CN109449008A - A kind of preparation method of the hollow core-shell structure electrode material of self-supporting and its application in lithium-sulfur cell and supercapacitor - Google Patents

A kind of preparation method of the hollow core-shell structure electrode material of self-supporting and its application in lithium-sulfur cell and supercapacitor Download PDF

Info

Publication number
CN109449008A
CN109449008A CN201811339232.4A CN201811339232A CN109449008A CN 109449008 A CN109449008 A CN 109449008A CN 201811339232 A CN201811339232 A CN 201811339232A CN 109449008 A CN109449008 A CN 109449008A
Authority
CN
China
Prior art keywords
electrode material
self
preparation
shell structure
supporting
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
CN201811339232.4A
Other languages
Chinese (zh)
Other versions
CN109449008B (en
Inventor
邵国胜
张鹏
苗富军
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.)
Zhengzhou New Century Material And Genome Engineering Research Institute Co Ltd
Original Assignee
Zhengzhou New Century Material And Genome Engineering Research Institute Co Ltd
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 Zhengzhou New Century Material And Genome Engineering Research Institute Co Ltd filed Critical Zhengzhou New Century Material And Genome Engineering Research Institute Co Ltd
Priority to CN201811339232.4A priority Critical patent/CN109449008B/en
Publication of CN109449008A publication Critical patent/CN109449008A/en
Application granted granted Critical
Publication of CN109449008B publication Critical patent/CN109449008B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M4/00Electrodes
    • H01M4/02Electrodes composed of, or comprising, active material
    • H01M4/36Selection of substances as active materials, active masses, active liquids
    • H01M4/58Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates
    • H01M4/583Carbonaceous material, e.g. graphite-intercalation compounds or CFx
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G11/00Hybrid capacitors, i.e. capacitors having different positive and negative electrodes; Electric double-layer [EDL] capacitors; Processes for the manufacture thereof or of parts thereof
    • H01G11/22Electrodes
    • H01G11/30Electrodes characterised by their material
    • H01G11/32Carbon-based
    • H01G11/40Fibres
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/05Accumulators with non-aqueous electrolyte
    • H01M10/052Li-accumulators
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/13Energy storage using capacitors

Abstract

The present invention relates to a kind of preparation method of the hollow core-shell structure electrode material of self-supporting and its applications in lithium-sulfur cell and supercapacitor.The preparation method of the hollow core-shell structure electrode material of the self-supporting includes: that precursor solution is carried out electrostatic spinning, carbonization treatment, Surface Oxidation Modification processing, coated with silica modification, phenolic resin coating modification, carbonization treatment, etching silicon dioxide.The preparation method of the hollow core-shell structure electrode material of self-supporting provided by the invention is allowed to combine with sulphur, can directly improve the electric conductivity of sulphur and prevent the diffusion and transfer of sulphur by constructing the carbon-based material of multilayered structure;Meanwhile the titanium dioxide on electrode material can be combined with element sulphur, formed chemical bonding between the two, be can be further improved the stability of sulphur anode, thus the captured sulfur result of electrode material can be improved, optimize the energy-storage property of lithium-sulfur cell.

