Three-dimensional graphene composite, preparation method for the same, and supercapacitor comprising the same

Abstract

The present invention relates to a three-dimensional graphene composite, a preparation method for the same, and a supercapacitor including the same, and more particularly to a three-dimensional graphene composite including at least one electrode material nanoparticle selected from a transition metal hydroxide, a transition metal oxide and a conducting polymer as adsorbed onto the surface of a three-dimensional graphene foam, a preparation method for the three-dimensional graphene composite, and a supercapacitor including the three-dimensional graphene composite.

Claims

1. A three-dimensional graphene composite comprising: a graphene foam having a three-dimensional structure with a plurality of pores; and an electrode material nanoparticle adsorbed onto the graphene foam, wherein the electrode material nanoparticle is a transition metal hydroxide, wherein the transition metal hydroxide is at least one selected from the group consisting of copper hydroxide (Cu(OH).sub.2) and manganese-aluminum hydroxide (MnAl(OH.sub.2).

2. A supercapacitor having an electrode using the three-dimensional graphene composite as claimed in claim 1.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIGS. 1A to 1T illustrate Example 1 using Ni.sub.xCo.sub.1-x(OH).sub.2 as an electrode material nanoparticle.

(2) FIGS. 2A to 2G illustrate Example 2 using Co(OH).sub.2 as an electrode material nanoparticle and an electrodeposition method.

(3) FIGS. 3A to 3F illustrate Example 3 using MnO.sub.2 as an electrode material nanoparticle.

(4) FIGS. 4A to 4G illustrate Example 4 using polyaniline as an electrode material nanoparticle.

(5) FIG. 5 shows the measurements of pseudocapacitive materials prepared in Examples 1 to 4 in regards to specific capacitance (F/g).

(6) FIG. 6 shows the measurements of pseudocapacitive materials prepared in Examples 1 to 4 in regards to energy density (Wh/kg).

(7) FIG. 7 shows the measurements of pseudocapacitive materials prepared in Examples 1 to 4 in regards to power density (kW/kg).

DETAILED DESCRIPTION

(8) Reference will be now made in detail to embodiments of the present disclosure with reference to the attached drawings. It will be understood that words or terms used in the specification and claims shall not be interpreted as the meaning defined in commonly used dictionaries. It will be further understood that the words or terms should be interpreted as having a meaning that is consistent with their meaning in the context of the relevant art and the technical idea of the disclosure.

(9) The present invention, according to a preferred embodiment, provides a three-dimensional graphene composite having an electro material nanoparticle adsorbed onto a three-dimensional graphene foam through immersion. The three-dimensional graphene composite includes: graphene foam having a three-dimensional structure with a plurality of pores; and an electrode material nanoparticle adsorbed onto the graphene foam, where the electrode material nanoparticle may include at least one selected from the group consisting of a transition metal hydroxide, a transition metal oxide, and a conducting polymer.

(10) The transition metal hydroxide may include at least one selected from the group consisting of nickel-cobalt hydroxide (NiCo(OH).sub.2), cobalt hydroxide (Co(OH).sub.2), nickel hydroxide (Ni(OH).sub.2), copper hydroxide (Cu(OH).sub.2), nickel-aluminum hydroxide (NiAl(OH).sub.2), manganese-aluminum hydroxide (MnAl(OH).sub.2), and cobalt-aluminum hydroxide (CoAl(OH).sub.2). The transition metal oxide may include at least one selected from the group consisting of manganese oxide (MnO.sub.2), nickel oxide (NiO), cobalt oxide (CoO), nickel-cobalt oxide (NiCO.sub.2O.sub.4), copper oxide (CuO), ruthenium oxide (RuO.sub.2), and iridium oxide (IrO.sub.2). The conducting polymer may include at least one selected from the group consisting of polyaniline, polyethylenedioxythiophene (poly(3,4-ethylenedioxythiophene), PEDOT), and polypyrrole.

(11) Further, the present invention provides a method for preparing a three-dimensional graphene composite including an electrode material nanoparticle adsorbed onto the surface of a graphene foam.

(12) First of all, there is performed a step of depositing graphene on a molded foam having a three-dimensional structure and then dissolving out the component to prepare a graphene foam having a three-dimensional structure. The molded foam may come in different shapes. Preferably, a nickel (Ni) foam having pores with an average diameter of 100 to 200 m may be used considering ease of purchase, feasibility of etching, etc. For supercapacitors, the optimal pore size is known in the range of about 20 to 50 m. It is preferable to use the initial molded foam having a pore size in the above-defined range, as a transition metal hydroxide is later adsorbed into the pores of the resulting three-dimensional graphene foam through immersion to cover the three-dimensional graphene foam.

(13) Graphene, which is emerging as an advanced material, refers to a graphite material consisting of one to five graphite sheets with a beehive (hexagonal) pattern. Graphene has a two-dimensional carbon structure being the thinnest material even known, only one atom thick. Graphene is known to be superior in properties to carbon nanotubes and particularly exhibits considerably goad electrical characteristics.

