New wide bandgap D-A polymer based on Benzothiadiazole-pyrrolo[3,4-b] dithieno[2,3-f:3’,2’-h]quinoxalindione and thiazole functionalized benzo[1,2-b:4,5-b’]dithiophene units for high performance ternary organic solar cells with over 16% efficiency

Author(s):  
Ganesh D Sharma ◽  
V. G. Alekseev ◽  
A Agrawal ◽  
I O Konstantinov ◽  
Mukhamed Lostambievich Keshtov ◽  
...  

We have designed a simple and new D-A copolymer P(PTQD-BDTTZ) denoted as P125 based on Benzothiadiazole-pyrrolo[3,4-b] dithieno[2,3-f:3’,2’-h]quinoxalindione donor unit and thiazole functionalized benzo[1,2-b:4,5-b’]dithiophene unit and its optical and electrochemical properties...

2019 ◽  
Vol 01 (01) ◽  
pp. 030-037 ◽  
Author(s):  
Jianyun Zhang ◽  
Wenrui Liu ◽  
Shengjie Xu ◽  
Xiaozhang Zhu

Recently, by elaborately designing nonfullerene acceptors and selecting suitable polymer donors great progresses have been made towards binary organic solar cells (OSCs) with power conversion efficiencies (PCEs) over 15%. Ternary organic photovoltaics by introducing a third component into the host binary system is recognized to be highly effective to elevate the performance through extending the light absorption, manipulating the recombination behavior of the carriers, and improving the morphology of the active layer. In this work, we synthesized a new electron-acceptor ZITI-4F matching it with the wide-bandgap polymer donor PBDB-T The PBDB-T:ZITI-4F-based OSC showed a high PCE of 12.33%. After introducing 40% of PC71BM as the third component, the ternary device achieved an improved PCE of 13.40% with simultaneously improved photovoltaic parameters. The higher performance of the ternary device can be attributed to the improved and more balanced charge mobility, reduced bimolecular recombination, and more favorable morphology. These results indicate that the cooperation of a fullerene-based acceptor and a nonfullerene acceptor to fabricate ternary OSCs is an effective approach to optimizing morphology and therefore to increase the performance of OSCs.


Nano Energy ◽  
2021 ◽  
pp. 106323
Author(s):  
Thavamani Gokulnath ◽  
Jungmin Choi ◽  
Ho-Yeol Park ◽  
Kyungmin Sung ◽  
Yeongju Do ◽  
...  

2019 ◽  
Vol 3 (3) ◽  
pp. 399-402 ◽  
Author(s):  
Yaxin Gao ◽  
Dan Li ◽  
Zuo Xiao ◽  
Xin Qian ◽  
Junliang Yang ◽  
...  

Dithieno[3,2-b:2′,3′-d]pyridin-5(4H)-one-based wide-bandgap copolymers gave high open-circuit voltages and decent power conversion efficiencies in nonfullerene organic solar cells.


2021 ◽  
pp. 129768
Author(s):  
Dou Luo ◽  
Xue Lai ◽  
Nan Zheng ◽  
Chenghao Duan ◽  
Zhaojin Wang ◽  
...  

2021 ◽  
Vol 60 (16) ◽  
pp. 8813-8817
Author(s):  
Shuting Pang ◽  
Zhiqiang Wang ◽  
Xiyue Yuan ◽  
Langheng Pan ◽  
Wanyuan Deng ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Zhenrong Jia ◽  
Shucheng Qin ◽  
Lei Meng ◽  
Qing Ma ◽  
Indunil Angunawela ◽  
...  

AbstractTandem organic solar cells are based on the device structure monolithically connecting two solar cells to broaden overall absorption spectrum and utilize the photon energy more efficiently. Herein, we demonstrate a simple strategy of inserting a double bond between the central core and end groups of the small molecule acceptor Y6 to extend its conjugation length and absorption range. As a result, a new narrow bandgap acceptor BTPV-4F was synthesized with an optical bandgap of 1.21 eV. The single-junction devices based on BTPV-4F as acceptor achieved a power conversion efficiency of over 13.4% with a high short-circuit current density of 28.9 mA cm−2. With adopting BTPV-4F as the rear cell acceptor material, the resulting tandem devices reached a high power conversion efficiency of over 16.4% with good photostability. The results indicate that BTPV-4F is an efficient infrared-absorbing narrow bandgap acceptor and has great potential to be applied into tandem organic solar cells.


2021 ◽  
Author(s):  
Lin Lin ◽  
Zeping Huang ◽  
Yuanqi Luo ◽  
Tingen Peng ◽  
Baitian He ◽  
...  

The synthesis and application as a cathode interlayer in organic photovoltaics of a fluorene derivative with pyridyl functional chains are presented.


2021 ◽  
Vol 13 (5) ◽  
pp. 6461-6469
Author(s):  
María Privado ◽  
Fernando G. Guijarro ◽  
Pilar de la Cruz ◽  
Rahul Singhal ◽  
Fernando Langa ◽  
...  

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