CN101262075B - Nickel hydrogen quick charging battery and its making method - Google Patents

Nickel hydrogen quick charging battery and its making method Download PDF

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Publication number
CN101262075B
CN101262075B CN2008100270537A CN200810027053A CN101262075B CN 101262075 B CN101262075 B CN 101262075B CN 2008100270537 A CN2008100270537 A CN 2008100270537A CN 200810027053 A CN200810027053 A CN 200810027053A CN 101262075 B CN101262075 B CN 101262075B
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China
Prior art keywords
battery
nickel
electrolyte
quick charging
weight
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Expired - Fee Related
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CN2008100270537A
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Chinese (zh)
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CN101262075A (en
Inventor
李中延
李群杰
陈华春
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Mcnair Technology Co Ltd
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Mcnair Technology Co Ltd
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    • 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
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50Manufacturing or production processes characterised by the final manufactured product

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  • Secondary Cells (AREA)

Abstract

The invention provides an Ni-MH fast charge battery which comprises an anode, a cathode, electrolyte and a battery separator; the anode comprises an active material, an additive and an adhesive; the active substance contains 3.7 to 4.3 percent of Zn<2+> and 1.3 to 1.7 percent of Co<2+> by weight proportion and is added with 6 percent of Ni(OH)2 of CoO by weight proportion; the additive is simple substance Ni which takes up 1 to 10 percent of total weight of Ni(OH)2; the electrolyte is two-element electrolyte consisting of two substances of KOH, NaOH or LiOH; the density of the electrolyte is 1.28g/ml, and molar concentration of OH<-> is 9.5mol/L. The Ni-MH fast charge battery can be charged with strong current in short time with high charging efficiency. The invention also provides a preparation method of the Ni-MH fast charge battery.

