EP0346397A1 - Hydrogel loaded active layer in pressure tolerant gas diffusion electrodes - Google Patents

Abstract

Gas diffusion electrodes (12) and electrochemical cells (10) generating or consuming gas and using said electrodes. The electrode (12) is composed of an electronically conductive and electrochemically active porous body defining respective gas and electrolyte contact surfaces (15, 17) with a material substantially impermeable to gas filling at least part of the volume of the pores of said body so as to prevent the passage of gas through this part. The material consists of a hydrophilic hydrogel insoluble in the electrolyte, ionically ionomeric conductor, formed by co-precipitation between at least two precursor polymers.

Description

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HYDROGEL LOADED ACTIVE LAYER IN PRESSURE TOLERANT GAS DIFFUSION ELECTRODES

BACKGROUND OF THE INVENTION

Field of. the Invention

This invention relates generally to gas diffusion electrodes and, more particularly, this invention relates to gas diffusion electrodes adapted for use in electrochemical cells utilizing an aqueous alkaline electrolyte and consuming or generating a gas via the electrochemical process occurring within the gas diffusion electrode.

Description of Related Art

The use of gas diffusion electrodes in fuel cells and metal-air batteries is well known. Gas diffusion electrodes have also been used in the electrolysis, either oxidation or reduction, of gaseous reactants. It is also possible to generate gases in such electrodes. In general, gas diffusion electrodes take the form of solid porous (gas and liquid permeable) bodies formed at least in part of an electronically conductive, electrochemically active material, and may include a catalyst. Such electrodes generally define an electrolyte contacting surface and a gas contacting surface. Electrochemical oxidation and reduction occur at the points in the electrode where the gas to be oxidized or reduced contacts both the electrode and the active material of the electrode. In the case of gas generation, electrolyte contacts the active material and gas is generated at this interface. Electrochemical cells utilizing such electrodes generally comprise the gas diffusion electrode, a spaced counter electrode, a liquid electrolyte (which is generally aqueous) which contacts both the counter electrode and the gas diffusion electrode, and a gas which contacts the gas diffusion electrode either (1) for reduction or oxidation of the gas or (2) produced via electrolytic generation. Circuit connections are disposed between the counter and gas diffusion electrodes. Additionally, the counter electrode may also be a gas diffusion electrode. A well known example of such a design is the H₂/θ2 fuel cell. Electrochemical batteries_r for example, the metal air type, commonly utilize either an aqueous alkaline or neutral (e.g., saline) electrolyte, while fuel cells may commonly utilize either acidic electrolytes or alkaline electrolytes. Other types of electrolytes are also use, depending upon the specific gas which is consumed or generated.

The use in electrochemical batteries of an oxygen-containing gas^' such as air which is reduced at the gas diffusion electrode. For example, hydrogen gas is oxidized in some fuel cells. The present invention is generally applicable to all such types of gas diffusion electrodes and cells.

The electronically conductive material in a gas diffusion electrode typically may be carbon. Additionally, a wide variety of catalyst such as platinum or transition metal organometallic catalysts (such as porphyrins) are available.

In various applications, it is desirable that either or both the liquid electrolyte and the gaseous electrode reactant be flowed through the body of the cell over the electrode surfaces. Flowing electrolyte and/or flowed gaseous reactant are of course accompanied by a pressure drop across the cell, especially on the electrode side. This can be lead to excess pressures either on the gas-side or the electrode-side of the electrode. Furthermore, it may be desirable in certain circumstances to operate at an elevated gas pressure with respect to the electrolyte pressure. One example of such a situation would be one in which the performance is increased by pressurizing the gaseous reactant. In battery and fuel cell applications, it is desirable to obtain as high a cell voltage as possible at any given current density. One means of accomplishing this is to utilize a relatively high gas pressure or flow rate.