(14) Such a very large surface area in relation to the volume and hence high electrical conductivity lead to a greatly enhanced electrical performance of graphene, and a higher electron mobility through the graphite sheets than other materials renders the graphene to emerge as one of the most promising materials suitable for electronic devices.

(15) However, graphene is poor in availability and processability and thus its applications have not been yet studied despite the worldwide attentions to graphene. Therefore, the inventors of the present invention contrive a novel material obtained by preparing a three-dimensional graphene foam indirectly using a three-dimensional molded foam and then adsorbing an electrode material nanoparticle selected from a transition metal hydroxide, a transition metal oxide, and a conducting polymer onto the three-dimensional graphene foam, only to overcome the poor availability and processability and offer economic feasibility and high electrical conductivity.

(16) In order to prepare a three-dimensional graphene foam with an optimal specific surface area using a molded foam, it is preferable to deposit graphene on the molded foam by a CVD method, that is, a chemical vapor deposition method. More specifically, a step is performed that includes adding a precursor of graphene, preferably methane (CH.sub.4) gas, hydrogen (H.sub.2) gas, or argon (Ar) gas, together with a nickel foam into a reaction chamber and then performing a heat treatment at a temperature range of 800 to 1,500 C., which is the optimal temperature range for activating the graphene precursor, to deposit graphene on the nickel foam.

(17) For immobilization of graphene, the graphene thus obtained is immersed in a methacryl resin solution, preferably a poly(methyl methacrylate) (PMMA) solution and then dried out. To eliminate the nickel component from the dried graphene-nickel foam, the graphene-nickel foam is dissolved in a FeCl.sub.3/HCl solution and subjected to the wet etching method to prepare a three-dimensional graphene foam having an optimal specific surface area.

(18) The subsequent step is preparing a solution containing the precursor of the electrode material nanoparticle and finally adsorbing the electrode material nanoparticle onto the surface of the graphene foam.

(19) The step of adsorbing the electrode material nanoparticle largely includes: (a) adding a reagent and distilled water to the solution to prepare a mixed solution and immersing the graphene foam into the mixed solution through chemical bath deposition to form the electrode material nanoparticle according to a reaction and adsorb the electrode material nanoparticle onto the surface of the graphene foam; or (b) immersing the graphene foam into the mixed solution and applying a voltage by a cyclic voltammetry method to electrodeposit the electrode material nanoparticle onto the surface of the graphene foam.

(20) The chemical bah deposition is one of the relatively simple thin film deposition methods that involves immersing an object material such as a substrate into an aqueous solution containing a desired deposition material or its precursor and applying heat or pressure to the object material to deposit the desired deposition material on the object material.

(21) The mixed solution may be prepared by mixing a precursor of the electrode material nanoparticle, a reagent, and distilled water together under agitation. A transition metal oxide/hydroxide, used as the transition metal nanoparticle, is a substance corresponding to a representative pseudocapacitor material. Examples of the transition metal oxide/hydroxide available may include MnO.sub.2, Mn.sub.3O.sub.4, Fe.sub.3O.sub.4, Fe.sub.2O.sub.3, CO.sub.2O.sub.3, CO.sub.3O.sub.4, NiO, CuO, SnO.sub.2, In.sub.2O.sub.3, In(OH).sub.3, Bi.sub.2O.sub.3, V.sub.2O.sub.3, TiO.sub.2, etc. According a preferred embodiment, the present invention uses a transition metal hydroxide or a transition metal oxide represented by the following chemical formula 1:
M.sub.xN.sub.1-x(OH).sub.2[Chemical Formula 1]

(22) (In the chemical formula 1, M and N are the same or different from each other, each representing a transition metal, and combine together at a stoichiometric ratio of x:1x, where 0x1)

(23) In this regard, M and N of the chemical formula 1 is preferably nickel (Ni) and cobalt (Co), respectively. More preferably, the stoichiometric ratio of nickel (Ni) to cobalt (Co) is at least one selected from the group consisting of 1:0, 2:1, 1:1, 1:2, and 0:1. Most preferably, the stoichiometric ratio of nickel (Ni) to cobalt (Co) is 1:2. This will be described in further detail later with reference to the Examples below.

(24) In addition, the reagent may be a reductant, which activates the functional groups to modify the surface of the three-dimensional graphene foam. As more functional groups, such as carboxy groups, hydroxyl groups and epoxy groups, are activated on the surface of the three-dimensional graphene foam, the final nucleation takes place more easily when adsorbing the transition metal hydroxide onto the surface of the three-dimensional graphene foam by the subsequent chemical bath deposition method. For this, the reductant is preferably an alkali solution, and most preferably urea or ammonium persulfate ((NH.sub.4).sub.2S.sub.2O.sub.8) in the aspect of achieving the reductive function.

(25) The subsequent step is immersing the three-dimensional graphene foam into the mixed solution prepared using the chemical bath deposition method to form the electrode material nanoparticle according to a reaction and adsorb the electrode material nanoparticle onto the surface of the three-dimensional graphene foam.