Description

Nickel hydrogen quick charging battery and manufacture method thereof
Technical field
The present invention relates to secondary cell and make the field, be meant the Ni-MH battery of electric current quick charge greatly especially.
Background technology
Ni-MH battery is the substitute products of early stage nickel-cadmium cell, similar on Ni-MH battery and the nickel-cadmium cell profile, and the positive pole of Ni-MH battery and nickel-cadmium cell are also basic identical, all be to be anodal with the nickel hydroxide, what the main distinction was the employing of nickel-cadmium battery negative pole plate is the cadmium active material, and Ni-MH battery is to be negative pole with the high energy hydrogen-storage alloy, so Ni-MH battery has bigger energy.Simultaneously Ni-MH battery is also similar substantially to nickel-cadmium cell aspect electrochemical properties, thus Ni-MH battery replacement nickel cadmium cell fully in use, and do not need equipment is carried out any transformation.It is the battery of at present environmental protection, does not re-use poisonous cadmium, can eliminate the pollution problem that heavy metal element brings environment.Ni-MH battery has bigger energy density ratio, this means to use Ni-MH battery can prolong the operating time of equipment effectively not for digital equipment increases under the situation of additional weight.Simultaneously Ni-MH battery is also similar substantially to nickel-cadmium cell aspect electrology characteristic, fully can the replacement nickel cadmium cell when practical application, and do not need equipment is carried out any transformation.Another advantage of Ni-MH battery is: reduced to exist in the nickel-cadmium cell " memory effect " greatly, this can use Ni-MH battery more easily.
At present, an important use of Ni-MH battery is to be applied in the field of power tools, because wireless chargeable electric tool fast development in recent years brings great convenience to people.And electric tool in use requires big flow discharge, in addition, also requires Ni-MH battery should have big flow charge function in order to shorten the charging interval.Yet the charging current that existing ni-mh secondary rechargeable battery can bear is little, and the charging consumption time is long, and large current charge efficient is low and security performance is low.
Summary of the invention
The object of the present invention is to provide a kind ofly can with big electric current battery be full of electricity at short notice, and the high nickel hydrogen quick charging battery of charge efficiency.
The present invention also aims to provide the manufacture method of above-mentioned nickel hydrogen quick charging battery.
For achieving the above object, solution of the present invention is:
A kind of nickel hydrogen quick charging battery comprises positive pole, negative pole, electrolyte and battery diaphragm;
Described positive pole comprises active material, additive, binding agent; Described active material is for containing Zn 2+(3.7-4.3wt%), Co 2+(1.3-1.7wt%), and add the Ni (OH) that percentage by weight is 6% CoO 2Described additive is a nickel simple substance, and content is Ni (OH) 2The 1%-10% of total weight;
Described electrolyte is two yuan of electrolyte being made up of two kinds of materials among KOH, NaOH or the LiOH.
Described density of electrolyte is 1.28g/ml, OH -Molar concentration is 9.5mol/L.
Described binding agent is a polytetrafluoroethylene.
The manufacture method of described nickel hydrogen quick charging battery may further comprise the steps:
The first step adopts and contains Zn 2+(3.7-4.3wt%), Co 2+(1.3-1.7wt%), and add the Ni (OH) that percentage by weight is 6% CoO 2As the positive active material of battery, add percentage by weight again and be 1%-10% nickel simple substance as additive, PTFE (polytetrafluoroethylene) dry powder blend that adds 0.5wt% becomes anodal material;
Second step was coated to the positive pole material on the anodal matrix, passed through roll-in and cut operation and make battery positive plate;
The 3rd step stacked gradually the formation electrode group of reeling with positive plate, diaphragm paper, negative plate, and electrode is assembled in the battery steel shell;
The 4th step, inject electrolyte, the enclosed cell housing changes into through overcharging and promptly to produce nickel hydrogen quick charging battery.
After adopting such scheme, though the present invention is structurally consistent with existing nickel-hydrogen secondary cell, but owing to added percentage by weight in positive pole is 6% CoO and the nickel simple substance of 1%-10%, and improved the prescription of electrolyte, thereby the charging current of bearing that the existing ni-mh secondary rechargeable battery of solution exists in charging process is little, the problem that the charging consumption time is long reaches the purpose of quick charge.
Description of drawings
Fig. 1 is the cutaway view of nickel hydrogen quick charging battery of the present invention.
Embodiment
Following embodiment is in order to describe nickel hydrogen quick charging battery provided by the invention in detail, lift the fact that comparative example proves that the charge efficiency of nickel hydrogen quick charging battery provided by the invention under the large current charge situation is improved simultaneously, but following examples and be not used in and limit interest field of the present invention.
Be that convenient the differentiation describe, this method is used contains Zn 2+, Co 2+Ni (OH) 2, all use " special Ni (OH) hereinafter 2" expression.The positive active material among the present invention and the addition of binding agent are with conventional interpolation scope of the prior art.
Embodiment 1:
With special Ni (OH) 2, CoO, nickel powder be by 100: 6: 6 part by weight mixing and stirring, evenly be coated on the matrix made of foaming nickel, through roll-in, cut, operation such as welding, make positive plate (because the manufacture method of battery positive plate is a known technology, and non-emphasis of the present invention, so will not describe in detail in the literary composition).。
