Alpha-FAPbI3 powder, preparation method thereof and perovskite solar cell
A solar cell and perovskite technology, which is applied in semiconductor/solid-state device manufacturing, circuits, photovoltaic power generation, etc., can solve problems such as methods to be improved, unfavorable for amplification, and long precipitation time, so as to solve the problem of irreproducible photovoltaic performance, Conducive to large-scale production and application, the effect of reducing production costs
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[0033] Preparation of α-FAPbI according to an embodiment of the present invention 3 The powder method obtains a mixed solution by mixing lead iodide, formamidine iodide and a solvent, wherein lead iodide and formamidine iodide can be synthesized in a laboratory, avoiding the use of high-purity reaction raw materials, thereby reducing costs, After normal temperature anti-solvent precipitation and solid-liquid separation, the FAPbI 3 Crystals are precipitated from the solution and a filter cake is obtained, thereby increasing the yield. Finally, the filter cake is heated at a temperature range of 110-150°C to prepare α-FAPbI 3 powder. Thus, adopt the preparation α-FAPbI of the present application 3 The powder method has the following advantages: (1) avoids the use of high-purity reaction raw materials, thereby reducing costs; (2) adopts antisolvent to separate out FAPbI at room temperature 3 Crystal, mild reaction conditions; (3) avoiding the use of a large amount of toxic so...
Embodiment 1
[0041] (1) Weigh 2.11g of iodoformamidine synthesized in the laboratory and 5.67g of lead iodide synthesized in the laboratory, then add 10mL of γ-butyrolactone in a 100mL single-necked flask to prepare 1.23mol / L of FAPbI 3 Precursor solution, place the flask in an ultrasonic cleaner and sonicate until the raw materials are completely dissolved and the solution turns into a bright yellow clear liquid;
[0042] (2) Put the rotor in the flask, stir vigorously on the magnetic stirrer, and slowly add 30mL of ethyl acetate to the flask, observe the formation of yellow powder precipitation, then filter the above solution to obtain yellow FAPbI 3 filter cake;
[0043] (3) Transfer the filter cake to an evaporating dish and put it on a heating plate for drying. When the temperature of the heating plate is 90°C, dry bright yellow δ-FAPbI can be obtained 3 Powder, dried at 150°C for a period of time to obtain dry bright black α-FAPbI 3 powder;
[0044] (4) Treatment of α-FAPbI in an ...
Embodiment 2
[0046] (1) Weigh 2.58g of iodoformamidine synthesized in the laboratory and 6.92g of lead iodide synthesized in the laboratory, then add 10mL of 2-methoxyethanol to a 100mL single-necked flask to prepare 1.5mol / L of FAPbI 3 Precursor solution, place the flask in an ultrasonic cleaner and sonicate until the raw materials are completely dissolved and the solution turns into a bright yellow clear liquid;
[0047] (2) Put the rotor in the flask, stir vigorously on a magnetic stirrer, and slowly add 50mL of ether to the flask, observe the formation of yellow powder precipitation, then filter the above solution to obtain yellow FAPbI 3 filter cake;
[0048] (3) Transfer the filter cake to an evaporating dish and put it on a heating plate for drying. When the temperature of the heating plate is 85° C., dry bright yellow δ-FAPbI can be obtained 3 Powder, dried at 150°C for a period of time to obtain dry bright black α-FAPbI 3 powder;
[0049] (4) Contains NH at 100°C 4 Treatment o...
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