CN106848215B - A kind of high-tap density lithium ion battery ternary material and its preparation method and application - Google Patents

A kind of high-tap density lithium ion battery ternary material and its preparation method and application Download PDF

Info

Publication number
CN106848215B
CN106848215B CN201611223385.3A CN201611223385A CN106848215B CN 106848215 B CN106848215 B CN 106848215B CN 201611223385 A CN201611223385 A CN 201611223385A CN 106848215 B CN106848215 B CN 106848215B
Authority
CN
China
Prior art keywords
lithium
nickel
cobalt
tap density
ion battery
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.)
Active
Application number
CN201611223385.3A
Other languages
Chinese (zh)
Other versions
CN106848215A (en
Inventor
阮殿波
周洲
李林艳
陈雪丹
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.)
Ningbo CRRC New Energy Technology Co Ltd
Original Assignee
Ningbo CRRC New Energy Technology 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 Ningbo CRRC New Energy Technology Co Ltd filed Critical Ningbo CRRC New Energy Technology Co Ltd
Priority to CN201611223385.3A priority Critical patent/CN106848215B/en
Publication of CN106848215A publication Critical patent/CN106848215A/en
Application granted granted Critical
Publication of CN106848215B publication Critical patent/CN106848215B/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
    • H01M4/62Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • 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
    • H01M4/362Composites
    • H01M4/364Composites as mixtures
    • 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
    • H01M4/48Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/50Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese
    • H01M4/505Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
    • 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
    • H01M4/48Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
    • H01M4/52Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron
    • H01M4/525Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
    • 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
    • H01M4/62Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/621Binders
    • H01M4/622Binders being polymers
    • H01M4/623Binders being polymers fluorinated polymers
    • 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
    • H01M4/62Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
    • H01M4/624Electric conductive fillers
    • H01M4/625Carbon or graphite
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Composite Materials (AREA)
  • Battery Electrode And Active Subsutance (AREA)

Abstract

The present invention relates to field of batteries, and in particular to a kind of high-tap density lithium ion battery ternary material and its preparation method and application.Ternary material prepared by the present invention due to offspring addition so that the gap between primary particle is reduced, a large amount of offspring by fill or intercalation in a manner of enter, more crypto set is accumulated between particle, therefore the tap density of material is greatly improved.Due to the addition of primary particle, reduce the problem of offspring is reunited because of a large amount of accumulation, increase the availability of offspring, the effective area contacted between particle and electrolyte is also increased simultaneously, to improve the chemical property of material, including specific capacity, multiplying power and cycle characteristics.