Hydrogen storing alloy powder, acetylene black, nickel powder are mixed by 100: 0.5: 0.5 part by weight, adding an amount of binding agent and water stirs, evenly be coated on the nickel plated steel strip, through oven dry, roll-in, cut, operation such as welding, make negative plate (because the manufacture method of cell negative plate is a known technology, and non-emphasis of the present invention, so will not describe in detail in the literary composition).
Add the LiOH of 1.5% (wt%) in the NaOH aqueous solution of 30% (wt%), stir, cooling promptly can be made into the electrolyte that this method is used.
Referring to Fig. 1, the battery diaphragm 3 that positive plate 1, negative plate 2 and polypropylene material are made stacks gradually the formation electrode group of reeling together, and electrode is assembled in the battery steel shell 4, injects electrolyte, the enclosed cell housing changes into through overcharging and promptly to produce nickel hydrogen quick charging battery.Make for convenience, make battery capacity and be about 2000mAh.
Comparative example 1:
In comparative example 1, do not add nickel powder as additive when making positive plate, other all identical with making embodiment 1 method is produced the nickel hydrogen quick charging battery of comparative example 1.
Comparative example 2:
In comparative example 2, do not add nickel powder as additive when making positive plate, use cobalt powder as additive.Other all identical with making embodiment 1 method is produced the nickel hydrogen quick charging battery of comparative example 2.
Comparative example 3:
In comparative example 3, do not use NaOH when making electrolyte, and use KOH.Other all identical with making embodiment 1 method is produced the nickel hydrogen quick charging battery of comparative example 3.
Comparative example 4:
In comparative example 4, do not use LiOH when making electrolyte, use KOH.Other all identical with making embodiment 1 method is produced the nickel hydrogen quick charging battery of comparative example 4.
Comparative example 5:
In comparative example 5, adding the nickel powder amount when making positive plate is 1wt%.Other all identical with making embodiment 1 method is produced the nickel hydrogen quick charging battery of comparative example 5.
Comparative example 6:
In comparative example 6, adding the nickel powder amount when making positive plate is 10wt%.Other all identical with making embodiment 1 method is produced the nickel hydrogen quick charging battery of comparative example 6.
Then, the battery of making embodiment 1 and comparative example 1-6 making was charged 14 hours with 200mA, discharge into 1.0V, circulate 3 times with 400mA, thus the nickel hydrogen quick charging battery that activation embodiment 1 and comparative example 1-6 make.
The battery examples that activated is respectively got 5 joints test, test result is got its mean value.
The charge efficiency method that detects under the battery large current charge situation is: with each embodiment and comparative example battery with the charging 30 minutes under the situation of-Δ V=10mV of 2C multiplying power, 0.5C multiplying power discharging is to 1.0V, the counting cell discharge capacity, and with this battery at 144 minutes (Δ V=10mV) of 0.5C multiplying power charging, 0.5C multiplying power discharging to the 1.0V discharge capacity of the cell relatively, thereby investigate its charge efficiency under the large current charge situation.At 144 minutes (Δ V=10mV) of 0.5C multiplying power charging, the 0.5C multiplying power discharging is represented with percentage to the ratio of 1.0V discharge capacity of the cell with the discharge capacity of the cell behind the large current charge and this battery.
The testing result of embodiment 1 and each comparative example battery is shown in subordinate list 1:
Subordinate list 1
The anodal nickel powder that adds The anodal cobalt powder that adds Used for electrolyte NaOH Used for electrolyte KOH Used for electrolyte LiOH Nickel powder adding proportion 1wt% Nickel powder adding proportion 6wt% Nickel powder adding proportion 10wt% Charge efficiency
Embodiment
1 Be Not Be Not Be Not Be Not 95%
Comparative example 1 Not Not Be Not Be Not Be Not 62%
Comparative example 2 Not Be Be Not Be Not Be Not 70%
Comparative example 3 Be Not Not Be Be Not Be Not 74%
Comparative example 4 Be Not Be Be Not Not Be Not 76%
Comparative example 5 Be Not Be Not Be Be Not Not 80%
The anodal nickel powder that adds The anodal cobalt powder that adds Used for electrolyte NaOH Used for electrolyte KOH Used for electrolyte LiOH Nickel powder adding proportion 1wt% Nickel powder adding proportion 6wt% Nickel powder adding proportion 10wt% Charge efficiency
Comparative example 6 Be Not Be Not Be Not Not Be 82%
By last expression, to compare with comparative example 1 battery that does not add nickel powder, the charge efficiency of comparative example 3-6 battery under the large current charge situation of having added nickel powder increases.
Compare with comparative example 3 batteries that added nickel powder, electrolyte uses the comparative example 4-6 battery of NaOH, and its charge efficiency under the large current charge situation is further enhanced.
Use comparative example 4 batteries of NaOH to compare with having added nickel powder with electrolyte, electrolyte uses the comparative example 5-6 battery of LiOH, and its charge efficiency under the large current charge situation is further improved.
But added example of making 1 battery that 6wt% nickel powder and electrolyte use NaOH and LiOH, with the battery comparison of above comparative example 1,2,3,4,5,6, its charge efficiency under the large current charge situation obtains maximum raising.
In sum, nickel hydrogen quick charging battery provided by the invention is because to have added percentage by weight in the positive pole be that the simple substance of 6% nickel is as additive, and electrolyte has used NaOH and two yuan of electrolyte of LiOH, thereby make the present invention with the charging 30 minutes under the situation of-Δ V=10mV of 2C multiplying power, its charge efficiency is up to 95%, realized with big electric current battery being full of electricity at short notice, and do not had the low and safety problem of charge efficiency.

