CN110828788A - Porous NiFe2O4Graphene composite material and preparation method and application thereof - Google Patents

Porous NiFe2O4Graphene composite material and preparation method and application thereof Download PDF

Info

Publication number
CN110828788A
CN110828788A CN201910954059.7A CN201910954059A CN110828788A CN 110828788 A CN110828788 A CN 110828788A CN 201910954059 A CN201910954059 A CN 201910954059A CN 110828788 A CN110828788 A CN 110828788A
Authority
CN
China
Prior art keywords
nife
porous
graphene
sio
layer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN201910954059.7A
Other languages
Chinese (zh)
Other versions
CN110828788B (en
Inventor
赵毅
吴初新
官轮辉
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fujian Institute of Research on the Structure of Matter of CAS
Original Assignee
Fujian Institute of Research on the Structure of Matter of CAS
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Fujian Institute of Research on the Structure of Matter of CAS filed Critical Fujian Institute of Research on the Structure of Matter of CAS
Priority to CN201910954059.7A priority Critical patent/CN110828788B/en
Publication of CN110828788A publication Critical patent/CN110828788A/en
Application granted granted Critical
Publication of CN110828788B publication Critical patent/CN110828788B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/362—Composites
    • H01M4/366—Composites as layered products
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00—Nanotechnology for materials or surface science, e.g. nanocomposites
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y40/00—Manufacture or treatment of nanostructures
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/052—Li-accumulators
    • H01M10/0525—Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00—Secondary cells; Manufacture thereof
    • H01M10/05—Accumulators with non-aqueous electrolyte
    • H01M10/054—Accumulators with insertion or intercalation of metals other than lithium, e.g. with magnesium or aluminium
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/36—Selection of substances as active materials, active masses, active liquids
    • H01M4/48—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/52—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
    • H01M4/523—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron for non-aqueous cells
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00—Electrodes
    • H01M4/02—Electrodes composed of, or comprising, active material
    • H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/624—Electric conductive fillers
    • H01M4/625—Carbon or graphite
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10—Energy storage using batteries

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nanotechnology (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Composite Materials (AREA)
  • Physics & Mathematics (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • General Physics & Mathematics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Battery Electrode And Active Subsutance (AREA)
  • Carbon And Carbon Compounds (AREA)

Abstract

The application discloses a porous NiFe2O4The graphene composite material is characterized by comprising a graphene layer and porous NiFe2O4A layer; the porous NiFe2O4The layers coat both surfaces of the graphene layer. The application also discloses a preparation method of the composite material and application thereofThe application is as follows. The nanocomposite has excellent electrical properties.

