A kind of graphene-supported nitrogen-doped carbon nanotube composite material and its preparation and application
A technology of nitrogen-doped carbon and composite materials, applied in fuel cell half-cells and primary battery half-cells, structural parts, electrical components, etc., can solve problems such as poor cycle stability and achieve excellent catalytic performance , Improve the conductivity and stability, and the effect of high cycle stability
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[0043] The invention provides a method for preparing a graphene-loaded nitrogen-doped carbon nanotube composite material, which is characterized in that it includes the following steps:
[0044] (1) with graphene oxide solution, the organic solution of transition metal salt and the organic solution of organic ligand, mix and stir for several hours, solid-liquid separation obtains solid, it is the precursor of graphene oxide supported metal organic framework material; Described The organic solution of the organic ligand also includes a nucleation promoter, and the nucleation promoter is used to promote the crystallization, nucleation and uniform dispersion of the metal-organic framework material on the graphene oxide surface;
[0045] (2) annealing the precursor obtained in step (1) in a reducing atmosphere to convert transition metal ions in the precursor into metal nanoparticles, and catalyze the conversion of organic ligands into nitrogen-doped carbon nanotubes, Obtain the s...
Embodiment 1
[0090] Example 1: Preparation of ZIF-67@GO-4
[0091] First, 2 ml of graphene oxide was ultrasonically dispersed in 10 ml of methanol, and then 291 mg of Co(NO 3 ) 2 ·6H 2 O and 657 mg of 2-methylimidazole were dissolved in 20 ml of methanol. After adding 10 μl of triethylamine to the 2-methylimidazole solution, the Co(NO 3 ) 2 ·6H 2 O and the 2-methylimidazole solution containing triethylamine were poured into the GO solution in turn, magnetically stirred at room temperature for 3 h, centrifuged and dried, and the obtained product was redispersed into 10 ml of methanol solution, and Co(NO) was added again. 3 ) 2 ·6H 2 O and 2-methylimidazole solution containing triethylamine, magnetic stirring for 3 h, repeated four times to obtain the ZIF-67@GO-4 precursor. figure 1 (b) and figure 1 (c) is the scanning electron microscope image of ZIF-67@GO-4, it can be seen from the figure that ZIF-67 is evenly distributed on both sides of GO.
Embodiment 2
[0092] Example 2: Preparation of GNCNTs-4
[0093] The ZIF-67@GO-4 in Example 1 was placed in the tube furnace, and the H 2 / Ar mixture (H 2 The volume percentage of the mixture is 5%), heated to 700°C at a rate of 2°C / min, kept at this temperature for 3h, cooled naturally, placed in 0.5M H 2 SO 4 48h, centrifugal drying to obtain GNCNTs-4 material. figure 1 (d) is the scanning electron microscope photo of GNCNTs-4. It can be seen from the figure that the CNTs are distributed on both sides of the graphene in a layered and multi-level structure. figure 1 (e), figure 1 (f) and figure 1 (g) is the transmission electron micrograph of GNCNTs-4, showing the successful preparation of CNTs. figure 1 (h), figure 1 (i), figure 1 (j) andfigure 1 (k) is the mapping characterization map of GNCNTs-4, showing the presence of C, N, and Co.
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