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30results about How to "Achieve large area growth" patented technology

Low-temperature direct preparation method of graphene under double-temperature-zone control, and double-temperature-zone tube furnace

InactiveCN102849733APrecise control of growth temperatureSimple growth processGrapheneHydrogenDefective graphene
The invention discloses a low-temperature direct preparation method of graphene under double-temperature-zone control, and a double-temperature-zone tube furnace. The method comprises the steps of dividing a vacuum reaction furnace into a high-temperature zone and a low-temperature zone, putting transition metal into the high-temperature zone, directly putting substrate material into the low-temperature zone, vacuumizing, injecting hydrogen gas into the vacuum reaction furnace, heating the low-temperature zone to 100-1,000 DEG C, heating the high-temperature zone to 1,000-1,100 DEG C, introducing carbon source into the vacuum reaction furnace, cracking the carbon source in the high-temperature zone, and performing chemical vapor deposition (CVD) for 5-180 min in the low-temperature zone while keeping constant hydrogen gas flow, to obtain graphene directly deposited on the substrate. The preparation method has the advantages of simple growth process, no need of catalysis, low growth temperature of 100-1,000 DEG C, no restriction on substrate material, and large-area growth of graphene. The grown graphene has low defect peak, high crystal quality, excellent light transmittance and electrical conductivity.
Owner:SHANDONG NORMAL UNIV

Process for preparing stretchable supercapacitor based on highly conductive graphene/nickel particle mixed structure

InactiveCN104882297APrecise control of growth temperatureDefect peak lowHybrid capacitor electrodesTransportation and packagingCvd grapheneCapacitance
The invention relates to a process for preparing a stretchable supercapacitor based on a highly conductive graphene/nickel particle mixed structure. Firstly, a chemical vapor deposition method is used for preparing spongy graphene material on a nickel foam, and the prepared graphene/nickel foam are immersed in an etching solution for slow reaction so that most of the nickel metal can be chemically displaced into various small nickel particles; secondly, the spongy graphene/nickel particle mixed structure is fished out from the etching solution by using a seal-type fishing method, cleaned and dried, and a pre-stretched elastic substrate slowly returns back to the original length or area; and thirdly, the prepared stretchable graphene/nickel particle mixed structure is used as electrode material, and an all-solid-state stretchable supercapacitor is prepared according to the elastomer/electrode/solid electrolyte/electrode/elastomer structure. According to the invention, the capacitance of a conventional capacitor is increased, contact resistance is reduced, the stretching stability, frequency and performance are excellent, the cost is low, and the method is controllable and suitable for mass production.
Owner:SHANDONG NORMAL UNIV

Carbon nano tube/porous ceramic hollow fiber composite ultrafiltration membrane as well as preparation method and application thereof

The invention discloses a carbon nano tube/porous ceramic hollow fiber composite ultrafiltration membrane as well as a preparation method and application thereof. The preparation method comprises the following steps: carrying out ultrasonic vibration on a hollow fiber ceramic membrane used as a carrier with absolute ethyl alcohol and washing the hollow fiber ceramic membrane with de-ionized water until the hollow fiber ceramic membrane is neutral; drying to obtain the treated carrier; coating a Ni(NO3)2 solution onto the treated carrier by using an impregnation coating method; after drying, putting the carrier into a muffle furnace to be roasted to obtain a hollow fiber membrane loaded with a nickel oxide catalyst; putting the hollow fiber membrane into a quartz reaction tube and introducing N2 and H2 into the quartz reaction tube to reduce a catalyst; and switching into hydrogen gas and raising the temperature, switching a gas flow into pure methane gas and carrying out a high-temperature reaction to obtain the product. The carbon nano tube/porous ceramic hollow fiber composite ultrafiltration membrane can be used for separating liquid-water emulsion liquid and bacteria, and has a very good effect of removing PM1 fine particles in atmosphere.
Owner:INST OF URBAN ENVIRONMENT CHINESE ACAD OF SCI

Molybdenum disulfide/gold nanoparticle mixed structure biosensor material and preparation method thereof

