Synthetic resins or natural rubbers -- part of the class 520 ser – Synthetic resins – Mixing of two or more solid polymers; mixing of solid...
Reexamination Certificate
2000-08-16
2002-10-22
Sellers, Robert E. L. (Department: 1712)
Synthetic resins or natural rubbers -- part of the class 520 ser
Synthetic resins
Mixing of two or more solid polymers; mixing of solid...
C429S309000, C429S312000
Reexamination Certificate
active
06469107
ABSTRACT:
BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention relates to ion-conductive polymer electrolyte compositions having a high electrical conductivity, and ion-conductive solid polymer electrolytes endowed with high conductivity and excellent shape retention.
2. Prior Art
Electrolytes used in secondary cells (batteries) and capacitors, for example, have up until now been primarily low-molecular-weight substances that are liquid at or above room temperature, such as water, ethylene carbonate, propylene carbonate, and tetrahydrofuran. In lithium-type cells in particular, use is commonly made of low-molecular-weight organic liquid electrolytes which tend to evaporate, ignite and burn rather easily. To ensure long-term stability, it is necessary to use a metal can as the outer cell enclosure and to increase the airtightness of the container. The result is a considerable rise in the weight of electrical and electronic components that use low-molecular-weight organic liquid electrolytes, and greater complexity of the production process.
Electrolytes can also be made of polymers. Such electrolytes have a very low volatility and thus are not prone to evaporation. Moreover, polymer electrolytes, as these are known, with a sufficiently high molecular weight can even be used as solid electrolytes that exhibit no fluidity at or above room temperature. They have the dual advantage of serving as a solvent for ion-conductive salts and of solidifying the electrolyte.
As an example of this type of polymer electrolyte, in 1978, Armond et al. at l'Université de Grenoble in France discovered that lithium perchlorate dissolves in solid polyethylene oxide, and reported that when the concentration of 1 M lithium salt is dissolved in polyethylene oxide having a molecular weight of about 2,000, the resulting complex shows an ionic conductivity of about 10
−7
S/cm at room temperature. Other groups also reported that when the concentration of 1 M lithium salt is dissolved at room temperature in liquid polyethylene oxide having a molecular weight of about 200, the ionic conductivity at room temperature is about 10
−4
to 10
−5
S/cm. Thus, it is known that polymeric substances such as polyethylene oxide with the ability to dissolve ion-conductive salts function as electrolytes.
Since then, similar research has been carried out on a broad range of largely polyethylene oxide-related polymeric substances, such as polypropylene oxide, polyethyleneimine, polyurethanes and polyesters.
The most thoroughly investigated of these substances, polyethylene oxide, is a polymer having a good ability to dissolve ion-conductive salts as noted above, but at the same time, a semi-crystalline polymer. Because of the latter nature, when a large amount of metallic salt is dissolved in polyethylene oxide, the salt forms a pseudo-crosslinked structure between the polymer chains that leads to crystallization of the polymer. As a result, the ionic conductivity is much lower than predicted.
The reason is as follows. When an ion conductor is dissolved in a linear polyether-based polymer matrix such as polyethylene oxide, the ion conductor migrates, at temperatures above the glass transition temperature of the polymer matrix, through amorphous regions of the polymer matrix along with the local movement of polymer chain segments. Since the cations accounting for ionic conductivity are strongly coordinated by the polymer chains, the local movement of the polymer chains has a strong influence on cation mobility. That local movement of polymer chains is called Brawnian motion.
Therefore, a linear polyether-based polymer such as polyethylene oxide is a poor choice as the matrix polymer for an ion-conductive polymer electrolyte. In fact, according to the literature to date, ion-conductive polymer electrolytes composed entirely of linear polymers such as polyethylene oxide, polypropylene oxide or polyethyleneimine generally have an ion conductivity at room temperature of about 10
−7
S/cm, and at best no more than about 10
−6
S/cm.
To obtain ion-conductive polymer electrolytes having a high conductivity, a molecule must be designed which allows the existence within the matrix polymer of many amorphous regions conducive to ion conductor mobility, and which does not crystallize even with the dissolution therein of ion-conductive salts to a high concentration.
One such method is the attempt to introduce a branched structure into polyethylene oxide, as described in N.Ogata et al., Journal of the Japan Textile Society, pp. 52-57, 1990. Their work demonstrates that ion-conductive solid polymer electrolytes composed of a polyethylene oxide derivative having a high ionic conductivity (about 10
−4
S/cm at room temperature) can indeed be synthesized. However, commercialization of such polymer electrolytes has not been achieved due to the sheer complexity of the method of polymer synthesis involved.
There have also been reports on methods of attaining ion conductivity by imparting to the matrix polymer a three-dimensional network structure so as to impede the formation of a crystalline structure. One example of the use of a polymer having a three-dimensional network structure as the polymer matrix is a method of polymerizing an acrylic monomer or methacrylic monomer containing a polyoxyalkylene component as disclosed in JP-A 5-25353. This method, however, has a number of problems including the low solubility of the ion-conductive salt in the monomer, which necessitates the addition of a third component such as vinylene carbonate, and the low physical strength of the resulting polymer.
SUMMARY OF THE INVENTION
Therefore, one object of the present invention is to provide an ion-conductive solid polymer electrolyte composition having a high conductivity. Another object of the invention is to provide an ion-conductive solid polymer electrolyte having a high conductivity, a semi-interpenetrating polymer network (semi-IPN) structure, and excellent shape retention.
The inventor has discovered that an ion-conductive polymer electrolyte composition composed primarily of a polymeric compound containing certain specific units, an ion-conductive salt, and a compound bearing crosslinkable functional groups has a high ion conductivity. The inventor has also found that this composition can be used to prepare an ion-conductive solid polymer electrolyte having a semi-IPN structure wherein molecular chains on the polymeric compound are entangled with a three-dimensional polymer network structure formed by crosslinking the crosslinkable functional group-bearing compound, and containing the ion-conductive salt. This polymer electrolyte has a dramatically improved shape retention. Moreover, because the matrix is amorphous rather than crystalline, the polymer electrolyte is endowed with a high ion conductivity, giving it an excellent performance as an ion-conductive solid polymer electrolyte.
Accordingly, the invention provides an ion-conductive polymer electrolyte composition comprising:
(A) a polymeric compound containing a unit of the following formula (1) and a unit of the following formula (2):
(B) an ion-conductive salt, and
(C) a compound having crosslinkable functional groups.
The invention also provides an ion-conductive solid polymer electrolyte prepared from the foregoing composition, wherein the polymer electrolyte has a semi-interpenetrating polymer network structure in which molecular chains on the polymeric compound (A) are entangled with a three-dimensional polymer network structure formed by crosslinking the crosslinkable functional group-bearing compound (C), and contains the ion-conductive salt (B).
REFERENCES:
patent: 4597838 (1986-07-01), Bammel
patent: 0 757 397 (1997-02-01), None
patent: 0 825 662 (1998-02-01), None
patent: 0 885 913 (1998-02-01), None
patent: A2-38451 (1990-02-01), None
patent: A2 2-95004 (1990-12-01), None
patent: 5-25353 (1993-02-01), None
patent: A10-204172 (1998-08-01), None
Ogata et al., Journal of Japan Textile Society, 46 (2), pp. 52-57, (1990). Abstract only.
Nissihinbo Industries, Inc.
Sellers Robert E. L.
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