WO2012140790A1 - リチウム二次電池用電極材およびリチウム二次電池 - Google Patents
リチウム二次電池用電極材およびリチウム二次電池 Download PDFInfo
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Definitions
- the present invention relates to an electrode material for a lithium secondary battery and a lithium secondary battery using the electrode material.
- a lithium secondary battery in which a negative electrode is formed using a material capable of occluding and releasing lithium ions can suppress dendrite deposition compared to a lithium battery in which a negative electrode is formed using metallic lithium. Therefore, it has been put on the market as a secondary battery with improved safety. In recent years, development of this lithium secondary battery for in-vehicle applications has been promoted, and all the improvement in performance of large current charge / discharge, high capacity, and long life by repetition thereof has become a major issue.
- lithium secondary batteries have been devised for this problem.
- a positive electrode material has been studied especially for an insulating oxide and a positive electrode material having high resistance.
- negative electrode materials capable of flowing a large current have been studied.
- the current density load of lithium secondary batteries has been reduced by increasing the specific surface area by reducing the particle size of the active material particles constituting the positive electrode material and the negative electrode material and by increasing the electrode area by electrode design.
- an additive was devised to prevent the formation of a resistive film by decomposition of the electrolyte.
- an alloy-based negative electrode having semiconductor characteristics a material in which a binder is devised in order to suppress the alloy composition, the addition of a conductive material, and the volume expansion of the alloy has been proposed.
- an electrode for a secondary battery having an electrode material having an active material powder, a conductive material formed of a carbon material and adhering to the surface of the active material powder, and a fibrous conductive material bonded to the conductive material Is known (Patent Document 1).
- the cycle life of several hundred cycles can be reduced to the 3000 to 4000 cycle level, but it is insufficient to realize 10 years and 5000 cycles or more for in-vehicle use. It was.
- polyimide as a binder for alloy-based negative electrodes and relieve the volume expansion of the alloy by strengthening the adhesive strength of the binder, it is possible to refine the active material of the alloy and prevent peeling from the current collector foil As a result, the amount of binder used has increased, and it has been difficult to satisfy the required performance as an in-vehicle battery, which has led to an increase in cost, which has led to an increase in cost.
- lithium metal oxide positive electrodes titanium oxide negative electrodes and alloy negative electrodes with insulation and semiconductor characteristics, and carbon negative electrodes with high contact resistance due to miniaturization even if they are conductive It has been difficult to improve capacity, high power and lifetime performance.
- the present invention has been made in order to cope with the above-described problems.
- the electrode material resistance can be made extremely low, the capacity can be increased in addition to the large current charge / discharge (high output), and the in-vehicle use.
- An object is to provide an electrode material for a lithium secondary battery that can achieve a usable cycle life and a lithium secondary battery using the electrode material.
- the electrode material for a lithium secondary battery of the present invention penetrates an organic electrolyte into an electrode group formed by winding or stacking via a separator between a positive electrode material in contact with a positive electrode plate and a negative electrode material in contact with a negative electrode plate. Used for secondary batteries that are immersed and repeatedly occluded / released lithium ions.
- the negative electrode material of the negative electrode plate includes the following component (a), component (b) and component (c). Each of these components has at least one phase selected from a graphene phase and an amorphous phase (hereinafter referred to as a graphene phase) as a surface phase, and the negative electrode material is a composite negative electrode active material obtained by fusing the surface phases together It is characterized by including.
- the graphene phase refers to a single plane 6-membered ring structure of sp 2 -bonded carbon atoms
- the amorphous phase refers to a structure in which this 6-membered ring structure is three-dimensionally formed.
- bonding refers to bonding due to disorder of the graphene phase and / or the amorphous phase.
- Component (a) is at least one active material selected from metal oxides and alloy materials encapsulating metals, coated with a carbon material and having at least a graphene phase on the surface
- Component (b) is a graphite-based carbon material having at least a graphene phase on the surface
- the component (c) is a carbon material other than the graphite-based carbon material and having at least a graphene phase on the surface.
- the active material is tin oxide powder encapsulating metal tin or silicon oxide powder encapsulating metal silicon.
- the positive electrode material includes a composite positive electrode active material obtained by fusion-bonding the graphene phases and the like on the surfaces of the components (d) and (e) shown below.
- Component (d) is an olivine-type lithium metal phosphate coated with a carbon material and having a graphene phase or the like at least on its surface
- Component (e) is a carbon material other than the graphite-based carbon material and having at least a graphene phase on the surface.
- the graphite-based carbon material is at least one carbon material selected from artificial graphite, natural graphite, graphitizable carbon material, and amorphous carbon material.
