CN106898770A - The method that ferrite vulcanization prepares flower-shaped lithium cell cathode material iron sulphur compound - Google Patents

The method that ferrite vulcanization prepares flower-shaped lithium cell cathode material iron sulphur compound Download PDF

Info

Publication number
CN106898770A
CN106898770A CN201710194102.5A CN201710194102A CN106898770A CN 106898770 A CN106898770 A CN 106898770A CN 201710194102 A CN201710194102 A CN 201710194102A CN 106898770 A CN106898770 A CN 106898770A
Authority
CN
China
Prior art keywords
ferrite
sulphur compound
lithium cell
iron sulphur
cathode material
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.)
Pending
Application number
CN201710194102.5A
Other languages
Chinese (zh)
Inventor
李苞
李凡
代冬梅
王新博
牛瑾
常照荣
汤宏伟
刘晓阳
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.)
Henan Normal University
Original Assignee
Henan Normal University
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 Henan Normal University filed Critical Henan Normal University
Priority to CN201710194102.5A priority Critical patent/CN106898770A/en
Publication of CN106898770A publication Critical patent/CN106898770A/en
Pending legal-status Critical Current

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
    • H01M4/581Chalcogenides or intercalation compounds thereof
    • H01M4/5815Sulfides
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y40/00Manufacture or treatment of nanostructures
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01GCOMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
    • C01G49/00Compounds of iron
    • C01G49/12Sulfides
    • 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
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/01Particle morphology depicted by an image
    • C01P2004/03Particle morphology depicted by an image obtained by SEM
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2004/00Particle morphology
    • C01P2004/30Particle morphology extending in three dimensions
    • C01P2004/32Spheres
    • C01P2004/34Spheres hollow
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01PINDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
    • C01P2006/00Physical properties of inorganic compounds
    • C01P2006/40Electric properties
    • 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

Abstract

The invention discloses the method that a kind of vulcanization of ferrite prepares flower-shaped lithium cell cathode material iron sulphur compound, using soluble ferric iron salt, glycol and diamines as raw material, there is micro-nano hollow ball structure ferrite by controlling reaction condition solvent heat to be obtained;Ferrite absolute ethyl alcohol is repeatedly washed, crystallinity ferrite hollow ball solid powder high is dried to obtain;Ferrite hollow ball solid powder is placed in tube furnace controls atmosphere ratio, heating rate and sintering temperature finally to prepare flower-shaped lithium cell cathode material iron sulphur compound.The present invention have the advantages that process is simple, it is easy to operate, be easy to regulate and control and it is with low cost, the characteristics of flower-shaped iron sulphur compound of gained is both easy to processing with micron ball, the characteristics of having nanometer sheet reactivity high again, and the excellent electrochemical performance of material, can be used as high-performance lithium cell negative electrode material, with preferable application prospect.

