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Preparation method of catalyst, and application of catalyst in metal-air battery

A catalyst, solvothermal reaction technology, applied in chemical instruments and methods, heterogeneous catalyst chemical elements, physical/chemical process catalysts, etc., can solve the problem of poor crystal formation, reduced electrocatalytic performance, low specific surface area And other issues

Active Publication Date: 2019-08-20
NINGBO INST OF MATERIALS TECH & ENG CHINESE ACADEMY OF SCI
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  • Abstract
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  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Calcination at high temperature will lead to the growth of oxide catalyst particles, serious agglomeration, and low specific surface area; thereby reducing the exposure of active sites and greatly reducing the catalytic performance of electrocatalysis
It will also lead to poor phase formation of the crystal form, and even only simple oxide composite materials can be prepared

Method used

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  • Preparation method of catalyst, and application of catalyst in metal-air battery
  • Preparation method of catalyst, and application of catalyst in metal-air battery
  • Preparation method of catalyst, and application of catalyst in metal-air battery

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preparation example Construction

[0036] The invention provides a method for preparing a perovskite type composite oxygen reduction catalyst, comprising the following steps:

[0037] A) After mixing the cerium source compound, the acid-base buffer, the surfactant and the solvent, performing a solvothermal reaction under airtight conditions to obtain a reaction solution;

[0038] B) adding a lanthanum source compound, a manganese source compound and a compound containing M to the reaction solution to obtain a mixed solution, and after adjusting the pH value of the mixed solution, perform a hydrothermal reaction to obtain a catalyst precursor;

[0039] C) Calcining the catalyst precursor to obtain a perovskite composite oxygen reduction catalyst, the chemical formula of the perovskite composite oxygen reduction catalyst is La 1-x m x MnO 3 -CeO 2 , M is selected from Sr and / or Ca, 0≤x<1.0.

[0040] In the invention, firstly, the cerium source compound, the acid-base buffer, the surfactant and the solvent are...

Embodiment 1

[0080] First, according to CeO 2 The amount of cerium nitrate dissolved in ethylene glycol, control CeO 2 Solid content is 10%; Add appropriate tetrabutylammonium bromide surfactant in above-mentioned solution again, control surfactant concentration is 0.1mmol / L; And add a certain amount of urea, control urea / CeO 2 The molar ratio is 0.4, fully stirred and mixed evenly to prepare a mixed solution. The above mixed solution was transferred to a polytetrafluoroethylene-lined stainless steel reactor, and subjected to solvothermal reaction at a certain temperature of 180° C. for 6 hours; the above reactor was lowered to room temperature to obtain the intermediate product of the first step.

[0081] At room temperature, add according to La to the above-mentioned first step reactor 0.7 Sr 0.3 MnO 3 Aqueous solutions of lanthanum nitrate, strontium nitrate, manganese nitrate in stoichiometric ratio, control CeO 2 / La 0.7 Sr 0.3 MnO 3The ratio is 2 / 3; and a mixed solvent of eth...

Embodiment 2

[0085] First, according to CeO 2 The amount of cerium nitrate dissolved in ethylene glycol, control CeO 2 Solid content is 3%; Add appropriate tetrabutylammonium bromide surfactant in above-mentioned solution again, control surfactant concentration is 0.01mmol / L; And add a certain amount of urea, control urea / CeO 2 The molar ratio is 0.2, fully stirred and mixed evenly to prepare a mixed solution. The above mixed solution was transferred to a polytetrafluoroethylene-lined stainless steel reaction kettle, and solvothermal reaction was carried out at a certain temperature of 85°C for 2 hours; the above reaction kettle was lowered to room temperature to obtain the intermediate product of the first step.

[0086] At room temperature, add LaMnO 3 Aqueous solutions of lanthanum nitrate and manganese nitrate in stoichiometric ratio to control CeO 2 / LaMnO 3 Proportioning is 0.1; And form the mixed solvent of ethylene glycol and deionized water, control ethylene glycol / water ratio...

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Abstract

The invention provides a preparation method of a perovskite composite oxygen reduction catalyst. The nano-composite oxygen reduction catalyst La1-xMxMnO3-CeO2 is successfully prepared by an intermittent stepwise improved solvothermal / hydrothermal synthesis process, M is selected from Sr and / or Ca, and x is equal to or more than 0 and less than 1.0 nm. A CeO2 material rich in oxygen vacancies is used to carry out surface oxygen vacancy modification on an elemental M-doped LaMnO3-based oxygen reduction catalyst in order to greatly improve the intrinsic electrochemical catalytic performances of the composite material, and the composite material is applied to an aluminum-air battery. The composite catalyst material prepared by the method has the advantages of small primary particles, uniform dispersion and high specific surface area; and the preparation method is simple, and facilitates large-scale batch production.

Description

technical field [0001] The invention belongs to the technical field of batteries, and in particular relates to a preparation method of a catalyst and its application in metal-air batteries. Background technique [0002] Among the many types of oxygen reduction catalysts, perovskite oxygen reduction catalysts have been considered as one of the catalysts with great potential to replace the noble metal Pt / C. The electrocatalytic performance of perovskite-type oxygen reduction catalysts is mainly influenced by crystal structure, surface properties, oxidation state and oxygen vacancy defects. For LnMnO with comparable surface area 3 (Ln=La series or Y) series perovskite oxides, in the alkaline system, the order of catalytic activity for oxygen reduction is La>Pr>Nd>Sm>Gd>Y>Dy>Yb; its catalytic activity is related to ion The radius is directly related to the LaMnO 3 exhibited the highest intrinsic oxygen reduction catalytic activity. For LaMnO 3 For perov...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J23/34B01J35/00H01M4/90H01M12/06
CPCB01J23/002B01J23/34H01M4/9016H01M12/06B01J2523/00B01J35/33B01J2523/24B01J2523/3706B01J2523/3712B01J2523/72
Inventor 薛业建颜杉杉刘兆平
Owner NINGBO INST OF MATERIALS TECH & ENG CHINESE ACADEMY OF SCI