CA1299936C - Current collector bonded to a solid polymer membrane - Google Patents
Current collector bonded to a solid polymer membraneInfo
- Publication number
- CA1299936C CA1299936C CA000544302A CA544302A CA1299936C CA 1299936 C CA1299936 C CA 1299936C CA 000544302 A CA000544302 A CA 000544302A CA 544302 A CA544302 A CA 544302A CA 1299936 C CA1299936 C CA 1299936C
- Authority
- CA
- Canada
- Prior art keywords
- foundation layer
- carbon atoms
- porous
- fluoropolymeric
- catalyst
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/30—Hydrogen technology
- Y02E60/50—Fuel cells
Landscapes
- Inert Electrodes (AREA)
- Fuel Cell (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
The invention is a method of forming an assembly of an ion permeable membrane, electrode, and current collector, comprising the steps of:
(a) forming a foundation layer of a porous electrically conductive material;
(b) at least partially coating a fluoropolymer binder on at least one surface of the conductive foundation layer;
(c) applying a particulate catalyst material over the fluoropolymer binder on the foundation layer;
(d) dispersing a polymeric material as a solution or dispersion over the catalyst material in a manner to obtain penetration of the polymeric material into the porous foundation layer to form a substantially continuous coating on the catalyst material and the at least partially coated foundation layer; and (e) applying heat and/or pressure to enhance the flow of the polymeric material into the foundation layer and around the catalyst material to obtain adherence of the catalyst material to the foundation layer and to sinter the polymer material into a substantially non-porous layer around the catalyst material.
33,070-A
The invention is a method of forming an assembly of an ion permeable membrane, electrode, and current collector, comprising the steps of:
(a) forming a foundation layer of a porous electrically conductive material;
(b) at least partially coating a fluoropolymer binder on at least one surface of the conductive foundation layer;
(c) applying a particulate catalyst material over the fluoropolymer binder on the foundation layer;
(d) dispersing a polymeric material as a solution or dispersion over the catalyst material in a manner to obtain penetration of the polymeric material into the porous foundation layer to form a substantially continuous coating on the catalyst material and the at least partially coated foundation layer; and (e) applying heat and/or pressure to enhance the flow of the polymeric material into the foundation layer and around the catalyst material to obtain adherence of the catalyst material to the foundation layer and to sinter the polymer material into a substantially non-porous layer around the catalyst material.
33,070-A
Description
lZ99936 CURRENT COLLECTOR BONDED TO A SOLID POLYMER MEMBRANE
The invention relates to an improved method of manufacturing a current collector/catalyst electrode/membrane assembly which has increased elec-~- trical conductivity in the area between the catalyst electrode and the current collector. Such assemblies are useful in a variety of applications including, for example, fuel cells, water electrolysis cells, chlor-alkali cells, and the like. The assembly produced according to the present invention is substantially structurally stable which allows the membrane portion to be substantially thinner than those presently available, thereby reducing the ionic resistance of the membrane.
It is highly desirable, given the harsh conditions of many of the applications for the membrane, that the membrane portion of the assembly have substantial structural integrity. Thinner membranes have been viewed as fragile and yet thinner membranes are desirable due to their reduced ionic resistance.
33,070A-F -1-1;!99936 This requires a balance between providing adequate structural support for the assembly and yet reducing the membrane's thickness to reduce the ionic resistance of the membrane without a sacrifice in the structural integrity.
References which have a bearing on this invention include U. S. Patent No . 4, 272,353, which discloses a surface abrading technique for scratching a solid polymer electrolyte (SPE) base member in preparation for subsequent treatment. U. S. Patent No.
4,272,560 describes a membrane having a cathode made of multiple coatings with a backing fabric; a dissolved copolymer is used in the fabrication of this electrode.
U. S. Patent No. 4,182,670 discloses a combined cathode and diaphragm utilizing a spray coating of a metal substrate with powdered metal; a polymer impregnated diaphragm is also described. An electrode body having impregnated powdered metal (typically noble metals) is described in U. S. Patent No. 3,276,911, and it also mentions a permeable ionic electrolytic material.
U. S. Patent No. 4,364,813 discloses catalytic particles deposited on an ion exchange material with a SPE membrane; additionally, this patent has an ion exchange feature mentioning a sulfonic group. U. S.
Patent No. 4,366,041 describes a cathode and diaphragm assembly with a sacrificial film made of wax.
~he present invention particularly describes a structurally stable electrode assembly which has lower ionic resistance in the membrane portion and which has higher electrical conductivity in the catalyst electrode and current collector portions. Membrane thinness is achieved without sacrifice of structural 33,070A-F -2-1Z!~9936 -integrity and yet resistance to ionic movement through the membrane is reduced.
While the foregoing refers in general terms to the present assembly, the structure thereof and the method of manufacture are exempliied in the detailed description of the preferred embodiments following.
The invention particularly resides in a method of forming an assembly of an ion permeable membrane, electrode, and current collector, comprising the steps of:
(a) forming the current collector from a foundation layer of a porous, electrically conductive material;
(b) at least partially coating a fluoro-polymer binder on at least one surface of the foundation layer;
(c) forming the electrode by applying a particulate catalyst material over the fluoropolymer binder on the foundation layer;
(d) applying a fluoropolymeric material as a solution or dispersion over the catalyst material in a manner to obtain penetration of the fluoropolymeric material into the porous foundation layer to form a substantially continuous coating on the catalyst material and the at least partially coated foundation layer; said fluoropolymeric material forming the ion permeable membrane, and (e) applying heat and/or pressure to the assembly to enhance the flow of the fluropolymeric material into the foundation layer and around the catalyst material to obtain adherence of the catalyst material to the foundation layer and to sinter the 33,070A-F -3-~...,' . ~. ~....
l;~g9936 .