(26) In this regard, the mixed solution into which the three-dimensional graphene foam is heated at 90 to 140 C. for 2 to 6 hours to accomplish a gradual adsorption, which can optimize the three steps of nucleation, binding and particle deposition to more efficiently adsorb the transition metal hydroxide.

(27) According to the above-described method, it is possible to prepare a final three-dimensional graphene composite having the electrode material nanoparticle, more specifically, nickel-cobalt hydroxide, nickel hydroxide, cobalt hydroxide, or manganese oxide adsorbed on the surface. The three-dimensional graphene composite can be used to form either a cathode electrode or an anode electrode, or both the cathode and anode electrodes and manufacture a supercapacitor.

(28) Such a hybrid composite made of transition metal hydroxide as a pseudocapacitor material and graphene as an electric double layer capacitor material can be used to prepare a supercapacitor with remarkably enhanced electrostatic performance and high energy density.

(29) Hereinafter, a detailed description will be given as to the three-dimensional graphene composite, preparation method for the same, and supercapacitor comprising the same according to the present invention with reference to exemplary embodiments, which are provided as the most preferable embodiments of the present invention and should not be construed as representing all the technical concepts of the present invention. It will be understood at the application time of the present invention that the present invention includes all the equivalents and modifications of the exemplary embodiments.

[Example 1] The Use of NixCo1-x(OH)2 as an Electrode Material Nanoparticle

(30) FIG. 1A shows a representation of the whole concept of the present example, FIG. 1B the coating process according to the chemical bath deposition method, and FIG. 1C the entire preparation process.

(31) Sample 1. Three-Dimensional Graphene Composite with Adsorbed Ni.sub.1Co.sub.0(OH).sub.2(Ni(OH).sub.2)

(32) A nickel foam 2 cm3 cm in size is put into a tube type furnace and, after addition of CH.sub.4, H.sub.2 and Ar gas, a heat treatment is carried out at an elevated temperature up to 1,000 C. for 3 hours to deposit graphene on the nickel foam. Then, the graphene-nickel foam thus obtained is immersed into a small amount of PMMA solution for about 10 seconds and then naturally dried out for about 3 hours.

(33) In order to eliminate the nickel component from the graphene-nickel foam, the graphene-nickel foam is immersed into a FeCl.sub.3/HCl solution and stood still for about 4 days to sufficiently dissolve the nickel contained in the foam into the solution.

(34) To remove the remaining FeCl.sub.3/HCl, the foam is sufficiently washed with distilled water until the pH becomes neutral, dried out and then exposed to acetone vapor at the room temperature for more than 4 days. This procedure completely removes the foam of the remaining PMMA to yield a graphene foam having a three-dimensional structure.

(35) After the preparation of the graphene foam, nickel (II) nitrate hexahydrate (Ni(NO.sub.3).sub.2.6H.sub.2O) and urea (CO(NH.sub.2).sub.2) are mixed at a weight ratio of 2:5 and added to 50 ml of distilled water. The resulting mixture is mechanically stirred for about 10 minutes to prepare a homogeneous mixed solution. The graphene foam is immersed into the mixed solution, which is then warmed up at 120 C. for about 4 hours. In this regard, for the purpose of uniform heat supply, the container containing the mixed solution is preferably surrounded with paraffin oil and continuously stirred with a magnetic stirrer. Subsequently, the mixed solution is naturally cooled down to the room temperature.

(36) After the hydroxide is all adsorbed onto the surface of the graphene foam, distilled water is used to wash the sample to eliminate all the residues from the surface of the sample.

(37) Sample 2. Three-Dimensional Graphene Composite with Adsorbed Ni.sub.0.66C.sub.0.33(OH).sub.2

(38) The procedures are performed in the same manner as described in Sample 1 to form a three-dimensional graphene composite with adsorbed nickel-cobalt hydroxide, excepting that the mixed solution is prepared by using nickel (II) nitrate hexahydrate (Ni(NO.sub.3).sub.2.6H.sub.2O) and cobalt (II) nitrate hexahydrate (Co(NO.sub.3).sub.2.6H.sub.2O) at a stoichiometric ratio of 2:1 to yield a final adsorbed hydroxide having a chemical formula of Ni.sub.0.66Co.sub.0.33(OH).sub.2, while the proportion of the nickel (II) nitrate hexahydrate (Ni(NO.sub.3).sub.2.6H.sub.2O) used in Sample 1 is 1.

(39) Sample 3. Three-Dimensional Graphene Composite with Adsorbed Ni.sub.0.50Co.sub.0.50(OH).sub.2

(40) The procedures are performed in the same manner as described in Sample 1 to form a three-dimensional graphene composite with adsorbed nickel-cobalt hydroxide, excepting that the mixed solution is prepared by using nickel (II) nitrate hexahydrate (Ni(NO.sub.3).sub.2.6H.sub.2O) and cobalt (II) nitrate hexahydrate (Co(NO.sub.3).sub.2.6H.sub.2O) at a stoichiometric ratio of 1:1 to yield a final adsorbed hydroxide having a chemical formula of Ni.sub.0.50Co.sub.0.50(OH).sub.2, while the proportion of the nickel (II) nitrate hexahydrate (Ni(NO.sub.3).sub.2.6H.sub.2O) used in Sample 1 is 1.

