A kind of preparation method of nontoxic and stable perovskite
A perovskite, stable technology, applied in the direction of chemical instruments and methods, inorganic chemistry, tin compounds, etc., can solve the problems affecting the application of solar cells, disadvantages, etc., achieve huge potential application value, simplify the reaction process, avoid equipment requirements and Effect of Reactive Atmosphere Requirements
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[0035] The invention discloses a preparation method of non-toxic and stable perovskite,
[0036] The preparation route is as follows,
[0037]
[0038] Among them, A and B are any halogen atoms, m, n, l, x, y, z are any constants greater than or equal to 0, and M and N are not 0 at the same time, L and X are not 0 at the same time; x is 0~ Any constant between 6, including two constants of 0 and 6 here. In particular, when x is 0, the reaction is:
[0039] ,
[0040] or
[0041] ,
[0042] The preparation method comprises the following steps,
[0043] S1. Weighing the reaction raw materials, putting the reaction raw materials into an organic solvent, heating the reaction and stirring for 2-12 hours. The organic solvent is 1,4-butyrolactone (GBL), and a very pure target product can be obtained by using this organic solvent. The reaction temperature is 25-220°C, and in this embodiment, the preferred reaction temperature is 70°C.
[0044] S2. Add a cleaning solvent...
Embodiment 1
[0049] Example 1: Cs 2 SnI 6 Synthesis
[0050] Weigh 1.036g of CsI and 0.744g of SnI respectively 2 , 0.508g of I 2 , take 5 ml of organic solvent 1,4-butyrolactone (GBL) or N,N-dimethylformamide (DMF), and add them in sequence to a 10 ml reaction bottle containing magnetons to form a mixed solution. Put the mixed solution on a magnetic hot plate and stir the reaction at 70°C, stop the reaction after 10 hours, add absolute ethanol to the reaction bottle and let it stand for 3-5 minutes, then remove the upper part of the solution in the reaction bottle to obtain a black precipitate , and then use absolute ethanol to wash the precipitate 3-5 times. After cleaning, place the precipitate in an oven at 70°C for 5-8 hours to obtain the final product. attached figure 1 It is the XRD test characterization diagram of the product obtained when using GBL and DMF as the reaction solvent, and the dotted line in the figure is the simulated Cs 2 SnI 6 data. When GBL was used as the...
Embodiment 2
[0051] Example 2: Cs 2 SnBr 6 synthesis
[0052] Weigh 0.85g of CsBr and 1.11g of SnBr respectively 2 , Measure 5ml of the organic solvent 1,4-butyrolactone, and sequentially add it into a 10ml reaction bottle containing magnetons to form a mixed solution. Place the mixed solution on a magnetic hot plate and stir the reaction at 70°C, stop the reaction after 10 hours, add absolute ethanol to the reaction bottle and let it stand for 3-5 minutes, then remove the upper part of the solution in the reaction bottle to obtain a precipitate, Next, use absolute ethanol to wash the precipitate 3-5 times. After cleaning, place the precipitate in an oven at 70° C. for 5-8 hours to obtain the final product. attached image 3 It is the XRD test characterization diagram of the product, and the dotted line in the figure is the simulated Cs 2 SnBr 6 Data, product XRD diffraction peaks and simulated Cs 2 SnBr 6 Data peaks coincide. The above results show that when using CsBr and SnBr ...
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