Description

A kind of high-tap density lithium ion battery ternary material and its preparation method and application
Technical field
The present invention relates to field of batteries, and in particular to a kind of high-tap density lithium ion battery ternary material and its preparation side Method and application.
Background technique
Practical anode material for lithium-ion batteries can be roughly divided into three categories according to its structure at present: the first kind It is the lithium metal oxide LiMO2 (M=Co, Ni, Mn) with six side's layer structures, representing material is cobalt acid lithium (LiCoO2) With the sour lithium of ternary nickel cobalt manganese (NCM), the sour lithium material of nickel cobalt aluminium (NCA) (NCM:LiNixCoyMnzO2, x+y+z=1 and NCA: LiNixCoyAlzO2, x+y+z=1);Second class is the material with spinel structure, and representing material mainly has LiMn2O4; Third class is the compound with polyanionic structure, and representing material mainly has the LiFePO 4 of olivine structural LiFePO4.Wherein ternary material becomes a kind of great application prospect due to energy density with higher and low cost Lithium ion battery material.But for the practical situations of ternary material, high rate performance and cycle performance need to be mentioned It is high.
Summary of the invention
In view of the above problems, the present invention provides a kind of lithium ion battery ternary electrode material with high-tap density, tool There are higher high rate performance and cycle performance.
The technical solution of present invention realization above-mentioned purpose are as follows: a kind of high-tap density lithium ion battery ternary material, it is described High-tap density lithium ion battery ternary material includes nickel cobalt aluminic acid lithium material, nickel-cobalt lithium manganate material, the nickel cobalt lithium aluminate Material is made of nickel cobalt lithium aluminate primary particle and nickel cobalt lithium aluminate offspring, and the nickel-cobalt lithium manganate material is by nickel cobalt mangaic acid Lithium primary particle and nickle cobalt lithium manganate offspring composition.
The material is that the primary particle and offspring by NCA or NCM collectively constitute, relative to common ternary material Material, due to the addition of offspring, so that the gap between primary particle is reduced, a large amount of offspring is to fill or intercalation Mode enters, and more crypto set is accumulated between particle, therefore the tap density of material is greatly improved.Due to adding for primary particle Enter, reduces the problem of offspring is reunited because of a large amount of accumulation, increase the availability of offspring, while The effective area contacted between particle and electrolyte is increased, to improve the chemical property of material, including specific capacity, multiplying power And cycle characteristics.
Further, by mass percentage: in the nickel cobalt aluminic acid lithium material, nickel cobalt lithium aluminate primary particle accounts for 30~ 70%, surplus is nickel cobalt lithium aluminate offspring;In the nickel-cobalt lithium manganate material, nickle cobalt lithium manganate primary particle accounts for 30~ 70%, surplus is nickle cobalt lithium manganate offspring.If if primary particle ratio not 30~70%, the specific volume of composite material Amount is reduced, and high rate performance is obviously deteriorated.
Further, the size of the nickel cobalt lithium aluminate primary particle and nickle cobalt lithium manganate primary particle be 600~ The size of 800nm, the nickel cobalt lithium aluminate offspring and nickle cobalt lithium manganate offspring is 200~400nm.Present invention selection Suitable particle, the material electrochemical performance prepared is more excellent, including specific capacity, multiplying power, cycle performance.
It is a further object to provide a kind of preparation method of high-tap density lithium ion battery ternary material, packets Include step:
(1) lithium source, nickel source, cobalt source, silicon source, manganese source are distributed in deionized water and obtain solution A;
(2) citric acid-ethylene glycol aqueous solution is added in solution A, forms colloidal sol;The colloidal sol is dried to obtain bulk Citric acid-glycerine, oxalic acid-ethylene glycol, tartaric acid-ethylene glycol, oxalic acid-glycerine, tartaric acid-the third three can be also added in gel The aqueous solution of one of alcohol;
(3) deionized water is cleaned 3~5 times after crushing bulk gel obtained in step (2), and heating obtains primary particle Presoma;
(4) deionized water is cleaned 3~5 times after crushing bulk gel obtained in step (2), then with organic solvent diafiltration 3~5 times, heating obtains offspring presoma, after organic solvent diafiltration, the metal residue and organic functional of particle surface Group can remove, and grain diameter reduces.
(5) primary particle presoma and offspring presoma obtained in mixing step (3) and step (4), are calcined Obtain high-tap density lithium ion battery ternary material;
Further, lithium source described in step (1) is one of lithium nitrate, lithium sulfate, lithium acetate or a variety of;The nickel Source is one of nickel nitrate, nickel sulfate, nickel acetate or a variety of;The cobalt source is one of cobalt nitrate, cobaltous sulfate, cobalt acetate Or it is a variety of;Source of aluminium is one of aluminum nitrate, aluminum sulfate, aluminum acetate or a variety of;The manganese source be manganese nitrate, manganese sulfate, One of manganese acetate is a variety of.