-3a-fluoropolymeric material into a substantially non-porous layer around the catalyst material.
33,070A-F -3a-A~
, ~
-~ 9 ~6 The foundation layer is an electrically conductive, hydraulically permeable matrix which acts as a current collector to transmit electrical energy to or from the electrode. It may be composed of a variety of substances, including carbon cloth, carbon paper, carbon felt, metallic screens, metallic felt, and porous metallic sheets. Preferably, however, the foundation layer is a carbon paper, which is readily available, performs well, is easily handled, and is relatively inexpensive.
The paper most preferably used in this invention is also one having low electrical resistivity, possessing sufficient strength for fabrication, and having adequate surface properties, such as roughness, to provide good bonding between the fluoropolymer binder and the foundation layer. It is also preferable to provide good electrical contact between the carbon paper and the catalytically active particles of the electrode.
As a beginning step, the foundation layer is at least partially coated with a suitable polymer binder.
This polymer binder can be a fluorocarbon polymer, such as polytetrafluoroethylene sold under the trademark of Teflon. Other suitable polymers can include thermo-plastic, non-ionic forms of sulfonic acid copolymers;
thermoplastic, non-ionic forms of carboxylic acid copolymers; and the like.
Particularly preferred as the fluoropolymer binder are thermoplastic, non-ionic forms of perfluor-inated polymers described in the following U. S. Patent Nos. 3,282,875; 3,909,378; 4,025,405; 4,065,366;
4,116,888; 4,123,336; 4,126,588; 4,151,052; 4,176,215;
33,070A-F -4-1~9936 4,178,218; 4,192,725; 4,209,635; 4,212,713; 4,251,333;
4,270,996; 4,329,435; 4,330,654; 4,337,137; 4,337,211;
4,340,680; 4,357,218; 4,358,412; 4,358,545; 4,417,969;
4,462,877; 4,470,889; 4,478,695; and published European Patent Application 0,027,009. Such polymers usually have equivalent weights of from 500 to 2000.
Particularly preferred for use as the fluoro-polymer binder are copolymers of monomer I with monomer II (as defined below). Optionally, a third type of monomer may be copolymerized with I and II.
The first type of monomer is represented by the general formula:
CF2-CZZ' (I) where:
Z and Z' are independently selected from -H, -Cl, -F, and -CF3 The second monomer consists of one or more monomers selected from compounds represented by the general formula:
(II) (CF2)a (cFRf)b-tcFRf.)c-o-[cF(cF2x)-cF2-o]n-cF=cF2 where:
Y is selected from -S02Z, -CN, -COZ, and -C(R3f)(R4f)OH;
Z is selected from -I, -Br, -Cl, -F, -OR and -NRlR2;
33,070A-F -5-~.ZW936 R is selected from a branched or linear alkyl radical having from 1 to 10 carbon atoms or an aryl radical;
R3f and R4f are independently selected from perfluoroalkyl radicals having from 1 to 10 carbon atoms;
R1 and R2 are independently selected from -H, a branched or linear alkyl radical havin~ from 1 to 10 carbon atoms or an aryl radical;
a is o-6;
b is 0-6;
c is 0 or 1;
provided a+b+c is not equal to 0;
,- 15 X is selected from -Cl, -Br, -F, or mixtures thereof when n~1;
n is 0 to 6; and Rf and Rf~ are independently selected from -F, -Cl, perfluoroalkyl radicals having from 1 to 10 carbon atoms, and fluorochloroalkyl radicals having from 1 to 10 carbon atoms.
Particularly preferred is when Y is -S02F or -CooCH3; n is 0 or 1; Rf and Rf~ are -F; X is -Cl or -F; and a+b+c is 2 or 3.
The third and optional monomer is one or more monomers selected from the compounds represented by the general formula:
(III) (CF2)a' (CFRf)b'-(CFR f)cl-o-[cF(cF2xl)-CF2-O]n,-CF=CF2 33,070A-F -6-where:
Y' is selected from -F, -Cl, or -Br;
a' and b' are independently 0-3;
c' is 0 or 1;
provided a'+b'+c' is not equal to 0;
n' is 0-6;
Rf and R'f are independently selected from -8r, -Cl, -F, perfluoroalkyl radicals having from 1 to lO
carbon atoms, and chloroperfluoroalkyl radicals having 0 from 1 to 10 carbon atoms; and X' is selected from -F, -Cl, -Br, or mixtures thereof when n'>1.
The binder is typically applied in a solution or dispersion to at least partially coat the foundation layer. The solution or dispersion can be applied to the foundation layer using a variety of methods well known in the art.
When the electrode is to be used in a fuel cell, preferably the binder is a hydrophobic material like polytetrafluoroethylene. When, however, the electrode is to be used in an electrolytic cell, such as a chlor-alkali cell, the binder is preferably a hydrophilic material like the copolymers formed from monomers I, II and, optionally III (described above).
The preferred loading, i.e. amount of application of the binder, is from 0.50 to 50 mg/cm2 of foundation area with a preferred range of from 2.5 to 30 mg/cm2 of foundation area.
When the binder is applied as a solution or a dispersion, the solvent/dispersant can be a variety of materials including, for example, water, methanol, 33,070A-F -7-~&
ethanol, and compounds represented by the general formula:
XCF2-CYZ-X ' wherein:
X is selected from F, Cl, Br, and I;
X' is selected from Cl, Br, and I;
Y and Z are independently selected from H, F, Cl, Br, I and R'; and R' is selected from perfluoroalkyl radicals and chloroperfluoroalkyl radicals having from 1 to 6 carbon atoms.
