The present invention relates to a positive electrode for lithium ion battery, a method for producing said positive electrode, and a lithium ion battery.
In general, lithium-containing transition metal oxides are used for a positive electrode active material for lithium ion battery. In particular, they are lithium cobaltate (LiCoO2), lithium nickelate (LiNiO2), lithium manganite (LiMn2O4) and the like. A combination of the lithium-containing transition metal oxides is proceeding in order to improve properties such as high capacity, cycle characteristic, storage characteristic, decreased internal resistance, rate performance, and safety. Specifically, lithium ion batteries, for large-size equipment use such as automobile use and load leveling use, require properties different from those of mobile phone use and mobile computer use. In particular, high capacity and low resistance are required for automobile use and high capacity and long lifetime are required for load leveling use.
Traditionally, the positive electrode for lithium ion battery is produced in a manner such that positive electrode active material and conductive material are mixed in organic solvent where binder dissolves, paste thereof is formed, the paste is coated on an aluminum foil, and then drying operation and pressing operation are conducted. The binder is necessary for maintaining adhesion between the positive electrode active material, the conductive material and the aluminum foil (current collector). Further, the conductive material is mixed in order to provide conductive property with the positive electrode active material which is poor at conductive property.
For example, such positive electrodes for lithium ion battery are disclosed in Patent documents 1 to 3. In these active materials, the positive electrode for lithium ion battery disclosed in Patent document 1 is produced in a manner such that paste of positive electrode active material is coated on an aluminum foil for a current collector where hydration and oxidation treatments are conducted on a surface. Further, the positive electrode active material paste used here includes positive electrode active material, conductive material such as carbon black and graphite, binder such as PTFE and solvent such as water (paragraphs 0016 to 0025 in the specification of Patent document 1).
Further, Patent document 2 discloses a positive electrode for lithium ion battery of an aluminum foil comprising a film containing compounds having ion permeability and carbon particulates as a lower layer, and a film containing binder, carbon particulates and positive electrode active material as a upper layer (paragraph 0009 and the like in the specification of Patent document 2).
Further, a positive electrode for lithium ion battery disclosed in Patent document 3 is produced in a manner such that positive electrode active material composition is coated on Al alloy positive electrode current collector. The positive electrode active material composition used here is produced in a manner such that positive electrode active material, polyvinylidene fluoride binder and carbon conductive material are dispersed in a solvent of N-methyl pyrrolidone (paragraphs 0031 and 0032 and the like in the specification of Patent document 3).
However, when the positive electrode for lithium ion battery is produced in a manner such that positive electrode active material mixed with conductive material, binder and the like is coated on a current collector such as aluminum foil, uneven distribution of conductive material, deactivation caused by covering of the binder over the positive electrode active material and the like are generated, and then a contact resistance of battery increases. Therefore, a problem that an output property of the battery deteriorates can be caused.
The present invention aims to provide a positive electrode for lithium ion battery reducing a contact resistance of a battery and achieving an excellent output property. Further, the present invention aims to provide a method for producing the positive electrode for lithium ion battery. Furthermore, the present invention aims to provide a lithium ion battery using the positive electrode for lithium ion battery.
The inventor has focused attention on a conductive property of the positive electrode active material and the aluminum foil of the current collector, and a method for bonding them, and diligently studied and eventually have found out, a positive electrode for lithium ion battery, using positive electrode active material including no conductive material and no binder, having non-traditional structure and properties, can be produced.
The present invention, produced on the basis of the above findings, in one aspect, is a positive electrode for lithium ion battery comprising a mixed layer comprising:
The present invention is, in one embodiment, the positive electrode for lithium ion battery, further comprising a layer of only the metal, where the mixed layer is formed on the layer of only the metal.
The present invention is, in another embodiment, the positive electrode for lithium ion battery, where the metal is aluminum or aluminum alloy.
The present invention is, in yet another embodiment, the positive electrode for lithium ion battery, where the positive electrode active material is a lithium-containing transition metal oxide.
The present invention is, in yet another embodiment, the positive electrode for lithium ion battery, where the transition metal in the lithium-containing transition metal oxide is one or more selected from the group consisting of Ni, Mn, Co and Fe.
The present invention is, in yet another embodiment, the positive electrode for lithium ion battery, where a crystal structure of the positive electrode active material has a layer structure or a spinel structure.
The present invention is, in another aspect, a method for producing a positive electrode for lithium ion battery, comprising a step of setting powder of positive electrode active material in a mold and casting molten metal on the powder in the mold.
The present invention is, in yet another aspect, a lithium ion battery using the positive electrode for lithium ion battery of the present invention.
The present invention can provide a positive electrode for lithium ion battery reducing a contact resistance of a battery and achieving an excellent output property.
