10 results about "Iodate" patented technology

The invention relates to a 1D / 2D dual-heterojunction catalyst, a preparation method thereof and application of the 1D / 2D dual-heterojunction catalyst in photo-assisted periodate activated degradation of bisphenol A. The preparation method comprises the following steps: mixing a concentrated hydrochloric acid solution with LiF, adding Ti3AlC2, carrying out a heating reaction, carrying out solid-liquid separation to obtain a solid phase, washing the solid phase to be neutral, and dispersing the solid phase in ethanol to obtain an MXene ethanol solution; adding a cerium source aqueous solution into an MXene ethanol solution, mixing, and placing in liquid nitrogen to obtain a mixed solution; mixing an organic ligand, ethanol and pure water to obtain a mixed solution, carrying out a mixed heating reaction on the mixed solution and the mixed solution, carrying out solid-liquid separation to obtain a precipitate, and freeze-drying to obtain powder; and heating and calcining the obtained powder in an inert atmosphere to obtain the 1D / 2D dual-heterojunction catalyst. According to the invention, photogenerated electron-hole recombination is effectively inhibited by constructing double heterojunctions, and ultrafast electron transfer is realized at the same time, so that the oxidation effect is enhanced, and the efficient photocatalytic activity of '1 + 1gt, 2' is realized.

The present application relates to a kind of 1D / 2D double heterojunction catalyst and its preparation method and its application in photo-assisted high iodate activation degradation bisphenol A.The preparation method of the present application: concentrated hydrochloric acid solution and LiF are mixed, Ti3AlC2 is added, heated reaction, solid-liquid separation is taken solid phase, after washing to neutral, dispersed in ethanol, to obtain MXene ethanol solution;Cerium source aqueous solution is added to MXene ethanol solution and mixed in liquid nitrogen, to obtain mixed solution;Organic ligand, ethanol and pure water are mixed to obtain mixed solution, the mixed solution and mixed solution are mixed and heated, solid-liquid separation is taken precipitate, freeze-drying is obtained powder;The obtained powder is heated and calcined under inert atmosphere, to obtain 1D / 2D double heterojunction catalyst.The present application effectively inhibits photo-generated electron hole recombination by constructing double heterojunction, while realizing ultrafast electron transfer, to enhance oxidation, realizes the high-efficiency photocatalytic activity of "1+1>2".

The application discloses a preparation method of a wide-bandgap perovskite photoactive layer, and comprises the following steps: S1, lead iodide powder, cesium iodide powder and ytterbium bromide powder are proportioned according to a proportioning molar ratio, and an inorganic target material is prepared by using a hot-press sintering process; S2, formamidinium hydriodide powder and methylammonium bromide powder are proportioned according to a proportioning molar ratio, and an organic target material is prepared by using a normal-temperature preparation process; S3, a pretreated substrate is placed on a magnetron sputtering sample table, the target materials prepared in steps S1 and S2 are respectively installed on corresponding radio frequency sputtering targets, and the background of a magnetron sputtering system is vacuumized; S4, high-purity argon gas is used as a sputtering gas, and a wide-bandgap perovskite thin film is prepared by using a magnetron co-sputtering method; the sputtering power of the inorganic target material prepared in step S1 is controlled, the sputtering power of the organic target material prepared in step S2 is controlled, and the thickness of the thin film is controlled, so that the high-quality thin film is prepared by using the differential target material preparation process.

The invention relates to a perovskite precursor solution, a perovskite thin film, a preparation method of the perovskite thin film and a photovoltaic module. The perovskite precursor solution comprises a perovskite precursor, an additive and a mixed solvent; the perovskite precursor is prepared from formamidine hydriodate and lead iodide; the additive comprises cesium iodide and methylamine hydrochloride; the mixed solvent is prepared from N, N-dimethyl formamide, N-methyl pyrrolidone and cyclohexyl pyrrolidone. The composition of the perovskite precursor solution is blended, the high-quality perovskite thin film with the micro-suede surface is spontaneously formed in the perovskite crystallization process, the micro-suede surface structure can increase the contact area between a perovskite layer and a subsequent functional layer, a tight mechanical interlocking effect is generated between the micro-suede surface structure and the interface of the functional layer, and the performance of the perovskite thin film is improved. Therefore, the interface adhesive force of the subsequent functional layer and the metal electrode is obviously improved, and the problem of performance degradation of the perovskite assembly caused by the packaging process is solved.

