Double-perovskite type intermediate temperature solid oxide fuel cell anode material and preparation method
A fuel cell cathode, solid oxide technology, applied in battery electrodes, circuits, electrical components, etc., can solve the problem of high thermal expansion coefficient, and achieve the effects of low thermal expansion coefficient, high electronic conductivity and low cost
Patent Information
- Authority / Receiving Office
- CN · China
- Current Assignee / Owner
- Publication Date
- 2015-09-09
- Estimated Expiration
- Not applicable · inactive patent
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Abstract
Description
technical field
[0001] The invention relates to the technical field of solid oxide fuel cells, in particular to a cathode material of a medium-temperature solid oxide fuel cell with a double perovskite structure and a preparation method thereof. Background technique
[0002] A solid oxide fuel cell is an electrochemical power generation device that directly converts chemical energy into electrical energy. It consists of a cathode, an anode, and an electrolyte. As the cathode material of solid oxide fuel cells, the material is required to have high electronic conductivity and suitable ion conductivity in an oxidizing atmosphere, good thermal and chemical stability, and high catalytic activity for oxygen reduction. The traditional high temperature solid oxide fuel cell cathode material is doped LaMnO 3-δ , this cathode material exhibits high performance only at high temperatures (~1000°C), when the temperature drops below 800°C, doped LaMnO 3-δ The polarization resistance of...
Examples
Embodiment 1
[0032] Cathodic material Sr for intermediate temperature solid oxidation fuel cells with double perovskite structure prepared by wet chemical method 2 CoFeO 5+δ . The preparation method is as follows:
[0033] 1) Using analytically pure Sr(NO 3 ) 2 , Co(NO 3 ) 2 ·6H 2 O, Fe(NO 3 ) 3 9H 2 O is the raw material, and the required experimental raw materials are weighed according to the stoichiometric ratio.
[0034] 2) With anhydrous ethylene glycol and citric acid (the molar ratio of the two is 1: 1) as complexing agent, take the complexing agent whose molar number is 1~3 times of the sum of all metal cations in the sample, and step 1 The weighed experimental raw materials were dissolved in deionized water together.
[0035] 3) Place the beaker containing the solution in step 2 on a magnetic stirrer and heat and stir until a gel is formed.
[0036] 4) Dry the gel sample obtained in step 3 in an oven at a temperature of 150-300° C. for 2-5 hours to form a xerogel.
[...
Embodiment 2
[0042] The raw material Sr(NO in embodiment 1 3 ) 2 replaced by Ca(NO 3 ) 2 , the rest of the raw materials and complexing agent remain unchanged, and Ca 2 CoFeO 5+δ cathode material. Ca 2 CoFeO 5+δ with La 0.9 Sr 0.1 Ga 0.8 Mg 0.2 o 3-δ Electrolyte materials also have a good chemical match.
Embodiment 3
[0044] The raw material Sr(NO in embodiment 1 3 ) 2 Replaced by Ba(NO 3 ) 2 , the rest of the raw materials and complexing agent remain unchanged, and Ba 2 CoFeO 5+δ cathode material.