An electrode binder for a nonaqueous secondary battery; and a nonaqueous secondary battery electrode. The electrode binder for a nonaqueous secondary battery contains a resin component and is water-soluble. The surface free energy γB at 23° C. is 70 mJ/m2 or less, and the dipole component γpB of the surface free energy is 26 mJ/m2 or less.
Provided is a transparent conducting film having a preferable optical property, a preferable electrical property, and further, a superior durability of folding. The transparent conducting film comprises a transparent substrate and a transparent conducting layer formed on at least one of main faces of the transparent substrate, wherein the transparent conducting layer contains a binder resin and a conducting fiber, a cut portion of the transparent conducting film has a straightness of 0.050 mm or less. Preferably, the transparent substrate is a resin film having an elongated resin film or cut out from an elongated film, and can be folded in with a folding axis in the direction perpendicular to the longitudinal direction of the elongated resin film.
A magnetic sensor includes: a sensitive layer made of a soft magnetic material with uniaxial magnetic anisotropy, the sensitive layer being configured to sense a magnetic field by a magnetic impedance effect; and a magnet layer made of a magnetized hard magnetic material and disposed to face the sensitive layer. The magnet layer is configured to apply a DC magnetic bias Hb in a direction intersecting a direction of the uniaxial magnetic anisotropy in the sensitive layer, the DC magnetic bias Hb having a greater value than an anisotropic magnetic field Hk of the sensitive layer.
Provided is a thermosetting resin composition which exhibits low water absorption and excellent reflow resistance properties without compromising heat resistance or moldability. This thermosetting resin composition contains a polyalkenylphenol compound (A), a polymaleimide compound (B), a liquid polybutadiene compound (C) and a radical initiator (D). The liquid polybutadiene compound (C) has structural units represented by formula (1)-1 and, optionally, structural units represented by formula (l)-2 and, optionally, structural units other than the structural units represented by formula (1)-1 and formula (1)-2. If the average number of structural units represented by formula (1)-1 per molecule is denoted by m, the average number of structural units represented by formula (1)-2 per molecule is denoted by n and the average number of structural units other than the structural units represented by formula (1)-1 and formula (1)-2 is denoted by w, the value of m/(m+n+w) is 0.15-1.
Provided is a thermosetting resin composition which exhibits low water absorption and excellent reflow resistance properties without compromising heat resistance or moldability. This thermosetting resin composition contains a polyalkenylphenol compound (A), a polymaleimide compound (B), a liquid polybutadiene compound (C) and a radical initiator (D). The liquid polybutadiene compound (C) has structural units represented by formula (1)-1 and, optionally, structural units represented by formula (l)-2 and, optionally, structural units other than the structural units represented by formula (1)-1 and formula (1)-2. If the average number of structural units represented by formula (1)-1 per molecule is denoted by m, the average number of structural units represented by formula (1)-2 per molecule is denoted by n and the average number of structural units other than the structural units represented by formula (1)-1 and formula (1)-2 is denoted by w, the value of m/(m+n+w) is 0.15-1.
[Problem] To provide an electroconductive ink suitable for an inexpensive carbon wiring substrate having a wide strain sensing range, and a carbon wiring substrate in which the electroconductive ink is used.
[Problem] To provide an electroconductive ink suitable for an inexpensive carbon wiring substrate having a wide strain sensing range, and a carbon wiring substrate in which the electroconductive ink is used.
[Solution] An electroconductive ink characterized by including a carbonaceous electroconductive material (A), a binder resin (B) including a cellulose compound (B1) and a poly N-vinyl compound (B2), and a solvent (C), the electroconductive ink including 0.5-23 parts by mass of the binder resin (B) with respect to 100 parts by mass of the carbonaceous electroconductive material (A), the mass blending ratio of the cellulose compound (B1) and the poly N-vinyl compound (B2) being 80:20 to 40:60, and the solvent (C) including water (C1). A carbon wiring substrate having a wiring pattern formed using the electroconductive ink.
C09D 11/106 - Printing inks based on artificial resins containing macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
H05K 1/09 - Use of materials for the metallic pattern
6.
