Classifications

• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
  • H01M8/00—Fuel cells; Manufacture thereof
  • H01M8/10—Fuel cells with solid electrolytes
  • H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
  • H01M8/1018—Polymeric electrolyte materials
  • H01M8/1067—Polymeric electrolyte materials characterised by their physical properties, e.g. porosity, ionic conductivity or thickness
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
  • H01M8/00—Fuel cells; Manufacture thereof
  • H01M8/04—Auxiliary arrangements, e.g. for control of pressure or for circulation of fluids
  • H01M8/04082—Arrangements for control of reactant parameters, e.g. pressure or concentration
  • H01M8/04089—Arrangements for control of reactant parameters, e.g. pressure or concentration of gaseous reactants
  • H01M8/04119—Arrangements for control of reactant parameters, e.g. pressure or concentration of gaseous reactants with simultaneous supply or evacuation of electrolyte; Humidifying or dehumidifying
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
  • H01M8/00—Fuel cells; Manufacture thereof
  • H01M8/10—Fuel cells with solid electrolytes
  • H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
  • H01M8/1018—Polymeric electrolyte materials
  • H01M8/102—Polymeric electrolyte materials characterised by the chemical structure of the main chain of the ion-conducting polymer
  • H01M8/1032—Polymeric electrolyte materials characterised by the chemical structure of the main chain of the ion-conducting polymer having sulfur, e.g. sulfonated-polyethersulfones [S-PES]
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
  • H01M8/00—Fuel cells; Manufacture thereof
  • H01M8/10—Fuel cells with solid electrolytes
  • H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
  • H01M8/1018—Polymeric electrolyte materials
  • H01M8/1041—Polymer electrolyte composites, mixtures or blends
  • H01M8/1046—Mixtures of at least one polymer and at least one additive
  • H01M8/1048—Ion-conducting additives, e.g. ion-conducting particles, heteropolyacids, metal phosphate or polybenzimidazole with phosphoric acid
• • H—ELECTRICITY
  • H01—ELECTRIC ELEMENTS
  • H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
  • H01M2300/00—Electrolytes
  • H01M2300/0017—Non-aqueous electrolytes
  • H01M2300/0065—Solid electrolytes
  • H01M2300/0082—Organic polymers
• • 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

