CN101438434A - Electrode active material with high stability and electrochemical device using the same - Google Patents
Electrode active material with high stability and electrochemical device using the same Download PDFInfo
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- CN101438434A CN101438434A CNA2007800160263A CN200780016026A CN101438434A CN 101438434 A CN101438434 A CN 101438434A CN A2007800160263 A CNA2007800160263 A CN A2007800160263A CN 200780016026 A CN200780016026 A CN 200780016026A CN 101438434 A CN101438434 A CN 101438434A
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- 229910052768 actinide Inorganic materials 0.000 claims description 6
- -1 actinide metals Chemical class 0.000 claims description 6
- 229910052783 alkali metal Inorganic materials 0.000 claims description 6
- 150000001340 alkali metals Chemical class 0.000 claims description 6
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 6
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 6
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- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
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Images
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-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
- H01M4/131—Electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/36—Accumulators not provided for in groups H01M10/05-H01M10/34
- H01M10/38—Construction or manufacture
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/04—Processes of manufacture in general
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/04—Processes of manufacture in general
- H01M4/0438—Processes of manufacture in general by electrochemical processing
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
- H01M4/134—Electrodes based on metals, Si or alloys
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
- H01M4/139—Processes of manufacture
- H01M4/1391—Processes of manufacture of electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/362—Composites
- H01M4/366—Composites as layered products
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- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
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- Y—GENERAL 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
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Abstract
Disclosed are an electrode active material, of which the stability is improved by adjusting an acid site of a surface of the electrode active material, an electrode containing the electrode active material, having a surface coated with a compound having an acid site, or mixed with the compound having the acid site and an electrode material, and an electrochemical device having the electrode to enhance its performance. By adjusting the acid site on the surface of the electrode active material, the side reaction with the electrolyte is decreased, and the structure stability of the electrode active material is secured, thereby enhancing the performance of the battery.
Description
Technical field
The present invention relates to a kind of adjusting and make stable improved electrode active material by the surface acidity site; A kind of electrode that comprises described electrode active material, this electrode surface are coated with the compound with acidic site or are mixed with the compound with acidic site; And a kind ofly comprise described electrode so that the electrochemical appliance that usefulness improves, for example lithium secondary battery.
Background technology
Because lithium secondary battery becomes commercialized, the exploitation of this battery is primarily aimed at and prepares a kind of for example active material of cathode of electrochemical properties such as capacity height, life-span length that has.Except electrochemical properties, also need to develop stability-enhanced active material of cathode really to guarantee the stability and the reliability of battery system under exceptional condition (for example be exposed to thermal environment, burn or overcharge).
LiMO
2(M is a kind of transition metal, comprise Ni, Mn, Co etc.) be widely used as the active material of cathode of lithium secondary battery, under charging or the state that overcharges, its can and the electrolyte reaction produce accessory substance, or the structure of destruction electrode active material, thereby cause battery efficiency to reduce.Therefore, many scientific workers have carried out many researchs by improving active material usefulness with stable oxide processing surface of active material, but these researchs can not increase the stability and the usefulness of electrode active material simultaneously.
Summary of the invention
Technical problem
Simultaneously, the inventor finds, if utilize conventional surface-modification method, is about to the particle surface that reactive low compound is coated in electrode active material, can guarantee the stability of electrode active material, but battery efficiency descends inevitably.Therefore, replace conventional surface-modification method, not only can improve the structural stability of electrode active material with the electrode coated surface of active material of compound, but also can stop the change of its physical characteristic with acid strength through regulating.Therefore, thus the inventor attempts adopting and a kind ofly can significantly reduce the novel surface modification method that improves battery efficiency with electrolytical reactivity.
Technical scheme
An object of the present invention is to provide a kind of electrode active material that comprises acidic site, described acidic site partly or entirely is formed at described electrode active material surface; A kind of electrode and a kind of electrochemical appliance, for example lithium secondary battery that comprises described electrode active material with described electrode.
One aspect of the present invention provides a kind of following electrode, and described electrode has one and applied the surface of the compound that contains acidic site or contained described compound; With a kind of electrochemical appliance, for example lithium secondary battery with described electrode.
Another aspect of the present invention provides a kind of a kind of method with electrode active material of the coat that acid strength is conditioned of producing, and said method comprising the steps of: (i) with (a) a kind of compound that can provide or accept proton or a kind ofly can provide or accept the compound of duplet and (b) a kind of compound reaction with acidic site; And (ii) the product of step (i) is coated on described electrode active material surface and dry described coat.
The invention is characterized in, acidic site partly or wholly is formed at and can embeds/removal lithium embedded ion or can insert/take off the particle surface of the electrode active material of inserting lithium ion, change the electrochemistry physical characteristic of described electrode active material thus.