Description

The preparation method of a kind of hollow core-shell structure electrode material of self-supporting and its in lithium sulphur electricity Application in pond and supercapacitor
Technical field
The invention belongs to electrode material fields, and in particular to a kind of preparation side of the hollow core-shell structure electrode material of self-supporting Method and its application in lithium-sulfur cell and supercapacitor.
Background technique
Currently in the case where the historical background for greatly developing clean energy resource is advocated in the whole world, energy density is higher for exploitation, cycle life It is longer, system cost is lower, the better energy storage technology of security performance has become an important research direction.Lithium-sulfur cell be with Element sulphur is as anode, a kind of lithium battery of the lithium metal as cathode.Elemental sulfur rich reserves in the earth have price The features such as cheap, environmental-friendly.Using sulphur as the lithium-sulfur cell of positive electrode, materials theory specific capacity and battery theory ratio Energy is higher, respectively reaches 1675mAh/g and 2600Wh/kg, the reason of significantly larger than commercial widely applied cobalt acid lithium battery By specific capacity (< 150mAh/g).Meanwhile sulphur is a kind of environment amenable element, is not polluted substantially to environment, it is comprehensive next It sees, lithium-sulfur cell is a kind of very promising lithium battery.
The application of lithium-sulfur cell still remains a series of problems at present, specifically includes that sulphur is non-conductive, the dissolution of polysulfide Lead to structural instability etc. with sulphur volume expansion in shuttle effect and charge and discharge process, factors above is likely to lead to battery Damage, to limit the development of lithium-sulfur cell.Therefore, key component of the sulphur anode as lithium-sulfur cell, is largely fixed The basic performance of lithium-sulfur cell.
Notification number is that the Chinese patent of CN106449159B discloses a kind of capacitor of carbon fiber package metal oxide It is that the intracavitary package metal oxide nano of carbon nano-fiber is prepared using electrostatic spinning technique with flexible electrode and preparation method Particle flexible membrane, volume change when being worked using carbon nano-fiber for metal oxide nanoparticles are provided cushion space, subtracted The bulk effect of small metal oxide.Captured sulfur result of the electrode material when being applied to lithium-sulfur cell is poor, is unfavorable for lithium sulphur The raising of battery high rate performance and cycle performance.
Summary of the invention
The purpose of the present invention is to provide a kind of preparation methods of the hollow core-shell structure electrode material of self-supporting, existing to solve There is the problem of the captured sulfur result difference of lithium-sulfur cell.
Second object of the present invention is to provide a kind of application of above-mentioned electrode material in lithium-sulfur cell, existing to solve There is the problem of high rate performance and poor circulation of lithium-sulfur cell.
Third object of the present invention is to provide a kind of application of above-mentioned electrode material in supercapacitor, to solve The problem of the energy storage capacity difference of existing supercapacitor.
To achieve the above object, the technical solution of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention It is:
A kind of preparation method of the hollow core-shell structure electrode material of self-supporting, comprising the following steps:
1) titanium tetrachloride, polyacrylonitrile are dissolved in solvent, obtain precursor solution, precursor solution is subjected to Static Spinning Silk, obtains polyacrylonitrile nanofiber cloth;
2) polyacrylonitrile nanofiber cloth is subjected under protective atmosphere carbonization treatment, obtains carbon nano-fiber/titanium dioxide Titanium composite material;
3) carbon nano-fiber/composite titania material is subjected to Surface Oxidation Modification processing, it is compound obtains surface modification Fiber;
4) it using surface modified composite fiber as active template, is immersed in alcohols solvent, ammonium hydroxide, water, just is then added Silester is reacted, and coated with silica modified composite fiber is obtained;
5) coated with silica modified composite fiber is immersed in alcohols solvent, ammonium hydroxide, water, resorcinol is then added It is reacted with formalin, obtains phenolic resin coating modification composite fibre;
6) phenolic resin coating modification composite fibre is subjected to carbonization treatment under protective atmosphere, it then will be after carbonization treatment Obtained product immerses in hydrofluoric acid, etch away coated with silica layer to get.