The most preferred solvents or dispersants are ,- 15 1,2-dibromotetrafluoroethane (commonly known as Freon 114 B 2) BrCF2-CF2Br and 1,2,3-trichlorotrifluoroethane (commonly known as Freon 113):
ClF2C-CC12F
Of these two materials, 1,2-dibromotetrafluoroethane is the most preferred solvent or dispersant.
The solution or dispersion used to apply the binder to the foundation layer may have a concentration of from 2 to 30 weight percent of polymer in the 3 solvent/dispersant. Preferably, the concentration is from 8 to 20 weight percent of polymer in the solvent/dispersant.
After the solution or dispersion has been applied to the foundation layer, the solvent can then be driven off using heat, a vacuum, or a combination of 33,070A-F -8--` 1299936 heat and a vacuum. Optionally, the solvent/dispersant may be allowed to evaporate under ambient conditions.
Preferably, the solvent is removed at an elevated temperature. In addition to removing the solvent/dispersant, the heat sinters the binder and causes it to more completely penetrate and surround the foundation layer. As an example, when polytetrafluoroethylene is used as the binder, exposure at a temperature of from 300C to 340C for about 20 minutes will suffice to remove the solvent/dispersant and to sinter the polytetrafluoroethylene.
The next step in the method of the present invention is the application of catalytically active and electrically conductive particles to the coated foundation layer. The composite structure will, ultimately, form what is commonly referred to as a solid polymer electrolyte, or SPE, when the composite is used in an electrochemical cell. The electrode can be ultimately used as either a cathode or as an anode.
Materials suitable for use as electro-catalytically active anode materials include, for example, metals or metal oxides of platinum group metals, such as ruthenium, iridium, rhodium, platinum, palladium, either alone or in combination with an oxide of a film-forming metal such as Ti or Ta. Other suitable activating oxides include cobalt oxide, either alone or in combination with other metal oxides, such as those described in U. S. Patent Nos. 3,632,498;
4,142,005; 4,061,549; and 4,214,971.
Materials suitable for use as electro-catalytically active cathode materials include, forexample, platinum group metals or metal oxides, such as 33,070A-F -9-lZ99936 --1 o ruthenium or ruthenium oxide. U. S. Patent No.
4,465,580 describes such cathodes.
The catalytic particles used in the present invention are preferably finely divided and have a preferred range of from 270 to smaller than 400 mesh size (U. S. Standard) (53 to less than 37 microns).
The metal powder is applied to the binder-coated foundation layer by methods known to those skilled in the art including, for example, spraying, forming a sheet of catalytic particles and pressing the sheet onto the foundation layer, or forming and applying the particles in the form of liquid dispersion, for example, an aqueous dispersion. A suitable loading of catalyst particles has been found to be from 0.2 to 20 mg/cm2 of foundation area with a preferred range of from 1.5 to 5.0 mg/cm2 of foundation area.
Separately, a copolymer is formed. One such suitàble polymer is the polymer formed from monomers I, II, and optionally III, as defined above. The polymer may be a thermoplastic, non-ionic precursor of a sulfonic acid copolymer or a thermoplastic, non-ionic precursor of a carboxylic acid copolymer, or a variety of other polymers as defined for use as the binder.
Preferably, the copolymer is formed into a solution or a dispersion with a solvent for application to the catalytically active particles. On mixing with a suitable solvent or dispersant, the polymer is applied to the catalyst particle coated foundation layer.
Utilizing a vacuum on one side of the foundation layer, the polymer in the solvent or dispersant is pulled onto the catalyst and into the foundation layer. While in one sense it can be described as coated on one side, 33,070A-F -10-the coating nevertheless sufficiently penetrates into the porous sheet.
In the step of bonding a fluoropolymer ontc the surface of the catalytic particle coated foundation layer, the most convenient procedure is the use of conventional organic solvents. Typical solvents used are 1,2-dibromotetrafluoroethane, methanol, ethanol, and the like. The polymeric material which is applied forms a substantially non-porous ion exchange layer.
The next step is the application of heat and/or pressure to remove the solvent/dispersant and to sinter the polymer, thereby forming the polymer into a substantially continuous sheet. In addition, the heat and/or pressure enhance the coating of the polymer around the catalyst particles and the foundation layer.
For example, exposure to a temperature in the range of from 260 to 320C is generally suitable to bond the polymer to the particles and the foundation layer. The temperature range is limited primarily by the onset of thermal degradation of the polymer caused by excessive heat. The pressure is preferably sufficiently high and sustained for an interval to achieve bonding. In one example, pressure may be applied up to about 5 kg/cm2 for about one minute at elevated temperature.
The next step in the manufacture of the improved electrode structure is to hydrolyze the structure from the non-ionic to the ionic form.
Hydrolysis may be accomplished by treating the polymer with a basic solution if the polymer is a thermo-plastic, non-ionic precursor of a sulfonic acid polymer or a thermoplastic, non-ionic precursor of a carboxylic acid polymer. In addition, if the polymer is a 33,070A-F -11--- 1~936 thermoplastic, non-ionic precursor of a carboxylic acid polymer, an acid solution may be used to hydrolyze the polymer. For example, in a thermoplastic, non-ionic precursor of a sulfonic acid polymer, the completed structure may be hydrolyzed in 25 weight percent sodium hydroxide for 16 hours at an elevated temperature of 80C.
