JP5841210B1 - Fuel cell - Google Patents

Abstract

A fuel cell and an air electrode material capable of improving an initial output are provided. In a fuel cell, an air electrode is represented by a general formula ABO3, and a main phase mainly composed of a perovskite oxide containing at least Sr at an A site, strontium sulfate and strontium chromate as main components. And a second phase as a component. The area occupation ratio of the second phase in the cross section of the air electrode 14 is 10.2% or less. [Selection] Figure 1

Description

  The present invention relates to a solid oxide fuel cell.

In recent years, attention has been focused on fuel cells from the viewpoint of environmental problems and effective use of energy resources. The fuel cell includes a fuel cell and an interconnector. A fuel cell generally has a fuel electrode, an air electrode, and a solid electrolyte layer disposed between the fuel electrode and the air electrode. The air electrode is composed of a perovskite oxide such as LSCF ((La, Sr) (Co, Fe) O ₃ ), LSF ((La, Sr) FeO ₃ ), LSC ((La, Sr) CoO ₃ ), for example. (See, for example, Patent Document 1).

JP 2006-32132 A

  However, in a fuel cell including an air electrode made of the above material, there is a problem that the initial output is likely to decrease. The present inventors have newly found that one of the causes of the decrease in the initial output is due to an inactive region generated inside the air electrode.

  The present invention is based on such new knowledge, and an object of the present invention is to provide a fuel cell that can improve the initial output.

The fuel cell according to the present invention includes a fuel electrode, an air electrode, and a solid electrolyte layer disposed between the fuel electrode and the air electrode. The air electrode includes a main phase and a second phase. The main phase is represented by the general formula ABO ₃ and contains a perovskite oxide containing at least Sr at the A site as a main component. The second phase is mainly composed of strontium sulfate and strontium chromate. The area occupation ratio of the second phase in the cross section of the air electrode is 10.2% or less.

  ADVANTAGE OF THE INVENTION According to this invention, the fuel cell and air electrode material which can improve an initial stage output are provided.

Sectional view showing the configuration of the fuel cell

  Next, embodiments of the present invention will be described with reference to the drawings. In the following description of the drawings, the same or similar parts are denoted by the same or similar reference numerals. However, the drawings are schematic, and the ratio of each dimension may be different from the actual one. Accordingly, specific dimensions and the like should be determined in consideration of the following description. Moreover, it is a matter of course that portions having different dimensional relationships and ratios are included between the drawings.

  In the following embodiments, a vertical stripe solid oxide fuel cell (SOFC) will be described as an example of the fuel cell.

(Configuration of fuel cell 10)
The configuration of the fuel cell (hereinafter abbreviated as “cell”) 10 will be described with reference to the drawings. FIG. 1 is a cross-sectional view showing the configuration of the cell 10.

  The cell 10 is a thin plate body made of a ceramic material. The thickness of the cell 10 is, for example, 300 μm to 3 mm, and the diameter of the cell 10 is, for example, 5 mm to 50 mm. A fuel cell can be formed by connecting a plurality of cells 10 in series by an interconnector.

  The cell 10 includes a fuel electrode 11, a solid electrolyte layer 12, a barrier layer 13, and an air electrode 14.

  The fuel electrode 11 functions as an anode of the cell 10. As illustrated in FIG. 1, the fuel electrode 11 includes a fuel electrode current collecting layer 111 and a fuel electrode active layer 112.

The anode current collecting layer 111 is a porous plate-like fired body containing a transition metal and an oxygen ion conductive material. The anode current collecting layer 111 may include, for example, nickel oxide (NiO) and / or nickel (Ni) and yttria-stabilized zirconia (8YSZ, 10YSZ, etc.). The thickness of the anode current collecting layer 111 can be set to 0.2 mm to 5.0 mm. The thickness of the anode current collecting layer 111 may be the thickest among the constituent members of the cell 10 when the anode current collecting layer 111 functions as a support substrate. In the anode current collecting layer 111, the volume ratio of Ni and / or NiO can be 35 to 65% by volume in terms of Ni, and the volume ratio of YSZ can be 35 to 65% by volume. The anode current collecting layer 111 may include yttria (Y ₂ O ₃ ) instead of YSZ.

