Patent Application
20050014051
The present invention relates to polymer electrolyte membranes for use in fuel cells, and more particularly, to the utilization of fullerene materials for enhancing the low relative humidity proton conductivity properties of such polymeric membranes.
A steadily increasing demand for portable electric power has stimulated interest in the development of more efficient and more powerful fuel cell devices. A polymer electrolyte membrane (PEM) fuel cell is a strong candidate as a portable power source for commercial applications primarily because of its low weight and high power density.
The operation of a PEM fuel cell relies upon the proton conductivity properties of a polymeric membrane positioned between the two electrodes of the cell, to transport protons internally from one electrode to the other. The membrane must also have no electronic conductivity, good chemical and mechanical stability, and sufficient gas impermeability to prevent cross over of the fuel. For many years now, the membrane of choice has been a sulfonated perfluoro polymer known as Nafion®, commercially available from DuPont. Nafion is a copolymer of tetrafluoroethylene and perfluoro-3,6-dioxa-4-methyl-7-octenesulfonyl fluoride, available in acid or ionomer form.
The major drawback to Nafion as the ideal polymer electrolyte membrane in fuel cells is that its proton conductivity depends on the water content in the membrane, in which proton transport is based on the diffusion of hydronium ion (H3O+). In order to retain its high proton conductivity, Nafion membrane requires the use of pre-humidified gases at an operating temperature under 80° C. Such requirements considerably increase the cost, size and complexity of PEM fuel cells using Nafion. Nafion membranes cannot perform under dry or low relative humidity conditions nor above the boiling point of water, despite the faster chemical reaction and increased output that would result from the higher temperature. Furthermore, operating at the lower temperature required by Nafion increases the risk of carbon monoxide poisoning of the fuel cell catalyst.
Various attemps have been made to develop water-free proton conductive membranes for PEM fuel cells that do not have the low temperature and high relative humidity requirements of Nafion. One such attempt, for example, is described in the Hinokuma et al. U.S. Pat. No. 6,495,290, issued Dec. 17, 2002, incorporated herein by reference. The proton conductors employed by Hinokuma et al. are based on fullerene derivatives containing acidic functional groups such as —OH or —SO3H, and are designed to operate under dry conditions over a wide range of temperatures. The proton conductors are described as being either compacted powder of the fullerene derivatives, or mixed with a small amount, generally 20 weight percent or less, of a film-forming polymeric material, such as polytetrafluoroethylene, polyvinylidene fluoride or polyvinyl alcohol. The patent cautions against employing the polymer in amounts any greater than 20 weight percent, at the risk of degrading the proton conductivity of the fullerene derivative. Furthermore, there is no hint in the Hinokuma et al. patent of using the fullerene derivative in combination with Nafion.
The present invention resides in the discovery that proton conductive fullerene materials, including but not limited to the fullerene derivatives described in the Hinokuma et al. U.S. Pat. No. 6,495,290, can be used in minor amounts, even as low as about 1% by weight, to enhance the low relative humidity proton conductivity properties of a variety of polymeric materials, even including Nafion itself. The proton conductive fullerene materials used in the present invention contain either bound water, or a plurality of functional groups with lone pair electrons, or a combination thereof, and may be incorporated into the polymeric material by doping or by mechanical mixing or by chemical reaction forming covalent bonds. The resulting proton conductors may be used as polymer electrolyte membranes in fuel cells operative over a wide range of relative humidity conditions and over a wide range of temperatures from below room temperature to above the boiling point of water.
The present invention includes the use of proton conductive fullerene materials to enhance the low relative humidity proton conductivity properties of polymeric materials. It also includes the proton conductors resulting from such use, as well as fuel cells employing such proton conductors.
In accordance with the present invention, proton conductive fullerene materials are employed to enhance the low relative humidity proton conductivity properties of polymeric materials for use as polymer electrolyte membranes in fuel cells. In this context, the term “low relative humidity” is used to signify relative humidities less than about 50%.
The proton conductive fullerene materials used in accordance with the present invention are fullerene materials containing bound water, or a plurality of functional groups with lone pair electrons, or a combination thereof. Fullerene materials containing a plurality of functional groups with lone pair electrons include, but are not limited to, all of the various fullerene derivatives described in the Hinokuma et al. U.S. Pat. No. 6,495,290, incorporated herein by reference, as having functional groups represented by the formula —XH where X is an arbitrary atom or atomic group having a bivalent bond, and more specifically by the formula —OH or —YOH where Y is an arbitrary atom or atomic group having a bivalent bond, and preferably the functional groups —OH, —OSO3H, —COOH, —SO3H or —OPO(OH)3. Other functional groups with lone pair electrons include basic functional groups, such as —NH2, ═NH and ≡N.
Fullerene materials containing bound water encompass just about all fullerene materials, with or without functional groups, even including C60 itself. This is so because all fullerenes inherently contain a certain amount of bound water in their molecules which is extremely difficult to drive out in its entirety. In this respect, all fullerenes and fullerene derivatives are inherently water carriers capable of supporting some degree of proton transport through the diffusion of hydronium ions. This is independent of the proton hopping mechanism of proton transport between functional groups that is exhibited by the fullerene derivatives. For this reason, C60 itself, even without functionalization, is included as a proton conductive fullerene material, and surprisingly has been found to be one of the preferred proton conductive fullerene materials for use in the present invention.
Other preferred proton conductive fullerene materials for use in the present invention are polyhydroxylated fullerene, polysulfonated fullerene and polyhydroxylated polysulfonated fullerene.