Further, drying temperature is 120~160 DEG C in step (2).
Further, citric acid-ethylene glycol described in step (2) and the metal ion molar ratio in solution A are 1~1.2: 1.
Further, step (3) and heating temperature in step (4) are 300~600 DEG C, and heating time is 3~6h.
Further, calcination temperature is 600~1000 DEG C in step (5), and calcination time is 10~15h.
It is a further object to provide a kind of applications of high-tap density lithium ion battery ternary material, by three First material and binder, conductive agent are uniformly mixed according to mass ratio for 6~8:0.8~1:1 ratio, and anode electrode is made.Together Soft carbon is fabricated to negative electrode by the method for sample, is added three First electrolyte is assembled into flexible packaged battery container.Chemical property, which is tested, in 0.5C and 5C multiplying power discharge capacity is respectively 166mAh/g and 129mAh/g, capacity attenuation rate is 8.9% after 2000 circulations.
The invention has the benefit that
Due to the addition of offspring so that the gap between primary particle is reduced, a large amount of offspring to fill or The mode of intercalation enters, and more crypto set is accumulated between particle, therefore the tap density of material is greatly improved.Due to primary grain The addition of son reduces the problem of offspring is reunited because of a large amount of accumulation, increases the availability of offspring, The effective area contacted between particle and electrolyte is also increased simultaneously, to improve the chemical property of material, including specific volume Amount, multiplying power and cycle characteristics.
Specific embodiment
The present invention is further detailed by the following examples.
Embodiment 1
Lithium nitrate, nickel sulfate, cobalt nitrate, aluminum nitrate, manganese nitrate are distributed in deionized water, are then added in the solution The ratio of citric acid-glycol water, citric acid and metal ion is 1:1, is formed after gel and removes moisture removal at 120 DEG C.Then By after drying blocky gel crush after use deionized water diafiltration 3 times, 300 DEG C heating 3 hours after obtain the forerunner of primary particle Body.It is first used after equally the blocky gel after drying is crushed deionized water diafiltration 3 times, then uses surfactant sodium dodecyl base again Benzene sulfonic acid diafiltration 3 times, 600 DEG C heating 3 hours after obtain the presoma of offspring.Obtained nickel cobalt lithium aluminate primary particle and The size of nickle cobalt lithium manganate primary particle is 600nm, the size of nickel cobalt lithium aluminate offspring and nickle cobalt lithium manganate offspring For 400nm.Then the two is mixed, nickle cobalt lithium manganate primary particle accounts for 70%, and surplus is nickle cobalt lithium manganate offspring, is placed in It is calcined 15 hours at 600 DEG C and obtains ternary material.By ternary material obtained, binder PVDF and conductive agent acetylene black according to matter Amount after mixing than 8:1:1, is fabricated to anode electrode.Graphite is fabricated to cathode by same method, is assembled into Soft Roll capacitor Device.It is respectively 185mAh/g and 159mAh/g that chemical property, which is tested, in 0.5C and 5C multiplying power discharge capacity.
Embodiment 2
Lithium sulfate, nickel nitrate, cobalt nitrate, aluminum nitrate, manganese nitrate are distributed in deionized water, are then added in the solution The ratio of citric acid-glycol water, citric acid and metal ion is 1.2:1, is formed after gel and removes moisture removal at 160 DEG C.So Afterwards by after drying blocky gel crush after use deionized water diafiltration 3 times, 600 DEG C heating 5 hours after obtain primary particle before Drive body.It is first used deionized water diafiltration 3 times after equally the blocky gel after drying is crushed, then uses surfactant sodium dodecyl again Base benzene sulfonic acid diafiltration 3 times, 500 DEG C heating 5 hours after obtain the presoma of offspring.Obtained nickel cobalt lithium aluminate primary particle Size with nickle cobalt lithium manganate primary particle is 700nm, the ruler of nickel cobalt lithium aluminate offspring and nickle cobalt lithium manganate offspring Very little is 300nm.Then the two is mixed, nickle cobalt lithium manganate primary particle accounts for 60%, and surplus is nickle cobalt lithium manganate offspring, sets It is calcined 12 hours at 800 DEG C and obtains ternary material.By ternary material obtained, binder PVDF and conductive agent acetylene black according to Mass ratio 8:1:1 after mixing, is fabricated to anode electrode.Graphite is fabricated to cathode by same method, is assembled into Soft Roll electricity Container.It is respectively 187mAh/g and 160mAh/g that chemical property, which is tested, in 0.5C and 5C multiplying power discharge capacity.
Embodiment 3
