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ORGANIC PROTON-TYPE IONIC LIQUID, TWO-DIMENSIONAL PEROVSKITE PURE-PHASE QUANTUM WELL FILM, PREPARATION METHOD AND USE THEREOF

20230022061 · 2023-01-26

    Inventors

    Cpc classification

    International classification

    Abstract

    Disclosed are an organic proton-type ionic liquid, a film with a two-dimensional perovskite pure-phase quantum well structure, a preparation method and use thereof. The chemical formula of the organic proton-type alkylamine acetate ionic liquid is RNH.sub.3.sup.+—RCOO.sup.−, where R represents an alkyl group of C4-8 or a phenyl group, preferably, the chemical formula of the organic proton-type alkylamine acetate ionic liquid is CH.sub.3(CH.sub.2).sub.3NH.sub.3.sup.+—CH.sub.2COO.sup.−. The organic proton-type alkylamino acetate ionic liquid disclosed in the present disclosure can be used to prepare perovskite material, the prepared perovskite film thereby can form a pure-phase single quantum well, and the crystal grain size of the film can reach the level of micrometers or even millimeters.

    Claims

    1. An organic proton-type alkylamine acetate ionic liquid, wherein a chemical formula of the organic proton-type alkylamine acetate ionic liquid is RNH.sub.3.sup.+—RCOO.sup.−, where R represents an alkyl group of C4-8 or a phenyl group.

    2. A method for preparing the organic proton-type alkylamine acetate ionic liquid, and the organic proton-type alkylamine acetate ionic liquid is a butylamine acetate ionic liquid, having a chemical formula of H.sub.3(CH.sub.2).sub.3NH.sub.3.sup.+—CH.sub.2COO.sup.−, comprising: 1. mixing a carboxyl group-containing organic acid and an amine group-containing organic amine in a molar ratio of the amine group and the carboxyl group of 1:1, then adding a same volume of a first diluent as the amine group-containing organic amine, cooling to 0° C. and stirring to react for 2-2.5 h to obtain a mixture; and 2. removing the first diluent and other organic impurities from the mixture by reduced pressure distillation at 80° C., then lowering the temperature to −4° C. for recrystallization, standing for 1 hour to obtain a solidified mixture, washing the solidified mixture with 1000 mL of a volatile anti-solvent for 3 times, then dissolving the solidified mixture in 100 mL of a second diluent, stirring for 30 min, and then removing the second diluent by reduced pressure distillation at 80° C. to obtain the organic proton-type alkylamine acetate ionic liquid.

    3. (canceled)

    4. The method according to claim 2, wherein the carboxyl group-containing organic acid comprises one or more of formic acid, acetic acid, propionic acid, butyric acid, pentanoic acid and hexanoic acid; the amine group-containing organic amine is one or more selected from aminomethane, (di)aminoethane, (di)aminopropane, (di)aminobutane, (di)aminopentane and (di)aminohexane; the first diluent is one or more selected from water, ethanol, methanol, propanol and isopropanol; and the volatile anti-solvent is an ethers reagent.

    5. The method according to claim 4, wherein the ethers reagent is diethyl ether.

    6. (canceled)

    7. (canceled)

    8. A two-dimensional perovskite pure-phase quantum well material prepared based on an organic proton-type alkylamine acetate ionic liquid, wherein a chemical formula of the two-dimensional perovskite pure-phase quantum well material is A.sub.aB.sub.bM.sub.mX.sub.x, where: A is a long carbon chain organic cation, and a-value ranges from 0 to 2.5; B is an amine group-containing monovalent cation, b-value satisfies 0≤(m−1)<b<(m+1), and m is any natural number; M is a divalent metal cation; and X is one or more of halogen ion, carboxylate ion and thiocyanate ion, and x-value satisfies (3m−1)<x<(3m+1).

