阅读说明：本技术 用于电解槽的含有分散催化剂的阳极组合物 (Anode composition containing dispersed catalyst for electrolytic cells ) 是由 安德鲁·T·豪格 约翰·E·阿布卢 克日什托夫·A·莱温斯基 安德鲁·J·L·斯坦巴克 孙福 于 2018-12-19 设计创作，主要内容包括：本文描述了与离聚物粘结剂一起分散用于电解槽中的多个针状颗粒。所述针状颗粒包括微结构化芯,所述微结构化芯具有位于所述微结构化芯的表面的至少一部分上的催化材料层。所述催化材料包含铱,并且所述微结构化芯包含多核芳族烃和杂环化合物中的至少一种。所述针状颗粒基本上不含铂。(Described herein are a plurality of acicular particles dispersed with an ionomer binder for use in an electrolysis cell. The acicular particles comprise a microstructured core having a layer of catalytic material on at least a portion of a surface of the microstructured core. The catalytic material comprises iridium, and the microstructured core comprises at least one of a polynuclear aromatic hydrocarbon and a heterocyclic compound. The acicular particles are substantially free of platinum.)

1. An electrode composition for an electrolytic cell, the electrode composition comprising:

(a) an ionomer binder; and

(b) less than 54 percent by solid volume of a plurality of acicular particles, wherein the plurality of acicular particles are dispersed throughout the electrode composition, and wherein the acicular particles comprise a microstructured core having a layer of catalytic material on at least a portion of the surface of the microstructured core, wherein the microstructured core comprises at least one of a polynuclear aromatic hydrocarbon, a heterocyclic compound, and combinations thereof, and the catalytic material comprises iridium, and wherein the acicular particles are substantially free of platinum.

2. The electrode composition of claim 1, wherein the catalytic material further comprises at least one of ruthenium or ruthenium oxide.

3. The electrode composition of any one of the preceding claims, wherein the iridium comprises iridium oxide.

4. The composition of any of the preceding claims, wherein the catalytic material layer comprises a nanostructured catalyst layer.

5. The composition of any of the preceding claims, wherein the polynuclear aromatic hydrocarbon comprises perylene red.

6. The composition of any one of the preceding claims, wherein the acicular particles have an aspect ratio of at least 3.

7. The composition of any one of the preceding claims, wherein the ionomer binder comprises at least one of: perfluorinated sulfonic acids, perfluorinated sulfonimide-acids, sulfonated polyimides, perfluorinated imides, sulfonated polytrifluoroethylenes, sulfonated hydrocarbon polymers, polysulfones, polyethersulfones, and combinations thereof.

8. The composition of any of the preceding claims, wherein the ionomer binder has an equivalent weight of no greater than 1100.

9. The electrode composition of any one of the preceding claims, wherein the layer of catalytic material on at least a portion of the surface of the microstructured core has a thickness of less than 100 nm.

10. A catalyst ink composition for an electrolytic cell, the composition comprising:

(a) an ionomer binder;

(b) a plurality of acicular particles less than 54 percent by solid volume, and wherein the acicular particles comprise a microstructured core having a layer of catalytic material on at least a portion of a surface of the microstructured core, wherein the microstructured core comprises at least one of a polynuclear aromatic hydrocarbon, a heterocyclic compound, and combinations thereof; wherein the catalytic material comprises iridium; and wherein the acicular particles are substantially free of platinum; and

(c) a solvent;

wherein the plurality of acicular particles are dispersed throughout the electrode composition.

11. An article of manufacture, comprising:

a substrate having a coating thereon, the coating comprising (a) an ionomer binder; and

(b) less than 54 percent by solid volume of a plurality of acicular particles, wherein the plurality of acicular particles are dispersed throughout the coating layer, and wherein the acicular particles comprise a microstructured core having a layer of catalytic material on at least a portion of the surface of the microstructured core, wherein the microstructured core comprises at least one of a polynuclear aromatic hydrocarbon, a heterocyclic compound, and combinations thereof; wherein the catalytic material comprises iridium; and wherein the acicular particles are substantially free of platinum.

12. Use of a composition for an anode of an oxygen evolution reaction, the composition comprising (a) an ionomer binder; and (b) a plurality of acicular particles, wherein the plurality of acicular particles are dispersed throughout the electrode composition, and wherein the acicular particles comprise a microstructured core having a layer of catalytic material on at least a portion of the surface of the microstructured core, wherein the microstructured core comprises at least one of a polynuclear aromatic hydrocarbon, a heterocyclic compound, and combinations thereof, and the catalytic material comprises iridium, and wherein the acicular particles are substantially free of platinum.

13. An electrolytic cell, comprising:

a proton exchange membrane having first and second opposed major surfaces;

a cathode on the first major surface of the proton exchange membrane;

an anode on the second major surface of the proton exchange membrane, wherein the anode comprises (a) an ionomer binder; and (b) a plurality of acicular particles, wherein the plurality of acicular particles are dispersed throughout the electrode composition, and wherein the acicular particles comprise a microstructured core having a layer of catalytic material on at least a portion of the surface of the microstructured core, wherein the microstructured core comprises at least one of a polynuclear aromatic hydrocarbon, a heterocyclic compound, and combinations thereof, and the catalytic material comprises iridium, and wherein the acicular particles are substantially free of platinum;

a first gas diffusion layer contacting the cathode;

a second gas diffusion layer contacting the anode; and

an electrical power source connected to the cathode and the anode.