Definitions

• the present invention generally relates to proton conducting polymers. More particularly, the present invention relates to proton conducting polymers for use in fuel cells.
• a fuel cell is an energy conversion device which electrochemically reacts fuels such as hydrogen and oxygen to produce an electrical current.
• fuels such as hydrogen and oxygen
• One particular type of a fuel cell is a fuel cell
• PEM fuel cell Proton Exchange Membrane (PEM) fuel cell.
• PEM fuel cells have an operating temperature of around 8O 0 C which makes them favorable for a number of applications, particularly automotive applications.
• a PEM fuel cell generally comprises one or more electrically connected membrane electrode assemblies (MEA).
• MEA membrane electrode assemblies
• Each MEA comprises an anode and a cathode separated by a solid electrolyte allowing for the transfer of protons there through.
• the solid electrolyte is typically in the form of a membrane.
• the MEAs are disposed between flow fields which provide for distribution of hydrogen across the surface of the anode opposite the membrane and the distribution of oxygen across the surface of the cathode opposite the membrane.
• catalysts are deposited on the surfaces of the electrodes.
• a typical catalyst used in PEM fuel cells is platinum.
• hydrogen is dissociated into hydrogen ions and electrons.
• the hydrogen ions permeate through the membrane to the cathode, while the electrons flow through an external circuit to the cathode.
• oxygen reacts with the hydrogen ions and electrons to form water.
• the flow of electrons from the anode to the cathode via the external circuit may be used as a source of power.
• the solid electrolyte as utilized in PEM fuel cells is an acidic proton conducting polymer.
• the acidity of the polymer allows the transfer of protons from the anode to the cathode while preventing the transfer of electrons therethrough.
• Sulfonated fluoropolymers are the most popular choice for the acidic proton conducting polymers used in PEM fuel cells.
• One of the most popular of these conductive polymers is Nafion® (registered trademark of DuPont).
• the popularity of sulfonated fluoropolymers is due to their high chemical resistivity, ability to be formed into very thin membranes, and high conductivity due to their ability to absorb water.
• the ability of the sulfonated fluoropolymers to absorb large quantities of water is due to the hydrophilic nature of the sulfonic groups within the polymer.
• the sulfonic groups provide for the creation of hydrated regions within the polymer, which allow the hydrogen ions to move more freely through the polymer due to a weaker attraction to the sulfonic group.
• the weaker attraction between the hydrogen ions and the sulfonic groups increases the conductivity of the polymer thereby increasing performance of the fuel cell.
• the conductivity of the hydrogen ions is directly proportional to the amount of hydration of the sulfonated fluoropolymer.
• the humidity of the air in a PEM fuel cell must be carefully monitored and controlled. If the air has too high of a humidity, the cell can become flooded with water created during operation of the fuel cell resulting in a decrease in performance due to clogging of the electrode pores. If the air has too low of a humidity, the electrolyte may dry out thereby decreasing the conductivity of the electrolyte resulting in decreased fuel cell performance. As such, control systems and humidification systems must be used in conjunction with PEM fuel cells. The use of these systems can adversely affect the cost, size, and mass of PEM fuel cell systems. As such, there is a need in the art for proton conducting polymers which exhibit high conductivity in low humidity environments.
• a proton conducting polymer comprising a proton donating polymer and an electron withdrawing species.
• the electron withdrawing species may comprise a Lewis acid.
• the Lewis acid may comprise a rare earth triflate.
• Triflate more formally known as trifluoromethanesulfonate, is a functional group with the formula CF 3 SO 3 .
• the group CF 3 SO 3 may be designated as OTf.
• Examples of rare earth triflates that may be used in accordance with the present invention include Sc(OTf) 3 , Y(OTf) 3 , and La(OTf) 3 .
• Lewis acids that may be used in accordance with the present invention include Sc(ClO 4 ) S , Pb(ClO 4 ) S , and Fe(OSO 2 CFs) 2 .
• the proton conducting polymer may exhibit a cationic conductivity greater than 0.015 S/cm at a relative humidity less than 25% at temperatures in the range of 4O 0 C to 8O 0 C.
• the proton donating polymer may comprises a sulfonic acid group.
• the proton conducting polymer may comprise sulfonated polysulfone.
• proton donating polymers that may be used in accordance with the present invention include sulfonated polyether ketones, sulfonated polystyrenes, sulfonated polyphenylenes, sulfonated trifluorostyrenes, sulfonated polyphosphazenes, sulfonated fluoropolymers, polyphenyl sulfides, polymers containing one or more fluorinated sulfonamide groups, zwitterionic ionenes, ionomers, sulfonated polyamides, sulfonated polyazoles, sulfonated silicones, polybenzoimidazole doped with phosphoric acid, nafion, and any derivatives thereof.
• the molar ratio between the proton donating acid groups and the Lewis acid is in the range of 0.1 to 3.0, more preferably 0.2 to 1.2.
• a fuel cell comprising an anode, a cathode, and a cationic exchange membrane comprising a proton donating polymer and an electron withdrawing species.
• the electron withdrawing species may comprise a Lewis acid.
• the Lewis acid comprises a rare earth triflate. Examples of rare earth triflates that may be used in accordance with the present invention include Sc(OTf) 3 , Y(OTf) 3 , and La(OTf) 3 .
• Lewis acids that may be used in accordance with the present invention include Sc(C104) 3 , Pb(C104) 3 , and Fe(OSO2CF 3 )2.
• the proton conducting polymer may exhibit a cationic conductivity greater than 0.015 S/cm at a relative humidity less than 25% at temperatures in the range of 4O 0 C to 8O 0 C.
• Figure 1 is a depiction of the mechanism in accordance with the present invention.
• Figure 2 is a plot showing the conductivity of the proton conducting polymer in accordance with the present invention as compared to sulfonated polysulfone.
• the proton conducting polymer may be used as the electrolyte in a fuel cell such as a PEM fuel cell, a direct methanol fuel cell, or any other type fuel cell that utilizes a proton conducting material as the electrolyte.
• the proton conducting polymer provides for high proton conductivity in low humidity environments.
• the proton conducting polymer generally comprises a proton donating polymer and an electron withdrawing species.
• the electron withdrawing species may comprise a Lewis acid.
• the proton conducting polymer may be doped with the Lewis acid.
• the ratio of the proton donating polymer to Lewis acid may be determined based on the molar ratio between the proton donating acid groups of the proton donating polymer and the Lewis acid. Preferably the molar ratio between the proton donating acid groups and the Lewis acid is in the range of 0.1 to 3.0, more preferably 0.2 to 1.2.