The use of a porous (e.g. typically 30-60% porosity) gas diffusion electrode, however,, poses difficult flow management problems. When gas pressure exceeds liquid electrolyte pressure by a sufficient amount, "blow-through" of gas through the electrode into the liquid electrolyte results. In conventional gas diffusion electrodes, this so-called "blow-through pressure" is usually much lower than is desirable for tolerance of substantial differential pressures between the gas and liquid sides of the cell.

For example, while it may be desirable to operate a cell at a gas vs. liquid differential pressure of up to 10 psi or more, typical air cathodes exhibit a gas blow-through pressure of less than about 0.25 psi. If the differential pressures exceeds the blow-through pressure, pumping of gas into the liquid electrolyte may result. (Typical blow-through pressures range from 0-1 psi, and are determined primarily by interfacial tension and pore size distribution) . Conversely, if the liquid electrolyte pressure is higher than the gas pressure and the differential pressure exceeds the liquid bleed-through pressure, liquid may be pumped into the gas side of the cell, which may result in liquid in the gas manifold with consequent pumping problems and a decrease in cell performance and useful cell life due to flooding of the active layer of the electrode. In gas-generating cells it is customary for the gas to be generated on the front face (electrolyte- side) of the electrode. The gas is thus generated as bubbles in the electrolyte, which can lead to removal of electrolyte from the cell and increased oh ic losses. Generation of gas in a gas diffusion electrode is more desirable because the gas can exit the cell directly through the back of the electrode. Operation in this mode would require a certain amount of pressure tolerance. Even higher pressure tolerance would be required if the gas is generated in a pressurized state.

If the differential pressure between the gas and liquid sides of an electrochemical cell using a porous gas diffusion electrode is to be maintained at a low level, impractical pressure management problems result, especially in view of the fact that pressure levels vary from point to point on each side of the electrode.

The problems described are not readily. amenable to correction by the use of a gas barrier material between the gas and electrolyte sides of the electrode, since such barriers tend to block the flow of electrolytic ions through the electrode and also strongly contribute to voltage losses or do not allow operation at a sufficiently high current density for the desire application. It is desirable to maintain the potential across the electrode at as positive a level as possible while maintaining as high a current density as possible. For example, it may be desired to operate a cell at a current density of up to as high as 500 mA/cm , typically at 100 mA/cm², while minimizing the voltage loss across the electrode. A voltage loss of less than 0.05 volts is preferred, with voltage losses of up to 0.25 volts being generally acceptable. One approach to solving these problems is disclosed in Juda and Ilan U.S. Patent No. 4,514,575 (September 30, 1986), which involves the use of nonionic polymeric hydrogel as a layer applied by painting onto the electrode side of the gas diffusion electrode. The maximum pressure tolerance disclose by the Juda, et al. patents is less than or equal to 40 inches of water

(1.44 psi or 10.0 kPa), which is significantly less than that possible with the present invention.

It is an object of the present invention to overcome one or more of the problems described above. According to the present invention, an ionomeric, ionically conductive, substantially gas impermeable material is disposed within the pore volume of a porous gas diffusion electrode adapted for use in a gas generating or consuming electrochemical cell utilizing a liquid electrolyte. The material comprises •a hydrophilic ionic polymer form by by coprecipitation Of at least two precursor polymers.

The invention also comprehends an electrochemical cell comprising the gas diffusion electrode spaced from a counter electrode and in contact with a liquid electrolyte. A gas to be oxidized, reduced or generated is in contact with the gas side of the electrode, and circuit connections are disposed between the counter and gas diffusion electrodes. The electrode and cell of the invention are capable of operating at very high gas v. electrolyte differential pressures at high current densities without significant voltage loss.

