KR20160150425A

KR20160150425A - Preparation method for the ultra thin cobalt oxide nanotubes-intercalated graphene composite

Info

Publication number: KR20160150425A
Application number: KR1020150088386A
Authority: KR
Inventors: 심재진; 웬방호아
Original assignee: 영남대학교 산학협력단
Priority date: 2015-06-22
Filing date: 2015-06-22
Publication date: 2016-12-30
Also published as: KR101743510B1

Abstract

The present invention relates to a process for preparing a mixed solution by mixing ethanol and an ionic liquid, and then dispersing the graphene oxide in the mixed solution to prepare a first mixture (first step); Preparing the mixed solution again, and dissolving the cobalt precursor to prepare a second mixture (second step); Mixing the first mixture and the second mixture, stirring the mixture, and adding an ammonia solution to prepare a slurry (third step); Heating the slurry to obtain a graphene composite (fourth step); And washing and drying the graphene composite (step 5). The present invention also provides a method for synthesizing a graphene composite having an ultrafine oxidized cobalt nanotube inserted therein.
Therefore, it is possible to produce a graphene complex in which ultrafine oxidized cobalt nanotubes are inserted by a one-step process through hydrothermal synthesis. When the prepared composite is used as an electrode for a supercapacitor, it has excellent electrochemical performance, can exhibit excellent discharge rate and improved cycle stability.

Description

Preparation method of ultra-thin cobalt oxide nanotubes-intercalated graphene composite

The present invention relates to a method for synthesizing a graphene composite having an ultrafine oxidized cobalt nanotube inserted therein by hydrothermal synthesis of a cobalt precursor and graphene.

An electrochemical capacitor is an energy storage device that stores and supplies electric energy by using a capacitor behavior caused by an electrochemical reaction between an electrode and an electrolyte. As compared with a conventional electrolytic capacitor and a secondary battery, an energy density and an output density are superior Has recently been attracting much attention as a new concept of energy storage power source capable of storing or supplying energy of a short period of time.

Cobalt oxide is a major magnetic and co-fuel p-type semiconductor (direct optical bandgap at 1.48 and 2.19 eV), which can be used in a variety of devices such as sensors, heterogenous catalysts, electrosensitive devices, lithium ion batteries, supercapacitors, And has attracted much attention.

Thus, considerable efforts have been made to produce nanostructured cobalt oxide through solvent-based synthesis, hydrothermal synthesis, physico-chemical synthesis, and electrochemical deposition based on a template, and a considerable effort has been made to produce nanostructured cobalt oxides of spherical, flake, rod, Cobalt nanowires, nanorods, nano needles and hollow spheres aligned with nanostructures have also become possible to fabricate by this method.

However, since the nanostructure is broken and undesired impurities or defects are produced by removing the template after the production by this method, there is a problem that it requires a complicated process as well as a porous template. Therefore, there is a need for a method of manufacturing an easily and various cobalt oxide nanotubes Is very urgently required.

Cobalt oxide, on the other hand, is considered to be a promising potential active material that can be used in supercapacitor electrodes due to its low conductivity and environmentally friendly, low cost and favorable dystrophic capacity.

Korean Patent Registration No. 10-0190987 discloses an electrode manufactured using lithium cobalt oxide powder. The lithium cobalt oxide powder used as an electrode active material for a lithium secondary battery is prepared by a liquid reaction (coprecipitation) (Positive electrode) for a lithium secondary battery manufactured by varying the ratio of ash and binder. However, a method of manufacturing an electrode for a supercapacitor capable of further increasing the charging / discharging efficiency through improvement of the manner of inserting cobalt oxide into graphene has not been disclosed at all, and the noble structure of the cobalt oxide is used to increase the non- There is still a need to do this.

The present invention provides a method for synthesizing a graphene composite having an ultrafine oxidized cobalt nanotube inserted therein, which is highly applicable to various electrode elements such as an electrode of a supercapacitor, a sensor catalyst, and a lithium ion battery .