    9. The two-dimensional perovskite pure-phase quantum well material according to claim 8, wherein: the long carbon chain organic cation is one or more of CH.sub.3CH.sub.2NH.sub.3.sup.+, CH.sub.3CH.sub.2CH.sub.2NH.sub.3.sup.+, CH.sub.3CH.sub.3CH.sub.2CH.sub.2NH.sub.3.sup.+, CH.sub.3CH.sub.2CH.sub.2CH.sub.2CH.sub.2NH.sub.3.sup.+ and CH.sub.3CH.sub.2CH.sub.2CH.sub.2CH.sub.2CH.sub.2NH.sub.3.sup.+; the amine group-containing monovalent cation is one or more of methylamine ion, formamidine ion, guanidine ion, and cesium ion; the divalent metal cation is one or more of lead ion, tin ion, copper ion, zinc ion, manganese ion and bismuth ion; and the halogen is one or more of F, Cl, Br, and I.

    10. The two-dimensional perovskite pure-phase quantum well material according to claim 8, wherein a chemical formula of the two-dimensional perovskite pure-phase quantum well material is A.sub.2B.sub.2M.sub.3X.sub.10.

    11. The two-dimensional perovskite pure-phase quantum well material according to claim 8, wherein a chemical formula of the two-dimensional perovskite pure-phase quantum well material is [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3)Pb.sub.2I.sub.7, [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3).sub.2Pb.sub.3I.sub.10, [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3).sub.3Pb.sub.4I.sub.13 or [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3).sub.4Pb.sub.5I.sub.16.

    12. A method for preparing a film with a two-dimensional perovskite pure-phase quantum well structure, comprising: 1. preparing materials in a molar ratio of the organic proton-type alkylamine acetate ionic liquid according to claim 1, BX and MX of 2:(m+1):m; 2. adding BX to a DMSO solution to prepare a DMSO mixture with a BX mass fraction of 1-35%; 3. adding the organic proton-type alkylamine acetate ionic liquid to the DMSO mixture prepared in step 2), mixing evenly, stirring at 25° C. for 2 h, and then adding MX; 4. then adding 1600 μL of a DMF reagent, heating to 65° C. and stirring until fully dissolved, and cooling to room temperature to obtain a mixed solution; and 5. subjecting the mixed solution prepared in step 4) to spin-coating with heating on the surface of a glass substrate in the air with a humidity of 20%-80%, and maintaining the temperature at 25° C.-250° C. to obtain the two-dimensional perovskite pure-phase quantum well film; wherein, X is one or more of halogen ion, carboxylate ion and thiocyanate ion; BX is a compound salt of a monovalent cation; and MX is a compound formed by a divalent metal cation and an X ion.

    13. The method according to claim 12, wherein the compound salt of the monovalent cation is one or more selected from a compound salt of methylamine ion, a compound salt of formamidine ion, a compound salt of guanidine ion and a compound salt of cesium ion.

    14. The method according to claim 12, wherein an addition amount of the DMF reagent in step 3) is 5-50 times an addition amount of the organic proton-type alkylamine acetate ionic liquid in volume.

    15. The method according to claim 12, wherein the spin-coating with heating comprises: heating the glass substrate to 80° C.-100° C., setting a spin-coating speed to 500-1000 rpm/min and performing spin-coating for 5-10 s, then setting a spin-coating speed to 2000-6000 rpm/min and performing spin-coating for 5-10 s, continuously heating the substrate between the two spin-coating steps, covering a film obtained after spin-coating with a petri dish with a diameter of 100 mm, and then subjecting to heat-treatment at 80° C.-120° C. for 5-10 min.

    16. The method according to claim 12, comprising: 1. preparing materials in a molar ratio of a butylamine acetate ionic liquid, methyl ammonium iodide and lead iodide of 2:4:3; 2. adding methyl ammonium iodide to a DMSO solution to prepare a DMSO mixture with a mass fraction of methyl ammonium iodide of 1-35 wt %; 3. adding the butylamine acetate ionic liquid to the DMSO mixture prepared in step 2), mixing evenly, stirring at 25° C. for 2 h, and then adding lead iodide powder; then adding a DMF reagent, heating to 65° C., stirring until fully dissolved, and cooling to room temperature to obtain a mixed solution; and 4. subjecting the mixed solution prepared in step 3) to spin-coating with heating on the surface of a glass substrate in the air with a humidity of 20%-80%, and maintaining the temperature at 25° C.-250° C.