Description

Porous NiFe2O4Graphene composite material and preparation method and application thereof
Technical Field
The invention belongs to the field of nano material preparation, and particularly relates to porous NiFe2O4Graphene composite material and preparation method and application thereof.
Background
Lithium Ion Batteries (LIBs) have enjoyed great success in the past few years in portable electronic products and electric vehicles. Recently, Sodium Ion Batteries (SIBs) have been used as LIB due to their abundant cost-effective sodium resourcesAlternative technologies are of increasing interest for their application in large-scale energy storage. In order to meet the increasing demand from the point of view of energy storage applications, it is crucial to explore new electrode materials with good safety, long-term cycling and high energy/power density of LIBs and SIBs. In the field of anode materials, commercial graphite for LIB has 372mA h g-1Low theoretical capacity of (a). Further, Na when inserted into the raw graphite+Large ionic radii of (a) lead to poor reversibility. Iron-based Metal Oxides (MOs), including Fe, in the pursuit of good quality anode materials2O3，Fe3O4，MFe2O4(M ═ Ni, Co, Mn, Zn, Mg, etc.), and has been widely studied because of its high capacity, good environment, and low cost. Wherein, NiFe2O4Has a theoretical capacity of 915mA h g-1. However, these anodes are in the presence of continuous Li+Or Na+Poor cell performance results from the inherently low conductivity and large volume changes during insertion/extraction. For example, pure NiFe2O4The sample exhibited a rapid capacity fade as LIB anode.
Disclosure of Invention
According to one aspect of the present invention, there is provided a porous NiFe2O4Graphene composite materials.
The porous NiFe2O4The graphene composite material is characterized by comprising a graphene layer and porous NiFe2O4A layer; the porous NiFe2O4The layers coat both surfaces of the graphene layer.
The NiFe2O4Is nanoparticle with particle size of 3-5 nm.
Optionally, the porous NiFe2O4NiFe in the layer2O4Has a porous structure and the pore size distribution is 1-10 nm.
Optionally, the porous NiFe2O4Layer opposite to the porous NiFe2O4The mass content of the graphene composite material is 80-92 wt%.
Optionally, theThe porous NiFe2O4Layer opposite to the porous NiFe2O4The mass content of the graphene composite material is 85-90 wt%, and more preferably 87 wt%.
Optionally, the porous NiFe2O4Layer opposite to the porous NiFe2O4The upper limit of the mass content of the graphene composite material is selected from 81 wt%, 82 wt%, 83 wt%, 84 wt%, 85 wt%, 86 wt%, 87 wt%, 88 wt%, 90 wt%, 91 wt%, or 92 wt%; the lower limit is selected from 80 wt%, 81 wt%, 82 wt%, 83 wt%, 84 wt%, 85 wt%, 86 wt%, 87 wt%, 88 wt%, 90 wt% or 91 wt%.
As a specific embodiment, a porous NiFe2O4The graphene composite material has the following structural general formula: g @ p-NiFe2O4Wherein G represents graphene, p-NiFe2O4NiFe representing porous structure2O4The compound comprises graphene as the innermost layer and NiFe as the outer layer2O4Which is coated on the surface of the graphene layer.
The NiFe2O4As porous compounds, with p-NiFe2O4Indicating that the pore size is 1-10 nm.
The NiFe2O4The content of the binder is 80 to 92 wt%, and more preferably 87 wt% based on the mass of the composite material.
According to another aspect of the present invention, there is provided a porous NiFe2O4A method for preparing a nanocomposite.
The porous NiFe2O4The preparation method of the nano composite material is characterized by comprising the following steps:
a) coating porous SiO on two surfaces of graphene layer2Layer to obtain G @ p-SiO2；
b) At G @ p-SiO2Coated with NiFe on both surfaces2O4Layer to obtain G @ p-SiO2@NiFe2O4；
c)G@p-SiO2@NiFe2O4Etching the-P to obtain G @ P-NiFe2O4I.e. the porous NiFe2O4A nanocomposite material.
Optionally, in step a), the G @ p-SiO2The content of the graphene in the graphene is 3-12 wt%.
Optionally, in step a), the G @ p-SiO2The upper limit of the content of the graphene in (b) is selected from 5 wt%, 6.3 wt%, 8 wt%, 10 wt% or 12 wt%; the lower limit is selected from 3 wt%, 5 wt%, 6.3 wt%, 8 wt% or 10 wt%.
Optionally, step a) comprises:
a21) dissolving a surfactant in a mixed solution containing water, ethanol and ammonia water to obtain a solution I;
a22) dispersing graphene oxide in the solution I, adding a silicon source, reacting, further annealing at 300-800 ℃ for more than 1 hour in an inert atmosphere to obtain G @ p-SiO2。
Optionally, the surfactant in step a21) is a cationic surfactant; the cationic surfactant is at least one selected from alkyl quaternary ammonium salts.
Optionally, the cationic surfactant is selected from at least one of cetyltrimethylammonium bromide (CTAB), cetyltrimethylammonium chloride, dodecyltrimethylammonium bromide, dodecyltrimethylammonium chloride.
Alternatively, the concentration of surfactant in said solution I in step a21) is between 0.5 and 1 wt%.
Optionally, the volume ratio of water, ethanol and ammonia water in the solution I in the step a21) is 1: (3-10): (0.01-0.04).
Optionally, the silicon source in step a22) is selected from ethyl orthosilicate.
Optionally, the inert atmosphere in step a22) is selected from at least one of nitrogen and noble gases.
Optionally, the upper limit of the temperature of the annealing in step a22) is selected from 350 ℃, 400 ℃, 450 ℃, 500 ℃, 550 ℃, 600 ℃, 650 ℃, 700 ℃, 750 ℃ or 800 ℃; the lower limit is selected from 300 deg.C, 350 deg.C, 400 deg.C, 450 deg.C, 500 deg.C, 550 deg.C, 600 deg.C, 650 deg.C, 700 deg.C or 750 deg.C.
Optionally, the annealing time in the step a22) is 1-24 hours.