In order to accomplish the above object, the present invention provides a method for manufacturing a semiconductor device, comprising: preparing a mixed solution by mixing ethanol and an ionic liquid, and then dispersing the graphene oxide in the mixed solution to prepare a first mixture; Preparing the mixed solution again, and dissolving the cobalt precursor to prepare a second mixture (second step); Mixing the first mixture and the second mixture, stirring the mixture, and adding an ammonia solution to prepare a slurry (third step); Heating the slurry to obtain a graphene composite (fourth step); And washing and drying the graphene composite (step 5). The present invention also provides a method for synthesizing a graphene composite having an ultrafine oxidized cobalt nanotube inserted therein.

Also, the mixed solution may be mixed in a volume ratio of ethanol: [bimm] [BF ₄ ] of 10: 20: 1.

The graphene oxide may be dispersed by ultrasonication in the mixed solution for 20 to 60 minutes.

The cobalt precursor may be any one selected from the group consisting of cobalt nitrate (Co (NO ₃ ) ₂ .6H ₂ O), cobalt chloride (CoCl ₂ ), and cobalt acetate (Co (CH ₃ COO) ₂ ).

Further, the first mixture and the second mixture may be mixed and stirred for 20 to 60 minutes.

In the third step, the slurry may be heated at 160 to 220 ° C for 6 to 12 hours.

Also, the drying in the above-mentioned five steps may be carried out at 50 to 70 ° C for 6 to 12 hours.

The cobalt oxide inserted into the graphene composite in the fifth step may be a nanotube having an average diameter of 15 to 25 nm and an average length of 1 to 10 탆.

The method of synthesizing a graphene composite having an ultrafine oxidized cobalt nanotube embedded therein according to the present invention can produce a graphene complex having ultrafine oxidized cobalt nanotubes inserted therein by a one-step process through hydrothermal synthesis. When the prepared composite is used as an electrode for a supercapacitor, it has excellent electrochemical performance, can exhibit excellent discharge rate and improved cycle stability.

FIG. 1 is an SEM image of a graphene composite having an ultrafine oxide cobalt nanotube inserted therein according to an embodiment of the present invention.
FIG. 2 is a transmission electron microscope (SEM) image of a graphene composite having an ultrafine oxide cobalt nanotube inserted therein according to an embodiment of the present invention.
FIG. 3 is an X-ray diffraction analysis graph of a graphene composite having an ultrafine oxide cobalt nanotube inserted therein according to an embodiment of the present invention.
FIG. 4 is a photograph of a high angle annular dark field-scanning transmission electron microscope (HAADF-STEM) image of a graphene composite with an ultrafine oxidized cobalt nanotube embedded therein according to an embodiment of the present invention. And an EDX mapping graph.
FIG. 5 is a graph of X-ray photoelectron spectroscopy of a graphene composite having an ultrafine oxide cobalt nanotube inserted therein according to an embodiment of the present invention.
6 is a graph showing the electrochemical properties of a graphene composite with an ultrafine oxide cobalt nanotube inserted therein according to an embodiment of the present invention.

The inventors of the present invention have found that cobalt oxide can greatly improve the electrochemical performance of an electrode such as an increase in specific capacitance while studying an electrode for a supercapacitor and also found that a mixture of a specific ionic liquid and ethanol, And the graphene was hydrothermally synthesized, the graphene composite was first synthesized by inserting the nano-sized cobalt oxide nanotubes into the graphene, thereby completing the present invention.

Hereinafter, the present invention will be described in more detail.

The present invention relates to a process for preparing a mixed solution by mixing ethanol and an ionic liquid, and then dispersing the graphene oxide in the mixed solution to prepare a first mixture (first step); Preparing the mixed solution again, and dissolving the cobalt precursor to prepare a second mixture (second step); Mixing the first mixture and the second mixture, stirring the mixture, and adding an ammonia solution to prepare a slurry (third step); Heating the slurry to obtain a graphene composite (fourth step); And washing and drying the graphene composite (step 5). The present invention also provides a method for synthesizing a graphene composite having an ultrafine oxidized cobalt nanotube inserted therein.

[Bimm] [BF ₄ ] is an ionic liquid, which contains 1-N-butyl-3-methylimidazolium as a cation and BF ₄ ^- as an anion . Nano-sized cobalt oxide nanotubes having an average diameter of 20 nm and an average length of 1 to 20 μm in the ionic liquid [bimm] [BF ₄ ] can be synthesized.

In the case of not performing sonication treatment within the above range, the graphene grains may not be uniformly dispersed.

