Patent Application
20060078783
1. Field of the Invention
The present invention relates to a gas blocking anode for a Direct Liquid Fuel Cell (DLFC) which uses a hydride fuel and specifically, to an anode which helps to prevent or at least substantially reduce, an increase of the electric resistance of the electrolyte in the fuel cell, which increase is caused by hydrogen bubbles in the electrolyte, and which bubbles result from, inter alia, a decomposition of the hydride fuel.
2. Discussion of Background Information
Direct liquid fuel cells are of considerable importance in the field of new energy conversion technologies. The most commonly used liquid fuel for a DLFC is methanol. The main disadvantages of such Direct Methanol Fuel Cells (DMFCs) are the toxicity of methanol and the very poor discharge characteristics at room temperature. As a result, DMFCs are not generally used for portable electronics applications and the like.
Fuels based on (metal) hydride and borohydride compounds such as, e.g., sodium borohydride (e.g., in alkaline solution) have a very high chemical and electrochemical activity. Consequently, DLFCs which use such fuels have extremely high discharge characteristics (current density, specific energy, etc.) even at room temperature.
Efficient operation of a DLFC which uses a (boro)hydride fuel requires continuous delivery of the (boro)hydride to the catalyst particles of the anode. For example, borohydride is electrochemically oxidized at the anode by direct reaction with formation of BO2− and water in accordance with the following equation:
BH4−+8OH−=BO2−+6H2O+8e− (1)
Side reactions include the electrochemical oxidation of the borohydride to H2 and the non-electrochemical decomposition of the borohydride (self-discharge). The decomposition of a borohydride compound occurs in accordance with the following equation:
BH4−+2H2O→BO2−+4H2↑ (2)
The formation of hydrogen gas as a result of the above side reactions causes several problems. One of these problems includes the passage of hydrogen gas through the anode into the electrolyte chamber, leading to the formation of hydrogen bubbles in the electrolyte and, in turn, to an increase of the electrical resistance of the electrolyte.
The present invention provides an anode for a direct liquid fuel cell in which hydrogen gas is generated as a result of a fuel oxidation or decomposition reaction, wherein that surface of the anode which is intended to face the electrolyte chamber of the fuel cell is substantially completely covered with a polymeric material which prevents at least about 80% of the generated hydrogen gas to pass through the polymeric material and into the electrolyte chamber.
In one aspect of the anode, at least about 85% of the hydrogen gas, e.g., at least about 90%, at least about 95%, or at least about 98% of the hydrogen gas may be prevented from entering the electrolyte chamber.
In another aspect, the electric area resistivity of the combination of the anode with the polymeric material may be not higher than about 1 Ohm·cm2, e.g., not higher than about 0.9 Ohm·cm2, not higher than about 0.85 Ohm·cm2, or not higher than about 0.8 Ohm·cm2. As used herein and in the appended claims, the terms “area resistivity” and “resistivity” are used interchangeably.
In yet another aspect, the surface of the anode may be covered with a single layer of polymeric material, or at least two layers of polymeric material may be arranged on the surface of the anode. For example, the at least two layers may comprise different polymeric materials.
In a still further aspect, the polymeric material may comprise one or more layers of polymeric material and may have a total thickness of not more than about 200 μm and/or a total thickness of at least about 25 μm.
In another aspect of the anode of the present invention, the polymeric material may comprise at least one polymer with a hydrophilic group. For example, the hydrophilic group may be an OH, a COOH and/or an SO3H group. Preferably, the at least one polymer with a hydrophilic group comprises OH groups. In yet another aspect, the at least one polymer with a hydrophilic group may comprise a homopolymer and/or a copolymer of vinyl alcohol, for example, a polymer having a weight average molecular weight of not more than about 100,000 and/or of not less than about 30,000. By way of non-limiting example, the copolymer of vinyl alcohol may comprise a copolymer of vinyl alcohol and one or more ethylenically unsaturated comonomers, e.g., a vinyl alcohol/ethylene copolymer. Also, the copolymer of vinyl alcohol may comprise at least about 50 mol-% of vinyl alcohol units.
In yet another aspect of the anode of the present invention, at least a part of the polymeric material may be capable of swelling in an aqueous solution.