The completed article is then ready for use.
As an example of typical size, it is not uncommon to encounter a membrane which is in a range of from 5 to 10 mils (0.125 to 0.25 mm) thick due to the need for structural integrity. The finished product can yield a membrane with a thickness in a range of from 1 to 2 mils (0.025 to 0.05), or even less. The resistance of ionic movement through the membrane is thus lowered by a significant amount.
In an alternate application, two similar sheets of equal size are positioned in contact with one another in a manner so that the foundation layers face toward the outside of the combination and the polymer layer on each sheet is contacted against the polymer layer on the other sheet. The coterminous sheets are then placed into a press and on the application of suitable pressure and/or heat, they are joined together.
33,070A-F -12-
The invention relates to an improved method of manufacturing a current collector/catalyst electrode/membrane assembly which has increased elec-~- trical conductivity in the area between the catalyst electrode and the current collector. Such assemblies are useful in a variety of applications including, for example, fuel cells, water electrolysis cells, chlor-alkali cells, and the like. The assembly produced according to the present invention is substantially structurally stable which allows the membrane portion to be substantially thinner than those presently available, thereby reducing the ionic resistance of the membrane.
It is highly desirable, given the harsh conditions of many of the applications for the membrane, that the membrane portion of the assembly have substantial structural integrity. Thinner membranes have been viewed as fragile and yet thinner membranes are desirable due to their reduced ionic resistance.
33,070A-F -1-1;!99936 This requires a balance between providing adequate structural support for the assembly and yet reducing the membrane's thickness to reduce the ionic resistance of the membrane without a sacrifice in the structural integrity.
References which have a bearing on this invention include U. S. Patent No . 4, 272,353, which discloses a surface abrading technique for scratching a solid polymer electrolyte (SPE) base member in preparation for subsequent treatment. U. S. Patent No.
4,272,560 describes a membrane having a cathode made of multiple coatings with a backing fabric; a dissolved copolymer is used in the fabrication of this electrode.
U. S. Patent No. 4,182,670 discloses a combined cathode and diaphragm utilizing a spray coating of a metal substrate with powdered metal; a polymer impregnated diaphragm is also described. An electrode body having impregnated powdered metal (typically noble metals) is described in U. S. Patent No. 3,276,911, and it also mentions a permeable ionic electrolytic material.
U. S. Patent No. 4,364,813 discloses catalytic particles deposited on an ion exchange material with a SPE membrane; additionally, this patent has an ion exchange feature mentioning a sulfonic group. U. S.
Patent No. 4,366,041 describes a cathode and diaphragm assembly with a sacrificial film made of wax.
~he present invention particularly describes a structurally stable electrode assembly which has lower ionic resistance in the membrane portion and which has higher electrical conductivity in the catalyst electrode and current collector portions. Membrane thinness is achieved without sacrifice of structural 33,070A-F -2-1Z!~9936 -integrity and yet resistance to ionic movement through the membrane is reduced.
While the foregoing refers in general terms to the present assembly, the structure thereof and the method of manufacture are exempliied in the detailed description of the preferred embodiments following.
The invention particularly resides in a method of forming an assembly of an ion permeable membrane, electrode, and current collector, comprising the steps of:
(a) forming the current collector from a foundation layer of a porous, electrically conductive material;
(b) at least partially coating a fluoro-polymer binder on at least one surface of the foundation layer;
(c) forming the electrode by applying a particulate catalyst material over the fluoropolymer binder on the foundation layer;
(d) applying a fluoropolymeric material as a solution or dispersion over the catalyst material in a manner to obtain penetration of the fluoropolymeric material into the porous foundation layer to form a substantially continuous coating on the catalyst material and the at least partially coated foundation layer; said fluoropolymeric material forming the ion permeable membrane, and (e) applying heat and/or pressure to the assembly to enhance the flow of the fluropolymeric material into the foundation layer and around the catalyst material to obtain adherence of the catalyst material to the foundation layer and to sinter the 33,070A-F -3-~...,' . ~. ~....
l;~g9936 .
-3a-fluoropolymeric material into a substantially non-porous layer around the catalyst material.
33,070A-F -3a-A~
, ~
-~ 9 ~6 The foundation layer is an electrically conductive, hydraulically permeable matrix which acts as a current collector to transmit electrical energy to or from the electrode. It may be composed of a variety of substances, including carbon cloth, carbon paper, carbon felt, metallic screens, metallic felt, and porous metallic sheets. Preferably, however, the foundation layer is a carbon paper, which is readily available, performs well, is easily handled, and is relatively inexpensive.
The paper most preferably used in this invention is also one having low electrical resistivity, possessing sufficient strength for fabrication, and having adequate surface properties, such as roughness, to provide good bonding between the fluoropolymer binder and the foundation layer. It is also preferable to provide good electrical contact between the carbon paper and the catalytically active particles of the electrode.
As a beginning step, the foundation layer is at least partially coated with a suitable polymer binder.
This polymer binder can be a fluorocarbon polymer, such as polytetrafluoroethylene sold under the trademark of Teflon. Other suitable polymers can include thermo-plastic, non-ionic forms of sulfonic acid copolymers;
thermoplastic, non-ionic forms of carboxylic acid copolymers; and the like.