Within this time range, a mixture can be made such that the graphene grains in the first mixture and the cobalt nitrate in the second mixture can react with each other.

A 30% ammonia solution may be added to the mixture to prepare a slurry.

In a third step, the slurry may be heated at 160-220 < 0 > C for 6-12 hours.

When hydrothermal method is used in the range of temperature and reaction time, cobalt oxide is formed in the form of ultrafine nanotubes and inserted into graphene to be synthesized as a graphene composite in which ultrafine oxidized cobalt nanotubes are inserted have.

After washing the synthesized graphene composites, the impurities or residues can be removed when the grains are dried in the above range to obtain a graphene composite in which ultrafine oxidized cobalt nanotubes are inserted.

When the cobalt oxide nanotubes of the size and shape are inserted into the graphene, the electrochemical performance required for the supercapacitor electrode can be increased, such as an increase in non-storage capacity and an increase in cycle stability, An increase in the electrochemical performance can not be expected if it is out of the above-mentioned form and size.

Hereinafter, the present invention will be described in more detail with reference to the following examples. However, the scope of the present invention is not limited to the following examples.

Example 1 Preparation of Graphene Composite with Cobalt Oxide Nanotube Inserted

All chemical reagents were analytical grade and used as received. Graphene oxide (GO) was prepared from graphene powder by the Hummer method, Nguyen VH, Nguyen TT, Shim JJ Synt Met 2015; 199: 276 -279).

The prepared graphene oxide was dispersed in 15 ml of a mixed solution of ethanol: ionic liquid [Bmim] [BF4] in a volume ratio of 14: 1 and ultrasonicated for 30 minutes to prepare a first mixture. The second mixture was prepared by dissolving cobalt nitrate (Co (NO ₃ ) ₂ .6H ₂ O) in a mixed solution prepared by the same process, followed by stirring for 30 minutes. After adding ammonia solution (30%) to the slurry state, the mixture was heated in an autoclave treated with TEFLON at 180 ° C for 10 hours to prepare a composite. The prepared composite was cooled at room temperature, washed, and dried at 60 ° C. for 6 hours to obtain a graphene composite having ultrafine oxidized cobalt nanotubes embedded therein.

EXPERIMENTAL EXAMPLE 1 Physical properties of a graphene composite having a cobalt oxide nanotube embedded therein

The morphology of the graphene composite with the ultrafine oxidized cobalt nanotubes prepared in the above-mentioned examples was examined by scanning electron microscopy (SEM) (Hitachi, S-4200), transmission electron microscopy &Quot; TEM ", Philips, CM-200) were accelerated at a voltage of 200 kV and observed. Also, X-ray photoelectron spectroscopy (XPS) (Thermo Scientific, K-Alpha) using monochromated irradiation using Al Kα was performed.

All measurements were carried out at room temperature in a triple-cell equipped with AutoLab (PGSTAT302N, Metrohm, Netherlands), using a working electrode, a counter electrode as a platinum plate, and a saturated calomel reference electrode (SCE) .

15 wt% acetylene black, 5 wt% polytetrafluorene-ethylene (5 wt%) were added to the graphene composite powder (5 mg, 80 wt%) having ultrafine oxidized cobalt nanotubes prepared in Example 1, a polytetrafluorene-ethylene (PTFE) binder was mixed and deposited on a 1.0 cm × 1.0 cm nickel foam current collector to prepare a graphene composite electrode having ultrafine oxide cobalt nanotubes inserted therein.

A 3M potassium hydroxide (KOH) solution was selected as the electrolyte.

The non-discharge capacity (C _s ) of the prepared electrode was calculated by calculating the charge / discharge curve according to the following equation (1).

Where C is the non-discharge capacity (F g ^-1 ) of the electrode, I is the discharge current, t is the discharge time, m is the amount of active material, and? V is the discharge potential range.

FIG. 1 is an SEM image of a graphene composite having an ultrafine oxide cobalt nanotube inserted therein according to an embodiment of the present invention.

FIG. 1 (a) is a SEM image of a pure cobalt oxide (Co ₃ O ₄ ) nanotube, and FIG. 1 (b) is an SEM photograph of a graphene composite having an ultrafine oxidized cobalt nanotube inserted therein.

Referring to FIG. 1, it was confirmed that the cobalt oxide was a uniform nanotube having an average length longer than 3 탆. The surfaces of the nanotubes were very smooth and clean. The graphene-doped ultra-thin oxide cobalt nanotubes had a hierarchical structure of cobalt oxide and graphene sheets.

FIG. 2 is a transmission electron microscope (SEM) image of a graphene composite having an ultrafine oxide cobalt nanotube inserted therein according to an embodiment of the present invention.

The morphology of the prepared graphene oxide cobalt nanotube-embedded graphene composites was confirmed by TEM photographs. The average diameter of the cobalt oxide nanotubes was 20 nm and uniformly applied to the surface of the graphene sheet. The cobalt oxide nanotubes were also firmly fixed to the surface of the oxidized graphene after long-time ultrasonic treatment of the sample for TEM photographing.

The strong interaction enabled very fast electron transfer between cobalt oxide and graphene.

FIG. 3 is an X-ray diffraction analysis graph of a graphene composite having an ultrafine oxide cobalt nanotube inserted therein according to an embodiment of the present invention.

Referring to FIG. 3, the diffraction pattern of the electrons in the selected zone showed a definite loop and point, which indicates the crystallinity of the graphene complex into which the ultrafine oxidized cobalt nanotubes are inserted.

FIG. 3F shows a wide-angle XRD pattern of the graphene complex into which the ultrafine oxidized cobalt nanotubes are inserted.

Except for the typical peak due to graphene, the other six distinct diffraction peaks are 21.5 (corresponding to the hkl values of (111), (220), (200), (400), (422) °, 31.2 °, 43.8 °, 49.4 °, 54.3 ° and 63.7 °, respectively.

The results show that the graphene complex with ultrafine oxidized cobalt nanotubes has a crystalline structure (JCPSD file no. 65-3103).

FIG. 4 is a photograph of a high angle annular dark field-scanning transmission electron microscope (HAADF-STEM) image of a graphene composite with an ultrafine oxidized cobalt nanotube embedded therein according to an embodiment of the present invention. And an EDX mapping graph.

Referring to FIG. 4 (a), it was confirmed that cobalt oxide and graphene were uniformly interconnected, and the results were consistent with those of the TEM photograph.

The EDX-STEM element mapping indicated the K-edge signals of oxygen, cobalt and carbon. Equivalent distribution of cobalt and oxygen indicates uniform deposition of cobalt oxide nanotubes and indicates that cobalt oxide nanotubes can be successfully inserted into the graphene through the hydrothermal synthesis process.

FIG. 5 is a graph of X-ray photoelectron spectroscopy of a graphene composite having an ultrafine oxide cobalt nanotube inserted therein according to an embodiment of the present invention.

XPS was performed to determine the surface information and the oxidation state of the detected elements.

Referring to FIG. 5, the compositions of the ultra-thin oxide cobalt nanotubes having graphene inserted therein and the carbon (C) 1s, cobalt (Co) 2p and O1s peaks at the center were shown. The spectrum of C 1s showed three peaks, which were due to the binding energy of the C = C, C-C and C = O bonds, and a small peak to the C = O bond confirmed the reduction of the oxidized graphene.

Referring to Figure 5c, the Co 2p spectrum coincided with two spin orbit lone electron pairs. This showed the characteristics of Co ²⁺ and Co ³⁺ .

The high resolution spectra of the O 1s region were dispersed into three peaks at 529.8, 530.9 and 532.4 eV of the bond bond. These are represented by O _I , O _II and O _III , respectively.

The component O _I was attributed to the typical metal-oxygen bond. The component O _II is due to oxygen in the hydroxyl group (-OH) at the surface of the cobalt oxide. O component _III is due to the large number of defects at a low oxygen coordination.

6 is a graph showing the electrochemical properties of a graphene composite with an ultrafine oxide cobalt nanotube inserted therein according to an embodiment of the present invention.

Referring to FIG. 6, a capacitor-voltage curve (hereinafter referred to as a "CV curve") measured at a scanning speed of 2 to 50 mV s ^-1 between -0.1 and 0.5 V of the potential window of the graphene composite electrode having the ultrafine oxidized cobalt nanotube inserted therein, ) Showed pseudocapacitance due to electrochemical reaction. The peaks of two pairs of redox reactions were identified in the CV curve, which is due to the redox process of cobalt oxide (Co ₃ O ₄ ).

The shape of the CV curve showed that the capacitive characteristics on the cobalt oxide were significantly different from the capacitances of the electrical double layer capacitors, and the CV curve was close to the ideal rectangular shape. It was also confirmed that the peak current increased as the scan speed increased from 2 to 50 mV s ^-1 .

6B shows Nyquist plots of about 5000 cycles of the graphene composite electrode into which the ultrafine oxidized cobalt nanotubes are inserted. Referring to the drawings, it was confirmed that a lower vertical line in the impedance curve and a higher vertical line in the higher frequency range indicate a higher electric capacity of the manufactured electrode.

A galvanostatic charge / discharge test was performed at various current densities to confirm the increase in the electrochemical performance of the graphene composite electrode with ultrafine oxidized cobalt nanotubes.

Referring to FIG. 6C, the graphene composite electrode having ultrafine oxide cobalt nanotubes embedded therein exhibited a good discharge rate, and in particular, 5 A g ^- ¹ The discharge capacity was 78.2% even at a high current rate of 25 A g < ^{-1 &} gt ;. The graphene composite electrode with ultrafine oxide cobalt nanotubes was found to have a discharge capacity of 89.2% of initial capacitance even after 5000 cycles of charging and discharging at a rate of 15 A g ^-1 .

As described above, the present invention provides a method for synthesizing graphene complex having ultrafine oxide cobalt nanotubes embedded therein by a single process by mixing an ionic liquid and ethanol under optimal conditions and hydrothermal synthesis. It was confirmed that nano-sized cobalt oxide nanotubes could not be produced except for the conditions of the ionic liquid and ethanol of the present invention. The graphene composite electrode with ultrafine oxidized cobalt nanotubes had a current of 5 and 25 A g ^-1 current And exhibited excellent non-electrochemical performance at 901 and 803 Fg < ^-1 > at the density. It was also confirmed that the electrochemical supercapacitor can exhibit excellent discharge rate and improved cycle stability.

While the invention has been described with reference to a limited number of embodiments, it is to be understood that the invention is not limited to the disclosed embodiments, but, on the contrary, is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the appended claims. Accordingly, the true scope of the present invention should be determined by the technical idea of the appended claims.

Claims

Preparing a mixed solution by mixing ethanol and an ionic liquid, and then dispersing the oxidized graphene in the mixed solution to prepare a first mixture (first step);
Preparing the mixed solution again, and dissolving the cobalt precursor to prepare a second mixture (second step);
Mixing the first mixture and the second mixture, stirring the mixture, and adding an ammonia solution to prepare a slurry (third step);
Heating the slurry to obtain a graphene composite (fourth step); And
And washing and drying the graphene composite (step 5). The method for synthesizing a graphene composite having an ultrafine oxidized cobalt nanotube inserted therein.

The method according to claim 1, wherein the mixed solution is prepared by mixing ethanol [bimm] [BF ₄ ] in a volume ratio of 10 to 20: 1.

The method for preparing a graphene composite according to claim 1, wherein the graft oxide is dispersed by ultrasonication in the mixed solution for 20 to 60 minutes to disperse the cobalt oxide nanotube.

The method of claim 1, wherein the cobalt precursor is selected from the group consisting of cobalt nitrate (Co (NO ₃ ) ₂ .6H ₂ O), cobalt chloride (CoCl ₂ ), and cobalt acetate (Co (CH ₃ COO) ₂ ) Wherein the cobalt oxide nanotubes are inserted into the microcatalyzed oxide nanotubes.

The method according to claim 1, wherein the first mixture and the second mixture are mixed and agitated for 20 to 60 minutes.

The method of claim 1, wherein the slurry is heated at 160 to 220 ° C for 6 to 12 hours in a third step.

The method of claim 1, wherein the drying in step 5 is performed at 50 to 70 ° C for 6 to 12 hours.

The ultrafine oxidized cobalt nanotube according to claim 1, wherein the cobalt oxide inserted into the graphene composite in the fifth step is a nanotube having an average diameter of 15 to 25 nm and an average length of 1 to 10 μm. Inserted graphene composite.