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56 results about "Mass activity" patented technology

Platinum and Platinum Based Alloy Nanotubes as Electrocatalysts for Fuel Cells

Electrocatalyst durability has been recently recognized as one of the most important issues that have to be addressed before the commercialization of the proton exchange membrane fuel cells (PEMFCs). The present invention is directed to a new class of cathode catalysts based on supportless platinum nanotubes (PtNTs) and platinum alloy nanotubes, for example, platinum-palladium nanotubes (PtPdNTs), that have remarkable durability and high catalytic activity. Due to their unique combination of dimensions at multiple length scales, the platinum nanotubes of the present invention can provide high platinum surface area due to their nanometer-sized wall thickness, and have the potential to eliminate or alleviate most of the degradation pathways of the commercial carbon supported platinum catalyst (Pt/C) and unsupported platinum-black (PtB) as a result of their micrometer-sized length. The platinum nanotube catalysts of the present invention asymptotically approach a maximum of about twenty percent platinum surface area loss in durability test, while the commercial PtB and Pt/C catalysts lose about fifty-one percent and ninety percent of their initial surface area, respectively. Moreover, the PtNT and PtPdNT catalysts of the present invention show higher mass activity and much higher specific activity than commercial Pt/C and PtB catalysts.
Owner:RGT UNIV OF CALIFORNIA

Metal material for proton exchange membrane fuel cell cathode catalyst and preparation method thereof

The invention provides a metal material for a proton exchange membrane fuel cell cathode catalyst. An alloy formed by platinum and gallium has a one-dimensional nanowire structure having the length of40-80nm and the diameter of 1-2nm, is provide. The invention also provides a preparation method of the metal material. Firstly Pt nanowires are obtained by reduction of the divalent metal platinum under the organic liquid condition, and a trivalent metal gallium compound and a reducing agent are added into the Pt nanowires and the alloy of Pt and Ga with the one-dimensional nanowire structure isobtained through reduction reaction. The structure of the Pt-Ga alloy material is the one-dimensional nanowire structure, the mass activity of the catalyst supported by carbon is more than nine timesof that of the Platinum-carbon nano-catalyst, the area activity of the catalyst is more than seven times than that of the Platinum-carbon nano-catalyst and the mass activity performance loss of the catalyst is only 15.7% when it is recycled 30000 times in oxygen atmosphere. Besides, the preparation method can realize high content doping of Ga element to Pt nanowires and the content is controllable, the use of the Pt element can be effectively reduced according to the requirements and the battery cost can be reduced; meanwhile, the reaction condition is mild and operation is simple.
Owner:HUNAN UNIV

Platinum-based monatomic electrocatalytic material as well as preparation method and application thereof

The invention provides a platinum-based monatomic electrocatalytic material as well as a preparation method and application thereof, belonging to the field of electrocatalysis. The platinum-based monatomic electrocatalytic material is prepared by taking an Anderson type heteropolyacid compound, dopamine or a salt thereof as raw materials, wherein the Anderson type heteropolyacid compound is Anderson type heteropolyacid or a hydrate thereof, and a salt of the Anderson type heteropolyacid or a hydrate thereof; and the structure of the Anderson type heteropolyacid is H8PtR6O24, and R is a transition metal. The electrocatalytic hydrogen evolution performance of the platinum-based monatomic electrocatalyst in an acid solution is equivalent to the electrocatalytic hydrogen evolution performance of commercial platinum carbon, and the electrocatalytic hydrogen evolution performance of the platinum-based monatomic electrocatalyst in an alkaline solution is remarkably higher than the electrocatalytic hydrogen evolution performance of the commercial platinum carbon. Meanwhile, the long-term durability of the platinum-based monatomic electrocatalyst in the acid solution and the alkaline solution is remarkably superior to the long-term durability of commercial platinum carbon, and the mass activity and the catalytic conversion frequency of the platinum-based monatomic electrocatalyst are also remarkably superior to the mass activity and the catalytic conversion frequency of the commercial platinum carbon. The platinum-based monatomic electrocatalyst prepared in the invention has high activity and long-term stable electrocatalytic performance in a wide pH range, and has wide application prospects.
Owner:WEST CHINA HOSPITAL SICHUAN UNIV

Metal nitrogen-carbon loaded low-platinum ordered alloy composite catalyst and preparation method thereof

