[go: up one dir, main page]

CN101587948A - Preparation method for LiTiO/C compound electrode material - Google Patents

Preparation method for LiTiO/C compound electrode material Download PDF

Info

Publication number
CN101587948A
CN101587948A CNA2009100437239A CN200910043723A CN101587948A CN 101587948 A CN101587948 A CN 101587948A CN A2009100437239 A CNA2009100437239 A CN A2009100437239A CN 200910043723 A CN200910043723 A CN 200910043723A CN 101587948 A CN101587948 A CN 101587948A
Authority
CN
China
Prior art keywords
electrode material
preparation
composite electrode
temperature
lithium
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
CNA2009100437239A
Other languages
Chinese (zh)
Other versions
CN101587948B (en
Inventor
张治安
李劼
赖延清
高宏权
王姣丽
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.)
YEXIANG JINGKE NEW ENERGY CO Ltd HUNAN
Central South University
Original Assignee
YEXIANG JINGKE NEW ENERGY CO Ltd HUNAN
Central South 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 YEXIANG JINGKE NEW ENERGY CO Ltd HUNAN, Central South University filed Critical YEXIANG JINGKE NEW ENERGY CO Ltd HUNAN
Priority to CN2009100437239A priority Critical patent/CN101587948B/en
Publication of CN101587948A publication Critical patent/CN101587948A/en
Application granted granted Critical
Publication of CN101587948B publication Critical patent/CN101587948B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • 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

Landscapes

  • Battery Electrode And Active Subsutance (AREA)
  • Inorganic Compounds Of Heavy Metals (AREA)

Abstract

本发明公开了一种Li4Ti5O12/C复合电极材料的制备方法,采用先低温预烧后高温二步煅烧固相反应法。包括以下步骤:(1)将含Ti化合物与无机锂盐按照一定配比,在有机溶剂介质中球磨混合;(2)空气气氛下,升温至300~700℃,保温2~8h后,随炉冷却至室温得到中间相产物;(3)将炭源与中间相产物进行球磨混合,在惰性保护性气氛下,升温至780℃~950℃保温2~20h,然后随炉冷却,即可制得Li4Ti5O12/C复合电极材料。本发明具有制备成本低廉,容易实现规模化生产的特点,合成的样品形貌规整、结构稳定,具有高的充放电倍率特性,且循环性能良好,可用作超级电容器、锂离子电池或者超级电容电池的电极材料。The invention discloses a preparation method of a Li 4 Ti 5 O 12 /C composite electrode material, which adopts a two-step solid-phase reaction method of pre-calcination at low temperature and then calcination at high temperature. The method comprises the following steps: (1) ball-milling and mixing the Ti-containing compound and the inorganic lithium salt in an organic solvent medium according to a certain ratio; (2) raising the temperature to 300-700° C. under an air atmosphere, keeping the temperature for 2-8 hours, and Cool to room temperature to obtain the mesophase product; (3) Mix the carbon source and the mesophase product by ball milling, raise the temperature to 780°C-950°C for 2-20 hours under an inert protective atmosphere, and then cool with the furnace to obtain Li 4 Ti 5 O 12 /C composite electrode material. The invention has the characteristics of low preparation cost and easy realization of large-scale production, and the synthesized samples have regular appearance, stable structure, high charge and discharge rate characteristics, and good cycle performance, and can be used as supercapacitors, lithium ion batteries or supercapacitors Electrode materials for batteries.