Lithium nitrate, nickel nitrate, cobalt nitrate, aluminum acetate, manganese nitrate are distributed in deionized water, are then added in the solution The ratio of citric acid-glycol water, citric acid and metal ion is 1.1:1, is formed after gel and removes moisture removal at 140 DEG C.So Afterwards by after drying blocky gel crush after use deionized water diafiltration 3 times, 400 DEG C heating 4 hours after obtain primary particle before Drive body.It is first used deionized water diafiltration 3 times after equally the blocky gel after drying is crushed, then uses surfactant sodium dodecyl again Base benzene sulfonic acid diafiltration 3 times, 400 DEG C heating 5 hours after obtain the presoma of offspring.Obtained nickel cobalt lithium aluminate primary particle Size with nickle cobalt lithium manganate primary particle is 700nm, the ruler of nickel cobalt lithium aluminate offspring and nickle cobalt lithium manganate offspring Very little is 300nm.Then the two is mixed, nickle cobalt lithium manganate primary particle accounts for 60%, and surplus is nickle cobalt lithium manganate offspring, sets It is calcined 15 hours at 1000 DEG C and obtains ternary material.Ternary material obtained, binder PVDF and conductive agent acetylene black are pressed After mixing according to mass ratio 7:0.9:1, it is fabricated to anode electrode.Graphite is fabricated to cathode by same method, is assembled into soft Packet capacitor.It is respectively 183mAh/g and 154mAh/g that chemical property, which is tested, in 0.5C and 5C multiplying power discharge capacity.
Embodiment 4
Lithium nitrate, nickel nitrate, cobalt nitrate, aluminum acetate, manganese nitrate are distributed in deionized water, are then added in the solution The ratio of citric acid-glycol water, citric acid and metal ion is 1:1, is formed after gel and removes moisture removal at 160 DEG C.Then By after drying blocky gel crush after use deionized water diafiltration 3 times, 600 DEG C heating 3 hours after obtain the forerunner of primary particle Body.It is first used after equally the blocky gel after drying is crushed deionized water diafiltration 3 times, then uses surfactant sodium dodecyl base again Benzene sulfonic acid diafiltration 3 times, 300 DEG C heating 3 hours after obtain the presoma of offspring.Obtained nickel cobalt lithium aluminate primary particle and The size of nickle cobalt lithium manganate primary particle is 800nm, the size of nickel cobalt lithium aluminate offspring and nickle cobalt lithium manganate offspring For 200nm.Then the two is mixed, nickle cobalt lithium manganate primary particle accounts for 70%, and surplus is nickle cobalt lithium manganate offspring, is placed in It is calcined 12 hours at 900 DEG C and obtains ternary material.By ternary material obtained, binder PVDF and conductive agent acetylene black according to matter Amount after mixing than 6:1:1, is fabricated to anode electrode.Graphite is fabricated to cathode by same method, is assembled into Soft Roll capacitor Device.It is respectively 188mAh/g and 162mAh/g that chemical property, which is tested, in 0.5C and 5C multiplying power discharge capacity.
Embodiment 5
Lithium nitrate, nickel nitrate, cobalt nitrate, aluminum acetate, manganese nitrate are distributed in deionized water, are then added in the solution The ratio of citric acid-glycol water, citric acid and metal ion is 1.2:1, is formed after gel and removes moisture removal at 160 DEG C.So Afterwards by after drying blocky gel crush after use deionized water diafiltration 3 times, 300 DEG C heating 3 hours after obtain primary particle before Drive body.It is first used deionized water diafiltration 3 times after equally the blocky gel after drying is crushed, then uses surfactant sodium dodecyl again Base benzene sulfonic acid diafiltration 3 times, 600 DEG C heating 3 hours after obtain the presoma of offspring.Obtained nickel cobalt lithium aluminate primary particle Size with nickle cobalt lithium manganate primary particle is 800nm, the ruler of nickel cobalt lithium aluminate offspring and nickle cobalt lithium manganate offspring Very little is 200nm.Then the two is mixed, nickle cobalt lithium manganate primary particle accounts for 70%, and surplus is nickle cobalt lithium manganate offspring, sets It is calcined 10 hours at 1000 DEG C and obtains ternary material.Ternary material obtained, binder PVDF and conductive agent acetylene black are pressed After mixing according to mass ratio 8:0.8:1, it is fabricated to anode electrode.Graphite is fabricated to cathode by same method, is assembled into soft Packet capacitor.It is respectively 183mAh/g and 167mAh/g that chemical property, which is tested, in 0.5C and 5C multiplying power discharge capacity.
This place embodiment is not exhaustive claimed midpoint of technical range and in embodiment technology In scheme to single or multiple technical characteristics it is same replacement be formed by new technical solution, equally all the present invention claims In the range of protection;Simultaneously the present invention program it is all enumerate or unlisted embodiment in, in the same embodiment each Parameter is merely representative of an example (i.e. a kind of feasible scheme) for its technical solution, and between parameters and is not present stringent Cooperation and qualified relation, wherein each parameter can be replaced mutually when stating and asking without prejudice to axiom and the present invention, special declaration Except.
The technical means disclosed in the embodiments of the present invention is not limited to the technical means disclosed in the above technical means, and further includes Technical solution consisting of any combination of the above technical features.The foregoing is a specific embodiment of the present invention, should refer to Out, for those skilled in the art, without departing from the principle of the present invention, can also make several Improvements and modifications, these modifications and embellishments are also considered to be within the scope of the present invention.