• the Lewis acid may be selected from any type Lewis acid compatible with the proton donating polymer. Some common Lewis acids include aluminium chloride, niobium pentachloride, and many metal ions are strong Lewis acids. However, to enable use in a fuel cell environment, the Lewis acid should not include metal ions which undergo hydrolysis to form basic salts in water.
• the Lewis acid may comprise one or more rare earth triflates. Examples of rare earth triflates that may be used in accordance with the proton conducting polymer include Sc(OTf) 3 , Y(OTf) 3 and La(OTf) 3 .
• the Lewis acid may also comprise one or more selected from Sc(C104) 3 , Pb(C104) 3 , and Fe(OSO2CF 3 )2.
• Lewis acids that may be used in accordance with the present invention include Lanthanoid triflates, such as Ce(OTf) 3 , Pr(OTf) 3 , Lanthanoids and chlorides, such as ScCb, YCb, YbCb, Lanthanoid tetraoxoclorides, such as Ce(Cl ⁇ 4) 3 , Y(C1O4) 3 , La(C104) 3 , chlorides containing Fe(II), Cd(II), Pb(II), or other Metal(III) elements, such as FeCb, tetraoxoclorides containing Fe(II), Cd(II), Pb(II), or other Metal(III) elements, such as Cu(C104) 3 , Zr(C104) 3 , Cd(Cl ⁇ 4)2, Fe(Cl ⁇ 4)2 and other triflates containing Fe(II), Cd(II), Pb(II), or other Metal(III) elements.
• the proton donating polymer may comprise a polymer including a sulfonic acid group or a phosphonic acid group.
• the proton donating polymer may comprise sulfonated polysulfone.
• Other proton donating polymers that may be used in accordance with the present invention include sulfonated polyether ketones, sulfonated polystyrenes, sulfonated polyphenylenes, sulfonated trifluorostyrenes, sulfonated polyphosphazenes, sulfonated fluoropolymers, sulfonated perfluoropolymers, polyphenyl sulfides, polymers containing one or more fluorinated sulfonamide groups, zwitterionic ionenes, ionomers, sulfonated polyamides, sulfonated polyazoles, sulfonated silicones, polybenzoimidazole doped with phosphoric
• protons move very easily under highly acidic conditions.
• the high acidity of the Lewis acid allows protons to move much more easier through the conductive polymer.
• the present inventors believe that the high acidity of the Lewis acid withdraws the electron from the proton donating group which allows the hydrogen ion to easily move through the conductive polymer.
• the electron density of proton donating polymer is moved toward the electron density of the Lewis acid. Since electron density between proton and one or more acid groups of the proton donating polymer may be decreased, ion bonding between proton and the one or more acid groups will weaken thereby allowing the proton to be easily detached. This mechanism is generally depicted in
• Lewis acids such as those described herein, are stable and are compatible in the humid environment. These Lewis acids can not be decomposed within the fuel cell environment. As such, they can remain "in-situ" within the membrane and/or other polymer electrolyte. This compatibility with an aqueous environment allows the fuel cell to benefit from the high acidity of a Lewis acid.
• the proton conducting polymer in accordance with the present invention may be prepared by mixing a proton donating polymer as described herein with a Lewis acid.
• the proton donating polymer and the Lewis acid may be in powder form and mechanically mixed together.
• the proton donating polymer and the Lewis acid may also dissolved in solution and mixed together with the solvent being evaporated off to obtain the proton conducting polymer.
• the proton conducting polymer may also be obtained by dipping the proton donating polymer into a Lewis acid solution with subsequent drying.
• the proton conducting polymer may be formed into a membrane as used in electrochemical cells.
• the proton donating polymer and the Lewis acid may be combined in solution and allowed to dry.
• the proton donating polymer and the Lewis acid may be dissolved in an organic solvent such as N,N-dimethylacetamide (DMAC) or dimethyl sulfoxide (DMSO). Some water may be added to the solution to aid in the dissolution of the Lewis acid. Once all of the proton donating polymer and the Lewis acid are dissolved the solvent is evaporated off to obtain the film. The solution may be heated to aid in dissolution of the proton donating polymer and the
• a membrane including the proton conducting polymer may also be obtained by preparing a membrane with the proton donating polymer and impregnating the membrane with the Lewis acid.
• the membrane may be impregnated with the Lewis acid by dipping the membrane into a Lewis acid solution with subsequent drying, spraying a Lewis acid solution onto the membrane with subsequent drying, or any other generally known deposition techniques.
• the proton conducting electrolyte When utilized as the proton conducting electrolyte in a fuel cell, the proton conducting electrolyte may be formed into an ion-exchange membrane as previously discussed and incorporated into a fuel cell. When incorporated into a fuel cell, the ion-exchange membrane is disposed between and in electrochemical communication with an anode and a cathode. During operation of the fuel cell, protons are transferred through the ion-exchange membrane from the anode to the cathode while electrons are transferred through an external circuit from the anode to the cathode.
• the ion-exchange membrane formed from the proton conducting polymer of the present invention may be utilized in a membrane electrode assembly (MEA).
• MEA membrane electrode assembly
• a MEA includes an anode, a cathode, and an ion-exchange membrane according disposed between the anode and cathode.
• One or more of the membrane electrode assemblies according to the present invention may be used in a fuel cell or other apparatus.
• a second pellet was created by die-casting approximately 0.5g to 1.Og of powder sulfonated polysulfone.
• the pellets had a height of approximately 10mm and a thickness of about 1.5 mm.
• Each pellet was separately placed in a temperature-humidity chamber which maintained a relative humidity of 20%.
• Ionic conductivity of the pellets were individually measured by the alternating current impedance (AC impedance) method. During testing, an electrical current was applied across each pellet via platinum electrodes in contact with the pellet. The ionic conductivity of the pellets were then measured at temperatures varying from 2O 0 C to 12O 0 C. The results of the experiment are shown in Figure 2.

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• Fuel Cell (AREA)
• Conductive Materials (AREA)
• Compositions Of Macromolecular Compounds (AREA)

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• 2007
  • 2007-05-08 US US11/745,782 patent/US7989116B2/en not_active Expired - Fee Related
• 2008
  • 2008-05-07 CN CN201610102196.4A patent/CN105720287A/zh active Pending
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