Description

The method that ferrite vulcanization prepares flower-shaped lithium cell cathode material iron sulphur compound
Technical field
The invention belongs to the synthesis technical field of lithium cell cathode material, and in particular to a kind of ferrite vulcanization prepares flower-shaped The method of lithium cell cathode material iron sulphur compound.
Background technology
Because lithium battery energy density is high, monomer voltage is high, good rate capability, small self discharge and the features such as environmental protection, It is widely used in the fields such as digital product, electric motor car and electric automobile.Transient metal sulfide has excellent light, electricity, half Conductor and magnetic property, are widely used in many fields.In recent years, transient metal sulfide attracts as new electrode material Increasing sight, wherein transient metal sulfide pyrite(FeS2)It is high with its energy density(890mAh/g), structure Stablize, safety non-toxic is pollution-free and cheap, receives the attention of researcher, be a kind of lithium electricity of great application prospect Pond negative material.But to there is self-conductance rate in iron sulphur compound relatively low, being formed in cyclic process many as negative material Sulfide is easily soluble in electrolyte and volume increases the shortcomings of causing material structure heavy damage in charge and discharge process, causes Stability and high rate performance in cyclic process is all poor, and them are hindered significantly in real-life application.Nano material Because causing that it has special property, can solve by some special structure designs with special pattern and size The problem that above-mentioned iron sulphur compound is faced as negative material.However, the method for the iron sulphur compound of synthesis is with very big at present Limitation, such as synthesis temperature is too high, is difficult to keep original pattern;And the low knot for being difficult to take into account material of synthesis temperature Brilliant degree, easily forms the material of undefined structure, and material property reduction is caused on the contrary.Therefore, current synthetic method is difficult to reality The practical application of existing iron sulphur compound.
The content of the invention
Present invention solves the technical problem that there is provided a kind of ferrite vulcanization prepares flower-shaped lithium cell cathode material iron sulphur The method of compound, property high is prepared using the ferrite hollow ball with special micro-nano structure under suitable vulcanization sintering temperature Energy iron sulphur compound, can obtain crystallinity iron sulphur compound higher, and the micro-nano of its presoma ferrite can be fully kept again Hollow ball structure, the micro-nano hollow ball structure has larger specific surface area, is conducive to storage lithium reaction, and micro-nano is hollow Spherical structure is conducive to slowing down iron sulphur compound in charge and discharge process because of the negative effect that volumetric expansion brings, and then puies forward probe into Processing high Iron and Sulfur The cycle performance of compound.
The present invention adopts the following technical scheme that ferrite vulcanization prepares flower-shaped cathode of lithium battery to solve above-mentioned technical problem The method of material iron sulphur compound, it is characterised in that concretely comprise the following steps:
(1)Soluble ferric iron salt is dissolved in molysite mixed solution is obtained in mixed solution of the alcohol with amine, wherein soluble ferric iron salt is chlorine Change one or more in iron, ferric sulfate, ferric nitrate or ferric acetate, alcohol and alcohol in the mixed solution of amine be ethylene glycol, propane diols, One or more in butanediol, hexylene glycol, tripropylene glycol, triethylene glycol or pentanediol, alcohol is with amine in the mixed solution of amine One or more in ethylenediamine, propane diamine, butanediamine, hexamethylene diamine, three propane diamine, triethylenediamine or pentanediamine;
(2)Molysite mixed solution is transferred to carry out solvent thermal reaction 6-36h and obtains with special in reactor in 100-300 DEG C The ferrite mixture of micro-nano hollow ball structure;
(3)Ferrite mixture centrifugation is obtained with special micro-nano hollow ball structure after repeatedly being washed with organic solvent Light green color ferrite, then be placed in baking oven dry, wherein organic solvent be absolute ethyl alcohol, acetone, hexamethylene, dimethyl sulfoxide or One or more in tetrahydrofuran;
(4)Dried ferrite is placed in tube furnace, in the mixing of sulfurous gas atmosphere or inert gas and sulfurous gas Under atmosphere, 300-600 DEG C of reaction 0.5-10h is warming up to the heating rate of 1-5 DEG C/min, is obtained with special after natural cooling The flower-shaped lithium cell cathode material iron sulphur compound of high-performance of micro-nano hollow ball structure.
Further preferably, step(1)Described in molysite mixed solution in soluble ferric iron salt concentration for >= 0.001mmol/L。
The present invention has the advantages that compared with prior art:
1st, the micron ball that the obtained high-performance lithium cell negative electrode material iron sulphur compound of the present invention is made up of nanometer sheet, with spy Different micro-nano hollow ball structure, micrometer structure is beneficial to the processing of later stage lithium cell cathode material, and nanometer sheet then ensure that material Material has reactivity higher and can slow down because of the negative effect that volumetric expansion brings;
2nd, the present invention with the ferrite with micro-nano hollow ball structure be presoma, after the nanometer sheet of high activity can be substantially reduced Phase prepares the sintering temperature of iron sulphur compound, can improve the crystallinity of material, the pattern of material can be kept again, and can have Effect reducing energy consumption;
3rd, the features such as obtained iron sulphur compound of the present invention has discharge capacity high, good rate capability and has extended cycle life, is one Plant high performance lithium cell cathode material;
4th, the present invention is prepared high-performance lithium cell negative electrode material iron sulphur compound by ferrite presoma, with equipment it is simple, Easy to operate and with low cost the features such as, it is easy to commercial application.
Brief description of the drawings
Fig. 1 is the scanning electron microscope (SEM) photograph with micro-nano hollow ball structure ferrite;
Fig. 2 is the scanning electron microscope (SEM) photograph of iron sulphur compound obtained in the embodiment of the present invention 1;
