Specifically, two parts on the button cell were arranged on each fulcrum, and an indenter was pressed against a part of the button cell located between the two parts from above. Next, the load applied to the button cell was increased by increasing the pressure contact force of the indenter, and the fracture load (MPa) when the button cell broke was measured.

A-6-3. Performance evaluation results:
As shown in FIG. 8, when the evaluation results of the cell samples 2, 4 and 5 are compared, it can be seen that the higher the tetragonal area ratio of zirconia in the active layer of the fuel electrode, the smaller the current density of the button cell. This means that the greater the proportion of zirconia belonging to the tetragonal crystal system in the active layer of the fuel electrode, the lower the ionic conductivity of the button cell. In this evaluation, when the zirconia square area ratio in the active layer was increased by 0.02, the current density of the button cell ^{decreased by 0.02 A / cm 2} , and the zirconia square area ratio in the active layer was reduced to 0. When it was increased by 06, the current density of the button cell decreased by ^{0.03 A / cm 2.} Moreover, when the evaluation results of the cell samples 4 and 5 were compared, the strength of the button cell was the same even if the tetragonal area ratio of zirconia in the active layer was changed. It is considered that this is because the thickness of the active layer in the button cell used in this evaluation is thinner than that of the substrate layer and the like.

Further, in the cell samples 1, 4 and 6, not only the tetragonal area ratio of zirconia in the active layer but also the tetragonal area ratio of zirconia in the substrate layer is high with respect to the cell samples 2, 4 and 5. It differs in that. According to the evaluation results of the cell samples 1, 4 and 6, the current density of the button cell was substantially the same as the evaluation results of the cell samples 2, 4 and 5. This means that increasing the tetragonal area ratio of zirconia in the active layer effectively lowers the ionic conductivity of the button cell rather than increasing the tetragonal area ratio of zirconia in the substrate layer of the fuel electrode. Means that you can. On the other hand, regarding the strength of the button cell, unlike the evaluation results of the cell samples 2, 4 and 5, the higher the tetragonal area ratio of zirconia in the substrate layer of the fuel electrode, the higher the strength of the button cell. I understand. This means that the higher the proportion of zirconia belonging to the tetragonal crystal system in the substrate layer of the fuel electrode, the higher the strength of the button cell. It also means that increasing the tetragonal area ratio of zirconia in the substrate layer can effectively improve the strength of the button cell rather than increasing the tetragonal area ratio of zirconia in the active layer of the fuel electrode. do.

Comparing the evaluation results of the cell samples 3 and 4, it can be seen that the current density decreases when the tetragonal area ratio of zirconia in the electrolyte layer is increased. In this evaluation, when the square area ratio of zirconia in the electrolyte layer is increased by 0.06, the current density of the button cell decreases by ^{0.13 A / cm 2.} Comparing the evaluation results of cell samples 3 and 4 with the evaluation results of cell samples 2, 4 and 5 described above, when changing the zirconia square area ratio in the electrolyte layer, the zirconia square area ratio in the active layer is changed. It can be seen that the current density of the button cell fluctuates greatly as compared with the case of changing, and it is difficult to bring the current density of the button cell close to a desired value.

A-7. Second performance evaluation:
FIG. 9 is an explanatory diagram showing a second performance evaluation result.

A-7-1. For each stack sample:
In the second performance evaluation, the relationship between the high temperature compatible portion and the low temperature compatible portion and the tetragonal area ratio of zirconia in a single cell was evaluated. For the second performance evaluation, stack samples (stack samples 1 to 4) of four fuel cell stacks were used. Each stack sample was prepared according to the method for manufacturing the fuel cell stack 100 of the above-described embodiment. The high temperature compatible portion and the low temperature compatible portion in each stack sample may be specified, for example, by actually measuring or specifying the temperature of the assembled fuel cell stack, or by simulating based on the design data of the fuel cell stack. Each stack sample was prepared by arranging each of the above-mentioned cell samples in each of the high temperature compatible portion and the low temperature compatible portion in the single cell.

As shown in FIG. 9, the four stack samples show the high-low relationship of the tetragonal area ratio of zirconia between the high-temperature-compatible portion and the low-temperature-compatible portion of the substrate layer, and the zirconia in the high-temperature-compatible portion and the low-temperature-compatible portion of the active layer. At least one of the high-low relations of the tetragonal area ratio is different from each other. In the stack sample 1, the tetragonal area ratio of zirconia in the high temperature compatible portion is higher than the tetragonal area ratio of zirconia in the low temperature compatible portion in both the substrate layer and the active layer. The stack sample 2 differs from the stack sample 1 in that the tetragonal area ratio of zirconia in the high temperature compatible portion and the low temperature compatible portion is the same for the substrate layer.

