CN101635354A - Method for preparing amorphous phase nickel hydroxide doped electrode active material of carbon nano tube - Google Patents

Method for preparing amorphous phase nickel hydroxide doped electrode active material of carbon nano tube Download PDF

Info

Publication number
CN101635354A
CN101635354A CN200910114321A CN200910114321A CN101635354A CN 101635354 A CN101635354 A CN 101635354A CN 200910114321 A CN200910114321 A CN 200910114321A CN 200910114321 A CN200910114321 A CN 200910114321A CN 101635354 A CN101635354 A CN 101635354A
Authority
CN
China
Prior art keywords
carbon nano
active material
nickel
electrode active
amorphous phase
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
CN200910114321A
Other languages
Chinese (zh)
Other versions
CN101635354B (en
Inventor
刘长久
李延伟
陈世娟
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.)
Guilin University of Technology
Original Assignee
Guilin University of Technology
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 Guilin University of Technology filed Critical Guilin University of Technology
Priority to CN2009101143213A priority Critical patent/CN101635354B/en
Publication of CN101635354A publication Critical patent/CN101635354A/en
Application granted granted Critical
Publication of CN101635354B publication Critical patent/CN101635354B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

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

Abstract

The invention discloses a method for preparing an amorphous phase nickel hydroxide doped electrode active material of a carbon nano tube. The amorphous phase nickel hydroxide doped electrode active material of the carbon nano tube is prepared by a rapid freezing chemical coprecipitation process through using nickel salt, strong base and the carbon nano tube as major materials, and surface active agent isooctyl phenol polyethoxylate (TX-100) and ethanol as auxiliary materials. The prepared electrode active material is prepared into a nickel electrode to form a hydrogen-nickel battery, and has high discharge specific capacity and favorable circulation performance. The method is simple and convenient to operate and the condition is easy to control; the prepared chemical material is stable in the electrochemical performance and is suitable for being used as the anode active material of an alkaline secondary battery.