In a still further aspect, the at least one polymer with a hydrophilic group may be at least partially crosslinked, for example, with a crosslinking agent which comprises a polymer that has at least one functional group which is capable of reacting with a functional group of the hydrophilic polymer. Preferably, the weight ratio of the at least one polymer with a hydrophilic group and the crosslinking agent ranges from about 2:1 to about 1:2.
In another aspect, the at least one polymer with a hydrophilic group may comprise a polymer having OH groups and the crosslinking agent may comprise a polymer selected from polyethylene glycol, polyethylene oxide and combinations thereof. For example, the polyethylene glycol may have a number average molecular weight of from about 300 to about 10,000, and the polyethylene oxide may have a number average molecular weight of from about 35,000 to about 200,000.
In yet another aspect, the at least one polymer with a hydrophilic group may be at least partially crosslinked with at least one crosslinking agent selected from a silicate, a pyrophosphate, a sugar alcohol, and an aldehyde. Non-limiting examples of these crosslinking agents include an alkali metal silicate, an alkali metal pyrophosphate, xylitol, sorbitol, and formaldehyde. By way of non-limiting example, the weight ratio of the at least one polymer with a hydrophilic group and the crosslinking agent may range from about 2:1 to about 1:2.
In yet another aspect of the anode of the present invention, the anode may comprise a metal mesh current collector, e.g., a nickel mesh current collector. Further, the anode may comprise a binder such as, e.g., polytetrafluoroethylene.
The present invention also provides an anode for a direct liquid fuel cell in which hydrogen gas is generated as a result of a fuel oxidation or decomposition reaction, wherein a surface of the anode which is intended to face an electrolyte chamber of the fuel cell is substantially completely coated with one or more layers of a material which comprises an at least partially crosslinked homopolymer and/or an at least partially crosslinked copolymer of vinyl alcohol with a content of vinyl alcohol units of at least about 50 mol-%. The one or more layers prevent at least about 90% of the generated hydrogen gas from penetrating the one or more layers into the electrolyte chamber. Also, the anode with the one or more layers thereon has an electric resistivity of not higher than about 0.9 Ohm·cm2.
In one aspect of this anode, the one or more layers may comprise at least two layers, a first layer in contact with the anode which comprises a copolymer of vinyl alcohol and one or more ethylenically unsaturated comonomers, and a second layer which is arranged on the first layer and comprises a vinyl alcohol homopolymer.
In another aspect of the anode, the one or more layers may comprise a vinyl alcohol homopolymer.
In yet another aspect, the one or more layers may have a total thickness of from about 25 μm to about 200 μm.
In a still further aspect, the vinyl alcohol polymer may be at least partially crosslinked with a crosslinking agent selected from polyethylene glycol and polyethylene oxide. By way of non-limiting example, the weight ratio of the vinyl alcohol polymer and the crosslinking agent may be from about 2:1 to about 1:2.
In another aspect, the vinyl alcohol polymer may be at least partially crosslinked with a crosslinking agent selected from sodium silicate, sodium pyrophosphate, sorbitol, xylitol, formaldehyde and combinations of two or more thereof.
In yet another aspect of the anode, the one or more layers may prevent at least about 95% of the generated hydrogen gas from penetrating the one or more layers, and the anode with the one or more layers thereon may have an electric resistivity of not higher than about 0.85 Ohm·cm2.
In another aspect, the anode may comprise a nickel mesh current collector.
The present invention also provides a direct liquid fuel cell which comprises an anode of the present invention as set forth above, including the various aspects thereof.
In one aspect, this fuel cell may comprise a metal hydride and/or a metal borohydride compound, for example, sodium borohydride in a fuel chamber thereof.
In another aspect, the electrolyte chamber of the fuel cell may comprise an aqueous alkali metal hydroxide, for example, aqueous potassium hydroxide.
The present invention also provides a direct liquid fuel cell for use with a liquid fuel that is prone to undergo decomposition with generation of hydrogen gas. The fuel cell comprises a cathode; an anode; an electrolyte chamber arranged between the cathode and the anode; a fuel chamber arranged on that side of the anode which is opposite to the side which faces the electrolyte chamber; and one or more layers of polymeric material which are arranged on that surface of the anode which faces the fuel chamber. These one or more layers of polymeric material prevent an at least substantial portion of the hydrogen gas that is present in the fuel chamber (when liquid fuel is present in the fuel chamber) from passing through the one or more layers into the electrolyte chamber.
In one aspect of the fuel cell, the fuel may comprise a metal hydride compound and/or a metal borohydride compound.
In another aspect, the anode may have a single layer of polymeric material thereon, or it may have at least two layers of polymeric material thereon.
In yet another aspect, at least about 90% of the hydrogen gas, for example, at least about 95% of the hydrogen gas, may be prevented from entering the electrolyte chamber.
In a still further aspect of the fuel cell, the electric resistivity of the anode with the polymeric material thereon may be not higher than about 1 Ohm·cm2, e.g., not higher than about 0.9 Ohm·cm2.
In another aspect, the one or more layers of polymeric material may have a total thickness of not more than about 200 μm and/or a total thickness of at least about 25 μm.
In another aspect of the fuel cell, the polymeric material may comprise at least one polymer with a hydrophilic group such as, e.g., one or more of OH, COOH and SO3H groups. In a preferred embodiment, the at least one polymer comprises at least OH groups. By way of non-limiting example, the at least one polymer may comprise a homopolymer and/or a copolymer of vinyl alcohol. The copolymer of vinyl alcohol may, for example, comprise at least about 50 mol-% of vinyl alcohol units.
In yet another aspect, the at least one polymer with a hydrophilic group may be at least partially crosslinked with a crosslinking agent which comprises a polymer that has at least one functional group which is capable of reacting with a functional group of the hydrophilic polymer. By way of non-limiting example, the weight ratio of the at least one polymer with a hydrophilic group and the crosslinking agent may range from about 2:1 to about 1:2. Further, the at least one polymer with a hydrophilic group may comprise a polymer having OH groups and the crosslinking agent may comprise a polymer selected from polyethylene glycol, polyethylene oxide and combinations thereof. Also, the at least one polymer with a hydrophilic group may be at least partially crosslinked with at least one crosslinking agent that is selected from an alkali metal silicate, an alkali metal pyrophosphate, a sugar alcohol, and an aldehyde.
In a still further aspect of the fuel cell, the anode may comprise a nickel mesh current collector and/or a binder which comprises polytetrafluoroethylene.
In another aspect, the electrolyte chamber of the fuel cell may comprise an aqueous alkali metal hydroxide such as, e.g., aqueous potassium hydroxide.
The present invention also provides a method of reducing or substantially preventing an increase in the electrical resistance of an electrolyte in an electrolyte chamber of a direct liquid fuel cell which comprises a cathode, an anode, an electrolyte chamber arranged between the cathode and the anode, and a fuel chamber arranged on that side of the anode which is opposite to the side of the electrolyte chamber. The increase in the electrical resistance is caused by hydrogen gas bubbles which are formed as a result of a generation of hydrogen gas by the liquid fuel in the fuel chamber and a migration of the hydrogen gas through the anode into the electrolyte chamber. The method comprises providing the surface of the anode which faces the electrolyte chamber with one or more layers of a polymeric material which prevent a substantial portion of the generated hydrogen gas from passing therethrough.
In one aspect of the method, the fuel may comprise a hydride compound and/or a borohydride compound, for example, an alkali metal borohydride. By way of non-limiting example, the fuel may comprise sodium borohydride which is dissolved and/or suspended in a liquid carrier.
In another aspect, at least about 90% of the hydrogen gas, e.g., at least about 95% of the hydrogen gas may be prevented from passing through the one or more layers of polymeric material.
In yet another aspect of the method, the electric resistivity of the anode with the one or more layers of polymeric material may be not higher than about 1 Ohm·cm2, e.g., not higher than about 0.85 Ohm·cm2.
In a still further aspect of the method, the surface of the anode may be provided with a single layer of polymeric material, or at least two layers of polymeric material may be arranged on the surface of the anode.
In another aspect, the one or more layers of polymeric material may have a total thickness of from about 25 μm to about 200 μm.
In a still further aspect, the polymeric material may comprise at least one polymer with a hydrophilic group selected from one or more of OH, COOH and SO3H groups. By way of non-limiting example, the at least one polymer may comprise OH groups.
In another aspect, the at least one polymer may comprise a homopolymer and/or a copolymer of vinyl alcohol. Preferably, this homo- and/or copolymer is at least partially crosslinked with a crosslinking agent which comprises a polymer that has at least one functional group which is capable of reacting with a functional group of the homopolymer/copolymer of vinyl alcohol. For example, the crosslinking agent may comprise a polyethylene glycol, a polyethylene oxide or a combination thereof. Alternatively or additionally, the crosslinking agent may comprise an alkali metal silicate, an alkali metal pyrophosphate, a sugar alcohol, and/or an aldehyde.
Other exemplary embodiments and advantages of the present invention may be ascertained by reviewing the present disclosure and the accompanying drawing.
The present invention is further described in the detailed description which follows, in reference to the noted plurality of drawings by way of non-limiting examples of exemplary embodiments of the present invention, in which like reference numerals represent similar parts throughout the several views of the drawings, and wherein:
The particulars shown herein are by way of example and for purposes of illustrative discussion of the embodiments of the present invention only and are presented in the cause of providing what is believed to be the most useful and readily understood description of the principles and conceptual aspects of the present invention. In this regard, no attempt is made to show structural details of the present invention in more detail than is necessary for the fundamental understanding of the present invention, the description taken with the drawings making apparent to those skilled in the art how the several forms of the present invention may be embodied in practice.
As illustrated in
In a conventional DLFC without the anode of the present invention, all or at least a substantial portion of the hydrogen gas formed at the anode 3 and/or in the body of the fuel chamber 2 will gradually pass through the (porous) anode and into the electrolyte chamber 5 where the hydrogen forms bubbles (usually, micro-bubbles) in the electrolyte. This, in turn, results in an increase of the electric resistance of the electrolyte. The anode of the present invention which is provided with the at least one layer of polymeric material 6 on that surface of the anode 3 which faces the electrolyte chamber 5 prevents all or at least a substantial portion (typically at least about 80%, preferably at least about 90%, and up to about 98 or close to about 100%, hereafter sometimes referred to as “gas-blocking efficiency”) of the hydrogen gas from reaching the electrolyte chamber, whereby an increase in the electric resistance of the electrolyte can be avoided to an at least substantial extent. The percentage of hydrogen gas which is prevented from reaching the electrolyte chamber may be determined according to the method which is described in the Examples below.
As set forth above, one side (major surface) of the anode 3 is substantially completely (and preferably completely) covered with at least one layer of polymeric material 6. Covering the anode with the polymeric material can be accomplished in various ways. For example, one or more films of polymeric material can be attached to the surface of the anode under pressure and/or by means of a suitable adhesive (applied, e.g. at the edges of the anode). Preferably, the one or more layers of polymeric material 6 are (successively) applied by a coating operation. For example, one or more solutions and/or suspensions of the desired polymeric material(s) may be applied onto the surface of the anode, and after the or each coating operation the solvent(s) may be at least partially removed, e.g., by heating and/or by applying a vacuum. A non-limiting example of a typical coating process is described in the Examples below. The polymeric material does not necessarily have to be in direct contact with the anode surface (although direct contact is preferred), as long as the polymeric material is capable of preventing a substantial portion of the hydrogen gas from entering the electrolyte chamber, and as long as the ionic conductivity of the combination of anode and polymeric layer is not significantly adversely affected by the lack of direct contact.
Where two or more layers of polymeric material (e.g., two, three or four layers of polymeric material) are applied, the layers may comprise the same or different polymer(s). Layers of the same polymer(s) may be of advantage, for example, if a single coating operation does not afford the desired thickness (and/or mechanical strength) of the polymeric material layer and/or if it is difficult to achieve a continuous coating film (substantially without any holes) with a single coating operation.
Two or more layers which comprise different polymers in at least two of the layers may be expedient for, e.g., imparting a combination of desired characteristics to the polymeric material. For example, a first layer of polymeric material which is in direct contact with the anode may comprise one or more polymers which provide a good adhesion to the anode surface, whereas a layer which comprises one or more polymers which is (are) different from the polymer(s) in the first layer and which layer is arranged on the first layer may provide other desired characteristics, for example, a high ionic conductivity. In this regard, it is preferred for the combination of anode and polymeric material to have an ionic resistivity of not substantially higher than about 1 Ohm·cm2, even more preferred of not higher than about 0.95 Ohm·cm2, particularly not higher than about 0.9 Ohm·cm2, not higher than about 0.85 Ohm·cm2, or not higher than about 0.8 Ohm·cm2. The ionic conductivity (resistivity) may be measured according to the method described in the Examples below.
Irrespective of whether one or two (or more) layers of polymeric material are provided on the anode surface, each of these layers may independently comprise a single polymer or a mixture of two or more polymers. Of course, if two or more layers are provided, these layers may have the same or a different thickness.
The one or more layers of polymeric material arranged on the anode will usually have a combined thickness of not more than about 0.2 mm, e.g., not more than about 0.15 mm. On the other hand, the combined thickness will preferably be not lower than about 0.025 mm, e.g., not lower than about 0.03 mm.
Suitable polymers for use in the one or more layers of polymeric material 6 include those which provide, alone or in combination, both a satisfactory ionic conductivity and a high gas-blocking efficiency (a low permeability for hydrogen gas), particularly in the conventional operating temperature range of a DLFC, i.e., from room temperature to about 60° C. Also, the one or more polymers should provide sufficient mechanical strength and maintain mechanical integrity to a sufficient extent even when exposed to an alkaline solution (in particular, an aqueous electrolyte) at a temperature of up to about 60° C. for extended periods of time. In this regard, an example of an aqueous electrolyte of the type conventionally used in a DLFC is aqueous potassium hydroxide solution (e.g., about 6M to about 7M KOH). Sufficient adhesion to the anode surface is also a desired characteristic. As mentioned above, it is not necessary for a single polymer to exhibit all of these desirable properties in order to be suitable for use in the present invention. A combination of two or more polymers which together provide these properties is equally suitable.
Examples of polymers which provide a satisfactory ionic conductivity include those which are able to dissolve or swell in aqueous solutions. A high gas-blocking efficiency may be achieved, for example, by crosslinking suitable polymer chains, which at the same time will increase the mechanical strength of the polymer layer.
Preferred polymers for use in the present invention include those which comprise one or more types of hydrophilic groups such as, e.g., OH, COOH and/or SO3H groups. Non-limiting examples of such polymers are homo- and copolymers which comprise units of vinyl alcohol, acrylic acid, methacrylic acid, and the like. Of course, polymers with different hydrophilic groups may also be useful. The term “hydrophilic groups” as used herein and in the appended claims is meant to encompass groups which have affinity for and/or are capable of interacting with, water molecules, e.g., by forming hydrogen bonds, ionic interactions, and the like. Preferred examples of polymers with hydrophilic groups for use in the present invention are polymers which comprise at least OH groups, in particular, the homo- and copolymers of vinyl alcohol.
Non-limiting examples of copolymers of vinyl alcohol comprise units of vinyl alcohol and units of one or more (e.g., one or two) ethylenically unsaturated comonomers. Preferred comonomers include C2-C8 alkenes such as, e.g., ethylene, propylene, butene-1, hexene-1, and octene-1. A particularly preferred comonomer is ethylene. In the copolymers of vinyl alcohol (or any other monomer which comprises hydrophilic groups) and comonomers without hydrophilic groups (e.g., alkenes and the like), the vinyl alcohol units will usually provide the desired ionic conductivity, and the comonomer(s) will preferably promote the adhesion of the polymer to the substrate (the anode surface).
In the copolymers of vinyl alcohol, the units of vinyl alcohol are preferably present in an amount of at least about 50 mol-%, particularly in copolymers where the comonomer(s) do not comprise any hydrophilic groups.
The average molecular weight of the homo- and copolymers of vinyl alcohol (or any other polymers) for use in the present invention is not particularly critical, but will usually be in the conventional range for this type of polymers, i.e., not significantly higher than about 100,000 and not significantly lower than about 30,000 (expressed as weight average molecular weight).
In order to increase the mechanical strength and the gas-blocking efficiency of a polymer with hydrophilic groups for use in the present invention, for example the homo- and copolymers of vinyl alcohol set forth above, it will usually be of advantage to crosslink the polymer chains. Suitable sites for crosslinking include the hydrophilic groups of the polymer molecules and/or any other functionalities (including ethylenically unsaturated bonds) that may be present in the polymer molecules. Suitable crosslinking agents include those which comprise in their molecule at least two (e.g., two, three, four of five) functional groups which are capable of reacting (or at least strongly interacting) with one or more types of functional groups present in the polymer molecule. The reaction between the functional groups preferably comprises a polycondensation (including a polyaddition), an ionic or free radical polymerization, or any other type of reaction which results in the formation of (preferably covalent) bonds between the reactants. The crosslinking agent may be of organic or inorganic nature, monomeric or polymeric, and two or more crosslinking agents may be employed, if desired.