The preparation method of the hollow core-shell structure electrode material of self-supporting provided by the invention passes through building multilayered structure Carbon-based material is allowed to combine with sulphur, can directly improve the electric conductivity of sulphur and prevent the diffusion and transfer of sulphur;Meanwhile electrode Titanium dioxide on material can be combined with element sulphur, form chemical bonding between the two, can be further improved sulphur anode Stability, thus the captured sulfur result of electrode material can be improved, optimize the energy-storage property of lithium-sulfur cell.In addition, side made above Method also has the characteristics that preparation process is simple, process is short, device dependence is low, is suitable for industrialization large-scale production.
In step 1), to further increase carbon, titanium dioxide and the synergy of sulphur, optimize the ratio of carbon and titanium dioxide Example, it is preferred that the additional amount that every gram of polyacrylonitrile corresponds to titanium tetrachloride is 0.1-1ml.
In step 2), carbonization treatment, which can satisfy presoma, can accordingly be converted into carbon-based material and metal oxide nano Particle, on this basis, to improve carbonization treatment efficiency, it is preferred that the temperature of the carbonization treatment is 900-1100 DEG C, The time of carbonization treatment is 1h.
In step 3), being handled by Surface Oxidation Modification can be improved the active site of material and improves wellability, Jin Eryou Conducive to the progress of subsequent step, from taking into account modification efficiency and modified effect aspect, it is preferred that at the Surface Oxidation Modification Reason is to immerse carbon nano-fiber/composite titania material in concentrated nitric acid to carry out immersion treatment.
Step 4) is the coating modification process of silica, for the being evenly coated property for improving silicon dioxide layer, it is preferred that every The dosage that gram polyacrylonitrile corresponds to ethyl orthosilicate is 1-5ml.
Step 5) is the coating modification process of phenolic resin, for the being evenly coated property for improving novolac resin layer, it is preferred that every The dosage that gram polyacrylonitrile corresponds to resorcinol is 0.1-0.5g, and the dosage of corresponding formalin is 0.15-0.75ml, the first The mass concentration of aldehyde solution is 35-40%.
Step 6) is the carbonisation of phenolic resin, to improve carbonization treatment efficiency, it is preferred that the temperature of the carbonization treatment Degree is 700-900 DEG C, and the time of carbonization treatment is 1h.In the step, by hf etching, it can be obtained in self-supporting The electrode material of empty core-shell structure characteristic, the electrode material have excellent three-dimensional conductive network and overlength 1-dimention nano knot Structure is conducive to the quick collection and transfer of electronics.In addition, the electrode material for preparing in this way while also having interconnects Three-dimensional porous structure and hollow core-shell structure feature, can greatly shorten ion dilation angle, be conducive in electrolyte from The quick transmission of son.
Further to prepare multilayer hollow core-shell structure electrode material, Hierarchical porosity gap structure is constructed, higher ratio is provided Surface area, and more active sites are provided for ionic adsorption, it is preferred that it is repeated in and carries out step 4) and step 5), then Step 6) is carried out again.
The electrode material prepared using the above method, since it is with good self-supporting characteristic, electrode production process In do not need collector, conductive agent and binder etc., furthermore continuous electronic conduction access is also advantageous to the fast of electronics Speed is collected and transfer, promotes the raising of high rate performance;Simultaneously the electrode material can directly as flexible substrate, it is convenient and other Dissimilar materials is compound, and then is conducive to the assembling of high performance electrode material.This three-dimensional porous structure can promote electrolyte to Electrode interior is quickly spread, and improves the ion diffusion rates of electrode material.
The technical solution of the application of above-mentioned electrode material of the invention in lithium-sulfur cell is:
Electrode material made from a kind of preparation method using the hollow core-shell structure electrode material of above-mentioned self-supporting is in lithium sulphur Application in battery.
Using the lithium-sulfur cell of above-mentioned electrode material, ideal captured sulfur result is may be implemented in the positive electrode of lithium-sulfur cell, The problems such as sulphur volume expansion and dissolution can not only be inhibited, it also can effectively avoid sulphur shuttle effect.With electrode material preparation Lithium-sulfur cell, the face load capacity and mass fraction of sulphur can respectively reach 6mg/cm2With 90% or more, and still there is good electricity Capacity and service life cycle show good electrochemical energy storage property.
The technical solution of the application of above-mentioned electrode material of the invention in supercapacitor is:
Electrode material made from a kind of preparation method using the hollow core-shell structure electrode material of above-mentioned self-supporting is super Application in capacitor.