Fig. 3 is the scanning electron microscope (SEM) photograph of iron sulphur compound obtained in the embodiment of the present invention 2;
Fig. 4 is the scanning electron microscope (SEM) photograph of iron sulphur compound obtained in the embodiment of the present invention 3;
Fig. 5 is the scanning electron microscope (SEM) photograph of iron sulphur compound obtained in the embodiment of the present invention 4;
Fig. 6 is the scanning electron microscope (SEM) photograph of iron sulphur compound obtained in the embodiment of the present invention 5.
Specific embodiment
The above of the invention is described in further details by the following examples, but this should not be interpreted as this The scope for inventing above-mentioned theme is only limitted to following embodiment, and all technologies realized based on the above of the present invention belong to this hair Bright scope.
Embodiment 1
By FeCl3•6H2O is dissolved in ethylene glycol and ethylenediamine, then mixed solution is transferred in reactor is carried out in 150 DEG C Solvent thermal reaction 24h, cooling, centrifugation, absolute ethyl alcohol are washed 3 times, are dried, and ferrite intermediate are obtained, then by dry iron alcohol Salt intermediate is placed in tube furnace, under argon gas and hydrogen sulfide gas mixed atmosphere, is warming up to the heating rate of 5 DEG C/min 300 DEG C of sintering 2h, natural cooling obtains iron sulphur compound, and Fig. 2 is the scanning electron microscope (SEM) photograph of iron sulphur compound obtained in the present embodiment.
Embodiment 2
By Fe2(SO4)3Be dissolved in propane diols and propane diamine, then mixed solution is transferred in reactor carried out in 150 DEG C it is molten Agent thermal response 24h, cooling, centrifugation, absolute ethyl alcohol are washed 3 times, are dried, and ferrite intermediate are obtained, then by dry ferrite Intermediate is placed in tube furnace, under argon gas and sulfur vapor mixed atmosphere, 450 DEG C of sintering is warming up to the intensification speed of 5 DEG C/min 2h, natural cooling obtains iron sulphur compound, and Fig. 3 is the scanning electron microscope (SEM) photograph of iron sulphur compound obtained in the present embodiment.
Embodiment 3
By Fe (NO)3Be dissolved in triethylene glycol and butanediamine, then mixed solution is transferred in reactor carried out in 150 DEG C it is molten Agent thermal response 24h, cooling, centrifugation, absolute ethyl alcohol are washed 3 times, are dried, and ferrite intermediate are obtained, then by dry ferrite Intermediate is placed in tube furnace, under argon gas and hydrogen sulfide gas mixed atmosphere, 600 is warming up to the heating rate of 1 DEG C/min DEG C sintering 2h, natural cooling obtains iron sulphur compound, and Fig. 4 is the scanning electron microscope (SEM) photograph of iron sulphur compound obtained in the present embodiment.
Embodiment 4
By FeCl3•6H2O is dissolved in pentanediol and ethylenediamine, then mixed solution is transferred in reactor is carried out in 300 DEG C Solvent thermal reaction 6h, cooling, centrifugation, tetrahydrofuran are washed 3 times, are dried, and ferrite intermediate are obtained, then by dry ferrite Intermediate is placed in tube furnace, under ammonium sulfide vapor atmosphere, 450 DEG C of sintering 0.5h is warming up to the heating rate of 2 DEG C/min, Natural cooling obtains iron sulphur compound, and Fig. 5 is the scanning electron microscope (SEM) photograph of iron sulphur compound obtained in the present embodiment.
Embodiment 5
By FeCl3•6H2O is dissolved in ethylene glycol and hexamethylene diamine, then mixed solution is transferred in reactor is carried out in 100 DEG C Solvent thermal reaction 36h, cooling, centrifugation, acetone are washed 3 times, are dried, and ferrite intermediate are obtained, then by dry ferrite Mesosome is placed in tube furnace, under nitrogen and hydrogen sulfide gas mixed atmosphere, 300 DEG C is warming up to the heating rate of 2 DEG C/min Sintering 10h, natural cooling obtains iron sulphur compound, and Fig. 6 is the scanning electron microscope (SEM) photograph of iron sulphur compound obtained in the present embodiment.
Embodiment 6
Electrochemical property test:In mass ratio it is 8 by active material, conductive agent and adhesive:1:1 ratio mixing, adds N- Methyl pyrrolidone is sized mixing and is made electrode slice, is dried and is weighed.The button electricity of CR2025 models is assembled into the glove box of argon gas Pond, in blue electrical measurement test system after standing a night(Wuhan Jin Nuo electronics limited company, CT2001A)On carry out constant current density Charge-discharge test, discharge current is 200mA/g, and electrochemical discharge the performance test results are shown in Table 1.
The electrochemical discharge the performance test results of table 1
Synthesis condition Embodiment 1 Embodiment 2 Embodiment 3 Embodiment 4 Embodiment 5
Discharge capacity mAh/g first 1500 1400 1200 1300 1400
100 circulation volume mAh/g 890 890 780 800 850
It is of the invention to be advantageous in that:The ferrite of the special construction obtained by early stage solvent heat, can be in relatively low burning Conversion reaction is carried out under junction temperature, and relatively low reaction temperature enables to its special appearance to be maintained, and then by control Atmosphere, heating rate and sintering temperature during conversion reaction, further the structure of control products therefrom, composition and pattern, obtain Obtain high performance lithium cell cathode material.Gained lithium cell cathode material specific capacity is high(200mA/g specific discharge capacities are 1400mAh/g), platform voltage is low(0.5V), cycle performance is excellent(100 circulation volume conservation rates are close to 70%).Institute of the present invention With method have the advantages that process is simple, it is easy to operate, be easy to regulation and control and it is with low cost, gained iron sulphur compound both have it is micro- Rice ball be easy to processing the characteristics of, and with nanometer sheet reactivity it is high the characteristics of, and material excellent electrochemical performance, can use Make high-performance lithium cell negative electrode material, with preferable application prospect.
Embodiment above describes general principle of the invention, principal character and advantage, the technical staff of the industry should Understand, the present invention is not limited to the above embodiments, simply original of the invention is illustrated described in above-described embodiment and specification Reason, under the scope for not departing from the principle of the invention, various changes and modifications of the present invention are possible, and these changes and improvements each fall within In the scope of protection of the invention.

