Patent Application
20130273427
The present invention relates to a secondary battery comprising an electrode assembly including a cathode, an anode and a separator interposed between the cathode and the anode, the secondary battery comprising a moisture scavenger.
Technological development and increased demand for mobile equipment have led to a sharp rise in the demand for secondary batteries as energy sources. Among these secondary batteries, lithium secondary batteries having high energy density and high operating voltage, long cycle lifespan and low self-discharge are commercially available and widely used.
In addition, increased interest in environmental issues has brought about a great deal of research associated with electric vehicles (EVs), hybrid electric vehicles (HEVs) and the like as alternatives to vehicles using fossil fuels such as gasoline vehicles and diesel vehicles which are major causes of air pollution. Nickel-metal hydride (Ni-MH) secondary batteries are generally used as power sources of electric vehicles (EVs) and hybrid electric vehicles (HEVs). However, a great deal of study associated with use of lithium secondary batteries with high energy density, discharge voltage and power stability is currently underway and some of such lithium secondary batteries are commercially available.
A lithium secondary battery has a structure in which a non-aqueous electrolyte comprising a lithium salt is impregnated into an electrode assembly comprising a cathode and an anode, each comprising an active material coated on a current collector, and a porous separator interposed therebetween.
In general, when moisture is present in a lithium secondary battery, the moisture decomposes into hydrogen gas during charge and discharge. As a result, a swelling phenomenon occurs. Furthermore, in serious cases, explosion may occur.
In addition, the presence of moisture in the battery may have great effects on battery safety. For this reason, removal of moisture is required in the process of producing the battery.
However, some porous substances may have a property of absorbing moisture in air, i.e., deliquescence.
Accordingly, there is an increasing need for methods of removing small amounts of moisture present in the battery.
Therefore, the present invention has been made to solve the above and other technical problems that have yet to be resolved.
As a result of a variety of extensive and intensive studies and experiments to solve the problems as described above, the present inventors discovered that a secondary battery comprising a moisture scavenger present in an electrode or an electrolyte can provide desired effects, as described later. The present invention has been completed based on this discovery.
In accordance with one aspect of the present invention, provided is a secondary battery comprising an electrode assembly including a cathode, an anode and a separator interposed between the cathode and the anode, the secondary battery comprising a moisture scavenger.
As described above, when the secondary battery, in particular, the lithium secondary battery contains moisture, phenomena associated with deterioration in safety such as explosion or swelling may occur.
Basically, moisture is removed by heating. However, it is difficult to completely remove moisture adsorbed on an active material or the like. Accordingly, the adsorbed moisture decomposes into hydrogen gas or causes problems associated with safety due to other electrochemical reactions during charge and discharge.
The secondary battery according to the present invention comprises a moisture scavenger, as described above, thereby solving these problems.
In one embodiment, the moisture scavenger may be present in the cathode or the anode. The electrode active material, conductive material or the like may function to absorb moisture, and moisture can thus be removed by adding a moisture scavenger together with the active material or conductive material to an electrode mix.
In another embodiment, the moisture scavenger may be contained in the electrolyte. The electrolyte sufficiently permeates into the cathode and the anode and electrochemically reacts with the electrode. Accordingly, moisture, which may be present in the electrode, can be removed by incorporating the moisture scavenger into the electrolyte.
Any moisture scavenger may be used without particular limitation so long as it is not involved in electrochemical reactions of the secondary battery and is capable of removing moisture. Non-limiting examples of the moisture scavenger include isocyanate compounds or silane compounds. An example of the isocyanate compounds includes ethyl isocyanate and an example of the silane compounds includes silazane.
The moisture scavenger may act as a resistant layer alone, and a reaction by-product of the moisture scavenger and moisture may act as a resistant layer. When excess moisture scavenger is used, electrochemical performance of the secondary battery may disadvantageously be deteriorated.
In one embodiment, when the moisture scavenger is contained in the cathode or the anode, a content thereof is preferably 0.1% to 10%, more preferably 0.1% to 3%, based on the total weight of the cathode mix or the anode mix.
In addition, when the moisture scavenger is contained in the electrolyte, a content thereof is preferably 0.1% to 10%, more preferably 0.1% to 3%, based on the total weight of the electrolyte.
The cathode for secondary batteries is fabricated by applying a mixture containing a cathode active material, a conductive material and a binder to a cathode current collector, followed by drying and pressing, and the mixture may optionally comprise a filler.
The cathode current collector is generally manufactured to have a thickness of 3 to 500 μm. Any cathode current collector may be used without particular limitation so long as it has suitable conductivity without causing adverse chemical changes in the fabricated battery. Examples of the cathode current collector include stainless steel, aluminum, nickel, titanium, sintered carbon, and aluminum or stainless steel surface-treated with carbon, nickel, titanium or silver. Similar to the anode current collector, the cathode current collectors include fine irregularities on the surfaces thereof so as to enhance adhesion to the cathode active material. In addition, the cathode current collector may be used in various forms including films, sheets, foils, nets, porous structures, foams and non-woven fabrics.