Had good using the supercapacitor of above-mentioned electrode material using the hollow core-shell structure electrode material of self-supporting Good three-dimensional continuous conduction channel can promote the quick collection of electronics and transfer, Hierarchical porosity gap structure are conducive to the quick of ion Diffusion has many advantages, such as that specific capacitance is high, stability is good, further improves the energy storage effect of supercapacitor.
Detailed description of the invention
Fig. 1 is the flow chart of the preparation method embodiment 1 of the hollow core-shell structure electrode material of self-supporting of the present invention;
Fig. 2 is the 1 the electrode obtained material of preparation method embodiment of the hollow core-shell structure electrode material of self-supporting of the present invention Optical photograph;
Fig. 3 is the 1 the electrode obtained material of preparation method embodiment of the hollow core-shell structure electrode material of self-supporting of the present invention SEM figure;
Fig. 4 is the 20 the electrode obtained material of preparation method embodiment of the hollow core-shell structure electrode material of self-supporting of the present invention SEM figure;
Fig. 5 is the forthright again of the lithium-sulfur cell that the Application Example 1 of electrode material of the invention in lithium-sulfur cell is related to It can curve;
Fig. 6 is the cyclicity for the lithium-sulfur cell that the Application Example 1 of electrode material of the invention in lithium-sulfur cell is related to It can curve;
Fig. 7 is the electricity for the supercapacitor that the Application Example 1 of electrode material of the invention in supercapacitor is related to Stream-voltage curve;
Fig. 8 is the electricity for the supercapacitor that the Application Example 1 of electrode material of the invention in supercapacitor is related to Pressure-discharge time curve.
Specific embodiment
The present invention constructs a kind of carbon substrate with multilayered structure mainly from the design angle of electrode material Material, is allowed to combine with sulphur, the electric conductivity of Lai Tigao sulphur and the diffusion and transfer for preventing sulphur.In addition, the multivalence gold such as titanium dioxide Chemical bonding can also be formed between the two, may further improve the stability of sulphur anode in conjunction with element sulphur by belonging to oxide.Its In, the Surface Oxidation Modification step of carbon nano-fiber, the soaking time in concentrated nitric acid is suitable in 48h or more;Surface oxidation changes Property after prepare coated with silica layer, the dosage that every gram of polyacrylonitrile correspond to ammonium hydroxide can be for 1-3ml, and the dosage of correspondence water can be with For 2-6ml, the reaction time is suitable in 4h or more, with being advisable with a thickness of 20-40nm for silicon dioxide layer;Prepare novolac resin layer Step, the dosage that every gram of polyacrylonitrile corresponds to ammonium hydroxide can be 1-3ml, and the dosage of corresponding water can be 2-6ml, and the reaction time is suitable Preferably in 12h or more, with being advisable with a thickness of 10-20nm for novolac resin layer.
Embodiments of the present invention are described further combined with specific embodiments below.Involved in following embodiment Reagent is commercially available customary commercial, and the mass concentration of concentrated nitric acid is 67-69%, and the mass concentration of ammonium hydroxide is 24-26%, and formaldehyde is molten The mass concentration of liquid is 35-40%.
The number-average molecular weight of polyacrylonitrile is 150000 (Mike woods reagents).
The embodiment 1 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, flow chart such as Fig. 1 institute Show, prepared using following steps:
1) 0.5ml titanium tetrachloride and 1g polyacrylonitrile are successively dissolved into 10ml n,N-Dimethylformamide, stirring is extremely Clarification, obtains precursor solution.
2) electrostatic spinning technique is utilized, 2ml precursor solution is poured into injector for medical purpose every time (syringe volume is 10ml;The a length of 2.5cm of syringe needle;Syringe tip outer diameter is 0.7mm;Distance of the syringe tip away from collecting board be 15cm), spinning is carried out under conditions of electrode voltage is 10kV, obtaining polyacrylonitrile nanofiber cloth, (polyacrylonitrile nano is fine The diameter of dimension is 200-300nm).
3) polyacrylonitrile nanofiber cloth (4cm*4cm) obtained by step 2) is placed in tube furnace, in inert atmosphere protection Under, 1000 DEG C are warming up to the rate of 5 DEG C/min by room temperature, high temperature cabonization processing is completed in 1000 DEG C of heat preservation 1h, obtains carbon and receive Rice fiber/composite titania material.
4) carbon nano-fiber/composite titania material is impregnated in 48h in concentrated nitric acid, then takes out and uses deionized water It repeatedly washs repeatedly, realizes that carbon nano-fiber surface is modified, increase active site and improve the wetting property with solution, obtain table Face modified composite fiber.
5) surface modified composite fiber obtained by step 4) is immersed in 20ml isopropanol as active template, and successively 2ml ammonium hydroxide, 4ml water and 4ml ethyl orthosilicate is added dropwise, 6h is kept, so that the silicon dioxide layer with a thickness of 50nm is uniformly wrapped Surface modified composite fiber surface is overlayed on, coated with silica modified composite fiber is obtained.
