A high-efficiency organic solar cell based on fluorinated electron donor and fluorinated electron acceptor

An organic solar cell and electron donor technology, which is applied in the field of solar cells, can solve the problems of the change of the morphology of the active layer, the drop of the open circuit voltage of the battery, and the small electron mobility, and achieves the enhancement of charge transfer, large short-circuit current density, and electron mobility. The effect of increased mobility

Active Publication Date: 2019-07-02
广州追光科技有限公司
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The above-mentioned fluorinated non-fullerene electron acceptors all have an aromatic condensed ring central unit, which is difficult to synthesize and high in cost, which is not conducive to the popularization and application of organic solar cells.
For this reason, Chinese patent 201710409496.1 discloses a non-fullerene electron acceptor DFPCIC with non-fused ring difluorobenzene as the central unit. The synthesis is simple, but its electron-withdrawing terminal group is unfluorinated cyanoindanone , the ICT effect is not strong enough, the absorption band edge is only 781nm, and the electron mobility is also small, 2.6×10 -5 cm 2 V - 1 the s -1
Therefore, the organic solar cell with DFPCIC as the electron acceptor has a PCE of 10.14%, and a short-circuit current density of only 15.66mA / cm 2 , to be further improved
[0005] In addition, the fluorination will reduce the energy level of the non-fullerene electron acceptor. If the energy level of the electron donor blended with it is not adjusted accordingly, it will inevitably cause a decrease in the open circuit voltage of the battery; there is another consideration The problem is that the fluorination strengthens the intermolecular interactions of the non-fullerene electron acceptors, which inevitably leads to a change in the morphology of the active layer, which has an important impact on the fill factor of the battery.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • A high-efficiency organic solar cell based on fluorinated electron donor and fluorinated electron acceptor
  • A high-efficiency organic solar cell based on fluorinated electron donor and fluorinated electron acceptor
  • A high-efficiency organic solar cell based on fluorinated electron donor and fluorinated electron acceptor

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0018] HF-PCIC is prepared by a simple Knoevenagel reaction using DF-PC-CHO as a raw material. The specific synthetic route is as follows:

[0019]

[0020] Among them, DF-PC-CHO is synthesized according to the method disclosed in Chinese patent 201710409496.1, and the specific synthesis steps of HF-PCIC are:

[0021] Add 0.3g of raw material DF-PC-CHO, 0.35g of fluorocyanindanone (IC-2F) and 50mL of dried chloroform into a two-necked round-bottomed flask, freeze the resulting mixed solution with liquid nitrogen, and then vacuumize it three times Nitrogen filled cycle. After thawing, 0.6 mL of pyridine was added under nitrogen atmosphere, and the resulting mixture was heated to reflux at 65°C for 12 hours. After the reaction was completed, the solvent was removed by rotary evaporation, and the crude product obtained was purified with a silica gel column using a n-hexane / dichloromethane mixture (1:3) as the eluent to obtain 0.27g of the final product HF-PCIC (dark brown sol...

Embodiment 2

[0024] The transparent conductive glass with strip-shaped ITO (cathode) etched on the surface is cleaned with cleaning agent, deionized water, acetone and isopropanol by ultrasonic oscillation, dried, and then treated with ultraviolet ozone for 15 minutes; then on the surface of the conductive glass A layer of ZnO was spin-coated at 3500 rpm for 60 seconds, and then annealed at 170° C. for 20 minutes. Then the sheet is transferred to the glove box, and the weight ratio of PBDB-TF:HF-PCIC (PBDB-TF can be prepared according to the document Advanced Materials, 2015, 27, 4655) is 1:1, and the total concentration is 20 mg / mL of chlorobenzene The mixed solution was spin-coated at a speed of 2000 rpm for 60 seconds to obtain an active layer with a thickness of 100 nm. Finally, a layer of MoO with a thickness of 10 nm was evaporated with an evaporation apparatus. 3 interface layer and a 100nm thick Ag electrode (anode), resulting in an effective area of ​​6mm 2 organic solar cells. ...

Embodiment 3

[0027]The transparent conductive glass with strip-shaped ITO (cathode) etched on the surface is cleaned with cleaning agent, deionized water, acetone and isopropanol by ultrasonic oscillation, dried, and then treated with ultraviolet ozone for 15 minutes; A layer of ZnO was spin-coated at 3500 rpm for 60 seconds, and then annealed at 170° C. for 20 minutes. Then the sheet was transferred to the glove box, and the chlorobenzene mixture with a weight ratio of PBDB-TF:HF-PCIC of 1:1.2 and a total concentration of 20mg / mL was spin-coated for 60 seconds at a speed of 2000rpm to obtain a layer of 100nm thick active layer. Finally, a layer of MoO with a thickness of 10 nm was evaporated with an evaporation apparatus. 3 interface layer and a 100nm thick Ag electrode (anode), resulting in an effective area of ​​6mm 2 organic solar cells.

[0028] When the light intensity is 100mW / cm 2 The current-voltage curve of the device is tested under the simulated sunlight of AM1.5, and the o...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention discloses a high-efficiency organic solar cell based on a fluorinated electron donor and a fluorinated electron acceptor, which comprises a substrate, a cathode, a cathode modification layer, an active layer, an anode modification layer and an anode, wherein the active layer is a fluorinated Blend film of electron donor PBDB‑TF and fluorinated electron acceptor HF‑PCIC. Utilize the widened absorption range and high electron mobility of HF-PCIC, and select the fluorinated electron donor PBDB-TF with good energy level matching and compatibility with HF-PCIC, the organic solar cell prepared by the present invention maintains high At the same time of open circuit voltage and fill factor, short circuit current density increased to 17.81mA / cm 2 , the highest power conversion efficiency (PCE) is 11.49%, which is significantly better than organic solar cells (PCE=10.14%) using unfluorinated electron donors and unfluorinated electron acceptors. In addition, HF‑PCIC is easy to synthesize, which is beneficial to reduce the cost of organic solar cells.

Description

technical field [0001] The invention relates to a solar cell, in particular to a high-efficiency organic solar cell based on a fluorinated electron donor and a fluorinated electron acceptor. Background technique [0002] In recent years, organic solar cells based on non-fullerene electron acceptors have made important progress, and the power conversion efficiency (PCE) of the cells has exceeded 13% (Journal of the American Chemical Society, 2017, 139, 7148), which is higher than that of the same industry. Efficiency values ​​for type fullerene cells. In order to further improve the efficiency of non-fullerene batteries, the light absorption range of non-fullerene electron acceptors should be extended to the near-infrared region, and the electron mobility should also be improved, so that the batteries can obtain greater short-circuit current density. [0003] Fluorinating the electron-withdrawing terminal groups of non-fullerene electron acceptors is an effective method to i...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Patents(China)
IPC IPC(8): H01L51/42H01L51/46
CPCH10K85/00H10K85/6576H10K30/00Y02E10/549
Inventor 施敏敏李水兴占玲玲陈红征
Owner 广州追光科技有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products