Optionally, the upper limit of the time of the annealing in step a22) is selected from 2 hours, 5 hours, 8 hours, 10 hours, 12 hours, 15 hours, 18 hours, 20 hours, or 24 hours; the lower limit is selected from 1 hour, 2 hours, 5 hours, 8 hours, 10 hours, 12 hours, 15 hours, 18 hours, or 20 hours. Optionally, step b) comprises:
g @ p-SiO2Adding the mixture into a solution containing ferric salt and nickel salt, dispersing uniformly, removing the solvent, and annealing at 300-500 ℃ for more than 1 hour in an inert atmosphere to obtain the G @ p-SiO2@NiFe2O4。
Optionally, the molar ratio of iron in the iron salt to nickel in the nickel salt is 2: (0.1-1).
Optionally, the molar ratio of iron in the iron salt to nickel in the nickel salt is 2: 1.
optionally, the concentration of the iron salt in the solution containing the iron salt and the nickel salt is 0.002-0.02 mol/L.
Optionally, the concentration of the nickel salt in the solution containing the iron salt and the nickel salt is 0.001-0.01 mol/L.
Alternatively, G @ p-SiO2The mass ratio of the iron ions to the nickel ions in the solution containing the iron salt and the nickel salt is respectively 1: (0.168-0.28), 1: (11.7-14.7).
Optionally, the upper limit of the temperature of the annealing in step b) is selected from 350 ℃, 400 ℃, 450 ℃ or 500 ℃; the lower limit is selected from 300 deg.C, 350 deg.C, 400 deg.C or 450 deg.C.
Optionally, the annealing time in the step b) is 1-12 hours.
Optionally, the upper limit of the time of the annealing in step b2) is selected from 2 hours, 5 hours, 8 hours, 10 hours or 12 hours; the lower limit is selected from 1 hour, 2 hours, 5 hours, 8 hours or 10 hours.
As an embodiment, the porous NiFe2O4A process for the preparation of a nanocomposite material, characterized in thatThe method comprises the following steps:
1. coating porous silicon dioxide on the surface of the graphene sheet layer to obtain a graphene porous silicon dioxide compound, and coating G @ p-SiO2Is represented by the formula G @ p-SiO2The content of the graphene in the graphene is 3-12 wt%;
2. g @ p-SiO2Adding the mixture into an ethanol solution containing ferric salt and nickel salt, uniformly dispersing, then completely evaporating the ethanol solvent, and annealing the obtained product in an inert atmosphere at the temperature of 300-500 ℃ for more than 1 hour to obtain the G @ SiO2@NiFe2O4A complex;
the molar ratio of iron to nickel in the ferric salt and the nickel salt is 2 (0.1-1), wherein the ferric salt is one or more of ferric nitrate and ferric carboxylate; the nickel salt is one or more of nickel nitrate or nickel carboxylate;
3. SiO in the product of the step 2 is dissolved in hot sodium hydroxide solution or hydrogen fluoride solution2Etching and removing to obtain G @ p-NiFe2O4I.e. said porous NiFe2O4A nanocomposite material.
Optionally, said porous NiFe2O4The nano composite material has the following structural general formula: g @ p-NiFe2O4；
Wherein G represents graphene, p-NiFe2O4NiFe representing porous structure2O4The compound comprises graphene as the innermost layer and NiFe as the outer layer2O4Which is coated on the surface of the graphene layer.
As a specific embodiment, a porous NiFe2O4The preparation method of the graphene composite material comprises the following steps:
1. coating porous silicon dioxide (p-SiO) on the surface of the graphene sheet layer (G)2) Obtaining the graphene porous silicon dioxide compound which is G @ p-SiO2Is represented by the formula G @ p-SiO2The content of the graphene in the graphene is 3-12 wt%;
2. g @ p-SiO2Adding into ethanol solution containing ferric salt and nickel salt, dispersing, and adding into ethanol solutionThe alcohol solvent is completely evaporated, the obtained product is placed in an inert atmosphere and annealed at the temperature of 300-500 ℃ for more than 1 hour, and the obtained G @ SiO2@NiFe2O4The molar ratio of iron to nickel in the ferric salt and the nickel salt is 2:1, the ferric salt is one or more of ferric nitrate and ferric carboxylate, the nickel salt is one or more of nickel nitrate and nickel carboxylate respectively, and the ferric carboxylate and the nickel carboxylate refer to corresponding carboxylate which can be dissolved in an ethanol solvent;
3. SiO in the product of the step 2 is dissolved in hot sodium hydroxide solution or hydrogen fluoride solution2Etching and removing to obtain G @ p-NiFe2O4I.e. said porous NiFe2O4A nanocomposite material.
Step 1, coating porous silicon dioxide (G @ p-SiO) on the surface of the graphene sheet layer2) The method comprises the following steps: cetyl Trimethyl Ammonium Bromide (CTAB) is first dissolved in H2O, ethanol and 1.5ml of concentrated aqueous ammonia (H)2O, ethanol and concentrated ammonia water in the volume ratio of 30:120:1.5), dispersing GO in the mixed solution, slowly adding tetraethyl orthosilicate (TEOS) and keeping the reaction solution to react completely, and then using H to react2O is washed and dried, and then the product is further annealed for more than 1 hour at the temperature of 300-800 ℃ in inert atmosphere to obtain G @ p-SiO2And (c) a complex.
According to yet another aspect of the present invention, there is provided a porous NiFe2O4Nanocomposite, porous NiFe prepared according to said method2O4Use of at least one of the nanocomposites in an electrode material.
According to yet another aspect of the present invention, there is provided a porous NiFe2O4Nanocomposite, porous NiFe prepared according to said method2O4Use of at least one of the nanocomposites in primary or secondary electrochemical generators, high energy generators, in electrochemiluminescence modulation systems.