Examples of the cathode current collector include, but are not limited to, layered compounds such as lithium cobalt oxide (LiCoO2) and lithium nickel oxide (LiNiO2) or these compounds substituted by one or more transition metals; lithium nickel manganese cobalt composite oxides with a layered structure represented by LiNixMnyCozO2; lithium manganese oxides represented by Li1+xMn2−xO4 (in which 0≦x≦0.33), LiMnO3, LiMn2O3 and LiMnO2; lithium copper oxide (Li2CuO2); vanadium oxides such as LiV3O8, LiFe3O4, V2O5 and Cu2V2O7; Ni-site type lithiated nickel oxides represented by LiNi1−xMxO2 (M=Co, Mn, Al, Cu, Fe, Mg, B or Ga, and 0.01≦x≦0.3); lithium manganese composite oxides represented by LiMn2−xMxO2 (M=Co, Ni, Fe, Cr, Zn or Ta, and 0.01≦x≦0.1), or Li2Mn3MO8 (M=Fe, Co, Ni, Cu or Zn); LiMn2O4 wherein Li is partially substituted by alkaline earth metal ions; disulfide compounds; and Fe2(MoO4)3.
In one embodiment, the cathode active material may comprise a lithium manganese composite oxide with a spinel structure, represented by the following Formula 1:
LixMyMn2−yO4−zAz (1)
wherein 0.9≦x≦1.2, 0<y<2, and 0≦z<0.2;
M is at least one element selected from the group consisting of Al, Mg, Ni, Co, Fe, Cr, V, Ti, Cu, B, Ca, Zn, Zr, Nb, Mo, Sr, Sb, W, Ti and Bi; and
A is at least one negative univalent or bivalent anion.
Specifically, the lithium manganese composite oxide may be lithium nickel manganese oxide represented by the following Formula 2:
LixNiyMn2−yO4 (2)
wherein 0.9≦x≦1.2, and 0.45≦y≦0.5.
More specifically, the lithium nickel manganese oxide may be LiNi0.5Mn1.5O4 or LiNi0.4Mn1.6O4.
The conductive material is commonly added in an amount of 1 to 50% by weight, based on the total weight of the mixture comprising the cathode active material. Any conductive material may be used without particular limitation so long as it has suitable conductivity without causing adverse chemical changes in the battery. Examples of suitable conductive materials include graphite such as natural graphite or artificial graphite; carbon black such as carbon black, acetylene black, Ketjen black, channel black, furnace black, lamp black and thermal black; conductive fibers such as carbon fibers and metallic fibers; metallic powders such as carbon fluoride powders, aluminum powders and nickel powders; conductive whiskers such as zinc oxide and potassium titanate; conductive metal oxides such as titanium oxide; and conductive materials such as polyphenylene derivatives.
The binder is a component which enhances binding of an electrode active material to the conductive material and the current collector. The binder is commonly added in an amount of 1 to 50% by weight, based on the total weight of the mixture comprising the cathode active material. Examples of the binder include polyvinylidene fluoride, polyvinyl alcohol, carboxymethylcellulose (CMC), starch, hydroxypropylcellulose, regenerated cellulose, polyvinyl pyrrolidone, tetrafluoroethylene, polyethylene, polypropylene, ethylene propylene diene terpolymer (EPDM), sulfonated EPDM, styrene butadiene rubbers, fluororubbers and various copolymers.
The filler is a component optionally used to inhibit expansion of the electrode. Any filler may be used without particular limitation so long as it does not cause adverse chemical changes in the manufactured battery and is a fibrous material. Examples of the filler include olefin polymers such as polyethylene and polypropylene; and fibrous materials such as glass fibers and carbon fibers.
Meanwhile, the anode is prepared by applying an anode active material to an anode current collector, followed by drying and pressing. The anode active material may comprise a conductive material, a binder, a filler and the like, as necessary.
The anode current collector is generally fabricated to have a thickness of 3 to 500 μm. There is no particular limit as to the anode current collector, so long as it has suitable conductivity without causing adverse chemical changes in the fabricated battery. Examples of the anode current collector include copper, stainless steel, aluminum, nickel, titanium, sintered carbon, and copper or stainless steel surface-treated with carbon, nickel, titanium or silver, and aluminum-cadmium alloys. Similar to the cathode current collector, if necessary, the anode current collector may be processed to form fine irregularities on the surface thereof so as to enhance adhesion to the anode active materials. In addition, the current collectors may be used in various forms including films, sheets, foils, nets, porous structures, foams and non-woven fabrics.
Examples of the anode active materials that can be used in the present invention include carbon such as non-graphitized carbon and graphitized carbon; metal composite oxides such as LixFe2O3(0≦x≦1), LixWO2(0≦x≦1) and SnxMe1−xMe′yOx(Me:Mn, Fe, Pb, Ge; Me′: Al, B, P, Si, Group I, II and III elements of the Periodic Table, halogen atoms; 0≦x≦1; 1≦y≦3; and 1≦z≦8); a lithium metal; lithium alloys; silicon-based alloys; tin-based alloys; metal oxides such as SnO, SnO2, PbO, PbO2, Pb2O3, Pb3O4, Sb2O3, Sb2O4, Sb2O5, GeO, GeO2, Bi2O3, Bi2O4, and Bi2O5; conductive polymers such as polyacetylene; and Li-Co-Ni based materials.
In one embodiment, corresponding to the lithium nickel manganese oxide as the high-voltage cathode active material, the anode active material may comprise lithium metal oxide represented by Formula 3:
LiaM′bO4−cAc (3)
wherein M′ is at least one element selected from the group consisting of Ti, Sn, Cu, Pb, Sb, Zn, Fe, In, Al and Zr;
a and b are determined depending on an oxidation number of M′ within ranges of 0.1≦a≦4 and 0.2≦b≦4;
c is determined depending on an oxidation number within a range of 0≦c≦0.2;5 and
A is at least one negative univalent or bivalent anion.
In one embodiment, the lithium metal oxide of Formula 3 may be lithium titanium oxide (LTO) represented by Formula 4 and specific examples thereof include Li0.8Ti22O4, Li2.67Ti1.33O4, LiTi2O4, Li1.33Ti1.67O4, Li1.14Ti1.71O4 and the like. There is no limitation as to the composition and type of the lithium metal oxide so long as it is capable of intercalating and deintercalating lithium ions. More specifically, the lithium metal oxide of Formula 3 may be Li1.33Ti1.67O4 or LiTi2O4 having a spinel structure which does not undergo change of crystal structural during charge and discharge, and is highly reversible.
LiaTibO4 (4)
wherein 0.5≦a≦3, and 1≦b≦2.5.
The separator is interposed between the cathode and the anode. As the separator, an insulating thin film having high ion permeability and mechanical strength is used. The separator typically has a pore diameter of 0.01 to 10 μm and a thickness of 5 to 300 μm As the separator, sheets or non-woven fabrics made of an olefin polymer such as polypropylene and/or glass fibers or polyethylene, which have chemical resistance and hydrophobicity, are used. When a solid electrolyte such as a polymer is employed as the electrolyte, the solid electrolyte may also serve as both the separator and the electrolyte.
The present invention provides a lithium secondary battery having a structure in which a lithium salt-containing electrolyte is impregnated in an electrode assembly having a structure in which a separator is interposed between the cathode and the anode.
The lithium salt-containing non-aqueous electrolyte is composed of a non-aqueous electrolyte and lithium. Examples of the electrolyte include, but are not limited to non-aqueous organic solvents, organic solid electrolytes, and inorganic solid electrolytes.
Examples of the non-protic organic solvents include N-methyl-2-pyrollidinone, propylene carbonate, ethylene carbonate, butylene carbonate, dimethyl carbonate, diethyl carbonate, ethylmethyl carbonate, gamma-butyrolactone, 1,2-dimethoxy ethane, 1,2-diethoxy ethane, tetrahydrofuran, 2-methyl tetrahydrofuran, dimethylsulfoxide, 1,3-dioxolane, formamide, dimethylformamide, dioxolane, acetonitrile, nitromethane, methyl formate, methyl acetate, phosphoric acid triester, trimethoxy methane, dioxolane derivatives, sulfolane, methyl sulfolane, 1,3-dimethyl-2-imidazolidinone, propylene carbonate derivatives, tetrahydrofuran derivatives, ether, methyl propionate and ethyl propionate.
Examples of the organic solid electrolytes include polyethylene derivatives, polyethylene oxide derivatives, polypropylene oxide derivatives, phosphoric acid ester polymers, poly agitation lysine, polyester sulfide, polyvinyl alcohol, polyvinylidene fluoride, and polymers containing ionic dissociation groups.
Examples of the inorganic solid electrolytes include nitrides, halides and sulphates of lithium such as Li3N, LiI, Li5NI2, Li3N-LiI-LiOH, LiSiO4, LiSiO4-LiI-LiOH, Li2SiS3, Li4SiO4, Li4SiO4-LiI-LiOH and Li3PO4-Li2S—SiS2.
The lithium salt is a material that is readily soluble in the above-mentioned non-aqueous electrolyte and may include, for example, LiCl, LiBr, LiI, LiClO4, LiBF4, LiB10Cl10, LiPF6, LiCF3SO3, LiCF3CO2, LiAsF6, LiSbF6, LiAlCl4, CH3SO3Li, CF3SO3Li, LiSCN, LiC(CF3SO2)3, (CF3SO2)2NLi, chloroborane lithium, lower aliphatic carboxylic acid lithium, lithium tetraphenyl borate and imide.
Additionally, in order to improve charge/discharge characteristics and flame retardancy, for example, pyridine, triethylphosphite, triethanolamine, cyclic ether, ethylenediamine, n-glyme, hexaphosphoric triamide, nitrobenzene derivatives, sulfur, quinone imine dyes, N-substituted oxazolidinone, N,N-substituted imidazolidine, ethylene glycol dialkyl ether, ammonium salts, pyrrole, 2-methoxy ethanol, aluminum trichloride or the like may be added to the non-aqueous electrolyte. If necessary, in order to impart incombustibility, the non-aqueous electrolyte may further include halogen-containing solvents such as carbon tetrachloride and ethylene trifluoride. Further, in order to improve high-temperature storage characteristics, the non-aqueous electrolyte may additionally include carbon dioxide gas and may further contain fluoro-ethylene carbonate (FEC), propene sultone (PRS) and the like.
In a preferred embodiment, the lithium salt-containing non-aqueous electrolyte can be prepared by adding a lithium salt such as LiPF6, LiClO4, LiBF4, LiN(SO2CF3)2, to a mixed solvent of a cyclic carbonate such as EC or PC as a highly dielectric solvent and linear carbonate such as DEC, DMC or EMC as a low-viscosity solvent.
The present invention provides a battery module comprising the secondary battery as a unit battery and a battery pack comprising the battery module.
The battery pack may be used as a power source of a middle or large sized device requiring high-temperature stability, long cycle properties and high rate properties.
Preferably, examples of middle and large sized devices include, but are not limited to, power tools powered by battery-driven motors; electric vehicles including electric vehicles (EVs), hybrid electric vehicles (HEVs) and plug-in hybrid electric vehicles (PHEVs); electric two-wheeled vehicles including electric bikes (E-bikes) and electric scooters (E-scooters); electric golf carts; power storage systems and the like.
As apparent from the fore-going, the secondary battery according to the present invention comprises a moisture scavenger, thereby advantageously removing moisture present in the battery and improving battery safety.
The above and other objects, features and other advantages of the present invention will be more clearly understood from the following detailed description taken in conjunction with the accompanying drawings, in which:
Now, the present invention will be described in more detail with reference to the following examples. These examples are provided only to illustrate the present invention and should not be construed as limiting the scope and spirit of the present invention.
90% by weight of LiNi0.5Mn1.504as a cathode active material, 5% by weight of Super-P (conductive material), and 5% by weight of PVdF (binder) were added to N-methyl-2-pyrrolidone (NMP) as a solvent to prepare a slurry, and the slurry was coated on an aluminum foil with a thickness of 20 μm, followed by drying and pressing, to produce a cathode.
Titanium isopropoxide was mixed with lithium hydroxide, followed by baking at a high temperature to prepare Li4/3Ti5/3O4, and 90% by weight of the prepared anode active material, 5% by weight of Super-P (conductive material) and 5% by weight of PVdF (binder) were added to NMP, to prepare an anode mixture slurry. The slurry was coated on an Al-foil with a thickness of 20 μm, followed by drying and pressing, to produce an anode.
The cathode and the anode were laminated using Celgard™ as a separator to produce a battery assembly, and a lithium non-aqueous electrolyte containing ethyl carbonate, dimethyl carbonate and ethyl methyl carbonate at a volume ratio of 1:1:1, and further containing 3 wt % of ethyl isocyanate, based on the total weight of the electrolyte as a moisture scavenger and 1M LiPF6 as a lithium salt was added to the battery assembly to produce a lithium secondary battery.
A lithium secondary battery was produced in the same manner as in Example 1, except that ethyl isocyanate was added as the moisture scavenger in an amount of 10 wt %, based on the total weight of the electrolyte.
A lithium secondary battery was produced in the same manner as in Example 1, except that the moisture scavenger was not added.
Lithium secondary batteries produced in Examples 1 to 3 and Comparative Example 1 were stored at 55° C. for four weeks and gas generation was analyzed. Results are shown in
As a result, as can be seen from
Although the preferred embodiments of the present invention have been disclosed for illustrative purposes, those skilled in the art will appreciate that various modifications, additions and substitutions are possible, without departing from the scope and spirit of the invention as disclosed in the accompanying claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2012-0038535 | Apr 2012 | KR | national |