    17. The two-dimensional perovskite pure-phase quantum well material according to claim 11, wherein: the long carbon chain organic cation is one or more of CH.sub.3CH.sub.2NH.sub.3.sup.+, CH.sub.3CH.sub.2CH.sub.2NH.sub.3.sup.+, CH.sub.3CH.sub.3CH.sub.2CH.sub.2NH.sub.3.sup.+, CH.sub.3CH.sub.2CH.sub.2CH.sub.2CH.sub.2NH.sub.3.sup.+ and CH.sub.3CH.sub.2CH.sub.2CH.sub.2CH.sub.2CH.sub.2NH.sub.3.sup.+; the amine group-containing monovalent cation is one or more of methylamine ion, formamidine ion, guanidine ion, and cesium ion; the divalent metal cation is one or more of lead ion, tin ion, copper ion, zinc ion, manganese ion and bismuth ion; and the halogen is one or more of F, Cl, Br, and I.

    18. The method according to claim 12, wherein the ionic liquid is a butylamine acetate ionic liquid, and a chemical formula of the butylamine acetate ionic liquid is CH.sub.3(CH.sub.2).sub.3NH.sub.3.sup.+—CH.sub.2COO.sup.−.

    Description

    BRIEF DESCRIPTION OF THE DRAWINGS

    [0056] FIG. 1 shows the appearance of the organic proton-type butylamine acetate ionic liquid.

    [0057] FIG. 2 is an ultrafast spectroscopic analysis spectrum of the two-dimensional perovskite pure-phase quantum well film prepared in Example 1.

    [0058] FIG. 3 is an ultrafast spectroscopic analysis spectrum of the two-dimensional perovskite pure-phase quantum well film prepared in Example 2.

    [0059] FIG. 4 is an ultrafast spectroscopic analysis spectrum of the two-dimensional perovskite pure-phase quantum well film prepared in Example 3.

    [0060] FIG. 5 is an ultrafast spectroscopic analysis spectrum of the two-dimensional perovskite pure-phase quantum well film prepared in Example 4.

    [0061] FIG. 6 is an ultrafast spectroscopic analysis spectrum of the two-dimensional perovskite pure-phase quantum well film prepared in Comparative Example 1.

    [0062] FIG. 7 is an ultrafast spectroscopic analysis spectrum of the two-dimensional perovskite pure-phase quantum well film prepared in Comparative Example 2.

    [0063] FIG. 8 is an ultrafast spectroscopic analysis spectrum of the two-dimensional perovskite pure-phase quantum well film prepared in Comparative Example 3.

    [0064] FIG. 9 is a scanning electron micrograph of the two-dimensional perovskite pure-phase quantum well film prepared in Example 1.

    [0065] FIG. 10 is a scanning electron micrograph of the two-dimensional perovskite pure-phase quantum well film prepared in Comparative Example 1.

    [0066] FIG. 11 is a nuclear magnetic resonance hydrogen spectrum of the proton-type butylamine acetate ionic liquid.

    DETAILED DESCRIPTION

    [0067] In order to enable those skilled in the art to better understand the technical solutions of the present disclosure, the present disclosure will be further described in detail below with reference to the accompanying drawings and specific embodiments.

    [0068] Source of Raw Materials.

    [0069] Except for the organic amine salt ionic liquid, the materials used in the embodiments of the present disclosure are all commercially available, and the purity is higher than 98-99%.

    [0070] The instruments and equipment used in the present disclosure are as follows: [0071] magnetic heating stirrer (1 set), freezing thermostat (1 set), rotary evaporator (1 set), mechanical pump (1 set), heating spin-coater (1 set), spin-coater (2 sets), and glove box (1 set).