Non-limiting and preferred examples of crosslinking agents for the crosslinking of homo- and copolymers of vinyl alcohol as well as other types of polymers include polymeric crosslinking agents such as, e.g., polyalkylene glycols, preferably polyethylene glycol, and polyethylene oxide, and monomeric species such as, e.g., alkali metal silicates and pyrophosphates (e.g., sodium or potassium silicate and sodium or potassium pyrophosphate), sugar alcohols (e.g., xylitol, sorbitol, etc.), and carbonyl compounds, in particular, aldehydes (e.g. formaldehyde).
In the case of polymeric crosslinking agents, the average molecular weight thereof is not particularly critical and commercially available materials may be employed. For example, the number average molecular weight of commercially available polyethylene glycols is typically in the range of from about 300 to about 10,000, whereas for commercially available polyethylene oxide the number average molecular weight is typically in the range of from about 35,000 to about 200,000.
When homo- and/or copolymers of vinyl alcohol are to be crosslinked for the purposes of the present invention, the weight ratio of these polymers and the crosslinking agent(s), e.g., the crosslinking agents set forth above, preferably ranges from about 2:1 to about 1:2. Of course, ratios outside this range may be used as well. One of ordinary skill in the art will be aware of or be able to readily ascertain suitable weight ratios for other polymers and/or other crosslinking agents.
The anode of the present invention may be any anode which is suitable for the present type of fuel and DLFC. The anode will usually comprise a porous material that is pervious to gaseous and liquid substances, and may have been produced by wet or dry technologies. Of course, the materials thereof should be able to withstand the chemical attack by the liquid fuel and should not catalyze a decomposition of the fuel to any appreciable extent. A non-limiting example of an anode for use in the present invention comprises a metal mesh current collector, e.g., a nickel or stainless steel mesh, which has attached to it a porous active layer. This active layer may comprise, by way of non-limiting example, activated carbon carrying a catalytically active material (such as a metal, for example Pt, Pd, Ru, Rh, to name just a few), and a binder, typically a polymeric material such as polytetrafluoroethylene, and the like. Of course, other materials for making the anode of the present invention may be used as well. For example, instead of the metal mesh, a metal foam, or hydrophilic carbon paper may be used.
The following non-limiting examples illustrate the production of anodes according to the present invention which are coated with polyethylene glycol-crosslinked vinyl alcohol homo- and copolymers. The anodes are composed of the following materials:
The coating materials used are as follows:
A solution is prepared by dissolving 7.31 g of PVA and 4.69 g of PEG in 88 g of de-ionized water under stirring and heating the mixture at 70° C. for 2 hours. One ml of the solution is applied onto one surface of the anode (20 cm2) and is then dried in air at ambient temperature for 20 min. Then 1 ml of the same solution is applied onto the first layer, whereafter the anode is transferred to an oven and dried at 120° C. for 2 hours.
The resistivity of the resultant coated anode is 0.8 Ohm·cm2, and the gas-blocking efficiency thereof is 99%.
A solution is prepared by dissolving 0.6 g of VAE and 0.4 g of PEG in 29 g of n-propanol/water (1:1) under stirring and heating the mixture at 70° C. for 2 hours. One ml of the solution is applied onto one surface of the anode (20 cm2) and then dried in air at ambient temperature for 20 min. Then 1 ml of the solution from Example 1 is applied onto the first layer, whereafter the anode is transferred to an oven and dried at 90° C. for 2 hours.
The resistivity of the resultant coated anode is 0.99 Ohm·cm2, and the gas-blocking efficiency thereof is 94%.
One ml of the solution from Example 2 is applied onto one surface of the anode (20 cm2) and is dried in air at ambient temperature for 20 min. Then 1 ml of the same solution is applied onto the first layer and the resultant coated anode is transferred to an oven and dried at 90° C. for 2 hours.