Usually known acidic site is the reactivity site that is present on the solid acid catalyst of zeolite for example, but solid acid catalyst induced chemical reaction, for example decomposition reaction.Yet in the present invention, but acidic site means the active region of the specific acid intensity of indication surface modification part, and described acidic site partly or entirely is formed at the surface of described active material by new surface-modification method.
Acid strength is according to how easily to supply with proton or how easily to accept duplet and determine.Therefore, the feature of acidic site is uncorrelated with surface texture usually, but relevant with the interatomic characteristic electron that constitutes the surface.
Owing to have positive charge or have the electronegativity difference, the electrode active material that is formed with acidic site on the surface reacts as the common acid material that partly has positive charge.Therefore, since with as the Bronsted acid of proton donor (
Acid) or as the reaction of the lewis acid (Lewis acid) of electron pair acceptor significantly reduce, so electrode active material can improve battery efficiency, can do following inferring this.
1) at first, the conventional electrodes surface of active material demonstrates alkalescent by lithium accessory substance or Hydrophilic Surface Treatment.Therefore, almost discern less than acidic site.
The battery of---particularly active material of cathode---for utilizing the conventional electrodes active material, the moisture that exists in electrode or the electrolyte can with lithium salts (LiPF for example
6) reaction generation strong acid HF.The HF that produces spontaneously reacts with apparent weakly alkaline electrode active material, with dissolving and degraded electrode active material composition.In addition, the resistance that can produce LiF and electrode on the cathode surface increases, and produces gas thus and therefore shortens battery life.Particularly, owing to the electrode dissolution velocity due to the HF at high temperature can increase, so HF becomes the principal element that influences battery life and maintenance.
By contrast, because electrode active material of the present invention has acidic site on its surface, so it can be used as acid material.So, reduce with the reaction of HX (X represents halogen), thereby make the problems referred to above be resolved substantially, guarantee the structural stability of electrode active material and improved the usefulness of battery.
In addition, 2) the second, use nonaqueous solvents based on carbonate as electrolyte in the conventional batteries.As hereinafter equation 1 is disclosed, because dipole moment, has positively charged carbon and electronegative oxygen based on the nonaqueous solvents of carbonate.In this example, if electrode active material surface existence can provide the lewis base of non-share electron pair, then lewis base has the carbon of positive charge with attack, thereby further activates the electric decomposition reaction of electrolytical parent.
Comparatively speaking, the electrode active material of the present invention with acidic site is can not provide non-share electron pair but the lewis acid that can accept non-share electron pair.Therefore, the above-mentioned side reaction that takes place with electrolyte is significantly reduced, thereby makes the battery efficiency deterioration reduce to minimum.
[reaction equation 1]
The acidic site that partly or entirely is formed at electrode active material of the present invention surface is meant conventional acidic site well known in the art.For example, it can be the lewis acid (being electron pair acceptor) that Bronsted acid (being proton donor) that proton can be provided maybe can be accepted non-share electron pair.
Acid strength can be used H
0Regulate in (Hammett (Hammett) indicator) indication, and can scope known in the art---for example-20 to 20 scope---.H
0Preferable range is-10 to 10, thereby prevents the degraded of electrode active material and inhibition and electrolytical side reaction by the adjustment of acidity site.
The method that forms acidic site on the electrode active material surface is unrestricted; Hereinafter will two embodiments be described by the mode of example.
1) embodiment 1
In this embodiment, handle the electrode active material surface with inorganic matter.
Because different metal (hetero-metal) element and/or partly or entirely be present in the electronegativity difference of the proton donor functional group on inorganic matter surface, the inorganic matter of handling on the electrode active material surface can change the electron distributions on electrode active material surface, thereby forms acidic site on the electrode active material surface.
Described inorganic matter is known in this field, for example pottery, metal or its compound.Described inorganic matter is unrestricted, as long as when there is this inorganic matter in the electrode active material surface, the electrochemical properties on described surface is changed.Especially, the compound that preferably contains the 13rd, 14,15 family's elements (for example B, Al, Ga, In, Ti etc.) or their mixture, described compound can improve the structural stability of electrode by the embedding of Li, and this is can easily it be mixed the electrode active material surface because Li atom size makes.
Available inorganic matter example can comprise the 13rd family's element, the 13rd family's element and at least a compound that is selected from following group element: alkaline-earth metal, alkali metal, the 14th family's element, the 15th family's element, transition metal, lanthanide series metal and actinide metals, scope of the present invention is not limited to this.For example, described inorganic matter can be M
1-xSi
xO
2(M is at least a element that is selected from transition metal; 0≤x＜1).