Particularly preferred as the fluoropolymer binder are thermoplastic, non-ionic forms of perfluor-inated polymers described in the following U. S. Patent Nos. 3,282,875; 3,909,378; 4,025,405; 4,065,366;
4,116,888; 4,123,336; 4,126,588; 4,151,052; 4,176,215;
33,070A-F -4-1~9936 4,178,218; 4,192,725; 4,209,635; 4,212,713; 4,251,333;
4,270,996; 4,329,435; 4,330,654; 4,337,137; 4,337,211;
4,340,680; 4,357,218; 4,358,412; 4,358,545; 4,417,969;
4,462,877; 4,470,889; 4,478,695; and published European Patent Application 0,027,009. Such polymers usually have equivalent weights of from 500 to 2000.
Particularly preferred for use as the fluoro-polymer binder are copolymers of monomer I with monomer II (as defined below). Optionally, a third type of monomer may be copolymerized with I and II.
The first type of monomer is represented by the general formula:
CF2-CZZ' (I) where:
Z and Z' are independently selected from -H, -Cl, -F, and -CF3 The second monomer consists of one or more monomers selected from compounds represented by the general formula:
(II) (CF2)a (cFRf)b-tcFRf.)c-o-[cF(cF2x)-cF2-o]n-cF=cF2 where:
Y is selected from -S02Z, -CN, -COZ, and -C(R3f)(R4f)OH;
Z is selected from -I, -Br, -Cl, -F, -OR and -NRlR2;
33,070A-F -5-~.ZW936 R is selected from a branched or linear alkyl radical having from 1 to 10 carbon atoms or an aryl radical;
R3f and R4f are independently selected from perfluoroalkyl radicals having from 1 to 10 carbon atoms;
R1 and R2 are independently selected from -H, a branched or linear alkyl radical havin~ from 1 to 10 carbon atoms or an aryl radical;
a is o-6;
b is 0-6;
c is 0 or 1;
provided a+b+c is not equal to 0;
,- 15 X is selected from -Cl, -Br, -F, or mixtures thereof when n~1;
n is 0 to 6; and Rf and Rf~ are independently selected from -F, -Cl, perfluoroalkyl radicals having from 1 to 10 carbon atoms, and fluorochloroalkyl radicals having from 1 to 10 carbon atoms.
Particularly preferred is when Y is -S02F or -CooCH3; n is 0 or 1; Rf and Rf~ are -F; X is -Cl or -F; and a+b+c is 2 or 3.
The third and optional monomer is one or more monomers selected from the compounds represented by the general formula:
(III) (CF2)a' (CFRf)b'-(CFR f)cl-o-[cF(cF2xl)-CF2-O]n,-CF=CF2 33,070A-F -6-where:
Y' is selected from -F, -Cl, or -Br;
a' and b' are independently 0-3;
c' is 0 or 1;
provided a'+b'+c' is not equal to 0;
n' is 0-6;
Rf and R'f are independently selected from -8r, -Cl, -F, perfluoroalkyl radicals having from 1 to lO
carbon atoms, and chloroperfluoroalkyl radicals having 0 from 1 to 10 carbon atoms; and X' is selected from -F, -Cl, -Br, or mixtures thereof when n'>1.
The binder is typically applied in a solution or dispersion to at least partially coat the foundation layer. The solution or dispersion can be applied to the foundation layer using a variety of methods well known in the art.
When the electrode is to be used in a fuel cell, preferably the binder is a hydrophobic material like polytetrafluoroethylene. When, however, the electrode is to be used in an electrolytic cell, such as a chlor-alkali cell, the binder is preferably a hydrophilic material like the copolymers formed from monomers I, II and, optionally III (described above).
The preferred loading, i.e. amount of application of the binder, is from 0.50 to 50 mg/cm2 of foundation area with a preferred range of from 2.5 to 30 mg/cm2 of foundation area.
When the binder is applied as a solution or a dispersion, the solvent/dispersant can be a variety of materials including, for example, water, methanol, 33,070A-F -7-~&
ethanol, and compounds represented by the general formula:
XCF2-CYZ-X ' wherein:
X is selected from F, Cl, Br, and I;
X' is selected from Cl, Br, and I;
Y and Z are independently selected from H, F, Cl, Br, I and R'; and R' is selected from perfluoroalkyl radicals and chloroperfluoroalkyl radicals having from 1 to 6 carbon atoms.
The most preferred solvents or dispersants are ,- 15 1,2-dibromotetrafluoroethane (commonly known as Freon 114 B 2) BrCF2-CF2Br and 1,2,3-trichlorotrifluoroethane (commonly known as Freon 113):
ClF2C-CC12F
Of these two materials, 1,2-dibromotetrafluoroethane is the most preferred solvent or dispersant.
The solution or dispersion used to apply the binder to the foundation layer may have a concentration of from 2 to 30 weight percent of polymer in the 3 solvent/dispersant. Preferably, the concentration is from 8 to 20 weight percent of polymer in the solvent/dispersant.
After the solution or dispersion has been applied to the foundation layer, the solvent can then be driven off using heat, a vacuum, or a combination of 33,070A-F -8--` 1299936 heat and a vacuum. Optionally, the solvent/dispersant may be allowed to evaporate under ambient conditions.
Preferably, the solvent is removed at an elevated temperature. In addition to removing the solvent/dispersant, the heat sinters the binder and causes it to more completely penetrate and surround the foundation layer. As an example, when polytetrafluoroethylene is used as the binder, exposure at a temperature of from 300C to 340C for about 20 minutes will suffice to remove the solvent/dispersant and to sinter the polytetrafluoroethylene.
The next step in the method of the present invention is the application of catalytically active and electrically conductive particles to the coated foundation layer. The composite structure will, ultimately, form what is commonly referred to as a solid polymer electrolyte, or SPE, when the composite is used in an electrochemical cell. The electrode can be ultimately used as either a cathode or as an anode.
