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Non-fullerene acceptor material based on chiral alkane chain and preparation method thereof

A technology of non-fullerene acceptors and alkane chains, which is applied in the field of organic solar cell material preparation, can solve the problems of being unsuitable for indoor photovoltaic devices, low external quantum efficiency, and large voltage loss, achieving mass production and improving short circuit Current, effect of high short-circuit current

Inactive Publication Date: 2021-07-27
HKUST SHENZHEN RES INST
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Its disadvantages are that the band gap is too narrow or the performance is too low, so it is not suitable for indoor photovoltaic device applications.
Moreover, most of the indoor organic photovoltaic devices reported now also have problems such as excessive voltage loss or low external quantum efficiency caused by the mismatch between the absorption spectrum and the emission spectrum of common indoor light sources (NatEnergy, 2019, 4, 768–775; Joule, 2020, 4, 1486–1500)

Method used

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  • Non-fullerene acceptor material based on chiral alkane chain and preparation method thereof
  • Non-fullerene acceptor material based on chiral alkane chain and preparation method thereof
  • Non-fullerene acceptor material based on chiral alkane chain and preparation method thereof

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Embodiment 1

[0037] R as mentioned above 1 for Ar is R 3 for

[0038] EG is When , the preparation of the acceptor material is as follows:

[0039] (1) 4,7-dibromo-5,6-dinitrobenzothiadiazole and compound A obtain compound B through stille coupling reaction:

[0040]

[0041] Synthesis of Compound B: In a 250ml round bottom flask, weigh 4,7-dibromo-5,6-dinitrobenzothiadiazole (10mmol) and tributyl (6-undecylthieno[3 ,2-b] Thiophen-2-yl) stannane (25mmol) was dissolved in 100ml of tetrahydrofuran, and bistriphenylphosphinepalladium dichloride (0.2mmol) was added to the system under the protection of argon. The mixture was refluxed at 80°C for 20 hours. Cool to room temperature, spin dry THF, extract with dichloromethane, and spin dry the solvent to obtain a crude product, which is separated and purified by silica gel column chromatography to obtain a rose-red solid (90% yield), which is compound B;

[0042] (2) Compound B, triphenylphosphine and o-dichlorobenzene undergo con...

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Abstract

The invention relates to a non-fullerene acceptor material based on a chiral alkane chain and a preparation method of the non-fullerene acceptor material. According to the invention, three optically pure non-fullerene small molecule acceptor materials (R, R)-Y6, (S, S)-Y6 and R, S) (-Y6 are synthesized, wherein the small molecule acceptors comprise fused ring benzothiadiazole central cores and electron withdrawing end groups, and small molecules are optically pure materials; when the synthesized optically pure acceptor material is applied to devices, the properties of the devices are different, and the light conversion efficiency of (S, S)-Y6 in the system is obviously higher than that of Y6 molecules of other two configurations and mixtures of the Y6 molecules; and the reported photoelectric conversion efficiency of Y6 molecules is generally about 16%, and under the same condition, when the S-configuration chiral alkane chain is applied to Y6, the efficiency can reach 16.5%.

Description

technical field [0001] The invention belongs to the technical field of preparation of organic solar cell materials, in particular to a non-fullerene acceptor material based on a chiral alkane chain and a preparation method thereof. Background technique [0002] With the increasingly serious energy problems, it is imminent to develop new energy sources, and solar energy has great development prospects because of its clean, non-polluting, inexhaustible and inexhaustible advantages. How to make better use of solar energy is a key solution to the energy crisis. Organic solar cells (OSCs) are a photovoltaic technology with great potential for commercialization due to their advantages of solution processing, roll-to-roll fabrication, light weight, good flexibility, and translucency. After more than two decades of development, the efficiency of single-layer heterojunction organic solar cells has reached 18%, which is attributed to the rapid development of new organic small molecul...

Claims

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Application Information

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IPC IPC(8): C07D513/22H01L51/42H01L51/46
CPCC07D513/22H10K85/657H10K30/00Y02E10/549
Inventor 殷俊力颜河
Owner HKUST SHENZHEN RES INST
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