14. A method of generating hydrogen and oxygen from water, the method comprising:

obtaining an electrolytic cell comprising an anode portion and a cathode portion and an ion-conducting membrane between the anode portion and the cathode portion, wherein the anode comprises an electrode composition, wherein the electrode composition comprises (a) an ionomer binder; and (b) a plurality of acicular particles, wherein the plurality of acicular particles are dispersed throughout the electrode composition, and wherein the acicular particles comprise a microstructured core having a layer of catalytic material on at least a portion of the surface of the microstructured core, wherein the microstructured core comprises at least one of a polynuclear aromatic hydrocarbon, a heterocyclic compound, and combinations thereof, and the catalytic material comprises iridium, and wherein the acicular particles are substantially free of platinum;

adding water to the anode portion of the electrolytic cell; and

a potential difference sufficient to generate hydrogen and oxygen from water is applied between the anode portion and the cathode portion.

15. A method of generating carbon monoxide and oxygen from carbon dioxide, the method comprising:

obtaining an electrolytic cell comprising an anode portion and a cathode portion and an ion-conducting membrane between the anode portion and the cathode portion, wherein the anode comprises the electrode composition, wherein the electrode composition comprises (a) an ionomer binder; and (b) a plurality of acicular particles, wherein the plurality of acicular particles are dispersed throughout the electrode composition, and wherein the acicular particles comprise a microstructured core having a layer of catalytic material on at least a portion of the surface of the microstructured core, wherein the microstructured core comprises at least one of a polynuclear aromatic hydrocarbon, a heterocyclic compound, and combinations thereof, and the catalytic material comprises iridium, and wherein the acicular particles are substantially free of platinum;

adding carbon dioxide to the cathode portion of the electrolytic cell; and

a potential difference is applied between the anode portion and the cathode portion sufficient to generate carbon monoxide and oxygen from carbon dioxide.

Technical Field

A composition comprising a dispersed catalyst for an anode of an electrolytic cell, the composition comprising a catalyst ink, an anode electrode, and a catalyst coated substrate.

Disclosure of Invention

There is great interest in achieving environmental cleanliness in the energy industry with energy from renewable resources. The desire to be able to convert and store renewable energy sources has increased the interest in hydrogen as a clean and environmentally friendly energy carrier. Also, the growth in mobility of hydrogen activation (e.g., power fuel cells) further drives the need for economical means of generating hydrogen.

Since renewable energy sources such as wind and solar are variable, Polymer Electrolyte Membrane (PEM) water electrolysis has emerged as an attractive fuel generation source to convert excess solar and wind energy into storable hydrogen fuel and generate additional usable hydrogen fuel for various power needs.

Accordingly, it is desirable to identify less expensive and/or more efficient electrolyzers.

In one aspect, an electrode composition for an electrolytic cell is described, the electrode composition comprising:

(a) an ionomer binder; and

(b) less than 54 percent by solid volume of a plurality of acicular particles, wherein the plurality of acicular particles are dispersed throughout the electrode composition, and wherein the acicular particles comprise a microstructured core having a layer of catalytic material on at least a portion of the surface of the microstructured core, wherein the microstructured core comprises at least one of a polynuclear aromatic hydrocarbon, a heterocyclic compound, and combinations thereof, and the catalytic material comprises iridium, and wherein the acicular particles are substantially free of platinum.

In another aspect, a catalyst ink composition is described, the catalyst ink comprising:

(a) an ionomer binder;

(b) a plurality of acicular particles less than 54% solids volume, and wherein the acicular particles comprise a microstructured core having a layer of catalytic material on at least a portion of a surface of the microstructured core, wherein the microstructured core comprises at least one of a polynuclear aromatic hydrocarbon, a heterocyclic compound, and combinations thereof, and the catalytic material comprises iridium, and the acicular particles are substantially platinum-free; and

(c) a solvent;

wherein the plurality of acicular particles are dispersed throughout the electrode composition.

In one embodiment, an article is provided. The article comprises:

a substrate having a coating thereon, the coating comprising (a) an ionomer binder; and (b) less than 54 percent by solid volume of a plurality of acicular particles, wherein the plurality of acicular particles are dispersed throughout the coating, and wherein the acicular particles comprise a microstructured core having a layer of catalytic material on at least a portion of the surface of the microstructured core, wherein the microstructured core comprises at least one of a polynuclear aromatic hydrocarbon, a heterocyclic compound, and combinations thereof, and the catalytic material comprises iridium, and the acicular particles are substantially free of platinum.

In one embodiment, an electrolytic cell is provided. The electrolytic cell comprises a proton exchange membrane having first and second opposed major surfaces;

a cathode on the first major surface of the proton exchange membrane;

an anode on the second major surface of the proton exchange membrane;

a gas diffusion layer contacting the cathode;

an anode gas diffusion layer contacting the anode; and

an electrical power source, wherein the anode comprises (a) an ionomer binder; and

and (b) a plurality of acicular particles, wherein the plurality of acicular particles are dispersed throughout the electrode composition, and wherein the acicular particles comprise a microstructured core having a layer of catalytic material on at least a portion of the surface of the microstructured core, wherein the microstructured core comprises at least one of a polynuclear aromatic hydrocarbon, a heterocyclic compound, and combinations thereof, and the catalytic material comprises iridium, and wherein the acicular particles are substantially free of platinum.

The above summary is not intended to describe each embodiment. The details of one or more embodiments of the invention are set forth in the detailed description below. Other features, objects, and advantages will be apparent from the description and from the claims.