Materials suitable for use as electro-catalytically active anode materials include, for example, metals or metal oxides of platinum group metals, such as ruthenium, iridium, rhodium, platinum, palladium, either alone or in combination with an oxide of a film-forming metal such as Ti or Ta. Other suitable activating oxides include cobalt oxide, either alone or in combination with other metal oxides, such as those described in U. S. Patent Nos. 3,632,498;
4,142,005; 4,061,549; and 4,214,971.
Materials suitable for use as electro-catalytically active cathode materials include, forexample, platinum group metals or metal oxides, such as 33,070A-F -9-lZ99936 --1 o ruthenium or ruthenium oxide. U. S. Patent No.
4,465,580 describes such cathodes.
The catalytic particles used in the present invention are preferably finely divided and have a preferred range of from 270 to smaller than 400 mesh size (U. S. Standard) (53 to less than 37 microns).
The metal powder is applied to the binder-coated foundation layer by methods known to those skilled in the art including, for example, spraying, forming a sheet of catalytic particles and pressing the sheet onto the foundation layer, or forming and applying the particles in the form of liquid dispersion, for example, an aqueous dispersion. A suitable loading of catalyst particles has been found to be from 0.2 to 20 mg/cm2 of foundation area with a preferred range of from 1.5 to 5.0 mg/cm2 of foundation area.
Separately, a copolymer is formed. One such suitàble polymer is the polymer formed from monomers I, II, and optionally III, as defined above. The polymer may be a thermoplastic, non-ionic precursor of a sulfonic acid copolymer or a thermoplastic, non-ionic precursor of a carboxylic acid copolymer, or a variety of other polymers as defined for use as the binder.
Preferably, the copolymer is formed into a solution or a dispersion with a solvent for application to the catalytically active particles. On mixing with a suitable solvent or dispersant, the polymer is applied to the catalyst particle coated foundation layer.
Utilizing a vacuum on one side of the foundation layer, the polymer in the solvent or dispersant is pulled onto the catalyst and into the foundation layer. While in one sense it can be described as coated on one side, 33,070A-F -10-the coating nevertheless sufficiently penetrates into the porous sheet.
In the step of bonding a fluoropolymer ontc the surface of the catalytic particle coated foundation layer, the most convenient procedure is the use of conventional organic solvents. Typical solvents used are 1,2-dibromotetrafluoroethane, methanol, ethanol, and the like. The polymeric material which is applied forms a substantially non-porous ion exchange layer.
The next step is the application of heat and/or pressure to remove the solvent/dispersant and to sinter the polymer, thereby forming the polymer into a substantially continuous sheet. In addition, the heat and/or pressure enhance the coating of the polymer around the catalyst particles and the foundation layer.
For example, exposure to a temperature in the range of from 260 to 320C is generally suitable to bond the polymer to the particles and the foundation layer. The temperature range is limited primarily by the onset of thermal degradation of the polymer caused by excessive heat. The pressure is preferably sufficiently high and sustained for an interval to achieve bonding. In one example, pressure may be applied up to about 5 kg/cm2 for about one minute at elevated temperature.
The next step in the manufacture of the improved electrode structure is to hydrolyze the structure from the non-ionic to the ionic form.
Hydrolysis may be accomplished by treating the polymer with a basic solution if the polymer is a thermo-plastic, non-ionic precursor of a sulfonic acid polymer or a thermoplastic, non-ionic precursor of a carboxylic acid polymer. In addition, if the polymer is a 33,070A-F -11--- 1~936 thermoplastic, non-ionic precursor of a carboxylic acid polymer, an acid solution may be used to hydrolyze the polymer. For example, in a thermoplastic, non-ionic precursor of a sulfonic acid polymer, the completed structure may be hydrolyzed in 25 weight percent sodium hydroxide for 16 hours at an elevated temperature of 80C.
The completed article is then ready for use.
As an example of typical size, it is not uncommon to encounter a membrane which is in a range of from 5 to 10 mils (0.125 to 0.25 mm) thick due to the need for structural integrity. The finished product can yield a membrane with a thickness in a range of from 1 to 2 mils (0.025 to 0.05), or even less. The resistance of ionic movement through the membrane is thus lowered by a significant amount.
In an alternate application, two similar sheets of equal size are positioned in contact with one another in a manner so that the foundation layers face toward the outside of the combination and the polymer layer on each sheet is contacted against the polymer layer on the other sheet. The coterminous sheets are then placed into a press and on the application of suitable pressure and/or heat, they are joined together.
33,070A-F -12-
Claims (11)
1. A method of forming an assembly of an ion permeable membrane, electrode, and current collector, comprising the steps of:
(a) forming the current collector from a foundation layer of a porous, electrically conductive material;
(b) at least partially coating a fluoro-polymer binder on at least one surface of the foundation layer;
(c) forming the electrode by applying a particulate catalyst material over the fluoropolymer binder on the foundation layer;
(d) applying a fluoropolymeric material as a solution or dispersion over the catalyst material in a manner to obtain penetration of the fluoropolymeric material into the porous foundation layer to form a substantially continuous coating on the catalyst material and the at least partially coated foundation layer; said fluoropolymeric material forming the ion permeable membrane, and (e) applying heat and/or pressure to the assembly to enhance the flow of the fluropolymeric material into the foundation layer and around the catalyst material to obtain adherence of the catalyst 33,070A-F -13-material to the foundation layer and to sinter the fluoropolymeric material into a substantially non-porous layer around the catalyst material.