Description

A kind of Li 4Ti 5O 12The preparation method of/C combination electrode material
Technical field
The invention belongs to the new energy materials technical field, be specifically related to a kind of Li as lithium ion battery, ultracapacitor or super capacitance cell 4Ti 5O 12The preparation method of/C combination electrode material.
Background technology
The world today, petroleum resources are day by day nervous, and environmental pollution is on the rise, and forces various countries to strive to find the novel energy of sustainable development.Along with Aero-Space, defence and military, communications and transportation, electronic information and instrument and meter, especially practical application such as electric automobile is urgent day by day to the demand of high power density, wide temperature range energy storage system, is the focus that the environmental protection energy storage device of representative has become current concern with lithium ion battery, ultracapacitor or super capacitance cell.The performance of electrode material and preparation technology are determining the performance of energy storage device to a great extent, so the research of battery material is particularly important.
Spinel lithium titanate (Li 4Ti 5O 12) theoretical embedding lithium current potential is 1.55V (vs.Li +/ Li), theoretical specific capacity is 175mAh/g, is a kind of " zero strain " material, volume changes hardly in the charge and discharge process, has advantages such as charging and discharging capabilities is good, cycle performance is good, charging/discharging voltage platform stable.Simultaneously, abundant, the cheap and more easily preparation of titanium resource.These advantages make it become the electrode material that lithium ion battery, ultracapacitor or super capacitance cell have prospect, and huge researching value and commercial application prospect are arranged.
Lithium ion battery has advantages such as high-energy-density, high working voltage, memory-less effect, is expected to one of major impetus source that becomes by electric automobile.At present, though the graphite-like carbon negative pole material successfully is applied in the lithium ion battery, because the current potential of the current potential of carbon electrode and lithium metal is very approaching, easily the precipitating metal lithium forms dendrite, has potential safety hazard; Lithium ion embeds repeatedly and deviates from simultaneously, and material structure can be damaged and cause capacity attenuation.And with Li 4Ti 5O 12As the lithium ion battery of negative material, cycle life is up to 4000 times, obviously greater than graphite cathode; Fail safe is also good than lithium metal and carbon negative pole.Toshiba Corp announces that in 2007 exploitation is based on Li 4Ti 5O 12Lithium ion battery " SCiB ", be intended to be used for the hybrid power field.U.S. EnerDel company has also showed employing Li in the AABC-07 meeting 4Ti 5O 12The hybrid vehicle lithium ion battery.
Ultracapacitor then is another high power energy storage device that is rapidly developed, and have strong, the advantage such as have extended cycle life of power density height, large current density ability, but energy density is lower.Typical ultracapacitor is that two electrodes are in the middle of active carbon (AC) electrode symmetric form capacitor that barrier film in addition constitutes.Asymmetric ultracapacitor then is a kind of novel energy-storing device between symmetry ultracapacitor and secondary cell that new development is got up, and compares with traditional charcoal/charcoal symmetry ultracapacitor, has more high-energy-density; Compare with battery, have more high power density and more long-life.(US 6252762, Journal of the Electrochemical Society, 2001,148 (8): the Li of A930~A939) for TelcordiaTechnologies 4Ti 5O 12Material constitutes Li 4Ti 5O 12The asymmetric ultracapacitor of/AC, energy density reaches tens Wh/kg, far above the energy density (5~10Wh/kg) of traditional symmetric form charcoal/charcoal super capacitor.On this basis, Deng Z H etc. (Journalof Power Sources, 2009,187:635~639) has studied with Li 4Ti 5O 12Be negative pole, constitute (LiMn 2O 4+ AC)/Li 4Ti 5O 12Super capacitance cell.
At present, the synthetic method of spinel lithium titanate is many, and high-temperature solid phase reaction method is arranged usually, molten salt growth method, sol-gel process etc.
High temperature solid-state is synthetic to be preparation Li 4Ti 5O 12Main method, usually by TiO 2With Li 2CO 3Or lithium salts such as lithium hydroxide makes through the high temperature solid-state method one-step calcination, and reaction temperature is generally 800~1000 ℃, reaction time 12~24h.This technology is fairly simple, has the large-scale production advantage.Yet these high-temperature solid phase reaction method shortcomings are that the reaction time is long, the energy consumption height; Simultaneously, because the reaction temperature height, temperature retention time is long, and inorganic lithium salt volatilizees easily, therefore in order to obtain the Li of desirable metering ratio 4Ti 5O 12, often need lithium excessive about 8% in the reaction raw materials.(the process engineering journal, 2005,5 (2): 170~174) by nLi: nTi=0.84 (mol ratio) accurately takes by weighing Li to people such as Yang Jianwen 2CO 3And TiO 2And be scattered in the ethanol, with three-head grinding machine continuously grinding 2h, remove ethanol, contain in the corundum boat, place in the tube furnace.In air, with Pt-Rh thermocouple measurement temperature, employing AI Artificial intelligence industry regulator control programming rate (5 ℃/min), temperature is kept 24h after reaching 950 ℃, slowly is cooled to below 100 ℃, uses three-head grinding machine continuously grinding 2h (in the air) again, 250 ℃ of oven dry make Li 4Ti 5O 12High temperature length consuming time, the energy consumption height, relatively poor with the product cycle performance that this technology makes.
Patent (ZL 200610109497.6) then adopts molten salt growth method, 500~1200 ℃ of reaction temperatures, reaction time 6~16h, cool to room temperature then with the furnace, after the taking-up of the product after the solid phase reaction, wash with distilled water, remove remaining low temperature melting salt, put in 80~100 ℃ the vacuum drying chamber and dry by the fire 24h, obtain the spinel lithium titanate material of particle diameter 50nm~100 μ m.
(Journal of Power Sources such as M Venkateswarlu, 2005,146:204~208) by Li: Ti=4: 5 atomic ratio mixes normal propyl alcohol titanium and lithium acetate in the 75ml ethanolic solution, stir 10min under the room temperature after solution become white by yellow.Solution is increased to 80 ℃, continues to stir the formation gel.At 60~70 ℃ of stable heating 20h, obtain Li 4Ti 5O 12Precursor powder, organic principle, wherein Li are removed in calcining under 800 ℃ of Oxygen Flow states 4Ti 5O 12Mean particle size is 39nm.But sol-gel process needs expensive organic alkoxide as reactant, and complex process, and is restive, therefore is difficult to realize that large-scale industrial production satisfies the wilderness demand of new energy field.
