A spiroindenoid hole-transporting small molecule and its application in perovskite solar cells
A technology for solar cells and hole transport, which is applied in circuits, photovoltaic power generation, electrical components, etc., can solve problems that limit large-scale applications, and achieve the effects of easy synthesis and purification, mild reaction conditions, and increased solubility
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Embodiment 1
[0057] The synthesis of compound A was achieved by two schemes:
[0058] Under argon, 1.14 g (1 mmol) of compound 6, 1.1 g (4.8 mmol) of 4,4'-dimethoxydiphenylamine, 0.036 g (0.039 mmol) of Pd 2 (dba) 3 , 0.032 g (0.158 mmol) of tri-tert-butylphosphine, 0.77 g (8 mmol) of sodium tert-butoxide and 20 mL of toluene were mixed and stirred, and the temperature was raised to 110° C. to react for 12 h. After the reaction was completed, toluene was evaporated to dryness, ethyl acetate and water were added, and after extraction, liquid separation, and drying over anhydrous sodium sulfate, neutral alumina was used, and a mixed solvent of n-hexane and ethyl acetate was used as the eluent, and the column was separated to obtain 1.00 g of yellow solid (yield 58%). LC-MS: C 115 H 102 N 6 O 10 , Calculated value: 1726.77, Measured value: [M] + = 1726.77. 1 H NMR(400MHz, DMSO)δ7.78(d,J=8.3Hz,4H),7.73(d,J=1.6Hz,4H),7.63(d,J=8.4Hz,4H),7.36(d,J =8.8Hz,4H),7.30(s,2H),7.11(dd,J=8.9,1.6Hz...
Embodiment 2
[0060] Synthesis of Example 2 Compound B:
[0061] Under argon, 1.14 g (1 mmol) of compound 6, 0.965 g (4.4 mmol) of N-phenyl-1-naphthylamine, 0.036 g (0.039 mmol) of Pd 2 (dba) 3 , 0.032 g (0.158 mmol) of tri-tert-butylphosphine, 0.77 g (8 mmol) of sodium tert-butoxide and 20 mL of toluene were mixed and stirred, and the temperature was raised to 110° C. to react for 12 h. After the reaction, toluene was evaporated to dryness, dichloromethane and water were added, and after extraction, liquid separation, and drying over anhydrous sodium sulfate, neutral alumina was used, and a mixed solvent of n-hexane and ethyl acetate was used as the eluent, and the column was separated. 0.98 g of yellow solid was obtained (yield 58%). LC-MS: C 123 H 94 N 6 O 2 , Calculated value: 1686.74, Measured value: [M] + = 1686.74. 1 H NMR (400MHz, DMSO) δ 8.18 (s, 4H), 7.94–7.78 (m, 14H), 7.69 (d, J=7.8Hz, 4H), 7.55 (t, J=9.7Hz, 8H), 7.46 –7.29(m, 26H), 7.13(d, J=8.0Hz, 6H), 7.06(t, J=7.3Hz...
Embodiment 3
[0064] Application of hole transport materials containing spiroindene structures in perovskite solar cell devices.
[0065] A perovskite solar cell device such as figure 1 shown, the layers are glass substrate 1, FTO cathode 2, dense TiO 2 Layer 3, perovskite layer 4, hole transport layer 5 and Au electrode 6, the hole transport layer 5 is prepared from the spiro ring hole transport small molecule material (eg compound A) as described above.
[0066] The preparation process of the perovskite solar cell device:
[0067] (1) Cleaning: The FTO glass substrate was ultrasonically cleaned with isopropanol, ethanol, and secondary water in turn to remove contaminants on the surface of the substrate, and the cleaned FTO glass substrate was blown dry with nitrogen. Treat with UV-ozone for 20min before use to further remove organic matter on the surface;
[0068] (2) Dense TiO 2 Layer preparation: prepare a 0.2 mol / L titanium tetrachloride aqueous solution, soak a clean FTO glass sub...
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