Inorganic matter with described acidic site can be by forming the heat treatment after the electrode active material surface modification.In this example, there is no particular restriction for heat treatment temperature, even also can more than the temperature that forms described acidic site.If hydroxyl still is present in described surface, just can not form the strong lewis acid site.Therefore, preferred temperature is at 400 ℃ or higher to eliminate hydroxyl.
There is no particular restriction for above-mentioned inorganic matter granularity and content, and they can do suitable adjusting in the normal ranges known in the art.
2) embodiment 2
In this embodiment, the surface of handling described electrode active material with the compound of organic metalloid (organic metalloid) compound or organo-metallic compound and inorganic matter.
Since each other organic metalloid (metal) compound of bonding and the electronegativity difference between the inorganic matter and/or and the organic substance of organic metalloid (metal) compound bonding between electronegativity difference, the compound of described organic metal compound or organo-metallic compound and electrode active material surface-treated inorganic matter can change the electrochemistry physical characteristic on described surface, thereby can form acidic site on described electrode active material surface.
In described compound, described organic metalloid (metal) compound and inorganic matter pass through chemical bond bonding each other, and the form and the kind of chemical bond are unrestricted.For example, it can be covalent bond or co-ordinate covalent bond.
If use the surface modifier of the compound of described organic metal compound or organo-metallic compound and inorganic matter, then can reduce the hydrolysis rate of inorganic constituents (for example inorganic alkoxide) as electrode active material or electrode.In addition, it can not only produce the more surface of homogeneous, but also the sustainable surface that is produced of keeping.Therefore, it can reduce to the battery efficiency deterioration minimum, described deterioration be since in the charging and discharging process electrode active material structural stability reduce and the cataclastic structure of described material due to.In addition, it can introduce surface reforming layer by utilizing inorganic compound contained in the organic-inorganic composition, thereby effectively increases the conductivity of electrode active material.
The organic-inorganic composition that introduce on described electrode active material surface can with contained moisture or carbon dioxide reaction in the air, generate the Li accessory substance, thereby prevent to cause the aging character of side reaction.Particularly, more effective by the serious Ni-based active material of cathode that changes of moisture.
In addition, it can reduce the side reaction contact surface between the negative electrode and electrolyte in the battery of being made up of the conventional electrodes active material, its surface is not changed, thereby has improved the stability of battery.
As mentioned above, can make one of organic-inorganic composition that acidic site partly or entirely results from described electrode active material particles surface can be the conventional organic metal compound or the organo-metallic compound of this area likewise known.In order to strengthen the effect of regulating acid strength and preventing aging character, preferably contain the electron-donating group that is useful on the increase bronsted acid sites.Described electron-donating group is not particularly limited on structural formula, substituting group and carbon atom number range.For example can be hydrogen or hydrocarbon.
The available organic metal compound or the example of organo-metallic compound can comprise the 14th family's element or the 14th family's element and at least a compound that is selected from following group element: alkaline-earth metal, alkali metal, the 13rd family's element, the 15th family's element, transition metal, lanthanide series metal and actinide metals, scope of the present invention is not limited to this.Described organic metal compound or organo-metallic compound are preferably silicon-containing compound (for example, silane, silanizing agent (silylizing agent), silane coupler, silane, single silane, silane polymer or their mixture).
Described organic metal compound can be represented by one of following formula 1-7.To described organic metal compound or organo-metallic compound without limits.
[formula 1]
SiH
4
[formula 2]
Si(OR)
4-xR
x (0.1≤x≤3)
[formula 3]
Si(OR)
4-(x+y)R
xZ
y (0.1≤x+y≤3.9)
[formula 4]
Si(OR)
4-xR
xSi (0.1≤x≤3)
[formula 5]
Si(OR)
4-(x+y)R
xZ
ySi (0.1≤x+y≤3.9)
[formula 6]
R
xM(OR)
4-x (1≤x≤3)
[formula 7]
R
xMZ
y(OR)
4-(x+y) (0.1≤x+y≤3.9)
Wherein, Z is a kind of element that is selected from halogen atom;
M is at least a element that is selected from alkaline-earth metal, alkali metal, transition metal, lanthanide series metal and actinide metals; And
R is a kind of substituting group, is selected from by halogen to replace or unsubstituted C
1-C
20Alkyl, thiazolinyl, alkynyl, vinyl, amino and sulfydryl.