6) it using coated with silica modified composite fiber obtained by step 5) as template, is immersed in 20ml ethyl alcohol, and 2ml ammonium hydroxide, 4ml water, 0.2g resorcinol and 0.3ml formalin is successively added dropwise, keeps carrying out for 24 hours to react fully, So that the novolac resin layer with a thickness of 20nm is evenly coated at coated with silica modified composite fiber surface, phenolic resin is obtained Coating modification composite fibre.
7) phenolic resin coating modification composite fibre obtained by step 6) is placed in tube furnace, under inert atmosphere protection, 900 DEG C are warming up to the rate of 5 DEG C/min by room temperature, high temperature cabonization processing is completed in 900 DEG C of heat preservation 1h, high temperature cabonization is handled Product is obtained afterwards to immerse in the hydrofluoric acid that mass concentration is 5%, keeps 6h, etches away silicon dioxide layer to get in carbon-coated The empty carbon-based composite nano-fiber material of core-shell structure, and still there is good three-dimensional self-supporting characteristic.
The embodiment 2 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 1), four chlorinations The additional amount of titanium is 0.1ml.
The embodiment 3 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 1), four chlorinations The additional amount of titanium is 0.2ml.
The embodiment 4 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 1), four chlorinations The additional amount of titanium is 1ml.
The embodiment 5 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 3), pyrocarbon The temperature for changing processing is 900 DEG C.
The embodiment 6 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 3), pyrocarbon The temperature for changing processing is 1100 DEG C.
The embodiment 7 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 1), four chlorinations The additional amount of titanium is 0.1ml, and in step 3), the temperature of high temperature cabonization processing is 900 DEG C.
The embodiment 8 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 1), four chlorinations The additional amount of titanium is 0.2ml, and in step 3), the temperature of high temperature cabonization processing is 900 DEG C.
The embodiment 9 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 1), four chlorinations The additional amount of titanium is 1ml, and in step 3), the temperature of high temperature cabonization processing is 900 DEG C.
The embodiment 10 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 1), four chlorinations The additional amount of titanium is 0.1ml, and in step 3), the temperature of high temperature cabonization processing is 1100 DEG C.
The embodiment 11 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 1), four chlorinations The additional amount of titanium is 0.2ml, and in step 3), the temperature of high temperature cabonization processing is 1100 DEG C.
The embodiment 12 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 1), four chlorinations The additional amount of titanium is 1ml, and in step 3), the temperature of high temperature cabonization processing is 1100 DEG C.
The embodiment 13 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 5), positive silicic acid The additional amount of ethyl ester is 1ml.
The embodiment 14 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 5), positive silicic acid The additional amount of ethyl ester is 2ml.
The embodiment 15 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 5), positive silicic acid The additional amount of ethyl ester is 3ml.
The embodiment 16 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 5), positive silicic acid The additional amount of ethyl ester is 5ml.
The embodiment 17 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 6), isophthalic two The dosage of phenol is 0.1g, and the dosage of formalin is 0.1ml.
The embodiment 18 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 6), isophthalic two The dosage of phenol is 0.1g, and the dosage of formalin is 0.15ml.
The embodiment 19 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, in step 6), isophthalic two The dosage of phenol is 0.5g, and the dosage of formalin is 0.75ml.
The embodiment 20 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, be repeated in step 5) and Step 6), number of repetition are primary, building double layer hollow core-shell structure.
The embodiment 21 of the preparation method of the hollow core-shell structure electrode material of self-supporting of the invention, with self-supporting hollow core The processing step of the preparation method embodiment 1 of shell structure electrode material is essentially identical, and difference is only that, be repeated in step 5) and Step 6), number of repetition are secondary, building multilayer hollow core-shell structure.
