Quasi-solid nanometer crystal solar battery and preparing method thereof
A technology of solar cells and nanocrystals, applied in the field of nanomaterials, can solve problems such as the inability to know the performance of electrolytes, the performance of solar cells, the influence of phase separation on the stability of solar cells, and the long-term stability of solar cells, etc., to achieve excellent coordination ability, good Solubility in organic solvents, the effect of solving phase separation problems
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Embodiment 1
[0046] Embodiment 1: Synthesis of 3-methyl-1 phenyl-4-(octadecanoyl)pyrazolone-5 (PMOP)
[0047] Add 7.0g (0.04mol) of 1-phenyl-3-methyl-pyrazolone-5 and 100ml of anhydrous 1,4-dioxane into a dry three-necked flask, heat and stir until dissolved, and add 9g of hydrogen The powder of calcium oxide and 1 g of barium hydroxide was cooled to room temperature, 15 ml (0.04 mol) of octadecanoyl chloride was added dropwise, and the mixture was stirred and refluxed for 2 hours. The reaction mixture was poured into 300ml of 0.5mol / L dilute hydrochloric acid, filtered with suction, and recrystallized twice with ethanol-water mixed solvent to obtain light pink needle-like crystals. Yield 65%. 1 H-NMR (400Hz, CDCl 3 )(δppm): 7.26-7.84 (5H, m, ArH), 2.73 (2H, t, CH 2 ), 2.48 (3H, s, CH 3 ), 1.74 (2H, m, CH 2 ), 1.24-1.43 (28H, m, (CH 2 ) 14 ), 0.88 (3H, t, CH 3 ). Its H 1 The nuclear magnetic resonance spectrum is shown in Figure 2.
Embodiment 2
[0048] Example 2: Synthesis of 3-methyl-1-phenyl-4-decanoylpyrazolone-5 (PMDP)
[0049] Add 0.01mol) 1-phenyl-3-methyl-pyrazolone-5 and 100ml anhydrous 1,4-dioxane in a dry there-necked flask, heat and stir until dissolved, add 9g calcium hydroxide and 1 g of barium hydroxide powder was cooled to room temperature, and 0.01 mol) of decanoyl chloride was added dropwise, and stirred and refluxed for 2 hours. The reaction mixture was poured into 100ml of 0.5mol / L dilute hydrochloric acid, filtered with suction, and recrystallized twice with ethanol-water mixed solvent to obtain white needle-like crystals. Yield 72%. 1 H-NMR (400Hz, CDCl 3 )(δppm): 7.29-7.85 (5H, m, ArH), 2.74 (2H, t, CHH 2 , 2.48 (3H, s, CH 3 ), 1.76 (2H, m, CH 2 ), 1.26-1.44 (12H, m, (CH 2 )6), 0.88 (3H, t, CH 3 ).
Embodiment 3
[0050] Embodiment 3: the synthesis of 3-methyl-4-octadecanoyl oxazolinone (OxOP)
[0051] Following the same method as in Example 1, but replacing 1-phenyl-3-methyl-pyrazolinone-5 with 3-methylazolinone-5, to prepare 3-methyl-4-octadecane Acyloxazolones (OxOP). The crude product of this product can be purified by recrystallization from ethanol. The melting point is 78-80°C.
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