Other objects and advantages of the invention will be apparent to those skilled in the art from a review of the following detailed description taken in conjunction with the drawings and the appended claims. BRIEF DESCRIPTION OF THE DRAWINGS

Fig 1. is a transverse sectional view of one embodiment of an electrochemical cell in which the invention may be utilized;

Fig. 2 is a schematic sectional view of a typical gas diffusion electrode with which the invention may be utilized;

Fig. 3 is a sectional view of an electrode holder useful in testing gas diffusion electrodes;

Fig. 4 is a schematic exploded perspective view of an electrode assembly adapted for use with the electrode holder of Fiq. 3;

Fig. 5 is a schematic transverse sectional view of an electrode as use in Figs. 3 and 4;

Fig» 6 is a series of polarization curves exhibited by an electrode made according to the invention; and

Fig. 7 is a polarization curve exhibited by another embodiment of an electrode made according to the invention.

DETAILED DESCRIPTION OF THE INVENTION

Fig. 1 illustrates a typical embodiment of an electrochemical battery utilizing a gas diffusion electrode. This particular cell is an aqueous alkaline lithium-air cell. It is to be understood that the present invention is not limited to use in electrochemical batteries, not to cells in which gas is consumed. Rather, the invention finds wide applicability in cells in which gas is either consumed or produced, via either consumed or produced, via either reduction or oxidation, in which any of various electrolytes are used, etc. The cell of Fig. 1 is described in detail in U.S. Patent No. 4,528,249 (July 9, 1985) the disclosure of which is incorporated by reference.

In Fig. 1, an electrochemical cell, generally designated 10, includes an anode 11, a gas consuming cathode 12, and a metal screen 13 interposed between the anode 11 and cathode 12 within an outer housing 14. In the embodiment of Fig. 1, the screen 13 is in electrical contact with the cathode 12, and is in mechanical (but not electrical) contact with the anode 11.

In the exemplary embodiment, the anode 11 comprises a lithium anode, which may comprose elemental lithium metal or lithium alloyed with alloying material such as small amounts of aluminum. The screen 13 is not in electrical contact with the anode 11, due to the presence of an insulating, porous lithium hydroxide (LiOH) film which is formed on the anode surface by contact thereof with humid air, and is well known in the art. It is to be noted, however, that this particular feature is peculiar to the aqueous lithium-air cell. In other types of metal-air batteries and fuel cells, either an electrically insulating porous separator layer or a simple electrolyte gap would be used. It should also be noted that the screen 13 is necessary to help restrain the gas diffusion electrode 12 against the gas pressure.

The cathode 12 is in this case an air cathode through which atmospheric air flows. Those skilled in the art, however, will recognize that such a cathode may operate with any oxygen-containing gas.

One surface 15 of the cathode 12 is exposed to ambient atmosphere (or a source of another oxygen- containing gas) in a chamber 16 of the housing 14, and the opposite surface 17 of the cathode 12 is contacted by the liquid electrolyte 18 which is flowed through a second chamber 19 in the housing 14 as by a suitable pump 20. In the illustrated embodiment, the electrode is provided from a reservoir 21 for suitable delivery when needed.

In Fig. 1, the anode 11 and cathode 12 each terminate in a respective terminal 26 or 28, and are connected to a load 30 through suitable circuit connections 32.

Typically, the cathode 12 comprises a structure formed of a suitable porous hydrophobic material, such as polytetrafluoroethylene (PTFE), mixed with carbon black, both pure and catalyst-containing. A preferred form of the cathode 12 is described below in connection with Fig. 2.

The screen 13 illustratively may comprise a woven metal wire screen formed of suitable non-corroding metal, which in the case of alkaline electrolyte may be nickel or silver plated nickel. If desired, the screen 13 may serve as a current collector if connected to the teminal 28. In the embodiments of Fig. 1 , liquid electrolyte, in this case an aqueous alkaline electrolyte such as aqueous lithium hydroxide, is flowed through the chamber 19 by means of the pump 20. As such, there is a pressure drop across the chamber 19 in the direction of flow.

Further, air is flowed through the chamber 16 by means not shown, and there is a small pressure drop across the chamber 16 in the direction of flow by virtue thereof. However, those skilled in the art will recognize that the pressures drop across the gas chamber 16 is small in comparison to that in the electrolyte chamber 19.

As set forth above, Fig. 1 is intented to be exemplary only, as the invention is applicable to any of a variety of types of gas diffusion electrodes and electrochemical cells. Fig. 2 is a schematic depiction of the structure of a preferred embodiment of the cathode 12. As shown in Fig. 2, the electrode 12 is formed essentially of a two or three component laminate defining the gas contacting surface 15 and the opposed electrolyte contacting surface 17. An electronically conductive porous gas carrier layer 40 defines the gas contacting surface 15 and typically is a mixture of a hydrophobic material such as porous PTFE (e.g. Teflon brand PTFE) with a carbon black such as Shawinigan black (Cheveron Chemical Co.. Olefins and Derivatives Div., Houston, TX) . A so-called "active layer" 42 comprises a layer 44 which comprises a mixture of carbon black, or catalyst supported on carbon black and PTFE. An optional layer 46 of catalyst is disposed on the layer 44 at an interface 50. As shown in the schematic of Fig. 2, layers 44 and 45 appear to be discrete layers, but in practice may define a single layer or two layers, since the catlayst is generally adsorbed onto the surface of the material of layer 44. In some cases, the material of the three layers 40, 44 and 46 may be intermixed in a single layer.

The entire structure of the electrode 12 of Fig. 2 is porous, generally exhibiting a porosity of 30- 60%.

A typical catalyst forming the layer 44 is heat-treated cobalt tetramethoxyphenyl porphyrin (CoTMPP) on a carbon black such as Vulcan XC-72 (Cabot Corp., Billerica, MA). The heat treatment is typically done at 400-1000°C in inert gas. The structure of CoTMPP is shown below:

This material is a currently preferred catalytic material. Other catalysts include platinum, Mn0₂ and transition metal macrocycles other than CoTMPP. The function of the layer 40 is to allow ready transmission of gas to the active layer 44. Its hydrophobicity also acts to repel liquid electrolyte which exists in the active layer 44 in order to avoid leakage of the liquid electrolyte into the gas side of the cell. It also provides electronic conductivity. The requisite consumption or generation of gas takes place in the active layer 44 where gas and liquid meet in the presence of the active material and optional catalyst, as is we°ll known in the art.

Fig. 3 illustrates an electrode holder useful in measuring characteristics of gas consuming or generating electrodes. The electrode nolder, generally designated 60, comprises a solid body 62 of a nonconductive material defining a gas inlet passage 64 communicating with a cell gas chamber 55 which in turn communicates with a gas outlet passage 68. (A typical material of construction for the body 62 is 3M's Kel-F brand chloro fluorocarbon polymer.) An annular electrode seat 70 is definded in the body 62 in order to position an electrode assembly (not shown in Fig. 3) which includes a gas diffusion electrode, generally designated 72, adjacent the cell chamber 66. A conductive (e.g. platinum) wire 74 contact the seat 70 and extends therefrom through the outlet passage 68. A threaded plug 76 of the same material as the body 62 retains an electrode assembly 80 (shown in Fig. 4) in place in the body 62.

Fig. 4 illlustrates the electrode assembly, generally designated 80, which includes the gas diffusion electrode 72 of Fig. 3. The electrode 72 is shown in schematic form in Fig. 4 and formed as a cylindrical disk defining gas and electrolyte contacting surfaces 82 and 84 respectively. These surfaces are analogous to surface 15 and 17 of Fig. 1. An annular conductive metal (e.g. platinum) ring 86 is disposed on the gas surface_, 82 between the gas surface 82 and an annular rubber gasket 88. A similar rubber gasket 90 is disposed on the electrolyte side of the electrode 72 between the electrolyte contacting surface 84 and an annular ring 92 of the same material as the body 62.

When the assembly 80 is in place in the seat 70 of the electrode holder 60, the ring 86 is in electrical contact with the wire 74 and acts as a current collector.

The electrode 72 as shown in Figs. 3 and 4 is schematic and these figures do not illustrate certain components such as the hydrophobic backing layer and associated screens. Fig. 5 illustrates an exploded sectional schematic view of a typical embodiment of the diffusion electrode 72. A silver plated nickel screen 100 is adjacent to and in contact with an electronically conductive hydrophobic backing layer 102, typically of Teflon brand PTFE plus carbon black, which defines the surface 82. An active layer 104, which may include a catalyst on carbon black, is adjacent to the layer 102 and defines the surface 84. A steel reinforcement screen 108 is adjacent the active layer 104. When constructed, the screen 100 is not a physical or electrical contact with the ring 186 and this merely acts as a physical restraint. The gas inlet passage 64 and gas outlet passage 68 are connected with gas flow regulating means (not shown) which regulate the flow of gas through the passages 64 and 68 and the cell chamber 66, and thus the gas pressure in the chamber 66 .

Those skilled in the art will recognize that the screens 100 and 108 may be embedded in the layer 102, and that the layers 102 and 104 may form a single homogenous layer if desired.

When the electrode 72 is in place in the assembly 80 in the electrode holder 60, a central circular segment of each of the electrode holder 60, a central circular segment of each of the electrode surfaces 82 and 84 is exposed to gas and electrolyte sources, respectively. The electrode holder body 62 is positioned in a test cell such that the electrode holder body 62 is positioned in a test cell such that the electrode surface 894 is exposed to a flowing or non- flowing (e.g. stirred) electrolyte,. The remainder of the cell and associated temperature control means, etc. are omitted for clarity.

For operation at elevated gas/electrolyte differential pressures, the steel screen 108 acts as a reinforcement to prevent physical rupture of the electrode 72. Flow-through of gas from the cell chamber 66 through the electrode 72 into the electrolyte side of the cell is prevented by a hydrophilic hydrogel polymer dispersed through at least a portion of the body of the electrode 72. The hydrogel is an ionomeric polymer which is substantially impermeable to the gross passage of gas and which is ionically conductive. It conducts hydroxide (OH^~) as well as water. It is also possible for bulk electrolyte to slowly diffuse through the hydrogel. The electrode 72 may be effectively wetted through the hydrogel, while the electrode 72 is virtually impermeable to gas flow by virtue of the presence of the hydrogel in the pore volume of the electrode.

The hydrogel-forming coprecipitation reaction takes place between at least two precursor polymers which can react together to coprecipitate to form a hydrophilic hydrogel which is insoluble or substantially insoluble in the electrolyte. Preferably, each precursor polymer is individually soluble in the electrolyte as this facilitates removal of any excess reactant present in the hydrogel.

At least one of the precursor polymers is an ionic polymer. Where the electrolyte is an alkaline electrolyte, it is preferred that a cationic polymer (e.g. containing ammonium or pyridinium groups, either pendent or part of the polymer claim) is reacted with an anionic or no-ionic polar polymer. In alkaline media, it is preferred that the ratio of the number of equivalents of the cationic to the anionic polymer be greater than 1. In acidic media, this ratio is typically reversed.

If both precursor polymers are ionic polymers, the reaction product may be referred to an an "ion pair bonded polymer".

The method of formation of the hydrogel layer is very simple, as is known in the art, and may conveniently be carried out by mixing of solutions of the polymers. The solvent is one in which the hydrogel is insoluble. As stated above, the ratios of the number of equivalent of the respective precursor polymers will generally be greater than one-, and typically in the range of 3-100:1, depending on the type of electrolyte to be used. In the case of an alkaline electrolyte, the ratio of the number of equivalent of the cationic polymer applied as compared to the weight of applied anionic polymer will generally be greater than one and may range as high as 100:1 or more. This is conveniently carried out by varing the concentrations of the polymers in their respective solutions, with use of approximately equal volumes of polymer solutions.

Any solvent which does not damage the electrode structures and in which the polymers are soluble may be used, including aqueous solvent, alcohols, ethers or other organic solvents. It is preferred, however, to use at least one and preferably both of the precursor polymers in low polarity organic solution whereby premature swelling of the polymers is avoided or minimized.

It is important that the coprecipitated hydrogel be swellable upon contact with electroylyte as this enhances the gas impermeability characteristics of the layer.

Although a wide variety of precursor polymers are applicable _r the currently preferred cationic polymer is poly (diallyl dimethyl ammonium chloride), abbreviated pDMDAAC. The currently preferred anionic polymer is poly (styrene sulfonic acid), abbreviated PSSA. Both materials are available for Polysciences of Warrington, Pennsylvania. pDMDAAC is available as a 15 wt. percent solids solution in water, while PSSA is available in a molecular weight of 70,000 in a 30 wt. percent solids solution in water. The equivalent weights for pDMDAAC and PSSA, respectively, are 161 and 185. Although the use of either of these materials probably would provide a pressure tolerant gas diffusion electrode in that neither microscopically passes gases, and both contain and pass ions, each of these polymers is independently soluble in the electrolyte and would promptly wash out of the electrode body once placed in use. However, the combination of the two polymers with opposite charges on the molecular strands thereof results in a coprecipitated, insoluble hydrophilic gel. This gel retains substantially all of the advantageous qualities of the original components, yet is insoluble in the electrolyte and should not wash out of the electrode. After exposure to water, such a hydrogel may contain up to 99.5 wt. percent (or more) water.

In a preferred form of the invention, the first precursor polymer is a cationic polymer and the second precursor polymer is an anionic polymer which is perfluorinated. A preferred perfluorinated polymer is a perfluorosulfonic acid polymer sold by DuPont under the trademark NAFION (equivalent weight = 1100). Nafion solution in lower alcohols from Aldrich was used. It is currently available from solution Technology, Mendenahall, PA. This is a chemically stable ion exchange resin.

Reaction of the cationic polymer with the perfluorinate polymer results in a partially fluorinated hydrogel. This hydrogel is expected to have the particular advantages of high oxygen solubility and low rates of chemical decomposition. In general, in electrochemical systems it is advantageous to utilize fluorinated components, especially perfluorinated materials, due to the extreme resistance to chemical attack for such materials. Furthermore, for systems using oxygen the relatively high solubility of oxygen in fluorocarbon materials is advantageous. In particular, the use of fluorinated species in gas diffusion electrodes provides twofold advantages. The high oxygen solubility results in improved electrode (e.g. cathode) voltages, while enhanced chemical stability results in the delay of failure of the device due to chemical attack of the fluroinated species.

The hydrogel is preferably preformed prior to incorporation into the electrode. Incorporation into the electrode may readily be carried out by simple mixing with the material of the active layer prior to forming the active material into the electrode. Preferably, a hydrogel-containing active layer is formed and subsequently joined to a hydrophobic layer in order that the hydrophobic layer be free of the hydrophilic gel, so that the function of the hydrophobic layer is not compromised.

EXAMPLES

The following specific examples are intended to illustrate the practice of the invention but are not to be considered limiting in any way.

The following generalized experimental procedure was followed in each example.

Cobalt tetramethoxyphenyl porphyrin (CoTMPP) was adsorbed on Vulcan XC-72 carbon (Cabot) by agitating a suspension of the latter in a solution of 10^~4 M

CoTMPP in acetone for at least 24 hours. The amount of the adsorbed macrocycle was calculated spectrophotometrically be determining its loss from the filtered solution. The solid catlayst/carbon was air- dried and then heat-treated to 450°C in a horizontal tube furnace under continuous flow of purified argon.