Yet, because Li 4Ti 5O 12The intrinsic electronic conductivity of material is lower by (about 10 -13S/cm), the Li of above-mentioned technology preparation 4Ti 5O 12Capacity attenuation is fast when high current charge-discharge, high rate performance is poor, has limited the application under the high current charge-discharge condition, and therefore improving its high rate performance becomes Li 4Ti 5O 12The key of practicalization.
Part Study person then be chosen in Li 4Ti 5O 12Material surface coated with conductive agent (mainly being carbon), the structure conductive network increases the electron conduction ability between the particle, improves electronic conductivity, improves the high current charge-discharge multiplying power property then.
Patent (CN 101378119A) adopts solid phase reaction that lithium salts and titanium dioxide are mixed, and makes lithium titanate at 750~1000 ℃ of roasting 8~20h.Then, the lithium titanate that utilizes the dipping steam seasoning will be coated with carbon source material places tube furnace, under inert gas shielding, at 750~1000 ℃ of roasting 0.5~5h, obtains the charcoal coating type lithium titanate.Coat charcoal behind the synthetic lithium titanate, the charcoal that is difficult to the processability homogeneous coats Li 4Ti 5O 12Electrode material; Twice high-temperature process length consuming time has also consumed big energy simultaneously.
Yu Haiying (SCI, 2007,28 (8): 1556~1560),, join Li with hard carbon material coalescence benzene (PAS) 2CO 3And TiO 2Mixture in, pour an amount of ethanol into, stir, dipping 12h places ball grinder with batch mixing, put into diameter and be 10 and the agate ball of 6mm some, at room temperature ball milling 3h takes out batch mixing and also places 80 ℃ baking oven, removes ethanol, siccative is placed quartz boat, at N 2In tube furnace, calcine under the gas shiled.After cooling, with product ball milling 30min again, make doped lithium titanate, high rate performance is improved.Yet said method adopts the charcoal source that adds in reaction raw materials, exists reaction to generate dephasign not exclusively, easily, causes problems such as capacity is not high, cycle performance difference.
(Journal of the Electrochemical Society, 2007,154 (7): 692-697) adopt thermal evaporation to decompose, be that the charcoal source is at Li with the toluene vapours to Cheng L etc. 4Ti 5O 12The surface coats balanced graphitized carbon, has improved Li 4Ti 5O 12Conductivity.But toluene is noxious substance, and its steam and air can form explosive mixture, meets naked light, high thermoae easy firing blast, causes operational danger and highly difficult.
Summary of the invention
At Li 4Ti 5O 12The problem of the electronic conductivity difference of material own the objective of the invention is to propose a kind of Li 4Ti 5O 12The preparation method of/C combination electrode can prepare the good Li of high-rate charge-discharge capability 4Ti 5O 12/ C combination electrode material improves the electron conduction ability of material.The present invention has that preparation cost is cheap, technology is simple, power consumption is few, the characteristics of accomplishing scale production easily.
The objective of the invention is to realize in the following manner.
A kind of Li 4Ti 5O 12The preparation method of/C combination electrode material may further comprise the steps:
(1) will contain Ti compound and inorganic lithium salt, ball milling mixes 2~6h in organic solvent medium, and vacuumize obtains presoma;
(2) under the air atmosphere, precursor is warming up to 300~700 ℃ of insulation 2~8h after, be cooled to room temperature obtain in the middle of the phase product;
(3) charcoal source and middle product are mutually carried out ball milling in organic solvent medium and mix 2~6h, under the inertia protective atmosphere, be warming up to 780 ℃~950 ℃ insulation 2~20h then, cooling promptly makes Li then 4Ti 5O 12/ C combination electrode material.
Described (2) are warming up to 400~650 ℃ of better heat preservation with precursor in the step.
Described (3) are warming up to 800 ℃~900 ℃ better heat preservation in the step.
The charcoal source is one or more in glucose, sucrose, starch, phenolic resins, epoxy resin, the polyacrylonitrile.
The content of C in combination electrode material is: 1~10wt%; Be preferably 1.5~5wt%.
The inertia protective atmosphere is one or more in nitrogen, argon gas, the hydrogen.
Organic solvent medium is one or more in acetone, isopropyl alcohol, n-butanol, normal propyl alcohol, the absolute ethyl alcohol.
Containing the Ti compound is unformed TiO 2, rutile TiO 2, Detitanium-ore-type TiO 2, in the metatitanic acid one or more; Inorganic lithium salt be in lithium hydroxide, lithium acetate, lithium nitrate, lithium carbonate, the lithium chloride one or more; Contain that the Li/Ti atomic ratio is 4.0~4.4: 5 in Ti compound and the inorganic lithium salt.
Li prepared according to the methods of the invention 4Ti 5O 12/ C combination electrode material is grey to black powder, the gram volume 〉=145mAh/g of material when 0.2C discharges and recharges, the gram volume 〉=120mAh/g of material when 3C discharges and recharges; Capability retention 〉=90% of 100 of material circulations when 1C discharges and recharges.
The present invention adopts two steps calcining solid phase reaction process, promptly carries out low temperature presintering earlier, and the phase product carries out high-temperature calcination again in the middle of making, suppress the volatilization that high temperature descends lithium salts for a long time, first on the other hand low temperature presintering, back high temperature crystallization on the one hand, reduce reaction temperature, shorten the reaction time, energy savings.Simultaneously, in middle phase product, add the charcoal source, save reaction raw materials on the one hand, prepare the Li that conducts electricity very well 4Ti 5O 12/ C material effectively suppresses further growing up of crystallite dimension under the high temperature on the other hand, effectively improves high rate performance.
Adopt the prepared Li of preparation method provided by the invention 4Ti 5O 12/ C combination electrode material has high charge, and has good cycle performance.The present invention has that preparation cost is cheap, technology is simple, the reaction power consumption is few; the characteristics of accomplishing scale production easily; synthetic regular, the Stability Analysis of Structures of sample topography; has high charge; and cycle performance is good, can be used as the electrode material of ultracapacitor, lithium ion battery or super capacitance cell.
Description of drawings
Fig. 1 is the XRD figure of embodiment 1, embodiment 2, embodiment 3;
Fig. 2 is the SEM figure of embodiment 1;
Fig. 3 is the SEM figure of embodiment 2;
Fig. 4 is the SEM figure of embodiment 3.
Embodiment
Below in conjunction with embodiment, the present invention is described in further detail, but these embodiment must not be interpreted as limiting the scope of the invention.
Embodiment 1
Take by weighing 7.62g and analyze pure Li 2CO 3, then by Li: Ti=4.12: 5 take by weighing the 20.00g rutile TiO 2, both being mixed the back add in the PTFE ball grinder, ball milling mixing 2h in anhydrous ethanol medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.
In being positioned in the high temperature resistance furnace with the crucible splendid attire, carry out the pre-burning reaction under the air conditions, the control heating rate is 5 ℃/min, is warming up to 650 ℃ of insulation 6h, cools to room temperature with the furnace and obtains middle phase product.