Drawings

The drawings are generally shown by way of example, and not by way of limitation, to the various embodiments discussed in this document.

FIG. 1 illustrates an exemplary membrane electrode assembly described herein;

FIG. 2 shows cell voltage versus current density for various anodes;

FIG. 3 shows cell voltage versus current density for various anodes; and is

Fig. 4 shows the current density versus electrode loading for examples 1-8 and comparative examples a-C at a cell voltage of 1.5 volts.

Detailed Description

Reference will now be made in detail to specific embodiments of the presently disclosed subject matter, examples of which are illustrated in the accompanying drawings. While the presently disclosed subject matter will be described in conjunction with the recited claims, it will be understood that the exemplary subject matter is not intended to limit the claims to the presently disclosed subject matter.

In this document, the terms "a", "an" or "the" are used to include one or more than one unless the context clearly indicates otherwise. The term "or" is used to refer to a non-exclusive "or" unless otherwise indicated. The expression "at least one of a and B" or "at least one of a or B" has the same meaning as "A, B or a and B". Also, it is to be understood that the phraseology or terminology employed herein, and not otherwise defined, is for the purpose of description only and not of limitation. Any use of section headings is intended to aid in the understanding of the document and should not be construed as limiting; information related to a section header may appear within or outside of that particular section. All publications, patents, and patent documents mentioned in this document are incorporated by reference herein in their entirety, as though individually incorporated by reference. In the event of inconsistent usages between this document and those documents so incorporated by reference, the usage in the incorporated reference should be considered supplementary to that of the document; for irreconcilable inconsistencies, the usage of the document controls.

As used herein, the term

"and/or" is used to indicate that one or both of the recited conditions may occur, for example, A and/or B includes (A and B) and (A or B);

"highly fluorinated" refers to a compound wherein at least 75%, 80%, 85%, 90%, 95%, or even 99% of the C-H bonds are replaced with C-F bonds and the remainder of the C-H bonds are selected from C-H bonds, C-Cl bonds, C-Br bonds, and combinations thereof;

"perfluorinated" means a group or compound derived from a hydrocarbon in which all hydrogen atoms have been replaced by fluorine atoms. However, the perfluorinated compounds may also contain other atoms than fluorine atoms and carbon atoms, such as oxygen atoms, chlorine atoms, bromine atoms, and iodine atoms; and is

"equivalent weight" (EW) of a polymer means the weight of the polymer that will neutralize one equivalent of base;

for certain chemical species, "substituted" means substituted with conventional substituents that do not interfere with the desired product or process, e.g., alkyl, alkoxy, aryl, phenyl, halo (F, Cl, Br, I), cyano, nitro, and the like;

"nanoscale catalyst particles" means particles of catalyst material having at least one dimension of about 10nm or less, or having a crystallite size of about 10nm or less, measured as the half width of the diffraction peak in a standard 2-theta x-ray diffraction scan; and is

"discrete" refers to discrete elements having separate bodies, but does not preclude contact between the elements;

also herein, the recitation of ranges by endpoints includes all numbers subsumed within that range (e.g. 1 to 10 includes 1.4, 1.9, 2.33, 5.75, 9.98, etc.).

Also, as used herein, the expression "at least one" includes one and all numbers greater than one (e.g., at least 2, at least 4, at least 6, at least 8, at least 10, at least 25, at least 50, at least 100, etc.).

The present invention relates to compositions useful in anodes for electrolytic cells. An electrolyzer is a device that can be used to produce hydrogen, carbon monoxide, or formic acid, etc., based on an input reactant (e.g., water or carbon dioxide).

An exemplary electrolytic cell is shown in fig. 1, which includes a membrane electrode assembly 100 having an anode 105. Adjacent anode 105 is a proton exchange membrane 104 having first and second opposing major surfaces. The cathode 103 is located adjacent to the proton exchange membrane 104 on a first major surface thereof, and the anode 105 is located adjacent to a second major surface of the proton exchange membrane 104. A gas diffusion layer 107 is located near the cathode 103. The proton exchange membrane 104 is electrically insulating and allows only hydrogen ions (e.g., protons) to pass through the membrane 104.

In operation for water electrolysis, water is introduced into the anode 105 of the membrane electrode assembly 100. At the anode 105, water is separated into molecular oxygen (O)₂) Hydrogen ion (H)⁺) And electrons. The hydrogen ions diffuse through the proton exchange membrane 104 while the potential 117 drives electrons to the cathode 103. At the cathode 103, the hydrogen ions combine with electrons to form hydrogen gas.

The ion-conducting membrane forms a durable, non-porous, non-electrically conductive mechanical barrier between the product gases, but it also readily transmits H⁺In some embodiments, the anode and cathode electrode layers are applied to GD L to form a catalyst coated backing layer (CCB), and the resulting CCB is sandwiched in the PEM to form a five-layer MEA five layers of anode GD L, anode electrode layer, PEM, cathode electrode layer, and cathode GD L in that order, in other embodiments, the anode and cathode electrode layers are applied on either side of the PEM, and the resulting Catalyst Coated Membrane (CCM) is sandwiched between two GD L to form a five-layer MEA.

The present disclosure relates to dispersion compositions containing electrode catalysts and articles made therefrom. The dispersion composition comprising an electrode catalyst comprises a plurality of acicular particles dispersed in an ionomer binder. The plurality of acicular particles are unoriented in the electrode composition. As used herein, "non-oriented" means that the acicular particles have randomly oriented long axes and no pattern is observed. These catalyst-containing dispersion compositions can be used in anodes for electrolytic cells.