Porous gas-fed electrodes were fabricated as follows: dilute (-2 mg/mL) Teflon T30 B aqueous suspension (DuPont) was slowly added to an aqueous suspension of the catalyst/carbon while the latter was ultrasoήically agitated. The mixed suspension was then filtered with a lμm pore size polycarbonate filter membrane. A polymeric hydrogel material was mixed with the supsension and then worked with spatula. The paste was shaped into a 1.75 cm diameter disk in a stainless steel die using hand pressure. This disk was then applied to another disk, -0.5 mm thick, of Teflon-carbon black hydrophobic porous sheet material (EΪtech Systems Corp., Fairport Harbor, OH) which contained a silver- plated Ni mesh. This dual layer disk was pressed at 380 kg/cm^ at room temperature and then air dried.

The gas-fed electrode was place in Teflon-Kel- F electrode holder as shown in Fig. 3. The gas (O2 or air) pressure was applied to the back-side (hydrophobic layer) of the electrode and was monitored at the outlet. A needle valve at the outlets was used to regulate the gas pressure. The O2 reduction measurements for the gas-fed electrodes were done galvanostatically in a concentrated alkaline electrolyte (0.5 M LiOH in 2:1 v/v/ 50% NaOH and 45% KOH) at 80°C with a research potentiostat (Stonehard Associates, Model BC1200). This potentiostat is equipped with positive feedback IR drop compensation and correction circuits. The IR drop correction adjustment is made while monitoring the potential on an oscilloscope, with the current repetitively interrupted for 0.1 us every 1.1 s. This procedure corrects for any IR drop that is external to the electrode itself. Nickel foil was used as the counter electrode and Hg/HgO, OH^~ reference electrode was used. The polarization curves were recorded under steady-state conditions.

An air cathode was prepared as generally described above with a hydrogel formed by reaction of pDMDAAC and PSSA, both in methanol solution, with a 10:1 pDMDAAC:PSSA weigth ratio (11.5:1 equivalent ratio). The cathode was tested for oxygen reduction with both air and oxygen at a gas/electrolyte differential pressure of 1 psi (5.9 kPa) at 100°C. Results are shown in Fig. 6. When operating with oxygen, measurements were taken both with increasing (Run 1) and decreasing (Run 2) current densities.

The relatively high potential exhibited with both air and oxygen and the low slope of both curves are excellent. The potential at 100 mA/cm² was —60 V vs. Hg/HgO, OH-. This is -10 V more positive than that obtained for an electrode prepared without hydrogel.

In the following example, an air cathode which could withstand an overpressure of at least 70 kPa (10.1 psi) without blow-through and which had relatively low polarization was prepared. As in the previous example, an ion-pair copolymer of pDMDAAC, containing quaternary amines, and Nafion brand fluorocarbon polymer, containing sulfonic acid groups, was used as an ingredient of the- active layer. This copolymer readily swells with H₂0 and forms a hydrogel. When used as a component of the active layer it fills the volume normally occupied by the liquid electrolyte. While the electrode in Fig. 6 was made from heat-treated CoTMPP on XC-72 carbon, the CoTMPP in this electrode was not heat- treated. The 0₂ reduction polarization behavior for this electrode is shown in Fig. 7. The electrode has also been tested with 70 kPa (10.1 psi) overpressure for about 16 hours at 100 mA/cm². No blow-through or significant variation of the potential were observed over this period.

Operation at high current densities (e.g. up to about 1 A/cm^ or more) is possible according to the invention.

Examination of the polarization curves presented above shows that according to the invention, very great increases in current (i.e. in current density) are available with only minor increases in the potential driving force over a wide range of current densities.

The forgoing detailed description is given for clearness of understanding, and no unnecessary limitations are to be inferred therefrom as modifications within the scope of the invention will be obvious those skilled in the art.

Claims

We claim:

1. A gas diffusion electrode adapted for use in a gas generating or consuming electrochemical cell utilizing a liquid electrolyte, said electrode comprising an electronically conductive and electrochemically active porous body defining respective gas and electrolyte contacting surfaces, with a substantially gas impermeable material filling at least a portion of the pore volume of said body so as to prevent gas passage there through, said material comprising an electrolyte-insoluble, ionomeric ionically conductive hydrophilic hydrogel formed by formed by coprecipitation between at least first and second precursor polymers.

2. The electrode of claim 1 wherein said first precursor polymer contains cationic groups and said second precursor polymer contains anionic or polar groups.

3. The electrode of claim 2 wherein said electrolyte is an alkaline aqeuous electrode and the ratio of the number of equivalents of said first precursor polymer to said second precursor polymer is greater than 1.

4. The electrode of claim 3 wherein said first precursor polymer comprises poly (dimethyl diallyl ammonium chloride) and said second precursor polymer comprises poly (styrene sulfonic acid).

5. The electrode of claim 4 wherein said ratio of the number of equivalents is in the range of about 3-100:1. 6. The electrode of claim 3 wherein said first precursor polymer is a cationic polymer -and said second precursor polymer is a perfluorinated anionic polymer.

7. The electrode of claim 6 wherein said second precursor polymer is a perfluorosulfonic acid polymer.

8. The electrode of claim 1 wherein.said porous body comprises a laminate of a porous hydrophobic layer defining said gas contacting surface, and a porous active layer defining said electrolyte contacting surface, said active layer comprising an electrochemically active material.

9. The electrode of claim 8 wherein said electrochemically active material comprises carbon.

10. The electrode of claim 8 wherein a catalyst is adsorbed on said active material.

11. The electrode of claim 10 wherein said catalyst is cobalt tetramethoxyphenyl porphyrin.

12. An electrochemical cell, comprising: (a) a gas diffusion electrode comprising an electronically conductive and electrochemically active porous body defining respective gas and electrolyte contracting surfaces, with a substantially gas impermeable material filling at least a portion of the pore volume of said body so as to prevent gas passage there through, said material comprising an electrolyte- insoluble, ionomeric ionically conductive hydrophilic hydrogel formed by coprecipitation between at least first and second precursor polymers; (b) a counter electrode spaced from said gas diffusion electrode;

(c) a liquid electrolyte in contact with said counter electrode and with said membrane on said electrolyte contacting surface of said gas diffusion electrode;

(d) either a gas to be consumed via oxidation or reduction or gas formed via electrolytic generation in contact with said gas contacting surface of said gas diffusion electrode; and,

(e) circuit connections between said gas diffusion electrode and said counter electrode.

13. The cell of claim 12 wherein said gas is an oxygen containing gas.

14. The cell of claim 13 wherein said gas is air.

15. The cell of claim 12 wherein at least one of said liquid electrolyte and said gas are flowed through said cell.

16. The cell of claim 12 wherein said first precursor polymer contains cationic groups and said second precursor polymer contains anionic or polar groups.

17. The cell of claim 16 wherein said electrolyte is an alkaline aqueous electrolyte and the ratio of the number of equivalents of said first precursor polymer to said second precursor polymer is greater than 1.

18. The cell of claim 17 wherein said first precursor polymer comprises poly (dimethyl diallyl ammonium chloride) and said second precursor polymer comprises poly (styrene sulfonic acid). 19. The cell of claim 18 wherein said ratio of the number of equivalents is in the range of about 3- 100:1.

20. The cell of claim 17 wherein said first precursor polymer is a cationic polymer and said second precursor polymer is a perfluorinated anionic polymer.

22. The cell of claim 12 wherein said porous body comprises a laminate of a porous hydrophobic layer defining said gas contacting surface, and a porous active layer defining said electrolyte contacting surface, said active layer comprising an electrochemically active material.

23. The cell of claim 22 wherein said electrochemically active material comprise carbon.

24. The cell of claim 22 wherein a catalyst is adsorbed on said active material.

25. The cell of claim 24 wherein said catalyst is cobalt tetramethoxyphenyl porphyrin.