scholarly journals Carboxylate substituted pyrazine: A simple and low-cost building block for novel wide bandgap polymer donor enables 15.3% efficiency in organic solar cells

Nano Energy ◽  
2021 ◽  
Vol 82 ◽  
pp. 105679
Author(s):  
Jingnan Wu ◽  
Qunping Fan ◽  
Minghai Xiong ◽  
Qiutang Wang ◽  
Kai Chen ◽  
...  
2020 ◽  
Vol 8 (35) ◽  
pp. 12265-12271
Author(s):  
Jong-Woon Ha ◽  
Hee Su Kim ◽  
Chang Eun Song ◽  
Hea Jung Park ◽  
Do-Hoon Hwang

A new heterocyclic aromatic structure, thieno[3,2-c]quinolin-4(5H)-one (TQO), was designed and synthesized as an electron-accepting building block for donor–acceptor-type copolymers.


ChemPhysChem ◽  
2019 ◽  
Vol 20 (20) ◽  
pp. 2668-2673 ◽  
Author(s):  
Ruihao Xie ◽  
Lei Ying ◽  
Kang An ◽  
Wenkai Zhong ◽  
Qingwu Yin ◽  
...  

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.


Polymer ◽  
2020 ◽  
Vol 188 ◽  
pp. 122131 ◽  
Author(s):  
Chang Eun Song ◽  
Hyobin Ham ◽  
Jiwoong Noh ◽  
Sang Kyu Lee ◽  
In-Nam Kang

2021 ◽  
Vol 405 ◽  
pp. 127033
Author(s):  
Jiangsheng Yu ◽  
Xin Liu ◽  
Hongtao Wang ◽  
Po-Chen Lin ◽  
Chu-Chen Chueh ◽  
...  

2015 ◽  
Vol 27 (18) ◽  
pp. 2938-2944 ◽  
Author(s):  
Lijun Huo ◽  
Tao Liu ◽  
Xiaobo Sun ◽  
Yunhao Cai ◽  
Alan J. Heeger ◽  
...  

2019 ◽  
Vol 39 (7) ◽  
pp. 636-641 ◽  
Author(s):  
Ismail Borazan ◽  
Yasin Altin ◽  
Ali Demir ◽  
Ayse Celik Bedeloglu

Abstract Polymer-based organic solar cells are of great interest as they can be produced with low-cost techniques and also have many interesting features such as flexibility, graded transparency, easy integration, and lightness. However, conventional wide bandgap polymers used for the light-absorbing layer significantly affect the power conversion efficiency of organic solar cells because they collect sunlight in a given spectrum range and due to their limited stability. Therefore, in this study, polymers with different bandgaps were used, which could allow for the production of more stable and efficient organic solar cells: P3HT as the wide bandgap polymer, and PTB7 and PCDTBT as low bandgap polymers. These polymers with different bandgaps were combined with PCBM to obtain increased efficiency and optimum photoactive layer in the organic solar cell. The obtained devices were characterized by measuring optical, photoelectrical, and morphological properties. Solar cells using the PTB7 and PCDTBT polymers had more rough surfaces than the reference cell using P3HT. The use of low-bandgap polymers improved Isc significantly, and when combined with P3HT, a higher Voc was obtained.


2019 ◽  
Vol 7 (10) ◽  
pp. 5234-5238 ◽  
Author(s):  
Nai-Yu Chen ◽  
Qihui Yue ◽  
Wenrui Liu ◽  
Hao-Li Zhang ◽  
Xiaozhang Zhu

A wide-bandgap polymer donor based on benzo[1,2-d:4,5-d′]bisthiazole is designed and synthesized delivering a PCE of 11.08% with a low energy loss of 0.50 eV.


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