(a) forming the current collector from a foundation layer of a porous, electrically conductive material;
(b) at least partially coating a fluoro-polymer binder on at least one surface of the foundation layer;
(c) forming the electrode by applying a particulate catalyst material over the fluoropolymer binder on the foundation layer;
(d) applying a fluoropolymeric material as a solution or dispersion over the catalyst material in a manner to obtain penetration of the fluoropolymeric material into the porous foundation layer to form a substantially continuous coating on the catalyst material and the at least partially coated foundation layer; said fluoropolymeric material forming the ion permeable membrane, and (e) applying heat and/or pressure to the assembly to enhance the flow of the fluropolymeric material into the foundation layer and around the catalyst material to obtain adherence of the catalyst 33,070A-F -13-material to the foundation layer and to sinter the fluoropolymeric material into a substantially non-porous layer around the catalyst material.
2. The method of Claim 1, wherein the fluoropolymeric material contains one or more solvents or dispersants selected from ethanol, methanol, water, and a compound represented by the general formula:
XCF2-CYZ-X ' wherein:
X is selected from F, C1, Br, and I;
X' is selected from C1, Br, and I;
Y and Z are independently selected from H, F, C1, Br, I, and R';
R' is selected from perfluoroalkyl radicals and chloroperfluoroalkyl radicals having from 1 to 6 carbon atoms, and;
XCF2-CYZ-X ' wherein:
X is selected from F, C1, Br, and I;
X' is selected from C1, Br, and I;
Y and Z are independently selected from H, F, C1, Br, I, and R';
R' is selected from perfluoroalkyl radicals and chloroperfluoroalkyl radicals having from 1 to 6 carbon atoms, and;
3. The method of Claim 2, wherein the solvent or dispersant is selected from 1,2-dibromotetra-fluoroethane and 1,2,3-trichlorotrifluoroethane.
4. The method of Claim 1, 2, or 3, wherein the catalyst particles are selected from ruthenium, iridium, rhodium, platinum, palladium, or oxides thereof either alone or in combination with an oxide of a film-forming metal, and cobalt oxide either alone or in combination with other platinum group metal or metal oxide.
5. The method of Claim 1, 2 or 3, including the step of making two similar sized assemblies, placing the two assemblies together such that the fluoro-polymeric surfaces are in intimate contact with each 33,070A-F -14-other, and applying heat and/or pressure to form a single planar assembly containing two current collectors and having a non-porous, ionically conductive polymer layer therebetween.
6. The method of Claim 1, wherein said fluoropolymer binder for the foundation layer is a thermoplastic, non-ionic precursor of a sulfonic acid copolymer having an equivalent weight range of from 500 to 2000.
7. The method of Claim 1, wherein said fluoropolymer binder for the foundation layer is a thermoplastic, non-ionic precursor of a carboxylic acid copolymer.
8. The method of Claim 1, wherein:
(a) said electrically conductive material is porous conductive graphite paper, (b) said fluoropolymeric binder is polytetra-fluoroethylene, and (c) said fluoropolymeric material is a sulfonic acid copolymer in thermoplastic powder form in a liquid solvent, and drawing a vacuum on the assembly to promote penetration of the fluoropolymeric material into the porous graphite paper.
(a) said electrically conductive material is porous conductive graphite paper, (b) said fluoropolymeric binder is polytetra-fluoroethylene, and (c) said fluoropolymeric material is a sulfonic acid copolymer in thermoplastic powder form in a liquid solvent, and drawing a vacuum on the assembly to promote penetration of the fluoropolymeric material into the porous graphite paper.
9. The method of Claim 1, including the step of exposing the fluoropolymeric material to a base or to an acid at a temperature and for a time sufficient to hydrolyze substantially all of the polymer.
10. The method of Claim 1, wherein the fluoropolymer binder is a copolymer formed from the polymerization of one or more monomers selected from the group of monomers represented by the general formula:
33,070A-F -15-CF2=CZZ' (I) where:
Z and Z' are independently selected from -H, -C1, -F, or -CF3;
with one or more monomers selected from a second group of monomers represented by the general formula:
(II) y-(CF2)a-(CFRf)b-(CFRf,)c-O-[CF(CF2X)-CF2-O]n-CF=CF2 where:
Y is selected from -SO2Z, -CN, -COZ, and -C(R3f)(R4f)OH;
Z is selected from -I, -Br, -C1, -F, -OR, and -NR1R2;
R is selected from a branched or linear alkyl radical having from 1 to 10 carbon atoms or an aryl radical;
R3f and R4f are independently selected from perfluoroalkyl radicals having from 1 to 10 carbon atoms;
R1 and R2 are independently selected from -H, a branched or linear alkyl radical having from 1 to 10 carbon atoms, and an aryl radical;
a is 0-6;
b is 0-6;
c is 0 or 1;
provided a+b+c is not equal to 0;
X is selected from -C1, -Br, -F, and mixtures thereof when n>1;
n is O to 6; and Rf and Rf' are independently selected from -F, -C1, perfluoroalkyl radicals having from 1 to 10 carbon atoms, and fluorochloroalkyl radicals having from 1 to 33,070A-F -16-10 carbon atoms, and optionally, one or more monomers selected from a third monomer represented by the general formula:
(III) Y'-(CF2)a'-(CFRf)b'-(CFR'f)c'-O-[CF(CF2X')-CF2-O]n,-CF=CF2 where:
Y' is selected from -F, -C1, or -Br;
a' and b' are independently 0-3;
c' is 0 or 1;
provided a'+b'+c' is not equal to 0;
n' is 0-6;
Rf and R'f are independently selected from -Br, -C1, -F, perfluoroalkyl radicals having from 1 to 10 carbon atoms, and chloroperfluoroalkyl radicals having from 1 to 10 carbon atoms; and X' is selected from -F, -C1, -Br, and mixtures thereof when n'>1.
