51 results about "Cesium bromide" patented technology

The invention relates to a method for preparing a high-quality quasi-two-dimensional perovskite thin film on a gallium nitride substrate, and relates to the technical field of semiconductors. The method for preparing the high-quality quasi-two-dimensional perovskite thin film on the gallium nitride substrate comprises the following steps: cleaning the gallium nitride substrate, and carrying out Plasma treatment; spin-coating a perovskite precursor solution on the processed gallium nitride substrate; the solute of the perovskite precursor solution is butylamine bromide powder, lead bromide powder and cesium bromide powder, and the solvent is a mixed solution of DMF (Dimethyl Formamide) and DMSO (Dimethylsulfoxide); adding a brominated metal salt into the perovskite precursor solution; and performing thermal annealing treatment on the perovskite thin film. According to the invention, a technology of growing a high-quality quasi-two-dimensional perovskite thin film by adopting a spin-coating process is adopted, and the high-quality thin film with uniform phase distribution is obtained by optimizing the proportion of a precursor solution and introducing inorganic salt to regulate and control growth kinetics.

The invention discloses a preparation method of a portable paper-based ratiometric fluorescence sensor APBA-CsPbBr3 at-UiO-66 / Ru, which comprises the following steps: 1, adding lead bromide and cesium bromide into N, N-dimethylformamide, then adding 5-bromovaleric acid and an oleylamine ligand, and stirring; 2, perfluorooctyltriethoxysilane is added, and a precursor solution is obtained; 3, adding zirconium chloride and terephthalic acid into N, N-dimethylformamide to obtain a homogeneous solution; 4, after heating, UiO-66 is obtained; 5, stirring the precursor solution, APBA, UiO-66 and tris (2, 2-dipyridyl) ruthenium chloride hexahydrate to obtain a composite material; and 6, dropwise adding the composite material solution into the filter paper. The APBA modified material is adopted as a recognition unit, the APBA modified material and the paper base construct a fluorescence sensing platform, visual quantitative analysis of oxytetracycline in water is achieved, and the device is convenient to carry, low in detection limit, high in anti-interference performance, easy and convenient to operate and suitable for on-site rapid detection of oxytetracycline.

The invention discloses a preparation method of a three-dimensional perovskite blue light film in an air environment. The preparation method comprises the following steps: S1, preparing a substrate modified by polyvinylpyrrolidone; s2, preparing a precursor solution of the three-dimensional perovskite blue light thin film; and S3, heating the precursor solution prepared in S2, and forming a film on a substrate modified by polyvinylpyrrolidone to prepare the three-dimensional perovskite blue light thin film. The preparation method comprises the following steps: modifying a substrate by polyvinylpyrrolidone and a precursor solution consisting of dimethyl sulfoxide containing cesium trifluoroacetate, lead bromide, rubidium chloride, triphenylphosphine oxide, 18-crown ether-6 and cesium bromide in different proportions, and combining a solvent treatment process in a spin coating process of the heated precursor solution and the spin coating process of the solution; and a series of perovskite blue light films are prepared in an air environment. The method provides a new reference for large-scale application of the perovskite light-emitting layer, especially the perovskite blue light-emitting layer, in light-emitting films and devices.

The invention discloses a preparation method and application of high-fluorescence quantum yield perovskite fluorescent powder based on amino acid, and belongs to the technical field of luminescent materials and display, the preparation method is used for preparing the perovskite fluorescent powder, and the preparation method comprises the following steps: dissolving potassium bromide in deionized water, then adding lead bromide, and carrying out ultrasonic dissolution to obtain a first solution; dissolving cesium bromide in another deionized water to obtain a second solution; mixing the first solution and the second solution, and standing to obtain a mixed solution; dropwise adding the mixed solution into absolute ethyl alcohol, and stirring to obtain a precursor solution; adding amino acid into the precursor solution, and stirring to obtain a precursor reaction suspension; and centrifuging the suspension, collecting the precipitate, centrifugally washing the precipitate with absolute ethyl alcohol, and drying the washed precipitate to obtain the perovskite fluorescent powder. The invention provides a green synthesis method of a water-ethanol system, which is combined with an amino acid synergistic passivation effect to realize low-cost preparation and improvement of luminous efficiency.

This invention provides a microgap suspension device and a microgap inverted suspension heat treatment process, comprising the following steps: adding p-aminobenzenesulfonic acid to a solvent, mixing thoroughly, and then adding carbon nanotubes to obtain a carbon nanotube dispersion; stirring the carbon nanotube dispersion under heating conditions to obtain a p-aminobenzenesulfonic acid-modified carbon nanotube dispersion; coating a substrate surface with a lead bromide solution, then coating the lead bromide surface with a cesium bromide solution, then coating the cesium bromide surface with the p-aminobenzenesulfonic acid-modified carbon nanotube dispersion; and finally performing heat treatment through a microgap suspension device to form a photoactive layer film. The microgap inverted suspension heat treatment process of this invention, through controllable height suspension heat treatment, ensures that the film is almost unconstrained by the rigidity of the substrate during thermal expansion and cooling contraction, thus making it suitable for flexible substrates as well. It also avoids direct contact damage to flexible substrates during high-temperature heat treatment.

The invention discloses a preparation method of a manganese-doped CsPbBr3 single crystal, and belongs to the field of inorganic perovskite preparation. The preparation method specifically comprises the following steps: dissolving cesium bromide, lead bromide and manganese bromide in a DMSO (dimethyl sulfoxide) solvent, adding bromohexanoic acid, and fully mixing in a water bath to obtain a mixed solution I; then methanol, cyclohexanol and DMF (N, N-dimethylformamide) are fully mixed, and a mixed solution II is obtained; mixing the mixed solution I and the mixed solution II, fully stirring in a water bath, and filtering by using a filter to obtain a precursor solution; and putting a seed crystal into the precursor solution, putting the precursor and the container into silicone oil, and obtaining the manganese-doped CsPbBr3 single crystal by adopting an inverse temperature crystallization method. The manganese-doped CsPbBr3 single crystal prepared by the invention has excellent photoelectric properties and stability, and can be used for low-temperature semiconductor radiation detectors.

The invention provides a cesium lead bromide quantum dot / single-layer molybdenum disulfide 0D / 2D heterojunction photoelectric sensor and a preparation method thereof, and belongs to the technical field of photoelectric devices. Constructing a patterned bottom electrode by adopting an Au / p + type silicon substrate / SiO2 structure; preparing a single-layer molybdenum disulfide (MoS2) film by a mechanical stripping method, and transferring the single-layer molybdenum disulfide (MoS2) film to the patterned silicon wafer electrode; and spin-coating the single-layer molybdenum disulfide film with the quantum dot solution, drying and annealing to obtain the cesium lead bromide quantum dot / single-layer molybdenum disulfide 0D / 2D heterojunction photoelectric sensor. According to the invention, CsPbBr3 QDs with efficient light absorption and single-layer MoS2 with high carrier mobility are integrated together, and CsPbBr3 QDs are used as an effective light absorbent to enhance a local electric field around MoS2. And by utilizing the synergistic effect of the CsPbBr3 QDs and the single-layer MoS2, the separation rate of photon-generated carriers in the heterojunction is accelerated, and the light absorption capability of the MoS2 device is improved. The p + type silicon substrate is combined with the annealing process, a Br-rich passivation ultra-clean II type heterojunction interface is constructed, and the charge separation efficiency and the environmental stability are remarkably improved.

The application relates to a large-size orthorhombic phase bromine lead cesium single crystal and a solution growth method and application thereof, and belongs to the technical field of crystal materials. The application comprises the following steps: (1) mixing water and dimethyl sulfoxide uniformly, adding cesium bromide and lead bromide to obtain a bromine lead cesium solution; (2) overheating the bromine lead cesium solution at 70-80 DEG C for 24-48h to obtain a bromine lead cesium growth solution; and (3) growing the bromine lead cesium seed in the bromine lead cesium growth solution or spontaneously nucleating and growing under a sealed condition to obtain a large-size orthorhombic phase bromine lead cesium single crystal. The application uses a mixed solution of water and dimethyl sulfoxide as a solvent of cesium bromide and lead bromide for the first time, lets water participate in the growth of the bromine lead cesium crystal, changes the inverse temperature crystallization property of the CsPbBr3 crystal, changes the solubility of the CsPbBr3 crystal from an inverse temperature curve into a positive temperature curve, realizes the temperature-reducing controlled growth of the crystal, and effectively avoids the generation of other by-products of the bromine lead cesium.

The present application relates to a kind of for CO2 reduction CsPbBr3 quantum dot / BiOCl heterojunction photocatalyst and its preparation method, the preparation method has the following steps: with bismuth oxychloride and lead nitrate is added to aqueous solution, freeze-drying after ultrasonic, by muffle furnace calcination, obtain precursor material;CsPbBr3 quantum dot / BiOCl heterojunction photocatalyst is obtained by two-step calcination method again by adding cesium bromide and potassium bromide, dissolving, ultrasonic, freeze-drying, by muffle furnace calcination its feature is.CsPbBr3 quantum dot / BiOCl heterojunction photocatalyst prepared has excellent performance and good cycle stability.The drug used in preparation is easily obtained and low in price, and preparation is simple and short in time.CsPbBr3 quantum dot / BiOCl heterojunction photocatalyst prepared can be successfully applied in the field of photocatalytic CO2 reduction.

The application discloses a 3D-printable all-inorganic perovskite flexible light-emitting gel and a preparation method and application thereof, and relates to the technical field of perovskite. The method comprises the following steps: dissolving cesium bromide in water to obtain a cesium bromide aqueous solution; adding photo-curing precursor components into the cesium bromide aqueous solution in a certain proportion, and stirring uniformly to obtain a photo-curing precursor mixed solution; obtaining a photo-curing composite hydrogel; obtaining a flexible high polymer gel containing cesium bromide; and performing a spontaneous crystallization reaction, and then performing heat treatment on the gel to remove residual solvents. The perovskite precursors with large solubility difference are introduced into the photo-curing base material in two steps, respectively, so that the compatibility problem of the perovskite and the flexible base material precursor is solved.

The application relates to a preparation method and application of a core-shell structure tin-based perovskite nanocrystal. The application adjusts the feeding ratio of a cesium source and a stannous source and the proportion of oleylamine and oleic acid, and through one-step hot injection, obtains a nanocrystal with a cesium bromide shell and a tin-based perovskite core; and further, a light emitting diode device is prepared by using the nanocrystal. The tin-based perovskite nanocrystal has a sustained and stable high fluorescence quantum yield, and the light emitting diode device prepared based on the nanocrystal has a very high light emitting efficiency.

The invention relates to an improved synthesis process of a cesium germanium bromide halogen perovskite material. The improved synthesis process comprises the following reaction steps: (1) constructing a condensation reflux device and a nitrogen pipeline; (2) weighing germanium dioxide, hydrobromic acid, concentrated hypophosphorous acid and absolute ethyl alcohol; (3) putting the three-neck flask into an oil bath pan, and connecting a condensation reflux device and a nitrogen gas path; (4) after germanium dioxide is completely dissolved, the solution in the flask is clarified; (5) injecting the cesium bromide solution into the three-neck flask in a nitrogen environment, heating, and reacting for a period of time; (6) cooling the solution to room temperature in a nitrogen environment, and collecting a yellow cesium germanium bromide crude product; and (8) refining the crude cesium germanium bromide to obtain refined cesium germanium bromide, wherein the impurity content is lower than 0.5%. According to the method, the cesium-germanium bromide solution and methylbenzene are used, so that the problem that divalent germanium ions and cesium bromide are not completely reacted is solved, and a good solution is provided for synthesizing a high-purity cesium-germanium bromide material.

The invention relates to the technical field of metal halide luminescent materials, and discloses a preparation method of a cesium-lead-bromine-chlorine blue-light quantum dot colloid and a preparation method of a blue-light film. The method comprises the following steps: dissolving cesium bromide and lead bromide in N, N-dimethylformamide, adding oleic acid and oleylamine to form a precursor solution, and injecting the precursor solution into a toluene anti-solvent to prepare CsPbBr3 quantum dot colloid; and then dropwise adding a toluene saturated solution of alkaline earth metal chloride (calcium chloride, strontium chloride, barium chloride or magnesium chloride) for post-treatment to realize ion exchange of Cl <-> and Br <-> and synergistic defect passivation, so that the emission peak is continuously adjustable in the range of 450-500 nm, the half-peak width is less than 30 nm, and the photoluminescence quantum yield is greater than 60%. And further mixing the quantum dot colloid with a polymethyl methacrylate toluene solution and forming a film to obtain a stable blue light quantum dot film which can be used for a backlight source or a display device.