According to yet another aspect of the present invention, there is provided a porous NiFe2O4Nano meterComposite material, porous NiFe prepared according to said method2O4Use of at least one of the nanocomposites in primary or secondary electrochemical generators, high energy generators, in electrode materials for electrochemiluminescence modulation systems.
According to still another aspect of the present invention, a secondary battery is provided.
The secondary battery is characterized in that the negative electrode material of the secondary battery contains the porous NiFe2O4Nanocomposite, porous NiFe prepared according to said method2O4At least one of the nanocomposites.
Optionally, the secondary battery includes a lithium ion battery, a sodium ion battery, or a potassium ion battery.
Optionally, the secondary battery comprises a positive electrode, a negative electrode and an electrolyte; the negative electrode includes: a current collector and a negative electrode material supported on the current collector; wherein the negative electrode material contains the composite material.
In the present invention, the "inert atmosphere" refers to at least one of nitrogen and a rare gas.
The beneficial effects that this application can produce include:
1) the invention provides porous NiFe2O4The nanocomposite is denoted G @ p-NiFe2O4The inner layer is graphene, and the surface of the graphene is coated with NiFe with a porous structure2O4In this microstructure, the internal graphene acts as a support for the porous NiFe2O4The matrix of the layer and can significantly improve NiFe2O4Is used for the electrical conductivity of (1). The more innovative part of the structure is an active ingredient NiFe2O4The porous structure is beneficial to rapid ion diffusion and buffering of volume change so as to keep structural stability and high rate performance. Thus, porous NiFe2O4The graphene composite material shows more excellent performance as an electrode material of lithium and sodium ion batteries. Especially when the ionic liquid is used as an electrode material of a sodium ion battery, the ionic radius of sodium ions is larger, so that the ionic liquid has ion diffusion and transmission characteristicsNiFe with higher demand and thus porous structure2O4In sodium ion battery application, the relative advantages are more prominent. In a lithium ion battery, G @ p-NiFe2O4Electrode at 1.5Ag-1After 1100 charge-discharge cycles at high rate, 240mAh g was still maintained-1The specific capacity of (A). In sodium ion batteries, at 0.2A g-1After 300 times of charge and discharge, the specific capacity is still maintained at 207mAhg-1. These properties are all superior to pure NiFe2O4、G@NiFe2O4And (4) comparison materials.
2) The active compound NiFe in the composite material provided by the invention2O4The content of the organic silicon compound has very important influence on the performance of the battery, namely directly influencing the specific capacity of the battery and influencing the microstructure of the composite material; active material NiFe for specific capacity of battery2O4The higher the content of the graphene is, the larger the corresponding theoretical specific capacity is, but the higher the content is, the less the content of the graphene is, the conductivity of the electrode is influenced, and the performance of the battery is severely restricted; for the microstructure of the composite material, if the active compound NiFe2O4If the content of (a) is too high, the graphene cannot play a supporting role, so that the volume of an active substance is changed violently and crushed in the charging and discharging processes, and the performance of the battery is influenced; if the content is too small, the specific capacity of one is too low, and the content and the specific capacity influence the ion transmission speed and the battery performance; in the present invention, the active material NiFe2O4The content in the entire composite material is selected from 70% to 90% by weight, and the battery performance is exhibited preferably, and particularly, the performance exhibited most preferably at a content of 87% by weight.
For the active material NiFe2O4Firstly, in the invention, the mass of the used graphene oxide is reduced due to oxygen radical cracking in the high-temperature annealing reduction process under the inert atmosphere, the mass content of the annealed and reduced graphene at 350 ℃ is reduced to 58 wt%, and the mass content of the annealed and reduced graphene is continuously increased along with the continuous increase of the annealing temperatureAnd gradually decreases, and the mass content of the powder is reduced to 45 wt% at 800 ℃. Therefore, in the invention, the reduction annealing temperature of the graphene and the input ratio of the graphene and the salt can be controlled, and the active substance NiFe in the target product can be accurately controlled2O4The content of (a). Of course, as the electrode material, NiFe is the active material2O4The higher the content in the whole composite material is expected to be, the better the content is, but the higher the content is, so that the content of graphene is too small, the conductivity is influenced, and finally the battery performance of the material is influenced2O4The content in the entire composite material is selected from 70 to 90 wt% to exhibit better battery performance, while the content of the most preferable battery performance is 87 wt% to exhibit the most preferable overall battery performance.
Drawings