33,070A-F -15-CF2=CZZ' (I) where:
Z and Z' are independently selected from -H, -C1, -F, or -CF3;
with one or more monomers selected from a second group of monomers represented by the general formula:
(II) y-(CF2)a-(CFRf)b-(CFRf,)c-O-[CF(CF2X)-CF2-O]n-CF=CF2 where:
Y is selected from -SO2Z, -CN, -COZ, and -C(R3f)(R4f)OH;
Z is selected from -I, -Br, -C1, -F, -OR, and -NR1R2;
R is selected from a branched or linear alkyl radical having from 1 to 10 carbon atoms or an aryl radical;
R3f and R4f are independently selected from perfluoroalkyl radicals having from 1 to 10 carbon atoms;
R1 and R2 are independently selected from -H, a branched or linear alkyl radical having from 1 to 10 carbon atoms, and an aryl radical;
a is 0-6;
b is 0-6;
c is 0 or 1;
provided a+b+c is not equal to 0;
X is selected from -C1, -Br, -F, and mixtures thereof when n>1;
n is O to 6; and Rf and Rf' are independently selected from -F, -C1, perfluoroalkyl radicals having from 1 to 10 carbon atoms, and fluorochloroalkyl radicals having from 1 to 33,070A-F -16-10 carbon atoms, and optionally, one or more monomers selected from a third monomer represented by the general formula:
(III) Y'-(CF2)a'-(CFRf)b'-(CFR'f)c'-O-[CF(CF2X')-CF2-O]n,-CF=CF2 where:
Y' is selected from -F, -C1, or -Br;
a' and b' are independently 0-3;
c' is 0 or 1;
provided a'+b'+c' is not equal to 0;
n' is 0-6;
Rf and R'f are independently selected from -Br, -C1, -F, perfluoroalkyl radicals having from 1 to 10 carbon atoms, and chloroperfluoroalkyl radicals having from 1 to 10 carbon atoms; and X' is selected from -F, -C1, -Br, and mixtures thereof when n'>1.
11. The method of Claim 10, wherein Y is -SO2F or -COOCH3; n is 0 or 1; Rf and Rf' are -F; X is -C1 or -F; and a+b+c is 2 or 3.
33,070A-F -17-
33,070A-F -17-
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA000544302A CA1299936C (en) | 1987-08-12 | 1987-08-12 | Current collector bonded to a solid polymer membrane |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA000544302A CA1299936C (en) | 1987-08-12 | 1987-08-12 | Current collector bonded to a solid polymer membrane |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1299936C true CA1299936C (en) | 1992-05-05 |
Family
ID=4136246
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000544302A Expired - Lifetime CA1299936C (en) | 1987-08-12 | 1987-08-12 | Current collector bonded to a solid polymer membrane |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA1299936C (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6428584B1 (en) | 1997-10-10 | 2002-08-06 | 3M Innovative Properties Company | Membrane electrode assemblies |
-
1987
- 1987-08-12 CA CA000544302A patent/CA1299936C/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6428584B1 (en) | 1997-10-10 | 2002-08-06 | 3M Innovative Properties Company | Membrane electrode assemblies |
| US6432571B1 (en) | 1997-10-10 | 2002-08-13 | 3M Innovative Properties Company | Membrane electrode assemblies |
| US6613106B1 (en) | 1997-10-10 | 2003-09-02 | 3M Innovative Properties Company | Membrane electrode assemblies |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0786156B1 (en) | Process of imprinting catalytically active particles on membrane | |
| JP3546055B2 (en) | Method of printing catalytically active particles on a membrane | |
| CA2121937C (en) | Membrane and electrode structure | |
| US5470448A (en) | High performance electrolytic cell electrode/membrane structures and a process for preparing such electrode structures | |
| US4992126A (en) | Method for making a current collector bonded to a solid polymer membrane | |
| US6238534B1 (en) | Hybrid membrane electrode assembly | |
| CA1315239C (en) | Solid polymer electrolyte electrode | |
| JP2011103308A (en) | Method for manufacturing catalyst coated film | |
| JP2010505222A (en) | Structure for gas diffusion electrode | |
| EP0305565B1 (en) | Current collector bonded to a solid polymer membrane | |
| JPH0248632B2 (en) | ||
| CA1293952C (en) | Method for forming a solid polymer electrolyte structure by pressing catalyst into membrane | |
| CA1299936C (en) | Current collector bonded to a solid polymer membrane | |
| JP4870328B2 (en) | Method for manufacturing membrane-electrode assembly | |
| FI84497B (en) | Collector which is bonded to a solid polymer membrane | |
| KR900007728B1 (en) | Current collector bonded to a solid polymer membrane | |
| JPS61230266A (en) | New gas diffusion electrode | |
| NO169465B (en) | POWER COLLECTOR CONNECTED TO A SOLID POLYMER MEMBRANE | |
| DE3784348T2 (en) | ELECTRIC COLLECTOR CONNECTED TO A SOLID POLYMER MEMBRANE. | |
| CA1323556C (en) | Method for forming a solid polymer electrolyte structure | |
| EP0064838A1 (en) | Composite membrane/electrode, electrochemical cell and electrolysis process | |
| CN1012687B (en) | Current collector combined with solid high-polymer membrane | |
| JPS6325076B2 (en) |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |