Optimization of Solubility, Film Morphology and Photodetector Performance by Molecular Side-Chain Engineering of Low-Bandgap Thienothiadiazole-Based Polymers

2014 ◽  
Vol 24 (48) ◽  
pp. 7605-7612 ◽  
Author(s):  
Ji Qi ◽  
Xiaokang Zhou ◽  
Dezhi Yang ◽  
Wenqiang Qiao ◽  
Dongge Ma ◽  
...  
2015 ◽  
Vol 3 (29) ◽  
pp. 7669-7676 ◽  
Author(s):  
Ying Sun ◽  
Chao Zhang ◽  
Qizan Huang ◽  
Bin Dai ◽  
Baoping Lin ◽  
...  

A naphthalene group was incorporated into the polymer side chain to help the active layer spontaneously form good film morphology.


ChemSusChem ◽  
2016 ◽  
Vol 9 (13) ◽  
pp. 1623-1633 ◽  
Author(s):  
Ning-Jiu Zhao ◽  
Mao-Jie Zhang ◽  
Ran Liang ◽  
Li-Min Fu ◽  
Wei Zhang ◽  
...  
Keyword(s):  

2020 ◽  
Vol 8 (42) ◽  
pp. 22335-22345
Author(s):  
Baofeng Zhao ◽  
Weiping Wang ◽  
Yuan Xie ◽  
Heng Zhao ◽  
Liuchang Wang ◽  
...  

Alkoxy-phenyl-modified twisted NFAs with optimized film morphology achieve enhanced performances in polymer solar cells.


2017 ◽  
Vol 8 (13) ◽  
pp. 2055-2062 ◽  
Author(s):  
Liuyong Hu ◽  
Wenqiang Qiao ◽  
Xiaokang Zhou ◽  
Jinfeng Han ◽  
Xiaoqin Zhang ◽  
...  

Enhancing the performance of polymer photodetectors by finely tuning the side chains of low-bandgap polymers.


2011 ◽  
Vol 95 (10) ◽  
pp. 2795-2804 ◽  
Author(s):  
Jung Feng Lee ◽  
Steve Lien Chung Hsu ◽  
Po I. Lee ◽  
Hung Yi Chuang ◽  
Ming Lun Yang ◽  
...  
Keyword(s):  

2013 ◽  
Vol 139 (12) ◽  
pp. 124904 ◽  
Author(s):  
Ming-Ming Huo ◽  
Ran Liang ◽  
Ya-Dong Xing ◽  
Rong Hu ◽  
Ning-Jiu Zhao ◽  
...  

2019 ◽  
Vol 7 (19) ◽  
pp. 5739-5747 ◽  
Author(s):  
Lei Lv ◽  
Jinde Yu ◽  
Xinyu Sui ◽  
Jianfei Wu ◽  
Xiaohan Dong ◽  
...  

Upon incorporating S⋯O noncovalent conformational locks and side chain engineering, the optical absorption and blend film morphology of molecular acceptors are effectively tuned, resulting in an enhanced photocurrent and thus a higher responsivity (from 70.5 mA W−1 to 291.3 mA W−1) for P3HT-based OPDs.


Polymers ◽  
2019 ◽  
Vol 11 (1) ◽  
pp. 55 ◽  
Author(s):  
Jinfeng Huang ◽  
Zhenkun Lin ◽  
Wenhuai Feng ◽  
Wen Wang

A series of bithiophene (2T)-based D-A1-D-A2 terpolymers with different A2 moieties were prepared via direct arylation reaction. In these terpolymers, pyrrolo[3,4-c]pyrrole-1,4-dione (DPP) was selected as the first electron-accepting (A1) moiety, 2,1,3-benzothiadiazole (BT) or fluorinated benzothiadiazole (FBT) or octyl-thieno[3,4-c]pyrrole-4,6-dione (TPD) or 2,1,3-benzoselendiazole (SeT) was selected as the second electron-accepting (A2) moiety, while bithiophene with hexyl side chain was used as the electron-donating moiety. The UV-vis absorption, electrochemical properties, blend film morphology, and photovoltaic properties were studied to explore the effects of the A2 moiety. It is shown that these terpolymer films exhibit broad absorption (350–1000 nm), full width at half-maximum of more than 265 nm and ordered molecular packing. Varying the A2 moiety could affect the energy levels and blend film morphology leading to different polymer solar cell (PSC) performances of these (2T)-based D-A1-D-A2 terpolymers. As a result, the highest Jsc of 10.70 mA/cm2 is achieved for Polymer 1 (P1) with BT as A2 moiety, while the higher highest occupied molecular orbital (HOMO) level limits the open circuit voltage (Voc) and leads to a power conversion efficiency (PCE) of 3.46%.


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