The invention discloses a metal nitrogen and carbon loaded low-platinum ordered alloy composite catalyst and a preparation method thereof, the composite catalyst comprises metal nitrogen and carbon and platinum alloy loaded on the metal nitrogen and carbon, the metal element in the metal nitrogen and carbon is one or more of iron, cobalt, nickel, copper and manganese; the platinum alloy comprises 2.0-8.6% of platinum and the balance of one or more elements of iron, cobalt, nickel, copper and manganese. The low-platinum-loading-capacity platinum-based ordered alloy loaded on metal nitrogen carbon is successfully prepared by regulating and controlling parameters such as heat treatment temperature, a nitrogen source and a carbon carrier. The metal nitrogen-carbon loaded platinum-iron ordered alloy composite catalyst prepared by the method shows excellent oxygen reduction activity and stability, the mass activity of the metal nitrogen-carbon loaded platinum-iron ordered alloy composite catalyst under the acidic condition of 0.9 V is 3 times that of commercial platinum-carbon, the mass activity of the metal nitrogen-carbon loaded platinum-iron ordered alloy composite catalyst under the alkaline condition is 6.9 times that of commercial platinum-carbon, and the performance of the metal nitrogen-carbon loaded platinum-iron ordered alloy composite catalyst keeps 82.55% of an initial value after 30000 circles of stability tests. The composite catalyst can be used for preparing a low-platinum membrane electrode of a fuel cell.
Owner:NANJING UNIV

Platinum-cobalt alloy catalyst for fuel cell, and preparation method thereof

The invention provides a platinum-cobalt alloy catalyst for a fuel cell, and a preparation method thereof. The platinum-cobalt alloy catalyst is prepared by adopting a polyol reduction method, and the preparation method specifically comprises the following steps: firstly, respectively adding a platinum precursor, a cobalt precursor, a carbon carrier and a reducing agent into polyol, carrying out ultrasonic dispersion to obtain a uniform solution, then transferring carbon carrier slurry into a round-bottom flask, respectively dropwise adding the platinum precursor, cobalt precursor and reducing agent solution, carrying out oil bath heating reaction, cooling, centrifuging, washing and carrying out vacuum drying; and grinding, adding an acid solution for etching, cooling, centrifuging, washing, and carrying out vacuum drying to obtain the high-performance platinum-cobalt alloy catalyst. The preparation method is simple in process, low in raw material cost and high in synthesis efficiency, the prepared carbon-loaded platinum-cobalt alloy electrocatalyst is excellent in oxygen reduction reaction activity, and a test result shows that the half-wave potential, the limiting current density, the electrochemical active area, the mass activity and the like of the synthesized platinum-cobalt alloy electrocatalyst are remarkably superior to those of commercial platinum-carbon.
Owner:郑州中科新兴产业技术研究院 +1

Mo-doped transition metal hydroxide electrocatalyst constructed through deep self-reconstruction as well as preparation method and application of Mo-doped transition metal hydroxide electrocatalyst

The invention discloses a Mo-doped transition metal hydroxide electrocatalyst constructed through deep self-reconstruction and a preparation method and application of the Mo-doped transition metal hydroxide electrocatalyst. The method comprises the following steps: activating a MoS2 nanosheet array under an overpotential condition, soaking the MoS2 nanosheet array in a transition metal salt solution for ion adsorption, and performing deep self-reconstruction by a cyclic voltammetry scanning method to obtain the catalyst. According to the method, raw materials are low in price, high-temperature sintering is not needed, energy consumption in the production process is low, and the production cost is low; and according to the method, a transition metal ion adsorption strategy and an electrochemical self-reconstruction strategy are adopted, the preparation process is simple, and the method is suitable for large-scale production. The deep self-reconstruction Mo-doped transition metal hydroxide electrocatalyst provided by the invention has excellent oxygen evolution reaction intrinsic activity, the overpotential under the current density of 10mA/cm<2> is 242mV, and the mass activity current density under the overpotential of 300mV is 1910A/g.
Owner:SOUTH CHINA UNIV OF TECH

Preparation of bifunctional catalyst diatomite domain limited cobalt-platinum-based composite material, and application of bifunctional catalyst diatomite domain limited cobalt-platinum-based composite material in electrocatalytic oxygen reduction reaction and oxygen evolution reaction

The invention discloses preparation of a diatomite (DTM) domain limited cobalt-platinum-based composite material (CoPt-x/DTM-C) prepared by a simple method, and electrocatalytic application thereof. The invention has the advantages that: (1) the preparation method is simple: firstly, Pt4 and Co2+ ions are adsorbed by the pores of DTM, then the Pt4 and Co2+ ions are reduced, and the structure of the catalyst prepared by the method cannot be damaged easily in the reaction; (2) the catalytic activity is high: in the oxygen reduction reaction, the mass activity and specific activity of the composite material are respectively 2.5 and 1.5 times as large as those of CoPt-x/C and are respectively 4.6 and 2.2 times as large as those of platinum-carbon; and in the oxygen evolution reaction, the overpotential of CoPt-x/DTM-C is reduced by 30 mV compared with that of the CoPt-x/C; and (3) the cost is low: the Pt content of the catalyst is low, the diatomite source is wide, and thus the cost of the catalyst is greatly reduced, and the commercial application prospect is good.
Owner:SOUTH CHINA UNIV OF TECH

Preparation method of dual-element Pt/PdPt/Pt sandwich tube wall porous nanotube and porous nanotube

The invention provides a porous nanotube with a rough surface and a dual-element Pt/PdPt/Pt interlayer tube wall and a preparation method of the porous nanotube. The Kirkendall effect is used for enabling platinum ions to generate a nucleation phenomenon on the surface of a palladium nanowire, internal palladium is gradually removed through gaps of a deposition layer, and then the hollow PdPt nanotube with the outer diameter being 8.6 nm and the wall thickness being about 2.2 nm is formed; the nanotube is further processed to form an interlayer structure with a tube wall element of Pt/PdPt/Pt. According to the product PdPt nanotube, the platinum element can be fully exposed on the inner side and the outer side of the nanotube wall, the utilization rate of platinum in the material is greatly increased, the tube wall interlayer contains the PdPt double elements, and the catalytic reaction activity is greatly improved through the stress and strain effect between the double metals. When the catalyst is used as a fuel cell cathode reaction catalyst, the reaction activity of the catalyst is greatly improved in an oxygen reduction reaction, the active specific surface area ECSA of the catalyst is 1.46 times that of commercial Pt/C sold in the market, the mass activity (MA) of the catalyst is 14.3 times that of the commercial Pt/C, and the actual specific activity (SA) of the catalyst is 9.64 times that of the commercial Pt/C.
Owner:YANSHAN UNIV

Substrate selection for catalyst

InactiveCN103252257AOptimal selection windowWiden selection windowCatalyst carriersCatalyst activation/preparationPlatinumHigh current density
In one embodiment, a method of forming a catalyst/substrate construction includes: identifying a catalyst having a specific activity, determining a surface area factor for supporting the catalyst based on the specific activity of the catalyst; selecting a substrate having the surface area factor; and applying the substrate to the catalyst to form the catalyst/substrate construction. In certain instances, the surface area factor may be determined according to the following equation: SA support  ( cm support 2 / cm planar 2 ) = [ ''  Baseline ''  ( A  /  mg Pt ) Mass   Activity   I   F Loading   ( mg Pt  /  cm 2 ) ]  [ Specific   Activity   ( [mu]   A  /  cm 2 ) 0.000001  ( A  /  [mu]A ) ] wherein the term "Baseline" refers to mass activity of 100 A per gram of platinum (Pt) for a comparative catalyst 5 nm Pt nano-particles dispersed on a carbon black support, the term "Mass Activity IF" refers to the activity required to achieve a high current density performance target of 1.5 A/cm2 at 0.67 V, at a platinum loading of 0.1 mg Pt/cm2. In another embodiment, the method also comprises a target superficial area corresponding to a superficial area factor calculated according to the following equation, wherein [sigma] represents catalyst layer thickness, [rho] represents substrate block density, and [u] represents catalyst use ratio percentage.
Owner:FORD GLOBAL TECH LLC

Inorganic-organic core-shell framework loaded low-dose precious metal palladium material and preparation thereof and application in electro-catalytic dechlorination hydrogenation reaction

The invention discloses an inorganic-organic core-shell framework loaded low-dosage precious metal palladium material and preparation thereof and application of the material in electro-catalytic dechlorination hydrogenation reaction. The preparation method comprises the following steps: polymerizing dopamine around a TiO2 one-dimensional nanorods which vertically grow on the surface of FTO and have an array structure by utilizing an in-situ auto-polymerization effect of the dopamine to form an inorganic-organic core-shell structure of TiO2 nanorod wrapped by the dopamine; and uniformly dispersing and loading an extremely low amount of palladium nanoparticles on the core-shell framework by adopting a chemical impregnation method to obtain an electrode material, wherein the loading capacity of precious metal palladium in the electrode material is only 0.29%, when the electrode material is used as a cathode to be applied to electro-catalysis of a dechlorination reaction of a chlorinated organic compound, the mass activity reaches up to 44.39 min<-1>g<-1>, the conversion rate of dechlorination of the chlorinated organic compound can reach up to 94%, very high electro-catalytic reaction activity is shown, and a relatively large application prospect is achieved in electro-catalytic hydrodechlorination.
Owner:ZHEJIANG UNIV OF TECH
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