D-A type chlorinated conjugated polymer as well as preparation method and application thereof
A conjugated polymer, D-A technology, applied in the field of solar cells, can solve problems such as cost and environmental pollution restrictions and popularization, and achieve the effects of low energy band gap, enhanced spectral absorption, and broadened spectral absorption.
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[0032] The preparation method of the solar cell device is not particularly limited, and the technical solution for the preparation of solar cells well known to those skilled in the art can be adopted. In the embodiment of the present invention, the preparation method of the solar cell device preferably includes the following steps:
[0033] S1: First, the glass with ITO sputtered on the surface is cleaned and treated with ultraviolet and ozone in order to obtain a clean ITO glass layer;
[0034] S2: Spin-coat ZnO and D-A conjugated polymer / PC sequentially on the ITO glass layer treated in step S1 71 BM, and then sequentially vapor-deposit MoO3 and Ag electrodes, and sequentially form ZnO electron transport layer, D-A conjugated polymer / PC on the ITO glass layer 71 BM active layer, MoO 3 The hole transport layer and the Ag electrode layer are prepared to obtain a solar cell device.
Embodiment 1
[0035] The compound of the structure shown in the formula II described in Example 1 is prepared by the following method:
[0036] Synthesis of S1, 4,7-dibromobenzo[c][1,2,5]thiadiazole: Add benzo[c][1,2,5]thiadiazole (3.12g, 22.8mmol) into a dry three-necked round-bottomed flask, then add hydrobromic acid (HBr) (60mL) to dissolve, and slowly add 46% liquid bromine (Br 2 ) (2.94mL, 57mmol), add Br 2 Afterwards, the reaction system was heated to 127° C. and refluxed for 12 hours. After the reaction was completed, it was cooled to room temperature, and then sodium bisulfite (NaHCO 3 ) aqueous solution to remove excess bromine, and use chloroform (CHCl 3 ) extraction, the organic layer was collected, and the organic layer was distilled under reduced pressure to obtain the crude product, and then the crude product was purified by silica gel column chromatography, and the mobile phase was dichloromethane to obtain 2.45g of the target product;
[0037] S2, 4,7-bis(4-hexylthiophen-...
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