Hollow-nanostructural Co2P@C composite material as well as preparation method and application thereof
A nanostructure and composite material technology, applied in the field of metal organic framework materials, nanomaterials, and nanocatalysis, can solve the problems that the OER performance of Co-based phosphides needs to be further improved.
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Embodiment 1
[0027] (1) Preparation of precursor Co-BTC
[0028] (a) Cobalt nitrate hexahydrate Co(NO 3 ) 2 ·6H 2 O (0.72mmol, 0.21g) was dissolved in the mixed solvent of 30ml ethylene glycol and 20ml ethanol, stirred until forming a red transparent solution;
[0029] (b) Add 0.2g of polyvinylpyrrolidone PVP to the solution obtained in (a), and stir until completely dissolved;
[0030] (c) Trimellitic acid H 3 BTC (0.34mmol, 0.07g) was added to the solution obtained in (b), ultrasonicated for 10 minutes, stirred evenly, put into the reaction kettle, kept at 150°C for 24h, and then naturally cooled to room temperature;
[0031] (d) Collect the product by centrifugation, wash the product three times with ethanol, and then dry it in a vacuum oven at 60°C for 12 hours to obtain the precursor Co-BTC;
[0032] (2) Preparation of Co with hollow nanostructure 2 P@C composite materials:
[0033] The Co-BTC material prepared by 0.1g step (1) and 1g sodium hypophosphite NaH 2 PO 2 Put them in...
Embodiment 2
[0037] (1) Preparation of precursor Co-BTC
[0038] (a) Cobalt nitrate hexahydrate Co(NO 3 ) 2 ·6H 2 O (0.72mmol, 0.21g) was dissolved in the mixed solvent of 30ml ethylene glycol and 20ml ethanol, stirred until forming a red transparent solution;
[0039] (b) Add 0.2g of polyvinylpyrrolidone PVP to the solution obtained in (a), and stir until completely dissolved;
[0040] (c) Trimellitic acid H 3 BTC (0.34mmol, 0.07g) was added to the solution obtained in (b), ultrasonicated for 10 minutes, stirred evenly, put into the reaction kettle, kept at 150°C for 24h, and then naturally cooled to room temperature;
[0041] (d) Collect the product by centrifugation, wash the product three times with ethanol, and then dry it in a vacuum oven at 60°C for 12 hours to obtain the precursor Co-BTC;
[0042] (2) Preparation of Co with hollow nanostructure 2 P@C composite materials:
[0043] The Co-BTC material prepared by 0.1g step (1) and 1g sodium hypophosphite NaH 2 PO 2 Put them ...
Embodiment 3
[0046] (1) Preparation of precursor Co-BTC
[0047] (a) Cobalt nitrate hexahydrate Co(NO 3 ) 2 ·6H 2 O (0.72mmol, 0.21g) was dissolved in the mixed solvent of 30ml ethylene glycol and 20ml ethanol, stirred until forming a red transparent solution;
[0048] (b) Add 0.2g of polyvinylpyrrolidone PVP to the solution obtained in (a), and stir until completely dissolved;
[0049] (c) Trimellitic acid H 3 BTC (0.34mmol, 0.07g) was added to the solution obtained in (b), ultrasonicated for 10 minutes, stirred evenly, put into the reaction kettle, kept at 150°C for 24h, and then naturally cooled to room temperature;
[0050] (d) Collect the product by centrifugation, wash the product three times with ethanol, and then dry it in a vacuum oven at 60°C for 12 hours to obtain the precursor Co-BTC;
[0051] (2) Preparation of Co with hollow nanostructure 2 P@C composite materials:
[0052] The Co-BTC material prepared by 0.1g step (1) and 1g sodium hypophosphite NaH 2 PO 2 Put them ...
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