FIG. 1 is a scheme showing the preparation of G @ p-NiFe2O4The scheme 1 shows that the outer surface of the graphene is coated with a porous silicon dioxide layer, and the scheme 2 shows that NiFe grows inside and outside the porous silicon dioxide layer2O4Nanoparticles, scheme 3 shows the removal of the porous silica layer by etching to obtain the target product, porous SiO in the figure2Denotes porous silica, NiFe2O4NPs denotes NiFe2O4And (3) nanoparticles.
FIG. 2 is the G @ p-NiFe prepared in example 12O4Representative Scanning Electron Micrographs (SEM) and Transmission Electron Micrographs (TEM); wherein, (a) and (b) are scanning electron micrographs, and (c) and (d) are transmission electron micrographs.
FIG. 3 is the G @ p-NiFe prepared in example 12O4Powder X-ray diffraction pattern (XRD) and thermogravimetric pattern (TG) of (a); wherein, (a) is XRD pattern, and (b) is TG pattern.
FIG. 4 is the G @ p-NiFe prepared in example 12O4Lithium ion battery performance of the electrode, at a current density of 1500mAg-1G @ p-NiFe2O4、G@NiFe2O4Pure NiFe2O4The cycle performance of (c).
FIG. 5 is the G @ p-NiFe prepared in example 12O4Sodium of electrodeIon Battery Performance, G @ p-NiFe2O4、G@NiFe2O4The electrode was at 200mA g-1Long term cycling stability.
Detailed Description
The present application will be described in detail with reference to examples, but the present application is not limited to these examples.
The raw materials in the examples of the present application were all purchased commercially, unless otherwise specified. The graphene oxide GO is prepared according to the literature (J.Mater.chem.,2011,21, 7376-.
The analysis method in the examples of the present application is as follows:
transmission electron microscopy analysis was performed using a transmission electron microscope (TEM, FEI Inc., USA, Tecnai F20).
Phase analysis of the compounds was performed using an X-ray powder diffractometer (XRD, Rigaku, Miniflex 600).
Scanning electron microscopy was performed using a field emission scanning electron microscope (FESEM, SU-8010, Hitachi, Japan).
Thermogravimetric analysis was performed using a simultaneous thermal analyzer (TG/DTA, STA449F3, Netzsch).
The battery performance test was performed using a battery test system (wuhan blue, CT 3001A).
Example 1
G@p-SiO2Synthesis of the composite material: 160mg of cetyltrimethylammonium bromide (CTAB) were dissolved in 30ml of H2O, 120ml ethanol and 1.5ml NH3.H2And O in a mixture. Then, 40mg of GO was dispersed in the above solution by ultrasonic waves, and then 1mL of Tetraethylorthosilicate (TEOS) was slowly added and kept stirring for 12 hours. By H2O washing and drying at 80 ℃, further annealing the product at 800 ℃ for 3 hours under Ar atmosphere to obtain G @ p-SiO2The composite comprises 6.3 wt% of graphene.
100mg of G @ p-SiO2(graphene composite with surface coated with porous silica) was added to a solution containing 0.5mmol of Fe (NO)3)3·9H2O and 0.25mmol Ni (NO)3)2·6H2O in 10mL of ethanol. After 10 minutes of sonication, the above solution was stirred at 45 ℃ to evaporate the ethanol. The product was annealed in Ar at 350 ℃ for 3 hours to give G @ SiO2@NiFe2O4Composite of NiFe2O4The content was 87 wt%, and was designated as p-N1.
Finally, the prepared G @ SiO2@NiFe2O4Etching with 1M NaOH solution at 50 deg.C for 12 hr to obtain G @ p-NiFe2O4And (c) a complex.
The product (80 wt%), conductive carbon black (10 wt%) and carboxymethyl cellulose (CMC10 wt%) were simultaneously put into an agate mortar for grinding, with deionized water as the dispersant and nickel foam as the current collector. And uniformly coating the ground slurry on the weighed dry foamed nickel, drying for 12 hours at 80 ℃ in vacuum, flattening and weighing the electrode plates, and obtaining the mass of the slurry on each electrode plate according to the mass difference before and after coating of the current collector. And continuously vacuum-drying the electrode plates for 2h at 80 ℃, and then putting the electrode plates into a glove box to be assembled with a button cell.
Assembling the button cell in a glove box filled with argon, wherein for a Lithium Ion Battery (LIB), the counter electrode and the diaphragm are respectively a lithium foil and a celgard 2300 membrane, and the electrolyte is 1M LiPF6In Ethylene Carbonate (EC): ethyl Methyl Carbonate (EMC): dimethyl carbonate (DMC), in a volume ratio of 1: 1: 1; for Sodium Ion Batteries (SIB), the counter electrode was sodium foil, the separator was a glass fiber membrane, and the electrolyte was 1M NaClO in EC4: diethyl carbonate (DEC) (1: 1 by volume) containing 10% by weight of Fluoroethylene (FEC). The cell was designated B-p-1.
The constant-current charge and discharge test mainly examines the charge and discharge specific capacity, the cycle performance and the rate capability of the lithium/sodium ion half-cell under different current densities. Cyclic voltammetry test at 0.2mV s on an electrochemical workstation (CHI660C)-1Is performed at the scanning rate of (1).
Example 2
The present embodiment is different from embodiment 1 in that:
G@p-SiO2synthesis of the composite material: 160mg of cetyltrimethylammonium bromide(CTAB) dissolved in 30ml H2O, 120ml ethanol and 1.5ml NH3.H2And O in a mixture. Then, 18.4mg of GO was dispersed in the above solution by ultrasonic waves, and then 1mL of Tetraethylorthosilicate (TEOS) was slowly added and kept stirring for 12 hours. By H2O washing and drying at 80 ℃, further annealing the product at 800 ℃ for 3 hours under Ar atmosphere to obtain G @ p-SiO2The composite comprises 3 wt% of graphene.