Negative electrode material for lithium ion secondary batteries, method for manufacturing the same, paste for negative electrode, negative electrode sheet, and lithium ion secondary
2/g, and an exothermic peak temperature in DTA measurement of 830° C. to 950° C. Also disclosed is a paste for negative electrodes, a negative electrode sheet, a lithium ion secondary battery and a method for manufacturing the negative electrode material.
An aluminum nitride sintered compact containing aluminum nitride crystal grains and composite oxide crystal grains containing a rare earth element and an aluminum element, wherein a median diameter of the aluminum nitride crystal grains is 2 μm or less; 10 to 200 intergrain voids having a longest diameter of 0.2 to 1 μm are dispersed in a region of a cross section of 100 μm in square; and the carbon atom content is less than 0.10% by mass. Also disclosed is a method of producing the aluminum nitride sintered compact.
C04B 35/581 - Shaped ceramic products characterised by their composition; Ceramic compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxides based on borides, nitrides or silicides based on aluminium nitride
H01L 21/48 - Manufacture or treatment of parts, e.g. containers, prior to assembly of the devices, using processes not provided for in a single one of the groups
8.
Oxygen reduction catalyst, electrode, membrane electrode assembly, and fuel cell
Provided are an oxygen reduction catalyst having a high electrode potential under a fuel cell operating environment, an electrode containing the oxygen reduction catalyst, a membrane electrode assembly in which a cathode is the electrode, and a fuel cell including the membrane electrode assembly. The oxygen reduction catalyst used here contains cobalt, sulfur, and oxygen as elements, has a CoS hexagonal structure in powder X-ray diffractometry, and having an S—Co/S—O peak area ratio of 2.1 to 8.9 in an S2p spectrum in X-ray photoelectron spectroscopic analysis.
2 cubic structure in powder X-ray diffractometry, and having an S—Co/S—O peak area ratio of 6 to 15 in an S2p spectrum in X-ray photoelectron spectroscopic analysis.
This collector plate includes a peripheral edge wall that surrounds a predetermined region, and is provided on at least one surface of the collector plate, in which a surface roughness (Ra) of a first surface which is an exposed surface of the peripheral edge wall on the side of one surface, which is measured along a direction perpendicular to an extension direction of the peripheral edge wall is greater than a surface roughness (Ra) of the first surface which is measured along the extension direction of the peripheral edge wall.
H01M 8/18 - Regenerative fuel cells, e.g. redox flow batteries or secondary fuel cells
H01M 8/026 - Collectors; Separators, e.g. bipolar separators; Interconnectors characterised by the configuration of channels, e.g. by the flow field of the reactant or coolant characterised by grooves, e.g. their pitch or depth
NATIONAL UNIVERSITY CORPORATION YOKOHAMA NATIONAL UNIVERSITY (Japan)
Inventor
Lee, Kunchan
Yamato, Yoshinori
Ota, Kenichiro
Ishihara, Akimitsu
Abstract
An object of the invention is to provide an oxygen reduction catalyst composed of a titanium oxynitride having high oxygen reduction capacity. The oxygen reduction catalyst of the invention is a titanium oxynitride that has a nitrogen element content of 8.0 to 15 mass %, has a crystal structure of anatase titanium dioxide in a powder X-ray diffraction measurement, and has a signal intensity ratio N—Ti—N/O—Ti—N in an X-ray photoelectron spectroscopic analysis of in the range of 0.35 to 0.70.
A heat sink (1A) is made of a composite material of aluminum and carbon particles (5). A plurality of fin portions (3) is integrally formed on a base plate portion (2) of the heat sink (1A) so as to protrude with respect to the base plate portion (2). The carbon particles (5) present in the fin portion (3) are oriented in the protrusion direction (P) of the fin portion (3) with respect to the base plate portion (2).
H01L 23/373 - Cooling facilitated by selection of materials for the device
H01L 23/367 - Cooling facilitated by shape of device
H01L 21/48 - Manufacture or treatment of parts, e.g. containers, prior to assembly of the devices, using processes not provided for in a single one of the groups
B23P 15/26 - Making specific metal objects by operations not covered by a single other subclass or a group in this subclass heat exchangers
14.
