Preparation method and application of iron-nitrogen-carbon catalyst
A carbon catalyst and catalyst technology, applied in structural parts, electrical components, battery electrodes, etc., can solve the problems of transition metal precursors and nitrogen sources without coordination structures, complex phase composition of catalysts, and difficulty in analyzing active centers, etc., to achieve Good stability and methanol poisoning resistance, excellent oxygen reduction catalytic performance, and simple preparation process
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Embodiment 1
[0033] Put 500 mg of pretreated commercial charcoal powder in a beaker, and add 200 mL of isopropanol to the beaker, and stir for 5 hours; then place 300 mg of iron phthalocyanine in another beaker, and add to this beaker 200 mL of tetrahydrofuran solution, stirred for 5 hours. The well-dispersed iron phthalocyanine solution was slowly added to the isopropanol solution dispersed with the carbon carrier, stirred ultrasonically rapidly for half an hour, and then the stirred mixture was stirred and dispersed at room temperature for 6 h. Then the obtained mixture solution was subjected to rotary evaporation at 40 °C until the solution was evaporated to dryness and the product was viscous. Afterwards, the viscous material was put into an oven at 80° C. and dried overnight to obtain an intermediate product for preparing the catalyst precursor.
[0034] The precursor obtained above was heat-treated at 400 °C with a heating rate of 2 °C min -1 , the holding time was 2 h, and the iro...
Embodiment 2
[0038] The operating conditions are the same as in Example 1, except that the added amount of iron phthalocyanine is 100 mg.
[0039] The iron-nitrogen-carbon oxygen reduction catalyst was thus prepared, and the half-wave potential of the oxygen reduction polarization curve was 0.88 V (vs. RHE), and the limiting diffusion current density was 5.19 mA cm -2 , the number of transferred electrons is 4.0, and it has good electrochemical stability and anti-methanol poisoning performance.
Embodiment 3
[0041] The operating conditions are the same as in Example 1, except that the amount of iron phthalocyanine added is 400 mg.
[0042] The iron-nitrogen-carbon oxygen reduction catalyst was thus prepared, and the half-wave potential of the oxygen reduction polarization curve was 0.85 V (vs. RHE), and the limiting diffusion current density was 5.83 mA cm -2 , the number of transferred electrons is 4.0, and it has good electrochemical stability and anti-methanol poisoning performance.
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