The stack sample 3 differs from the stack sample 1 in that the tetragonal area ratio of zirconia in the high temperature compatible portion is lower than the tetragonal area ratio of zirconia in the low temperature compatible portion in both the substrate layer and the active layer. .. The stack sample 4 is different from the stack sample 1 in that the tetragonal area ratio of zirconia in the high temperature compatible portion and the low temperature compatible portion is the same in both the substrate layer and the active layer.

A-7-2. Evaluation items and evaluation methods:
In the second performance evaluation, the deterioration rate (%) and the OCV (open circuit voltage) decrease amount (mV) of each stack sample were evaluated. As an evaluation of the deterioration rate, first, the initial voltage of the fuel cell stack when the ^{current density was 0.37 A / cm 2 was measured before the start of the power generation operation.} Next, after performing power generation operation at 700 ° C. for 100 hours, ^{the output voltage of the fuel cell stack when the current density is 0.37 A / cm 2} is measured, and the difference between the initial voltage and the output voltage with respect to the initial voltage is measured. The ratio was taken as the deterioration rate of the fuel cell stack. If the deterioration rate was 0.5% or less, it was evaluated as "○", and if the deterioration rate exceeded 0.5%, it was evaluated as "×". As the amount of decrease in OCV, the amount of decrease in OCV of the fuel cell stack before and after the durability test of the deterioration rate was measured. OCV is an index of the oxygen partial pressure difference between the air electrode and the fuel electrode in the fuel cell stack. It means that the airtightness with the fuel electrode has decreased. If the OCV decrease is 0 mV, it is evaluated as the best "○", if the OCV decrease is more than 0 mV and 5 mV or less, it is evaluated as good "Δ", and if the OCV decrease is more than 5 mV, it is rejected. × ”was evaluated.

A-7-3. Performance evaluation results:
As shown in FIG. 9, in the stack sample 1, the deterioration rate was evaluated as “◯”, and the OCV reduction amount was evaluated as the best “◯”. Further, in the stack sample 2, the deterioration rate was evaluated as “◯”, but the OCV reduction amount was evaluated as good “Δ”. From these facts, in particular, by making the tetragonal area ratio of zirconia in the high temperature compatible portion higher than the tetragonal area ratio of zirconia in the low temperature compatible portion for the active layer of the fuel electrode, the current concentration in the single cell is suppressed and the fuel It can be seen that the acceleration of deterioration of the battery stack can be suppressed. Further, by making the tetragonal area ratio of zirconia in the high temperature compatible portion of the substrate layer of the fuel electrode higher than the tetragonal area ratio of zirconia in the low temperature compatible portion, the strength of the single cell is improved, and the air electrode and the fuel electrode are combined. It can be seen that the airtightness between the two can be ensured.

In the stack samples 3 and 4, the deterioration rate was evaluated as "x", and the OCV reduction amount was evaluated as good "Δ". From these facts, in both the substrate layer and the active layer, when the zirconia tetragonal area ratio in the high temperature compatible portion is less than or equal to the zirconia tetragonal area ratio in the low temperature compatible portion, current concentration in a single cell occurs. However, it can be seen that the acceleration of deterioration of the fuel cell stack cannot be suppressed.

B. Modification example:
The technique disclosed in the present specification is not limited to the above-described embodiment, and can be transformed into various forms without departing from the gist thereof, and for example, the following modifications are also possible.

The configuration of the single cell 110, the power generation unit 102, or the fuel cell stack 100 in the above embodiment is merely an example and can be variously modified. For example, in the above embodiment, the number of single cells 110 included in the fuel cell stack 100 is only an example, and the number of single cells 110 is appropriately determined according to the output voltage and the like required for the fuel cell stack 100. The thickness of each member (layer) is just an example and can be deformed in various ways. For example, the thickness of the electrolyte layer 112 may be thicker than 10 μm.

Further, the material constituting each member in the above embodiment is merely an example, and each member may be composed of another material. For example, the fuel electrode 116 may contain zirconia, and zirconia includes not only YSZ but also CSZ and the like.

Further, in the above embodiment, the city gas is reformed to obtain a hydrogen-rich fuel gas FG, but the fuel gas FG may be obtained from other raw materials such as LP gas, kerosene, methanol, and gasoline. Pure hydrogen may be used as the fuel gas FG.

Further, in the above embodiment (or a modified example, the same applies hereinafter), all the single cells 110 included in the fuel cell stack 100 are configured to satisfy the first to third conditions. If at least one single cell 110 included in the stack 100 has such a configuration, it is possible to prevent the current density from becoming non-uniform due to the temperature difference in the single cell 110. Further, in the above embodiment, the single cell 110 may be configured not to satisfy at least one of the second to third conditions.