The Application Example 1 of electrode material of the invention in lithium-sulfur cell, including sulphur anode, cathode of lithium, diaphragm, electrolysis Liquid, sulphur anode include the 1 the electrode obtained material of preparation method embodiment of sulphur and the hollow core-shell structure electrode material of self-supporting, are used Conventional melt consolidates sulphur mode (being uniformly mixed electrode material and sulphur in closed container, keep the temperature 12h at 150 DEG C), the face of sulphur Load capacity and weight percent are respectively 6mg/cm2With 90%;Cathode of lithium is common metal lithium piece;Diaphragm is Celgard 2400;It is 2% vinylene carbonate, 1M LiPF that electrolyte, which is containing mass concentration,6Ethylene carbonate/diethyl carbonate (body Product is than being 3:7) mixed solution, being built into specification is the button-shaped lithium-sulfur cell of CR 2025 (by lithium-sulfur cell before being tested Stand 6h).
The Application Example 2-21 of electrode material of the invention in lithium-sulfur cell uses the hollow core-shell structure electricity of self-supporting The preparation method embodiment 2-21 the electrode obtained material of pole material, Application Example 1 of the reference electrode material in lithium-sulfur cell Construct corresponding lithium-sulfur cell.
The Application Example 1 of electrode material of the invention in supercapacitor, uses specification for CR2025 button mode Construct symmetric form supercapacitor.Wherein the preparation method of the hollow core-shell structure electrode material of the direct self-supporting of positive and negative anodes is implemented 1 the electrode obtained material of example, electrolyte are 1M KOH aqueous solution, and diaphragm is conventional glass fibers diaphragm.
The Application Example 2-21 of electrode material of the invention in supercapacitor, uses the hollow core-shell structure of self-supporting The preparation method embodiment 2-21 the electrode obtained material of electrode material, application implementation of the reference electrode material in supercapacitor Example 1 constructs corresponding symmetric form supercapacitor.
Test example 1
The optical photograph of the 1 the electrode obtained material of preparation method embodiment of the hollow core-shell structure electrode material of self-supporting is as schemed Shown in 2, in figure, electrode material can be cut into the shapes such as disc as needed, show good Scalability;Tweezers can be used The disc electrode material of black is picked up, shows that it, with good self-supporting, can be used as flexible substrate use.
The SEM of 1 the electrode obtained material of preparation method embodiment schemes the electrode fig. 3, it is shown that embodiment preparation Material has good three-dimensional self-supporting characteristic and hollow core-shell structure.
The SEM figure of 20 the electrode obtained material of preparation method embodiment is as shown in Figure 4, it can be seen that it is with double layer hollow Core-shell structure, and the appearance regularity and consistency of material are preferable, show good three-dimensional self-supporting characteristic.It is indicated above that With electrode material shown in Fig. 3 (hollow core-shell structure carbon nano-fiber) for template, related procedure according to the invention can be at Function synthesis has the carbon nano-fiber materials of double layer hollow core-shell structure.
Test example 2
The electrochemistry for the lithium-sulfur cell that Application Example 1 of this test example detecting electrode material in lithium-sulfur cell is related to Can, as a result as shown in Figure 5 and Figure 6, the chemical property and the lithium of the lithium-sulfur cell that other lithium-sulfur cell Application Examples are related to Sulphur battery is suitable.
In fig. 5 and fig., in 27 DEG C of insulating boxs, testing result illustrates this hollow nucleocapsid for the detection of assembly device Structure carbon nano-fiber has good captured sulfur result as the electrode material of lithium-sulfur cell, can be effectively improved the electric conductivity of sulphur And its utilization rate is improved, it especially can be good at inhibiting the dissolution of sulphur to shuttle to a certain extent, therefore device entirety body Reveal good high rate performance and cyclical stability, is 1000mAh/g in 0.1C condition discharge capacity.
Test example 3
The electrification for the supercapacitor that Application Example 1 of this test example detecting electrode material in supercapacitor is related to Learn performance, as a result as shown in Figure 7 and Figure 8, the electrochemistry for the supercapacitor that other supercapacitor applications embodiments are related to It can be suitable with the supercapacitor.
In Fig. 7 and Fig. 8, the testing conditions of device are room temperature condition, close to the cyclic voltammetry curve and triangular symmetrical of rectangle Charging and discharging curve all illustrate that hollow core-shell structure carbon nano-fiber has ideal electricity as the electrode material of supercapacitor Hold energy storage characteristic, embodies multiplying power energy storage characteristic outstanding.
By the above test result it is found that the hollow core-shell structure electrode material of self-supporting provided by the invention is being applied to lithium sulphur There is good captured sulfur result, corresponding lithium-sulfur cell device has capacitance outstanding, high rate performance and circulation when battery Stability.When being applied to supercapacitor, good energy storage effect is shown.