Description

The preparation method of amorphous phase nickel hydroxide doped electrode active material of carbon nano tube
Technical field
The present invention relates to a kind of preparation method of battery material, particularly relate to a kind of preparation method of amorphous phase nickel hydroxide doped electrode active material of carbon nano tube.
Background technology
But Ni-H cell is described as first-selected electric vehicle power accumulator because of its high-energy-density, long-life fast charging and discharging, excellent comprehensive characteristic such as pollution-free.In the Ni-H cell, the performance of positive active material is the key that cell integrated combination property improves, and especially as the electric motor car power accumulator, the specific capacity of nickel electrode and electric conductivity also need further to improve.
Summary of the invention
The preparation method who the purpose of this invention is to provide a kind of amorphous phase nickel hydroxide doped electrode active material of carbon nano tube.
Concrete steps are as follows:
(1) calculates the consumption of nickel salt, alkali and carbon nano-tube according to the amount of required preparation target product;
(2) with above-mentioned raw materials weighing in proportion, and wiring solution-forming;
(3) in the nickel salt solution for preparing, add surfactant isooctylphenol APEO (TX-100), ethanol and carbon nano-tube sequentially, ultrasonic concussion 30-60 minute, form the mixed liquor that even carbon nanotube is disperseed;
(4) control reaction temperature is 50-60 ℃, and adding is 2: 1 strong base solutions with the mol ratio of nickel salt in the mixed liquor that step (3) makes, and reaction is 2-3 hour under strong agitation;
(5) step (4) product snap frozen, filtration, washing, drying, grinding are disperseed, can obtain amorphous phase nickel hydroxide doped electrode active material of carbon nano tube.
Described highly basic is a kind of in NaOH and the potassium hydroxide; The concentration of NaOH and potassium hydroxide is respectively 1-4mol/L and 1-5mol/L.
Described nickel salt is a kind of in nickelous sulfate and the nickel nitrate; The concentration of nickelous sulfate and nickel nitrate is respectively 0.5-1mol/L and 0.1-1mol/L.
Described carbon nano-tube is that caliber is the multi-walled carbon nano-tubes of 30-50nm.
Advantage of the present invention is:
1. adopt the method to the product snap frozen, the nickel hydroxide that system is equipped with has noncrystalline structure, and structural disorder and a large amount of faults of construction of height make material have the active material utilization of more electro-chemical activity center and Geng Gao.
2. carbon nano-tube conductive network inner at amorphous phase nickel hydroxide and that the surface forms not only can improve the inner and intergranular conductivity of nickel hydroxide particle, and can also suppress the efflorescence of nickel electrode active material in the charge and discharge cycles process effectively.
3. have the high and good characteristic of cyclic reversibility of specific capacity with this material as the alkaline secondary cell of positive electrode, and the preparation method is simple, condition is easy to control.
Embodiment
Embodiment 1:
By the mass percent of carbon nano-tube in the target product nickel hydroxide is 1% to take by weighing carbon nano-tube and join in the nickel sulfate solution of 0.5mol/L, carbon nano-tube is that caliber is the multi-walled carbon nano-tubes of 30-40nm, add surfactant isooctylphenol APEO (TX-100) and the absolute ethyl alcohol that volume ratio is respectively above-mentioned solution 1% and 2% simultaneously and make dispersant, ultrasonic concussion 30 minutes forms the mixed liquor that even carbon nanotube is disperseed.Above-mentioned mixed liquor is placed reactor, 60 ℃ of control bath temperatures, the mol ratio of adding and nickel salt is that the sodium hydroxide solution strong agitation of 2: 1 1mol/L was reacted 2 hours.After reaction finishes, the gained precipitation was transferred in 0 ℃ of frozen water snap frozen rapidly 5 minutes, suction filtration is washed with distilled water to neutrality, is dried to constant weight in 60 ℃, grinds and disperses to be the finished product amorphous phase nickel hydroxide doped electrode active material of carbon nano tube.Products therefrom is indicated as amorphous phase nickel hydroxide through X-ray diffraction analysis.Products obtained therefrom is made simulated battery discharge and recharge under the 0.1C multiplying power, its discharge capacity is 316mAhg -1
Embodiment 2:
By the mass percent of carbon nano-tube in the target product nickel hydroxide is 2% to take by weighing carbon nano-tube and join in the nickel nitrate solution of 1mol/L, carbon nano-tube is that caliber is the multi-walled carbon nano-tubes of 40-50nm, add surfactant isooctylphenol APEO (TX-100) and the absolute ethyl alcohol that volume ratio is respectively above-mentioned solution 2% and 5% simultaneously and make dispersant, ultrasonic concussion 50 minutes forms the mixed liquor that even carbon nanotube is disperseed.Above-mentioned mixed liquor is placed reactor, 50 ℃ of control bath temperatures, the mol ratio of adding and nickel salt is that the potassium hydroxide solution strong agitation of 2: 1 3mol/L was reacted 3 hours.After reaction finishes, the gained precipitation was transferred in 0 ℃ of frozen water snap frozen rapidly 8 minutes, suction filtration is washed with distilled water to neutrality, is dried to constant weight in 80 ℃, grinds and disperses to be the finished product amorphous phase nickel hydroxide doped electrode active material of carbon nano tube.Products therefrom is indicated as amorphous phase nickel hydroxide through X-ray diffraction analysis.Products obtained therefrom is made simulated battery discharge and recharge under the 0.1C multiplying power, its discharge capacity is 305mAhg -1

Claims (2)

1. the preparation method of an amorphous phase nickel hydroxide doped electrode active material of carbon nano tube is characterized in that concrete steps are:
(1) calculates the consumption of nickel salt, alkali and carbon nano-tube according to the amount of required preparation target product;
(2) with above-mentioned raw materials weighing in proportion, and wiring solution-forming;
(3) in the nickel salt solution for preparing, add surfactant isooctylphenol APEO, ethanol and carbon nano-tube sequentially, ultrasonic concussion 30-60 minute, form the mixed liquor that even carbon nanotube is disperseed;
(4) control reaction temperature is 50-60 ℃, and adding is 2: 1 strong base solutions with the mol ratio of nickel salt in the mixed liquor that step (3) makes, and reaction is 2-3 hour under strong agitation;
(5) step (4) product snap frozen, filtration, washing, drying, grinding are disperseed, can obtain amorphous phase nickel hydroxide doped electrode active material of carbon nano tube;
Described highly basic is a kind of in NaOH and the potassium hydroxide; The concentration of NaOH and potassium hydroxide is respectively 1-4mol/L and l-5mol/L;
Described nickel salt is a kind of in nickelous sulfate and the nickel nitrate; The concentration of nickelous sulfate and nickel nitrate is respectively 0.5-1mol/L and 0.1-1mol/L.
2. preparation method according to claim 1 is characterized in that described carbon nano-tube is that caliber is the multi-walled carbon nano-tubes of 30-50nm.
CN2009101143213A 2009-08-19 2009-08-19 Method for preparing amorphous phase nickel hydroxide doped electrode active material of carbon nano tube Expired - Fee Related CN101635354B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2009101143213A CN101635354B (en) 2009-08-19 2009-08-19 Method for preparing amorphous phase nickel hydroxide doped electrode active material of carbon nano tube