100mg of G @ p-SiO2(graphene composite with surface coated with porous silica) was added to a solution containing 0.3mmol of Fe (NO)3)3·9H2O and 0.15mmol Ni (NO)3)2·6H2O in 10mL of ethanol. After 10 minutes of sonication, the above solution was stirred at 45 ℃ to evaporate the ethanol. The product was dried at 300 ℃ under N2And carrying out medium annealing for 12 hours. Finally, the prepared G @ SiO2@NiFe2O4Etching with 1M NaOH solution at 50 deg.C for 12 hr to obtain G @ p-NiFe2O4Composite of NiFe2O4The content was 92% by weight, and the product was designated p-N2.
A battery B-p-2 was prepared in the same manner as in example 1, using p-N2.
Example 3
The present embodiment is different from embodiment 1 in that:
G@p-SiO2synthesis of the composite material: 160mg of cetyltrimethylammonium bromide (CTAB) were dissolved in 30ml of H2O, 120ml ethanol and 1.5ml NH3.H2And O in a mixture. Then, 81.3mg of GO was dispersed in the above solution by ultrasonic waves, and then 1mL of Tetraethylorthosilicate (TEOS) was slowly added and kept stirring for 12 hours. By H2O washing and drying at 80 ℃, further annealing the product at 800 ℃ for 12 hours under Ar atmosphere to obtain G @ p-SiO2The composite comprises 12 wt% of graphene.
100mg of G @ p-SiO2(graphene composite with surface coated with porous silica) was added to a solution containing 0.4mmol of Fe (NO)3)3·9H2O and 0.2mmol Ni (NO)3)2·6H2O in 10mL of ethanol. After 10 minutes of sonication, the above solution was stirred at room temperature to evaporate the ethanol. The product was dried at 500 ℃ under N2Intermediate annealing for 1 hour to obtain G @ SiO2@NiFe2O4A composite, finally preparing the prepared G @ SiO2@NiFe2O4Etching with 1M NaOH solution at 50 deg.C for 12 hr to obtain G @ p-NiFe2O4Composite of NiFe2O4The content was 80% by weight, and the product was designated p-N3.
A battery B-p-3 was produced in the same manner as in example 1, using p-N3.
Example 4
The present embodiment is different from embodiment 1 in that: the ferric nitrate salt and the nickel nitrate salt were replaced with ferric acetate and nickel acetate, respectively, and the product was designated as p-N4.
A battery B-p-4 was prepared in the same manner as in example 1, using p-N4.
Example 5
The present embodiment is different from embodiment 1 in that: g @ p-SiO2The annealing temperature in the synthesis of the composite material was 350 ℃ for 24 hours, and the product was designated as p-N5.
A battery B-p-5 was produced in the same manner as in example 1, using p-N5.
Comparative example 1
1) Pure NiFe2O4The preparation of (1):
containing 1mmol of Fe (NO) by evaporation3)3·9H2O and 0.5mmol Ni (NO)3)·2.6H2O in 10mL ethanol and annealing the mixture at 350 deg.C for 3h under Ar to prepare pure NiFe2O4The sample, noted D-p-N1.
2)G@NiFe2O4Synthesis of the composite material:
1mmol of Ni (NO)3)2·6H2O and 2mmol Fe (NO)3)3·9H2O was added to 70ml ethanol containing 40mg GO. After stirring for 30 minutes, the pH of the solution was adjusted to 10.0. Then, will beThe resulting mixture was transferred to a 100mL Teflon lined stainless steel autoclave and held at 180 ℃ for 20 hours. The precipitate was vacuum filtered, washed with water and ethanol, and dried at 80 ℃ for 12 hours to give G @ NiFe2O4The complex, labeled D-p-N2.
The prepared samples are respectively manufactured into button batteries by the same method as that of the embodiment 1, and are marked as D-B-p-1 and D-B-p-2, and the battery performance test is carried out by the same test method.
Example 6 sample characterization and Performance testing
The samples obtained in examples 1-4 and comparative example were characterized and tested for performance.
FIG. 2 is the G @ p-NiFe prepared in example 12O4Representative Scanning Electron Micrographs (SEM) (fig. (a) and (b)), and Transmission Electron Micrographs (TEM) (fig. (c) and (d)). As can be seen from SEM and TEM images, NiFe with porous structure2O4The nano-particles are coated with graphene and NiFe2O4The size of the nano particles is uniform and is concentrated in 3-5 nm; the pore size distribution is concentrated in the range of 1-10 nm. The morphology, particle size and pore size distribution of the samples p-N2-p-N5 are all similar to those of p-N1.
FIG. 3 is the G @ p-NiFe prepared in example 12O4Powder X-ray diffraction pattern (XRD) (a) and thermogravimetric pattern (TG) (b). XRD and electron diffraction pattern prove that the material contains NiFe2O4Crystal phase, NiFe can be identified2O4The phase of the card is consistent with that of the JCPDS No.10-0325 standard card. The TG plot indicates the NiFe content in the samples prepared in this example 12O4The mass fraction of (a) is 87%. FIG. 4 is the G @ p-NiFe prepared in example 12O4Lithium ion battery performance of the electrode, at a current density of 1500mAg-1G @ p-NiFe2O4(sample p-N1), G @ NiFe2O4(sample D-p-N2), pure NiFe2O4(sample D-p-N1). At 1.5Ag-1After 1100 cycles at high rate of G @ p-NiFe2O4、G@NiFe2O4Respectively keeping 240mA h g and 170mA h g-1The specific capacity of (A). Preparation of samples p-N2-p-N5The prepared lithium ion battery had cycle performance similar to that of sample p-N1.
FIG. 5 is the G @ p-NiFe prepared in example 12O4Sodium ion Battery Performance of the electrode, G @ p-NiFe2O4、G@NiFe2O4The electrode was at 200mA g-1Long term cycling stability. At 0.2Ag-1After 300 cycles at a rate of G @ p-NiFe2O4、G@NiFe2O4Respectively keeping 207 and 142mA h g-1The specific capacity of (A). The cycling performance of the sodium ion batteries prepared from samples p-N2-p-N5 was similar to that of sample p-N1.
Although the present application has been described with reference to a few embodiments, it should be understood that various changes, substitutions and alterations can be made herein without departing from the spirit and scope of the application as defined by the appended claims.