(41) Sample 4. Three-Dimensional Graphene Composite with Adsorbed Ni.sub.0.33Co.sub.0.66(OH).sub.2

(42) The procedures are performed in the same manner as described in Sample 1 to form a three-dimensional graphene composite with adsorbed nickel-cobalt hydroxide, excepting that the mixed solution is prepared by using nickel (II) nitrate hexahydrate (Ni(NO.sub.3).sub.2.6H.sub.2O) and cobalt (II) nitrate hexahydrate (Co(NO.sub.3).sub.2.6H.sub.2O) at a stoichiometric ratio of 1:2 to yield a final adsorbed hydroxide having a chemical formula of Ni.sub.0.33Co.sub.0.66(OH).sub.2, while the proportion of the nickel (II) nitrate hexahydrate (Ni(NO.sub.3).sub.2.6H.sub.2O) used in Sample 1 is 1.

(43) Sample 5. Three-Dimensional Graphene Composite with Adsorbed Ni.sub.0Co.sub.1(OH).sub.2

(44) The procedures are performed in the same manner as described in Sample 1 to form a three-dimensional graphene composite with adsorbed nickel-cobalt hydroxide, excepting that the mixed solution is prepared by using cobalt (II) nitrate hexahydrate (Co(NO.sub.3).sub.2.6H.sub.2O) alone to yield a final adsorbed hydroxide having a chemical formula of Ni.sub.0Co.sub.1(OH).sub.2, while the proportion of the nickel (II) nitrate hexahydrate (Ni(NO.sub.3).sub.2.6H.sub.2O) used in Sample 1 is 1.

REFERENCES

(45) Cobalt-nickel electrodes using different electron collectors as suggested by the following references are given as Comparative Examples. Ref. 1-1. One-dimensional (1D) ultralayered mesoporous nickel-cobaltite (NiCo.sub.2O.sub.4) nanowires electrode (Yuan, C.; Li, J.; Hou, L.; Yang, L.; Shen, L.; Zhang, X. J. Mater. Chem. 2012, 22, 16084-16090.) Ref. 1-2. NiCo.sub.2O.sub.4 nanowire-graphene oxide nanocomposites electrode (Carriazo, D.; Patino, J.; Gutierrez, M. C.; Ferrer, M. L.; del Monte, F. RSC Adv. 2013, 3, 13690-13695.) Ref. 1-3. NiCo.sub.2O.sub.4 and reduced graphene oxide (RGO) nanocomposites electrode (Wang, H.-W.; Hu, Z.-A.; Chang, Y.-Q.; Chen, Y.-L.; Wu, H.-Y.; Zhang, Z.-Y.; Yang, Y.-Y. J. Mater. Chem. 2011, 21, 10504-10511.) Ref. 1-4. Hierarchical porous spinel nickel cobaltite (NiCo.sub.2O.sub.4) nanowires electrode (Jiang, H.; Ma, J.; Li, C. Chem. Commun. 2012, 48, 4465-4467.) Ref. 1-5. mesoporous nickel cobaltite (NiCO.sub.2O.sub.4) nanosheets (with Ni Foam) (Yuan, C.; Li, J.; Hou, L.; Zhang, X.; Shen, L.; Lou, X. W. D. Adv. Funct. Mater. 2012, 22, 4592-4597.) Ref. 1-6. Template-free hierarchical porous nickel cobalt oxides (NiCo.sub.2O)(with Ni Foam) (Chang, J.; Sun, J.; Xu, C.; Xu, H.; Gao, L. Nanoscale 2012, 4, 6786-6791.) Ref. 1-7. nickel cobaltite (NiCO.sub.2O.sub.4) microspherical superstructures constructed by one-dimension nanowires (Wu, T.; Li, J.; Hou, L.; Yuan, C.; Yang, L.; Zhang, X. Electrochim. Acta 2012, 81, 172-178.) Ref. 1-8. Nickel Cobaltite Nanowire NiCoO.sub.2 (by hydrothermal and thermal-decomposition processes) (Wang, H.; Gao, Q.; Jiang, L. Small 2011, 7, 2454-2459.) Ref. 1-9. Kulkarni, S. B.; Jagadale, A. D.; Kumbhar, V. S.; Bulakhe, R. N.; Joshi, S. S.; Lokhande, C. D. Int. Hydrogen Energy 2013, 38, 4046-4053 Ref. 1-10. Ghosh, D.; Giri, S.; Das, C. K. ACS Sustainable Chem. Eng. 2013, 1, 1135-1142 Ref. 1-11. Salunkhe, R. R.; Jang, K.; Lee, S.-w.; Yu, S.; Ahn, H. J. Mater. Chem. 2012, 22, 21630-21635

Experiment 1. Preparation of Electrode and Charge/Discharge Testing

(46) The three-dimensional graphene composites prepared in Samples 1 to 5 are used as a working electrode, with an Ag/AgCl electrode used as a reference electrode and a Pt electrode as a relative electrode. Using a 1M KOH solution, the measurement is carried out at the room temperature. The testing is performed at the voltage interval ranging from 0 V to 0.5 V and the current density of 60 A/g to calculate the specific capacitance.