Acicular particles

Acicular particles disclosed herein are discrete elongated particles comprising a plurality of microstructured cores, wherein at least a portion of the surface of the microstructured cores comprises a layer of catalytic material.

The microstructured core is an elongated particle comprising an organic compound that acts as a support for the catalytic material disposed thereon. Although elongated, the shape of the microstructured core of the present disclosure need not be linear, and may be bent, curled, or curved at the ends of the structure, or the structure itself may be bent, curled, or curved along its entire length.

The microstructured core is made of an organic compound. Organic compounds include planar molecules with chains or rings, and pi electron densities are widely delocalized over the planar molecules. Organic compounds suitable for use in the present disclosure typically crystallize in a herringbone configuration. Preferred compounds include those that can be broadly classified as polynuclear aromatic hydrocarbons and heterocyclic compounds. Polynuclear aromatics are described in "Organic Chemistry" by Morrison and Boyd (third edition, Allyn and Bacon inc., Boston, 1974, chapter 30), and heterocyclic aromatics are described in Morrison and Boyd, chapter 31, supra. Among the preferred classes of polynuclear aromatic hydrocarbons of the present disclosure are naphthalene, benzanthrene, perylene, anthracene, coronene, pyrene, and derivatives of the compounds in the aforementioned classes. Preferred organic compounds are the commercially available perylene red pigments, N' -di (3, 5-xylyl) perylene-3, 4:9,10 bis (diimide), hereinafter referred to as perylene red. Among the classes of heterocyclic aromatic compounds preferred for the present disclosure are phthalocyanines, porphyrins, carbazoles, purines, pterins, and derivatives of the foregoing classes of compounds. Representative examples of phthalocyanines particularly useful in the present disclosure are phthalocyanines and metal complexes thereof, such as copper phthalocyanine. A representative example of a porphyrin useful in the present disclosure is a porphyrin.

Methods for manufacturing needle-like elements are known in the art. For example, methods for manufacturing organic microstructured elements are disclosed in "Materials Science and Engineering", a158(1992), pages 1-6; J.Vac.Sci.Technol.A,5, (4), 1987, July/August, pages 1914-16; J.Vac.Sci.Technol.A,6, (3),1988, May/August, pages 1907-11; "Thin Solid Films", Vol.186, 1990, pp.327-47; mat. journal of science, 25, 1990, pages 5257-68; "Rapid quenching Metals", Proc. of the Fifth int. Conf. on Rapid quenching Metals, Wurzburg, Germany (Fifth Rapid quenching Metals International conference record, Utzburg, Germany) (9, 3, 7, 1984), S. Steeb et al, eds., Elsevier Science Publishers B.V., New York (Elez scientific Press, N.Y.) (1985), p.1117-24; photo.sci.and eng, 24, (4), july/august, 1980, pages 211-16; and U.S. patent applications 4,568,598(Bilkadi et al) and 4,340,276(Maffitt et al), the disclosures of which are incorporated herein by reference. Robbie et al, "contamination of Thinfilms with high porosity microspheres" (manufacture of films with Highly Porous microstructure), "J.Vac.Sci.Tech.A., Vol.13, p.3, 1995, May/June, p.1032-35 and K.Robbie et al," First Thin Film reaction of Bianisoropic Medium (Realization of the First Film of a bi-anisotropic Medium) ", J.Vac.Sci.Tech.A., Vol.13, Vol.6, 1995, November/December, p.2991-93.

For example, the organic compound is coated onto the substrate using techniques known in the art, including, for example, vacuum vapor deposition (e.g., vacuum evaporation, sublimation, and chemical vapor deposition) and solution or dispersion coating (e.g., dip, spray, spin, knife or blade coating, rod, roll, and flow coating (i.e., pouring a liquid onto a surface and letting the liquid flow over the surface)). The organic compound layer is then processed (e.g., annealed, plasma etched) such that the layer undergoes a physical change, wherein the organic compound layer grows to form a microstructured layer comprising a dense array of discrete oriented single crystal or polycrystalline microstructured cores. Following this approach, the microstructured core long axis is oriented generally perpendicular to the substrate surface.

In one embodiment, the organic compound is vapor coated onto the substrate. The substrate may vary and is selected to be compatible with the heating process. Exemplary substrates include polyimide and metal foil. The temperature of the substrate during vapor deposition may vary depending on the organic compound selected. For perylene red, substrate temperatures near room temperature (25 ℃) are satisfactory. The rate of vacuum vapor deposition can be varied. The thickness of the deposited organic compound layer may vary and the thickness selected will determine the major dimensions of the resulting microstructure after the annealing step is performed. The thickness of the layer is generally in the range of about 1 nanometer to about 1 micron, and preferably in the range of about 0.03 microns to about 0.5 microns. The organic compound layer is then heated, optionally under reduced pressure, for a sufficient temperature and time to cause a physical change in the deposited organic compound, thereby producing a microlayer comprising a pure single-crystal or polycrystalline microstructured core. These single crystal or polycrystalline microstructures are used to support a layer of catalytic material, thereby forming the acicular particles of the present disclosure.