Claims (10)

1. Porous NiFe2O4The graphene composite material is characterized by comprising a graphene layer and porous NiFe2O4A layer; the porous NiFe2O4The layers coat both surfaces of the graphene layer.
2. Porous NiFe according to claim 12O4Graphene composite material, characterized in that the porous NiFe2O4NiFe in the layer2O4Has a porous structure and the pore size distribution is 1-10 nm;
preferably, the porous NiFe2O4Layer opposite to the porous NiFe2O4The mass content of the graphene composite material is 80-92 wt%;
preferably, the porous NiFe2O4Layer opposite to the porous NiFe2O4The mass content of the graphene composite material is 85-90 wt%.
3. Porous NiFe2O4The preparation method of the graphene composite material is characterized by comprising the following steps:
a) coating porous SiO on two surfaces of graphene layer2Layer to obtain G @ p-SiO2；
b) At G @ p-SiO2Coated with NiFe on both surfaces2O4Layer to obtain G @ p-SiO2@NiFe2O4；
c)G@p-SiO2@NiFe2O4Etching the-P to obtain G @ P-NiFe2O4I.e. the porous NiFe2O4Graphene composite materials.
4. Porous NiFe according to claim 32O4The preparation method of the nano composite material is characterized in that in the step a), G @ p-SiO2The content of the graphene in the graphene is 3-12 wt%;
preferably, step a) comprises:
a21) dissolving a surfactant in a mixed solution containing water, ethanol and ammonia water to obtain a solution I;
a22) dispersing graphene oxide in the solution I, adding a silicon source, reacting, further annealing at 300-800 ℃ for more than 1 hour in an inert atmosphere to obtain G @ p-SiO2；
Preferably, the surfactant in step a21) is a cationic surfactant; the cationic surfactant is selected from at least one of alkyl quaternary ammonium salt;
preferably, the cationic surfactant is selected from at least one of cetyl trimethyl ammonium bromide, cetyl trimethyl ammonium chloride, dodecyl trimethyl ammonium bromide and dodecyl trimethyl ammonium chloride;
preferably, the concentration of surfactant in said solution I in step a21) is between 0.5 and 1 wt%;
preferably, the volume ratio of water, ethanol and ammonia water in the solution I in the step a21) is 1: (3-10): (0.01-0.04);
preferably, the silicon source in step a22) is selected from ethyl orthosilicate;
preferably, the inert atmosphere in step a22) is selected from at least one of nitrogen and noble gases;
preferably, step b) comprises:
g @ p-SiO2Adding the mixture into a solution containing ferric salt and nickel salt, dispersing uniformly, removing the solvent, and annealing at 300-500 ℃ for more than 1 hour in an inert atmosphere to obtain the G @ p-SiO2@NiFe2O4；
Preferably, the molar ratio of the iron in the iron salt to the nickel in the nickel salt is 2 (0.1-1).
5. Porous NiFe according to claim 32O4The preparation method of the nano composite material is characterized by comprising the following steps:
1. coating porous silicon dioxide on the surface of the graphene sheet layer to obtain a graphene porous silicon dioxide compound, and coating G @ p-SiO2Is represented by the formula G @ p-SiO2The content of the graphene in the graphene is 3-12 wt%;
2. g @ p-SiO2Adding the mixture into an ethanol solution containing ferric salt and nickel salt, uniformly dispersing, then completely evaporating the ethanol solvent, and annealing the obtained product in an inert atmosphere at the temperature of 300-500 ℃ for more than 1 hour to obtain the G @ SiO2@NiFe2O4A complex;
the molar ratio of iron to nickel in the ferric salt and the nickel salt is 2 (0.1-1), wherein the ferric salt is one or more of ferric nitrate and ferric carboxylate; the nickel salt is one or more of nickel nitrate or nickel carboxylate;
3. SiO in the product of the step 2 is dissolved in hot sodium hydroxide solution or hydrogen fluoride solution2Etching and removing to obtain G @ p-NiFe2O4I.e. said porous NiFe2O4A nanocomposite material.
6. Porous NiFe according to claim 32O4A process for the preparation of a nanocomposite material,characterized in that the porous NiFe2O4The nano composite material has the following structural general formula: g @ p-NiFe2O4；
Wherein G represents graphene, p-NiFe2O4NiFe representing porous structure2O4The compound comprises graphene as the innermost layer and NiFe as the outer layer2O4Which is coated on the surface of the graphene layer.
7. Porous NiFe according to claim 1 or 22O4Nanocomposite, porous NiFe prepared according to the method of any one of claims 3 to 62O4Use of at least one of the nanocomposites in an electrode material.
8. Porous NiFe according to any one of claims 1 or 22O4Nanocomposite, porous NiFe prepared according to the method of any one of claims 3 to 62O4Use of at least one of the nanocomposites in primary or secondary electrochemical generators, high energy generators, electrochemiluminescence modulation systems.
9. Porous NiFe according to claim 1 or 22O4Nanocomposite, porous NiFe prepared according to the method of any one of claims 3 to 62O4Use of at least one of the nanocomposites in an electrode material for primary or secondary electrochemical generators, high energy generators, electrochemiluminescence modulation systems.
10. A secondary battery characterized in that a negative electrode material for the secondary battery contains the porous NiFe as claimed in claim 1 or 22O4Nanocomposite, porous NiFe produced according to the method of any one of claims 3 to 162O4At least one of a nanocomposite;
preferably, the secondary battery includes a lithium ion battery, a sodium ion battery, or a potassium ion battery.
CN201910954059.7A 2019-10-09 2019-10-09 Porous NiFe2O4Graphene composite material and preparation method and application thereof Active CN110828788B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910954059.7A CN110828788B (en) 2019-10-09 2019-10-09 Porous NiFe2O4Graphene composite material and preparation method and application thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910954059.7A CN110828788B (en) 2019-10-09 2019-10-09 Porous NiFe2O4Graphene composite material and preparation method and application thereof