Claims (4)

1. a nickel hydrogen quick charging battery comprises positive pole, negative pole, electrolyte and battery diaphragm; It is characterized in that:
Described positive pole comprises active material, additive, binding agent; Described active material is to contain the zinc ion Zn that percentage by weight is 3.7%-4.3% 2+Divalent cobalt ion Co with 1.3%-1.7% 2+, and add the hydroxide nickel (OH) that percentage by weight is 6% cobalt oxide CoO 2Described additive is a nickel simple substance, and content is hydroxide nickel (OH) 2The 1%-10% of total weight;
Described electrolyte is two yuan of electrolyte being made up of two kinds of materials among potassium hydroxide KOH, NaOH NaOH or the lithium hydroxide LiOH.
2. nickel hydrogen quick charging battery as claimed in claim 1 is characterized in that: density of electrolyte is 1.28g/mL, hydroxide ion OH -Molar concentration is 9.5mol/L.
3. nickel hydrogen quick charging battery as claimed in claim 1 is characterized in that: described binding agent is a polytetrafluoroethylene.
4. method of making nickel hydrogen quick charging battery as claimed in claim 1 is characterized in that: may further comprise the steps:
The first step adopts and contains the zinc ion Zn that percentage by weight is 3.7%-4.3% 2+Divalent cobalt ion Co with 1.3%-1.7% 2+, and add the hydroxide nickel (OH) that percentage by weight is 6% cobalt oxide CoO 2As the positive active material of battery, add percentage by weight again and be 1%-10% nickel simple substance as additive, add percentage by weight and be 0.5% PolytetrafluoroethylDry Dry-powder and be mixed into anodal material;
Second step was coated to anode sizing agent on the anodal matrix, passed through roll-in and cut operation and make battery positive plate;
The 3rd step stacked gradually the formation electrode group of reeling with positive plate, diaphragm paper, negative plate, and electrode is assembled in the battery steel shell;
The 4th step, inject electrolyte, the enclosed cell housing changes into through overcharging and promptly to produce nickel hydrogen quick charging battery.
CN2008100270537A 2008-03-27 2008-03-27 Nickel hydrogen quick charging battery and its making method Expired - Fee Related CN101262075B (en)

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Application Number Priority Date Filing Date Title
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Application Number Priority Date Filing Date Title
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CN101262075B true CN101262075B (en) 2010-07-28

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101794913A (en) * 2010-03-23 2010-08-04 欧阳宁 Maintenance-free nickel/metal hydride (MH-Ni) battery and manufacturing method thereof
CN102148376A (en) * 2011-02-25 2011-08-10 深圳市豪鹏科技有限公司 Secondary battery anode piece and preparation method thereof
CN107146878B (en) * 2017-05-18 2020-01-14 深圳市量能科技有限公司 Nickel battery pole piece, nickel battery and preparation method thereof

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Denomination of invention: Nickel hydrogen quick charging battery and its making method

Effective date of registration: 20170712

Granted publication date: 20100728

Pledgee: Dongguan rural commercial bank Limited by Share Ltd. Songshan Lake Science and Technology Branch

Pledgor: DONGGUAN MCNAIR TECHNOLOGY Co.,Ltd.|DONGGUAN MCNAIR NEW POWER Co.,Ltd.|TECHNICAL INSTITUTE OF LITHIUM BATTERY ENERGY-SAVING TECHNOLOGY OF MCNAIR, DONGGUAN.

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Granted publication date: 20100728

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