    [0072] Preparation of Organic Proton-Type Butylamine Acetate Ionic Liquid: [0073] 1) the acetic acid and 1-aminobutane were mixed in a molar ratio of 1:1, then the same volume of ethanol as 1-aminobutane was added, the temperature was cooled to 0° C. and stirred for 2 h to obtain a mixture; and [0074] 2) the ethanol and water were removed from the mixture by reduced pressure distillation at 80° C., then the temperature was lowered to −4° C. for recrystallization, a solidified mixture was obtained after standing for 1 h, the mixture was washed with 1000 mL of diethyl ether for 3 times, then the mixture was dissolved in 100 mL of ethanol, stirred for 30 min, and then the ethanol was removed by reduced pressure distillation at 80° C. to obtain an organic proton-type butylamine acetate ionic liquid (CH.sub.3(CH.sub.2).sub.3NH.sub.3.sup.+—CH.sub.2COO.sup.−).

    [0075] As shown in the subgraph on the right side of FIG. 1, the organic proton-type butylamine acetate ionic liquid prepared by the present disclosure is a colorless and transparent liquid with good fluidity and special aromatic odor, which is a new type of environmentally friendly and pollution-free organic amine salt for low-dimensional perovskite. The subgraph on the left side of FIG. 1 is a common organic halogen organic amine salt, which is white powder or massive crystal in appearance.

    [0076] FIG. 11 is a nuclear magnetic resonance hydrogen spectrum of the organic proton-type butylamine acetate ionic liquid, indicating that the product is an ionic product composed of butylamine and acetate.

    Example 1

    [0077] Preparation of Two-Dimensional Perovskite Pure-Phase Quantum Well Film (m-Value is 2, a Narrow Quantum Well Structure with a Broad Band-Gap):

    [0078] 82.94 mg of butylamine acetate ionic liquid CH.sub.3(CH.sub.2).sub.3NH.sub.3.Math.CH.sub.2COO.sup.− was drawn, 148.72 mg of methyl ammonium iodide CH.sub.3NH.sub.3I was weighed, then the two were preferentially mixed in 400 μL of DMSO solution, stirred fully at 25° C. for about 2 h. When the solution was uniform, 287.48 mg of PbI.sub.2 powder was weighed, and then 1600 μL of DMF reagent was drawn to be added in the solution to obtain a mixture, the mixture was continued to heat and stir at 65° C. until it was completely dissolved, and finally cooled to room temperature for use. The mixture was subjected to heating coating in the air with a humidity of 20%-80%, the glass substrate was maintained smooth and tidy during the entire coating process, and the temperature was maintained at 25° C.-250° C. First, the glass substrate was heated to 80-100° C., the spin-coating speed was set to 500-1000 rpm/min, and the spin-coating time was 5-10 s, secondly, the spin-coating speed was set to 2000-6000 rpm/min, the spin-coating time was 5-10 s, the substrate was heated continuously between the two spin-coating steps. The film obtained after spin-coating was covered with a petri dish with a diameter of 100 mm, and then subjected to a heat treatment at 80-120° C. Finally, a flat and smooth two-dimensional perovskite pure-phase quantum well film with micron-level grains was obtained, as shown in FIG. 9, of which the chemical formula is [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3)Pb.sub.2I.sub.7. FIG. 10 is a two-dimensional perovskite multiphase quantum well film prepared by butylamine iodine.