Press Li 4Ti 5O 12The target carbon content is that 2wt% adds starch 0.46g respectively in the/C composite material, and ball milling mixing 2h in the anhydrous ethanol medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.Dry back in atmosphere furnace at N 2Be warming up to 800 ℃ of insulation 6h under the protective atmosphere, cool off with stove then.Products therefrom is Li 4Ti 5O 12/ C combination electrode material.
Material property characterizes:
The crystal structure of Japan Rigaku 3014 type X-ray diffractometer analysis of material is with scanning electron microscopy (Japan, JSM-6360) pattern of observation material.With the C content in the leco CS-600 charcoal sulphur analyzer working sample.
Electrochemical property test:
Electrode slice is with assembling all prepares as follows to the lithium half-cell: with embodiment 1 prepared Li 4Ti 5O 12/ C combination electrode material, conductive black, binding agent evenly mix according to mass ratio at 8: 1: 1, drip an amount of solvent (NMP), after fully grinding slurry evenly is coated on the 10 μ m Copper Foil collectors, 120 ℃ of following vacuumize 12h strike out diameter and are the electrode thin slice about 0.8cm then.In being full of the glove box of argon gas work electrode, barrier film, metal lithium sheet be assembled into the lithium half-cell is carried out electrochemical property test, barrier film is Celgard 2400, and electrolyte is LiPF 6/ EC-DMC-EMC, wherein: DMC: EMC: EC=1: 1: 1 (W/W), LiPF 6Concentration 1.0M.
Take out the back and carry out the constant current charge and discharge with blue electricity (LAND) series battery test macro and test, the test voltage scope is 0.8~2.8V, with a certain multiplying power electric current constant-current discharge to 0.8V, again with same electric current constant current charge to 2.8V.
XRD detects and is spinelle Li 4Ti 5O 12Characteristic peak.The SEM of JSM-6360 sem observation particle size as can be known is more even, regular, and is spherical in shape or class is spherical.Using leco CS-600 charcoal sulphur analyzer to detect C content is 1.29%.
Press the Li of embodiment 1 method and proportioning preparation 4Ti 5O 12Gram volume is 156.4mAh/g under the/C combination electrode material 0.2C charging and discharging currents, and gram volume is 146.5mAhg under the 0.5C charging and discharging currents -1, gram volume is 133mAh/g under the 3C charging and discharging currents.Capability retention 〉=94% of 100 of material circulations when 1C discharges and recharges.
Embodiment 2
Take by weighing 7.62g and analyze pure Li 2CO 3, then by Li: Ti=4.12: 5 take by weighing the unformed TiO of 20.00g 2, both being mixed the back add in the PTFE ball grinder, ball milling mixing 2h in isopropanol medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.
In being positioned in the high temperature resistance furnace with the crucible splendid attire, carry out the pre-burning reaction under the air conditions, the control heating rate is 5 ℃/min, is warming up to 650 ℃ of insulation 6h, cools to room temperature with the furnace and obtains middle phase product.
Press Li 4Ti 5O 12The target carbon content is that 3wt% adds glucose 0.69g respectively in the/C composite material, and ball milling mixing 2h in the isopropanol medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.Dry back in atmosphere furnace at N 2Be warming up to 800 ℃ of insulation 8h under the protective atmosphere, cool off with stove then.Products therefrom is Li 4Ti 5O 12/ C combination electrode material.
The material property sign is identical with embodiment 1 with electrochemical property test.
Press the Li of embodiment 2 methods and proportioning preparation 4Ti 5O 12Gram volume is 152.4mAh/g under the/C combination electrode material 0.2C charging and discharging currents, and gram volume is 141.3mAhg under the 0.5C charging and discharging currents -1, gram volume is 129.4mAh/g under the 3C charging and discharging currents.Capability retention 〉=95% of 100 of material circulations when 1C discharges and recharges.
Embodiment 3
Take by weighing 7.62g and analyze pure Li 2CO 3, then by Li: Ti=4.12: 5 take by weighing 20.00g anatase TiO 2, both being mixed the back add in the PTFE ball grinder, ball milling mixing 2h in isopropanol medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.
In being positioned in the high temperature resistance furnace with the crucible splendid attire, carry out the pre-burning reaction under the air conditions, the control heating rate is 5 ℃/min, is warming up to 680 ℃ of insulation 6h, cools to room temperature with the furnace and obtains middle phase product.
Press Li 4Ti 5O 12The target carbon content is that 2wt% adds glucose 0.46g respectively in the/C composite material, and ball milling mixing 2h in the isopropanol medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.Dry back is warming up to 900 ℃ of insulation 6h under argon shield atmosphere in atmosphere furnace, cool off with stove then.Products therefrom is Li 4Ti 5O 12/ C combination electrode material.
The material property sign is identical with embodiment 1 with electrochemical property test.
Press the Li of embodiment 3 methods and proportioning preparation 4Ti 5O 12Gram volume is 157.4mAh/g under the/C combination electrode material 0.2C charging and discharging currents, and gram volume is 145.2mAhg under the 0.5C charging and discharging currents -1, gram volume is 128.4mAh/g under the 3C charging and discharging currents.Capability retention 〉=92% of 100 of material circulations when 1C discharges and recharges.
Embodiment 4
Take by weighing 7.62g and analyze pure Li 2CO 3, then by Li: Ti=4.12: 5 take by weighing 20.00g anatase TiO 2, both being mixed the back add in the PTFE ball grinder, ball milling mixing 2h in anhydrous ethanol medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.
In being positioned in the high temperature resistance furnace with the crucible splendid attire, carry out the pre-burning reaction under the air conditions, the control heating rate is 5 ℃/min, is warming up to 650 ℃ of insulation 2h, cools to room temperature with the furnace and obtains middle phase product.
Press Li 4Ti 5O 12The target carbon content is that 5wt% adds phenolic resins 1.15g respectively in the/C composite material, and ball milling mixing 2h in the anhydrous ethanol medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.Dry back is warming up to 850 ℃ of insulation 6h under argon shield atmosphere in atmosphere furnace, cool off with stove then.Products therefrom is Li 4Ti 5O 12/ C combination electrode material.
Electrochemical property test is identical with embodiment 1.
Press the Li of embodiment 4 methods and proportioning preparation 4Ti 5O 12Gram volume is 150.6mAh/g under the/C combination electrode material 0.2C charging and discharging currents, and gram volume is 142.2mAhg under the 0.5C charging and discharging currents -1, gram volume is 127.4mAh/g under the 3C charging and discharging currents.Capability retention 〉=95% of 100 of material circulations when 1C discharges and recharges.
Embodiment 5
Take by weighing 7.62g and analyze pure Li 2CO 3, then by Li: Ti=4.12: 5 take by weighing 20.00g anatase TiO 2, both being mixed the back add in the PTFE ball grinder, ball milling mixing 2h in anhydrous ethanol medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.