ActiveCN106525812AEnhanced chemisorptionEnable separation and detectionRaman scatteringChemisorptionMolybdenum disulfide
The invention discloses a molybdenum disulfide/gold nanoparticle mixed structure biosensor material and a preparation method thereof. The molybdenum disulfide/gold nanoparticle mixed structure biosensor material comprises a glass fiber paper substrate, two-dimensional molybdenum disulfide adhered to the glass fiber paper substrate and gold nanoparticles adhered to the two-dimensional molybdenum disulfide. Molybdenum disulfide growth temperature is accurately controlled. Grown molybdenum disulfide has low defect peak and high crystalline quality. Grown molybdenum disulfide size is only limited by CVD cavity, and large-area growth of molybdenum disulfide can be realized. The molybdenum disulfide/metal particle mixed structure with grown metal particles has extremely high chemisorption and physical strengthening mechanisms. By the etching method for growth of gold particles, etching time can be controlled to accurately control size of the gold particles. In addition, the gold particles can uniformly grow on the whole material, which is beneficial to detection of biomolecules. The prepared biosensor can simultaneously realize separation and detection of biomolecules. The method is simple and controllable, is low-cost, and has high application value.
Owner:SHANDONG NORMAL UNIV

Bent optical fiber ATR (attenuated total reflectance) glucose sensor reinforced on basis of silver nanoparticles

The invention discloses a bent optical fiber ATR (attenuated total reflectance) glucose sensor reinforced on the basis of silver nanoparticles. The bent optical fiber ATR glucose sensor comprises an optical fiber. The optical fiber comprises an optical fiber core and optical fiber cladding, the optical fiber cladding wraps the outer periphery of the optical fiber core, optical fiber connectors which are used for being connected with external components are respectively connected to two ends of the optical fiber, a bent sensitive area is formed in the middle of the optical fiber, and the silver nanoparticles grow on the outer surface of the portion, which is positioned in the sensitive area, of the optical fiber. The optical fiber is a multi-mode optical fiber. The optical fiber core and the optical fiber cladding are made of silver halide materials, and light with the wavelength ranging from 4 micrometers to 18 micrometers can be transmitted through the optical fiber core and the optical fiber cladding. The portion, which is positioned in the sensitive area, of the optical fiber is of a U-shaped structure or a single-ring structure or a structure with two or more rings. The diameter of each silver nanoparticle ranges from 20 nanometers to 100 nanometers. The bent optical fiber ATR glucose sensor has the advantages that the bent optical fiber ATR glucose sensor is simple in structure and operation, small in size, easy to process and low in cost, and can be subcutaneously implanted into a human body, so that the blood glucose concentration of the human body can be continuously monitored in an online manner and can be directly measured in vivo, and the requirement on continuously monitoring the blood glucose concentration of the human body in real time can be met.
Owner:TIANJIN UNIV

Preparation method of all-inorganic lead-free metal halide perovskite nanowire and high-performance infrared detection application of nanowire

InactiveCN110171845AAchieve an effective responseEasy to operateNanotechnologyTin halidesSource materialEffective response
The invention relates to a preparation method of an all-inorganic lead-free metal halide perovskite nanowire and a high-performance infrared detection application of the nanowire. The nanowire is grown by a three-temperature-zone gas phase method, and the three temperature zones include the upstream source zone, the midstream source zone and the growth zone. A SnX2 source material is placed in theupstream source zone for providing a Sn source material; a CsX source material is placed in the midstream source zone for providing a CsX source material; a freshly stripped fluorophlogopite substrate is placed in the growth zone for growing the nanowire. A metal mask plate and electron beam evaporation are adopted for positioning and vapor deposition of metal electrodes to construct an infrareddetector. By means of the method, the new all-inorganic lead-free metal halide perovskite nanowire material which is free of toxicity, free of lead and environmentally friendly can be prepared, the forbidden band width is made continuously adjustable through energy band engineering, and effective response to near-infrared light is successfully realized. In the adopted chemical vapor deposition method, conditions are simple, and the cost is low. By adopting the electrode positioning method with the metal mask plate to prepare the infrared detector, the operation is convenient.
Owner:SHANDONG UNIV