    Example 2

    [0079] Preparation of Two-Dimensional Perovskite Pure-Phase Quantum Well Film:

    [0080] 56.78 mg of butylamine acetate ionic liquid CH.sub.3(CH.sub.2).sub.3NH.sub.3.sup.+—CH.sub.2COO.sup.− was drawn, 135.89 mg of methyl ammonium iodide CH.sub.3NH.sub.3I was weighed, then the two were preferentially mixed in 400 μL of DMSO solution, stirred fully at 25° C. for about 2 h. When the solution was uniform, 295.51 mg of PbI.sub.2 powder was weighed, and then 1600 μL of DMF reagent was drawn to be added in the solution to obtain a mixture, the mixture was continued to heat and stir at 65° C. until it was completely dissolved, and finally cooled to room temperature for use. The mixture was subjected to heating coating in the air with a humidity of 20%-80%, the glass substrate was maintained smooth and tidy during the entire coating process, and the temperature was maintained at 25° C.-250° C. First, the glass substrate was heated to 80-100° C., the spin-coating speed was set to 500-1000 rpm/min, and the spin-coating time was 5-10 s, secondly, the spin-coating speed was set to 2000-6000 rpm/min, the spin-coating time was 5-10 s, the substrate was heated continuously between the two spin-coating steps. The film obtained after spin-coating was covered with a petri dish with a diameter of 100 mm, and then subjected to a heat treatment at 80-120° C. Finally, a flat and smooth two-dimensional perovskite pure-phase quantum well film with micron-level grains was obtained with a chemical formula of [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3).sub.2Pb.sub.3I.sub.10.

    Example 3

    [0081] Preparation of Two-Dimensional Perovskite Pure-Phase Quantum Well Film (m-Value is 4, a Broad Quantum Well Structure with a Narrow Band-Gap):

    [0082] 43.18 mg of butylamine acetate ionic liquid CH.sub.3(CH.sub.2).sub.3NH.sub.3.sup.+—CH.sub.2COO.sup.− was drawn, 129.06 mg of methyl ammonium iodide CH.sub.3NH.sub.3I was weighed, then the two were preferentially mixed in 400 μL of DMSO solution, stirred fully at 25° C. for about 2 h. When the solution was uniform, 299.36 mg of PbI.sub.2 powder was weighed, and then 1600 μL of DMF reagent was drawn to be added in the solution to obtain a mixture, the mixture was continued to heat and stir at 65° C. until it was completely dissolved, and finally cooled to room temperature for use. The mixture was subjected to heating coating in the air with a humidity of 20%-80%, the glass substrate was maintained smooth and tidy during the entire coating process, and the temperature was maintained at 25° C.-250° C. First, the glass substrate was heated to 80-100° C., the spin-coating speed was set to 500-1000 rpm/min, and the spin-coating time was 5-10 s, secondly, the spin-coating speed was set to 2000-6000 rpm/min, the spin-coating time was 5-10 s, the substrate was heated continuously between the two spin-coating steps. The film obtained after spin-coating was covered with a petri dish with a diameter of 100 mm, and then subjected to a heat treatment at 80-120° C. Finally, a flat and smooth two-dimensional perovskite pure-phase quantum well film with micron-level grains was obtained, of which the chemical formula is [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3).sub.3Pb.sub.4I.sub.13.

    Example 4

    [0083] Preparation of Two-Dimensional Perovskite Pure-Phase Quantum Well Film (m-Value is 5, a Broad Quantum Well Structure with a Narrow Band-Gap):

    [0084] 34.84 mg of butylamine acetate ionic liquid CH.sub.3(CH.sub.2).sub.3NH.sub.3.sup.+—CH.sub.2COO.sup.− was drawn, 124.92 mg of methyl ammonium iodide CH.sub.3NH.sub.3I was weighed, then the two were preferentially mixed in 400 μL of DMSO solution, stirred fully at 25° C. for about 2 h. When the solution was uniform, 295.51 mg of PbI.sub.2 powder was weighed, and then 1600 μL of DMF reagent was drawn to be added in the solution to obtain a mixture, the mixture was continued to heat and stir at 65° C. until it was completely dissolved, and finally cooled to room temperature for use. The mixture was subjected to heating coating in the air with a humidity of 20%-80%, the glass substrate was maintained smooth and tidy during the entire coating process, and the temperature was maintained at 25° C.-250° C. First, the glass substrate was heated to 80-100° C., the spin-coating speed was set to 500-1000 rpm/min, and the spin-coating time was 5-10 s, secondly, the spin-coating speed was set to 2000-6000 rpm/min, the spin-coating time was 5-10 s, and the substrate was heated continuously between the two spin-coating steps. The film obtained after spin-coating was covered with a petri dish with a diameter of 100 mm, and then subjected to a heat treatment at 80-120° C. Finally, a flat and smooth two-dimensional perovskite pure-phase quantum well film with micron-level grains was obtained, of which the chemical formula is [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3).sub.4Pb.sub.5I.sub.16.