Claims (9)

1. a kind of high-tap density lithium ion battery ternary material, it is characterised in that: the high-tap density lithium ion battery three First material includes nickel cobalt aluminic acid lithium material, nickel-cobalt lithium manganate material, and the nickel cobalt aluminic acid lithium material is by the primary grain of nickel cobalt lithium aluminate Son and nickel cobalt lithium aluminate offspring composition, the nickel-cobalt lithium manganate material is by nickle cobalt lithium manganate primary particle and nickle cobalt lithium manganate Offspring composition;
The preparation method of the high-tap density lithium ion battery ternary material, comprising steps of
(1) lithium source, nickel source, cobalt source, silicon source, manganese source are distributed in deionized water and obtain solution A;
(2) citric acid-ethylene glycol aqueous solution is added in solution A, forms colloidal sol;The colloidal sol is dried to obtain blocky solidifying Glue;
(3) deionized water is cleaned 3~5 times after crushing bulk gel obtained in step (2), and heating obtains primary particle forerunner Body;
(4) deionized water is cleaned 3~5 times after crushing bulk gel obtained in step (2), then with organic solvent diafiltration 3~5 Secondary, heating obtains offspring presoma;
(5) primary particle presoma and offspring presoma obtained in mixing step (3) and step (4), calcining obtain height Tap density lithium ion battery ternary material.
2. a kind of high-tap density lithium ion battery ternary material according to claim 1, it is characterised in that: press quality hundred Point ratio: in the nickel cobalt aluminic acid lithium material, nickel cobalt lithium aluminate primary particle accounts for 30~70%, and surplus is the secondary grain of nickel cobalt lithium aluminate Son;In the nickel-cobalt lithium manganate material, nickle cobalt lithium manganate primary particle accounts for 30~70%, and surplus is the secondary grain of nickle cobalt lithium manganate Son.
3. a kind of high-tap density lithium ion battery ternary material according to claim 1, it is characterised in that: the nickel cobalt The size of lithium aluminate primary particle and nickle cobalt lithium manganate primary particle be 600~800nm, the nickel cobalt lithium aluminate offspring and The size of nickle cobalt lithium manganate offspring is 200~400nm.
4. a kind of high-tap density lithium ion battery ternary material according to claim 1, it is characterised in that: step (1) Described in lithium source be one of lithium nitrate, lithium sulfate, lithium acetate or a variety of;The nickel source is nickel nitrate, nickel sulfate, nickel acetate One of or it is a variety of;The cobalt source is one of cobalt nitrate, cobaltous sulfate, cobalt acetate or a variety of;Source of aluminium be aluminum nitrate, One of aluminum sulfate, aluminum acetate are a variety of;The manganese source is one of manganese nitrate, manganese sulfate, manganese acetate or a variety of.
5. a kind of high-tap density lithium ion battery ternary material according to claim 1, it is characterised in that: step (2) Middle drying temperature is 120~160 DEG C.
6. a kind of high-tap density lithium ion battery ternary material according to claim 1, it is characterised in that: step (2) Described in metal ion molar ratio in citric acid-ethylene glycol and solution A be 1~1.2:1.
7. a kind of high-tap density lithium ion battery ternary material according to claim 1, it is characterised in that: step (3) It is 300~600 DEG C with heating temperature in step (4), heating time is 3~6h.
8. a kind of high-tap density lithium ion battery ternary material according to claim 1, it is characterised in that: step (5) Middle calcination temperature is 600~1000 DEG C, and calcination time is 10~15h.
9. a kind of capacitor, it is characterised in that: by high-tap density lithium ion battery ternary material as described in claim 1 with Binder, conductive agent are uniformly mixed according to mass ratio for 6~8:0.8~1:1, and anode electrode is made, positive electrode and negative electrode are assembled Obtain capacitor.
CN201611223385.3A 2016-12-27 2016-12-27 A kind of high-tap density lithium ion battery ternary material and its preparation method and application Active CN106848215B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201611223385.3A CN106848215B (en) 2016-12-27 2016-12-27 A kind of high-tap density lithium ion battery ternary material and its preparation method and application