A kind of preparation method of spongy graphene/zinc oxide hybrid structure flexible gas sensor

The invention relates to a preparation method of a flexible gas-sensitive sensor with a spongy graphene / zinc oxide mixed structure. The preparation method comprises the following steps of: firstly placing foam metal into a heating area of a vacuum reaction furnace, vacuumizing, simultaneously heating to a preset temperature, charging hydrogen into the vacuum reaction furnace; after heating to the preset temperature, introducing a carbon source and simultaneously keeping the flow of the hydrogen constant, thus obtaining a substrate directly deposited with graphene after 10-180 minutes; then soaking the prepared graphene / foam metal in etching solution, displacing off the foam metal, fishing out flexible graphene from the etching solution, cleaning, and fishing the graphene out by using a flexible substrate; finally, with the flexible substrate coated with conductive graphene as a cathode, a platinum sheet as a counter electrode, and Ag / Cl as a reference electrode, in the filling solution, adopting by taking Zn-containing solution as electrolyte, carrying out electrolytic growth to obtain a zinc-oxide nano structure. The preparation method has the beneficial effects that the sensitivity and the response speed are improved, and the development prospect on the aspects of environmental monitoring and chemical-gas detection and the like is important.
Owner:SHANDONG NORMAL UNIV

A large-area method for preparing self-supporting high-performance oxygen evolution electrodes at room temperature

The invention discloses a method of large-area preparation of a self-supporting high-performance oxygen evolution electrode at the room temperature, and belongs to the field of electrolyzed water catalysis and oxygen evolution. The method comprises the steps that a layer of alkaline oxide is arranged on a conductive substrate in a loading mode, the conductive substrate and the layer of alkaline oxide are soaked in a transition metal mixed salt solution, a reaction is conducted for a period of time at the room temperature, finally ultra-thin sheet-shaped transition mono-metal and multi-metal hydroxide perpendicularly grows on the conductive substrate in an oriented mode, and then the self-supporting high-performance oxygen evolution electrode is obtained. The method is not limited by substrate materials, and large-area growth can be achieved; the method is conducted at the room temperature, and the energy cost is saved; the method has the universality and can achieve perpendicular and oriented growth of most of two-dimensional sheet-shaped transition mono-metal and multi-metal hydroxide; and part of electrodes prepared according to the method have the quite high electro-catalysis oxygen evolution activity, are much superior to commercial RuO2 catalytic agents, and can be applied to the fields of industrial water electrolysis, metal-air cells and fuel cells.
Owner:QINGDAO UNIV

A Porous Single Crystal Gallium Nitride Micro/Nanotube Array with Controllable Inner Diameter and Its Preparation Method

The invention relates to an inner-diameter-controllable porous mono-crystalline gallium nitride micro / nano-tube array and a preparation method thereof. The preparation method comprises the following steps: enabling a gallium source to be in contact with a nitrogen source at a reducing atmosphere, reacting to generate gallium nitride gaseous molecules, and performing epitaxial growth on the gallium nitride gaseous molecules by using a zinc oxide micro / nano-wire array as a template to prepare the inner-diameter-controllable porous mono-crystalline gallium nitride micro / nano-tube array, wherein reaction conditions of the epitaxial growth are as follows: the reaction temperature is 850-1050 DEG C, and the reaction time takes 0.5-5 hours. The gallium nitride micro / nano-tube array disclosed by the invention is special in morphology, uniform in size and controllable in inner diameter, and large-area growth can be achieved. Compared with a conventional method for preparing the gallium nitride micro / nano-tube array, by adopting the method disclosed by the invention, synthesis steps of gallium nitride micro / nano-tubes can be simplified, the production cost can be lowered, and moreover, a special porous surface structure can be formed. The preparation method is simple in process and convenient to operate, is easy to perform large-scale production, and has relatively low requirements for an experimental environment.
Owner:THE NAT CENT FOR NANOSCI & TECH NCNST OF CHINA