(47) To evaluate the electrical characteristics as an electrode material, an electronic-chemical analyzer (ZIVE SP2 LAB analytical equipment, Korea) is used at the current density of 60 A/g to calculate the specific capacitance in the unit of farad (F). The measurement results are presented in the graph of FIG. 1G and Table 1.

(48) TABLE-US-00001 TABLE 1 Specific Composition capacitance (Ni:Co) (F/g) Sample 1 1:0 130 Sample 2 2:1 280 Sample 3 1:1 596 Sample 4 1:2 1280 Sample 5 0:1 1130

(49) Referring to Table 1, the three-dimensional graphene composite electrode according to the present invention exhibits a specific electrostatic capacity of 125 F/g or greater at the stoichiometric ratio of nickel to cobalt. Particularly, the maximum specific capacitance is 1280 F/g at the nickel-to-cobalt stoichiometric ratio of 1:2 and 1847 F/g at the nickel-to-cobalt stoichiometric ratio of 1:2 and the current density of 5 A/g. In this case, the energy density is 62 Wh/kg and the power density is 11 kW/kg. It is therefore possible to determine the optimal stoichiometric ratio of nickel to cobalt adsorbed onto the three-dimensional graphene composite as a supercapacitor electrode.

(50) Referring to FIG. 1H, it can be seen that the maximum specific capacitance and the energy density of Example 1 are greater than those of the electron collectors disclosed in other reference documents.

(51) Although the electrodes of Ref. 1 to 6 are superior in performance to the electrode of the present invention, the electrode of Ref. 6 which contains nickel foam leads to inefficiency that its industrial use for the capacitor actually increases the weight. Contrarily, it is more ideal to apply the present invention using a graphene foam lighter than the nickel foam in the industrial use.

Experiment 2. Surface Observation of Three-Dimensional Graphene Composite

(52) The surface of the three-dimensional graphene composite prepared in Example 1 is observed with a field emission scanning electron microscope (FESEM; JSM-7001F, JEOL, Japan). The results are presented in FIG. 1D, where (a), (b) and (c) are images at low magnification; and (d) and (f) are images at high magnification.

Experiment 3. Observation of XRD, XPS Peeks for Examples

(53) The respective three-dimensional graphene composite materials prepared according to Samples 1 to 5 are determined in regards to the structure using an X-ray diffractometer (XRD; Ultima (Cu-K radiation), Rigaku) and an X-ray photoelectron spectroscope (XPS; ESCALAB 250 (Thermo Fisher Scientific, UK)). The peek graphs are shown in FIGS. 1E and 1F.

(54) On the other hand, a separate testing is carried out on the composite prepared using a nickel hydroxide as an electrode material nanoparticle. The entire concept of using a nickel hydroxide as an electrode material nanoparticle is illustrated in FIG. 1I.

Experiment 4. Preparation of Electrode Using Nickel Hydroxide and Charge/Discharge Testing

(55) An electrode is prepared in the same manner as described in Sample 1 and then used as a working electrode, with an Ag/AgCl electrode used as a reference electrode and a Pt electrode as a relative electrode. Using a 1M KOH solution, the measurement is carried out at the room temperature.

(56) The testing is performed at the voltage interval ranging from 0 V to 0.55 V and the scan rate of 20 to 100 mV/s to calculate the specific capacitance.

(57) To evaluate the electrical characteristics as an electrode material, the same equipment as mentioned in Experiment 1 is used at the scan rate of 20 mV/s to calculate the specific capacitance in the unit of farad (F) (FIGS. 1M and 1N).

(58) TABLE-US-00002 TABLE 2 Specific Energy Power Electron capacitance density density collector (F/g) (Wh/kg) (kW/kg) Sample 1 130 16 4.6 Stainless 50 5.5 1.8 steel

(59) Referring to Table 2, the supercapacitor electrode according to Sample 1 which enables to use the three-dimensional graphene foam in an electron collector can exhibit a specific capacitance of 130 F/g, which is considerably far higher than the maximum specific capacitance of 50 F/g obtainable with the reference material, stainless steel, as the electron collector.

Experiment 5. Analysis on the Surface, Structure and Chemical Bonds of Electrode Using Nickel Hydroxide

(60) As for the nickel hydroxide/graphene foam composite prepared according to Sample 1, the surface is observed with a scanning electrode microscope (FIG. 1J), the composite structure is analyzed using the X-ray diffractometer (FIG. 1K), and the chemical bonds are identified by the X-ray photoelectron spectroscopy (FIG. 1L).

(61) On the other hand, a separate testing is carried out on the composite prepared using a cobalt hydroxide as an electrode material nanoparticle. The entire concept of using a cobalt hydroxide as an electrode material nanoparticle is illustrated in FIG. 10.

