2D expanded conjugated polymers with non-fullerene acceptors for efficient polymer solar cells

2018 ◽  
Vol 6 (7) ◽  
pp. 1753-1758 ◽  
Author(s):  
Shuguang Wen ◽  
Weichao Chen ◽  
Gongyue Huang ◽  
Wenfei Shen ◽  
Huizhou Liu ◽  
...  

2D expanded conjugated polymers show a power conversion efficiency of 8.03% in non-fullerene solar cell devices with a high JSC of over 17 mA cm−2.

2018 ◽  
Vol 42 (3) ◽  
pp. 1626-1633 ◽  
Author(s):  
M. L. Keshtov ◽  
S. A. Kuklin ◽  
A. R. Khokhlov ◽  
I. O. Konstantinov ◽  
N. V. Nekrasova ◽  
...  

The increase in the fluorine atoms in the copolymer improves the power conversion efficiency of the polymer solar cell.


2015 ◽  
Vol 3 (26) ◽  
pp. 13632-13636 ◽  
Author(s):  
Yuhang Liu ◽  
Joshua Yuk Lin Lai ◽  
Shangshang Chen ◽  
Yunke Li ◽  
Kui Jiang ◽  
...  

A series of tetraphenyl carbon-group (tetraphenylmethane, tetraphenylsilane and tetraphenylgermane) core based 3D-structure non-fullerene electron acceptors were synthesized and polymer solar cell performances were tested. A power conversion efficiency of up to 4.3% was achieved.


RSC Advances ◽  
2017 ◽  
Vol 7 (28) ◽  
pp. 17076-17084 ◽  
Author(s):  
Xiangzhi Li ◽  
Xiaoyuan Liu ◽  
Po Sun ◽  
Yaomiao Feng ◽  
Haiquan Shan ◽  
...  

Incorporation of a different number of fluorine atoms on the donor portion of naphthalene diimide (NDI) based donor–acceptor conjugated polymers significantly affected the solar cell's power conversion efficiency from 0.67% to 2.50%.


2019 ◽  
Vol 43 (14) ◽  
pp. 5325-5334 ◽  
Author(s):  
M. L. Keshtov ◽  
S. A. Kuklin ◽  
I. O. Konstantinov ◽  
I. E. Ostapov ◽  
E. E. Makhaeva ◽  
...  

The overall power conversion efficiency of the polymer solar cell based on P13 (DPP/BTQx ratio is 1/1) showed the highest value of 9.20% with a Voc of 0.86 V, Jsc of 15.74 mA cm−2, and FF of 0.68.


2016 ◽  
Vol 4 (21) ◽  
pp. 8097-8104 ◽  
Author(s):  
Yahui Liu ◽  
Wenchao Zhao ◽  
Yang Wu ◽  
Jicheng Zhang ◽  
Guangwu Li ◽  
...  

Two conjugated polymers (P1, P2) were designed and used as donor materials for polymer solar cells. The open-circuit voltage was significantly improved to 0.85 V. The synergistic effect of combined carboxylate and fluoro functional groups promoted the PCE to as high as 9.26%.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
S. Wageh ◽  
Mahfoudh Raïssi ◽  
Thomas Berthelot ◽  
Matthieu Laurent ◽  
Didier Rousseau ◽  
...  

AbstractPoly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) mixed with single-wall nanotubes (SWNTs) (10:1) and doped with (0.1 M) perchloric acid (HClO4) in a solution-processed film, working as an excellent thin transparent conducting film (TCF) in organic solar cells, was investigated. This new electrode structure can be an outstanding substitute for conventional indium tin oxide (ITO) for applications in flexible solar cells due to the potential of attaining high transparency with enhanced conductivity, good flexibility, and good durability via a low-cost process over a large area. In addition, solution-processed vanadium oxide (VOx) doped with a small amount of PEDOT-PSS(PH1000) can be applied as a hole transport layer (HTL) for achieving high efficiency and stability. From these viewpoints, we investigate the benefit of using printed SWNTs-PEDOT-PSS doped with HClO4 as a transparent conducting electrode in a flexible organic solar cell. Additionally, we applied a VOx-PEDOT-PSS thin film as a hole transporting layer and a blend of PTB7 (polythieno[3,4-b] thiophene/benzodithiophene): PC71BM (phenyl-C71-butyric acid methyl ester) as an active layer in devices. Zinc oxide (ZnO) nanoparticles were applied as an electron transport layer and Ag was used as the top electrode. The proposed solar cell structure showed an enhancement in short-circuit current, power conversion efficiency, and stability relative to a conventional cell based on ITO. This result suggests a great carrier injection throughout the interfacial layer, high conductivity and transparency, as well as firm adherence for the new electrode.


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