A biosensor material with molybdenum disulfide/gold nanoparticle hybrid structure and its preparation method

The invention discloses a molybdenum disulfide / gold nanoparticle mixed structure biosensor material and a preparation method thereof. The molybdenum disulfide / gold nanoparticle mixed structure biosensor material comprises a glass fiber paper substrate, two-dimensional molybdenum disulfide adhered to the glass fiber paper substrate and gold nanoparticles adhered to the two-dimensional molybdenum disulfide. Molybdenum disulfide growth temperature is accurately controlled. Grown molybdenum disulfide has low defect peak and high crystalline quality. Grown molybdenum disulfide size is only limited by CVD cavity, and large-area growth of molybdenum disulfide can be realized. The molybdenum disulfide / metal particle mixed structure with grown metal particles has extremely high chemisorption and physical strengthening mechanisms. By the etching method for growth of gold particles, etching time can be controlled to accurately control size of the gold particles. In addition, the gold particles can uniformly grow on the whole material, which is beneficial to detection of biomolecules. The prepared biosensor can simultaneously realize separation and detection of biomolecules. The method is simple and controllable, is low-cost, and has high application value.
Owner:SHANDONG NORMAL UNIV

Low-temperature direct preparation method of graphene under double-temperature-zone control, and double-temperature-zone tube furnace

InactiveCN102849733BPrecise control of growth temperatureSimple growth processGrapheneHydrogenDefective graphene
The invention discloses a low-temperature direct preparation method of graphene under double-temperature-zone control, and a double-temperature-zone tube furnace. The method comprises the steps of dividing a vacuum reaction furnace into a high-temperature zone and a low-temperature zone, putting transition metal into the high-temperature zone, directly putting substrate material into the low-temperature zone, vacuumizing, injecting hydrogen gas into the vacuum reaction furnace, heating the low-temperature zone to 100-1,000 DEG C, heating the high-temperature zone to 1,000-1,100 DEG C, introducing carbon source into the vacuum reaction furnace, cracking the carbon source in the high-temperature zone, and performing chemical vapor deposition (CVD) for 5-180 min in the low-temperature zone while keeping constant hydrogen gas flow, to obtain graphene directly deposited on the substrate. The preparation method has the advantages of simple growth process, no need of catalysis, low growth temperature of 100-1,000 DEG C, no restriction on substrate material, and large-area growth of graphene. The grown graphene has low defect peak, high crystal quality, excellent light transmittance and electrical conductivity.
Owner:SHANDONG NORMAL UNIV

Method for producing down-converting luminescent material

The invention discloses a manufacturing method of a down-conversion luminescent material. The manufacturing method comprises the forming steps that 1, multi-target magnetron sputtering equipment is provided; 2, a plurality of target materials are mounted and selected according to to-be-formed rare earth doped oxide, the matrix material of the rare earth doped oxide is rare earth vanadate or rare earth niobate, the target materials comprise matrix rare earth oxide targets, vanadium oxide targets or niobium oxide targets and doped rare earth targets, wherein the matrix rare earth oxide targets,the vanadium oxide targets or the niobium oxide targets correspond to the matrix material, and the doped rare earth targets correspond to a rare earth doped material; 3, a substrate is placed on a base sheet base of a co-sputtering reaction chamber; 4, vacuumizing is conducted on the co-sputtering reaction chamber; and 5, sputtering gas is introduced, and a sputtering technology with the substratetemperature being room temperature to 400 DEG C is conducted, so that the rare earth doped oxide is formed on the surface of the substrate. According to the manufacturing method of the down-conversion luminescent material, large area growth of the down-conversion luminescent material at the low temperature can be achieved, the manufacturing method can be compatible with a microelectronic technology, the technology of the manufacturing method is simple, the cost is low, and the manufacturing method can be effectively combined with the preparation process of solar cells.
Owner:HANSHAN NORMAL UNIV
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