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Production of graphene-based composite nanostructures obtained by growing ZnO nanorods or microrods on suspended unsupported graphene nanosheets

A technology of graphene nanosheets and zinc oxide nanorods, applied in the direction of zinc oxide/zinc hydroxide, etc., can solve the problems of lengthy and problematic implementation

Active Publication Date: 2021-04-13
UNIV DEGLI STUDI DI ROMA LA SAPIENZA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The different production steps also include a large number of processes, which makes their implementation lengthy and problematic

Method used

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  • Production of graphene-based composite nanostructures obtained by growing ZnO nanorods or microrods on suspended unsupported graphene nanosheets
  • Production of graphene-based composite nanostructures obtained by growing ZnO nanorods or microrods on suspended unsupported graphene nanosheets
  • Production of graphene-based composite nanostructures obtained by growing ZnO nanorods or microrods on suspended unsupported graphene nanosheets

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0080] The preparation of embodiment 1-GNP

[0081] GNPs were produced using graphite intercalation compounds (GICs) as precursors according to methods similar to those reported in [13–15]. Briefly, the GIC was thermally expanded at 1150 °C for 5 s in a muffle furnace. Then 20 mg of expanded graphite was immersed in ethanol (instead of acetone or acetone-DMF mixture or acetone-NMP mixture as described in [13-15]) and pulsed through the probe for a total time between 15 and 30 minutes. The needle was sonicated for exfoliation in the liquid phase, the oscillation amplitude of the probe was fixed at 70% and the temperature of the suspension was controlled at 15 °C by using a recirculating bath connected to a thermal cryostat. Sonication produces a colloidal suspension of GNPs with a lateral dimension of 1 μm to 5 μm and a thickness of 1 nm to 20 nm. The solvent was then removed by centrifugation.

Embodiment 2

[0082] Example 2 - Deposition of a seed layer on GNPs by magnetic stirring

[0083] The solution for deposition was prepared by dissolving zinc acetate dihydrate (concentration between 0.001 M and 0.010 M) in isopropanol with magnetic stirring at 400-600 rpm for 20 to 60 minutes. Before depositing the seed layer, the GNPs obtained in the previous step were rinsed with isopropanol and the solvent was removed by centrifugation. The GNPs were then dispersed in the solution by vigorous stirring in a centrifuge tube to form a seed layer. The suspension was then transferred to a glass beaker and magnetically stirred at 250 rpm for 30 min to obtain a uniform coating of the GNPs by the seed layer. The suspension was then further centrifuged (3095 g, 30 minutes) to remove the seed layer growth solution. The obtained precipitate was then heat-treated in a muffle furnace at a temperature of 200° C. to 400° C. for a period of 10 minutes to 60 minutes to obtain GNPs coated with ZnO nanop...

Embodiment 3

[0085] Example 3 - Deposition of a seed layer on GNPs by probe sonication

[0086] The solution used to deposit the seed layer was obtained as described in Example 2. Suspensions of GNPs were prepared as described in Example 2. The suspension was then transferred to a glass beaker and sonicated by an ultrasonic probe for a period of 5 min to 30 min, fixing the probe oscillation amplitude between 20% and 80% of the maximum value. The suspension was then further centrifuged (3095 g, 30 minutes) to remove the seed layer growth solution. The obtained precipitate was then heat-treated in a muffle furnace at a temperature of 200° C. to 400° C. for a period of 10 minutes to 60 minutes to obtain GNPs coated with ZnO nanoparticles constituting a seed layer.

[0087] Figure 2 shows images obtained under a scanning electron microscope of GNPs coated with a seed layer obtained by probe sonication. Compared with Example 2, it can be noted that the size of the nanoparticles providing the...

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Abstract

An innovative approach enables the control of the morphology of ZnO nanostructures and the coating density of graphene flakes to produce zinc oxide microrods or nanorods (possibly doped with metals) decorated with enhanced electrical, electronic and mechanical properties. properties of graphene nanosheets. The method is carried out in aqueous or hydroalcoholic suspensions and leads to the production of nanomaterials that can be used as fillers in polymer matrices to obtain nanocomposites with specific electrical, electromagnetic and electromechanical properties. Proper definition of process conditions and the use of deposition of seed layers on GNP surfaces where appropriate and the use of growth techniques with continuous mixing of suspensions enables control of the morphology of the nanostructures and makes it possible to obtain a high and uniform coating of GNP surfaces density.

Description

[0001] The present invention relates to the field of nanotechnology, more precisely to an innovative method for the production of graphene nanosheets decorated with nanorods or microrods (possibly doped with metal) of zinc oxide, which have improved electrical performance, electrical and mechanical properties. Graphene nanosheets (GNPs) are uniformly coated on their entire surface (on both sides of the sheet) with nanorods (NR) or microrods (MR) of zinc oxide (ZnO), possibly doped with metals. The morphological properties of the ZnO nanostructures and the coating density of the GNP surface can be controlled during the growth process. [0002] The method is carried out in aqueous or hydroalcoholic suspensions and leads to the production of nanomaterials that can be used as fillers in polymer matrices to obtain nanocomposites with specific electrical, electromagnetic and electromechanical properties . [0003] The method used in the present invention is simple, economically favo...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C01G9/02
CPCC01G9/02C01P2004/03C01P2004/16
Inventor 玛丽亚·塞布丽娜·萨尔托钱德拉坎斯·雷迪·钱德拉亚加里乔瓦尼·德贝利斯
Owner UNIV DEGLI STUDI DI ROMA LA SAPIENZA