Experiment 6. Preparation of Electrode Using Cobalt Hydroxide and Charge/Discharge Testing

(62) An electrode is prepared in the same manner as described in Sample 5 and then used as a working electrode, with an Ag/AgCl electrode used as a reference electrode and a Pt electrode as a relative electrode. Using a 1M KOH solution, the measurement is carried out at the room temperature.

(63) The testing is performed at the voltage interval ranging from 0.2 V to 0.4 V and the current density of 5 to 25 A/g to calculate the specific capacitance.

(64) To evaluate the electrical characteristics as an electrode material, the same equipment as mentioned in Experiment 1 is used at the current density of 5 A/g to calculate the specific capacitance in the unit of farad (F) (FIGS. 1S and 1T).

(65) TABLE-US-00003 TABLE 3 Specific Energy Power Electron capacitance density density collector (F/g) (Wh/kg) (kW/kg) Sample 5 1130 49 10 Stainless 630 21 9 steel

(66) Referring to Table 3, the supercapacitor electrode according to Sample 5 which enables to use the three-dimensional graphene foam in an electron collector can exhibit a specific capacitance of 1130 F/g, which is considerably far higher than the maximum specific capacitance of 630 F/g obtainable with the reference material, stainless steel, as the electron collector.

(67) On the other hand, FIG. 1T(b) shows the comparison in the performance as a function of the energy density between the electron collectors according to Ref. 1-1 (A. D. Jagadale, V. S. Kumbhar, D. S. Dhawale, C. D. Lokhande, Performance evaluation of symmetric supercapacitor based on cobalt hydroxide [Co(OH).sub.2] thin film electrodes, Electrochim. Acta 98 (2013) 32) and Ref. 1-2 (M. Jayalakshmi, K. Balasubramanian, Simple capacitors to supercapacitors Anoverview, Int. J. Electrochem. Sci. 3 (2008) 1196).

Experiment 7. Analysis on the Surface, Structure and Chemical Bonds of Electrode Using Cobalt Hydroxide

(68) As for the cobalt hydroxide/graphene foam composite prepared according to Sample 5, the surface is observed with a scanning electrode microscope (FIG. 1P), the composite structure is analyzed using the X-ray diffractometer (FIG. 1Q), and the chemical bonds are identified by the X-ray photoelectron spectroscopy (FIG. 1R).

[Example 2] Nanoflake-Like Composite Using Co(OH)2 Adsorbed as an Electrode Material Nanoparticle Through Electrodeposition

(69) Example 2 involves depositing a nanoflake-like cobalt hydroxide on the surface of a graphene foam by a novel deposition method, electrodeposition, while Example 1 involves depositing a nanorod-like cobalt hydroxide on the surface of a graphene foam by the chemical bath deposition method. The whole concept of Example 2 is illustrated in FIG. 2A.

(70) The prepared graphene foam is immersed into an aqueous solution of cobalt salt, which solution is neutral. Preferably, the cobalt hydroxide is slowly deposited by circulating the electric current 20 to 50 cycles according to the potentio dynamic electrodepositioncyclic voltammetry method at the potential ranging from 1.2 V to 0 V and the scan rate of 50 mV/s. The preparation method using the cyclic voltammetry is illustrated in FIG. 2B.

(71) In this regard, sodium sulfate (Na.sub.2SO.sub.4) may be added as a conducing material that is a kind of reagent in order to evenly adsorb the cobalt hydroxide on the surface of the graphene foam and enhance the adsorption yield. This can enhance the electrical conductivity of the aqueous solution of cobalt salt.

Experiment 1. Preparation of Cobalt Hydroxide/Graphene Foam Composite Using Electrodeposition

(72) The preparation method for graphene foam is the same as described in Example 1.

(73) After the preparation of the graphene foam, a 0.1M aqueous solution of cobalt (II) nitrate hexahydrate (Co(NO.sub.3).sub.2.6H.sub.2O) is prepared and the graphene foam is immersed into the aqueous solution. Then, adsorption is performed for 20 to 50 cycles according to the potentio-dynamic electrodeposition method using cyclic voltammetry at a potential ranging from 1.2 V to 0 V and a defined scan rate.

(74) Subsequently, distilled water is used to eliminate the reaction residues from the surface of the hydroxide/graphene foam sample to prepare the final nanoflake type cobalt hydroxide/graphene foam composite.

Experiment 2. Charge/Discharge Testing on Electrode Using Cobalt Hydroxide

(75) The electrode prepared is used as a working electrode, with an Ag/AgCl electrode used as a reference electrode and a Pt electrode as a relative electrode. Using a 1M KOH solution, the measurement is carried out at the room temperature.

(76) The testing is performed at the voltage interval ranging from 0.2 V to 0.4 V and the current density of 9 to 45 A/g to calculate the specific capacitance.

(77) To evaluate the electrical characteristics as an electrode material, the same equipment as mentioned in Example 1 is used at the current density of 9 A/g to calculate the specific capacitance in the unit of farad (F) (FIGS. 2F and 2G)

(78) TABLE-US-00004 TABLE 4 Specific Energy Power Electron capacitance density density collector (F/g) (Wh/kg) (kW/kg) Experiment 1 1030 37 12 Stainless 410 steel

(79) Referring to Table 4, the supercapacitor electrode according to Example 2 which enables to use the three-dimensional graphene foam in an electron collector can exhibit a specific capacitance of 1030 F/g, which is considerably far higher than the maximum specific capacitance of 410 F/g obtainable with the reference material, stainless steel, as the electron collector.

Experiment 3. Analysis on the Surface, Structure and Chemical Bonds of Electrode Using Cobalt Hydroxide

(80) As for the cobalt hydroxide/graphene foam composite prepared according to Experiment 1, the surface is observed with a scanning electrode microscope (FIG. 2C), the composite structure is analyzed using the X-ray diffractometer (FIG. 2D), and the chemical bonds are identified by the X-ray photoelectron spectroscopy (FIG. 2E).

[Example 3] The Use of MnO2 as an Electrode Material Nanoparticle

(81) The procedures are performed in the same manner as described in Example 1 to adsorb an electrode material nanoparticle onto the surface of the graphene foam using the chemical bath deposition method, excepting that manganese oxide (MnO.sub.2) is used as the electrode material nanoparticle.

Experiment 1. Preparation of Manganese Oxide/Graphene Foam Composite

(82) The procedures are performed in the same manner as described in Example 1, excepting that a manganese salt is used as a precursor of the electrode material nanoparticle, with ammonium persulfate used as a reductant. The entire concept of Example 3 is illustrated in FIG. 3A.

(83) The procedures of preparing a graphene foam is performed in the same manner as described in Example 1, except for the solution prepared after the completion of the graphene foam. More specifically, manganese sulfate (MnSO.sub.4) and ammonium persulfate ((NH.sub.4).sub.2S.sub.2O.sub.8) are mixed together at a ratio of 2:5, and 50 ml of distilled water is added to the mixture. After 10-minute mechanical agitation, a mixed solution is completed.

(84) The graphene foam is immersed into the mixed solution, which is then warmed up at 90 C. for 4 hours. In this regard, for the purpose of uniform heat supply, the container containing the mixed solution is preferably surrounded with paraffin oil and continuously stirred with a magnetic stirrer. Subsequently, the mixed solution is naturally cooled down to the room temperature. After the formation of an oxide, distilled water is used to wash the oxide/graphene foam sample to eliminate all the residues from the surface of the sample.

Experiment 2. Charge/Discharge Testing on Electrode Using Manganese Oxide

(85) The electrode prepared is used as a working electrode, with an Ag/AgCl electrode used as a reference electrode and a Pt electrode as a relative electrode. Using a 1M Na.sub.2SO.sub.4 solution, the measurement is carried out at the room temperature.

(86) The testing is performed at the voltage interval ranging from 0 V to 1.0 V and the scan rate of 10 to 125 mV/s to calculate the specific capacitance.

(87) To evaluate the electrical characteristics as an electrode material, the same equipment as mentioned in Example 1 is used at the scan rate of 10 mV/s to calculate the specific capacitance in the unit of farad (F) (FIGS. 3E and 3F)

(88) TABLE-US-00005 TABLE 5 Specific Energy Power Electron capacitance density density collector (F/g) (Wh/kg) (kW/kg) Experiment 1 670 34.1 17.5 Stainless 440 8.7 9.7 steel

(89) Referring to Table 5, the supercapacitor electrode according to Example 3 which enables to use the three-dimensional graphene foam in an electron collector can exhibit a specific capacitance of 670 F/g, which is considerably far higher than the maximum specific capacitance of 440 F/g obtainable with the reference material, stainless steel, as the electron collector.

(90) Further, when compared with other electron collectors reported in Ref. 3-1 (L. Deng, G. Zhu, J. Wang, L. Kang, Z-H Liu, Z. Yang, Z. Wang, J. Power Sources 196 (2011) 10782), Ref. 3-2 (J. Zhu, W. Shi, N. Xiao, X. Rui, H. Tan, X. Lu, H. H. Hng, J. Ma, Q. Yan, ACS Appl. Mater. Interfaces, 4 (2012) 2769), Ref. 3-3 (Q. Qu, P. Zhang, B. Wang, Y. Chen, S. Tian, Y. Wu, R. Holze, J. Phys. Chem. C, 113 (2009) 14020), Ref. 3-4 (Y. Cheng, H. Zhang, S. Lu, C. V. Varanasi, J. Liu, Nanoscale, 5 (2013) 1067-73), Ref. 3-5 (K. Chiang, S. Zhang, C. Peng, G. Z. Chen, J. Electrochem. Soc., 156 (2009) A846.), Ref. 3-6 (Z. Lei, J. Zhang, X. S. Zhao, J. Mater. Chem., 22 (2012) 153), Ref. 3-7 (L. Yuan, X-H. Lu, X. Xiao, T. Zhai, J. Dai, F. Zhang, B. Hu, X. Wang, L. Gong, J. Chen, C. Hu, Y. Tong, J. Zhou, Z. L. Wang, ACS Nano, 6 (2012) 656), etc., the electron collector using the supercapacitor electrode according to Example 3 is enhance in the energy density, which can be seen from FIG. 3F.