Claims (10)

1. a kind of preparation method of the hollow core-shell structure electrode material of self-supporting, which comprises the following steps:
1) titanium tetrachloride, polyacrylonitrile are dissolved in solvent, obtain precursor solution, precursor solution is subjected to electrostatic spinning, Obtain polyacrylonitrile nanofiber cloth;
2) polyacrylonitrile nanofiber cloth is subjected under protective atmosphere carbonization treatment, it is multiple obtains carbon nano-fiber/titanium dioxide Condensation material;
3) carbon nano-fiber/composite titania material is subjected to Surface Oxidation Modification processing, obtains surface modified composite fiber;
4) it using surface modified composite fiber as active template, is immersed in alcohols solvent, ammonium hydroxide, water, positive silicic acid is then added Ethyl ester is reacted, and coated with silica modified composite fiber is obtained;
5) coated with silica modified composite fiber is immersed in alcohols solvent, ammonium hydroxide, water, resorcinol and first is then added Aldehyde solution is reacted, and phenolic resin coating modification composite fibre is obtained;
6) phenolic resin coating modification composite fibre is subjected under protective atmosphere carbonization treatment, then will be obtained after carbonization treatment Product immerse hydrofluoric acid in, etch away coated with silica layer to get.
2. the preparation method of the hollow core-shell structure electrode material of self-supporting as described in claim 1, which is characterized in that step 1) In, the additional amount that every gram of polyacrylonitrile corresponds to titanium tetrachloride is 0.1-1ml.
3. the preparation method of the hollow core-shell structure electrode material of self-supporting as described in claim 1, which is characterized in that step 2) In, the temperature of the carbonization treatment is 900-1100 DEG C, and the time of carbonization treatment is 1h.
4. the preparation method of the hollow core-shell structure electrode material of self-supporting as described in claim 1, which is characterized in that step 3) In, the Surface Oxidation Modification processing is to immerse carbon nano-fiber/composite titania material in concentrated nitric acid to carry out at immersion Reason.
5. the preparation method of the hollow core-shell structure electrode material of self-supporting as described in claim 1, which is characterized in that step 4) In, the dosage that every gram of polyacrylonitrile corresponds to ethyl orthosilicate is 1-5ml.
6. the preparation method of the hollow core-shell structure electrode material of self-supporting as described in claim 1, which is characterized in that step 5) In, the dosage that every gram of polyacrylonitrile corresponds to resorcinol is 0.1-0.5g, and the dosage of corresponding formalin is 0.15-0.75ml, The mass concentration of the formalin is 35-40%.
7. the preparation method of the hollow core-shell structure electrode material of self-supporting as described in claim 1, which is characterized in that step 6) In, the temperature of the carbonization treatment is 700-900 DEG C, and the time of carbonization treatment is 1h.
8. such as the preparation method of the hollow core-shell structure electrode material of self-supporting of any of claims 1-7, feature It is, is repeated in and carries out step 4) and step 5), then carry out step 6) again.
9. electrode material made from a kind of preparation method of the hollow core-shell structure electrode material of self-supporting as described in claim 1 Application in lithium-sulfur cell.
10. electrode material made from a kind of preparation method of the hollow core-shell structure electrode material of self-supporting as described in claim 1 Expect the application in supercapacitor.
CN201811339232.4A 2018-11-12 2018-11-12 Preparation method and application of self-supporting hollow core-shell structure electrode material Active CN109449008B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201811339232.4A CN109449008B (en) 2018-11-12 2018-11-12 Preparation method and application of self-supporting hollow core-shell structure electrode material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201811339232.4A CN109449008B (en) 2018-11-12 2018-11-12 Preparation method and application of self-supporting hollow core-shell structure electrode material