Claims (2)

1. the method that ferrite vulcanization prepares flower-shaped lithium cell cathode material iron sulphur compound, it is characterised in that concretely comprise the following steps:
(1)Soluble ferric iron salt is dissolved in molysite mixed solution is obtained in mixed solution of the alcohol with amine, wherein soluble ferric iron salt is chlorine Change one or more in iron, ferric sulfate, ferric nitrate or ferric acetate, alcohol and alcohol in the mixed solution of amine be ethylene glycol, propane diols, One or more in butanediol, hexylene glycol, tripropylene glycol, triethylene glycol or pentanediol, alcohol is with amine in the mixed solution of amine One or more in ethylenediamine, propane diamine, butanediamine, hexamethylene diamine, three propane diamine, triethylenediamine or pentanediamine;
(2)Molysite mixed solution is transferred to carry out solvent thermal reaction 6-36h and obtains with special in reactor in 100-300 DEG C The ferrite mixture of micro-nano hollow ball structure;
(3)Ferrite mixture centrifugation is obtained with special micro-nano hollow ball structure after repeatedly being washed with organic solvent Light green color ferrite, then be placed in baking oven dry, wherein organic solvent be absolute ethyl alcohol, acetone, hexamethylene, dimethyl sulfoxide or One or more in tetrahydrofuran;
(4)Dried ferrite is placed in tube furnace, in the mixing of sulfurous gas atmosphere or inert gas and sulfurous gas Under atmosphere, 300-600 DEG C of reaction 0.5-10h is warming up to the heating rate of 1-5 DEG C/min, is obtained with special after natural cooling The high performance lithium ionic cell cathode material iron sulphur compound of micro-nano hollow ball structure.
2. the method that ferrite vulcanization according to claim 1 prepares flower-shaped lithium cell cathode material iron sulphur compound, its It is characterised by:Step(1)Described in molysite mixed solution in the concentration of soluble ferric iron salt be >=0.001mmol/L.
CN201710194102.5A 2017-03-28 2017-03-28 The method that ferrite vulcanization prepares flower-shaped lithium cell cathode material iron sulphur compound Pending CN106898770A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201710194102.5A CN106898770A (en) 2017-03-28 2017-03-28 The method that ferrite vulcanization prepares flower-shaped lithium cell cathode material iron sulphur compound