This invention discloses a high-fluorescence quantum yield all-inorganic perovskite thin film, its preparation method, and its applications, belonging to the field of lead-free perovskite optoelectronic device technology. The thin film preparation method includes the following steps: dissolving tin dibromide and cesium bromide in an organic solvent to obtain a precursor solution; adding N-(diphenylphosphino)-P,P-diphenylphosphineamide; coating the obtained perovskite precursor solution onto a substrate; and then annealing to obtain a high-fluorescence quantum yield all-inorganic perovskite thin film, which is a CsSnBr3 perovskite thin film. The CsSnBr3 perovskite thin film prepared using the method of this invention exhibits a high fluorescence quantum yield and improved film coverage. The high-fluorescence quantum yield CsSnBr3 perovskite thin film prepared by this invention can be applied to perovskite light-emitting devices, perovskite solar cells, perovskite photodetectors, and other fields.

The application discloses a cesium copper bromide-silver bromide heterojunction photocatalyst and a preparation method and application thereof, and belongs to the technical field of photocatalytic material for preventing and treating air pollution. The preparation method comprises the following steps: dissolving cesium bromide and copper bromide in dimethyl sulfoxide, and obtaining cesium copper bromide by using an anti-solvent recrystallization method; dispersing the cesium copper bromide into an isopropyl alcohol solution, adding a silver nitrate-isopropyl alcohol solution, sealing the obtained mixed solution, continuously stirring under light irradiation, and obtaining the cesium copper bromide-silver bromide heterojunction photocatalyst through centrifugation, washing and drying. The cesium copper bromide-silver bromide heterojunction photocatalyst provided by the application has stronger photocatalytic reduction capacity, and can greatly improve the activity of the cesium copper bromide-silver bromide in photocatalytic reduction of carbon dioxide.

The invention discloses a method for recycling copper from a waste lithium battery to synthesize perovskite nanocrystals and application of the perovskite nanocrystals, and the method specifically comprises the following steps: dissolving a negative electrode containing copper foil and carbon powder by using sulfuric acid, evaporating to dryness to obtain a copper sulfate and carbon powder mixture, and then carbonizing to obtain cuprous oxide; cuprous oxide and hydrobromic acid are mixed and react to obtain cuprous bromide; cuprous bromide and cesium bromide are mixed, then the mixture is ground, the ground mixture is placed in a vacuum environment to be heated, annealing treatment is conducted after heating, and perovskite powder is obtained; perovskite powder is dissolved in a solvent, a paper-based substrate is coated with the solution, and perovskite nanocrystals are formed after annealing treatment. The carbon powder participates in the preparation process of the perovskite nanocrystals, so that the structural stability of the perovskite nanocrystals is remarkably improved, and meanwhile, the recycled copper can optimize the lattice structure of perovskite and enhance the chemical stability of the perovskite nanocrystals.

The invention provides a preparation method of a perovskite thin film, a perovskite / silicon laminated cell and a preparation method. The method comprises the following steps: depositing lead iodide and cesium bromide on a crystal silicon bottom cell through thermal evaporation to obtain an inorganic composite film, processing the inorganic composite film by using a fused bis-heterocyclic compound solution to obtain a mesoporous structure composite film, preparing an ammonium salt layer on the mesoporous structure composite film, and annealing to form a perovskite film. The solution can promote recrystallization of lead iodide, bicyclic sulfur / nitrogen atoms are coordinated with lead ions to form a five-membered ring chelate, nucleation of lead iodide is delayed, layered stacking is hindered by a bicyclic rigid structure, and vertically-oriented nano-channels are synergistically formed to assist ammonium salt diffusion. R2 long-chain alkyl groups are orderly stacked on a perovskite (001) crystal face to reduce surface energy, the crystal is promoted to preferentially nucleate on the (001) face and vertically and orderly grow, an R1 group, perovskite A-site cations and halide ions form hydrogen bonds, ion escape during annealing is inhibited, defects are reduced, and finally the quality of the perovskite thin film and the performance of the laminated cell are improved.

The invention relates to a preparation method of Na+ / Cu2+ ions co-doped cesium lead bromide perovskite quantum dots, products and applications thereof, which belongs to the technical field of modification research of perovskite quantum dots. The invention discloses a preparation method of Na+ / Cu2+ ions co-doped cesium lead bromide (CsPbBr3) perovskite quantum dots, which adopts lead bromide (PbBr2), oleic acid (OA), oleylamine (OAm), sodium ion precursors and copper ion precursors for the reaction preparation in octadecene (ODE), in which copper ions (Cu2+) and sodium ions (Na+) substitute A and B crystal sites in cesium lead bromide (CsPbBr3) perovskite fluorescent quantum dots respectively. The quantum dots have been effectively improved in photoluminescence quantum yield, thermal stability, etc., and can be used as an active layer to fabricate light emitting diodes which achieve the tuning of emission color from green to blue.

