Crosslinked porous La1-xCaxCoO3 oxygen evolution reaction catalyst preparation method
A catalyst and oxygen precipitation technology, applied in the direction of metal/metal oxide/metal hydroxide catalyst, catalyst activation/preparation, physical/chemical process catalyst, etc., can solve problems such as low specific surface area, increased cost, and many additives , to achieve the effect of increasing the specific surface area, low cost, and improving the apparent activity
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[0029] A kind of cross-linked porous La of the present invention 1-x Ca x CoO 3 The preparation method of oxygen evolution reaction catalyst, the chemical formula of described catalyst is La 0.6 Ca 0.4 CoO 3 or La 0.5 Ca 0.5 CoO 3 , its preparation method comprises the following steps:
[0030] 1) Liquid preparation: Weigh soluble La(NO 3 ) 3 .6H 2 O or LaCl 3 , Ca(NO 3 ) 2 .4H 2 O or CaCl 2 and Co(NO 3 ) 2 .6H 2 O or CoCl 2 .6H 2 O dissolves in volume V 1 In distilled water, stir continuously with a magnetic stirrer to make metal precursor solution A, wherein the sum of the amount of soluble La salt and soluble Ca salt is equal to the amount of soluble Co salt, and the metal precursor solution The total concentration of metal ions in A is 0.5-1.0mol / L; weigh citric acid, pore-forming agent sucrose or glucose to a volume of V 2 in distilled water to make solution B; where V 1 :V 2 =3:2, the amount of substance of citric acid is equal to the sum of the a...
Embodiment 1
[0036] 1) Cross-linked porous perovskite La 0.6 Ca 0.4 CoO 3 Preparation of Catalyst for Oxygen Evolution Reaction
[0037] Accurately weigh 0.6mmol La(NO 3 ) 3 .6H 2 O, 0.4mmol Ca(NO 3 ) 2 .4H 2 O, 1mmol Co(NO 3 ) 2 .6H 2 O was dissolved in 30ml of distilled water and stirred on a magnetic stirrer for 15min; in addition, 2mmol of citric acid and 3mmol of sucrose were weighed and dissolved in 20ml of distilled water and stirred evenly to form solution B; Solution B was added dropwise to the metal cation nitrate mixed solution to form a sol solution; the sol solution was placed in a magnetic stirrer and stirred in a constant temperature water bath at a temperature of 80°C, and most of the water was evaporated to form a wet gel; then in an oven at 100°C Dry the dry gel; place the dry gel in a muffle furnace, and calcinate it in an air atmosphere at 650°C for 2 hours to obtain a cross-linked porous La 0.6 Ca 0.4 CoO 3 catalyst powder.
[0038] 2) Testing the cross-...
Embodiment 2
[0049] With reference to the preparation method and test method of the catalyst of Example 1, the difference is that the calcination temperature is 675 ° C, and the cross-linked porous La 0.6 Ca 0.4 CoO 3 catalyst powder.
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