Electrode material, electrode of redox flow battery, and redox flow battery
An electrode material including a conductive sheet containing carbon nanotubes having an average fiber diameter of 1 μm or less; a liquid inflow member that is formed on a first surface of the conductive sheet such that an electrolyte solution that is passed therethrough flows into the conductive sheet; and a liquid outflow member that is formed on a second surface of the conductive sheet and out of which flows the electrolyte solution that has passed through the conductive sheet; wherein, when using a sheet surface of the conductive sheet as a reference plane, the Darcy permeability, in an in-plane direction, inside the liquid inflow member, is at least 100 times the Darcy permeability, in a normal direction, through the conductive sheet.
A redox flow battery is provided, including an ion-exchange membrane, a current collector plate, and an electrode that is disposed between the ion-exchange membrane and the current collector plate. The electrode includes a main electrode layer in which an electrolytic solution flows from a surface on the current collector plate side to a surface on the ion-exchange membrane side, and the main electrode layer includes a plurality of main electrode pieces which are arranged in parallel in a plane direction.
A redox flow electrode according to one aspect of the present invention is a redox flow battery electrode disposed between an ion exchange membrane and a bipolar plate, wherein the electrode includes a conductive sheet containing carbon nanotubes having an average fiber diameter of 1 μm or less, and a porous sheet that is laminated to the conductive sheet and is formed from fibers having an average fiber diameter of greater than 1 μm.
Provided in the present invention is a redox flow battery including a positive electrode, a negative electrode and a separation membrane, wherein a positive electrode electrolyte composed of an aqueous solution containing vanadium ions is supplied into a positive electrode chamber, and a negative electrode electrolyte composed of an aqueous solution containing vanadium ions is supplied into a negative electrode chamber, to carry out charging and discharging of the battery. In the redox flow battery, zirconium or titanium coated with a noble metal or a compound thereof is used as a positive electrode material, and when the positive electrode material is zirconium coated with a noble metal or a compound thereof, the positive electrode electrolyte and the negative electrode electrolyte contain sulfuric acid; and when the positive electrode material is titanium coated with a noble metal or a compound thereof, the positive electrode electrolyte contains nitric acid.
Catalysts of the present invention are not corroded in acidic electrolytes or at high potential and have excellent durability and high oxygen reducing ability. The catalyst includes a metal oxycarbonitride containing two metals M selected from the group consisting of tin, indium, platinum, tantalum, zirconium, titanium, copper, iron, tungsten, chromium, molybdenum, hafnium, vanadium, cobalt, cerium, aluminum and nickel, and containing zirconium and/or titanium. Also disclosed is a process for producing the catalyst.
2. A sum total thickness of the metal foils in the electrode plates is 0.2 to 2 mm. The electrode plates are welded to each other in a portion where the undercoat layer is formed and no active material layer is formed. Further, at least one of the electrode plates is welded to the metal tab lead in a portion where the undercoat layer is formed and no active material layer is formed.
H01G 11/28 - Electrodes characterised by their structure, e.g. multi-layered, porosity or surface features arranged or disposed on a current collector; Layers or phases between electrodes and current collectors, e.g. adhesives
H01G 11/38 - Carbon pastes or blends; Binders or additives therein
H01G 11/72 - Current collectors specially adapted for integration in multiple or stacked hybrid or EDL capacitors
H01G 11/26 - Electrodes characterised by their structure, e.g. multi-layered, porosity or surface features
H01G 11/86 - Processes for the manufacture of hybrid or EDL capacitors, or components thereof specially adapted for electrodes
H01M 4/133 - Electrodes based on carbonaceous material, e.g. graphite-intercalation compounds or CFx
H01M 4/587 - Carbonaceous material, e.g. graphite-intercalation compounds or CFx for inserting or intercalating light metals
H01M 10/0525 - Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
Provided is a method of culturing green algae which promotes the growth of the green algae which is in a state of being a green swarm cell by irradiating the green algae that accumulate astaxanthin with an artificial light. The green algae are grown in a liquid medium while maintaining a state in which the color of a culture solution of the green algae is green or brown by alternately and continuously radiating a red illumination light and a blue illumination light.
C12N 1/12 - Unicellular algae; Culture media therefor
C12N 13/00 - Treatment of microorganisms or enzymes with electrical or wave energy, e.g. magnetism, sonic waves
C12P 23/00 - Preparation of compounds containing a cyclohexene ring having an unsaturated side chain containing at least ten carbon atoms bound by conjugated double bonds, e.g. carotenes
Provided is a method of culturing green algae which promotes the growth of the green algae which is in a state of being a green swarm cell by irradiating the green algae that accumulate astaxanthin with an artificial light. The green algae are grown in a liquid medium while maintaining a state in which the color of a culture solution of the green algae is green or brown by intermittently radiating a blue illumination light while continuously radiating a red illumination light.
C12N 1/12 - Unicellular algae; Culture media therefor
C12N 13/00 - Treatment of microorganisms or enzymes with electrical or wave energy, e.g. magnetism, sonic waves
C12P 23/00 - Preparation of compounds containing a cyclohexene ring having an unsaturated side chain containing at least ten carbon atoms bound by conjugated double bonds, e.g. carotenes
Provided is a method of culturing green algae which promotes the growth of the green algae which is in a state of being a green swarm cell by irradiating the green algae that accumulate astaxanthin with an artificial light. The green algae are grown in a liquid medium while maintaining a state in which the color of a culture solution of the green algae is green or brown by intermittently radiating a red illumination light while continuously radiating a blue illumination light.
C12N 1/12 - Unicellular algae; Culture media therefor
C12N 13/00 - Treatment of microorganisms or enzymes with electrical or wave energy, e.g. magnetism, sonic waves
C12P 23/00 - Preparation of compounds containing a cyclohexene ring having an unsaturated side chain containing at least ten carbon atoms bound by conjugated double bonds, e.g. carotenes
24.
Light-emitting diode and method of manufacturing the same
A light-emitting diode and manufacturing method, including a flat portion and a mesa structure. An inclined side surface is formed by wet etching such that a cross-sectional area of the mesa structure is continuously reduced toward a top surface. A protective film covers the flat portion, the inclined side surface, and a peripheral region of the top surface of the mesa structure. The protective film includes an electrical conduction window arranged around a light emission hole and from which a compound semiconductor layer is exposed. A continuous electrode film contacts the exposed compound semiconductor layer, covers the protective film formed on the flat portion, and has the light emission hole on the top surface. A transparent conductive film is formed between a reflecting layer and the layer at a position that corresponds to the electrical conduction window and in a range surrounded by the electrical conduction window.
H01L 29/06 - Semiconductor bodies characterised by the shapes, relative sizes, or dispositions of the semiconductor regions
H01L 31/00 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof
H01L 33/24 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the semiconductor bodies with a particular shape, e.g. curved or truncated substrate of the light emitting region, e.g. non-planar junction
H01L 33/20 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the semiconductor bodies with a particular shape, e.g. curved or truncated substrate
H01L 33/38 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the electrodes with a particular shape
H01L 33/44 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the coatings, e.g. passivation layer or anti-reflective coating
H01L 33/00 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof
H01L 33/06 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the semiconductor bodies with a quantum effect structure or superlattice, e.g. tunnel junction within the light emitting region, e.g. quantum confinement structure or tunnel barrier
H01L 33/10 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the semiconductor bodies with a light reflecting structure, e.g. semiconductor Bragg reflector
A plant-cultivating method is provided which comprises a step (A) of irradiating a plant with a red light and a step (B) of irradiating a plant with a blue light, wherein the step (A) and the step (B) are independently carried out for a predetermined period of time under cultivation conditions such that a fertilizer is used for each of the step (A) and the step (B), of which at least the fertilizer used for the step (A) is applied in the form of a nutritious liquid containing fertilizer ingredients and further carbon dioxide added therein. Preferably, a nutritious liquid is applied at each of the step (A) and the step (B), and the nutritious liquid applied at the step (A) contains carbon dioxide at a concentration higher than that in the nutritious liquid applied at the step (B).
A plant-cultivating method is provided which comprises a red light irradiation step (A) and a blue light irradiation step (B), wherein the step (A) and the step (B) are independently carried out for a predetermined period of time under cultivation conditions such that the humidity in a cultivation atmosphere at the step (A) is higher than that at the step (B). Preferably the humidities in a cultivation atmosphere at the step (A) and the step (B) are in the ranges of 60%-90% and 40%-60%, respectively.
A plant-cultivating method is provided which comprises a red light irradiation step (A) and a blue light irradiation step (B), wherein the step (A) and the step (B) are independently carried out for a predetermined period of time under cultivation conditions such that the temperature in a cultivation atmosphere at the step (A) is lower than that at the step (B). Preferably, the temperatures in a cultivation atmosphere at the step (A) and the step (B) are in the ranges of 12° C. to 19° C. and 20° C. to 25° C., respectively.
A plant-cultivating method is provided which comprises a step (A) of irradiating a plant with a red light and a step (B) of irradiating a plant with a blue light, and a step (C) of irradiating a plant with a light predominantly comprised of far-red light wherein the step (A), the step (B) and the step (C) are independently and separately carried out for a predetermined period of time. The light irradiated at each of the steps (A), (B) and (C) has at least 60%, based on the total emission intensity of the light, of an emission intensity ratio of red light, blue light or far-red light.
A plant-cultivating method is provided which comprises a red light irradiation step (A) and a blue light irradiation step (B), wherein the step (A) and the step (B) are independently carried out for a predetermined period of time under cultivation conditions such that amounts of nitrogen, phosphorus and potassium as fertilizer ingredients as used at the step (B) are smaller than amounts of nitrogen, phosphorus and potassium as fertilizer ingredients, respectively, as used at the step (A). Preferably, fertilizer ingredients are applied in amounts such that a growth medium at the step (B) contains 10-15 me/L of nitrogen, 1-4 me/L of phosphorus and 2-6 me/L of potassium, and a growth medium at the step (A) contains 15-20 me/L of nitrogen, 3-6 me/L of phosphorus and 6-9 me/L of potassium.
A plant-cultivating method is provided which comprises a red light irradiation step (A) and a blue light irradiation step (B), wherein the step (A) and the step (B) are independently carried out for a predetermined period of time under cultivation conditions such that a fertilizer is used at each of the step (A) and the step (B), of which at least the fertilizer used at the step (B) is applied in the form of a nutritious liquid containing fertilizer ingredients and further an increased amount of dissolved oxygen, which nutritious liquid is prepared by adding oxygen therein. Preferably, a nutritious liquid is applied at each of the step (A) and the step (B), and the nutritious liquid applied at the step (B) contains dissolved oxygen at a content higher than that in the nutritious liquid applied at the step (A).
3, has an angle of repose in the range of 20° to 50° inclusive, and has a particle size (D90) in the volume-based particle size distribution measured using laser diffraction of 120 μm or less. The average surface interval (d002) of a surface (002) of the carbon material after graphitization, measured using x-ray diffraction, is in the range of 0.3354 nm-0.3450 nm inclusive.
In a direct-liquid fuel cell supplied directly with a liquid fuel, a process for producing an electrode catalyst for a direct-liquid fuel cell is provided which is capable of suppressing decrease in cathode potential caused by liquid fuel crossover and providing an inexpensive and high-performance electrode catalyst for a direct-liquid fuel cell. The process for producing an electrode catalyst for a direct-liquid fuel cell includes Step A of mixing at least a transition metal-containing compound with a nitrogen-containing organic compound to obtain a catalyst precursor composition, and Step C of heat-treating the catalyst precursor composition at a temperature of from 500 to 1100° C. to obtain an electrode catalyst, wherein part or entirety of the transition metal-containing compound includes, as a transition metal element, at least one transition metal element M1 selected from Group IV and Group V elements of the periodic table.
A catalyst carrier production process includes a step (a) of mixing a transition metal compound (1), a nitrogen-containing organic compound (2), and a solvent to provide a catalyst carrier precursor solution; a step (b) of removing the solvent from the catalyst carrier precursor solution; and a step (c) of the thermally treating a solid residue obtained in the step (b) at a temperature of 500 to 1100° C. to provide a catalyst carrier; wherein the transition metal compound (1) is partly or wholly a compound including a transition metal element (M1) selected from the group 4 and 5 elements of the periodic table as a transition metal element; and at least one of the transition metal compound (1) and the nitrogen-containing organic compound (2) includes an oxygen atom.
A method for producing a fuel cell electrode catalyst including a metal element selected from aluminum, chromium, manganese, iron, cobalt, nickel, copper, strontium, yttrium, tin, tungsten, and cerium and having high catalytic activity through heat treatment at comparatively low temperature. The method including: a step (1) of mixing at least a certain metal compound (1), a nitrogen-containing organic compound (2), and a solvent to obtain a catalyst precursor solution, a step (2) of removing the solvent from the catalyst precursor solution, and a step (3) of heat-treating a solid residue, obtained in the step (2), at a temperature of 500 to 1100° C. to obtain an electrode catalyst; a portion or the entirety of the metal compound (1) being a compound containing, as the metal element, a metal element M1 selected from aluminum, chromium, manganese, iron, cobalt, nickel, copper, strontium, yttrium, tin, tungsten, and cerium.
A negative electrode material for a lithium ion battery, in which a fine particle (A) containing an element selected from Si, Sn, Ge and In and a carbon particle (B) obtained by heat-treating a petroleum-based coke and/or a coal-based coke at a temperature of 2,500° C. or more are connected through a chemical bond such as urethane bond, urea bond, siloxane bond and ester bond. Also disclosed are a negative electrode sheet obtained by coating a current collector with a paste containing the negative electrode material, a binder and a solvent, and then drying and pressure-forming the paste; and a lithium ion battery incorporating the negative electrode sheet.
H01M 4/133 - Electrodes based on carbonaceous material, e.g. graphite-intercalation compounds or CFx
H01M 10/0525 - Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
H01M 10/0569 - Liquid materials characterised by the solvents
H01M 4/134 - Electrodes based on metals, Si or alloys
H01M 4/36 - Selection of substances as active materials, active masses, active liquids
H01M 4/38 - Selection of substances as active materials, active masses, active liquids of elements or alloys
H01B 1/12 - Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances organic substances
H01L 29/06 - Semiconductor bodies characterised by the shapes, relative sizes, or dispositions of the semiconductor regions
H01L 21/00 - Processes or apparatus specially adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
H01L 33/06 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the semiconductor bodies with a quantum effect structure or superlattice, e.g. tunnel junction within the light emitting region, e.g. quantum confinement structure or tunnel barrier
H01L 33/32 - Materials of the light emitting region containing only elements of group III and group V of the periodic system containing nitrogen
H01L 33/20 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the semiconductor bodies with a particular shape, e.g. curved or truncated substrate
H01L 33/38 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the electrodes with a particular shape
37.
Light-emitting diode and light-emitting diode lamp
H01L 33/12 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the semiconductor bodies with a stress relaxation structure, e.g. buffer layer
H01L 33/00 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof
H01L 29/06 - Semiconductor bodies characterised by the shapes, relative sizes, or dispositions of the semiconductor regions
H01L 33/06 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the semiconductor bodies with a quantum effect structure or superlattice, e.g. tunnel junction within the light emitting region, e.g. quantum confinement structure or tunnel barrier
A01G 7/04 - Electric or magnetic treatment of plants for promoting growth
H01L 33/30 - Materials of the light emitting region containing only elements of group III and group V of the periodic system
H01L 33/12 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the semiconductor bodies with a stress relaxation structure, e.g. buffer layer
H01L 33/16 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the semiconductor bodies with a particular crystal structure or orientation, e.g. polycrystalline, amorphous or porous
39.
Metal oxide electrocatalyst, use thereof, and process for producing metal oxide electrocatalysts
A metal oxide electrode catalyst which includes a metal oxide (Y) obtained by heat treating a metal compound (X) under an oxygen-containing atmosphere. The valence of the metal in the metal compound (X) is smaller than the valence of the metal in the metal oxide (Y). Further, the metal oxide electrocatalyst has an ionization potential in the range of 4.9 to 5.5 eV.
B01J 23/00 - Catalysts comprising metals or metal oxides or hydroxides, not provided for in group
C01B 13/14 - Methods for preparing oxides or hydroxides in general
H01B 1/02 - Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of metals or alloys
A transparent-substrate light-emitting diode (10) has a light-emitting layer (133) made of a compound semiconductor, wherein the area (A) of a light-extracting surface having formed thereon a first electrode (15) and a second electrode (16) differing in polarity from the first electrode (15), the area (B) of a light-emitting layer (133) formed as approximating to the light-extracting surface and the area (C) of the back surface of a light-emitting diode falling on the side opposite the side for forming the first electrode (15) and the second electrode (16) are so related as to satisfy the relation of A>C>B. The light-emitting diode (10) of this invention, owing to the relation of the area of the light-emitting layer (133) and the area of the back surface (23) of the transparent substrate and the optimization of the shape of a side face of the transparent substrate (14), exhibits high brightness and high exoergic property never attained heretofore and fits use with an electric current of high degree.
H01L 27/15 - Devices consisting of a plurality of semiconductor or other solid-state components formed in or on a common substrate including semiconductor components with at least one potential-jump barrier or surface barrier, specially adapted for light emission
H01L 29/26 - Semiconductor bodies characterised by the materials of which they are formed including, apart from doping materials or other impurities, elements provided for in two or more of the groups , , , ,
H01L 21/00 - Processes or apparatus specially adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
A method for producing a carbon fiber, comprising a step of dissolving or dispersing [I] a compound containing Co element; [II] a compound containing at least one element selected from the group consisting of Ti, V, Cr, and Mn; and [III] a compound containing at least one element selected from the group consisting of W and Mo in a solvent to obtain a solution or a fluid dispersion, a step of impregnating a particulate carrier with the solution or the fluid dispersion to prepare a catalyst, and a step of bringing a carbon source into contact with the catalyst in a vapor phase.
A light-emitting diode includes a substrate, a compound semiconductor layer including a p-n junction-type light-emitting part formed on the substrate, an electric conductor disposed on the compound semiconductor layer and formed of an electrically conductive material optically transparent to the light emitted from the light-emitting part and a high resistance layer possessing higher resistance than the electric conductor and provided in the middle between the compound semiconductor layer and the electric conductor. In the configuration of a light-emitting diode lamp, the electric conductor and the electrode disposed on the semiconductor layer on the side opposite to the electric conductor across the light-emitting layer are made to assume an equal electric potential by means of wire bonding. The light-emitting diode abounds in luminance and excels in electrostatic breakdown voltage.
Catalyst layers include an electrocatalyst having high oxygen reduction activity that is useful as an alternative material to platinum catalysts. Uses of the catalyst layers are also disclosed. A catalyst layer of the invention includes an electrode substrate and an electrocatalyst on the surface of the electrode substrate, and the electrocatalyst is formed of a metal compound obtained by hydrolyzing a metal salt or a metal complex.
A lightweight, compact high-performance fuel cell separator is provided with enhanced output density and capable of being stacked without a gas seal member. Embodiments include a separator having a corrugated electrically conducting flow path. A recess and projection are formed on front and rear surfaces, each constituting a gas flow path alternately arrayed abreast in a plane.
3 or less, wherein filaments having a diameter within ±20% of the mean fiber diameter occupies 65% (on a number basis) or more of the total. The production method involves thermal decomposition of a carbon source at 800 to 1,300° C. in the presence of, as a catalyst, a transition metal compound having a vapor pressure of 0.13 kPa (1 mmHg) or more at 150° C. and spraying of the carbon source and the transition metal compound in gas form toward the reactor inner wall to allow reaction to proceed. The vapor grown carbon fiber having a larger aspect ratio has excellent dispersibility, and when added in a resin, a smaller amount contributes to enhancement in electroconductivity and thermal conductivity, as compared with a case using conventional one.
C01B 31/10 - Preparation by using gaseous activating agents
D01F 9/12 - Carbon filaments; Apparatus specially adapted for the manufacture thereof
D01F 9/127 - Carbon filaments; Apparatus specially adapted for the manufacture thereof by thermal decomposition of hydrocarbon gases or vapours
B82B 1/00 - Nanostructures formed by manipulation of individual atoms or molecules, or limited collections of atoms or molecules as discrete units
B82B 3/00 - Manufacture or treatment of nanostructures by manipulation of individual atoms or molecules, or limited collections of atoms or molecules as discrete units