The invention relates to the technical field of nano material preparation, and discloses formamidine acetate doped CsPbBr3 perovskite nanocrystals and a water phase preparation method thereof.The method comprises the steps that firstly, lead bromide, cesium bromide, formamidine acetate and dimethylacetamide are mixed, and a uniformly-doped precursor solution containing formamidine acetate is prepared under the ultrasonic concussion condition; sequentially adding oleylamine and 5-bromovaleric acid into the precursor solution according to a specific sequence, and carrying out ultrasonic-assisted in-situ surface ligand modification; and finally, rapidly injecting the precursor solution into deionized water, inducing crystallization by using the polarity difference of the solvent, centrifuging to remove the precipitate, and taking the supernatant to obtain the target product. According to the preparation method disclosed by the invention, the structural stability of the CsPbBr3 nanocrystal is remarkably improved through doping of formamidine acetate (FA) to a lattice A site and synergistic coordination of acetate. The obtained nanocrystal has a cubic crystal phase structure and can be stably dispersed in a water phase system, and the technical problem that a traditional perovskite material is easy to decompose when meeting water is solved.

The invention discloses a preparation method of a CsPbBr3 single crystal, and belongs to the technical field of novel nano materials. According to the technical scheme, the preparation method comprises the following steps: firstly, dissolving cesium bromide and lead bromide in a DMSO solvent, adding 4-bromobutyric acid, and cooling and stirring to obtain a mixed solution I; sufficiently mixing absolute methanol, cyclohexanol and DMF (Dimethyl Formamide) to obtain a mixed solution II; fully mixing the mixed solution I and the mixed solution II to obtain a precursor solution; and placing a seed crystal in the precursor solution, then putting the precursor solution and the container into preheated silicone oil, and preparing the CsPbBr3 single crystal by adopting a temperature inversion crystallization method. According to the method, methanol and 4-bromobutyric acid are introduced into a precursor solution, the solubility of the precursor solution can be reduced by introducing methanol, the slope of a solubility curve of CsPbBr3 at 85-90 DEG C is reduced, the growth speed of CsPbBr3 is reduced, the crystal quality is improved, the solubility curve of CsPbBr3 is monotonically reduced by introducing 4-bromobutyric acid, and the crystal quality is improved. The CsPbBr3 can be separated out at the temperature of about 60 DEG C, so that the growth temperature is reduced. The high-quality CsPbBr3 single crystal is obtained through the growth of the process disclosed by the invention.

This invention provides a co-encapsulation method for highly stable perovskite quantum dots, comprising the following preparation steps: S1, mixing and grinding a low-crystallinity all-silica zeolite carrier, cesium bromide, and lead bromide to obtain a precursor mixture; S2, heating the precursor mixture to allow the cesium, lead, and halogen components to enter the pores of the low-crystallinity all-silica zeolite carrier, and crystallizing under the confinement of the pores to form CsPbBr3 perovskite quantum dots; S3, contacting the product obtained in step S2 with an aqueous potassium chloride solution and performing hydrothermal treatment to obtain zeolite-encapsulated CsPbBr3 perovskite quantum dots containing lead hydroxide chloride. This invention can reduce the adverse effects of chlorine sources on direct halogen exchange in the perovskite quantum dot bulk lattice and promote the participation of chlorine sources in the formation of a stable protective structure at the carrier interface, thereby improving the stability of perovskite quantum dots.

The invention discloses a porous gallium nitride / cesium lead bromide heterojunction and a preparation method and application thereof, and belongs to the technical field of semiconductors. A sapphire substrate and a magnesium-doped p-type GaN sheet are adopted, and a high-temperature annealing technology is utilized to prepare a porous GaN structure, so that the specific surface area and porosity of a GaN material are increased, the surface wettability of GaN is improved, a solution can form a film more conveniently, and an ideal physical support is provided for permeation and deposition of a CsPbBr3 precursor solution. PbBr2 and CsBr solutions are spin-coated on the surface of the porous GaN through a multi-step method, pores of the porous GaN can be filled with the solutions, a CsPbBr3 thin film is formed after annealing, and finally construction of a three-dimensional heterojunction in the pores is achieved. The heterojunction can effectively separate photon-generated carriers and improve the photoelectric conversion efficiency; the carrier transmission efficiency and collection efficiency are improved, and the carrier transmission path is improved; and the response range of ultraviolet light is widened.

The present invention belongs to the technical field of perovskite thin films, and relates to a surfactant-assisted synthesis of perovskite thin films and a solar cell prepared and assembled therefrom. In the present invention, an aqueous solution of tin dioxide quantum dots is coated on a substrate and then sintered; the obtained tin dioxide electron layer is soaked in an aqueous solution of titanium tetrachloride and then calcined; a solution of lead bromide in N,N-dimethylformamide is coated on the obtained tin dioxide-titanium oxychloride composite electron transport layer and then annealed; an aqueous solution of cesium bromide containing a surfactant is coated on the obtained lead bromide thin film and then annealed; a conductive paste is coated on the obtained CsPbBr3 perovskite thin film and then heat-treated to obtain a surfactant-assisted synthesis of perovskite thin film. The present invention improves problems such as poor film quality and serious charge recombination existing in CsPbBr3 all-inorganic solar cells through a surfactant, thereby improving the performance of the battery.

The invention provides a preparation method of zinc-doped perovskite quantum dots and application of the zinc-doped perovskite quantum dots in a photovoltaic film. The preparation method of the Zn-PQD comprises the following steps: dissolving cesium bromide, lead bromide and a zinc dopant in N, N-dimethylformamide, adding oleic acid and oleylamine, and stirring until the materials are completely dissolved to obtain a precursor solution; ethyl acetate is added into the precursor solution, and Zn-PQD is formed. The energy band gap of the PQD is regulated and controlled by doping Zn, visible light absorption is increased, the photon transition rate is increased, and the fluorescence efficiency and stability of the PQD are improved. According to the Zn-doped CsPbBr3 quantum dots, Pb is partially replaced by Zn, perovskite crystal lattices are gradually shrunk, a transition energy band is reduced, and the fluorescence efficiency is greatly improved. And the Zn-PQD / EVA film is obtained through compounding with the EVA, so that the stability of the Zn-PQD is improved, the light transmittance of the EVA is improved by improving light absorption, and the photoelectric conversion efficiency of the solar cell is improved.

This invention belongs to the field of photocatalytic materials technology, specifically relating to a manganese ferrite / silver hexabromobismuthate dicesium heterojunction photocatalyst, its preparation method, and its application. The mass ratio of manganese ferrite to cesium hexabromobismuthate dicesium heterojunction photocatalyst is 1:3 to 1:7. The preparation method includes: dissolving manganese chloride and ferric chloride hydrate in deionized water, then adding sodium hydroxide, and obtaining manganese ferrite using a hydrothermal method; dissolving silver bromide and bismuth bromide in hydrobromic acid, heating in an oil bath, then adding cesium bromide, and obtaining cesium hexabromobismuthate dicesium using an acid precipitation method; and dissolving manganese ferrite and cesium hexabromobismuthate dicesium in an ethanol solution, and obtaining the manganese ferrite / silver hexabromobismuthate dicesium heterojunction photocatalyst using a mechanical stirring method. The formation of the heterojunction can significantly improve the photocatalytic reduction activity of carbon dioxide by manganese ferrite / silver hexabromobismuthate dicesium.

The invention discloses preparation of a bright and stable CsPbBr3-coated MS-Al composite material and application of a pore channel microenvironment regulation and control strategy to a light emitting diode, and the preparation method comprises the following steps: 1, taking deionized water, hydrochloric acid, Pluronic P123 and tetraethyl orthosilicate (TEOS) as raw materials, and obtaining a mesoporous molecular sieve MS through a hydrothermal method; 2, sodium metaaluminate (NaAlO2) is used as a modifier, and the mesoporous molecular sieve MS-Al is obtained through a post-modification impregnation method. And 3, taking cesium bromide (CsBr), lead bromide (PbBr2) and the mesoporous molecular sieve MS-Al as raw materials, and preparing a product CsPbBr3-coated MS-Al through solid-phase grinding and high-temperature calcination methods. By forming a mesoporous coating structure, the CsPbBr3 quantum dots are uniformly distributed in MS-Al pore channels, and the luminescence property and stability of the material are effectively improved. The prepared CsPbBr3-coated MS-Al composite material has the photoluminescence quantum yield of 81%, and meanwhile has the excellent anti-interference capability on environmental factors. The luminance of a light-emitting diode (LED) prepared from the light-emitting layer is still 90% of that of an initial state when the LED continuously works for more than 600 hours under the working current of 23 mA and the operating voltage of 3.11 V.