Publications (2)

Publication Number Publication Date
CN109449008A true CN109449008A (en) 2019-03-08
CN109449008B CN109449008B (en) 2020-08-14

Family

ID=65551960

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201811339232.4A Active CN109449008B (en) 2018-11-12 2018-11-12 Preparation method and application of self-supporting hollow core-shell structure electrode material

Country Status (1)

Country Link
CN (1) CN109449008B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111508723A (en) * 2020-04-29 2020-08-07 陕西科技大学 Carbon cloth loaded carbon coated WO3Electrode material, preparation method and application thereof
CN111986931A (en) * 2020-07-24 2020-11-24 华南理工大学 Manganese oxide nano-structure electrode material and preparation method and application thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105633379A (en) * 2016-03-03 2016-06-01 大连理工大学 Core-shell structured carbon/sulfur composite positive electrode material, preparation method and application therefor
US20170141382A1 (en) * 2015-11-18 2017-05-18 GM Global Technology Operations LLC Forming sulfur-based positive electrode active materials
CN108305995A (en) * 2017-12-19 2018-07-20 华南师范大学 A kind of preparation method of hollow hemisphere type lithium sulfur battery anode material
CN108682816A (en) * 2018-05-18 2018-10-19 华中科技大学 A kind of high face carrying capacity lithium sulphur composite positive pole and preparation method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20170141382A1 (en) * 2015-11-18 2017-05-18 GM Global Technology Operations LLC Forming sulfur-based positive electrode active materials
CN105633379A (en) * 2016-03-03 2016-06-01 大连理工大学 Core-shell structured carbon/sulfur composite positive electrode material, preparation method and application therefor
CN108305995A (en) * 2017-12-19 2018-07-20 华南师范大学 A kind of preparation method of hollow hemisphere type lithium sulfur battery anode material
CN108682816A (en) * 2018-05-18 2018-10-19 华中科技大学 A kind of high face carrying capacity lithium sulphur composite positive pole and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111508723A (en) * 2020-04-29 2020-08-07 陕西科技大学 Carbon cloth loaded carbon coated WO3Electrode material, preparation method and application thereof
CN111986931A (en) * 2020-07-24 2020-11-24 华南理工大学 Manganese oxide nano-structure electrode material and preparation method and application thereof

Also Published As

Publication number Publication date
CN109449008B (en) 2020-08-14

Similar Documents

Publication Publication Date Title
CN108520985B (en) Method for prolonging cycle life of zinc battery and application thereof
CN110323074B (en) Asymmetric all-solid-state fibrous flexible supercapacitor and preparation method thereof
EP3454399A1 (en) Method for preparing boron-doped porous carbon sphere
CN108615865B (en) Lithium-sulfur battery positive electrode material and preparation method thereof
CN106602012B (en) Flexible thin film electrode and preparation method and application thereof
CN107221716A (en) A kind of chargeable water system Zinc ion battery
CN107221454B (en) A kind of all-solid-state flexible supercapacitor and preparation method thereof based on porous carbon fiber cloth
CN106571451A (en) Lithium ion battery anode material, and preparation method thereof
CN110048174B (en) Gel battery electrolyte membrane and preparation method and application thereof
CN105098160A (en) Hollow porous graphene-doped carbon/silicon nanofiber lithium battery anode material and preparation method thereof
CN111362254A (en) Preparation method and application of nitrogen-doped carbon nanotube-loaded phosphorus-doped cobaltosic oxide composite material
CN100547707C (en) A kind of ultracapacitor and manufacture method thereof
CN109979763A (en) Folding stack-type one dimension fibre shape flexibility energy storage device and preparation method thereof
CN105118974A (en) Silicon-based negative electrode material and preparation method thereof
CN105552342A (en) Flexible negative electrode with MnO2 attached onto carbon fiber of lithium ion battery and preparation method of flexible negative electrode
CN106784745A (en) The sodium-ion battery method for manufacturing electric spinning of cobaltosic oxide carbon nano-fiber
CN103762091A (en) Cellular porous manganese dioxide nanofiber preparing method and application of cellular porous manganese dioxide nanofiber in supercapacitor
CN109727781A (en) A kind of self-supporting flexible super capacitor electrode material and preparation method
CN109742370A (en) A kind of self-supporting carried by nano carbon fiber molybdenum disulfide composite material and preparation method and application
Wang et al. Robust Room‐Temperature Sodium‐Sulfur Batteries Enabled by a Sandwich‐Structured MXene@ C/Polyolefin/MXene@ C Dual‐functional Separator
CN111170307B (en) Nanocarbon modified hollow activated carbon microtube and preparation method and application thereof
CN109192927A (en) A kind of sulfurized polyacrylonitrile film and binder free lithium-sulphur cell positive electrode prepared therefrom with hollow tubular nanofiber
CN112467113A (en) Preparation method of nitrogen-doped carbon-coated silicon dioxide nanotube composite material
CN106848282B (en) Negative electrode material for non-aqueous electrolyte secondary battery and preparation method and application thereof
CN109449008A (en) A kind of preparation method of the hollow core-shell structure electrode material of self-supporting and its application in lithium-sulfur cell and supercapacitor

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