Single-phase perovskite-based solid electrolyte, solid oxide fuel cell comprising same, and method for manufacturing same

Patent metadata

Field	Value
Publication number	US-2018198150-A1
Application number	US-201515506419-A
Country	US
Kind code	A1
Filing date	Jun 16, 2015
Priority date	Aug 28, 2014
Publication date	Jul 12, 2018
Grant date	—

Abstract

This invention relates to a single-phase perovskite-based solid electrolyte, a solid oxide fuel cell including the same, and a method of manufacturing the same. The method of the invention includes stirring and pulverizing a mixed oxide including lanthanum oxide (La 2 O 3 ), strontium carbonate (SrCO 3 ), gallium oxide (Ga 2 O 3 ) and magnesium oxide (MgO); and obtaining an LSGM powder by subjecting the pulverized mixed oxide to primary calcination at a first temperature and then secondary calcination at a second temperature that is higher than the first temperature.

First claim

1 . A method of manufacturing a single-phase perovskite-based solid electrolyte, comprising:
stirring and pulverizing a mixed oxide comprising lanthanum oxide (La 2 O 3 ), strontium carbonate (SrCO 3 ), gallium oxide (Ga 2 O 3 ) and magnesium oxide (MgO); and obtaining an LSGM powder by subjecting the pulverized mixed oxide to primary calcination at a first temperature and then to secondary calcination at a second temperature that is higher than the first temperature.

2 . The method of claim 1 , wherein the LSGM powder has a composition of La 0.8 Sr 0.2 Ga 0.8 Mg 0.2 O 3-δ (0≤δ≤0.2).

3 . The method of claim 1 , wherein the lanthanum oxide (La 2 O 3 ) has a purity of 99.99% or more, the strontium carbonate (SrCO 3 ) has a purity of 99.7% or more, the gallium oxide (Ga 2 O 3 ) has a purity of 99.0% or more, and the magnesium oxide (MgO) has a purity of 99.0% or more.

4 . The method of claim 1 , wherein the mixed oxide comprises 100 parts by weight of the lanthanum oxide (La 2 O 3 ), 15 to 30 parts by weight of the strontium carbonate (SrCO 3 ), 50 to 65 parts by weight of the gallium oxide (Ga 2 O 3 ), and 3 to 9 parts by weight of the magnesium oxide (MgO), which are mixed together.

5 . The method of claim 1 , wherein the stirring and pulverizing the mixed oxide further comprises:
subjecting the mixed oxide to planetary ball milling in a zirconia container containing zircon balls and then to pulverization using a mortar and pestle.

6 . The method of claim 1 , further comprising subjecting the mixed oxide to planetary ball milling and then to pulverization using a mortar and pestle, after the primary calcination and before the secondary calcination.

7 . The method of claim 1 , further comprising subjecting the mixed oxide to planetary ball milling and then to pulverization using a mortar and pestle, after the secondary calcination.

8 . The method of claim 1 , wherein the first temperature ranges from 900° C. to 1,200° C. and the second temperature ranges from 1,400° C. to 1,600° C.

9 . The method of claim 1 , wherein the lanthanum oxide (La 2 O 3 ) is thermally treated at 800° C. to 1,300° C. and maintained in an atmosphere that blocks a reaction with water in order to prevent conversion into La(OH) 3 .

10 . A method of manufacturing a solid oxide fuel cell, comprising:
preparing an anode diffusion layer slurry and an anode reaction layer slurry using NiO, GDC (Gadolinia-Doped Ceria) and a carbon material; preparing a buffer layer slurry using LDC (Lanthanum-Doped Ceria); preparing an electrolyte layer slurry using an LSGM powder obtained by the method of claim 1 ; subjecting the anode diffusion layer slurry, the anode reaction layer slurry, the buffer layer slurry and the electrolyte layer slurry to tape casting to form respective films, which are then sequentially stacked, thus obtaining an anode-supported electrolyte assembly; manufacturing an anode-supported electrolyte-sintered assembly by subjecting the anode-supported electrolyte assembly to primary calcination at a first temperature and then to secondary calcination at a second temperature higher than the first temperature; and applying a cathode slurry comprising LSCF (Lanthanum-Strontium-Cobalt-Ferrite Oxide) and the LSGM powder on the anode-supported electrolyte-sintered assembly and then performing sintering.

