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Carbon-resistant and sulfur poisoning-resistant solid-state oxide fuel cell positive electrode and preparation method thereof

A solid oxide and fuel cell technology, applied in battery electrodes, circuits, electrical components, etc., can solve the problems of cumbersome and repetitive impregnation methods, poor catalytic activity, and low electrocatalytic activity, and achieve excellent anti-carbon deposition and anti-sulfur poisoning , good structural stability, high electrocatalytic activity

Inactive Publication Date: 2019-07-26
CHANGSHU INSTITUTE OF TECHNOLOGY +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, the catalytic activity of Cu for fuel oxidation is worse than that of Ni, and CuO x With a low melting point (1326°C), it is difficult to prepare Cu-based anodes by oxide blending, sintering and reduction
Although copper-based anodes and cerium-based anodes have good anti-carbon deposition and anti-sulfur poisoning effects, they have low electrocatalytic activity or low electrical conductivity. Later studies found that introducing Cu and doped cerium oxide into the anode by impregnation method can Significantly improve the electrocatalytic activity and anti-carbon deposition and anti-sulfur poisoning performance of the electrode, but the impregnation method is cumbersome and the repeatability is not good, which is not conducive to large-scale production

Method used

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  • Carbon-resistant and sulfur poisoning-resistant solid-state oxide fuel cell positive electrode and preparation method thereof
  • Carbon-resistant and sulfur poisoning-resistant solid-state oxide fuel cell positive electrode and preparation method thereof
  • Carbon-resistant and sulfur poisoning-resistant solid-state oxide fuel cell positive electrode and preparation method thereof

Examples

Experimental program
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Effect test

Embodiment 1

[0026] Cerium nitrate, samarium nitrate and copper nitrate are dissolved in deionized water to form a 1.0M nitrate solution, wherein the molar ratio of cerium ions to samarium ions is 4:1, and the molar content of copper ions accounting for all metal ions is 10%. Glycine is then added to the nitrate solution, wherein the molar ratio of glycine to nitrate in the solution is 1:2. Stir well at room temperature, heat on an electric furnace, concentrate until spontaneous combustion to obtain a light brown powder. Then heat treatment at 700 ° C for 4 h to obtain light brown CSCO (copper samarium co-doped cerium oxide) powder, the scanning electron microscope picture of the powder section is figure 1 shown.

[0027] The obtained CSCO powder was ball-milled for 72 hours, and the ball-milling medium was alcohol, and then vacuum-dried at 60° C. for 24 hours. The ball-milled powder and polystyrene monodisperse microspheres with a particle size of 0.3 μm were ultrasonically mixed in an ...

Embodiment 2

[0031] Dissolve cerium nitrate, gadolinium nitrate and copper nitrate in deionized water to form a 1.0M nitrate solution, wherein the molar ratio of cerium ions to gadolinium ions is 4:1, and the molar content of copper ions in all metal ions is 10%. Glycine is then added to the nitrate solution, wherein the molar ratio of glycine to nitrate in the solution is 1:2. Stir well at room temperature, heat on an electric furnace, concentrate until spontaneous combustion to obtain a light brown powder. Then heat treatment at 800°C for 5h to obtain light brown CGCO (copper-gadolinium co-doped cerium oxide) powder.

[0032] The prepared CGCO powder was ball-milled for 72 hours, and the ball-milling medium was alcohol, and then vacuum-dried at 50°C for 48 hours. The vacuum-dried powder and ethyl cellulose were ultrasonically mixed in alcohol medium at a mass ratio of 9:1 for 6 hours, and then vacuum-dried at 50°C for 48 hours. Put 0.6g of the obtained powder into a stainless steel mold ...

Embodiment 3

[0035] Cerium nitrate, samarium nitrate and copper nitrate are dissolved in deionized water to form a 0.5M nitrate solution, wherein the molar ratio of cerium ions to samarium ions is 4:1, and the molar content of copper ions accounting for all metal ions is 5%. Then stearic acid is added to the nitrate solution, wherein the molar ratio of stearic acid to nitrate in the solution is 2:1. Stir well at room temperature, heat on an electric furnace, concentrate until spontaneous combustion to obtain a light brown powder. Then heat treatment at 500 °C for 8 h to obtain light brown CSCO powder.

[0036] The obtained CSCO powder was ball-milled for 96 hours, the ball-milling medium was acetone, and then vacuum-dried at 70° C. for 12 hours. The milled powder and polystyrene monodisperse microspheres with a particle size of 0.3 μm were ultrasonically mixed in an acetone medium at a mass ratio of 6:1 for 1 h, and then vacuum-dried at 70° C. for 24 h. Put 0.45g of the powder obtained b...

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Abstract

The invention discloses a carbon-resistant and sulfur poisoning-resistant solid-state oxide fuel cell positive electrode and a preparation method thereof. Copper and samarium co-doped cerium oxide orcopper gadolinium co-doped cerium oxide powder is prepared by preparation of copper ions and samarium or gadolinium doped cerium oxide-based oxide, doped cerium oxide powder is used as precursor powder to prepare porous ceramic, a part of copper is permeated from lattices to obtain the carbon-resistant and sulfur poisoning-resistant solid-state oxide fuel cell positive electrode after hydrogen reduction on the porous ceramic. The conductivity of the positive electrode is improved, the three-phase reaction interface of the positive electrode is added, the carbon-resistant and sulfur poisoning-resistant solid-state oxide fuel cell positive electrode has favorable structure stability and excellent carbon-resistant and sulfur poisoning-resistant performance, and agglomeration can be prevented.According to the preparation method, copper is introduced to the positive electrode by ion doping and desolvation effect, a positive electrode-supported solid-state oxide fuel cell can be directly prepared by a traditional pressing or curtain coating and sintering method, the complicated process of the copper-containing positive electrode prepared by an impregnation reduction method is prevented,and the industrialization implementation becomes probable.

Description

technical field [0001] The invention relates to a fuel cell anode and a preparation method thereof, in particular to an anti-carbon deposition and anti-sulfur poisoning solid oxide fuel cell anode and a preparation method thereof. Background technique [0002] Fuel cell technology can directly convert the chemical energy of the fuel into electrical energy through the electrochemical reaction process, which can greatly reduce pollution, and because it is not limited by the Carnot cycle, its energy utilization rate can reach 40% to 60%. At the same time, by utilizing its thermal energy, the conversion rate of energy can be as high as more than 80%. These advantages make fuel cell technology very likely to become an important means of power supply in the near future. The final product of fuel cells using hydrogen as the optimal fuel is water, which has little pollution to the environment. However, there are many problems to be solved in the acquisition, storage and transporta...

Claims

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Application Information

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IPC IPC(8): H01M4/88H01M4/90
CPCH01M4/88H01M4/8875H01M4/8885H01M4/9016H01M4/9041Y02E60/50
Inventor 王志成张波陈鹏刘冠鹏苏建刚杨沛霖陶石张惠国钱斌冯金福
Owner CHANGSHU INSTITUTE OF TECHNOLOGY
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