The catalytic material of the present invention comprises iridium. The iridium may be iridium metal, iridium oxide and/or iridium-containing compounds such as IrO_xWherein x can be in the range of 0-2. In one embodiment, the catalytic material further comprises ruthenium, which may be in the form of ruthenium metal, ruthenium oxide, and/or may be a ruthenium-containing compound, such as iridium oxide, RuO_xWherein x may be in the range of 0-2. In water-based electrolyzer applications, platinum-based anodes tend to be less efficient in oxygen evolution than their iridium counterparts. Thus, the acicular particles are substantially free of platinum (meaning that the composition contains less than 1, 0.5, or even 0.1 atomic percent platinum in the catalytic material). Iridium and/or ruthenium include alloys thereof, and intimate mixtures thereof.

The iridium and ruthenium may be disposed on the same microstructured core or may be disposed on separate microstructured cores.

The catalytic material is disposed on at least one surface (more preferably at least two or even three surfaces) of the plurality of microstructured cores. The catalytic material is disposed in a continuous layer over the entire surface such that electrons can continuously move from one portion of the acicular particles to another portion of the acicular particles. The catalytic material layer on the surface of the organic compound creates a large number of reaction sites for oxygen evolution at the anode.

In one embodiment, a catalytic material is deposited onto the surface of an organic compound, initially forming a nanostructured catalyst layer, wherein the layer comprises nanoscale catalyst particles or a catalyst thin film. In one embodiment, the nanoscale catalyst particles are particles having at least one dimension equal to or less than about 10nm, or having a crystallite size of about 10nm or less, as measured by the diffraction peak half-width of a standard 2-theta x-ray diffraction scan. The catalytic material may further be deposited onto the surface of the organic compound to form a thin film comprising nano-sized catalyst particles, which may or may not be in contact with each other.

In one embodiment, the thickness of the layer of catalytic material on the surface of the organic compound may vary, but is typically in the range of at least 0.3nm, 0.5nm, 1nm, or even 2 nm; and no greater than 5nm, 10nm, 20nm, 40nm, 60nm, or even 100nm on the sides of the microstructured core.

In one embodiment, the catalytic material is applied to the microstructured core by vacuum deposition, sputtering, physical vapor deposition, or chemical vapor deposition.

In one embodiment, the acicular particles of the present disclosure are formed by: the microstructured core is first produced on a substrate as described above, a layer of catalytic material is applied to the microstructured core, and the catalytically coated microstructured core is then removed from the substrate to form loose acicular particles. Such methods of making microstructured cores and/or coating them with catalytic materials are disclosed, for example, in U.S. patent 5,338,430(Parsonage et al); 5,879,827(Debe et al); 5,879,828(Debe et al); 6,040,077(Debe et al); and 6,319,293(Debe et al); 6,136,412(Spiewak et al); and 6,482,763(Haugen et al), which are incorporated herein by reference. Such methods of removing a catalyst coated microstructured core from a substrate are disclosed, for example, in U.S. patent application 25001/0262828(Noda et al), which is incorporated herein by reference.

While these multiple acicular particles may have a variety of shapes, the shape of the individual acicular particles is preferably uniform. Shapes include rods, cones, cylinders, and slats. In one embodiment, the acicular particles have a large aspect ratio, defined as the ratio of length (major dimension) to diameter or width (minor dimension). In one embodiment, the acicular particles have an average aspect ratio of at least 3,5, 7, 10 or even 20 and at most 60, 70, 80 or even 100. In one embodiment, the acicular particles have an average length of greater than 250nm, 300nm, 400nm, or even 500nm (nanometers); and less than 750 nanometers, 1 micron, 1.5 microns, 2 microns, or even 5 microns. In one embodiment, the acicular particles have an average diameter (or width) of greater than 15nm, 20nm, or even 30 nm; and less than 100 nanometers, 500 nanometers, 750 nanometers, 1 micron, 1.5 microns, or even 2 microns. Such length and diameter (or width) measurements may be obtained by Transmission Electron Microscopy (TEM).

In one embodiment, the size, i.e., length and cross-sectional area, of the acicular particles is generally consistent from particle to particle. As used herein, the term "uniform" with respect to size means that the major dimension of the cross-section of an individual acicular particle varies by no more than about 23% from the average of the major dimension, and the minor dimension of the cross-section of an individual acicular particle varies by no more than about 28% from the average of the minor dimension. The uniformity of the acicular particles provides uniformity in the characteristics and performance of the article containing the acicular particles. Such properties include optical, electrical and magnetic properties. For example, electromagnetic wave absorption, scattering and trapping are highly dependent on the uniformity of the microlayers.

Ionomer binders

The ionomer binder is a polymer electrolyte material that may or may not be the same polymer electrolyte material of the electrochemical cell membrane. Ionomer binders are used to aid in ion transport through the electrodes. The ionomer binder is a solid polymer and thus its presence in the electrode inhibits the transport of reactants to the electrocatalyst. In a water electrolyser, the reactant fluid is liquid water, not gas. It is believed that reactant water transport through the PEM electrolyser electrodes is much faster than when gaseous reactants are used. Thus, as the present disclosure relates to an electrolytic cell, it is believed that more ionomers can be used in the electrode compositions disclosed herein without reducing high current operation. From a cost perspective, it may be advantageous to have a higher percentage of ionomer in the electrode, and/or to be able to achieve optimal performance. In one embodiment, the electrode composition comprises less than 54, 52, 50, or even 48 percent by solid volume of the acicular particles relative to the total solid volume of the electrode composition (i.e., comprising acicular particles and ionomer binder), and/or alternatively, comprises greater than 46, 48, 50, or even 52 percent by solid volume of the ionomer relative to the total solid volume of the electrode composition.

