1048results about How to "Inhibitory complex" patented technology

The invention discloses a preparation method of a visible light catalyst. Compared with the prior art, the invention adopts inexpensive, non-toxic and harmless urea as the raw material, with no need for highly toxic raw materials. By controlling the calcination temperature, C3N4 can be prepared, thus being in favor of environment protection. The invention also provides a preparation method of a visible light catalyst, comprising the steps of: preparing C3N4 according to the above process; mixing the obtained C3N4 with a modifier in a solvent for reaction, drying the reaction product, thus obtaining the visible light catalyst. The modifier can be an Fe source compound, a Cu source compound, a Zn source compound, a V source compound, a W source compound, a Pt source compound, an Au source compound or a Pd source compound. The method of the invention employs an immersion method for C3N4 metal ion modification, so that metal ions can adsorb the C3N4 surface, thus inhibiting photoinduced charge recombination. Therefore, the visible light catalyst prepared by the preparation method provided in the invention has a high photo catalytic performance.

The invention provides a perovskite thin-film solar cell with a three-dimensional ordered mesopore support layer. The perovskite thin-film solar cell with the three-dimensional ordered mesopore support layer comprises a transparent conducting substrate, a compact layer, the three-dimensional ordered mesopore support layer, a perovskite light absorbing layer, a hole transporting layer and a counter electrode layer which are sequentially laminated to form a laminating layer, wherein the three-dimensional ordered mesopore support layer is filled with the perovskite light absorbing layer, the hole transporting layer and the counter electrode layer; the three-dimensional ordered mesopore support layer is of a three-dimensional ordered mesopore material prepared by using water-soluble colloidal crystal microspheres as a template; the aperture dimension of the three-dimensional ordered mesopore support layer depends on the dimension of the water-soluble colloidal crystal microspheres; and the perovskite light absorbing layer is prepared through materials of an ABXmY3-m type crystal structure. The perovskite thin-film solar cell has the advantages that the three-dimensional ordered mesopore support layer of which the aperture is uniform and adjustable, the specific surface area is relatively large and a good electronic transmission channel is arranged is provided and reaches high photoelectric conversion efficiency and outstanding repeatability and stability; and the preparation method has the advantages that the conditions are mild and controllable, the preparation method is simple and needs a little cost, and large-scale commercial production can be popularized.

The invention relates to a silver-modified carbon nitride composite photocatalytic material and a preparation method thereof. The preparation method comprises: dissolving dicyanodiamide or melamine in deionized water or dimethyl sulfoxide and performing ultrasonic dispersing, so as to obtain a dicyanodiamide or melamine dispersion liquid; dissolving silver nitrate in deionized water and stirring uniformly, so as to obtain a silver nitrate solution; slowly dropwise adding the silver nitrate solution into the above dicyanodiamide or melamine dispersion liquid under the condition of magnetic stirring, and continuing stirring the solution, so as to obtain a mixed precursor solution; using anhydrous ethanol and deionized water repeatedly wash the obtained mixed precursor solution for multiple times, and performing vacuum drying; and putting the obtained product in a proper crucible and covering, putting in a high-temperature furnace, and sintering for a period under the condition of nitrogen protection, so as to obtain a powdery sample. The advantages comprise that the raw material source is wide, the preparation technology is simple and practicable, and the cost is relatively low; and the prepared composite photocatalytic material has relatively good photocatalytic degradation effect on organic dye rhodamine B under irradiation of visible light.

This invention discloses one photoelectric reactor to degrade organic pollute and one method to remove the pollute assistant with catalyze reactor, wherein, the reactor is located with conductive multi-hole materials load compound semi-conductor photo catalyze positive and negative electrodes; the optimized catalyze can be used as light source; it uses conductive solid electrolyte applied to degrade pollute with gas and liquid and to separate metal ions.

A hybrid solar cell with an aluminum-doped zinc oxide nanorod as the electron transfer layer is composed of a transparent conducting glass substrate, the aluminum-doped zinc oxide nanorod electron transfer layer, a layered perovskite-like hybrid material CH3NH3PbX3(wherein X is Cl, or Br or I),2,2',7,7'-Tetrakis[N,N-di(4-methoxyphenyl)amino]-9,9'-spirobifluorene hole transfer layer and an Au metal back electrode layer, wherein all the parts form a laminated structure in sequence. The hybrid solar cell with the aluminum-doped zinc oxide nanorod as the electron transfer layer has the advantages that due to the fact that the aluminum-doped zinc oxide nanorod is used as the electron transfer layer in the hybrid solar cell, the specific surface area is large, electron-transport capacity is high, electron-hole combination is effectively restrained, and photoelectric conversion efficiency is high; the manufacturing method and technique are simple, reaction temperature is low, efficiency is high, raw materials are rich, cost is low, and environmental friendliness is achieved. The hybrid solar cell with the aluminum-doped zinc oxide nanorod as the electron transfer layer is suitable for industrialized large-scale production.