11 . The method of claim 10 , wherein the preparing the anode diffusion layer slurry and the anode reaction layer slurry further comprises:
mixing zircon balls, NiO, GDC, the carbon material, toluene, ethanol, and a dispersant in a container, thus obtaining a mixed solution; and mixing the mixed solution with a binder solution.

12 . The method of claim 11 , wherein the anode diffusion layer slurry comprises 100 parts by weight of NiO, 62 to 72 parts by weight of GDC, 10 to 47 parts by weight of the carbon material, 75 to 110 parts by weight of toluene, 50 to 70 parts by weight of ethanol, 3 to parts by weight of the dispersant, and 75 to 95 parts by weight of the binder solution.

13 . The method of claim 11 , wherein the anode reaction layer slurry comprises 100 parts by weight of NiO, 62 to 72 parts by weight of GDC, 0 to 30 parts by weight of the carbon material, 70 to 90 parts by weight of toluene, 45 to 65 parts by weight of ethanol, 2 to 6 parts by weight of the dispersant, and 60 to 95 parts by weight of the binder solution.

14 . The method of claim 10 , wherein the preparing the buffer layer slurry further comprises:
providing LDC, toluene, ethanol, a dispersant and a binder solution so as to comprise 100 parts by weight of LDC, 75 to 85 parts by weight of toluene, 15 to 25 parts by weight of ethanol, 0.5 to 1.5 parts by weight of the dispersant, and 45 to 55 parts by weight of the binder solution, and mixing zircon balls, LDC, toluene, ethanol and the dispersant in a container, thus obtaining a mixed solution; and mixing the mixed solution with the binder solution.

15 . The method of claim 10 , wherein the preparing the electrolyte layer slurry further comprises:
providing the LSGM powder, toluene, ethanol, a dispersant and a binder solution so as to comprise 100 parts by weight of the LSGM powder, 75 to 85 parts by weight of toluene, 15 to 25 parts by weight of ethanol, 0.5 to 1.5 parts by weight of the dispersant, and 45 to 55 parts by weight of the binder solution and mixing zircon balls, the LSGM powder, toluene, ethanol and the dispersant in a container, thus obtaining a mixed solution; and mixing the mixed solution with the binder solution.

16 . The method of claim 10 , wherein the cathode slurry comprises 100 parts by weight of LSCF, 95 to 105 parts by weight of LSGM, 76 to 90 parts by weight of terpineol, and 3 to 15 parts by weight of ethylene cellulose.

17 . A solid oxide fuel cell, comprising:
an anode diffusion layer comprising NiO, GDC (Gadolinia-Doped Ceria) and a carbon material; an anode reaction layer formed on the anode diffusion layer and comprising NiO, GDC and the carbon material; a buffer layer formed on the anode reaction layer and comprising LDC (Lanthanum-Doped Ceria); an electrolyte layer formed on the buffer layer and comprising an LSGM powder obtained by the method of claim 1 ; and a cathode formed on the electrolyte layer and comprising LSCF (Lanthanum-Strontium-Cobalt-Ferrite Oxide) and the LSGM powder.

Assignees

• Korea Inst Ind Tech

Inventors

• Kim Ho Sung
• Kim Kyeong Joon
• Choi Seung Woo
• Kim Min Young
• Kim Yu Sin

Classifications

• C01P2002/72

  by d-values or two theta-values, e.g. as X-ray diagram · CPC title

• C01P2006/80

  Compositional purity · CPC title

• C01P2002/34

  perovskite-type (ABO3) · CPC title

• C01P2006/40

  Electric properties · CPC title

• H01M8/1213 Primary

  characterised by the electrode/electrolyte combination or the supporting material · CPC title