The positive electrode for lithium ion battery of an embodiment of the present invention comprises a mixed layer comprising metal forming a current collector, and positive electrode active material dispersed in a state of layer in the metal forming the current collector. The mixed layer may compose the positive electrode singularly. Further, the mixed layer may be formed on a metal layer forming a current collector, and these two layers may compose the positive electrode.
As raw materials for positive electrode active material for lithium ion battery, without being limited particularly, various compounds useful for positive electrode active material for general positive electrode for lithium ion battery can be used. In particular, it is preferable to use lithium-containing transition metal oxides such as lithium cobaltate (LiCoO2), lithium nickelate (LiNiO2) and lithium manganate (LiMn2O4). The transition metal in the lithium-containing transition metal oxide is preferably one or more selected from the group consisting of Ni, Mn, Co and Fe. The lithium ratio to all metals in the lithium-containing transition metal oxide is over 1.0 to below 1.3. This is because it is difficult to maintain stable crystal structure if the ratio is 1.0 or less, and high capacity of the battery cannot be secured if the ratio is 1.3 or more. A crystal structure of the positive electrode active material in such a mixed layer is not limited as long as lithium can be inserted to and removed from, but a layer structure or a spinel structure is preferable.
The current collector is formed with a conductive material, consisting of metal having excellent conductive property. The conductive material is, as described below, cast on the powder of the positive electrode active material after melted in a production process of the positive electrode. Therefore, the conductive material, in which a melting point of the conductive material is a temperature such that negatively affects a property of the positive electrode active material, is not preferable. Further, it is necessary for the conductive material to be a metal having greater ionization tendency than a metal element composing the positive electrode active material. Accordingly, as conductive materials composing the current collector, aluminum, magnesium, manganese, zinc, or an alloy comprising at least one species thereof may be used, and aluminum and aluminum alloy (for example, Al—Mn series, Al—Mg series, Al—Zn—Mg series) are especially preferable among them. Further, a configuration of the current collector is not limited in particular, and it may be in the form of foils, plates and the like.
The mixed layer is, as described below, a mixed layer of positive electrode active material and metal composing the current collector, formed in a manner such that positive electrode active material in powder form is bedded in a mold, molten metal to be constituent material of the current collector is poured on the positive electrode active material, and then they are solidified. Accordingly, the mixed layer has a structure where the metal gets through the interval between particles of the positive electrode active material and becomes solid. Further, the positive electrode active material in the mixed layer is dispersed in layers in the metal composing the current collector. The positive electrode active material dispersed in layers is not limited, but it is preferably dispersed evenly.
The positive electrode for lithium ion battery of the embodiment of the present invention, as described above, comprises the mixed layer of the positive electrode active material and the metal composing the current collector. Accordingly, the positive electrode active material has an excellent adhesion property with the current collector and an excellent conductive property even though binder or conductive material is not included.
The mixed layer has a thickness of, for example, 10 μm to 60 μm, though it differs according to a size of the positive electrode to be formed, an average particle size of the positive electrode active material powder, a hardness of the surface of the positive electrode active material bedded on the mold, materials, amount and temperature of the molten metal to be poured, and the like.
A composition of the mixed layer can be determined by a quantitative analysis of each element of the materials (Li, Ni, Mn and the like) with ICP-MS (ICP mass spectroscope). Further, the thickness of the mixed layer can be determined by an observation with SEM (scanning electron microscope).
[Manufacturing Method for Positive Electrode for Lithium Ion Battery]
Next, manufacturing method for positive electrode for lithium ion battery of the embodiment of the present invention is explained.
First, powder of the positive electrode active material is formed. The present invention can use a method to oxidize a mixture or a coprecipitate containing metal composing the positive electrode active material for forming the positive electrode active material powder. The mixture can be formed by mixing compounds of each element with a general method, and the coprecipitate can be formed with a general method (coprecipitation with hydroxide or carbonate).
In particular, firstly, raw materials of various types are mixed in a manner such that metal elements composing crystals of the positive electrode active material exist in the crystal structure at an intended composition ratio, and then they are defined as raw material mixtures. The raw material includes a lithium compound and compounds of other metal elements.
Examples of the lithium compound may include, but not limited to, lithium carbonate, lithium hydroxide, lithium oxide, lithium chloride, lithium nitrate, lithium sulfate, lithium hydrogen carbonate, lithium acetate, lithium fluoride, lithium bromide, lithium iodide and lithium peroxide. Above all, lithium carbonate is preferable because it is easy to handle and it is inexpensive.
When Ni, Mn, Co, Mg, Al, Ti, Cr, Fe, Cu or Zr is employed as other metal elements contained in the positive electrode active material, carbonate, nitrate, hydroxide, chloride, oxide and the like, of the metal elements, can be used as the raw materials in a similar way.
The mixing method will be explained. The mixing method may include, but not limited to, a method where powdered raw materials are directly mixed, a method where raw materials are mixed after dissolved or suspended in water and/or organic solvent.