This invention relates to the field of alkali metal-chlorine secondary battery technology, and discloses an electrolyte additive, an electrolyte, and an alkali metal-chlorine secondary battery. The additive contains components A, B, and C in a mass ratio of 1:0.2-2.0:0.5-3.0; component A is selected from at least one of ethyl viologen dibromide, benzyl viologen diiodide, and 1,4-phenylenediamine hydroiodate; component B is selected from at least one of 3-(4-iodophenyl)-3-(trifluoromethyl)-3H-bisacrylidine, 1-bromo-2-fluorobenzene, and 4-(benzyloxy)-1-bromo-2-fluorobenzene; and component C is selected from at least one of 3-(trifluoromethyl)phenyltrimethylammonium bromide, (3-fluoro-4-iodophenyl)methylamine, and 3-iodobenzylamine. The electrolyte provided by this invention, when applied in an alkali metal-chlorine secondary battery system, exhibits high reversible capacity, cycle stability, and environmental adaptability.

The invention discloses a methylamine formamidino perovskite single crystal, a preparation method thereof and an X-ray detector, and belongs to the technical field of perovskite single crystal X-ray detectors. Methyl iodide amine, formamidino hydriodate and lead iodide are used as raw materials, anhydrous acetic acid is used as an additive, growth is carried out in a solvent through a seed crystal method, and the methylamine formamidino perovskite single crystal is obtained. Anhydrous acetic acid and formamidine generate hydrogen-bond interaction, formamidine is pulled to enter crystal lattices, so that phase separation is eliminated, acetate and Pb coordinate to delay formation of a lead-iodine framework, the speed of methylamine and formamidine entering the crystal lattices is balanced, meanwhile, the stability of a methylamine formamidine perovskite precursor solution is improved, stable growth of methylamine formamidine perovskite single crystals is achieved, and the methylamine formamidine perovskite single crystals are obtained. The single crystal has the advantages of high crystallinity, low defect density, large size and favorable X-ray response performance. The methylamine formamidine perovskite single crystal is high in controllability in the growth process, and the preparation method is high in operability, simple and easy to implement, short in preparation period, low in equipment requirement and low in cost.

The invention discloses a multifunctional hair cosmetic active raw material as well as a preparation method and application thereof. The active raw material is cystine dimaleate amide. The disulfide bond-containing molecule with a symmetric maleic acid structure is used as a sulfydryl reconnection reagent, so that a traditional oxidized sulfydryl reconnection reagent represented by hydrogen peroxide, bromate, iodate and the like is avoided, the content of the disulfide bond in hair is maintained while the hair is shaped, and particularly, after multiple times of perming, the hair is more comfortable to use. Compared with the prior art that a large amount of disulfide bonds are consumed after perming, the supplement and the shaping method are used for perming, so that the hair can be effectively and repeatedly permed according to the willingness of consumers, and the hair styles can be changed for multiple times.

This invention relates to a 3D dual heterojunction catalyst hydrogel, its preparation method, and its application in photo-assisted periodate-activated degradation of organic pollutants. The preparation method of the 3D dual heterojunction catalyst hydrogel of this invention involves: mixing acid and LiF, adding Ti3AlC2 for heating and reaction, separating the solid phase, dispersing the obtained solid phase in an organic solvent to obtain an MXene solution; mixing a cobalt salt solution with the MXene solution and placing it in liquid nitrogen to obtain a precursor solution; mixing and stirring a dimethylimidazole aqueous solution with the precursor solution; separating the solid and liquid phases of the reaction solution to obtain the precipitate, calcining it under an inert atmosphere, mixing it with chitosan colloid, and adding an alkaline solution dropwise to obtain the 3D dual heterojunction catalyst hydrogel. This invention combines the excellent conductivity of MXene with the synergistic effect of the large specific surface area of ​​MOF and Cs, realizing an ultrafast electron transport channel and significantly improving the utilization efficiency of photogenerated carriers.

The invention provides an electrolyte, a battery, a battery pack and electric equipment, the electrolyte comprises azabowl-ene alkyl ammonium iodate, and the azabowl-ene alkyl ammonium iodate comprises a compound with a structure as shown in a formula 1. The electrolyte provided by the invention can inhibit lithium precipitation and self discharge of the battery, and improve the cycle life and other performances of the battery.