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2009101143213A CN101635354B (en) 2009-08-19 2009-08-19 Method for preparing amorphous phase nickel hydroxide doped electrode active material of carbon nano tube

Publications (2)

Publication Number Publication Date
CN101635354A true CN101635354A (en) 2010-01-27
CN101635354B CN101635354B (en) 2011-05-11

Family

ID=41594462

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2009101143213A Expired - Fee Related CN101635354B (en) 2009-08-19 2009-08-19 Method for preparing amorphous phase nickel hydroxide doped electrode active material of carbon nano tube

Country Status (1)

Country Link
CN (1) CN101635354B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103943372A (en) * 2014-05-08 2014-07-23 扬州大学 Nickel hydroxide/multi-walled carbon nanotube composite material and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103943372A (en) * 2014-05-08 2014-07-23 扬州大学 Nickel hydroxide/multi-walled carbon nanotube composite material and preparation method thereof

Also Published As

Publication number Publication date
CN101635354B (en) 2011-05-11

Similar Documents

Publication Publication Date Title
CN107221716B (en) Rechargeable aqueous zinc ion battery
CN107275606B (en) Carbon-coated spinel lithium manganate nanocomposite and preparation method and application thereof
CN102826617B (en) Spherical nickel hydroxide material and preparation method thereof
CN101567447B (en) LiFePO4 lithium ion battery anode material coated with C and metal oxide and preparation method
CN103779559B (en) Anode material for lithium-ion batteries Li 2mn 1-Xm xsiO 4the preparation method of/C
CN107611411B (en) Preparation method and application of three-dimensional hierarchical porous nitrogen-doped carbon-coated silicon composite material
CN105789584A (en) Cobalt selenide/carbon sodium ion battery composite negative electrode material as well as preparation method and application of cobalt selenide/carbon-sodium ion battery composite negative electrode material
CN102208614B (en) Method for preparing lithium ion battery cathode material coated iron sesquioxide
CN107732180B (en) A kind of preparation method for water system sodium-ion battery anode composite material
CN102633300A (en) Carbon-coated lithium titanate cathode material as well as preparation method and applications thereof
CN109755498B (en) Iron-based negative electrode additive for alkaline secondary battery, preparation method, iron-based negative plate using additive and application of iron-based negative plate
CN103008653B (en) Carbon coated lead composite material and preparation method thereof
CN109461592A (en) The preparation method of 3D hierarchical structure flexibility carbon cloth load MOF-LDH mixing array electrode material for super capacitor
CN105591087A (en) Preparation method of nickel hydroxide/graphene composite material for nickel-metal hydride battery positive pole
CN111600006B (en) Preparation method of rod-like tin-antimony alloy as negative electrode material of lithium ion battery
CN113104824A (en) Se doped Fe2Preparation method of P self-supporting sodium ion battery cathode material
CN108172744B (en) Sb for lithium-sulfur battery diaphragm2Se3Method for preparing composite material
CN102774893B (en) Preparation method of nano petaline Ni(OH)2
CN109802127B (en) Preparation method of silver-doped ferroferric oxide nano composite material
CN103359796A (en) Preparation method of supercapacitor cobaltous oxide electrode material
CN109004233B (en) Preparation method and application of layered double hydroxide-loaded lithium metal negative electrode composite copper foil current collector
CN108598405B (en) Preparation method of three-dimensional graphene tin oxide carbon composite negative electrode material
CN108281620B (en) Preparation method of negative electrode material titanium dioxide of sodium-ion battery
CN103531809A (en) Preparation method and application of core-shell structural particle and graphene composite material
CN104124447B (en) A kind of New Co (OH) F lithium ion battery cathode material and its preparation method

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
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20110511

Termination date: 20110819