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710194102.5A CN106898770A (en) 2017-03-28 2017-03-28 The method that ferrite vulcanization prepares flower-shaped lithium cell cathode material iron sulphur compound

Publications (1)

Publication Number Publication Date
CN106898770A true CN106898770A (en) 2017-06-27

Family

ID=59193549

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201710194102.5A Pending CN106898770A (en) 2017-03-28 2017-03-28 The method that ferrite vulcanization prepares flower-shaped lithium cell cathode material iron sulphur compound

Country Status (1)

Country Link
CN (1) CN106898770A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108878844A (en) * 2018-06-30 2018-11-23 苏州思创源博电子科技有限公司 A kind of preparation method of lithium battery iron sulphur negative electrode material
CN108899490A (en) * 2018-06-19 2018-11-27 苏州思创源博电子科技有限公司 A kind of preparation method of carbon-encapsulated iron sulphur composite negative pole material
CN111318259A (en) * 2020-02-05 2020-06-23 江苏大学 Iron alkoxide As5+Preparation method and application of ion remover
CN115231621A (en) * 2022-08-26 2022-10-25 浙江理工大学 Nano microspheric iron disulfide material and preparation method and application thereof

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1454851A (en) * 2002-04-17 2003-11-12 国际商业机器公司 Synthesizing of magnetite nano particles and method for forming iron-base nano material
CN102760877A (en) * 2012-07-23 2012-10-31 浙江大学 Transition metal sulfide/graphene composite material, and preparation method and application thereof
CN103145535A (en) * 2013-03-25 2013-06-12 北京化工大学 Diethylene glycol ferrous alkoxide with three-dimensional pattern multi-stage structure and preparation method thereof
CN104045117A (en) * 2014-06-16 2014-09-17 上海电力学院 Synthesis method of multi-form FeS2 pyrite photoelectric material
CN105932256A (en) * 2016-06-20 2016-09-07 华南理工大学 Graphene-based FeS 2 nano material and preparation and application thereof
CN106058176A (en) * 2016-06-21 2016-10-26 中南民族大学 Preparation method of microsphere structure lithium ion battery cathode material
CN106099126A (en) * 2016-06-11 2016-11-09 北京化工大学 A kind of flower-like structure cobalt sulfide/carbon composite and preparation method thereof

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1454851A (en) * 2002-04-17 2003-11-12 国际商业机器公司 Synthesizing of magnetite nano particles and method for forming iron-base nano material
CN102760877A (en) * 2012-07-23 2012-10-31 浙江大学 Transition metal sulfide/graphene composite material, and preparation method and application thereof
CN103145535A (en) * 2013-03-25 2013-06-12 北京化工大学 Diethylene glycol ferrous alkoxide with three-dimensional pattern multi-stage structure and preparation method thereof
CN104045117A (en) * 2014-06-16 2014-09-17 上海电力学院 Synthesis method of multi-form FeS2 pyrite photoelectric material
CN106099126A (en) * 2016-06-11 2016-11-09 北京化工大学 A kind of flower-like structure cobalt sulfide/carbon composite and preparation method thereof
CN105932256A (en) * 2016-06-20 2016-09-07 华南理工大学 Graphene-based FeS 2 nano material and preparation and application thereof
CN106058176A (en) * 2016-06-21 2016-10-26 中南民族大学 Preparation method of microsphere structure lithium ion battery cathode material