In being positioned in the high temperature resistance furnace with the crucible splendid attire, carry out the pre-burning reaction under the air conditions, the control heating rate is 5 ℃/min, is warming up to 600 ℃ of insulation 6h, cools to room temperature with the furnace and obtains middle phase product.
Press Li 4Ti 5O 12The target carbon content is that 3wt% adds starch 0.69g respectively in the/C composite material, and ball milling mixing 2h in the anhydrous ethanol medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.Dry back is warming up to 850 ℃ of insulation 6h under argon shield atmosphere in atmosphere furnace, cool off with stove then.Products therefrom is Li 4Ti 5O 12/ C combination electrode material.
Electrochemical property test is identical with embodiment 1.
Press the Li of embodiment 5 methods and proportioning preparation 4Ti 5O 12Gram volume is 156.7mAh/g under the/C combination electrode material 0.2C charging and discharging currents, and gram volume is 139.2mAhg under the 0.5C charging and discharging currents -1, gram volume is 130.1mAh/g under the 3C charging and discharging currents.Capability retention 〉=94% of 100 of material circulations when 1C discharges and recharges.
Embodiment 6
Take by weighing 7.62g and analyze pure Li 2CO 3, then by Li: Ti=4.12: 5 take by weighing the unformed TiO of 20.00g 2, both being mixed the back add in the PTFE ball grinder, ball milling mixing 2h in anhydrous ethanol medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.
In being positioned in the high temperature resistance furnace with the crucible splendid attire, carry out the pre-burning reaction under the air conditions, the control heating rate is 5 ℃/min, is warming up to 600 ℃ of insulation 8h, cools to room temperature with the furnace and obtains middle phase product.
Press Li 4Ti 5O 12The target carbon content is that 5wt% adds starch 1.15g respectively in the/C composite material, and ball milling mixing 2h in the anhydrous ethanol medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.Dry back is warming up to 900 ℃ of insulation 4h under nitrogen+hydrogen shield atmosphere in atmosphere furnace, cool off with stove then.Products therefrom is Li 4Ti 5O 12/ C combination electrode material.
Electrochemical property test is identical with embodiment 1.
Press the Li of embodiment 6 methods and proportioning preparation 4Ti 5O 12Gram volume is 151.3mAh/g under the/C combination electrode material 0.2C charging and discharging currents, and gram volume is 139.2mAhg under the 0.5C charging and discharging currents -1, gram volume is 128.1mAh/g under the 3C charging and discharging currents.Capability retention 〉=94% of 100 of material circulations when 1C discharges and recharges.
Embodiment 7
Take by weighing 7.77g and analyze pure Li 2CO 3, then by Li: Ti=4.2: 5 take by weighing the unformed TiO of 20.00g 2, both being mixed the back add in the PTFE ball grinder, ball milling mixing 2h in anhydrous ethanol medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.
In being positioned in the high temperature resistance furnace with the crucible splendid attire, carry out the pre-burning reaction under the air conditions, the control heating rate is 5 ℃/min, is warming up to 600 ℃ of insulation 6h, cools to room temperature with the furnace and obtains middle phase product.
Press Li 4Ti 5O 12The target carbon content is that 5wt% adds starch 1.15g respectively in the/C composite material, and ball milling mixing 2h in the anhydrous ethanol medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.Dry back is warming up to 900 ℃ of insulation 4h under nitrogen+hydrogen shield atmosphere in atmosphere furnace, cool off with stove then.Products therefrom is Li 4Ti 5O 12/ C combination electrode material.
Electrochemical property test is identical with embodiment 1.
Press the Li of embodiment 7 methods and proportioning preparation 4Ti 5O 12Gram volume is 151.3mAh/g under the/C combination electrode material 0.2C charging and discharging currents, and gram volume is 139.2mAhg under the 0.5C charging and discharging currents -1, gram volume is 128.1mAh/g under the 3C charging and discharging currents.Capability retention 〉=94% of 100 of material circulations when 1C discharges and recharges.
Embodiment 8
Take by weighing 8.74g LiOHH 2O, then by Li: Ti=4.16: 5 take by weighing 20.00g rutile TiO 2, both being mixed the back add in the PTFE ball grinder, ball milling mixing 2h in absolute ethyl alcohol and isopropyl alcohol (weight ratio 1: 1) medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.
In being positioned in the high temperature resistance furnace with the crucible splendid attire, carry out the pre-burning reaction under the air conditions, the control heating rate is 5 ℃/min, is warming up to 580 ℃ of insulation 3h, cools to room temperature with the furnace and obtains middle phase product.
Press Li 4Ti 5O 12The target carbon content is that 3wt% adds starch 0.69g respectively in the/C composite material, and ball milling mixing 2h in absolute ethyl alcohol and isopropyl alcohol (weight ratio 1: the 1) medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.Dry back is warming up to 850 ℃ of insulation 6h under nitrogen+hydrogen shield atmosphere in atmosphere furnace, cool off with stove then.Products therefrom is Li 4Ti 5O 12/ C combination electrode material.
Electrochemical property test is identical with embodiment 1.
Press the Li of embodiment 8 methods and proportioning preparation 4Ti 5O 12Gram volume is 157.6mAh/g under the/C combination electrode material 0.2C charging and discharging currents, and gram volume is 141.2mAhg under the 0.5C charging and discharging currents -1, gram volume is 130.4mAh/g under the 3C charging and discharging currents.Capability retention 〉=91% of 100 of material circulations when 1C discharges and recharges.
Embodiment 9
Take by weighing 8.57g LiOHH 2O, then by Li: Ti=4.08: 5 take by weighing the unformed TiO of 20.00g 2, both being mixed the back add in the PTFE ball grinder, ball milling mixing 2h in absolute ethyl alcohol and isopropyl alcohol (weight ratio 1: 1) medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.
In being positioned in the high temperature resistance furnace with the crucible splendid attire, carry out the pre-burning reaction under the air conditions, the control heating rate is 5 ℃/min, is warming up to 600 ℃ of insulation 2h, cools to room temperature with the furnace and obtains middle phase product.
Press Li 4Ti 5O 12The target carbon content is that 6wt% adds sucrose 1.38g respectively in the/C composite material, and ball milling mixing 2h in absolute ethyl alcohol and isopropyl alcohol (weight ratio 1: the 1) medium puts into 120 ℃ of dry 8h of vacuum drying chamber then.Dry back is warming up to 900 ℃ of insulation 5h under nitrogen+hydrogen shield atmosphere in atmosphere furnace, cool off with stove then.Products therefrom is Li 4Ti 5O 12/ C combination electrode material.
Electrochemical property test is identical with embodiment 1.
Press the Li of embodiment 9 methods and proportioning preparation 4Ti 5O 12Gram volume is 149.6mAh/g under the/C combination electrode material 0.2C charging and discharging currents, and gram volume is 138.7mAhg under the 0.5C charging and discharging currents -1, gram volume is 130.2mAh/g under the 3C charging and discharging currents.Capability retention 〉=95% of 100 of material circulations when 1C discharges and recharges.