    Comparative Example 1

    [0085] a. The n-butylamine iodide CH.sub.3(CH.sub.2).sub.3NH.sub.3I, methylamine chloride CH.sub.3NH.sub.3Cl, and lead iodide PbI.sub.2 were dissolved in methylamine acetate in a molar ratio of 2:3:4, and stirred at 60° C. for 1 h-24 h to obtain a precursor solution with a concentration of 200 mg.Math.mL.sup.−1; b. The precursor solution was preheated to 50° C.-100° C., and then spin-coated for 10 s-60 s on a heating spin-coater at 60° C.-130° C., and the heating was continued during the whole spin-coating process, and then gradient annealing was performed at 60° C.-100° C. for 3 min-10 min to obtain a mixed multi-quantum well perovskite film with no fixed chemical formula. Its main components include [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3)Pb.sub.2I.sub.7, [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3).sub.2Pb.sub.3I.sub.10, [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3).sub.3Pb.sub.4I.sub.13, [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3).sub.4Pb.sub.5I.sub.16 and CH.sub.3NH.sub.3PbI.sub.3.

    Comparative Example 2

    [0086] a. The n-butylamine iodide CH.sub.3(CH.sub.2).sub.3NH.sub.3I, methylamine chloride CH.sub.3NH.sub.3C1, and lead iodide PbI.sub.2 were dissolved in DMF at the molar ratio of 2:3:4, and stirred at 60° C. for 1 h-24 h to prepare a precursor solution with a concentration of 200 mg.Math.mL.sup.−1; b. The precursor solution was preheated to 50° C.-100° C., and then spin-coated for 10 s-60 s on a room-temperature spin-coater at 60° C.-130° C., and then gradient annealing was performed at 60° C.-100° C. for 3 min-10 min to obtain a mixed multi-quantum well perovskite film with no fixed chemical formula. Its main components include [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3)Pb.sub.2I.sub.7, [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3).sub.2Pb.sub.3I.sub.10, [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3).sub.3Pb.sub.4I.sub.13, [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3).sub.4Pb.sub.5I.sub.16 and CH.sub.3NH.sub.3PbI.sub.3.

    Comparative Example 3

    [0087] a. The butylamine acetate ionic liquid CH.sub.3(CH.sub.2).sub.3NH.sub.3.sup.+.Math.CH.sub.3COO.sup.−, methylamine chloride CH.sub.3NH.sub.3C1, and lead iodide PbI.sub.2 were dissolved in DMF at the molar ratio of 2:3:4, and stirred at 60° C. for 1 h-24 h to prepare a precursor solution with a concentration of 200 mg.Math.mL.sup.−1; b. The precursor solution was preheated to 50° C.-100° C., and then spin-coated for 10 s-60 s on a room-temperature spin-coater at 60° C.-130° C., and then gradient annealing was performed at 60° C.-100° C. for 3 min-10 min to obtain a mixed multi-quantum well perovskite film with no fixed chemical formula. The main components include [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3)Pb.sub.2I.sub.7, [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3).sub.2Pb.sub.3I.sub.10, [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3).sub.3Pb.sub.4I.sub.13, [CH.sub.3(CH.sub.2).sub.3NH.sub.3].sub.2(CH.sub.3NH.sub.3).sub.4Pb.sub.5I.sub.16 and CH.sub.3NH.sub.3PbI.sub.3.