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
金双玲: "纳米结构锂离子电池负极材料的设计、制备及性能研究", 《中国博士学位论文全文数据库工程科技II辑》 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108899490A (en) * 2018-06-19 2018-11-27 苏州思创源博电子科技有限公司 A kind of preparation method of carbon-encapsulated iron sulphur composite negative pole material
CN108878844A (en) * 2018-06-30 2018-11-23 苏州思创源博电子科技有限公司 A kind of preparation method of lithium battery iron sulphur negative electrode material
CN111318259A (en) * 2020-02-05 2020-06-23 江苏大学 Iron alkoxide As5+Preparation method and application of ion remover
CN115231621A (en) * 2022-08-26 2022-10-25 浙江理工大学 Nano microspheric iron disulfide material and preparation method and application thereof

Similar Documents

Publication Publication Date Title
CN106532012B (en) A kind of sulphur-biomass carbon/transition metal combination electrode material and its preparation method and application
CN109378449A (en) NiCo for lithium sulfur battery anode material2S4The preparation method of coated porous carbon skeleton
CN106058215B (en) Dodecahedron porous C o3The preparation method of ZnC/C composite materials and the application in lithium ion battery
CN106898770A (en) The method that ferrite vulcanization prepares flower-shaped lithium cell cathode material iron sulphur compound
CN107731560B (en) Li5FeO4The preparation method and lithium-ion capacitor of prelithiation agent and lithium-ion capacitor
CN109616331B (en) Core-shell type nickel hydroxide nanosheet/manganese cobalt oxide composite electrode material and preparation method thereof
CN107403918A (en) A kind of preparation method for coating nitrogen-doped graphene ternary material
CN105655548A (en) Method for uniform carbon coating on lithium iron phosphate surface
CN109360953A (en) A kind of method synthesizing vulcanization lithium/carbon composite material and the lithium-sulfur cell using the material
CN104803423B (en) A kind of preparation method and applications of porous cobaltosic oxide material
CN110364366A (en) A kind of high-performance electric chemistry capacitor anode material molybdenum dioxide and nitrogen-doped carbon composite material and preparation method and application
CN110429265A (en) A kind of lithium ion battery MEG/Si/C composite negative pole material and preparation method thereof
CN111056544B (en) Sodium iron phosphate composite material and preparation method and application thereof
CN110828820B (en) Positive electrode material of potassium ion battery and preparation method thereof
CN107706397A (en) Nickel-cobalt-manganese ternary combination electrode material of modified carbon nano-tube modification and preparation method thereof
CN106960947A (en) Composite, its preparation method and application
CN106129383B (en) A kind of ball-shaped lithium-ion battery anode material and its synthetic method with two phase gradient distributed architecture of nanoscale
CN103337616B (en) Metal oxide coated lithium titanate negative pole material and preparation method thereof
CN108075120B (en) Preparation method of spherical lithium titanate material
CN110311135A (en) A kind of metal sulfide hollow ball that can load sulphur, preparation method and application
CN107742706B (en) Preparation method and application of graphene composite metal boride and sulfur composite nano material
CN111463415B (en) Positive host material and preparation method and application thereof
CN112820549A (en) Phosphorus-doped heterogeneous nickel-cobalt sulfide composite material and preparation method and application thereof
CN104953114B (en) Cobaltosic oxide-stannic disulfide nano-complex preparation method
CN104362291B (en) A kind of lithium-enriched cathodic material of lithium ion battery and preparation method thereof and lithium ion battery

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
WD01 Invention patent application deemed withdrawn after publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20170627