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201611223385.3A CN106848215B (en) 2016-12-27 2016-12-27 A kind of high-tap density lithium ion battery ternary material and its preparation method and application

Publications (2)

Publication Number Publication Date
CN106848215A CN106848215A (en) 2017-06-13
CN106848215B true CN106848215B (en) 2019-09-13

Family

ID=59135570

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201611223385.3A Active CN106848215B (en) 2016-12-27 2016-12-27 A kind of high-tap density lithium ion battery ternary material and its preparation method and application

Country Status (1)

Country Link
CN (1) CN106848215B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107706373B (en) * 2017-09-19 2020-05-22 合肥国轩高科动力能源有限公司 High-nickel ternary material for lithium ion battery and preparation method thereof
CN110416511B (en) 2019-07-19 2020-12-25 宁德新能源科技有限公司 Positive electrode material, and positive electrode and electrochemical device comprising same
CN116404160B (en) * 2023-03-28 2024-06-21 江门市科恒实业股份有限公司 High-Wen Mengsuan-resistant lithium positive electrode material and preparation method thereof

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101117623B1 (en) * 2009-06-05 2012-02-29 에스비리모티브 주식회사 Positive electrode for rechargeable lithium battery and rechargeable lithium battery including the positive electrode
CN103943822B (en) * 2014-05-13 2017-03-29 南通瑞翔新材料有限公司 A kind of lithium rechargeable battery nickel-base anode active material and preparation method thereof
CN107316995A (en) * 2017-05-27 2017-11-03 广东烛光新能源科技有限公司 A kind of anode material for lithium-ion batteries and preparation method thereof
CN107316997A (en) * 2017-05-27 2017-11-03 广东烛光新能源科技有限公司 Anode material for lithium-ion batteries and preparation method thereof

Also Published As

Publication number Publication date
CN106848215A (en) 2017-06-13

Similar Documents

Publication Publication Date Title
US10522816B2 (en) Lithium secondary battery
EP3588630A1 (en) Positive electrode plate and lithium ion battery
CN111200109B (en) Battery with a battery cell
CN102544481B (en) Lithium ion battery and cathode material thereof
WO2017190367A1 (en) Secondary battery and preparation method therefor
US9263729B2 (en) Lithium secondary battery
Yang et al. Understanding voltage decay in lithium-rich manganese-based layered cathode materials by limiting cutoff voltage
CN105161693B (en) A kind of high circulation lithium electricity polynary positive pole material NCM and preparation method thereof
KR101980974B1 (en) Method for producing negative electrode and secondary battery, and secondary battery
KR20150143681A (en) Non-aqueous electrolyte secondary battery
WO2016202169A2 (en) High energy density lithium ion battery
CN106233498B (en) Nonaqueous electrolytic solution secondary battery
CN102694201A (en) Lithium ion battery
US20190334160A1 (en) Secondary battery
WO2013008475A1 (en) Nonaqueous electrolyte secondary battery
JP7211900B2 (en) Positive electrode material for secondary battery, and secondary battery using the same
CN111799470B (en) Positive pole piece and sodium ion battery
CN111200159B (en) Battery with a battery cell
CN109860584B (en) High-energy density lithium ion secondary battery
CN106848215B (en) A kind of high-tap density lithium ion battery ternary material and its preparation method and application
CN103117410A (en) 1.5V rechargeable lithium battery and preparation method thereof
JP2015088343A (en) Method for manufacturing positive electrode active material for nonaqueous electrolyte secondary batteries
CN105514364A (en) Modified lithium ion battery cathode material capable of improving cycle performance and preparation method thereof
JP2005197073A (en) Positive electrode for lithium secondary battery
CN104584279A (en) Nonaqueous electrolyte secondary 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
GR01 Patent grant
GR01 Patent grant