The another kind of organic-inorganic composition that can make acidic site partly or entirely result from described electrode active material particles surface can be a kind of conventional inorganic matter that produces acidic site, and the generation of this acidic site is because between above-mentioned organic metalloid (metal) compound and the inorganic matter due to the difference of chemical bond number.Any compound that contains inorganic matter all can use, and this be there is no concrete restriction.For example, can use above-mentioned inorganic constituents.In this example, in order to prevent that electrode active material from because of the conductivity due to the introducing of organic-inorganic composition reduces, preferably using conducting metal, containing the oxide of conducting metal, the hydroxide that contains conducting metal or their mixture.
The organic-inorganic composition of being made up of described organic metalloid (metal) compound and inorganic matter is not the simple mixtures of organic substance and inorganic matter, but their chemical bonding mixture.For example, it can comprise metal-organic metalloid (metal) compound, metal oxide-organic metalloid (metal) compound (Al
2O
3-SiOCH
3) and hydroxide-organic metalloid (metal) compound (AlOOH-Si-CH
3).
In forming the compound of acidic site, the ratio of component of organic metalloid (metal) compound and inorganic matter is in the scope of 0 weight %-95 weight % than 5 weight %-100 weight %.
In addition, organic and inorganic compound of the present invention also can comprise additive well known in the art except comprising said components.
There is no particular restriction for the method that is used to produce the electrode active material that comprises organic-inorganic compounding coat.In one embodiment, the surface portion ground of electrode active material or the compound that contained acidic site fully apply.
According to embodiment preferred, described method can may further comprise the steps: (i) will contain the compound of inorganic matter or contain organic compound and organic metalloid (metal) compound, perhaps they are scattered in a kind of solvent, and (ii) in described mixture or dispersion soln, add electrode active material, it is stirred and drying.
The compound that contains inorganic matter that uses can be the water-soluble or water-fast compound that contains the routine of at least a above-mentioned element (alkoxide, nitrate, acetate etc. that for example, contain above-mentioned inorganic matter).
Described solvent can comprise conventional solvent well known in the art (for example, organic solvent is as water, alcohol or its mixture).
Employed lining can be conventional active material of cathode well known in the art and conventional active material of positive electrode with the electrode active material of the above-mentioned compound that makes.
In this example, the method with the electrode coated surface of active material of complex solution of having mixed inorganic matter and organic metalloid (metal) compound can comprise solvent evaporated method, coprecipitation, the precipitation method, sol-gel process, absorbing and filtering method, sputtering method, CVD method etc.In these methods, preferred spraying process.
When in electrode active material, adding described organic metalloid (metal) compound and inorganic matter or contain the mixed solution of compound of inorganic matter, the electrode active material of preferred per 100 weight portions adds the mixed solution of 0.05 to 20 weight portion, and scope of the present invention is not limited to this number range.If mixed solution is excessive, will there be the exhibiting high surface processing layer in the electrode active material surface, thereby makes lithium can not be free to migrate to electrode active material, makes the electrochemical characteristic deterioration of electrode active material thus.In addition, if mixed solution is very not enough, the effect of acidic site will be very weak so.Can pass through the conventional method drying then through the electrode active material that applies.
If necessary, can add the process that the electrode active material of dry gained is annealed.In this example, heat-treatment temperature range is more than 100 ℃, but is not limited to this especially.Preferably, this scope is 100 ℃ to 600 ℃.In addition, described heat treatment can be carried out under atmosphere or inert gas conditions.
Can't obtain required effect by conventional method, this is because in ignition process (hotfiring process), described organic substance be heat-labile and/or part burned.Therefore, firing temperature is restricted.By contrast, in the present invention, organic thermal instability is compensated by inorganic constituents, therefore can provide the electrode active material with thermal stability.In addition, owing to can prepare described electrode active material, therefore can improve economic benefit and productivity gain by simplifying the preparation method by conventional drying method or low temperature methods of printing.
Surface by the electrode active material of method for preparing has inorganic or the organic and inorganic composite bed, and wherein said inorganic or organic and inorganic composite bed can produce acidic site.
Can verify and obtain to have the acidic site (see figure 9) by experiment by the surface inorganic or electrode active material that the organic-inorganic composition modification obtains.Particularly, described organic-inorganic composition not only demonstrates the bonding state (see figure 7) of organic substance and inorganic matter, but also relatively increased the bronsted acid sites of inorganic matter, thereby increased the acid strength (see figure 9) of electrode active material by the electron-donating group that exists in the organic substance in the compound.
The invention provides a kind of electrode that contains above-mentioned electrode active material.In this example, described electrode is preferably a kind of by HF or the remarkable negative electrode that changes of moisture.
In addition, the present invention also provides a kind of following electrode, and the surface-coated of this electrode has compound or this electrode with described acidic site to contain the compound with described acidic site.
