Low-band gap copolymers based on diketopyrrolopyrrole and dibenzosilole and their application in organic photovoltaics

2017 ◽  
Vol 146 ◽  
pp. 73-81 ◽  
Author(s):  
Yeon Hee Ha ◽  
Jisu Hong ◽  
Tae Kyu An ◽  
Hui-Jun Yun ◽  
Kyunghun Kim ◽  
...  
RSC Advances ◽  
2015 ◽  
Vol 5 (81) ◽  
pp. 66005-66012 ◽  
Author(s):  
Mohamed Shaker ◽  
Jong-Hoon Lee ◽  
Cuc Kim Trinh ◽  
Wonbin Kim ◽  
Kwanghee Lee ◽  
...  

Synthesis of promising new composition low band gap small molecules based on the push–pull (donor–acceptor) system, which displayed power conversion efficiency of up to 3.24%.


2013 ◽  
Vol 103 (17) ◽  
pp. 173901 ◽  
Author(s):  
Kouhei Yonezawa ◽  
Hayato Kamioka ◽  
Takeshi Yasuda ◽  
Liyuan Han ◽  
Yutaka Moritomo

2012 ◽  
Vol 48 (55) ◽  
pp. 6933 ◽  
Author(s):  
Jae Woong Jung ◽  
Jea Woong Jo ◽  
Feng Liu ◽  
Thomas P. Russell ◽  
Won Ho Jo

RSC Advances ◽  
2014 ◽  
Vol 4 (85) ◽  
pp. 44902-44910 ◽  
Author(s):  
M. G. Murali ◽  
Arun D. Rao ◽  
Praveen C. Ramamurthy

Novel low band gap conjugated polymers (PBDTTBIandPBDTBBT) are designed and synthesized for polymer solar cell applications.


ACS Nano ◽  
2012 ◽  
Vol 6 (6) ◽  
pp. 5539-5548 ◽  
Author(s):  
Silvio Osella ◽  
Akimitsu Narita ◽  
Matthias Georg Schwab ◽  
Yenny Hernandez ◽  
Xinliang Feng ◽  
...  

Green ◽  
2011 ◽  
Vol 1 (1) ◽  
Author(s):  
Eva Bundgaard ◽  
Ole Hagemann ◽  
Mikkel Jørgensen ◽  
Frederik C. Krebs

AbstractIn this paper we present the design and synthesis of 25 new low band gap polymers. The polymers were characterized by UV-vis spectroscopy which showed optical band gaps of 2.0–0.9 eV. The polymers which were soluble enough were applied in organic photovoltaics, both small area devices with a spin coated active layer and in large area modules where all layers including the active layer were either roll-to-roll coated or printed. These experiments showed that the design of polymers compatible with roll-toroll coating is not straightforward and that there are various issues such as donor/acceptor fitting within the polymer, side chains to ensure solubility and HOMO/LUMO level alignment with the acceptor (e.g. [60]PCBM) to take into consideration.


2012 ◽  
Vol 116 (17) ◽  
pp. 9838-9844 ◽  
Author(s):  
Giulia Grancini ◽  
Nicola Martino ◽  
Maria Rosa Antognazza ◽  
Michele Celebrano ◽  
Hans-Joachim Egelhaaf ◽  
...  

2013 ◽  
Vol 51 (21) ◽  
pp. 4550-4557 ◽  
Author(s):  
Ching-Chih Chang ◽  
Chih-Ping Chen ◽  
Ho-Hsiu Chou ◽  
Chuang-Yi Liao ◽  
Shu-Hua Chan ◽  
...  

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