Claims (9)

1、一种Li4Ti5O12/C复合电极材料的制备方法,其特征在于,所述制备方法包括以下步骤:1. A preparation method of Li 4 Ti 5 O 12 /C composite electrode material, characterized in that the preparation method comprises the following steps: (1)将含Ti化合物与无机锂盐,在有机溶剂介质中球磨混合2~6h,真空干燥得到前驱体;(1) Mixing the Ti-containing compound and the inorganic lithium salt by ball milling in an organic solvent medium for 2 to 6 hours, and drying in vacuum to obtain a precursor; (2)空气气氛下,将前躯体升温至300~700℃保温2~8h后,冷却至室温得到中间相产物;(2) Under an air atmosphere, heat the precursor to 300-700°C for 2-8 hours, then cool to room temperature to obtain the mesophase product; (3)将炭源与中间相产物在有机溶剂介质中进行球磨混合2~6h,真空干燥,然后在惰性保护性气氛下,升温至780℃~950℃保温2~20h,然后冷却,即制得Li4Ti5O12/C复合电极材料。(3) Mix the carbon source and the mesophase product by ball milling in an organic solvent medium for 2 to 6 hours, dry in vacuum, and then raise the temperature to 780°C to 950°C for 2 to 20 hours under an inert protective atmosphere, and then cool to prepare Obtain Li 4 Ti 5 O 12 /C composite electrode material. 2、根据权利要求1所述的Li4Ti5O12/C复合电极材料的制备方法,其特征在于:所述的(2)步中将前躯体升温至400~650℃保温。2. The preparation method of Li 4 Ti 5 O 12 /C composite electrode material according to claim 1, characterized in that: in the step (2), the temperature of the precursor is raised to 400-650°C and kept warm. 3、根据权利要求1所述的Li4Ti5O12/C复合电极材料的制备方法,其特征在于:所述的(3)步中升温至800℃~900℃保温。3. The preparation method of Li 4 Ti 5 O 12 /C composite electrode material according to claim 1, characterized in that: in the step (3), the temperature is raised to 800°C-900°C and kept warm. 4、根据权利要求1所述的Li4Ti5O12/C复合电极材料的制备方法,其特征在于,所述的炭源为葡萄糖、蔗糖、淀粉、酚醛树脂、环氧树脂、聚丙烯腈中的一种或几种。4. The preparation method of Li 4 Ti 5 O 12 /C composite electrode material according to claim 1, characterized in that the carbon source is glucose, sucrose, starch, phenolic resin, epoxy resin, polyacrylonitrile one or more of them. 5、根据权利要求1或4所述的Li4Ti5O12/C复合电极材料的制备方法,其特征在于:C在复合电极材料中的含量为:1~10wt%。5. The preparation method of Li 4 Ti 5 O 12 /C composite electrode material according to claim 1 or 4, characterized in that: the content of C in the composite electrode material is: 1-10wt%. 6、根据权利要求5所述的Li4Ti5O12/C复合电极材料的制备方法,其特征在于,C在复合电极材料中的含量为:1.5~5wt%。6. The preparation method of Li 4 Ti 5 O 12 /C composite electrode material according to claim 5, characterized in that the content of C in the composite electrode material is 1.5-5 wt%. 7、根据权利要求1所述的Li4Ti5O12/C复合电极材料的制备方法,其特征在于,所述的惰性保护性气氛是氮气、氩气、氢气中的一种或几种。7. The preparation method of Li 4 Ti 5 O 12 /C composite electrode material according to claim 1, characterized in that the inert protective atmosphere is one or more of nitrogen, argon and hydrogen. 8、根据权利要求1所述的Li4Ti5O12/C复合电极材料的制备方法,其特征在于,所述的有机溶剂介质为丙酮、异丙醇、正丁醇、正丙醇、无水乙醇中的一种或几种。8. The preparation method of Li 4 Ti 5 O 12 /C composite electrode material according to claim 1, characterized in that, the organic solvent medium is acetone, isopropanol, n-butanol, n-propanol, no One or more of water and ethanol. 9、根据权利要求1所述的Li4Ti5O12/C复合电极材料的制备方法,其特征在于,所述的含Ti化合物为无定型TiO2、金红石型TiO2、锐钛矿型TiO2、偏钛酸中的一种或几种;无机锂盐为氢氧化锂、乙酸锂、硝酸锂、碳酸锂、氯化锂中一种或几种;含Ti化合物与无机锂盐中Li/Ti原子比为4.0~4.4∶5。9. The preparation method of Li 4 Ti 5 O 12 /C composite electrode material according to claim 1, characterized in that the Ti-containing compound is amorphous TiO 2 , rutile TiO 2 , anatase TiO 2. One or more of metatitanic acid; the inorganic lithium salt is one or more of lithium hydroxide, lithium acetate, lithium nitrate, lithium carbonate, lithium chloride; Li/ The atomic ratio of Ti is 4.0-4.4:5.
CN2009100437239A 2009-06-19 2009-06-19 A kind of preparation method of Li4Ti5O12/C composite electrode material Expired - Fee Related CN101587948B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2009100437239A CN101587948B (en) 2009-06-19 2009-06-19 A kind of preparation method of Li4Ti5O12/C composite electrode material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2009100437239A CN101587948B (en) 2009-06-19 2009-06-19 A kind of preparation method of Li4Ti5O12/C composite electrode material