The invention provides a silver-based metal halide microcrystal, a preparation method thereof and application of the microcrystal in a deep ultraviolet photoelectric detector, and belongs to the technical field of semiconductor nanomaterials. The preparation method comprises the following steps: dissolving cesium bromide and silver bromide by adopting dimethyl sulfoxide and N, N-dimethyl formamide to form a precursor saturated solution, coating the precursor saturated solution on the surface of a carrier, and in an anti-solvent evaporative crystallization process, influencing the supersaturation degree of the precursor saturated solution by utilizing methanol to drive the solute of the precursor saturated solution to separate out CsAgBr2 crystals, thereby obtaining the CsAgBr2 / CsAgBr2 / CsAgBr2 / CsAgBr2 / CsAgBr2 / CsAgBr2 composite material. Obtaining a carrier loaded with a precursor crystal; the carrier loaded with the precursor crystal is annealed, so that the internal stress of the precursor crystal can be released, the crystallinity of the precursor crystal is improved, and the crystallization quality of the silver-based metal halide microcrystal is improved. The method provided by the invention is simple and convenient to operate, does not need expensive equipment, ultrahigh vacuum and other harsh conditions, is easier to control and implement in the preparation process, and is beneficial to large-scale production.

The invention relates to a metal organic gel type composite adsorbent as well as a preparation method and application thereof. The metal organic gel type composite adsorbent comprises metal organic gel and hygroscopic salt, the hygroscopic salt comprises any one or a combination of at least two of calcium chloride, magnesium chloride, sodium chloride, barium chloride, cesium chloride, lithium bromide, calcium bromide, magnesium bromide, sodium bromide, barium bromide or cesium bromide. According to the preparation method of the metal organic gel type composite adsorbent, synthesis conditions are mild, large-scale preparation is easy, a reaction product is blocky gel, a final product is a granular integral adsorbent after drying, the adsorbent has efficient water vapor adsorption capacity, and the adsorbent has good application prospects. The metal organic gel type composite adsorbent has excellent adsorption and desorption performance and good cycle stability on water vapor.

The present invention discloses a composition for preparing deep blue light-emitting quasi-two-dimensional perovskites and its application. The raw materials for preparing the composition include cesium bromide, lead bromide, lead chloride, and 2-acryloyloxyethyl N-butylcarbamate. By introducing 2-acryloyloxyethyl N-butylcarbamate as a key additive, the present invention precisely inhibits the overgrowth of the high-n phase (i.e., the perovskite phase with a higher number of layers) in the quasi-two-dimensional perovskites, thereby achieving fine tuning of the optical properties of the perovskite material. When the perovskite thin film emits deep blue light, its photoluminescence quantum yield (PLQY) reaches 93.4%.

The invention discloses a preparation method of a one-dimensional cesium-lead-bromine nanowire film, a film material, an element and equipment. The preparation method comprises the following steps: preparing a first solution containing a proper amount of acetone, toluene and a surfactant; weighing lead bromide and cesium bromide in a molar ratio of 1: 1, and grinding into uniform powder; in a constant-temperature water bath, adding the powder into the first solution, and stirring for reaction; after the reaction is finished, separating and washing to obtain a pure cesium-lead-bromine nanowire; dispersing the cesium-lead-bromine nanowires in a mixed solvent of normal octane and normal hexane to obtain a nanowire dispersion liquid required for preparing the thin film; and coating the nanowire dispersion liquid on a substrate, and drying at room temperature to obtain the uniform one-dimensional cesium-lead-bromine nanowire film with high polarization luminescence and polarization response. According to the invention, the preparation process of the one-dimensional cesium-lead-bromine nanowire film is optimized, and the preparation of the macroscopic orientation cesium-lead-bromine nanowire film with high polarization luminescence and polarization response is realized, so that the preparation of an optical device with good anisotropy and polarization performance is realized.