It is also without particular limitation as the method for the electrode of the constituent of electrode that preparation comprises the compound with acidic site, and this electrode can be made by conventional method.In a preferred embodiment, to contain the compound of organic/inorganic substance or contain organic compound and organic metalloid (metal) compound, perhaps it is dispersed in the solvent, and described electrode active material added to mixes or disperse in the solution of gained to form electrode slurry.Then, slurry added to prepare electrode on the current-collector, and with pole drying.
In this example, in mixed process, mixed solution or dispersion soln and electrode active material be mixed with electrode slurry after, this slurry is added on the current-collector.
By described organic-inorganic composition can be implemented by conventional method as the method for coating composition electrogenesis in the next life utmost point of electrode of the present invention.For example, will contain the compound of inorganic matter or contain organic compound and described organic metalloid (metal) compound, this mixture will be added to preformed electrode surface, and then with pole drying.In this example, described preformed electrode can be by the conventional known method preparation in this area.
In addition, the present invention also provides a kind of anode, negative electrode, spacer and electrolyte electrochemical device of containing, and the one of wherein said anode and/or negative electrode or both are contained above-mentioned electrode active material or above-mentioned electrode.
Described electrochemical appliance comprises all devices that carry out electrochemical reaction, and their instantiation comprises primary cell and secondary cell, fuel cell, solar cell and the capacitor of all kinds.For secondary cell, preferred lithium secondary batteries comprises lithium metal secondary batteries, lithium rechargeable battery, lighium polymer secondary battery and lithium ion polymer secondary cell.
Electrochemical appliance of the present invention can be made according to any conventional method known in the art.In one embodiment, described electrochemical appliance can be by inserting a porous spacer, electrolyte being injected this electrochemical appliance case then and prepare between negative electrode in battery case and anode.
There is no particular restriction to be used for the electrolyte of electrode and spacer, can use the electrolyte and the spacer that are usually used in electrochemical appliance.
That the electrochemical appliance (for example lithium secondary battery) that is made by the present invention can be made into is cylindric, coin, prism-shaped or bag shape, but is not limited to described shape.
In addition, the present invention also provides the production method of the electrode active material that a kind of surface acid intensity is conditioned.In one embodiment, said method comprising the steps of: (i) make (a) a kind of compound that can provide or accept proton, perhaps a kind ofly can provide or accept the compound of duplet and (b) a kind of compound reaction with acidic site; And (ii) the product of step (i) is coated to the surface of described electrode active material and dry described coat.But the present invention is not limited to such scheme.
The described compound that proton (or duplet) can be provided or accept proton (or duplet) can be used as the regulatory factor of compound acid strength in particular range that routinize.In this example, can by the functional group that exists in the content of controlling described compound, the described compound with and combination regulate described acid strength.
Described compound of the present inventionly proton (or duplet) can be provided or accept the compound of proton (duplet) that there is no particular restriction for can be used for, as long as can provide proton (or duplet) or accept proton (duplet).Preferably regulate the acid strength of being regulated on described electrode active material surface-20 to 20 (promptly-20＜H
0＜20), preferably-10 to 10 (promptly-10＜H
0＜10) in the scope.
Description of drawings
Take the following drawings into consideration, aforementioned and other purposes of the present invention, feature and advantage will be more clear by following detailed description.
Fig. 1 is the curve chart of the charging of the lithium secondary battery that shown that the active material of cathode that utilizes embodiment 1 is produced;
Fig. 2 is the curve chart of the charging of the lithium secondary battery that shown that the active material of cathode that utilizes embodiment 2 is produced;
Fig. 3 is the curve chart of the charging of the lithium secondary battery that shown that the active material of cathode that utilizes embodiment 3 is produced;
Fig. 4 is the curve chart of the charging of the lithium secondary battery that shown that the active material of cathode that utilizes comparing embodiment 1 is produced;
Fig. 5 is the curve chart of the charging of the lithium secondary battery that shown that the active material of cathode that utilizes comparing embodiment 2 is produced;
Fig. 6 is the curve chart of the charging of the lithium secondary battery that shown that the active material of cathode that utilizes comparing embodiment 3 is produced;
Fig. 7 is the IR spectrogram that has shown that surface characteristics that the active material of cathode that makes among the embodiment 1 produces with temperature and measuring condition changes;
Fig. 8 is the IR spectrogram that has shown that surface characteristics that the active material of cathode that makes in the comparing embodiment 1 produces with temperature and measuring condition changes;
Fig. 9 has shown the acidic site of active material of cathode of embodiment 1-3 and comparing embodiment 1-3 and the IR spectrogram of acid strength thereof.
Embodiment
With reference to embodiment and comparing embodiment, hereinafter will be described in further detail the present invention.Yet, be understood that these embodiment only are used for explanation, and non-limiting scope of the present invention.
1-1. the preparation of active material of cathode
With 0.8mol% aluminium isopropoxide and 0.8mol%CH
3Si (OCH
3)
3Place the 200ml absolute ethyl alcohol, and stirred 18 hours.Then, in mixture, add 100g LiCoO
2, then mixture was stirred 80 minutes.Filter this mixture to obtain electrode active material with vacuum filter.With vacuum drying chamber that the electrode active material of gained is dry under 130 ℃, thus make active material with treated surface.
1-2. the production of negative electrode
The active material of cathode, conductive agent and the adhesive that the make ratio with 95:2.5:2.5 is added in the nmp solvent with the preparation cathode slurry.After adding to slurries on the 20 μ m aluminium foils, make this aluminium foil dry under 130 ℃ in vacuum drying chamber again, thereby make negative electrode.
1-3. the production of lithium secondary half-cell
The electrode that obtains is rolled processing obtains 25% porosity, then it is struck out coin to form button cell.At this moment, electrode of opposite is made of the Li metal, and uses following electrolyte, i.e. 1M LiPF in this electrolyte
6Be dissolved in the solvent that contains EC that ratio is 1:2 and EMC.
Except again with the active material of drying 300 ℃ of annealing, obtained active material of cathode with same procedure as embodiment 1.Then, with same procedure, produce active material of cathode, used the negative electrode of this active material of cathode and have the button cell of described negative electrode as embodiment 1.
The active material of cathode that will be only except again makes with aluminium isopropoxide has obtained active material of cathode with the same procedure as embodiment 1 400 ℃ of annealing.Then, with same procedure, produce active material of cathode, used the negative electrode of this active material of cathode and have the button cell of described negative electrode as embodiment 1.
Comparing embodiment 1
Except with conventional LiCoO
2Replace having beyond the active material of cathode of treated surface as active material of cathode, with produce negative electrode as the same procedure of embodiment 1 and have as described in the button cell of negative electrode.
Comparing embodiment 2
Except only preparing the active material of cathode, obtain active material of cathode with same procedure as embodiment 1 with aluminium isopropoxide.Then, with produce active material of cathode as the same procedure of embodiment 1, used as described in active material of cathode negative electrode and have as described in the button cell of negative electrode.
Comparing embodiment 3
Except only using CH
3Si (OCH
3)
3Beyond the preparation active material of cathode, obtain active material of cathode with same procedure as embodiment 1.Then, with produce active material of cathode as the same procedure of embodiment 1, used the negative electrode of this active material of cathode and have as described in the button cell of negative electrode.
EXPERIMENTAL EXAMPLE 1: the surface physical characteristic analysis of electrode active material
For the physical characteristic of analyzing surface modified electrode active material of the present invention is carried out following experiment.
With having of obtaining of embodiment 1 through the active material of cathode on the surface of organic-inorganic composition modification as sample, and (be LiCoO with the conventional electrodes active material
2) in contrast.
Use the IR spectrometer above-mentioned active material of cathode of observation under following state respectively: in room temperature and the atmosphere, room temperature and vacuum, 50 ℃ and vacuum, 100 ℃ and vacuum, 200 ℃ and vacuum and 300 ℃ and vacuum.The result shows, comparing embodiment 1 and 2 active material of cathode do not occur 2800 to 3000cm
-1Near alkyl (CH
2CH
3) (see figure 8), but the alkyl (see figure 7) has appearred in active material of cathode of the present invention.Therefore, the compound that has described organic substance and inorganic matter in the surface modifying material that exists in the susceptible of proof active material of cathode of the present invention.
EXPERIMENTAL EXAMPLE 2: the acidic site analysis of electrode active material
For the surface characteristic of analyzing surface modified electrodes active material of the present invention is carried out following experiment.
Following material is as sample: by having of obtaining of embodiment 1 by the active material of cathode on the surface of organic-inorganic composition modification and the active material of cathode that obtains by embodiment 3 with mineral-modified surface through containing acidic site; Following material is with comparing: the conventional active material of cathode that is obtained by comparing embodiment 1 (is LiCoO
2) and only have a active material of cathode through the surface of inorganic matter or organic substance modification by what comparing embodiment 2 and 3 obtained.
Make above-mentioned active material of cathode absorption compound CH
3CN measures their acidic site then respectively with the IR spectrometer.As a reference, because Compound C H
3CN is a kind of alkali compounds with non-share electron pair, and the compound that therefore can be had an acidic site absorbs by the surface through neutralization, therefore can occur the change at peak in the IR spectrum.Can measure the acid strength of compound thus with acidic site.
Experimental result shows, adopted the comparing embodiment 1 of conventional active material of cathode active material of cathode, adopted only to have through the active material of cathode of the comparing embodiment 2 of the active material of cathode on mineral-modified surface and adopted and only had the special change that does not all demonstrate the IR data through the active material of cathode of the comparing embodiment 3 of the active material of cathode on the surface of organic substance modification.Comparatively speaking, have the active material of cathode of the embodiment 3 on mineral-modified surface only and have active material of cathode through the embodiment 1 on the surface of organic and inorganic compound complex modification through containing acidic site, 2200 to 2400cm
-1Near have the cyano group peak.Therefore, susceptible of proof, described electrode activity is formed with the acidic site (see figure 9) on the surface.
Particularly, the active material of cathode that only has among the embodiment 3 by identical mineral-modified surface is compared with the active material of cathode in the comparing embodiment 2, though the active material of cathode of comparing embodiment 2 can prevent to take place with electrolytical side reaction, but this active material of cathode can not promote the formation of acidic site, therefore still can make battery efficiency deterioration (see figure 5).Yet, used the battery efficiency of the active material of cathode of embodiment 3 (see figure 3) that is enhanced with acidic site.Therefore, the formation of susceptible of proof acidic site is a factor relevant with battery efficiency.
EXPERIMENTAL EXAMPLE 3: the efficiency evaluation of lithium secondary battery
For the usefulness of lithium secondary battery that evaluation utilizes surface of the present invention to have the electrode active material production of acidic site is carried out following experiment.
The button cell of embodiment 1-3 that employing is had the active material of cathode production of acidic site is tested.Test as the sample of correspondence with the button cell of comparing embodiment 1-3 simultaneously, the sample surfaces of wherein said correspondence is unmodified, and perhaps the surface is only through inorganic matter or organic substance modification.
Making each sample is being that 0.5C, charge/discharge scope are to carry out constant current and constant voltage (CC/CV) charge/discharge cycle under the condition of 3-4.5V in current density under 50 ℃.The gained result is shown in each cycle charging/discharge curve of Fig. 1-6.
Test result shows, for the battery of embodiment 1-3 of active material of cathode production that employing has acidic site, kept charge in cyclic process.In other words, its cycle characteristics significantly improves (Fig. 1-3) as can be known.Simultaneously, for the battery of the comparing embodiment 1-3 of the active material of cathode production of adopting surperficial no acidic site, its charge/discharge characteristics variation (Fig. 4-6) as can be known.
Be considered to reality and embodiment preferred the most at present though the present invention has described, it should be understood that to the invention is not restricted to disclosed embodiment and accompanying drawing.On the contrary, the present invention is intended to cover the purport of claims and various modifications and the conversion scheme in the scope.
Industrial applicability
From aforementioned content as seen, by regulating the acidic site on electrode active material surface, can reduce The structural stability of electrode active material is guaranteed in electrode active material and electrolytical side reaction, from And the raising battery efficiency.
Claims (23)
1. electrode active material that contains acidic site, wherein said acidic site partly or entirely is formed at the surface of described electrode active material.
2. the electrode active material of claim 1, wherein said acidic site is Bronsted acid or lewis acid.
3. the electrode active material of claim 1, wherein said acid strength is with Hammett indicator (H
0) indication intensity-10 to 10 scope.
4. the electrode active material of claim 1, wherein said acidic site is by forming with inorganic compound or with the surface that the compound that contains organic metal compound or organo-metallic compound and inorganic matter is handled described electrode active material.
5. the electrode active material of claim 4, wherein said acidic site are to form owing to the different metallic element that partially or completely is present in described inorganic matter surface with for one of electronegativity difference of proton functional group or both.
6. the electrode active material of claim 4, the wherein said electrode active material of handling with inorganic matter is heat-treated under 400 ℃ or higher temperature.
7. the electrode active material of claim 4, wherein said inorganic matter comprises
(a) the 13rd family's element; Perhaps
(b) the 13rd family's element and at least a compound that is selected from following group element: alkaline-earth metal, alkali metal, the 14th family's element, the 15th family's element, transition metal, lanthanide series metal and actinide metals.
8. the electrode active material of claim 4, wherein said acidic site be owing to organic metal compound of bonding each other and the electronegativity difference between the inorganic matter and/or and the organic substance of organic metal compound or organo-metallic compound bonding between electronegativity difference form.
9. the electrode active material of claim 4, wherein said organic metal compound or organo-metallic compound comprise
(a) the 14th family's element; Or
(b) the 14th family's element and at least a compound that is selected from following group element: alkaline-earth metal, alkali metal, the 13rd family's element, the 15th family's element, transition metal, lanthanide series metal and actinide metals.
10. the electrode active material of claim 4, wherein said organic metal compound or organo-metallic compound comprise at least a electron-donating group.
11. the electrode active material of claim 4, wherein said organic metal compound is a silicon-containing compound.
12. the electrode active material of claim 11, wherein said siliceous organic metal compound comprises at least a following material that is selected from: silane, silanizing agent, silane coupler, silane, single silane and silane polymer.
13. the electrode active material of claim 4, wherein said organic metal compound or organo-metallic compound are represented with one of following formula 1-7:
[formula 1]
SiH
4；
[formula 2]
Si(OR)
4-xR
x(0.1≤x≤3)；
[formula 3]
Si(OR)
4-(x+y)R
xZ
y(0.1≤x+y≤3.9)；
[formula 4]
Si(OR)
4-xR
xSi(0.1≤x≤3)；
[formula 5]
Si(OR)
4-(x+y)R
xZ
ySi(0.1≤x+y≤3.9)；
[formula 6]
R
xM (OR)
4-x(1≤x≤3); With
[formula 7]
R
xMZ
y(OR)
4-(x+y)(0.1≤x+y≤3.9)，
Wherein, Z is a kind of element that is selected from halogen atom;
M is at least a following element that is selected from: alkaline-earth metal, alkali metal, transition metal, lanthanide series metal and actinide metals; And
R is a kind of substituting group, is selected from by halogen to replace or unsubstituted C
1-C
20Alkyl, thiazolinyl, alkynyl, vinyl, amino and sulfydryl.
14. the electrode active material of claim 4, the ratio of component of wherein said organic metal compound or organo-metallic compound and described inorganic matter is in the scope of 0 weight %-95 weight % than 5 weight %-100 weight %.
15. the electrode active material of claim 4, wherein said inorganic compound or the described content that contains the compound of described organic metal compound or organo-metallic compound and inorganic matter are the mixture to the described electrode active material use of per 100 weight portions 0.05 to 20 weight portion.
16. electrode that comprises each described electrode active material of claim 1-15.
17. the electrode of claim 16, wherein said electrode are negative electrode.
18. the electrode of claim 16, the reactivity between wherein said electrode active material and the HX (X is one of F, Cl, Br and I) is owing to the acidic site that partly or entirely is formed at described electrode active material surface reduces.
19. being coated with compound or this electrode with acidic site, an electrode, this electrode surface comprise described compound with acidic site.
20. one kind comprises anode, negative electrode, spacer and electrolyte electrochemical device, wherein said anode and negative electrode the two or one of comprise claim 1-15 each electrode active material or be the electrode of claim 19.
21. the electrochemical appliance of claim 20, wherein said electrochemical appliance are lithium secondary battery.
22. a production has the method for the electrode active material of the coat that acid strength is conditioned,
Said method comprising the steps of:
(i) make (a) a kind of compound that can provide or accept proton or a kind ofly can provide or accept the compound of duplet and (b) a kind of compound reaction with acidic site; And
(ii) the product with step (i) is coated on the electrode active material surface, and dry described coat.
23. the method for claim 22, wherein said acid strength is with Hammett indicator (H
0) be designated as in-10 to 10 the scope.
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|---|---|---|---|---|
| CN103247819A (en) * | 2012-02-06 | 2013-08-14 | 三星Sdi株式会社 | Lithium secondary battery |
| CN104054195A (en) * | 2012-03-05 | 2014-09-17 | 株式会社Lg化学 | Method for coating inorganic particles on lithium secondary battery substrate, and lithium secondary battery including substrate coated by the method |
| CN108370025A (en) * | 2015-11-16 | 2018-08-03 | 氢氦锂有限公司 | For energy storage, catalysis, the synthetic surface functionalization acidified metal oxide material of photovoltaic and sensor application |
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Also Published As
| Publication number | Publication date |
|---|---|
| KR100984591B1 (en) | 2010-09-30 |
| DE112007001087T5 (en) | 2009-02-19 |
| KR20070108086A (en) | 2007-11-08 |
| CA2651235C (en) | 2014-12-09 |
| CA2651235A1 (en) | 2007-11-15 |
| CN101438434B (en) | 2017-09-15 |
| JP5761725B2 (en) | 2015-08-12 |
| DE112007001087B4 (en) | 2019-11-28 |
| KR20090013841A (en) | 2009-02-05 |
| JP5450057B2 (en) | 2014-03-26 |
| JP2009535781A (en) | 2009-10-01 |
| WO2007129842A1 (en) | 2007-11-15 |
| JP2014013770A (en) | 2014-01-23 |
| CN102916163A (en) | 2013-02-06 |
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