Useful polymer electrolyte materials can contain anionic functional groups such as sulfonate groups, carbonate groups, or phosphonate groups bonded to the polymer backbone, as well as combinations and mixtures thereof. In one embodiment, the anionic functional group is preferably a sulfonate group. The polymer electrolyte material can include an imide group, an amide group, or another acidic functional group, as well as combinations and mixtures thereof.

Examples of useful polymer electrolyte materials are highly fluorinated, typically perfluorinated, fluorocarbon materials. Such fluorocarbon materials can be copolymers of tetrafluoroethylene with one or more types of fluorinated acid-functional comonomers. Fluorocarbon resins have high chemical stability with respect to halogens, strong acids and bases, and thus they can be advantageously used. For example, when high oxidation resistance or acid resistance is required, a fluorocarbon resin having a sulfonate group, a carbonate group, or a phosphonate group, and particularly a fluorocarbon resin having a sulfonate group can be used advantageously.

Exemplary fluorocarbon resins containing sulfonate groups include perfluorosulfonic acid (e.g., Nafion), perfluorosulfonimide acid (PFIA), sulfonated polyimide, sulfonated polytrifluoroethylene, sulfonated hydrocarbon polymers, polysulfone, and polyethersulfone. Other fluorocarbon resins include perfluoroimides such as Perfluoromethylimide (PFMI) and Perfluorobutylimide (PFBI). In one embodiment, the fluorocarbon resin is a polymer containing multiple primary forming groups per side chain.

Commercially available polymer electrolyte materials include, for example, those available under the trade designation "DYNEON" from 3M company of St.Paul, MN, Minnesota, DuPont Chemicals (Wilmington, DE), under the trade designation "NAIFON" from Asahi Glass Co., L td., Tokyo, Japan, under the trade designation "F L EMION", from Asahi Glass Co., Ltd, of Tokyo, Japan, and from electro-Chemical Co., Inc. of Walker, Inc., of Massachusetts, Inc., and those available under the trade designation "ACIP L EX" from Asahi Chemical company of Wookup, Japan (Asahi Kasei Chemicals, Tokyo, Japan), and from Milwauk Chemical Co., Inc., of Wako, Inc., of Massachusetts.

In one embodiment, the polymer electrolyte material is selected from perfluorox imides, where X can be, but is not limited to, methyl, butyl, propyl, phenyl, and the like.

Typically, the equivalent weight of the ionically conductive polymer is at least about 400, 500, 600, or even 700; and no greater than about 825, 900, 1000, 1100, 1200, or even 1500.

In one embodiment, the ratio of ionomer binder to acicular particles is from 1:100 to 1:1 by weight, more preferably from 1:20 to 1:2 by weight.

In one embodiment, the ratio of ionomer binder to acicular particles is from 1:10 to 1:10 by volume, more preferably from 1:3 to 3:1 by volume.

Solvent(s)

Typically, a plurality of microstructured elements are applied along with an ionomer binder, and various solvents in dispersion form, such as inks or pastes.

Exemplary solvents include water, ketones (such as acetone, tetrahydrofuran, methyl ethyl ketone, and cyclohexanone), alcohols (such as methanol, isopropanol, propanol, ethanol, and propylene glycol butyl ether), polyols (such as glycerol and ethylene glycol), hydrocarbons (such as cyclohexane, heptane, and octane), dimethyl sulfoxide, and fluorinated solvents (such as heptadecafluorooctane sulfonate), and partially or perfluorinated alkanes or tertiary amines (such as those available under the trade designation "3M OVEC ENGINNERED F L UID" or "3M F L UORONEOIRT E L RONIC L IQUID" liquid from 3M company (3M Co., St.Paul, MN), St.P.M.).

In one embodiment, the catalyst ink composition is an aqueous dispersion optionally comprising water and one or more solvents, and optionally a surfactant.

In one embodiment, the catalyst ink composition comprises from 0.1 to 50 wt%, 5 to 40 wt%, 10 to 25 wt%, and more preferably 1 to 10 wt% solvent/solids weight (i.e., the plurality of acicular particles and ionomer binder).

Article of manufacture

In one embodiment, the catalyst composition is applied to a substrate such as a Polymer Electrolyte Membrane (PEM) or a gas diffusion layer (GD L), or a transfer substrate, and subsequently transferred to a PEM or GD L.

PEM is known in the art the PEM may comprise any suitable polymer electrolyte typically bearing anionic functional groups bonded to a common backbone, typically sulfuric acid groups, but may also include carboxylic acid groups, imide groups, amide groups, or other acidic functional groups exemplary polymer electrolytes include those mentioned above for ionomer binders polymer electrolytes are typically cast to have a thickness of less than 250 microns, more typically less than 175 microns, more typically less than 125 microns, in some embodiments less than 100 microns, and in some embodiments about 50 microns (film) (i.e., a MEMBRANE (MEMBRANE)), PEM may be composed of a polymer electrolyte, or a polymer electrolyte may be absorbed into a porous carrier (such as PTFE.) examples of known PEMs include those available under the trade designation "nafn sa members" from souton chemical company (e.i.pount, podu, usa, inc., and sekun co. (r.r.r.r.r.r.r.r. poa.m., inc., fava.p.r., inc., fak, inc., n. pfm.