The present invention allows for significant flexibility in selection of the base polymeric material whose proton conductivity properties are to be enhanced by incorporation of the proton conductive fullerene materials. The selection will generally be made based upon the other requisite properties for a fuel cell polymer electrolyte membrane, such as no electronic conductivity, good chemical and mechanical stability, and sufficient gas impermeability to prevent cross over of the fuel. Since Nafion is well known to exhibit these properties and has long been the membrane of choice for PEM fuel cell applications, it is the logical preferred polymeric material for use in the present invention. Other preferred polymeric materials include sulfonated perfluoro polymers in general, polyethylene oxide, polystyrene and sulfonated polystyrene.
The requisite amount of proton conductive fullerene material to be incorporated into the polymeric material for enhancing the low relative humidity proton conductivity properties of the polymeric material, is surprisingly small, particularly in view of the negative teachings in this regard of the Hinokuma et al. U.S. Pat. No. 6,495,290, cautioning against adding polymer to fullerene derivatives in amounts any greater than 20 weight percent, at the risk of degrading the proton conductivity of the fullerene derivative. The present invention employs the reverse approach and adds the fullerene material to the polymer in a minor amount relative to the polymer. This amount will generally be less than about 30% by weight, and in most instances, within the range of from about 1 to about 10% by weight.
The actual incorporation of the fullerene material into the base polymeric material may be carried out in a variety of ways, depending upon the form of the starting materials. For example, if the base polymer is already in membrane or film form, such as the commercially available Nafion membrane, the fullerene material may be doped into the polymeric material by soaking the membrane in a doping solution of the fullerene material. Alternatively, the components may be mixed together in solution, for example, using supercritical CO2, and then either casting a composite film or membrane, or evaporating the solvent to form a powder and then pelletizing the powder into a pelletized membrane. In some instances, it may be desirable to covalently link the fullerene material to the polymeric material through chemical reaction there-between.
Other additives may desirably be incorporated into the polymeric material in conjunction with the fullerene material. For example, when using a relatively high loading of fullerene that may cause the final membrane to become brittle, it may be desirable to add a brittleness inhibiting amount of a plasticizer for the polymeric material, such as low molecular weight polyethylene oxide, low molecular weight polyethylene imine, or carbon disulfide. Also, it may be desirable to aid the incorporation of the requisite amount of the fullerene material into the polymeric material by the addition of a fullerene-uptake adjuvant, such as silica, alumina or titania. Silica, in amounts up to about 10% by weight, has been found to be particularly suitable for this purpose.
The invention is further illustrated by way of the following examples.
Nafion 117 membrane obtained from DuPont was first boiled for 30 minutes with 3% hydrogen peroxide solution to remove organic impurities. The film was then rinsed several times with de-ionized water. The film was then boiled with IM sulfuric acid for an hour to remove inorganic minerals. The membrane was again rinsed with de-ionized water and soaked in isopropyl alcohol until use. 1 wt % of dried C60(OH)12 was mixed with 0.8 g of Nafion ionomer solution obtained from DuPont. The wet membrane was soaked in a closed vial filled with this mixture of C60(OH)12 and Nafion ionomers for 24 hours. The membrane was then removed from the vial and dried in the vacuum oven. The resulting product was a Nafion membrane doped with 1 wt % C60(OH)12.
Example 1 was repeated, substituting C60 (OSO3H)4(OH)8 for the C60 (OH)12, to obtain a Nafion membrane doped with 1 wt % C60 (OSO3H)4(OH)8.
Example 1 was repeated, substituting C60 for the C60(OH)12, to obtain a Nafion membrane doped with 1 wt % C60.
A composite membrane consisting of polyethylene oxide and 1 wt % C60(OSO3H)4(OH)8 was prepared by mixing the two ingredients together in solution and then solution casting the membrane on Teflon sheet.
Example 4 was repeated, this time increasing the amount of C60(OSO3H)4(OH)8 to 20 wt %
A composite membrane consisting of sulfonated polystyrene and 10 wt % C60(OSO3H)4(OH)8 was prepared by mixing the two ingredients together in solution and then solution casting the membrane on Teflon sheet.
The proton conductivities of the membranes prepared in accordance with Examples 1-5, as well as that of a bare Nafion membrane, were measured at 30° C. (i.e., low temperature) at varying relative humidities ranging from 20% to 100%.
The PEM fuel cell performance of the membranes prepared in accordance with Examples 2 and 3, as well as that of a bare Naflon membrane, were measured at 120° C. (i.e., high temperature) and 25% relative humidity (i.e., low relative humidity), with the fuels being hydrogen and air, the pressure being ambient, and the platinum loading being 0.2 mg cm−2.
The proton conductivities of the membranes prepared in accordance with Examples 1-3 and 6, as well as that of a bare Nafion membrane and a bare sulfonated polystyrene membrane, were also measured at 120° C. (i.e., high temperature) and 25% relative humidity (i.e., low relative humidity). The results are listed in Table 1, below.
From the proton conductivity data listed in Table 1, it can be seen that the incorporation of the fullerene materials into the membranes, in the case of both the Nafion membrane and the sulfonated polystyrene membrane, increases the high temperature, low relative humidity proton conductivity of the membrane by an order of magnitude.
It is apparent from the above test results that the proton conductors with enhanced low relative humidity proton conductivity properties in accordance with the present invention, are well suited for use as polymer electrolyte membranes in fuel cells. An example of a fuel cell using the proton conductor of this invention is shown in
This application claims the benefit of U.S. Provisional Application No. 60/477,971, filed Jun. 12, 2003, and U.S. Provisional Application No. 60/500,603, filed Sep. 5, 2003.
This invention was made with Government support under Government Contract No. DAAD19-03-C-0024, awarded by the United States Department of Defense. The Government has certain rights in the invention.
| Number | Date | Country | |
|---|---|---|---|
| 60477971 | Jun 2003 | US | |
| 60500603 | Sep 2003 | US |