- the component (c) or the component (e) is at least one selected from acetylene black, ketjen black, powder containing graphite crystals, and conductive carbon fibers.
- the conductive carbon fiber is at least one fiber selected from carbon fiber, graphite fiber, vapor-grown carbon fiber, carbon nanofiber, and carbon nanotube.
- the lithium secondary battery of the present invention is obtained by infiltrating or immersing an organic electrolyte in an electrode group formed by winding or laminating a separator between a positive electrode material in contact with a positive electrode plate and a negative electrode material in contact with a negative electrode plate.
- the positive electrode material is the positive electrode material of the present invention
- the negative electrode material is the negative electrode material of the present invention
- the positive electrode material and the negative electrode material are lithium of the present invention. It is an electrode material for secondary batteries.
- the electrode material for a lithium secondary battery according to the present invention is an olivine-type lithium metal phosphate positive electrode material in which the positive electrode material has a graphene phase or the like on the surface.
- the negative electrode material is a metal oxide or alloy material negative electrode material including a metal having a graphene phase or the like on the surface.
- lithium secondary batteries using these as electrodes can be charged and discharged with a large current compared to (a) powder-mixed contact electrodes, and (b) high utilization of active material is improved.
- C No change in conductivity due to expansion / contraction due to charge / discharge cycle
- e Due to the presence of various carbon materials on the positive and negative electrode powder surfaces, Since there is no generation of a resistance film, there is almost no increase in resistance during charging and discharging, and a longer life can be achieved.
- the negative electrode material the surface layer of silicon or tin oxide powder containing metal silicon or metal tin is covered with a carbon material having a graphene phase, etc., and the graphite-based carbon material and this graphene phase are bonded by carbon atoms. Therefore, the negative electrode active material becomes a powder surrounded by a fused graphene phase or the like. As a result, the short life due to volume expansion, which is a major problem with silicon and tin-based materials, can be improved by the strong bonding of carbon materials.
- olivine-type lithium metal phosphates and silicates having relatively high resistance titanium oxides known as insulators, and metal oxide negative electrode powders having semiconductor properties
- a graphene phase or the like is covered with a carbon material, and the graphene phase or the like is fused with a graphene phase or the like of a conductive carbon material.
- the surface of the active material is covered with a carbon material, so that the electron energy distribution of the atoms that make up the powder close to the insulator and the powder with semiconductor properties is conductive. It is considered that there is an effect that electrons from carbon atoms constituting the carbon material are attracted to the valence band that exhibits the effect of changing the electron distribution to that of a conductive material.
- the conductive material combined with the carbon material on the surface of the active material works to secure the electrolytic solution, and as a result, exerts an effect on capacity development at the time of large current charge / discharge.
- FIG. 1 is a schematic view of a Si—SiO 2 / carbon-based conductive material composite negative electrode material that is an example of the present invention.
- FIG. It is a transmission electron micrograph which shows the state by which the graphene phase etc. were united.
- FIG. 1 shows a schematic diagram of a Si—SiO 2 / carbon-based conductive material composite negative electrode material which is an example of an electrode material for a lithium secondary battery of the present invention.
- FIG. 1A shows a Si—SiO 2 active material coated with a graphene phase and the like
- FIG. 1B shows a carbon material which is a negative electrode carbon-based main material
- FIG. 1C shows a state in which graphene phases and the like are fused and bonded.
- FIG. 2 is a transmission electron micrograph showing a state in which graphene phases and the like are fused.
- an active material 4 capable of occluding and releasing lithium ions is a powder in which metal silicon 2 is included in an oxide (SiO—SiO 2 ) 1 (average particle diameter of 100 to 100). 500 nm) is covered with a carbon material 3 having a layer thickness of several nanometers. The surface of the carbon material 3 is composed of a graphene phase or the like.
- the active material 4 is surrounded by the graphite-based carbon material 5 to obtain a composite active material 7 containing the active material therein.
- the composite active material 7 has an average particle size of 3 to 10 ⁇ m, preferably 3 to 7 ⁇ m.
- a graphene phase or the like 8a on the surface of acetylene black 6a and a graphene or the like 8b on the surface of the carbon nanotube 6b are overlapped and fused to form a fused phase 8 such as a graphene phase.
- graphene and the like are fused together on the surfaces of the carbon materials. In this way, electrical conductivity is improved by overlapping and fusing each other.
- AB represents acetylene black
- CNT represents carbon nanotube
- magnification is 3.2 million.
- the negative electrode for a lithium secondary battery includes the composite active material 7 and a binder.
- Materials for the negative electrode material 4 capable of occluding and releasing lithium ions forming the composite active material 7 include carbon materials, lithium-aluminum alloys, silicon-based or tin-based lithium alloys, oxide mixtures thereof, and titanium. A lithium acid etc. or these mixed systems can be mentioned. Among these, it is preferable to use a carbon material because of its low irreversible capacity, but in recent years lithium titanate, silicon or tin oxide, and silicon or tin metal mixtures are being used as high-capacity materials. In the present invention, it is considered that the use of a metal oxide encapsulating a metal, an alloy material encapsulating a metal, or the like has a great effect.
- the negative electrode material 4 in which a carbon material having a graphene phase or the like is arranged on the powder surface of tin or silicon oxide containing metal tin or silicon is preferable.
- Examples of the positive electrode material for lithium secondary batteries include layered or spinel lithium-containing metal oxides and solid solutions thereof, lithium-containing metal phosphate compounds, lithium-containing metal silicates, and fluorides thereof. Of these, lithium-containing metal phosphate compounds are preferred, and olivine-type lithium metal phosphate is particularly suitable for the purposes of the present invention.
- a positive electrode material for a lithium secondary battery is mainly composed of an olivine type lithium metal phosphate and includes the material and a binder.
- the lithium-containing metal phosphate compound include LiFePO 4 , LiCoPO 4 , and LiMnPO 4, and examples of the siliceous oxide include LiFeSiO 4 .
- the fluoride include Li 2 FePO 4 ⁇ F.
- the lithium-containing compound include LiTi 2 (PO 4 ) 3 and LiFeO 2 .
- LiFePO 4 which is an olivine type lithium metal phosphate as a lithium-containing metal phosphate compound in terms of electrochemical characteristics, safety and cost.
- the carbon material covering the surface of the positive electrode or negative electrode active material that can be used in the present invention can be selected from either a crystalline system or an amorphous system. An amorphous carbon material is particularly preferable. Further, the coating on the surface of the positive electrode or the negative electrode active material can be easily obtained by treating the positive electrode or the negative electrode active material with a gas or liquid containing hydrocarbon and then firing the treated product in a reducing atmosphere. The carbon material covering the surface of the positive electrode or the negative electrode active material is in close contact with the surface of the active material, and a graphene phase or the like is formed on the surface of the carbon material. These phases can be formed by firing in a reducing atmosphere.
- the thickness of the carbon material coating layer is 1 to 10 nm, preferably 2 to 5 nm. If it is out of the range of 10 nm or more, the carbon material layer is thick and the diffusion of lithium ions to the surface of the active material which is the battery reaction site is reduced, resulting in a decrease in high output characteristics.
- the negative electrode graphite-based carbon material that can be used in the present invention has, when subjected to heat treatment in an inert atmosphere, a hexagonal network plane composed of carbon atoms, a graphite structure that is a structure in which so-called graphene phases are laminated with regularity on the surface. Carbon materials that are easy to develop, so-called soft carbon, can be used.
- the average particle size of the negative electrode graphite carbon material is preferably 5 to 10 ⁇ m, and the mixing ratio of the negative electrode material constituting material can be 60 to 95% by mass, preferably 70 to 80% by mass.
- the carbon material other than the graphite-based carbon material that can be used in the present invention and having a graphene phase or the like on at least the surface thereof is at least one conductive material selected from conductive carbon powder and conductive carbon fiber.
- the conductive carbon powder is preferably at least one selected from powders containing acetylene black, ketjen black, and graphite crystals.
- carbon fiber it is carbon fiber which has electroconductivity.
- the fiber diameter of the carbon fiber is preferably 5 nm to 200 nm, and more preferably 10 nm to 100 nm.
- the fiber length is preferably 100 nm to 50 ⁇ m, more preferably 1 ⁇ m to 30 ⁇ m.
- the lithium battery using the lithium secondary battery electrode material of the present invention not only the output characteristics and long life of the battery, but also a combination of electrode materials that are highly effective as a high-capacity material as a compact and lightweight battery that will be required for automotive use in the future.
- the positive electrode material olivine-type LiFePO 4 coated with a carbon material such as graphene phase on the powder surface is used, which has a long life, low cost, and high safety.
- conductive acetylene black and carbon are added to the positive electrode main material. It is preferable to use it in combination with a nanotube.
- the opposing negative electrode material is coated with carbon material such as graphene phase on the surface of metallic silicon, tin-encapsulated silicon, or tin oxide powder.
- carbon material such as graphene phase on the surface of metallic silicon, tin-encapsulated silicon, or tin oxide powder.
- conductive carbon acetylene black, carbon nanotubes, etc.
- graphite-based carbon material artificial graphite or graphite powder
- amorphous carbon material with carbon coating on the surface Think best.
- a separator that can be used is to electrically insulate the positive electrode and the negative electrode to hold the electrolytic solution.
- the separator include synthetic resin films, fibers or inorganic fibers. Specific examples thereof include polyethylene and polypropylene films, woven and nonwoven fabrics made of these resins, glass fibers and cellulose fibers. And so on.
- the electrolytic solution in which the electrode group described above is immersed it is preferable to use a nonaqueous electrolytic solution containing lithium salt or an ion conductive polymer.
- a nonaqueous electrolytic solution containing lithium salt examples include ethylene carbonate (EC), propylene carbonate (PC), diethyl carbonate (DEC), dimethyl carbonate (DMC), and methyl ethyl carbonate (MEC).
- the binder is a material that is physically and chemically stable under the atmosphere in the battery, and contains fluorine such as polytetrafluoroethylene, polyvinylidene fluoride, and fluororubber.
- fluorine such as polytetrafluoroethylene, polyvinylidene fluoride, and fluororubber.
- Thermoplastic resins such as resin, polypropylene, and polyethylene can be used.
- Acrylic resin materials, styrene / butadiene based materials and the like can also be used.
- the electrode for the lithium secondary battery has the above electrode material and the like and other members selected as necessary.
- other members include current collectors that collect current from electrode materials.
- An example of the current collector is a metal thin film.
- the positive electrode current collector may be an aluminum foil
- the negative electrode current collector may be a copper foil.
- Example 1 A positive electrode of a lithium secondary battery was produced by the following method.
- An olivine type lithium iron phosphate (LiFePO 4 ) coated with an amorphous carbon material of several nm and having a secondary particle size of 0.5 to 2 ⁇ m is used as a positive electrode active material.
- To 94 parts by mass of the obtained composite positive electrode active material 6 parts by mass of polyvinylidene fluoride was added as a binder.
- a positive electrode mixture (positive electrode slurry).
- An aluminum foil having a thickness of 20 ⁇ m and a width of 150 mm is prepared.
- the positive electrode slurry was applied to both sides of the aluminum foil and dried.
- the positive electrode for lithium secondary batteries was obtained by pressing and cutting.
- the total thickness of the positive electrode when pressed after applying and drying the positive electrode slurry on both sides of the aluminum foil was 160 ⁇ m.
- Example 2 A negative electrode of a lithium secondary battery was produced by the following method. An amorphous carbon material was coated to a thickness of several nm on the surface of silicon oxide powder containing metallic silicon. 90 parts by mass of graphite-based carbon material (soft carbon) whose surface is coated with an amorphous carbon material to a thickness of several nm is mixed with 10 parts by mass of the obtained silicon oxide powder to obtain a mixed powder. It was. The graphite-based carbon material was treated with a hydrocarbon-containing gas or liquid, and then the treated product was fired in a reducing atmosphere to coat the amorphous carbon material to a thickness of several nm.
- graphite-based carbon material soft carbon
- the graphite-based carbon material was treated with a hydrocarbon-containing gas or liquid, and then the treated product was fired in a reducing atmosphere to coat the amorphous carbon material to a thickness of several nm.
- a composite negative electrode active material was obtained.
- 5 parts by mass of polyvinylidene fluoride as a binder is added, and N-methylpyrrolidone as a dispersion solvent is added thereto and kneaded to prepare a negative electrode mixture (negative electrode slurry).
- a copper foil having a thickness of 10 ⁇ m and a width of 150 mm is prepared. The slurry was applied and dried, and then pressed and cut to obtain a negative electrode for a lithium secondary battery. The total thickness of the negative electrode when pressed after applying and drying the negative electrode slurry on both sides of the copper foil was 120 ⁇ m.
- Comparative Example 1 Comparative Example 1 in which the olivine-type lithium iron phosphate (LiFePO 4 ) as a main material, acetylene black as a conductive material, and carbon nanotubes were mixed and mixed at room temperature in the positive electrode of Example 1 at a room temperature.
- the positive electrode plate was prepared.
- Other manufacturing methods were manufactured in the same manner as in Example 1.
- Comparative Example 2 In the negative electrode of Example 2, a carbon-coated carbon material as a main material, a carbon-coated silicon oxide containing metal silicon, an acetylene black as a conductive material, and a carbon nanotube were mixed and mixed without being combined. As a negative electrode plate of Comparative Example 2. However, polyimide was used as the binder, the ratio was 15 parts by mass, and the other production methods were produced in the same manner as in Example 2.
- the positive and negative electrode plates produced in Examples 1 and 2 and Comparative Examples 1 and 2 were combined to produce a 3.4 V-0.5 Ah aluminum laminated film pack type lithium ion battery.
- As the electrolytic solution one obtained by dissolving 1 mol / l of lithium hexafluorophosphate (LiPF 6 ) in a solution mixed at a volume ratio of EC and MEC of 30:70 was used.
- a PE resin-made film having a thickness of 20 ⁇ m was used as a separator for the positive and negative electrode plates.
- each battery is adjusted to 50% charged state and discharged at 0.1, 0.5, 1, 1.5 and 2.5A for 10 seconds from the circuit release, and the voltage after 10 seconds is Measured and obtained a value obtained by calculating the slope of the straight line by the least square method from the IV characteristic line in which the relationship between the current value and the voltage drop from the open circuit voltage at each discharge current is plotted. Comparison was made as a direct current resistance value at 50% charge. The results are shown in Table 2.
- the combination of the positive electrode plate of Example 1 and the negative electrode plate of Example 2 made it possible to provide a battery with low resistance, high output, high capacity and long life for in-vehicle use. This is because carbon materials fuse and superimpose their respective graphene phases, etc., improving and maintaining the electron conductivity between the electrodes and reducing the reaction resistance of lithium ions, and large charge / discharge is the carbon conductive material in the electrodes. It can be considered that this is the result of maintaining the same state over a long period of time without any obstruction phenomenon with respect to the electronic network and electrode reaction state.
- the electrode material for a lithium secondary battery of the present invention is a lithium secondary battery that can be repeatedly charged and discharged with a large current, has a cycle performance of 10 years, 5000 to 10000 cycle level, and can be applied to industrial batteries such as in-vehicle use. Deployment is possible.
Abstract
Description
近年、このリチウム二次電池を車載用途にと開発が進められており、大電流充放電と高容量化、さらにその繰り返しによる長寿命化のすべての性能向上が大きな課題となっている。
正極材および負極材を構成する活物質粒子の小粒径化による比表面積の増加や、電極設計による電極面積の増加等の工夫により、リチウム二次電池の電流密度負荷低減がなされてきた。
これらの工夫によって高容量化や大電流充放電は向上したが、リチウム二次電池の長寿命対策に対しては不十分であった。このため、正極ではリチウム金属酸化物の金属元素の置換配合比やドープ金属の置換が検討された。また、炭素系負極では電解液の分解による抵抗被膜の生成防止を工夫した添加剤が提案された。半導体特性を有する合金系負極では、合金組成や導電材の添加、さらには合金の体積膨張を抑制するために結着剤に工夫を施したものが提案された。例えば、活物質粉末と、炭素材料から形成され活物質粉末の表面に付着する導電材料と、導電材料に結合した繊維状導電材料とをもつ電極材料を有することを特徴とする二次電池用電極が知られている(特許文献1)。
抵抗の高いリチウム金属酸化物正極、また絶縁、半導体特性を有するチタン酸化物負極や合金系負極、さらには導電性があっても微細化により接触抵抗が大きい炭素系負極をそれぞれ用いた電池の高容量化、高出力および寿命性能を改善することは困難であった。
上記負極板の負極材は、以下に示す成分(a)、成分(b)および成分(c)を含む。これら各成分はグラフェン相およびアモルファス相から選ばれた少なくとも1つの相(以下、グラフェン相等という)を表面相として有し、上記負極材はこの表面相同士を融合結合させて得られる複合負極活物質を含むことを特徴とする。ここで、グラフェン相とはsp2結合炭素原子の平面6員環構造一層をいい、アモルファス相とはこの6員環構造が3次元的に構成されたものをいい、これらが融合結合するとは、グラフェン相および/またはアモルファス相の乱れによって結合することを言う。
成分(a)は、炭素材が被覆されて、少なくとも表面にグラフェン相等を有する、金属を内包した金属酸化物および合金材から選ばれた少なくとも1つの活物質であり、
成分(b)は、少なくとも表面にグラフェン相等を有する黒鉛系炭素材であり、
成分(c)は、上記黒鉛系炭素材以外であり、少なくとも表面にグラフェン相等を有する炭素材である。
特に上記活物質が金属スズを内包したスズ酸化物の粉体、または金属シリコンを内包したシリコン酸化物の粉体であることを特徴とする。
成分(d)は、炭素材が被覆されて、少なくとも表面にグラフェン相等を有するオリビン形リチウム金属燐酸化物であり、
成分(e)は、黒鉛系炭素材以外であり、少なくとも表面にグラフェン相等を有する炭素材である。
また、上記成分(c)または成分(e)は、アセチレンブラック、ケッチェンブラック、黒鉛結晶を含む粉体、および導電性カーボン繊維から選ばれた少なくとも1つであることを特徴とする。
特に上記導電性カーボン繊維が、カーボン繊維、グラファイト繊維、気相成長炭素繊維、カーボンナノファイバーおよびカーボンナノチューブから選ばれた少なくとも1つの繊維であることを特徴とする。
炭素材3が被覆されている活物質4を、黒鉛などの黒鉛系炭素材5と、アセチレンブラック6aおよびカーボンナノチューブ6b等の黒鉛系炭素材以外の炭素材6と混合して焼成することにより、炭素材同士の表面のグラフェン相等が相互に重ね合わさって融合する。それとともに活物質4が黒鉛系炭素材5で包囲されて活物質を内部に含む複合活物質7が得られる。この複合活物質7の平均粒子径は3~10μmであるが、好ましくは3~7μmである。
図2に示すように、炭素材同士の表面でグラフェン等が相互に融合されている。このように、相互に重ね合わされて融合していることにより電気伝導性が向上する。図2において、ABはアセチレンブラックを、CNTはカーボンナノチューブをそれぞれ表し、倍率は320万倍である。
リチウム二次電池用負極は、複合活物質7と結着材とを含んで構成される。
これらの中で、不可逆容量が小さいなどの理由から、炭素材を用いることが好ましいが、近年チタン酸リチウムやシリコンまたはスズ酸化物およびシリコンまたはスズ金属混合体が高容量材料として用いられつつある。
本発明では、金属を内包した金属酸化物、金属を内包した合金材等を用いることが大きな効果をもたらすものと考えられる。これらの例としては、チタン酸リチウムやスズまたはシリコン金属および酸化物混合体が挙げられる。
また、本発明ではスズまたはシリコン系負極の短寿命を解決するため、金属スズまたはシリコンを内包したスズまたはシリコン酸化物の粉体表面にグラフェン相等を有する炭素材を配した負極材4が好ましい。
これらの中で、電気化学特性、安全性やコスト面で、リチウム含有金属リン酸化合物としてのオリビン形リチウム金属燐酸化物であるLiFePO4を用いることが好ましい。
また、正極または負極活物質表面への被覆は、正極または負極活物質を炭化水素を含んだガスまたは液体で処理した後に、この処理物を還元性雰囲気で焼成することにより容易に得られる。
正極または負極活物質表面を被覆する炭素材は、当該活物質の表面に密接しており、かつ該炭素材表面にグラフェン相等が形成されている。これらの相の形成は、還元雰囲気下において焼成を行なうことで形成できる。炭素材の被覆層の厚さは1~10nm、好ましくは2~5nmである。10nm以上の範囲外となると、炭素材層が厚く電池反応部位である活物質の表面へのリチウムイオンの拡散が低下し、結果高出力特性が低下する。
負極黒鉛系炭素材の平均粒子径は5~10μmであることが好ましく、負極材構成材料の配合比で60~95質量%、好ましくは70~80質量%配合することができる。
導電性カーボン粉体としては、具体的にはアセチレンブラック、ケッチェンブラック、および黒鉛結晶を含む粉体から選ばれた少なくとも1つであることが好ましい。
カーボン繊維としては、導電性を有するカーボン繊維である。例えば、カーボン繊維、グラファイト繊維、気相成長炭素繊維、カーボンナノファイバーおよびカーボンナノチューブのうちの少なくとも1種類を含有することが好ましい。カーボン繊維の繊維径としては5nm~200nmであることが好ましく、10nm~100nmであることがより好ましい。また、繊維長が100nm~50μmであることが好ましく、1μm~30μmであることがより好ましい。
また、負極材構成材料の配合割合で、導電材は1~12質量%、好ましくは4~8質量%配合することができる。
すなわち、正極材としては長寿命で低コスト、かつ安全性の高い、粉体表面にグラフェン相等の炭素材被覆を施したオリビン形LiFePO4を用い、この正極主材にさらに導電性アセチレンブラックとカーボンナノチューブとを結合させて用いることが好ましい。
リチウム塩を含む非水電解液における非水溶媒としては、エチレンカーボネート(EC)、プロピレンカーボネート(PC)、ジエチルカーボネート(DEC)、ジメチルカーボネート(DMC)、メチルエチルカーボネート(MEC)等が挙げられる。
また、上記非水溶媒に溶解できるリチウム塩としては、六フッ化リン酸リチウム(LiPF6)、ホウ四フッ化リチウム(LiBF4)、トリフルオロメタンスルホン酸リチウム(LiSO3CF4)等が挙げられる。
リチウム二次電池の正極を以下の方法で製造した。
数nmの非晶質炭素材が被覆された、二次粒子径が0.5~2μmのオリビン型リン酸鉄リチウム(LiFePO4)を正極活物質とする。
この活物質90質量部に、導電材として10質量部のアセチレンブラックおよびカーボンナノチューブ(アセチレンブラック/カーボンナノチューブ=8/2(質量比))を加えて、700℃で1時間還元性雰囲気で焼成した。
得られた複合正極活物質94質量部に、結着剤として6質量部のポリフッ化ビニリデンを添加した。これに分散溶媒として、N-メチルピロリドンを添加し、混練して、正極合剤(正極スラリー)を作製した。
20μm厚さで、150mm幅のアルミニウム箔を準備する。上記正極スラリーを該アルミニウム箔の両面に塗布、乾燥した。その後、プレス、裁断してリチウム二次電池用の正極を得た。アルミニウム箔の両面に正極スラリーを塗布・乾燥後、プレスした時の正極総厚さは160μmであった。
リチウム二次電池の負極を以下の方法で製造した。
金属シリコンを内包したシリコン酸化物の粉体表面に非晶質炭素材を数nmの厚さに被覆した。
得られたシリコン酸化物粉末10質量部に対して、表面に非晶質炭素材を数nmの厚さに被覆した黒鉛系炭素材(ソフトカーボン)90質量部を混合して混合粉体を得た。この黒鉛系炭素材は、炭化水素を含んだガスまたは液体で処理した後に、この処理物を還元性雰囲気で焼成することにより、非晶質炭素材を数nmの厚さに被覆した。
この混合粉体98質量部に対して、アセチレンブラックおよびカーボンナノチューブを2質量部(アセチレンブラック/カーボンナノチューブ=1/1(質量比))とを混合して1100℃で1時間還元性雰囲気で焼成することで複合負極活物質を得た。
この複合負極活物質粉体95質量部に結着剤として5質量部のポリフッ化ビニリデンを添加し、これに分散溶媒としてN-メチルピロリドンを添加し混練して、負極合剤(負極スラリー)を作製した。
10μm厚さで、150mm幅の銅箔を準備する。当該スラリーを用いて塗工乾燥を行ない、その後、プレス、裁断してリチウム二次電池用の負極を得た。銅箔の両面に負極スラリーを塗布・乾燥後、プレスした時の負極総厚さは120μmであった。
実施例1の正極において、主材であるオリビン型リン酸鉄リチウム(LiFePO4)と導電材であるアセチレンブラックとカーボンナノチューブとを複合化せずに室温で混合して混ぜたものを比較例1の正極板として作製した。その他の作製方法は実施例1と同一の方法で作製した。
実施例2の負極において、主材であるカーボン被覆された炭素材と金属シリコン内包のカーボン被覆シリコン酸化物と導電材であるアセチレンブラックとカーボンナノチューブとを複合化せずに混合して混ぜたものを比較例2の負極板として作製した。ただし、結着剤としてポリイミドを用いて、その割合は15質量部とし、その他の作製方法は実施例2と同一の方法で作製した。
2 金属シリコン
3 炭素材
4 炭素材が被覆されている活物質
5 黒鉛系炭素材
6 黒鉛系炭素材以外の炭素材
7 複合活物質
8 グラフェン相等
Claims (12)
- 正極板および負極板間にセパレータを介して、捲回または積層してなる電極群に有機電解液を浸透または浸漬させてリチウムイオンの吸蔵・放出を繰返し行なう二次電池に用いられるリチウム二次電池用電極材であって、
前記負極板の負極材は以下に示す成分(a)、成分(b)および成分(c)を含み、前記各成分はグラフェン相およびアモルファス相から選ばれた少なくとも1つの相を表面相として有し、前記負極材はこの表面相同士を融合結合させて得られる複合負極活物質を含み、
成分(a)は、炭素材が被覆されて、少なくとも表面にグラフェン相およびアモルファス相から選ばれた少なくとも1つの相を有する、金属を内包した金属酸化物および合金材から選ばれた少なくとも1つの活物質であり、
成分(b)は、少なくとも表面にグラフェン相およびアモルファス相から選ばれた少なくとも1つの相を有する黒鉛系炭素材であり、
成分(c)は、前記黒鉛系炭素材以外であり、少なくとも表面にグラフェン相およびアモルファス相から選ばれた少なくとも1つの相を有する炭素材であることを特徴とするリチウム二次電池用電極材。 - 前記活物質が金属スズを内包したスズ酸化物の粉体であることを特徴とする請求項1記載のリチウム二次電池用電極材。
- 前記活物質が金属シリコンを内包したシリコン酸化物の粉体であることを特徴とする請求項1記載のリチウム二次電池用電極材。
- 前記黒鉛系炭素材が、人造黒鉛、天然黒鉛、易黒鉛化炭素材、および非晶質炭素材から選ばれた少なくとも1つの炭素材であることを特徴とする請求項1記載のリチウム二次電池用電極材。
- 前記成分(c)は、アセチレンブラック、ケッチェンブラック、黒鉛結晶を含む粉体、および導電性カーボン繊維から選ばれた少なくとも1つの炭素材であることを特徴とする請求項1記載のリチウム二次電池用電極材。
- 前記導電性カーボン繊維が、カーボン繊維、グラファイト繊維、気相成長炭素繊維、カーボンナノファイバーおよびカーボンナノチューブから選ばれた少なくとも1つの繊維であることを特徴とする請求項5記載のリチウム二次電池用電極材。
- 正極板に接触する正極材および負極板に接触する負極材間にセパレータを介して、捲回または積層してなる電極群に有機電解液を浸透または浸漬させてリチウムイオンの吸蔵・放出を繰返し行なう二次電池に用いられるリチウム二次電池用電極材であって、
前記正極板の正極材は以下に示す成分(d)および成分(e)を含み、前記各成分はグラフェン相およびアモルファス相から選ばれた少なくとも1つの相を表面相として有し、前記正極材はこの表面相同士を融合結合させて得られる複合正極活物質を含み、
成分(d)は、炭素材が被覆されて、少なくとも表面にグラフェン相およびアモルファス相から選ばれた少なくとも1つの相を有するオリビン形リチウム金属燐酸化物であり、
成分(e)は、黒鉛系炭素材以外であり、少なくとも表面にグラフェン相およびアモルファス相から選ばれた少なくとも1つの相を有する炭素材であることを特徴とするリチウム二次電池用電極材。 - 前記成分(e)は、アセチレンブラック、ケッチェンブラック、黒鉛結晶を含む粉体、および導電性カーボン繊維から選ばれた少なくとも1つであることを特徴とする請求項7記載のリチウム二次電池用電極材。
- 前記導電性カーボン繊維が、カーボン繊維、グラファイト繊維、気相成長炭素繊維、カーボンナノファイバーおよびカーボンナノチューブから選ばれた少なくとも1つの繊維であることを特徴とする請求項8記載のリチウム二次電池用電極材。
- 正極板に接触する正極材、および負極板に接触する負極材間にセパレータを介して、捲回または積層してなる電極群に有機電解液を浸透または浸漬させてリチウムイオンの吸蔵・放出を繰返し行なうリチウム二次電池において、
前記負極板の負極材が請求項1記載のリチウム二次電池用電極材であることを特徴とするリチウム二次電池。 - 正極板に接触する正極材、および負極板に接触する負極材間にセパレータを介して、捲回または積層してなる電極群に有機電解液を浸透または浸漬させてリチウムイオンの吸蔵・放出を繰返し行なうリチウム二次電池において、
前記正極板の正極材が請求項7記載のリチウム二次電池用電極材であることを特徴とするリチウム二次電池。 - 正極板に接触する正極材および負極板に接触する負極材間にセパレータを介して、捲回または積層してなる電極群に有機電解液を浸透または浸漬させてリチウムイオンの吸蔵・放出を繰返し行なうリチウム二次電池において、
前記負極板の負極材が請求項1記載のリチウム二次電池用電極材であり、
前記正極板の正極材が請求項7記載のリチウム二次電池用電極材であることを特徴とするリチウム二次電池。
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Also Published As
Publication number | Publication date |
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CN102934266A (zh) | 2013-02-13 |
KR101907700B1 (ko) | 2018-10-12 |
US9413003B2 (en) | 2016-08-09 |
EP2698851B1 (en) | 2018-12-12 |
CA2786012A1 (en) | 2012-10-24 |
EP2698851A4 (en) | 2014-10-01 |
EP2698851A1 (en) | 2014-02-19 |
JPWO2012140790A1 (ja) | 2014-07-28 |
JP5834273B2 (ja) | 2015-12-16 |
CA2786012C (en) | 2020-03-31 |
KR20130142877A (ko) | 2013-12-30 |
CN102934266B (zh) | 2016-04-20 |
US20120328923A1 (en) | 2012-12-27 |
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