GD L is also known in the art in one embodiment, the anode GD L is a sintered metal fiber nonwoven or felt, such as those disclosed in CN 203574057(Meekers et al) and WO2016/075005(Van Haver et al), coated or impregnated with a metal comprising at least one of titanium, platinum, gold, iridium, or combinations thereof.

The transfer substrate is a temporary carrier that is not intended for the end use of the electrode, but rather is used to support and/or protect the electrode during manufacture or storage. The transfer substrate is removed from the electrode article prior to use. The transfer substrate comprises a backing that is typically coated with a release coating. The electrode is disposed on the release coating, which allows for easy and clean removal of the electrode from the transfer substrate. Such transfer substrates are known in the art. Backings are typically constructed of PTFE, polyimide, polyethylene terephthalate, polyethylene naphthalate (PEN), polyester, and similar materials with or without release agent coatings.

Examples of release agents include urethanes (carbamates or urethanes), silicones, fluorocarbons, fluorosilicones, and combinations thereof. Urethane strippers typically have long side chains and relatively high softening points. Exemplary urethane release agents are polyethylene stearyl urethane available under the trade designation "ESCOAT P20" from Anderson Development Co of aldrin, michigan (andreson Development Co. (Adrian, Mich.)), and RA-95H, RA-95HS, RA-155, and RA-585S in various grades from Mayzo Inc.

Illustrative examples of surface-applied (i.e., topically-applied) release agents include polyvinyl urethanes such as disclosed in U.S. Pat. No. 2,532,011(Dahlquist et al), reactive silicones, fluoride polymers, epoxy silicones such as disclosed in U.S. Pat. Nos. 4,313,988(Bany et al) and 4,482,687(Kessel et al), polyorganosiloxane-polyurea block copolymers such as disclosed in U.S. Pat. No. 5,512,650 (L eir et al), and the like.

Silicone release agents typically comprise an organopolysiloxane polymer that contains at least two crosslinkable reactive groups, such as two ethylenically unsaturated organic groups. In some embodiments, the silicone polymer comprises two terminal crosslinkable groups, for example two terminal ethylenically unsaturated groups. In some embodiments, the silicone polymer comprises a pendant functional group, such as a pendant ethylenically unsaturated organic group. In some embodiments, the silicone polymer has a vinyl equivalent weight of no greater than 20,000 grams/equivalent, such as no greater than 15,000 grams/equivalent, or even no greater than 10,000 grams/equivalent. In some embodiments, the silicone polymer has a vinyl equivalent weight of at least 250 grams/equivalent, such as at least 500 grams/equivalent, or even at least 1000 grams/equivalent. In some embodiments, the silicone polymer has a vinyl equivalent weight of 500 to 5000 grams per equivalent, such as 750 to 4000 grams per equivalent, or even 1000 to 3000 grams per equivalent.

Commercially available silicone polymers include those available under the trade designation "DMS-V" from Gelest Inc. (Gelest Inc.), such as DMS-V05, DMS-V21, DMS-V22, DMS-V25, DMS-V31, and DMS-V33. other commercially available silicone polymers containing an average of at least two ethylenically unsaturated organic groups include "SY L-OFF 2-7170" and "SY L-OFF 7850" (from Dow Corning Corporation), "VVMS-T11" and "SIT 7900" (from Gelest Inc. (Gelest Inc.), "SI L MER VIN 70", "SI L MER 100", and "SI L MER VIN 200" (from Silty Corporation (Aldrich)), and 2,4,6, 8-tetramethyl-2, 4,6, 8-tetraethoxysilane (8-alkenyl-tetrakissiloxane) (Aldrich Inc.)).

Commercially available ethylenically unsaturated fluorosilicone polymers are commercially available from Dow Corning corporation of Midland, Mich under the series trade names, including, for example, "SY L-OFFFOPS-7785" and "SY L-OFFFOPS-7786" (available from Dow Corning Corp. (Midland, MI) other ethylenically unsaturated fluorosilicone polymers are commercially available from General Electric company of Olbani, N.Y. (Albancy, NY)) and from Veksa chemical company of Germany (Wacker Chemie (Germany)), additional useful ethylenically unsaturated fluorosilicone polymers are described as component (e) in column 5, lines 67 to 7 of U.S. patent 5,082,706(Tangney), when mixed with a suitable crosslinker, the fluorosilicone useful fluorosilicone polymer in forming a coating composition is disclosed as particularly useful under the trade names "SY-L" (available from Dow Corp.). and other useful crosslinkers are disclosed in U.S. Corning corporation of Corp 3932 (available from Corksa Corksman, Corp.). Corp.

The electrode composition may be initially mixed together in an ink, paste, or dispersion, thus, the electrode composition in one or more layers, each layer having the same composition or some layers having different compositions, may be subsequently applied to the PEM, GD L, or transfer article.

After coating, the coated substrate is typically dried to at least partially remove the solvent from the electrode composition, leaving the electrode layer on the substrate.

In one embodiment, the composition comprises less than 54, 52, 50, or even 48 percent by solid volume of the acicular particles relative to the total solid volume of the composition (i.e., comprising acicular particles and ionomer binder). If there are not enough acicular particles in the resulting electrode, there will be insufficient conductivity and performance may be reduced. Thus, in one embodiment, the composition comprises at least 1, 5, 10, 20 or even 25% by solid volume of acicular particles relative to the total solid volume of the composition to be performed.

