Cobalt metaphosphate/nitrogen carbon oxygen reduction catalyst and preparation method and application thereof
A cobalt metaphosphate and catalyst technology, applied in structural parts, electrical components, battery electrodes, etc., can solve the problems of low initial potential and half-wave potential, and achieve a simple method, cheap and easily available raw materials, and promotion of electrocatalytic activity. Effect
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Embodiment 1
[0027] (1) Accurately weigh 582.10 mg Co(NO 3 ) 2 ·6H 2 The O solid was dissolved in 20 mL of methanol solution, then sonicated and magnetically stirred until a clear pink solution of cobalt nitrate in methanol was obtained.
[0028] (2) 2 mL of ATMP aqueous solution with a mass concentration of 50 wt.% was slowly added dropwise to the above cobalt nitrate methanol solution, reacted for 15 minutes to obtain a mixed solution, and then centrifuged, washed, and dried to obtain pink cobalt metaphosphate. Coordination polymer precursors.
[0029] (3) The cobalt metaphosphate coordination polymer precursor formed in step 2 was placed in a tube furnace, and calcined at 700 °C for 1 h under a protective gas atmosphere to obtain a cobalt metaphosphate / nitrogen carbon oxygen reduction catalyst.
[0030] figure 1 According to the X-ray diffraction pattern of the product obtained in Example 1 of the present invention, all X-ray powder diffraction peaks can be indexed as Co(PO 3 ) 2 ...
Embodiment 2
[0032] (1) Accurately weigh 1164.2 mg Co(NO 3 ) 2 ·6H 2 The O solid was dissolved in 20 mL of methanol solution, then sonicated and magnetically stirred until a clear pink solution of cobalt nitrate in methanol was obtained.
[0033] (2) 2 mL of ATMP aqueous solution with a mass concentration of 55 wt.% was slowly added dropwise to the above cobalt nitrate methanol solution, reacted for 30 minutes to obtain a mixed solution, and then centrifuged, washed, and dried to obtain pink cobalt metaphosphate. Coordination polymer precursors.
[0034] (3) The cobalt metaphosphate coordination polymer precursor formed in step 2 was placed in a tube furnace, and calcined at 800 °C for 1 h in a protective gas atmosphere to obtain a cobalt metaphosphate / nitrogen carbon oxygen reduction catalyst.
Embodiment 3
[0036](1) Accurately weigh 1746.18 mg Co(NO 3 ) 2 ·6H 2 The O solid was dissolved in 20 mL of methanol solution, then sonicated and magnetically stirred until a clear pink solution of cobalt nitrate in methanol was obtained.
[0037] (2) 2 mL of ATMP aqueous solution with a mass concentration of 60 wt.% was slowly added dropwise to the above cobalt nitrate methanol solution, reacted for 60 minutes to obtain a mixed solution, and then centrifuged, washed, and dried to obtain pink cobalt metaphosphate. Coordination polymer precursors.
[0038] (3) The cobalt metaphosphate coordination polymer precursor formed in step 2 was placed in a tube furnace, and calcined at 900 °C for 2 h under a protective gas atmosphere to obtain a cobalt metaphosphate / nitrogen carbon oxygen reduction catalyst.
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