Further, the method for manufacturing the fuel cell stack 100 in the above embodiment is merely an example, and the fuel cell stack 100 may be manufactured by another manufacturing method.

Further, in the above embodiment, the SOFC that generates power by utilizing the electrochemical reaction between hydrogen contained in the fuel gas and oxygen contained in the oxidizing agent gas is targeted, but the present invention comprises an electrolysis reaction of water. It is also applicable to an electrolytic cell unit, which is the smallest unit of a solid oxide fuel cell (SOEC) that generates hydrogen by utilizing it, and an electrolytic cell stack having a plurality of electrolytic cell units. The configuration of the electrolytic cell stack is not described in detail here because it is known as described in, for example, Japanese Patent Application Laid-Open No. 2016-81813, but is generally the same as the fuel cell stack 100 in the above-described embodiment. It is a configuration. That is, the fuel cell stack 100 in the above-described embodiment may be read as an electrolytic cell stack, and the power generation unit 102 may be read as an electrolytic cell unit. However, during the operation of the electrolytic cell stack, a voltage is applied between both electrodes so that the air electrode 114 is positive (anode) and the fuel electrode 116 is negative (cathode), and the voltage is applied through the communication hole 108. Water vapor as a raw material gas is supplied. As a result, an electrolysis reaction of water occurs in each electrolytic cell unit, hydrogen gas is generated in the fuel chamber 176, and hydrogen is taken out of the electrolytic cell stack through the communication hole 108. Even in the electrolytic cell unit and the electrolytic cell stack having such a configuration, if the fuel electrode 116 has the configuration of the above embodiment as in the above embodiment, the current density is non-uniform due to the temperature difference in the single cell 110. Can be suppressed.

22: Bolt 24: Nut 26: Insulation sheet 27: Gas passage member 28: Main body 29: Branch 100: Fuel cell stack 102: Power generation unit 104, 106: End plate 108: Communication hole 110: Single cell 112: Electrolyte layer 114: Air pole 116: Fuel pole 120: Separator 121: Hole 124: Joint 130: Air pole side frame 131: Hole 132: Oxidizing agent gas supply communication hole 133: Oxidizing agent gas discharge communication hole 134: Air pole side current collection Body 135: Collector element 140: Fuel pole side frame 141: Hole 142: Fuel gas supply communication hole 143: Fuel gas discharge communication hole 144: Fuel pole side current collector 145: Electrode facing part 146: Interconnector facing part 147 : Connecting part 149: Spacer 150: Interconnector 161: Oxidizing agent gas introduction manifold 162: Oxidizing agent gas discharge manifold 166: Air chamber 171: Fuel gas introduction manifold 172: Fuel gas discharge manifold 176: Fuel chamber 310: Substrate layer 320: Active layer FG: Fuel gas FOG: Fuel off gas OG: Oxidating agent gas OOG: Oxidating agent off gas

Claims (3)

A plurality of electrochemical reaction single cells including an air electrode, a fuel electrode, and an electrolyte layer arranged between the air electrode and the fuel electrode in a first direction are provided, and the fuel electrode contains zirconia. Including, in the electrochemical reaction cell stack,
At least one of the plurality of electrochemical reaction single cells has a high temperature cell portion and a low temperature which are different in position in the first directional view and have different temperatures during the electrochemical reaction. There is a cell part,
The high temperature cell portion has a higher temperature during the electrochemical reaction than the low temperature cell portion.
In case of performing Raman analysis on the layer comprising zirconia, wavenumber 440 cm ^-1 or more, the integral value of the intensity in the range of 690 cm ^-1 or less as the first integrated value, the wave number is 185cm ^-1 or more, 380 cm ^{- When} the integral value of the intensity in the range of 1 or less is the second integral value,
A first, which is a ratio of the second integral value to the first integral value in the first fuel pole portion included in the high temperature cell portion among the fuel poles included in the at least one electrochemical reaction single cell. The ratio of is larger than the second ratio, which is the ratio of the second integrated value to the first integrated value in the second fuel electrode portion included in the low temperature cell portion.
It is characterized by an electrochemical reaction cell stack. In the electrochemical reaction cell stack according to claim 1,
The electrolyte layer contains zirconia and
The difference between the second ratio and the first ratio in the electrolyte layer is smaller than the difference between the second ratio and the first ratio in the fuel electrode.
It is characterized by an electrochemical reaction cell stack. In the electrochemical reaction cell stack according to claim 1 or 2.
The difference between the second ratio and the first ratio in the electrolyte layer is 0.02 or less.
It is characterized by an electrochemical reaction cell stack.

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