Publications (2)

Publication Number Publication Date
CN101587948A true CN101587948A (en) 2009-11-25
CN101587948B CN101587948B (en) 2011-05-18

Family

ID=41372080

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2009100437239A Expired - Fee Related CN101587948B (en) 2009-06-19 2009-06-19 A kind of preparation method of Li4Ti5O12/C composite electrode material

Country Status (1)

Country Link
CN (1) CN101587948B (en)

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102201570A (en) * 2010-03-25 2011-09-28 清华大学 Preparation method for electrode material of lithium battery
CN102364729A (en) * 2011-11-10 2012-02-29 中南大学 High-power Li4Ti5O12/activated carbon composite electrode material and preparation method thereof
CN102522535A (en) * 2011-12-15 2012-06-27 深圳市金润能源材料有限公司 Lithium ion battery cathode material and preparation method thereof
CN102569766A (en) * 2011-12-12 2012-07-11 长沙东旭环保科技有限公司 Method for preparing nanoscale lithium titanate and carbon composite electrode material
CN102906025A (en) * 2010-05-21 2013-01-30 纳幕尔杜邦公司 Process for making titanium compounds
CN102997651A (en) * 2012-11-30 2013-03-27 龙能科技(苏州)有限公司 Pusher furnace for preparing lithium titanate negative electrode materials of lithium ion battery and method
CN103296257A (en) * 2013-06-05 2013-09-11 深圳市斯诺实业发展有限公司永丰县分公司 Preparation method of modified lithium titanate negative material of lithium-ion battery
CN103311528A (en) * 2013-06-14 2013-09-18 天奈(镇江)材料科技有限公司 Spinel lithium titanate inserted carbon nanotube electrode material and preparation method thereof
CN103456939A (en) * 2013-07-24 2013-12-18 湖南大学 Method for preparing cathode material carbon-coated lithium titanate for lithium ion battery from metatitanic acid
CN104169220A (en) * 2012-03-16 2014-11-26 帝化株式会社 Lithium titanate and production method and use for same
CN104617287A (en) * 2014-04-25 2015-05-13 上海应用技术学院 Preparation method of oxygen-vacancy-type nano lithium titanate used as lithium-ion battery anode material
CN105914344A (en) * 2016-04-13 2016-08-31 武汉理工大学 High temperature-stable lithium iron fluorphosphate type lithium ion battery material and preparation method thereof
CN106207150A (en) * 2016-09-23 2016-12-07 湖南桑顿新能源有限公司 A kind of atomizing freeze drying prepares the method for lithium cell negative pole material lithium titanate
CN107437618A (en) * 2016-05-27 2017-12-05 松下知识产权经营株式会社 Electrochemical appliance
CN108565427A (en) * 2018-04-16 2018-09-21 合肥国轩电池材料有限公司 A kind of preparation method of carbon/lithium titanate composite material
DE112018000205T5 (en) 2017-02-21 2019-08-14 International Advanced Research Centre For Powder Metallurgy And New Materials (Arci) A METHOD FOR PRODUCING A POWERFUL LITHIUM TITANATE ANODE MATERIAL FOR APPLICATIONS OF LITHIUM-ION ACCUMULATORS

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100530780C (en) * 2006-12-29 2009-08-19 深圳市贝特瑞电子材料有限公司 Composite lithium titanate electrode material and preparation method thereof
CN101378119A (en) * 2008-10-06 2009-03-04 天津巴莫科技股份有限公司 Method for preparing carbon-coating type lithium titanate for lithium ion battery

Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9425458B2 (en) 2010-03-25 2016-08-23 Tsinghua University Method for making lithium-ion battery electrode material
CN102201570B (en) * 2010-03-25 2013-11-06 清华大学 Preparation method for electrode material of lithium battery
CN102201570A (en) * 2010-03-25 2011-09-28 清华大学 Preparation method for electrode material of lithium battery
CN102906025A (en) * 2010-05-21 2013-01-30 纳幕尔杜邦公司 Process for making titanium compounds
CN102364729A (en) * 2011-11-10 2012-02-29 中南大学 High-power Li4Ti5O12/activated carbon composite electrode material and preparation method thereof
CN102569766A (en) * 2011-12-12 2012-07-11 长沙东旭环保科技有限公司 Method for preparing nanoscale lithium titanate and carbon composite electrode material
CN102522535A (en) * 2011-12-15 2012-06-27 深圳市金润能源材料有限公司 Lithium ion battery cathode material and preparation method thereof
CN104169220A (en) * 2012-03-16 2014-11-26 帝化株式会社 Lithium titanate and production method and use for same
CN102997651A (en) * 2012-11-30 2013-03-27 龙能科技(苏州)有限公司 Pusher furnace for preparing lithium titanate negative electrode materials of lithium ion battery and method
CN102997651B (en) * 2012-11-30 2015-09-16 龙能科技(苏州)有限公司 Prepare pusher furnace and the method thereof of lithium titanate anode material for lithium ion battery
CN103296257B (en) * 2013-06-05 2015-06-24 深圳市斯诺实业发展有限公司 Preparation method of modified lithium titanate negative material of lithium-ion battery
CN103296257A (en) * 2013-06-05 2013-09-11 深圳市斯诺实业发展有限公司永丰县分公司 Preparation method of modified lithium titanate negative material of lithium-ion battery
CN103311528A (en) * 2013-06-14 2013-09-18 天奈(镇江)材料科技有限公司 Spinel lithium titanate inserted carbon nanotube electrode material and preparation method thereof
CN103456939A (en) * 2013-07-24 2013-12-18 湖南大学 Method for preparing cathode material carbon-coated lithium titanate for lithium ion battery from metatitanic acid
CN103456939B (en) * 2013-07-24 2015-12-23 湖南大学 Metatitanic acid is utilized to prepare the method for the coated lithium titanate of lithium ion battery negative material carbon
CN104617287A (en) * 2014-04-25 2015-05-13 上海应用技术学院 Preparation method of oxygen-vacancy-type nano lithium titanate used as lithium-ion battery anode material
CN105914344A (en) * 2016-04-13 2016-08-31 武汉理工大学 High temperature-stable lithium iron fluorphosphate type lithium ion battery material and preparation method thereof
CN107437618B (en) * 2016-05-27 2022-01-28 松下知识产权经营株式会社 Electrochemical device
CN107437618A (en) * 2016-05-27 2017-12-05 松下知识产权经营株式会社 Electrochemical appliance
CN106207150A (en) * 2016-09-23 2016-12-07 湖南桑顿新能源有限公司 A kind of atomizing freeze drying prepares the method for lithium cell negative pole material lithium titanate
DE112018000205T5 (en) 2017-02-21 2019-08-14 International Advanced Research Centre For Powder Metallurgy And New Materials (Arci) A METHOD FOR PRODUCING A POWERFUL LITHIUM TITANATE ANODE MATERIAL FOR APPLICATIONS OF LITHIUM-ION ACCUMULATORS
US11001506B2 (en) 2017-02-21 2021-05-11 International Advanced Research Centre For Powder Metallurgy And New Materials (Arci) Method of producing high performance lithium titanate anode material for lithium ion battery applications
CN108565427B (en) * 2018-04-16 2020-06-26 合肥国轩电池材料有限公司 Preparation method of carbon/lithium titanate composite material
CN108565427A (en) * 2018-04-16 2018-09-21 合肥国轩电池材料有限公司 A kind of preparation method of carbon/lithium titanate composite material

Also Published As

Publication number Publication date
CN101587948B (en) 2011-05-18

Similar Documents

Publication Publication Date Title
CN101587948A (en) Preparation method for LiTiO/C compound electrode material
CN100530780C (en) Composite lithium titanate electrode material and preparation method thereof
CN103022459B (en) Preparation method of graphene/lithium titanate composite anode material
CN104425808B (en) A kind of compound negative electrode material of lithium ion battery and preparation method thereof and lithium ion battery
CN103682332B (en) Compound negative material of a kind of lithium ion battery and preparation method thereof and lithium ion battery
CN101572305B (en) A preparation method of LiFePO4/C cathode material with high rate performance
CN103078100B (en) A kind of lithium sodium manganate cathode material and preparation method thereof
CN101635348B (en) Tantalum-containing lithium ion battery cathode material lithium titanate preparation method
CN102328952B (en) Preparation method for spherical lithium titanate material
CN101159328A (en) LiFePO4/C nano composite positive pole material and preparation method thereof
CN102034971B (en) Lithium iron phosphate/polypyridine composite cathode material and preparation method thereof for lithium ion battery
CN101591012B (en) Preparation method of lithium iron phosphate as cathode material of lithium ion battery
CN113659141A (en) SiO @ Mg/C composite material and preparation method and application thereof
CN102496707A (en) Preparation method of nano-grade-carbon-clad spinel lithium titanate battery cathode material
CN103151506A (en) Preparation method of nanoscale zirconium-doped lithium titanate material
CN102120610A (en) Lithium ion battery cathode material as well as preparation method and application thereof
CN107093739A (en) Kalium ion battery positive electrode potassium Mn oxide and preparation method thereof
CN105789607A (en) Preparation method of lithium titanate anode material doped with rare earth
CN103378355A (en) Alkali metal secondary battery as well as negative active substance, negative material and negative electrode thereof, and preparation method of negative active substance
CN108767214A (en) A kind of preparation method of alumina-graphite alkene composite lithium ion battery cathode material
CN108281620B (en) A kind of preparation method of sodium ion battery anode material titanium dioxide
CN105261736A (en) Preparation method of monodisperse lithium iron phosphate and lithium cobalt iron phosphate core-shell structure composite cathode material
CN100426568C (en) Method of synthesizing lithium ion cathode material lithium titanium oxide using solvent heating method
CN102306769A (en) Preparation method of lithium iron phosphate/lithium vanadium phosphate composite material
CN102569808B (en) A modification method of high-rate lithium-rich cathode material

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20110518

Termination date: 20160619

CF01 Termination of patent right due to non-payment of annual fee