If the coating is applied to a transfer substrate, the electrode is typically transferred to the surface of the PEM. In one embodiment, the coated transfer substrate is pressed against the PEM with heat and pressure, after which the coated transfer substrate is removed and discarded, leaving the electrode bonded to the surface of the PEM.

In one embodiment, the coating is incorporated into an electrolytic cell, such as the water electrolysis cell described in FIG. 1.

In addition to a membrane electrode assembly comprising a cathode gas diffusion layer, a cathode, a proton exchange membrane, an anode and an anode gas diffusion layer, the cell may further comprise a cathode gasket in contact with the cathode gas diffusion layer.

The membrane electrode assembly is typically mounted between a set of flow field plates, which enable reactant water to be distributed to the anode electrode, product oxygen to be removed from the anode and product hydrogen to be removed from the cathode, and voltage and current to be applied to the electrodes. Flow field plates are typically non-porous plates comprising flow channels, have low permeability to reactants and products, and are electrically conductive.

The flow field and MEA assembly can be repeated to provide a stack of repeating units that are typically electrically connected in series.

The battery assembly may also include a set of current collectors and compression hardware.

In the case of water input, the operation of the electrolyzer produces hydrogen and oxygen, and consumes water and electrical energy. A voltage of 1.23V or higher needs to be applied across the cell to electrochemically generate hydrogen and oxygen from water under standard conditions. As the cell voltage increased to 1.23V and above, current began to appear between the anode and cathode. The electron current is proportional to the water consumption rate and the production of hydrogen and oxygen.

The electrolytic cells of the present disclosure can have any suitable operating current density consistent with the membrane electrode assemblies described herein, for example, 0.001A/cm at 80 ℃²To 30A/cm²、0.5A/cm²To 25A/cm²、1A/cm²To 20A/cm²、2A/cm²To 10A/cm²Within the range of, or less than, equal to, or greater than 0.001A/cm²、0.01A/cm²、0.1A/cm²、0.5A/cm²、1A/cm²、2A/cm²、3A/cm²、4A/cm²、5A/cm²、6A/cm²、7A/cm²、8A/cm²、9A/cm²、10A/cm²、11A/cm²、12A/cm²、13A/cm²、14A/cm²、15A/cm²、16A/cm²、17A/cm²、18A/cm²、19A/cm²、20A/cm²、22A/cm²、24A/cm²、26A/cm²、28A/cm²Or 30A/cm²Or a greater range of operating current densities.

Generally, the measured current density is an approximately proportional measure of the absolute catalytic activity of the anode electrode. The relationship between current density and catalytic activity is especially true at low electrode overpotentials. With all other components and operating conditions fixed, a higher current density at a given cell voltage indicates a higher absolute catalyst activity. It is generally believed that increasing the catalyst surface area per unit planar area would be expected to increase the absolute catalyst activity proportionately by increasing the number of active catalytic sites per unit planar area. Methods for increasing the catalyst surface area per unit electrode planar area include (1) increasing the catalyst (i.e., Ir) content of the electrode (i.e., higher Ir area loading per unit electrode planar area) and (2) increasing the catalyst (i.e., Ir) surface area per unit Ir content (i.e., higher specific surface area, m per gram Ir electrochemical surface²). Without being bound by theory, the specific surface area (m) is expected²/g) will increase with decreasing thickness of the Ir metal film on the whisker, since the fraction of Ir metal increases at the surface of the film rather than within the bulk of the film. Based on PR149 whisker geometry, significantly greater absolute incremental area gain is expected to occur when the Ir film thickness on the PR149 whisker support is reduced below about 10 nm.

Traditionally, it is expected that there may be a limit to the minimum practical catalyst coating thickness on the whisker support below which the catalyst may be substantially deactivated. The operation of the anode electrode for electrolysis cells requires electronic conduction within the electrode to effect the electrochemical oxygen evolution reaction. In electrodes comprising catalyst-coated acicular particles and ionomers and not comprising any other electron conductor, it is believed that electron conduction within the electrode occurs only within the metal catalyst. As the thickness decreases, the catalyst thin film may not be thermodynamically stable, but may take the form of individual grains that do not contact each other. If the catalyst is in the form of individual crystallites that are not in contact with each other, a portion of the catalyst material will not be electrochemically active due to a lack of electron conduction and performance will be lost.

In the present disclosure, it was unexpectedly found that the use of dispersed acicular particles in an electrolytic cell anode resulted in a monotonic increase in current density at a particular voltage as the thickness of catalytic material on the microstructured core decreased. This enables the use of less catalytic material.

In various embodiments, the present disclosure provides methods of using an electrolytic cell. The method may be any suitable method using any embodiment of the electrolytic cell described herein. For example, the method may include applying an electrical potential across the anode and the cathode. In one embodiment, the anode may be used for oxygen evolution reactions, for example in water electrolysis or carbon dioxide electrolysis. In one embodiment, in water electrolysis using an acidic membrane electrode assembly, water (e.g., any suitable water, such as deionized water) may be provided to the anode, and oxygen may be generated on the anode side and hydrogen on the cathode side. In one embodiment, in water electrolysis using an alkaline membrane electrode assembly, water may be provided to the cathode side, and oxygen may be generated on the anode side and hydrogen may be generated on the cathode side. In one embodiment, in carbon dioxide electrolysis, carbon dioxide may be provided to the cathode side, thereby producing oxygen on the anode side and carbon monoxide on the cathode side.

Exemplary embodiments of the present disclosure include, but are not limited to, the following.