Next, an oxidation treatment (for example, calcination under oxidation atmosphere) is conducted to provided raw material mixture under an appropriate condition and then the powder of the positive electrode active material of the present invention can be provided.
Further, an averaged particle size of the powder of the positive electrode active material to be used is preferably not greater than 10 μm though it depends on properties required for the battery. It is because, in the case that the averaged particle size is not greater than 10 μm, the molten metal substantially can mix with the powder of the positive electrode active material when the molten metal is poured. It is also because properties required for the battery can be largely satisfactory.
Next, a mold is prepared and the powder of the positive electrode active material is evenly bedded in the mold. A configuration and a size of the mold are not limited. Further, constituent material of the mold can include, but not limited to, for example, cast iron, copper alloy, aluminum alloy, steel, other special alloy and the like.
Next, the molten metal as a constituent material of the current collector is poured on the powder in the mold. At this time, when, for example, aluminum is used as the molten metal, it does not negatively affect properties of the positive electrode active material because its melting point is 660° C. The poured molten metal goes into the powder of the positive electrode active material in the mold. In this way, the molten metal mixes with the positive electrode active material and the mixed layer in which the positive electrode active material is dispersed in a state of layer is formed. Further, a part of the molten metal may be formed to overlap on the mixed layer.
Next, a mixture composed of the positive electrode active material and the molten metal is solidified to form a mixed layer by cooling the positive electrode active material and the molten metal in the mold, and then the positive electrode for lithium ion battery having the mixed layer is formed. Further, in the case as described above that a part of the molten metal is formed to overlap on the mixture, a layer of metal only, forming the current collector, is additionally formed on the mixed layer.
The lithium ion battery can be produced by using thus obtained positive electrode for lithium ion battery according to publicly known means.
The positive electrode for lithium ion battery of the present invention is, as described above, produced in a manner such that powdered positive electrode active material is set in the mold and the molten metal is poured on the material. Accordingly, it does not include conductive materials or binders. Thus, the contact resistance of the battery is reduced and the output property becomes excellent. Therefore, it is particularly useful for large-scale use such as automobile use and load leveling use in which high capacity, low resistance and long lifetime are required.
Examples of the present invention will be provided as follows for better understanding of the present invention and its advantages, but the following examples are intended to be non-limiting to the present invention.
Carbonate which is a precursor was formed by wet coprecipitation method using solution of nitrate of Ni, Mn and Co and lithium carbonate. After drying this, powder of positive electrode active material was formed by conducting a oxidation treatment. Contained amounts of Li, Ni, Mn and Co in the powder of the positive electrode active material was measured with ICP-MS, and it was determined that Ni:Mn:Co was 1:1:1 and a ratio of Li and all metals (Li/all metals ratio) was 1.05. Further, by the measurement with XRD (X-ray diffractometer), it was determined that the positive electrode active material had a layer structure. Further, by the measurement with laser diffraction particle size distribution, it was determined that the average particle size of the positive electrode active material was 6 μm.
The powder of the positive electrode active material was dispersed evenly on the bottom of the mold being set on the level and having the thickness of 100 μm. Next, melted aluminum was poured on the powder in the mold, and then cooled to produce the positive electrode for lithium ion battery.
As comparative examples, the same positive electrode active material as used in the working examples was formed. Next, carbon black as conductive material and PVDF as binder were prepared. Next, the positive electrode active material, the conductive material and the binder were weighed at the ratio of 85:8:7. Subsequently, the positive electrode active material and the conductive material were mixed in organic solvent (N-methyl pyrrolidone) where the binder dissolved, paste thereof was formed, the paste was coated on an aluminum foil as the current collector, and then drying operation and pressing operation were conducted. In this way, the positive electrode for lithium ion battery was produced. A thickness of the positive electrode was just about 100 μm.
A 2032 coin cell for use in evaluation, in which Li was used as a counter electrode, was prepared with using the positive electrode for lithium ion battery of working example and comparative example. With a solution obtained by dissolving 1M-LiPF6 in EC-DMC (1:1) as an electrolytic solution, the charge and discharge operation was conducted under the charge condition of 4.3V and the discharge condition of 3.0V. A resistance was estimated by a voltage reduction between ending of the charge and beginning of the discharge. As a result, the electrode resistance of working example was 0.5 mΩ and the electrode resistance of comparative example was 1.3 mΩ. This shows that a contact resistance of the battery using the positive electrode for lithium ion battery produced by the producing method of the present invention (working example) is less than that of the battery using the positive electrode for lithium ion battery produced by the traditional coating method (comparative example). Therefore, it is found that, if the positive electrode for lithium ion battery of the present invention is used, the contact resistance of the battery is reduced and the output property becomes excellent.
Number | Date | Country | Kind |
---|---|---|---|
2009-287556 | Dec 2009 | JP | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
---|---|---|---|---|
PCT/JP2010/071724 | 12/3/2010 | WO | 00 | 6/6/2012 |
Publishing Document | Publishing Date | Country | Kind |
---|---|---|---|
WO2011/074431 | 6/23/2011 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
2165128 | Cheesman | Jul 1939 | A |
4443186 | Shell | Apr 1984 | A |
4469654 | Haskett et al. | Sep 1984 | A |
5393622 | Nitta et al. | Feb 1995 | A |
5478674 | Miyasaka | Dec 1995 | A |
6037095 | Miyasaka | Mar 2000 | A |
6123911 | Yamaguchi et al. | Sep 2000 | A |
6423447 | Ohsaki et al. | Jul 2002 | B1 |
6582854 | Qi et al. | Jun 2003 | B1 |
6984469 | Kweon et al. | Jan 2006 | B2 |
7410728 | Fujimoto et al. | Aug 2008 | B1 |
8623551 | Kawahashi et al. | Jan 2014 | B2 |
8748041 | Satoh et al. | Jun 2014 | B2 |
20020106561 | Lee et al. | Aug 2002 | A1 |
20030082448 | Cho et al. | May 2003 | A1 |
20030211391 | Cho et al. | Nov 2003 | A1 |
20040110063 | Uchitomi et al. | Jun 2004 | A1 |
20040197658 | Kase et al. | Oct 2004 | A1 |
20050079416 | Ohzuku et al. | Apr 2005 | A1 |
20050142442 | Yuasa et al. | Jun 2005 | A1 |
20050158546 | Shizuka | Jul 2005 | A1 |
20060083989 | Suhara et al. | Apr 2006 | A1 |
20060121350 | Kajiya et al. | Jun 2006 | A1 |
20060127765 | Machida et al. | Jun 2006 | A1 |
20060204849 | Saito et al. | Sep 2006 | A1 |
20060233696 | Paulsen et al. | Oct 2006 | A1 |
20060281005 | Cho et al. | Dec 2006 | A1 |
20070015058 | Takezawa et al. | Jan 2007 | A1 |
20070141469 | Tokunaga et al. | Jun 2007 | A1 |
20070202405 | Shizuka et al. | Aug 2007 | A1 |
20070248883 | Oda et al. | Oct 2007 | A1 |
20070298512 | Park et al. | Dec 2007 | A1 |
20080044736 | Nakura | Feb 2008 | A1 |
20080081258 | Kim et al. | Apr 2008 | A1 |
20090117464 | Cho et al. | May 2009 | A1 |
20090117469 | Hiratsuka et al. | May 2009 | A1 |
20090148772 | Kawasato et al. | Jun 2009 | A1 |
20090233176 | Kita et al. | Sep 2009 | A1 |
20090286164 | Wada et al. | Nov 2009 | A1 |
20090289218 | Kajiya et al. | Nov 2009 | A1 |
20090299922 | Malcus et al. | Dec 2009 | A1 |
20090305136 | Yada et al. | Dec 2009 | A1 |
20100015514 | Miyagi et al. | Jan 2010 | A1 |
20100019194 | Fujiwara et al. | Jan 2010 | A1 |
20100112447 | Yamamoto et al. | May 2010 | A1 |
20100143583 | Honda et al. | Jun 2010 | A1 |
20100183922 | Cho et al. | Jul 2010 | A1 |
20100209757 | Ooyama et al. | Aug 2010 | A1 |
20100209771 | Shizuka et al. | Aug 2010 | A1 |
20110031437 | Nagase et al. | Feb 2011 | A1 |
20110033749 | Uchida et al. | Feb 2011 | A1 |
20110250499 | Hiratsuka | Oct 2011 | A1 |
20120034525 | Satoh et al. | Feb 2012 | A1 |
20120231342 | Satoh et al. | Sep 2012 | A1 |
20120231343 | Nagase et al. | Sep 2012 | A1 |
20120292562 | Kajiya et al. | Nov 2012 | A1 |
20120319036 | Kajiya et al. | Dec 2012 | A1 |
20120319037 | Kawahashi et al. | Dec 2012 | A1 |
20120319039 | Satoh et al. | Dec 2012 | A1 |
20120319040 | Okamoto et al. | Dec 2012 | A1 |
20120321956 | Kawahashi et al. | Dec 2012 | A1 |
20120326080 | Okamoto et al. | Dec 2012 | A1 |
20120326098 | Satoh | Dec 2012 | A1 |
20120326099 | Satoh | Dec 2012 | A1 |
20120326101 | Satoh | Dec 2012 | A1 |
20120326102 | Satoh | Dec 2012 | A1 |
20130001463 | Okamoto et al. | Jan 2013 | A1 |
20130004849 | Satoh | Jan 2013 | A1 |
20130043428 | Kawahashi et al. | Feb 2013 | A1 |
20130143121 | Kobayashi et al. | Jun 2013 | A1 |
20130175470 | Kajiya et al. | Jul 2013 | A1 |
20130221271 | Nagase et al. | Aug 2013 | A1 |
20130316239 | Okamoto | Nov 2013 | A1 |
20140306152 | Okamoto | Oct 2014 | A1 |
20140339465 | Okamoto | Nov 2014 | A1 |
20140339466 | Okamoto | Nov 2014 | A1 |
Number | Date | Country |
---|---|---|
1520621 | Aug 2004 | CN |
1701451 | Nov 2005 | CN |
1710735 | Dec 2005 | CN |
101478044 | Jul 2009 | CN |
0794155 | Sep 1997 | EP |
0903796 | Mar 1999 | EP |
1244164 | Sep 2002 | EP |
1391950 | Feb 2004 | EP |
1450423 | Aug 2004 | EP |
1742281 | Jan 2007 | EP |
2023426 | Feb 2009 | EP |
2207226 | Jul 2010 | EP |
2207227 | Jul 2010 | EP |
2219251 | Aug 2010 | EP |
2533333 | Dec 2012 | EP |
4-328277 | Nov 1992 | JP |
7-29603 | Jan 1995 | JP |
7-211311 | Aug 1995 | JP |
8-138669 | May 1996 | JP |
09-82325 | Mar 1997 | JP |
9-120813 | May 1997 | JP |
10-83815 | Mar 1998 | JP |
10-116618 | May 1998 | JP |
10-188986 | Jul 1998 | JP |
10-206322 | Aug 1998 | JP |
10-208744 | Aug 1998 | JP |
10-302779 | Nov 1998 | JP |
10-321224 | Dec 1998 | JP |
11-67205 | Mar 1999 | JP |
11-273676 | Oct 1999 | JP |
11-292542 | Oct 1999 | JP |
11-307094 | Nov 1999 | JP |
11-345615 | Dec 1999 | JP |
2000-72445 | Mar 2000 | JP |
2000-149945 | May 2000 | JP |
2000-215884 | Aug 2000 | JP |
2000-348721 | Dec 2000 | JP |
2001-110420 | Apr 2001 | JP |
2001-148249 | May 2001 | JP |
2001-223008 | Aug 2001 | JP |
2001-266851 | Sep 2001 | JP |
2002-63901 | Feb 2002 | JP |
2002-164053 | Jun 2002 | JP |
2002-203552 | Jul 2002 | JP |
2002-216745 | Aug 2002 | JP |
2002-260655 | Sep 2002 | JP |
2002-298914 | Oct 2002 | JP |
3334179 | Oct 2002 | JP |
2003-7299 | Jan 2003 | JP |
2003-17052 | Jan 2003 | JP |
2003-81637 | Mar 2003 | JP |
2003-151546 | May 2003 | JP |
2004-6264 | Jan 2004 | JP |
2004-146374 | May 2004 | JP |
2004-172109 | Jun 2004 | JP |
2004-193115 | Jul 2004 | JP |
2004-214187 | Jul 2004 | JP |
2004-227790 | Aug 2004 | JP |
2004-273451 | Sep 2004 | JP |
2004-355824 | Dec 2004 | JP |
2004-356094 | Dec 2004 | JP |
2005-11713 | Jan 2005 | JP |
2005-53764 | Mar 2005 | JP |
2005-56602 | Mar 2005 | JP |
2005-60162 | Mar 2005 | JP |
2005-75691 | Mar 2005 | JP |
2005-183366 | Jul 2005 | JP |
2005-235624 | Sep 2005 | JP |
2005-243636 | Sep 2005 | JP |
2005-251700 | Sep 2005 | JP |
2005-285572 | Oct 2005 | JP |
2005-289700 | Oct 2005 | JP |
2005-302507 | Oct 2005 | JP |
2005-302628 | Oct 2005 | JP |
2005-324973 | Nov 2005 | JP |
2005-327644 | Nov 2005 | JP |
2005-332707 | Dec 2005 | JP |
2005-347134 | Dec 2005 | JP |
2006-4724 | Jan 2006 | JP |
2006-19310 | Jan 2006 | JP |
2006-54159 | Feb 2006 | JP |
2006-107818 | Apr 2006 | JP |
2006-107845 | Apr 2006 | JP |
2006-127923 | May 2006 | JP |
2006-127955 | May 2006 | JP |
2006-134816 | May 2006 | JP |
2006-134852 | May 2006 | JP |
2006-156126 | Jun 2006 | JP |
2006-156235 | Jun 2006 | JP |
2006-164758 | Jun 2006 | JP |
2006-286614 | Oct 2006 | JP |
3835266 | Oct 2006 | JP |
2006-302542 | Nov 2006 | JP |
2006-351379 | Dec 2006 | JP |
2007-48744 | Feb 2007 | JP |
2007-95443 | Apr 2007 | JP |
2007-194202 | Aug 2007 | JP |
2007-214138 | Aug 2007 | JP |
2007-226969 | Sep 2007 | JP |
2007-227368 | Sep 2007 | JP |
2007-257890 | Oct 2007 | JP |
2007-280723 | Oct 2007 | JP |
2008-13405 | Jan 2008 | JP |
4070585 | Apr 2008 | JP |
2008-103132 | May 2008 | JP |
2008-181708 | Aug 2008 | JP |
2008-192547 | Aug 2008 | JP |
2008-266136 | Nov 2008 | JP |
2008-277106 | Nov 2008 | JP |
4175026 | Nov 2008 | JP |
2008-544468 | Dec 2008 | JP |
2009-117365 | May 2009 | JP |
2009-135070 | Jun 2009 | JP |
2009-151959 | Jul 2009 | JP |
4287901 | Jul 2009 | JP |
2009-289726 | Dec 2009 | JP |
2010-15959 | Jan 2010 | JP |
2010-47466 | Mar 2010 | JP |
2010-192200 | Sep 2010 | JP |
2011-44364 | Mar 2011 | JP |
2012-169224 | Sep 2012 | JP |
2012-243572 | Dec 2012 | JP |
2013-152911 | Aug 2013 | JP |
10-2010-0060362 | Jun 2010 | KR |
363940 | Jul 1999 | TW |
02086993 | Oct 2002 | WO |
03003489 | Jan 2003 | WO |
2004064180 | Jul 2004 | WO |
2007072759 | Jun 2007 | WO |
2008084679 | Jul 2008 | WO |
2009011157 | Jan 2009 | WO |
2009060603 | May 2009 | WO |
2009063838 | May 2009 | WO |
2009128289 | Oct 2009 | WO |
2010049977 | May 2010 | WO |
2010113512 | Oct 2010 | WO |
2010113583 | Oct 2010 | WO |
2011007751 | Jan 2011 | WO |
2011065391 | Jun 2011 | WO |
2011108720 | Sep 2011 | WO |
2012098724 | Jul 2012 | WO |
2012132071 | Oct 2012 | WO |
2012132072 | Oct 2012 | WO |
2012157143 | Nov 2012 | WO |
Entry |
---|
International Preliminary Report on Patentability mailed Nov. 22, 2012 in co-pending PCT application No. PCT/JP2011/054938. |
International Preliminary Report on Patentability mailed Nov. 22, 2012 in co-pending PCT application No. PCT/JP2011/055111. |
International Search Report mailed Nov. 1, 2011 in co-pending PCT application No. PCT/JP2011/066722. |
International Search Report mailed Apr. 10, 2012 in co-pending PCT application No. PCT/JP2011/079535. |
Office Action-Restriction-mailed Mar. 12, 2013 in co-pending U.S. Appl. No. 13/508,887. |
Office Action mailed Mar. 13, 2013 in co-pending U.S. Appl. No. 13/582,091. |
International Search Report mailed Jun. 8, 2010 in co-pending PCT application No. PCT/JP2010/053443. |
International Preliminary Report on Patentability mailed Nov. 17, 2011 in co-pending PCT application No. PCT/JP2010/053443. |
International Search Report mailed May 24, 2011 in co-pending PCT application No. PCT/JP2011/053271. |
International Search Report/Written Opinion Mar. 8, 2011 in co-pending PCT application No. PCT/JP2010/071723. |
International Preliminary Report on Patentability mailed Jul. 12, 2012 in co-pending PCT application No. PCT/JP2010/071723. |
International Search Report/Written Opinion mailed Jan. 25, 2011 in corresponding PCT application No. PCT/JP2010/071724. |
International Preliminary Report on Patentability issued Jul. 10, 2012 in corresponding PCT application No. PCT/JP2010/071724. |
International Search Report mailed Jan. 24, 2012 in co-pending PCT application No. PCT/JP2011/072860. |
International Search Report mailed Apr. 26, 2011 in co-pending PCT application No. PCT/JP2011/052394. |
International Preliminary Report on Patentability mailed Oct. 11, 2012 in co-pending PCT application No. PCT/JP2011/052394. |
International Search Report mailed May 10, 2011 in co-pending PCT application No. PCT/JP2011/052399. |
International Preliminary Report on Patentability mailed Oct. 11, 2012 in co-pending PCT application No. PCT/JP2011/052399. |
International Search Report mailed Nov. 15, 2011 in co-pending PCT application No. PCT/JP2011/069042. |
International Search Report/Written Opinion mailed Jun. 7, 2011 in co-pending PCT application No. PCT/JP2011/054935. |
International Preliminary Report on Patentability mailed Oct. 11, 2012 in co-pending PCT application No. PCT/JP2011/054935. |
International Search Report mailed Jun. 7, 2011 in co-pending PCT application No. PCT/JP2011/054938. |
International Search Report/Written Opinion mailed May 17, 2011 in co-pending PCT application No. PCT/JP2011/054942. |
International Preliminary Report on Patentability issued Oct. 2, 2012 in co-pending PCT application No. PCT/JP2011/054942. |
International Search Report/Written Opinion mailed Jun. 7, 2011 in co-pending PCT application No. PCT/JP2011/054934. |
International Preliminary Report on Patentability mailed Oct. 11, 2012 in co-pending PCT application No. PCT/JP2011/054934. |
International Search Report/Written Opinion mailed May 17, 2011 in co-pending PCT application No. PCT/JP2011/054941. |
International Preliminary Report on Patentability issued Oct. 2, 2012 in co-pending PCT application No. PCT/JP2011/054941. |
International Search Report mailed May 10, 2011 in co-pending PCT application No. PCT/JP2011/055111. |
International Search Report/Written Opinion mailed May 17, 2011 in co-pending PCT application No. PCT/JP2011/053710. |
International Preliminary Report on Patentability issued Oct. 2, 2012 in co-pending PCT application No. PCT/JP2011/053710. |
International Search Report/Written Opinion mailed May 24, 2011 in co-pending PCT application No. PCT/JP2011/054777. |
International Preliminary Report on Patentability issued Oct. 2, 2012 in co-pending PCT application No. PCT/JP2011/054777. |
International Search Report mailed May 24, 2011 in co-pending PCT application No. PCT/JP2011/054781. |
Written Opinion mailed Jun. 24, 2011 in co-pending PCT application No. PCT/JP2011/054781. |
International Preliminary Report on Patentability mailed Oct. 11, 2012 in co-pending PCT application No. PCT/JP2011/054781. |
International Search Report/Written Opinion mailed May 24, 2011 in co-pending PCT application No. PCT/JP2011/054779. |
International Preliminary Report on Patentability issued Oct. 2, 2012 in co-pending PCT application No. PCT/JP2011/054779. |
Electrochimica Acta, vol. 51, 2006, pp. 5581-5586, “Preparation and electrochemical properties of LiCoO2—LiNi0.5Mn0.5O2—Li2MnO3 solid solutions with high Mn contents”, Sun, et al. |
Office Action mailed Jun. 10, 2013 in co-pending U.S. Appl. No. 13/508,887. |
Office Action mailed Jul. 29, 2013 in co-pending U.S. Appl. No. 13/576,548. |
Office Action mailed Aug. 1, 2013 in co-pending U.S. Appl. No. 13/581,546. |
Office Action mailed Jul. 17, 2013 in co-pending U.S. Appl. No. 13/581,814. |
Office Action mailed Jun. 19, 2013 in co-pending U.S. Appl. No. 13/582,096. |
Office Action mailed Jul. 12, 2013 in co-pending U.S. Appl. No. 13/582,101. |
Office Action mailed Jul. 15, 2013 in co-pending U.S. Appl. No. 13/582,113. |
Office Action mailed Aug. 13, 2013 in co-pending U.S. Appl. No. 13/582,067. |
International Preliminary Report on Patentability mailed Oct. 10, 2013 in co-pending PCT application No. PCT/JP0212/057974. |
Office Action mailed Dec. 4, 2013 in co-pending U.S. Appl. No. 13/508,880. |
Final Rejection mailed Jan. 9, 2014 in co-pending U.S. Appl. No. 13/576,548. |
Notice of Allowance mailed Nov. 6, 2013 in U.S. Appl. No. 13/582,091 (now US Patent No. 8,623,551. |
Int. J. Electrochem. Sci., vol. 4, 2009, pp. 1770-1778, “Improved High Rate Cycling of Li-rich Li(1.10)Ni(1/3)Co(1/3)Mn(1/3)O(2) Cathode for Lithium Batteries”, Santhanam, et al. |
Notice of Allowance mailed Mar. 20, 2014 in co-pending U.S. Appl. No. 13/258,120. |
Final Rejection mailed Feb. 27, 2014 in co-pending U.S. Appl. No. 13/856,514. |
Final Rejection mailed Jan. 27, 2014 in co-pending U.S. Appl. No. 13/581,546. |
Final Rejection mailed Jan. 24, 2014 in co-pending U.S. Appl. No. 13/582,067. |
Final Rejection mailed Jan. 27, 2014 in co-pending U.S. Appl. No. 13/581,814. |
Final Rejection mailed Feb. 20, 2014 in co-pending U.S. Appl. No. 13/582,096. |
Final Rejection mailed Feb. 7, 2014 in co-pending U.S. Appl. No. 13/582,101. |
Final Rejection mailed Feb. 18, 2014 in co-pending U.S. Appl. No. 13/582,113. |
European communication issued May 9, 2014 in co-pending European patent application No. EP 11739870.1. |
European communication issued May 9, 2014 in co-pending European patent application No. EP 11750704.6. |
Chinese communication dated May 12, 2014 in co-pending Chinese patent application No. CN 201180008573.3. |
European communication issued May 22, 2014 in co-pending European patent application No. EP 11750705.3. |
European communication issued May 6, 2014 in co-pending European patent application No. EP 11845955.1. |
International Search Report mailed Dec. 25, 2012 in co-pending PCT application No. PCT/JP2012/074263. |
International Search Report mailed Dec. 25, 2012 in co-pending PCT application No. PCT/JP2012/074266. |
International Search Report mailed Aug. 27, 2013 in co-pending PCT application No. PCT/JP2013/064941. |
Final Rejection mailed Jun. 18, 2014 in co-pending U.S. Appl. No. 13/508,880. |
Office Action mailed Jul. 1, 2014 in co-pending U.S. Appl. No. 13/576,548. |
Office Action mailed Jul. 8, 2014 in co-pending U.S. Appl. No. 13/576,753. |
International Preliminary Report on Patentability mailed Sep. 26, 2013 in co-pending PCT application No. PCT/JP2011/053271. |
International Preliminary Report on Patentability mailed Oct. 10, 2013 in co-pending PCT application No. PCT/JP2011/072860. |
International Preliminary Report on Patentability mailed Aug. 1, 2013 in co-pending PCT application No. PCT/JP2011/069042. |
Japanese Communication mailed Oct. 1, 2013 in co-pending Japanese patent application No. JP 2012-503253. |
Japanese Communication mailed Oct. 1, 2013 in co-pending Japanese patent application No. JP 2012-503255. |
Japanese Communication mailed Oct. 1, 2013 in co-pending Japanese patent application No. JP 2012-503252. |
International Preliminary Report on Patentability mailed Jun. 13, 2013 in co-pending PCT application No. PCT/JP2011/066722. |
International Search Report mailed Jun. 5, 2012 in co-pending PCT application No. PCT/JP2012/057974. |
International Journal of Inorganic Materials 3 (2001), pp. 323-329, “Structural and electrochemical properties of Li—Ni—Co oxides synthesized by wet chemistry via a succinic-acid-assisted technique”, Castro-Garcia, et al. |
Office Action mailed Oct. 3, 2013 in co-pending U.S. Appl. No. 13/258,120. |
Final Rejection mailed Sep. 19, 2013 in co-pending U.S. Appl. No. 13/508,887. |
Office Action mailed Sep. 17, 2013 in co-pending U.S. Appl. No. 13/856,514. |
International Preliminary Report on Patentability mailed Jul. 31, 2014 in co-pending PCT application No. PCT/JP2012/074263. |
International Preliminary Report on Patentability mailed Jul. 31, 2014 in co-pending PCT application No. PCT/JP2012/074266. |
Journal of the Electrochemical Society, 151 (11), 2004, pp. A1899-A1904, “Synthesis, Thermal, and Electrochemical Properties of AIPO4-Coated LiNi0.8Co0.1Mn0.1O2 Cathode Materials for Li-Ion Cell”, Cho, et al. |
Journal of the Electrochemical Society, 155 (3), 2008, pp. A239-A245, “Storage Characteristics of LiNi0.8Co0.1+xMn0.1-xO2 (x=0, 0.03, and 0.06) Cathode Materials for Lithium Ion Batteries”, EOM, et al. |
Machine English translation for CN 1710735 (2005), 9 pages, European Patent Office, http://translationportal.epo.org . . . , retrieved from the internet Oct. 6, 2014. |
Final Rejection mailed Sep. 18, 2014 in co-pending U.S. Appl. No. 13/508,887. |
Office Action mailed Sep. 18, 2014 in co-pending U.S. Appl. No. 13/856,514. |
Office Action mailed Oct. 9, 2014 in co-pending U.S. Appl. No. 13/695,663. |
Office Action mailed Oct. 2, 2014 in co-pending U.S. Appl. No. 13/582,089. |
Office Action mailed Oct. 3, 2014 in co-pending U.S. Appl. No. 13/581,730. |
European communication dated Nov. 5, 2014 in co-pending European patent application No. EP 11856183.6. |
European communication dated Oct. 27, 2014 in co-pending European patent application No. EP 10839166.5. |
European communication dated Oct. 20, 2014 in co-pending European patent application No. EP 12763420.2. |
Office Action mailed Nov. 5, 2014 in co-pending U.S. Appl. No. 13/582,087. |
Office Action mailed Nov. 14, 2014 in co-pending U.S. Appl. No. 13/582,096. |
Number | Date | Country | |
---|---|---|---|
20120244434 A1 | Sep 2012 | US |