Publications (2)

Publication Number Publication Date
CN110828788A true CN110828788A (en) 2020-02-21
CN110828788B CN110828788B (en) 2021-08-10

Family

ID=69548802

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910954059.7A Active CN110828788B (en) 2019-10-09 2019-10-09 Porous NiFe2O4Graphene composite material and preparation method and application thereof

Country Status (1)

Country Link
CN (1) CN110828788B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022019605A1 (en) * 2020-07-21 2022-01-27 삼성에스디아이주식회사 Porous composite, anode and lithium battery each including same, and method for preparing same

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102276244A (en) * 2011-05-19 2011-12-14 东华大学 Alcohol-heating method for preparing cobalt nickel ferrite / graphene magnetic nano composite powder
CN102779994A (en) * 2012-07-23 2012-11-14 浙江大学 Iron-based complex oxide/graphene composite and preparation method and application thereof
CN103871755A (en) * 2014-03-05 2014-06-18 南京理工大学 N-doped graphene/nickel ferrite nanometer compound material and preparation thereof
CN104051729A (en) * 2014-07-04 2014-09-17 电子科技大学 Preparation method of NiFe2O4/graphene composite material for lithium battery cathode
WO2018085936A1 (en) * 2016-11-10 2018-05-17 Polyvalor, Limited Partnership Piezoelectric composite, ink and ink cartridge for 3d printing, bifunctional material comprising the piezoelectric composite, manufacture and uses thereof
CN110182858A (en) * 2019-07-09 2019-08-30 南京林业大学 The hollow NiCo of high-sequential2O4The preparation method of electrode material

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102276244A (en) * 2011-05-19 2011-12-14 东华大学 Alcohol-heating method for preparing cobalt nickel ferrite / graphene magnetic nano composite powder
CN102779994A (en) * 2012-07-23 2012-11-14 浙江大学 Iron-based complex oxide/graphene composite and preparation method and application thereof
CN103871755A (en) * 2014-03-05 2014-06-18 南京理工大学 N-doped graphene/nickel ferrite nanometer compound material and preparation thereof
CN104051729A (en) * 2014-07-04 2014-09-17 电子科技大学 Preparation method of NiFe2O4/graphene composite material for lithium battery cathode
WO2018085936A1 (en) * 2016-11-10 2018-05-17 Polyvalor, Limited Partnership Piezoelectric composite, ink and ink cartridge for 3d printing, bifunctional material comprising the piezoelectric composite, manufacture and uses thereof
CN110182858A (en) * 2019-07-09 2019-08-30 南京林业大学 The hollow NiCo of high-sequential2O4The preparation method of electrode material

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022019605A1 (en) * 2020-07-21 2022-01-27 삼성에스디아이주식회사 Porous composite, anode and lithium battery each including same, and method for preparing same

Also Published As

Publication number Publication date
CN110828788B (en) 2021-08-10

Similar Documents

Publication Publication Date Title
CN110224129B (en) MOFs derivative coated NCM ternary positive electrode material and preparation method thereof
CN105895886B (en) A kind of sodium-ion battery transition metal phosphide/porous anode composite and preparation method thereof
CN111180709B (en) Carbon nano tube and metal copper co-doped ferrous oxalate lithium battery composite negative electrode material and preparation method thereof
Zhang et al. Phosphorus-modified Fe 4 N@ N, P co-doped graphene as an efficient sulfur host for high-performance lithium–sulfur batteries
CN112349885B (en) Modified lithium ion battery positive electrode material and preparation method thereof
CN113540466B (en) Metal boride and borate composite coated modified nickel-cobalt-manganese ternary material precursor and preparation method thereof
Chen et al. MOF-derived bimetal oxides NiO/NiCo 2 O 4 with different morphologies as anodes for high-performance lithium-ion battery
CN110600697A (en) Sulfur positive electrode material with core-shell structure, preparation method of sulfur positive electrode material, lithium-sulfur battery positive electrode piece and lithium-sulfur battery
CN111591971B (en) Titanium lithium phosphate nanocomposite, preparation method and application in aqueous battery
CN113651303A (en) Preparation method of nano flaky iron phosphate and LiFePO prepared by using same4Positive electrode active material/C
CN111342020B (en) Silicon-based negative electrode material, preparation method thereof and lithium ion battery
CN115064665B (en) Doped modified carbon-coated sodium titanium phosphate composite material and preparation method and application thereof
CN113036101A (en) Carbon-coated pyrophosphate and preparation method and application thereof
CN110571431B (en) Li2FeSiO4@ mesoporous carbon lithium ion battery cathode material and preparation method thereof
CN111933904A (en) Bimetal sulfide and preparation method thereof, compound and preparation method thereof, lithium-sulfur positive electrode material and lithium-sulfur battery
CN111653750A (en) Preparation method of carbon nitride modified molybdenum disulfide lithium ion battery cathode material
CN102157727B (en) Preparation method for nano MnO of negative electrode material of lithium ion battery
CN108400296A (en) Heterogeneous element doped ferroferric oxide/graphene negative material
CN110828788B (en) Porous NiFe2O4Graphene composite material and preparation method and application thereof
CN116177556B (en) Sodium-electricity positive electrode material, precursor thereof, preparation method and application
CN107845787B (en) Pomegranate-shaped Fe3O4Preparation method of @ N-C lithium battery negative electrode material
CN113346087B (en) Hybrid phosphate open framework material composite high-nickel positive electrode material and preparation method thereof
CN115140783A (en) Ternary positive electrode material precursor and preparation method and application thereof
CN112002893B (en) Research of taking antimony-based composite metal sulfide as potassium ion battery negative electrode material
CN110828787B (en) NiFe2O4Nano composite material and preparation method and application thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant