Patent Application
20080118846
This application claims the benefit of Korean Application No. 2006-113991, filed Nov. 17, 2006, in the Korean Intellectual Property Office, the disclosure of which is incorporated herein, by reference.
1. Field of the Invention
Aspects of the present invention relate to lithium rechargeable batteries.
2. Description of the Related Art
Lithium rechargeable batteries have recently drawn attention for use as power sources for portable electronic devices. Lithium rechargeable batteries use an organic electrolyte solution, have a high energy density, and have a discharge voltage that is twice as high as a conventional alkaline battery. Rechargeable lithium batteries contain a positive active material, for example lithium-transition element composite oxides capable of intercalating lithium, such as, LiCoO2, LiMn2O4, LiNiO2, LiNi1−xCoxO2 (0<x<1), LiMnO2, and the like. Rechargeable lithium batteries contain a negative active material, for example various carbon-based materials, such as, artificial graphite, natural graphite, and hard carbon, which can all intercalate and deintercalate lithium ions. Recently, batteries having high-capacity and improved cycle-life characteristics have been researched, but as yet, they have not approached a satisfactory performance level.
Various embodiments of the present invention provide a rechargeable lithium battery that has a high capacity and improved cycle-life characteristics.
According to various embodiments of the present invention, provided is a rechargeable lithium battery including a positive electrode including a positive active material, a negative electrode including a negative active material, and a non-aqueous electrolyte. The positive electrode has an active-mass density of about 3.7 to 4.1 g/cc. The non-aqueous electrolyte includes a nitrile-based compound additive, a non-aqueous organic solvent, and a lithium salt.
Additional aspects and/or advantages of the invention will be set forth in part in the description which follows and, in part, will be obvious from the description, or may be learned by practice of the invention.
These and/or other aspects and advantages of the invention will become apparent and more readily appreciated from the following description of the embodiments, taken in conjunction with the accompanying drawings of which:
Reference will now be made in detail to the present embodiments of the present invention, examples of which are illustrated in the accompanying drawings, wherein like reference numerals refer to the like elements throughout. The embodiments are described below in order to explain the aspects of present invention, by referring to the figure.
Aspects of the present invention relate to a rechargeable lithium battery that includes a positive electrode with a high active-mass density. The rechargeable lithium battery has improved cycle-life characteristics and reliability at high temperatures. The rechargeable lithium battery, according to an exemplary embodiment of the present invention, includes a positive electrode including a positive active material, a negative electrode including a negative active material, and a non-aqueous electrolyte.
The positive electrode has an active-mass density of about 3.7 to 4.1 g/cc. The non-aqueous electrolyte includes a nitrile-based compound additive, a non-aqueous organic solvent, and a lithium salt. Generally, a positive electrode having a high active-mass density is used to provide a high-capacity battery. However, if the active-mass density of a positive electrode is increased, room temperature cycle-life characteristics may be degraded. For this reason, the active-mass density of a positive electrode, used in the related art rechargeable lithium batteries, is about 3.6 g/cc. On the contrary, according to aspects of the present invention, the nitrile-based compound additive can provide a high-capacity battery, as well as improved cycle-life characteristics, at room temperature, even though the positive electrode has a relatively higher active-mass density of about 3.7 to 4.1 g/cc.
Examples of the nitrile-based compound include, at least one selected from the group consisting of succinonitrile, glutaronitrile, adiponitrile, pimelonitrile, suberonitrile, and combinations thereof. According to various embodiments, adiponitrile may be appropriate.
The nitrile-based compound additive ranges from about 0.01 to 10 wt %, based on the total weight of the non-aqueous electrolyte. The nitrile-based compound additive may be used in an amount of about 0.5 to 5 wt %. When the amount of the nitrile-based compound additive is less than about 0.01 wt %, enhanced battery performance may not be realized. When the amount of the nitrile-based compound additive is more than 10 wt %, electrolyte ion conductivity may be reduced, and side-reactions may be increased, resulting in a small initial capacity.
The non-aqueous electrolyte can include a non-aqueous organic solvent and a lithium salt, as well as the nitrile-based compound additive. The non-aqueous organic solvent acts as a medium for transmitting ions that take part in the electrochemical reactions of the battery.
The non-aqueous organic solvent may include a solvent that is carbonate-based, ester-based, ether-based, ketone-based, alcohol-based, or aprotic. Examples of the carbonate-based solvent may include dimethyl carbonate (DMC), diethyl carbonate (DEC), dipropyl carbonate (DPC), methylpropyl carbonate (MPC), ethylpropyl carbonate (EPC), methylethyl carbonate (MEC), ethylene carbonate (EC), propylene carbonate (PC), butylene carbonate (BC), and the like. Examples of the ester-based solvent may include n-methyl acetate, n-ethyl acetate, n-propyl acetate, dimethylacetate, methylpropinonate, ethylpropinonate, γ-butyrolactone, decanolide, valerolactone, mevalonolactone, caprolactone, and the like. Examples of the ether-based solvent include dibutyl ether, tetraglyme, diglyme, dimethoxyethane, 2-methyltetrahydrofuran, tetrahydrofuran, and the like. Examples of the ketone-based solvent include cyclohexanone, and the like. Examples of the alcohol-based solvent include ethyl alcohol, isopropyl alcohol, and the like. Examples of the aprotic solvent include: nitriles, such as, R—CN (where R is a C2 to C20 linear, branched, or cyclic hydrocarbon, a double bond, an aromatic ring, or an ether bond); amides, such as dimethylform amide; dioxolanes, such as, 1,3-dioxolane, sulfolanes, and the like.
The non-aqueous organic solvent may be used singularly or in a mixture. When the organic solvent is used in a mixture, a mixture ratio may be controlled in accordance with a desired battery performance.
The carbonate-based solvent may include a mixture of a cyclic carbonate and a linear carbonate. The cyclic carbonate and the linear carbonate can be mixed together in a volume ratio of about 1:1 to 1:9. When the mixture is used as an electrolyte, the electrolyte performance may be enhanced.
The electrolyte may further include mixtures of carbonate-based solvents and aromatic hydrocarbon-based solvents. The carbonate-based solvents and the aromatic hydrocarbon-based solvents can be mixed together in the volume ratio of about 1:1 to 30:1.
The aromatic hydrocarbon-based organic solvent may be represented by Formula 1.
In Formula 1, R1 to R6 are independently selected from the group consisting of hydrogen, a halogen, a C1 to C10 alkyl, a haloalkyl, and combinations thereof.
The aromatic hydrocarbon-based organic solvent may include, but is not limited to, at least one selected from the group consisting of benzene, fluorobenzene, 1,2-difluorobenzene, 1,3-difluorobenzene, 1,4-difluorobenzene, 1,2,3-trifluorobenzene, 1,2,4-trifluorobenzene, chlorobenzene, 1,2-dichlorobenzene, 1,3-dichlorobenzene, 1,4-dichlorobenzene, 1,2,3-trichlorobenzene, 1,2,4-trichlorobenzene, iodobenzene, 1,2-diiodobenzene, 1,3-diiodobenzene, 1,4-diiodobenzene, 1,2,3-triiodobenzene, 1,2,4-triiodobenzene, toluene, fluorotoluene, 1,2-difluorotoluene, 1,3-difluorotoluene, 1,4-difluorotoluene, 1,2,3-trifluorotoluene, 1,2,4-trifluorotoluene, chlorotoluene, 1,2-dichlorotoluene, 1,3-dichlorotoluene, 1,4-dichlorotoluene, 1,2,3-trichlorotoluene, 1,2,4-trichlorotoluene, iodotoluene, 1,2-diiodotoluene, 1,3-diiodotoluene, 1,4-diiodotoluene, 1,2,3-triiodotoluene, 1,2,4-triiodotoluene, xylene, and combinations thereof.
The non-aqueous electrolyte may further include an overcharge inhibition additive, such as, ethylene carbonate, pyrocarbonate, and the like.
The lithium salt can be dissolved in the non-aqueous organic solvent, to supply lithium ions in the rechargeable lithium battery. The lithium salt may facilitate a basic operation in the rechargeable lithium battery, and can facilitate the transmission of lithium ions between positive and negative electrodes. Non-limiting examples of the lithium salt include at least one supporting electrolyte salt selected from the group consisting of LiPF6, LiBF4, LiSbF6, LiAsF6, LiCF3SO3, LiN(SO2C2F5)2, LiN(CF3SO2)2, LiC4F9SO3, LiClO4, LiAlO4, LiAlCl4, LiN(CxF2x+1SO2)(CyF2y+1SO2) (where x and y are natural numbers), LiCl, LiI, lithium bisoxalate borate, and combinations thereof. The lithium salt may be used at about a 0.1 to 2.0M concentration. When the lithium salt concentration is less than about 0.1M, the performance of the electrolyte may be compromised, due to a reduction in the conductivity of the electrolyte. When the lithium salt concentration is more than about 2.0M, lithium ion mobility may be reduced, due to an increase in the viscosity of the electrolyte.
The negative active material in the negative electrode may include at least one selected from the group consisting of a carbonaceous material, a lithium metal, a lithium alloy, a material capable of forming a lithium-containing compound, and combinations thereof. According to various embodiments, the carbonaceous material may be appropriate for the negative active material.
The carbonaceous material may be amorphous carbon or crystalline carbon. The amorphous carbon may be a soft carbon (carbon obtained by sintering at a low temperature), a hard carbon (carbon obtained by sintering at a high temperature), mesophase pitch carbide, fired coke, and the like. The crystalline carbon may be shaped or unshaped. The shaped crystalline carbon may be shaped as a sheet, a flake, a sphere, or a fiber. The crystalline carbon may be natural graphite or artificial graphite.
The carbonaceous material has an Lc (crystallite size) of at least about 10 nm, as found through X-ray diffraction. According to various embodiments, the carbonaceous material has an Lc (crystallite size) of from about 10 to 1500 nm, as found through X-ray diffraction. The carbonaceous material exhibits an exothermic peak at about 700° C. or more. The exothermic peak differentiates a crystalline and an amorphous carbon. The exothermic peak at about 700° C. or more, indicates a crystalline carbon, and therefore, the maximum value of exothermic temperature need not be limited.
The crystalline carbon may be a carbon prepared by carbonizing mesophase spherical particles, then graphitizing the produced carbonized material. Further, the carbonaceous material may be a graphite fiber prepared by carbonizing a mesophase pitch fiber and then graphitizing the produced carbonized material.
The lithium alloy includes lithium and a metal selected from the group consisting of Na, K, Rb, Cs, Fr, Be, Mg, Ca, Sr, Ba, Ra, Al, and Sn.
The material capable of reversibly forming a lithium-containing compound, by reaction with lithium ions, can include tin oxide (SnO2), titanium nitrate, silicon (Si), and the like, but is not limited thereto.
The negative electrode may be fabricated as follows. A negative active material composition is prepared by mixing a negative active material, a binder, and optionally a conductive agent. Then the composition is applied on a negative current collector. The composition and current collector are then dried and compressed. The negative electrode manufacturing methods are well known, and thus, are not described in detail, herein.
Examples of the binder include polyvinylalcohol, carboxylmethyl cellulose, hydroxypropyl cellulose, diacetyl cellulose, polyvinylchloride, polyvinylpyrrolidone, polytetrafluoroethylene, polyvinylidene fluoride, polyethylene, polypropylene, and combinations thereof, but are not limited thereto.
Any electrically conductive material may be used as a conductive agent, so long as it has suitable electrical conductivity and chemical stability. Examples of the conductive agent include: natural graphite; artificial graphite; carbon black; acetylene black; ketjen black; a carbon fiber; a metal powder; a metal fiber including copper, nickel, aluminum, silver, and the like; and a polyphenylene derivative.
The solvent can include N-methylpyrrolidone, but is not limited thereto.
The current collector may be selected from the group consisting of a copper foil, a nickel foil, a stainless steel foil, a titanium foil, a nickel foam, a copper foam, a polymer substrate coated with a conductive metal, and combinations thereof.
The positive electrode includes a positive active material, such as a lithiated intercalation compound capable of intercalating and deintercalating lithium. Examples of the lithiated intercalation compound include a composite oxide including lithium and a metal selected from the group consisting of cobalt, manganese, nickel, and combinations thereof. More specifically, the lithiated intercalation compound can be exemplified by compounds of Formulas 2 to 25.
LiaA1−bBbD2, Formula 2
wherein, 0.95≦a≦1.1 and 0≦b≦0.5.
LiaE1−bBbO2−cFc, Formula 3
wherein, 0.95≦a≦1.1, 0≦b≦0.5, and 0≦c≦0.05.
LiE2−bBbO4−cFc, Formula 4
wherein, 0≦b≦0.5, and 0≦c≦0.05.
LiaNi1−b−cCObBcDα, Formula 5
wherein, 0.95≦a≦1.1, 0≦b≦0.5, 0≦c≦0.05, and 0<α<2.
LiaNi1−b−cCobBcO2−αFα, Formula 6
wherein, 0.95≦a≦1.1, 0≦b≦0.5, 0≦c≦0.05, and 0<α<2.
LiaNi1−b−cCobBcO2−αF2, Formula 7
wherein, 0.95≦a≦1.1, 0≦b≦0.5, 0≦c≦0.05, and 0<α<2.
LiaNi1−b−cMnbBcDα, Formula 8
wherein, 0.95≦a≦1.1, 0≦b≦0.5, 0≦c≦0.05, and 0<α<2.
LiaNi1−b−cMnbBcO2−αFα, Formula 9
wherein, 0.95≦a≦1.1, 0≦b≦0.5, 0≦c≦0.05, and 0<α<2.
LiaNi1−b−cMnbBcO2−αF2, Formula 10
wherein, 0.95≦a≦1.1, 0≦b≦0.5, 0≦c≦0.05, and 0<α<2.
LiaNibEcGdO2, Formula 11
wherein, 0.90≦a≦1.1, 0≦b≦0.9, 0≦c≦0.5, and 0.001≦d≦0.1.
LiaNibCocMndGeO2, Formula 12
wherein, 0.90≦a≦1.1, 0≦b≦0.9, 0≦c≦0.5, 0≦d≦0.5, and 0.001≦e≦0.1.
LiaNiGbO2, Formula 13
wherein, 0.90≦a≦1.1 and 0.001≦b≦0.1.
LiaCoGbO2, Formula 14
wherein, 0.90≦a≦1.1 and 0.001≦b≦0.1.
LiaMnGbO2, Formula 15
wherein, 0.90≦a≦1.1 and 0.001≦b≦0.1.
LiaMn2GbO4, Formula 16
wherein, 0.90≦a≦1.1 and 0.001≦b≦0.1.
QO2 Formula 17
QS2 Formula 18
LiQS2 Formula 19
V2O5 Formula 20
LiV2O5 Formula 21
LiIO2 Formula 22
LiNiVO4 Formula 23
Li3−fJ2(PO4)3 (0≦f≦3) Formula 24
Li3−fFe2(PO4)3 (0≦f≦2) Formula 25
In Formulas 2 to 25: A is selected from the group consisting of Ni, Co, Mn, and combinations thereof; B is selected from the group consisting of Al, Ni, Co, Mn, Cr, Fe, Mg, Sr, V, a rare earth element, and combinations thereof; D is selected from the group consisting of O, F, S, P, and combinations thereof; E is selected from the group consisting of Co, Mn, and combinations thereof; F is selected from the group consisting of F, S, P, and combinations thereof; G is a transition element or a lanthanide element selected from the group consisting of Al, Cr, Mn, Fe, Mg, La, Ce, Sr, V, and combinations thereof; Q is an element selected from the group consisting of Ti, Mo, Mn, and combinations thereof; I is an element selected from the group consisting of Cr, V, Fe, Sc, Y, and combinations thereof; and J is an element selected from the group consisting of V, Cr, Mn, Co, Ni, Cu, and combinations thereof.
The lithiated intercalation compound may include a coating layer on the surface thereof, or may be mixed with another lithiated intercalation compound having a coating layer. The coating layer includes at least one coating element-containing compound selected from the group consisting of a coating element-containing hydroxide, a coating element-containing oxyhydroxide, a coating element-containing oxycarbonate, a coating element-containing hydroxycarbonate, and combinations thereof. The coating element-containing compound may be amorphous or crystalline. Examples of the coating element include at least one selected from the group consisting of Mg, Al, Co, K, Na, Ca, Si, Ti, V, Sn, Ge, Ga, B, As, Zr, and combinations thereof. The coating layer may be formed by any coating method that does not have an unfavorable effect on properties of the positive active material. Examples of suitable coating methods include spray coating, and dipping. Since such a coating method is well known in this art, a detailed description is not provided.
The positive electrode can be fabricated as follows. A positive active material composition is prepared by mixing a positive active material, a binder, and a conductive agent. The composition is then applied on a positive current collector, such as aluminum foil, then dried and compressed. The positive electrode manufacturing method is well known, and thus it is not described in detail herein. The active-mass density of the positive electrode may be controlled during the fabrication of the positive electrode by altering a compressing pressure, compressing time, and a compressing temperature. The compressing pressure, compressing time, and compressing temperature are not specifically limited. However, they may be controlled such that the fabricated positive electrode may have an active-mass density of about 3.7 to 4.1 g/cc.
Any electrically conductive material maybe used as a conductive agent, so long as it has suitable electrical conductivity and chemical stability. Examples of the conductive agent include: natural graphite; artificial graphite; carbon black; acetylene black; ketjen black; a carbon fiber; a metal powder; a metal fiber including copper, nickel, aluminum, silver, or the like; and a polyphenylene derivative.
Examples of the binder include polyvinyl alcohol, carboxylmethyl cellulose, hydroxypropylene cellulose, diacetylene cellulose, polyvinylchloride, polyvinylpyrrolidone, polytetrafluoroethylene, polyvinylidene fluoride, polyethylene, polypropylene, and combinations thereof, but are not limited thereto.
The solvent may be N-methylpyrrolidone, but is not limited thereto.
The rechargeable lithium battery generally includes a positive electrode, a negative electrode, and an electrolyte. The battery may further include a separator. The separator may include any material used in conventional lithium secondary batteries. Non-limiting examples of suitable separator materials include polyethylene, polypropylene, polyvinylidene fluoride, and multi-layers thereof, such as, a polyethylene/polypropylene double-layered separator, a polyethylene/polypropylene/polyethylene triple-layered separator, or a polypropylene/polyethylene/polypropylene triple-layered separator.
Rechargeable lithium batteries may be classified as lithium ion batteries, lithium ion polymer batteries, and lithium polymer batteries, according to the presence of a separator and the kind of electrolyte used in the battery. The rechargeable lithium batteries may have a variety of shapes and sizes, including cylindrical, prismatic, or coin-type, and may be a thin film battery or may be rather bulky in size. Structures and fabricating methods for lithium ion batteries, are well known in the art.
The following Examples 1-9 illustrate aspects of the present invention in more detail. These examples, however, should not in any sense be interpreted as limiting the scope of the present invention.
1.3M LiPF6 was dissolved in a mixed solvent of ethylene carbonate (EC), dimethyl carbonate (DMC), and ethylmethyl carbonate (EMC), in a volume ratio of 30:30:40, and then adiponitrile was added thereto, to prepare an electrolyte solution. The adiponitrile (AN) was added in an amount of 1 wt % of the total weight of the electrolyte solution.
An LiCoO2 positive active material, a polyvinylidene fluoride binder, and a Super-P conductive material were mixed in a weight ratio of 94:3:3 in an N-methylpyrrolidone solvent, to prepare a positive active material slurry. The positive active material slurry was coated on an aluminum current collector and then dried and compressed, to fabricate positive electrodes.
The compressing was performed by controlling the compressing pressure, time, and temperature, to fabricate positive electrodes having active-mass densities as shown in Table 1.
A graphite negative active material and a polyvinylidene fluoride binder were mixed in a weight ratio of 94:6 in an N-methylpyrrolidone solvent, to prepare a negative active material slurry. The slurry was coated on a copper current collector, dried, and compressed, to fabricate a negative electrode. When X-ray diffraction was measured using CuKα, the graphite negative active material had an Lc of about 100 nm. The graphite negative active material showed an exothermic peak at 700° C. or more.
Rechargeable lithium battery cells were fabricated using the above positive electrodes, negative electrode, and electrolyte solution, according to a conventional method.
1.3M LiPF6 was dissolved in a mixed solvent of ethylene carbonate (EC), dimethyl carbonate (DMC), and ethylmethyl carbonate (EMC), in a volume ratio of 30:30:40, and then adiponitrile was added thereto, to prepare an electrolyte solution.
An LiCoO2 positive active material, a polyvinylidene fluoride binder, and a Super-P conductive material were mixed in a weight ratio of 94:3:3 in an N-methylpyrrolidone solvent, to prepare a positive active material slurry. The positive active material slurry was coated on an aluminum current collector, and then dried and compressed to fabricate positive electrodes.
The compressing was performed by controlling the compressing pressure, time, and temperature, to fabricate positive electrodes having active-mass densities as shown in Table 1.
A graphite negative active material and a polyvinylidene fluoride binder were mixed in a weight ratio of 94:6 in an N-methylpyrrolidone solvent, to prepare a negative active material slurry. The slurry was coated on a copper current collector, dried, and compressed to fabricate a negative electrode.
Rechargeable lithium battery cells were fabricated using the above positive electrodes, negative electrode, and electrolyte solution, according to a conventional method.
A rechargeable lithium battery cell was fabricated according to the same method as in Example 1, except that a positive electrode was fabricated to have an active-mass density of 3.6 g/cc.
A rechargeable lithium battery cell was fabricated according to the same method as in Example 1, except that a positive electrode was fabricated to have an active-mass density of 3.65 g/cc.
The fabricated rechargeable lithium battery cells, according to Examples 1 to 9 and Comparative Examples 1 to 13, were charged at 0.2 C and discharged at 0.2 C, for a formation process, and then charged at 0.5 C and discharged at 0.2 C for a standard process. In the following Table 1, cell capacity refers to a third-cycle discharge capacity for a standard process.
The battery cells were also charged and discharged at 1.0 C for 300 cycles, at a normal temperature of 25° C. and at a high temperature of 45° C. The cycle-life test results are shown in the following Table 1. In Table 1, the cycle-life was evaluated by the 300th cycle discharge capacity ratio, relative to the first cycle discharge capacity.
As shown by the measurement results of Comparative Examples 1 to 11 in Table 1, as the active-mass densities of the positive electrodes were increased, the 300th cycle-life at both 25° C. and 45° C. was significantly decreased. However, the cells including the adiponitrile in the electrolyte solution, according to Examples 1 to 9, showed only a slightly reduced discharge capacity, at the 300th cycle at 25° C. and 45° C. In other words, the cells including the adiponitrile showed an improved cycle-life, even though the active-mass density of the positive electrode was increased. The measured results, of Comparative Examples 12 and 13, show that cycle-life improvements, according to the use of adiponitrile, were not obtained in the case where the active-mass density of the positive electrode was less than 3.7 g/cc. That is to say, the cycle-life improvements, according to the use of the adiponitrile, were realized when using a positive electrode having a high active-mass density of 3.7 g/cc or more.
Rechargeable lithium battery cells were fabricated according to the same method as in Example 5, except that the adiponitrile amount was varied, as shown in the following Table 2.
The fabricated rechargeable lithium battery cells, according to Examples 10 to 16, were charged at 0.2 C and discharged at 0.2 C, for a formation process, and then charged at 0.5 C and discharged at 0.2 C for a standard process. In the following Table 2, capacity refers to a third-cycle discharge capacity for a standard process.
The battery cells were also charged and discharged at 1.0 C for 300 cycles at a normal temperature of 25° C. The cycle-life test results are shown in the following Table 2. In the following Table 2, the cycle-life was evaluated by the 300th cycle discharge capacity ratio, relative to the first cycle discharge capacity.
Furthermore, in order to evaluate the cycle-life depending on the adiponitrile amount when the positive electrode has the same high active-mass density of 3.9 g/cc, the cycle-life and capacity of cells, according to Example 5 and Comparative Example 7, are also provided in Table 2.
As shown in Table 2, when the adiponitrile amount ranges from 0.1 to 10 wt %, the 300th cycle-life is improved as compared with Comparative Example 7 without the adiponitrile.
Rechargeable lithium battery cells were fabricated, according to the same method as in Example 7, except that the adiponitrile amount was varied, as shown in the following Table 3.
The fabricated rechargeable lithium battery cells, according to Examples 17 to 23, were charged at 0.2 C and discharged at 0.2 C, for a formation process, and then charged at 0.5 C and discharged at 0.2 C for a standard process. In the following Table 3, capacity refers to a third-cycle discharge capacity for a standard process.
The battery cells were also charged and discharged at 1.0 C for 300 cycles at a normal temperature of 25° C. The cycle-life test results are shown in the following Table 3. In Table 3, the cycle-life was evaluated by the 300th cycle discharge capacity ratio, relative to the first cycle discharge capacity.
Furthermore, in order to evaluate the cycle-life depending on the adiponitrile amount when the positive electrode has the same high active-mass density of 4.0 g/cc, the cycle-life and capacity of cells, according to Example 7 and Comparative Example 9, are also provided in Table 3.
As shown in Table 3, when the adiponitrile amount ranges from 0.1 to 10 wt %, the 300th cycle-life is improved, as compared with Comparative Example 9 (without the adiponitrile).
When results of Comparative Examples 7 and 9 in Tables 2 and 3 are compared, the cells, without the adiponitrile and including a positive electrode having a higher active-mass density (3.9 g/cc vs. 4.00 g/cc), have an increased capacity, but the 300th cycle-life at a normal temperature was decreased by 7% (62% vs. 55%). On the contrary, the results of Examples 5, 10 to 16, 7, and 17 to 23 show similar cycle-life characteristics, indicating that cycle-life characteristics are more improved when the electrolyte includes the adiponitrile.
Rechargeable lithium battery cells were fabricated according to the same method as in Example 1, except that succinonitrile (SN) was used instead of the adiponitrile, and the active-mass density of the positive electrodes were varied, as shown in the following Table 4.
The fabricated rechargeable lithium battery cells, according to Examples 24 to 34, were charged at 0.2 C and discharged at 0.2 C, for a formation process, and then charged at 0.5 C and discharged at 0.2 C for a standard process. In the following Table 4, cell capacity refers to a third-cycle discharge capacity for a standard process.
The battery cells were also charged and discharged at 1.0 C for 300 cycles, at a normal temperature of 25° C. The cycle-life test results are shown in the following Table 4. In Table 4, the cycle-life was evaluated by the 300th cycle discharge capacity ratio, relative to the first cycle discharge capacity.
Furthermore, in order to evaluate the cycle-life depending on the use of the succinonitrile, the cycle-life and capacity of cells, according to Comparative Examples 1 to 11, are also provided in Table 4.
As shown in the measurement results of Comparative Examples 1 to 15 in Table 4, as the active-mass density of the positive electrode was increased, the 300th cycle-life at 25° C. was significantly decreased. However, the cells including the succinonitrile in the electrolyte solution, according to Examples 24 to 32, showed little reduction in discharge capacity, at the 300th cycle at 25° C. In other words, the cells including the succinonitrile showed improved cycle-life characteristics, even though the active-mass densities of the positive electrodes were increased. The results of Comparative Examples 14 and 15 show that such cycle-life improvements, according to the use of the succinonitrile, were not obtained when the active-mass density of the positive electrode was less than 3.7 g/cc. That is to say, such cycle-life improvements, according to the use of the succinonitrile, were realized when using a positive electrode having a high active-mass density of 3.7 g/cc or more.
As described above, the rechargeable lithium batteries, including a nitrile-based compound additive in an electrolyte, have high capacity as well as improved cycle-life characteristics at room temperature, even though the positive electrodes have high active-mass densities of 3.7 to 4.1 g/cc.
Although a few embodiments of the present invention have been shown and described, it would be appreciated by those skilled in the art that changes may be made in this embodiment without departing from the principles and spirit of the invention, the scope of which is defined in the claims and their equivalents.
| Number | Date | Country | Kind |
|---|---|---|---|
| 10-2006-0113991 | Nov 2006 | KR | national |