Experiment 3. Analysis on the Surface, Structure and Chemical Bonds of Electrode Using Manganese Oxide

(91) As for the manganese oxide/graphene foam composite prepared according to Experiment 1, the surface is observed with a scanning electrode microscope (FIG. 3B), the composite structure is analyzed using the X-ray diffractometer (FIG. 3C), and the chemical bonds are identified by the X-ray photoelectron spectroscopy (FIG. 3D).

[Example 4] The Use of Polyaniline as an Electrode Material Nanoparticle

(92) The electrode material nanoparticle is adsorbed onto the surface of the graphene foam, provided that polyaniline among the conducting polymers is used as the electrode material nanoparticle. The entire concept of Example 4 is illustrated in FIG. 4A, and the preparation method of Example 4 is shown in FIG. 4B.

(93) In Example 4, as different from the other Examples, the solution prepared to form polyaniline on the surface of the graphene foam contains an aniline monomer and an initiator for polymerization of the monomer into the polymer as a reagent. For ensuring an even adsorption of the polyaniline, it is preferable to perform the step of immersing the graphene foam into the solution at a relatively low temperature of 4 to 25 C.

Experiment 1. Preparation of Polyaniline/Graphene Foam Composite

(94) The procedures are performed in the same manner as described in the other Examples to prepare a graphene foam, excepting that the prepared solution contains 0.1 M aniline (C.sub.6H.sub.5NH.sub.2) monomer and 0.1 M ammonium persulfate. More specifically, 1 to 3 ml of an aqueous solution of ammonium persulfate is added to 50 ml of an aqueous solution of aniline monomer, and the mixed solution is mechanically stirred for 1 to 5 minutes. The graphene foam is immersed into the mixed solution, which is then subjected to the fast reaction for about 10 minutes. In this regard, the mixed solution is continuously stirred with a magnetic stirrer to effectively induce the reaction uniform.

(95) After the formation of polyaniline, distilled water is used to eliminate the reaction residues from the surface of the oxide/graphene foam sample.

Experiment 2. Charge/Discharge Testing on Electrode Using Polyaniline

(96) The electrode prepared is used as a working electrode, with an Ag/AgCl electrode used as a reference electrode and a Pt electrode as a relative electrode. Using a 1M H.sub.2SO.sub.4 solution, the measurement is carried out at the room temperature.

(97) The testing is performed at the voltage interval ranging from 0.2 V to 0.8 V and the scan rate of 10 to 100 mV/s to calculate the specific capacitance.

(98) To evaluate the electrical characteristics as an electrode material, the same equipment as mentioned in Example 1 is used at the scan rate of 10 mV/s to calculate the specific capacitance in the unit of farad (F) (FIGS. 4F and 4G)

(99) TABLE-US-00006 TABLE 6 Specific Energy Power Electron capacitance density density collector (F/g) (Wh/kg) (kW/kg) Experiment 1 1024 60 3 Stainless 410 steel

(100) Referring to Table 6, the supercapacitor electrode according to Example 4 which enables to use the three-dimensional graphene foam in an electron collector can exhibit a specific capacitance of 1024 F/g, which is considerably far higher than the maximum specific capacitance of 410 F/g obtainable with the reference material, stainless steel, as the electron collector.

Experiment 3. Analysis on the Surface, Structure and Chemical Bonds of Electrode Using Polyaniline

(101) As for the polyaniline/graphene foam composite prepared according to Experiment 1, the surface is observed with a scanning electrode microscope (FIG. 40), the composite structure is analyzed using the X-ray diffractometer (FIG. 4D), and the chemical bonds are identified by the X-ray photoelectron spectroscopy (FIG. 4E).

(102) Further, the embodiments discussed have been presented by way of example only and not limitation. Thus, the breadth and scope of the invention(s) should not be limited by any of the above-described exemplary embodiments, but should be defined only in accordance with the following claims and their equivalents. Moreover, the above advantages and features are provided in described embodiments, but shall not limit the application of the claims to processes and structures accomplishing any or all of the above advantages.

(103) Additionally, the section headings herein are provided for consistency with the suggestions under 37 CFR 1.77 or otherwise to provide organizational cues. These headings shall not limit or characterize the invention(s) set out in any claims that may issue from this disclosure. Specifically and by way of example, although the headings refer to a Technical Field, the claims should not be limited by the language chosen under this heading to describe the so-called technical field. Further, a description of a technology in the Background is not to be construed as an admission that technology is prior art to any invention(s) in this disclosure. Neither is the Brief Summary to be considered as a characterization of the invention(s) set forth in the claims found herein. Furthermore, any reference in this disclosure to invention in the singular should not be used to argue that there is only a single point of novelty claimed in this disclosure. Multiple inventions may be set forth according to the limitations of the multiple claims associated with this disclosure, and the claims accordingly define the invention(s), and their equivalents, that are protected thereby. In all instances, the scope of the claims shall be considered on their own merits in light of the specification, but should not be constrained by the headings set forth herein.