Provided is a hybrid solar cell with Cs mingling with ZnO as an electron transfer layer. The hybrid solar cell with the Cs mingling with the ZnO as the electron transfer layer is composed of a transparent conductive glass substrate, a Cs mingling with ZnO nanorod electron transfer layer, layered perovskite hybrid materials CH3NH3PbX3(wherein X is C1, Br or I), a 2, 2', 7 and 7'- four [N, N - two (four - methoxy phenyl) amidogen] - 9, 9' - spirobifluorene hole transport layer and an Au metal back electrode layer which sequentially form a layered structure in a combining mode. The hybrid solar cell with the Cs mingling with the ZnO as the electron transfer layer has the advantages that the Cs mingling with the ZnO as the electron transfer layer is used in the hybrid solar cell, compared with zinc oxide, 2-3 orders of magnitude of electronic transmission capacity are improved, the recombination of electron-hole is effectively constrained, and the photoelectric conversion efficiency is high; the preparing method of the hybrid solar cell is simple in process, low in reaction temperature, high in efficiency, rich in raw material, low in cost, environmentally friendly, free of pollution, and suitable for industrial mass production.

The invention discloses a perovskite solar cell and a preparation method thereof. The perovskite solar cell comprises a transparent conductive substrate, a hole transport layer, a decoration layer, a perovskite layer, an electron transport layer, a barrier layer and a metal electrode. The surfaces of PEDOT: PSS, NiOx and the hole transport layer are decorated by ionic liquid based on imidazole, atomic force microscope graphs before and after the decoration are compared, and the decorated surface appearance is more smooth, which is conducive to inhibiting the compounding of dark current. The perovskite layer is a new perovskite material 3MAI: PbAc2.xH2O (x is not smaller than 0 and is not greater than 3), and is prepared by quickly preheating a substrate and heating a perovskite precursor solution, namely instant heating assisted spray coating technology (HASP) at a low temperature (lower than 100 DEG C), which is conducive to increasing the grain size of perovskite and reducing the defects between perovskite grains so as to greatly improve the efficiency of the perovskite battery. The photoelectric conversion efficiency of the final battery device is greater than 19%, the flexible device efficiency is 10.8%, no hysteresis effect is formed, and thus the preparation method has a broad application prospect.

The invention discloses a preparation method and application of a cadmium sulfide/graphite like carbon nitride (CdS/g-C3N4) composite visible light catalyst. The preparation method of the catalyst is a chemical precipitation method which is performed in an alkaline environment, wherein g-C3N4 is taken as a matrix, and CdCl2 and Na2S are taken as raw materials. The weight ratio of CdS to g-C3N4 in CdS/g-C3N4 is (1:2)-(5:1), and when the composite visible light catalyst is used for visible light catalysis treatment of methylene blue and methyl violet solutions, a better degradation effect can be obtained; and furthermore, the catalyst can still keep higher catalytic activity after being reused for five times. The composite visible light catalyst disclosed by the invention has important significance for development of the visible light catalyst, and also has good application prospects in treatment of dye wastewater.

The invention belongs to the technical fields of material preparation and photocatalysis, and discloses a phenyl ring modified graphite-like carbon nitride photocatalyst, and a preparation method and an application thereof. The method comprises the following steps: 1, dissolving nitrogen-containing organic micro-molecules and a phenyl ring-containing compound in a solvent, and evaporating the obtained solution until the solution is dry in order to obtain a mixed precursor; and 2, roasting the mixed precursor to obtain the phenyl ring modified graphite-like carbon nitride photocatalyst, wherein the nitrogen-containing organic micro-molecules are one or more of urea and melamine; and the phenyl ring-containing compound is one or more of trimesic acid, phenol, benzoic acid and benzaldehyde. The electron structure of the photocatalyst is changed by phenyl ring modification, so the pi electron delocalization of graphite-like carbon nitride is excited, the absorption of visible lights is improved, compounding of photon-generated carriers is inhibited, and the photocatalytic hydrogen production performance is improved. The method has the advantages of simple preparation, no expensive device and good practical application prospect.

The invention discloses a method for controlling virtual reality interaction according to the head motion of a user. The method comprises the following steps of setting preset direction and distance threshold values and acceleration values for judging and triggering the corresponding execution operation according to the direction, distance and acceleration of the head motion of the user in a display system supporting the virtual reality interaction; and triggering the content of the corresponding execution operation set in the display system when the conditions that the space position change direction and distance of video playing equipment change, the space position change direction meets the preset direction, the space position change distance is greater than or equal to the distance threshold value, and the component of the acceleration value in the preset direction is greater than or equal to the acceleration threshold value are detected in the display system. The method provided by the invention has the advantage that the control of the virtual reality interaction according to the head motion of the user is realized.

The invention discloses a preparation method of a ZnO-doped TiO2 hollow sphere composite photocatalyst, comprising the following steps of: preparing Zn<2+> doped carbon/titanium dioxide nuclear-shell particles by adopting a template method and a hydrolytic cladding method, and then calcinating the nuclear-shell particles to obtain the ZnO-doped TiO2 nano hollow sphere composite photocatalyst. The photocatalyst can be used for catalyzing and degrading cationic dyes under ultraviolet or solar visible light. By utilizing low-cost titanium sources, zinc sources and carbon spheres for preparing the ZnO-doped TiO2 nano hollow sphere composite photocatalyst, the preparation method has the advantages of low cost of raw materials, simple process, short preparation period, less energy consumption and belongs to green synthetic technologies. After TiO2 hollow spheres are doped and compounded by utilizing ZnO, absorption spectrums generate red shift by utilizing the interface coupling effect of the TiO2 hollow spheres and the ZnO so that the spectral response range of the photocatalyst is broadened, and the utilization rate of solar energy is improved; and meanwhile, the method can also inhibit the compounding of photon-generated carriers and improve the activity of the photocatalyst by utilizing the high conductivity of ZnO particles.

The invention provides a platinum supported nitrogen-doped molybdenum disulfide photocatalyst and a preparation method thereof. The method comprises the following steps: with sodium molybdate and thioacetamide as raw materials, preparing molybdenum disulfide nanoplates via a hydrothermal method; performing thermal treatment on the molybdenum disulfide nanoplates in an ammonia atmosphere to obtain nitrogen-doped molybdenum disulfide nanoplates; and finally, loading precious metal platinum on the nitrogen-doped molybdenum disulfide nanoplates via a photo reduction method to obtain the platinum supported nitrogen-doped molybdenum disulfide photocatalyst. With the platinum supported nitrogen-doped molybdenum disulfide photocatalyst, molybdenum disulfide is taken as a photocatalyst to produce hydrogen from water by visible light catalytic decomposition for the first time. The platinum supported nitrogen-doped molybdenum disulfide photocatalyst has excellent visible light catalytic hydrogen production capability and excellent stability. The preparation method is simple to operate, the photocatalyst is good in repeatability, and the application of molybdenum disulfide in the aspects of photocatalysis and electrochemistry is expanded.

The invention discloses a preparation method of a nanosheet self-assembled C-doped (BiO)2CO3 microsphere visible light catalyst, which comprises the following steps: (1) dissolving a bismuth-containing precursor, a soluble carbonate and a doping carbon source in a water solution, stirring for 30 minutes, transferring the obtained mixed solution into a high-pressure hydrothermal kettle, and carrying out hydrothermal reaction at 120-250 DEG C for 3-100 hours; and (2) after the hydrothermal reaction finishes, cooling, filtering out the precipitate, respectively washing the precipitate with deionized water and ethanol, and drying to obtain the nanosheet self-assembled C-doped (BiO)2CO3 microspheres. According to the C-doped (BiO)2CO3 prepared by the method disclosed by the invention, the doping C element reduces the energy gap of (BiO)2CO3, and the (BiO)2CO3 has visible light catalytic activity. The experimental result proves that the NO removal rate of the bismuthyl carbonate photocatalyst disclosed by the invention is 30-45%, which indicates that the bismuthyl carbonate photocatalyst has high visible light catalytic activity.

The invention discloses a method for preparing TiO2/BiVO4 composite photocatalyst by a MH (microwave-hydrothermal) method. The method comprises the steps as follows: Bi(NO3)3 5H2O and (NH4)2TiF6 are resolved in HNO3 to form mother salt solution A, NH4VO3 is resolved in NaOH solution to form mother salt solution B, the mother salt solution A and the mother salt solution B are mixed uniformly to form precursor solution, the precursor solution is placed in a microwave hydrothermal reaction kettle for microwave hydrothermal reaction and is cooled after the reaction is over, and yellow sediment in the reaction kettle is taken out and is washed and dried. According to the invention, TiO2/BiVO4 powder is synthesized quickly through a microwave-hydrothermal synthesis technology, and the photocatalysis performance of the powder is better because TiO2 particles are carried on the surface of BiVO4 to serve as an electron acceptor, and then compounding of a photon-generated carrier is inhibited, further the photocatalysis efficiency of pure-phase BiVO4 powder can be improved.

The invention relates to the field of titanium dioxide photocatalysis, in particular to researches in application of a titanium dioxide nanotube modified through metal doping to the field of photocatalysis. The invention provides a simple and feasible preparation method of a copper-doped TiO2 nanotube catalyst. According to the preparation method provided by the invention, low-concentration copper is effectively doped into a titanium dioxide nanotube array through adoption of a constant-voltage electrodeposition method; and the copper inside the titanium dioxide nanotube exists in the form of copper oxide; the copper-doped TiO2 nanotube catalyst has a good photocatalytic activity under ultraviolet light and sunlight; and the composition of electron hole pairs contained in titanium dioxide is effectively inhibited through copper doping, and therefore the photocatalytic property of the titanium dioxide nanotube is enhanced. The preparation method of the photocatalyst is a constant-voltage electrochemical deposition method, in which copper sulfate is taken as electrolyte, and a preparation process is simple; and in addition, the prepared copperdoped TiO2 nanotube catalyst has a stable property and can be used repeatedly.

The invention discloses a preparation method of ordered mesoporous titania/silver photocatalyst, relating to a preparation method of titania/silver and aiming to solve the technical problems of small specific surface area, poor orderliness and low photocatalytic activity of mesoporous titania/silver photocatalyst prepared by prior arts. The preparation method comprises the steps of silver solution preparation, titanium precursor preparation, titania/silver gel preparation, and heat treatment. The inventive photocatalyst has specific surface area of 120-160 m<2>/g, has the advantages of uniform mesopores and high catalytic activity; can be applied to photocatalysis field, and water treatment field of lake, ocean, municipal sewage and industrial sewage.

The invention discloses a water disposing method to remove pollution, which comprises the following steps: (1) detecting pollution content; adding water purification agent with quality rate at 1-10: 1 corresponding to pollution; (2) irradiating the disposed flow through ultrasonic reactor with inflow frequency of at 10KHz-10MHz and acoustic intensity at 0.1W-12W for 1-30min; (3) sedimenting; filtering; draining. The water purification agent is ferrate or ferrate composite agent, which improves removing rate of organic pollution effectively.

The invention discloses a flower-shaped mesoporous titanium dioxide material and a preparation method and application thereof. The material is prepared by the following method: 1) adding a template agent into a diluent, adding concentrated hydrochloric acid, and stirring evenly; 2) adding a titanium source into the solution, and stirring; 3) placing the solution in the conditions of the relative humidity above 60% at the temperature of 40-80 DEG C for 12h-24h, crystallizing at 80-90 DEG C for 6-12h; and 4) refluxing a sample to remove a surface active agent, and drying to obtain the flower-shaped mesoporous titanium dioxide. According to the method, high-temperature calcinations is not needed, the reaction synthesis temperature is lower than 100 DEG C, and the obtained flower-shaped mesoporous titanium dioxide material has the advantages of good monodispersity, high specific surface area and controllable crystalline phase and the like. The flower-shaped mesoporous titanium dioxide material can be used for negative electrode materials of a lithium ion battery, has high charge and discharge specific capacity, stable cycle performance, excellent high rate performance and very good photocatalytic activity, and can be used in the fields of degradation of organic pollutants, photocatalytic water splitting for hydrogen production, dye-sensitized solar cells and the like.

The invention discloses a perovskite solar cell with a high fill factor and a method for preparing the perovskite solar cell. The perovskite solar cell is sequentially provided with a transparent conductive substrate, a hole transport layer, a perovskite thin film, an interface passivation layer, an electron transport layer and a cathode from bottom to top. The interface passivation layer is madefrom alkali metal halide or alkaline earth metal halide on the perovskite thin film by means of evaporation, and the thickness of the interface passivation layer ranges from 1 nm to 5 nm; the electrontransport layer is a C<60> thin film formed on the interface passivation layer by means of evaporation, and the thickness of the C<60> thin film ranges from 10 nm to 20 nm; the cathode is a metal thin film formed on the electron transport layer by means of evaporation, and the thickness of the metal thin film ranges from 50 nm to 120 nm; the perovskite thin film is made from methylamine lead halide or formamidine lead halide; conductive thin films are arranged on the transparent conductive substrate. The perovskite solar cell and the method have the advantages that the shortcoming of incapability of preparing large-area solar cell devices by the aid of existing spin-coating technologies can be overcome by the aid of the perovskite solar cell and the method; the interface passivation layeris prepared by the aid of processes for carrying out evaporation on the alkali metal halide or the alkaline earth halide, accordingly, current carrier recombination at interfaces of perovskite lightabsorption layers and the electron transport layer can be reduced, the efficiency of the perovskite solar cell can be improved, and mass production of large-area cells further can be implemented.

The invention relates to a method for preparing visible light photocatalyst Bi2O3/TiO2, comprising the following steps: (1) adding cetyl trimethyl ammonium bromide to anhydrous ethanol, and ultrasonically dissolving the cetyl trimethyl ammonium bromide to the anhydrous ethanol to form transparent solution A; (2) adding tetrabutyl titanate to the solution A, and ultrasonically dissolving the tetrabutyl titanate to the solution A to form light yellow transparent solution B; (3) heating the solution B to 75-85 DEG C, adding bismuth nitrate pentahydrate to the solution B, and ultrasonically dispersing the bismuth nitrate pentahydrate to the solution B to form light yellow sol; (4) standing the light yellow sol at 25-45 DEG C to form light yellow gel; (5) aging the light yellow gel at 80-100 DEG C to form light yellow particles; and (6) heating light yellow particles from the room temperature to 450-550 DEG C, calcining the light yellow particles for 5-8h, and cooling the calcined light yellow particles to room temperature naturally to obtain compound semiconductor with visible light catalytic activity. The method for preparing the visible light photocatalyst of Bi2O3/TiO inhibits the combination of the light induced electrons and the hole, improves the quantum efficiency of the photocatalytic reaction and the utilization of solar energy, is easy to operate, has low cost and lays a foundation for the light catalytic technology to be practical. The photocatalyst Bi2O3/TiO2 has high visible light catalytic performance.

The invention discloses a method for preparing a B-doped g-C3N4 photocatalyst through nonmetal liquid-phase doping, and belongs to the technical field of hydrogen production through photocatalytic materials. According to the prepared organic polymer semiconductor material g-C3N4 photocatalyst, cheap chemical material urea is taken as a reactant source, sodium tetraphenylborate is taken as a doping source, PEI (polyethyleneimine) is taken as a surface charge modifier, and the B-doped g-C3N4 photocatalyst is successively prepared with a pyrolysis and polymerization method easy to operate. The nonmetal liquid-phase doping modified g-C3N4 photocatalyst has novel organization structure appearance, good response of visible light with wavelength larger than 420 nm and good photocatalytic hydrogen generation property, and promotes solar energy conversion into new energy under the photocatalysis action at a low cost; the provided preparation method has the advantages of cheap raw materials, simple and convenient technology and the like and has an important research value and a wide industrialized application prospect.

The invention discloses a method for controlling virtual reality interaction according to use eye actions. The method comprises the steps that a residence time threshold value, for selecting interaction corresponding to a corresponding execution operation, of the pupils of the user eyes and the least blinking frequency, for judging and triggering the corresponding execution operation, of the user eyes within one second are set in a display system supporting virtual reality interaction; the retention time of the pupil in the interaction area corresponding to the corresponding execution operation is detected in the display system, and when the retention time reaches or exceeds the retention time threshold value, interaction corresponding to the corresponding execution operation is selected; the blinking frequency of the user eyes within one second is detected, and when the blinking frequency of the user eyes within one second reaches or exceeds the least blinking frequency within one second, content, arranged in the display system, of the corresponding execution operation is triggered. According to the method, control of the user eye actions over virtual reality interaction is achieved.