    [0088] The two-dimensional perovskite pure-phase quantum well films prepared in Examples 1, 2, 3, 4 and Comparative Examples 1, 2, and 3 were subjected to ultrafast spectroscopy analysis. The equipment name and test conditions are as follows: ultrafast system HELIOS-TA spectrometer, the laser source is a Coherent Legend regenerative amplifier (150 fs, 1 KHz, 800 nm) injected by a Coherent Vitesse oscillator (100 fs, 80 MHz). Broadband probe pulse (420-780 nm) is generated by focusing a small part (about 10 mj) of a basic 800 nm laser pulse onto a 2 mm sapphire plate to obtain FIG. 2, FIG. 3, FIG. 4, FIG. 5, FIG. 6, FIG. 7 and FIG. 8, respectively.

    [0089] It can be seen from the figures that the two-dimensional perovskite pure-phase quantum well film prepared in Example 1 has a single perovskite pure-phase quantum well with an n-value of 2, i.e. the distribution width of the quantum well is two lead-iodine octahedrons on average, it is well distributed with no quantum wells with other n values, and the purity is close to 100%. According to the scanning electron micrographs, it can be seen that the grain size of the perovskite film has reached the micron level with a high crystallinity, the film is dense and has no holes, and the surface is smooth and flat.

    [0090] The two-dimensional perovskite pure-phase quantum well film prepared in Example 2 has a single perovskite pure-phase quantum well with an n value of 3, i.e. the distribution width of the quantum well is three lead-iodine octahedrons on average, it is well distributed with no quantum wells with other n values, and the purity is close to 100%.

    [0091] The two-dimensional perovskite pure-phase quantum well film prepared in Example 3 has a single perovskite pure-phase quantum well with an n value of 4, i.e. the distribution width of the quantum well is four lead-iodine octahedrons on average, it is well distributed with no quantum wells with other n values, and the purity is more than 98%.

    [0092] The two-dimensional perovskite pure-phase quantum well film prepared in Example 4 has a single perovskite pure-phase quantum well with an n value of 5, i.e. the distribution width of the quantum well is five lead-iodine octahedrons on average, it is well distributed with no quantum wells with other n values, and the purity is more than 98%.

    [0093] The two-dimensional perovskite multiphase quantum well film prepared in Comparative Example 1 has a target quantum well width of 4, but a complex multiphase quantum well film is actually obtained, which contains phases with various widths of 2, 3, 4 and infinite three-dimensional perovskite parts, and even impurity phases such as lead iodide. It can be seen from the scanning electron micrographs that the perovskite film has a smaller grain size in the nanometer range, and the crystallinity of the grain is average, the film has a small number of holes and a high surface roughness.

    [0094] The two-dimensional perovskite multiphase quantum well film prepared in Comparative Example 2 has a target quantum well width of 4, but a complex multiphase quantum well film is actually obtained, which contains phases with various widths of 2, 3, 4 and infinite three-dimensional perovskite parts, even the content of infinity phase is more, and there are still impurity phases such as lead iodide.

    [0095] The two-dimensional perovskite multiphase quantum well film prepared in Comparative Example 3 has a target quantum well width of 4, but a complex multiphase quantum well film is actually obtained, which contains phases with various widths of 2, 3, 4 and infinite three-dimensional perovskite parts, even the content of infinity phase is more, and there is still a small amount of impurity phases such as lead iodide.

    [0096] It can be seen that the films prepared in Examples 1-3 are significantly better than the films prepared in Comparative Examples 1 and 2 in terms of crystallinity, grain size, especially the width distribution and purity of quantum wells.

    [0097] The foregoing description of the disclosed embodiments enables those skilled in the art to implement or use the present disclosure. Various modifications to these embodiments will be obvious to those skilled in the art, and the general principles defined herein can be implemented in other embodiments without departing from the spirit or scope of the present disclosure. Therefore, the present disclosure will not be limited to the embodiments shown in this document, but should conform to the widest scope consistent with the principles and novel features disclosed in this document.