The resistivity of the resultant coated anode is 0.88 Ohm·cm2, and the gas-blocking efficiency thereof is 89%.
The resistivity of the coated anodes in the above Examples may be determined as follows:
Method Basics
The method is based on a DC applied to an ionic conductor in a porous object and a simultaneous measurement of the potential difference of the electrolyte across the object in the thickness direction thereof. A four-electrode cell is used for measurements. Two of the electrodes are “current source” auxiliary electrodes and the two others are identical “potential sense” reference electrodes.
The resistance of a porous object impregnated with an electrolyte is determined as resistance difference between capillaries of the “potential sense” electrodes with and without the object under measurement. The resistance R is calculated according to equation (1):
R=R1−R0=(ΔE 1−ΔE0)/I, (1)
where R1 and ΔE1 are resistance and potential difference, respectively with object, and R0 and ΔE0 are resistance and potential difference without object. I is the source current. Two measurements are carried out: one for electrolyte without object and another one with object impregnated with electrolyte. R0 also includes an empiric temperature correction: R0(t2)=R0(t1)*[1−0.017(t2−t0)] (for the temperature range of 20-27° C.). The area resistivity p of the object (anode) is calculated according to equation (2):
ρ=R·S (2)
where S is the object surface area.
Equipment and Materials
Procedure
5. By means of control interface select galvanostatic mode of operation and program the following steps:
The duration of each step is 1 s (total duration 10 s). The potential read-out frequency is 0.2 s. Start program, print data table, plot ΔE (mV) vs. I (mA). Approximate branches of E(I) by linear lines for positive and for negative current values. Absolute values of slopes are equal to the resistance R0.
The gas-blocking efficiency (E GBL) of the gas-blocking layer (GBL) of the coated anodes of the above Examples may be determined as follows.
E GBL is calculated according to equation (3):
where V GBL is the volume of hydrogen gas that penetrates into the electrolyte chamber, and V is the total volume of hydrogen gas that is produced at the anode/in the fuel chamber.
In order to determine E GBL, it is necessary to generate hydrogen gas at a constant pre-determined rate and to measure its flow from the side of the GBL. For this purpose, a triple-chamber cell, shown in
The cell 12 is produced from alkali-resistant plastic Delrin™ and is equipped with standard 4 cm2 electrodes 13, 15. It is assembled using bolts and is leak-proofed by rubber O-rings. A Ni plate serves as counter electrode 15; a porous polypropylene membrane 14 (Celgard™) which is glued in a standard electrode frame is used as separator. The anode 13 with the GBL to be tested is arranged in the cell 12. The cell is filled with 4M KOH solution; the level thereof must be the same in all three chambers of the cell 12. The anode 13 to be tested must be totally immersed in electrolyte.
Cell 12 is connected to a test assembly as shown in
E GBL is calculated as the volume of hydrogen gas that enters the central chamber of the cell 12 divided by the known total volume of generated hydrogen gas.
A gas outlet of the central chamber of cell 12 is connected to a water-filled Drexel bottle 16 (equipped with thermometer 19) by a silicon rubber tube. The hydrogen gas from the central chamber pushes water from Drexel bottle 16 into a beaker 18 placed on balance 17. The volume of hydrogen gas per time unit from the central chamber of cell 12 is obtained from the weight change of beaker 18 with time.
Equipment and Materials
Measurement Procedure
Example of Measurement and Calculation of E GBL
The total hydrogen gas generation rate V under a total current of I=0.4 A (0.1 A/cm2·4 cm2) taking into account the temperature correction at t=25° C. is equal to:
F=96500 Coulombs/mol is Faraday's number.
E GBL expressed in percent is equal to:
It is noted that the foregoing examples have been provided merely for the purpose of explanation and are in no way to be construed as limiting of the present invention. While the present invention has been described with reference to an exemplary embodiment, it is understood that the words that have been used are words of description and illustration, rather than words of limitation. Changes may be made, within the purview of the appended claims, as presently stated and as amended, without departing from the scope and spirit of the present invention in its aspects. Although the invention has been described herein with reference to particular means, materials and embodiments, the invention is not intended to be limited to the particulars disclosed herein. Instead, the invention extends to all functionally equivalent structures, methods and uses, such as are within the scope of the appended claims.