  The anode active layer 112 is disposed between the anode current collecting layer 111 and the solid electrolyte layer 12. The anode active layer 112 is a porous plate-like fired body containing a transition metal and an oxygen ion conductive material. The anode active layer 112 may contain NiO and / or Ni and yttria-stabilized zirconia, like the anode current collecting layer 111. The thickness of the anode active layer 112 can be 5.0 μm to 30 μm. In the anode active layer 112, the volume ratio of Ni and / or NiO can be 25 to 50% by volume in terms of Ni, and the volume ratio of YSZ can be 50 to 75% by volume. Thus, the anode active layer 112 may have a higher YSZ content than the anode current collecting layer 111. The anode active layer 112 may contain a zirconia-based material such as scandia-stabilized zirconia (ScSZ) instead of YSZ.

The solid electrolyte layer 12 is disposed between the fuel electrode 11 and the barrier layer 13. The solid electrolyte layer 12 is a dense plate-like fired body. The solid electrolyte layer 12 has a function of transmitting oxygen ions generated at the air electrode 14. The solid electrolyte layer 12 contains zirconium (Zr). The solid electrolyte layer 12 may contain Zr as zirconia (ZrO ₂ ). The solid electrolyte layer 12 may contain ZrO ₂ as a main component.

The solid electrolyte layer 12 may contain additives such as Y ₂ O ₃ and / or Sc ₂ O ₃ in addition to ZrO ₂ . These additives function as stabilizers. In the solid electrolyte layer 12, mol compositional ratio of ZrO ₂ stabilizer (stabilizer: ZrO ₂₎ is 3: 97 to 20: can be set to about 80. That is, examples of the material for the solid electrolyte layer 12 include yttria-stabilized zirconia such as 3YSZ, 8YSZ, and 10YSZ, and zirconia-based materials such as ScSZ. The thickness of the solid electrolyte layer 12 can be 3 μm to 30 μm.

The barrier layer 13 is disposed between the solid electrolyte layer 12 and the air electrode 14. The barrier layer 13 is a dense plate-like fired body. The barrier layer 13 has a function of suppressing the formation of a high resistance layer between the solid electrolyte layer 12 and the air electrode 14. Examples of the material of the barrier layer 13 include cerium (Ce) and a ceria-based material containing a rare earth metal oxide dissolved in Ce. Specifically, examples of the ceria-based material include GDC ((Ce, Gd) O ₂ : Gadolinium doped ceria), SDC ((Ce, Sm) O ₂ : samarium doped ceria) and the like. The thickness of the barrier layer 13 can be 3 μm to 20 μm.

  The air electrode 14 is disposed on the barrier layer 13. The air electrode 14 functions as a cathode of the cell 10. The thickness of the air electrode 14 can be 10 μm to 100 μm. The air electrode 14 is a porous body, and the porosity of the air electrode 14 can be set to 25% to 50%.

The air electrode 14 is represented by the general formula ABO ₃ and includes a main phase mainly composed of a perovskite oxide containing Sr at the A site. Such a perovskite oxide includes a perovskite complex oxide containing lanthanum and a perovskite complex oxide not containing lanthanum. Examples of the perovskite complex oxide containing lanthanum include LSCF (lanthanum strontium cobalt ferrite: (La, Sr) (Co, Fe) O ₃ ), LSF (lanthanum strontium ferrite: (La, Sr) FeO ₃ ), And LSC (lanthanum strontium cobaltite: (La, Sr) CoO ₃ ) and the like. Examples of the perovskite complex oxide not containing lanthanum include SSC (Samarium Strontium Cobaltite: (Sm, Sr) CoO ₃ ). The density of the main phase ^can be ^{5.5g / cm 3 ~8.5g / cm 3} . In the present embodiment, “A contains B as a main component” means that 70% or more of A is composed of B.

The air electrode 14 includes a second phase mainly composed of strontium sulfate (SrSO ₄ ) and strontium chromate (SrCrO ₄ ). In the second phase, constituent elements of the main phase (for example, La and Co) may be dissolved. The second phase may contain impurities other than SrSO ₄ and SrCrO ₄ . The density of the second phase may be smaller than the density of the main phase. For example, the density of the second phase ^can be ^{3.2g / cm 3 ~5.2g / cm 3} .

  The area occupation ratio of the second phase in the cross section of the air electrode 14 is 10.2% or less. Thereby, since the inactive area | region which generate | occur | produces inside the air electrode 14 is reduced, it can suppress that an initial stage output falls. Furthermore, since the reaction between the second phase and the main phase during energization can be suppressed, it is possible to suppress the deterioration of the air electrode 14 from proceeding.

  In the present embodiment, the “area occupation ratio of the object X in the cross section of the air electrode 14” means the entire region excluding the pores included in the air electrode 14 (that is, the solid phase of the air electrode 14). The ratio of the total area of the object X to the area shall be said.

The area occupation ratio of the second phase in the cross section of the air electrode 14 is preferably 0.2% or more, and more preferably 0.36% or more. Thereby, since the second phase mainly composed of SrSO ₄ and SrCrO ₄ functions as a sintering aid, the skeleton of the air electrode 14 having a porous structure can be strengthened. As a result, the occurrence of cracks in the air electrode 14 during energization can be suppressed, so that the durability of the air electrode 14 can be improved.

  The average equivalent circle diameter of the constituent particles of the second phase in the cross section of the air electrode 14 is preferably 0.05 μm or more and 2.5 μm or less. Thereby, the durability of the air electrode 14 can be further improved. The average equivalent circle diameter is an arithmetic average value of the diameters of circles having the same area as the particles constituting the second phase.

(Calculation method of area occupancy)
Next, a method for calculating the area occupation ratio of the second phase in the cross section of the air electrode 14 will be described.

(1) FE-SEM image First, the cross section of the air electrode 14 magnified by a magnification of 10000 times by a FE-SEM (Field Emission Scanning Electron Microscope) using an in-lens secondary electron detector. To get. Specifically, the FE-SEM image can be obtained by FE-SEM (model: ULTRA55) manufactured by Zeiss (Germany) set to acceleration voltage: 1 kV and working distance: 2 mm. The cross section of the air electrode 14 is preferably preliminarily subjected to ion milling processing by IM4000 of Hitachi High-Technologies Corporation after the precision mechanical polishing.

In the FE-SEM image, the main phase (LSCF) and the second phase (SrSO ₄ and SrCrO ₄ ) are different in the brightness difference between the pores, the main phase is “gray white”, the second phase is “gray”, and the pores are “ “Black”. Such ternarization by light and dark difference can be realized by classifying the luminance of an image into 256 gradations.

  However, the method of discriminating the main phase, the second phase, and the pores is not limited to using the light / dark difference in the FE-SEM image. For example, after obtaining element mapping of the same field of view by SEM-EDS (Scanning Electron Microscope Energy Dispersive X-ray Spectrometry), each particle in the image is identified by comparing with the FE-SEM image. The second phase and the pores can be ternized with high accuracy.

(2) Analysis of FE-SEM Image Next, the FE-SEM image is subjected to image analysis using image analysis software HALCON manufactured by MVTec (Germany). In the analysis image, the second phase can be specified by a predetermined method (for example, a method surrounded by a line).

(3) Calculation of area occupation ratio Next, the total area of the second phase specified in the analysis image is calculated.

  Next, the ratio of the total area of the second phase to the total area of the region excluding the pores (that is, the solid phase of the air electrode 14) is calculated. The ratio of the total area of the second phase calculated in this way is the area occupation ratio of the second phase.

  In addition, the area occupation rate of the main phase can also be calculated by using the above method.

(Air electrode material)
The air electrode material constituting the air electrode 14 is preferably a mixed material of perovskite oxide powder, SrSO ₄ powder, and SrCrO ₄ powder represented by the general formula ABO ₃ and containing Sr at the A site. Examples of the perovskite complex oxide containing Sr at the A site include LSCF, LSF, LSC, and SSC as described above.

The addition amount of SrSO ₄ powder and SrCrO ₄ powder in the air electrode material is preferably 11.7% by weight or less. Thereby, the area occupation ratio of the second phase in the cross section of the air electrode 14 can be controlled to 10.2% or less. Further, the addition amount of SrSO ₄ powder and SrCrO ₄ powder in the air electrode material is more preferably 0.05% by weight or more. Thereby, the area occupation ratio of the second phase in the cross section of the air electrode 14 can be controlled to 0.2% or more.

Moreover, the density of the second phase in the air electrode 14 can be made smaller than the density of the main phase by making the average density of the SrSO ₄ powder and the SrCrO ₄ powder smaller than the density of the perovskite oxide powder.

Further, by adjusting the particle sizes of the SrSO ₄ powder and the SrCrO ₄ powder, the average equivalent circle diameter of the constituent particles of the second phase in the air electrode 14 and the area occupation ratio of the second phase can be adjusted. By adjusting the particle size of the SrSO ₄ powder and the SrCrO ₄ powder using an airflow classifier, precise classification including an upper limit value and a lower limit value is possible.

(Manufacturing method of cell 10)
Next, an example of a method for manufacturing the cell 10 will be described. However, various conditions such as the material, particle size, temperature, and coating method described below can be changed as appropriate. Hereinafter, the “molded body” refers to a member before firing.

  First, a slurry is prepared by adding polyvinyl alcohol (PVA) as a binder to a mixture of NiO powder, YSZ powder, and a pore-forming agent (for example, PMMA (polymethyl methacrylate resin)). Next, this slurry is dried and granulated with a spray dryer to obtain a fuel electrode current collecting layer powder. Next, a molded body of the fuel electrode current collecting layer 111 is formed by molding the fuel electrode powder by a die press molding method.

  Next, polyvinyl alcohol is added to a mixture of NiO powder, YSZ powder, and a pore-forming agent to prepare a slurry. Next, this slurry is printed on the molded body of the anode current collecting layer 111 by a printing method to form a molded body of the anode active layer 112.

  Next, a slurry is prepared by mixing the YSZ powder with a mixture of water and a binder in a ball mill for 24 hours. Next, this slurry is applied onto the molded body of the fuel electrode active layer 112 and dried to form a molded body of the solid electrolyte layer 12. However, a tape lamination method, a printing method, or the like can be used instead of the coating method.

  Next, a slurry is prepared by mixing a mixture of water and a binder with the GDC powder in a ball mill for 24 hours. Next, the slurry is applied on the solid electrolyte layer 12 compact and then dried to form the barrier layer 13 compact. However, a tape lamination method, a printing method, or the like can be used instead of the coating method.

  As a result, a laminate of the molded bodies of the fuel electrode 11, the solid electrolyte layer 12, and the barrier layer 13 is completed.

  Next, a co-fired body of the porous fuel electrode 11, the dense solid electrolyte layer 12 and the barrier layer 13 is formed by co-sintering the laminate of the molded bodies at 1300 to 1600 ° C. for 2 to 20 hours. .

  Next, a slurry is prepared by mixing the air electrode material, water, and binder described above with a ball mill for 24 hours. Next, this slurry is applied onto the co-fired barrier layer 13 and then dried to form a molded body of the air electrode 14. And the air electrode 14 is formed by baking the molded object of the air electrode 14 for 1 hour-20 hours with an electric furnace (oxygen-containing atmosphere, 900 degreeC-1100 degreeC).

(Other embodiments)
The present invention is not limited to the embodiment described above, and various modifications or changes can be made without departing from the scope of the present invention.

  (A) In the above embodiment, the cell 10 includes the fuel electrode 11, the solid electrolyte layer 12, the barrier layer 13, and the air electrode 14. However, the present invention is not limited to this. The cell 10 only needs to include the fuel electrode 11, the solid electrolyte layer 12, and the air electrode 14, and other layers may be interposed between the layers. Specifically, a porous barrier layer may be interposed between the barrier layer 13 and the air electrode 14.

  (B) Although the vertical stripe-shaped cell 10 has been described in the above embodiment, the cell 10 may be a fuel electrode support type, a flat plate shape, a cylindrical shape, a horizontal stripe shape, or the like. Note that the cell 10 may have an elliptical cross section.

  Examples of the fuel battery cell according to the present invention will be described below, but the present invention is not limited to the examples described below.

[Sample No. 1-No. 20 production]
In the following manner, the sample No. of the fuel electrode support type cell having the fuel electrode current collecting layer as the support substrate was used. 1-No. 20 was produced.

  First, a fuel electrode current collecting layer (NiO: 8YSZ = 50: 50 (Ni volume% conversion)) having a thickness of 500 μm is formed by a die press molding method, and a fuel electrode active layer (NiO: 8YSZ = 20 μm thickness) is formed thereon. 45:55 (Ni volume% conversion)) was formed by a printing method.

  Next, an 8YSZ electrolyte having a thickness of 5 μm and a GDC barrier film having a thickness of 5 μm were sequentially formed on the fuel electrode active layer to prepare a laminate.

  Next, the laminate was co-sintered at 1400 ° C. for 2 hours to obtain a co-fired body.

Next, a slurry was prepared by mixing the air electrode material shown in Table 1, water, and a binder with a ball mill for 24 hours. And after apply | coating this slurry on a barrier film | membrane, it baked at 1000 degreeC for 2 hours, and produced the 30-micrometer-thick air electrode. As shown in Table 1, LSCF, LSF, and SSC were used as the main components of the air electrode material, and different amounts of SrSO ₄ powder and SrCrO ₄ powder were added for each sample.

[Measurement of area occupancy]
First, the air electrode of each sample was subjected to precision mechanical polishing, and then subjected to ion milling using IM4000 manufactured by Hitachi High-Technologies Corporation.

  Next, the FE-SEM image which shows the cross section of the air electrode expanded by 10,000 times by FE-SEM using the in-lens secondary electron detector was acquired.

  Next, the analysis image was acquired by analyzing the FE-SEM image of each sample with image analysis software HALCON manufactured by MVTec (Germany).

Next, the area occupation ratio of the second phase containing SrSO ₄ and SrCrO ₄ was calculated using the analysis image. The calculation results of the area occupancy ratio of the second phase are as shown in Table 1.

[Component analysis of the second phase]
Next, component analysis of the second phase was performed, and it was confirmed that the main components of the second phase were SrSO ₄ and SrCrO ₄ .

  First, a TEM image of an air electrode cross section was obtained by TEM (Transmission Electron Microscope). And the position of the 2nd phase was confirmed with reference to the TEM image.

  Next, by EDX (Energy Dispersive X-ray Spectroscopy: Energy Dispersive X-ray Spectroscopy), the EDX spectrum in the first region on the second phase confirmed by the TEM image and the second region on the second phase ( An EDX spectrum in a region away from the first region was acquired. By semi-quantitatively analyzing these EDX spectra, constituent materials of the second phase can be inferred. Characteristic X-rays of Sr, S, O, and Cu were detected in the EDX spectrum in the first region, and characteristic X-rays of Sr, Cr, O, and Cu were detected in the EDX spectrum in the second region. The characteristic X-ray of Cu was detected because the component of the sample holder of the analyzer was detected and not a constituent material of the second phase.

Next, the crystal structure (lattice constant, lattice type, crystal orientation) of the constituent particles of the second phase was analyzed by SAED (Selected Area Electron Diffraction). By analyzing the lattice constant, lattice type, and crystal orientation based on the SAED image, it was confirmed that the second phase was mainly composed of SrSO ₄ and SrCrO ₄ .

[Confirmation of microcracks in air electrode after firing]
At the time when each sample was completed by firing the air electrode, the presence or absence of microcracks was observed by observing the cross section of the air electrode with an electron microscope. The observation results are summarized in Table 1.

[Confirmation of microcracks in air electrode after performance evaluation test and durability test]
About each sample, it heated up to 750 degreeC, supplying nitrogen gas to the fuel electrode side, and air to the air electrode side, and when 750 degreeC was reached, reduction processing was performed for 3 hours, supplying hydrogen gas to a fuel electrode. . For each sample, the output density (initial output) at a rated current density of 0.2 A / cm ² at a temperature of 750 ° C. was measured. The measurement results are summarized in Table 1.

  Next, the voltage drop rate per 1000 hours was measured as the deterioration rate. The measurement results are summarized in Table 1.

  Subsequently, the presence or absence of cracks was observed by observing the cross section of the air electrode with an electron microscope after 1000 hours had elapsed. The observation results are summarized in Table 1.

表１に示すように、空気極断面における第二相（ＳｒＳＯ_４及びＳｒＣｒＯ_４）の面積占有率が１０．２％以下に抑えたサンプルでは、初期出力を０．１５Ｗ／ｃｍ^２以上に向上させることができた。これは、空気極内部の不活性領域を低減することができたためである。

As shown in Table 1, in the sample in which the area occupancy of the second phase (SrSO ₄ and SrCrO ₄ ) in the air electrode cross section is suppressed to 10.2% or less, the initial output is improved to 0.15 W / cm ² or more. I was able to. This is because the inactive area inside the air electrode could be reduced.

Moreover, as shown in Table 1, in the sample in which the area occupation ratio of the second phase in the air electrode cross section was 0.20% or more, generation of microcracks after firing could be suppressed. This is because the added SrSO ₄ and SrCrO ₄ improve the sinterability of the air electrode and strengthen the skeleton of the porous structure.

Moreover, as shown in Table 1, in the sample in which the area occupancy of the second phase in the air electrode cross section was 0.36% or more, generation of microcracks could be suppressed even after the durability test. This is because the SrSO ₄ and SrCrO ₄ that is added is improved sinterability of the air electrode further because the skeleton of the porous structure has been strengthened.

  Further, as shown in Table 1, the deterioration rate could be suppressed to 1.5% or less in the sample having the average equivalent circle diameter of the particles constituting the second phase of 0.05 μm or more and 2.5 μm or less.

DESCRIPTION OF SYMBOLS 10 Fuel cell 11 Fuel electrode 111 Fuel electrode current collection layer 112 Fuel electrode active layer 12 Solid electrolyte layer 13 Barrier layer 14 Air electrode

Claims (6)

An anode,
An air electrode that is represented by the general formula ABO ₃ and includes a main phase mainly composed of a perovskite oxide containing at least Sr at the A site, and a second phase mainly composed of strontium sulfate and strontium chromate;
A solid electrolyte layer disposed between the fuel electrode and the air electrode;
With
The area occupancy of the second phase in the cross section of the air electrode is 10.2% or less.
Fuel cell. The area occupancy of the second phase is 0.20% or more.
The fuel battery cell according to claim 1. The area occupancy of the second phase is 0.36% or more.
The fuel battery cell according to claim 1. The average equivalent circle diameter of the second phase in the cross section is 0.05 μm or more and 2.5 μm or less.
The fuel cell according to any one of claims 1 to 3. The density of the second phase is smaller than the density of the main phase,
The fuel cell according to any one of claims 1 to 4. The perovskite oxide is LSCF.
The fuel cell according to any one of claims 1 to 5.

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