Design and synthesis of new low band gap organic semiconductors for photovoltaic applications

2014 ◽  
Author(s):  
M. G. Murali ◽  
Udaya Kumar Dalimba
2017 ◽  
Vol 60 (9) ◽  
pp. 819-828 ◽  
Author(s):  
Huan-Huan Gao ◽  
Yanna Sun ◽  
Xiangjian Wan ◽  
Bin Kan ◽  
Xin Ke ◽  
...  

2006 ◽  
Vol 39 (13) ◽  
pp. 4289-4297 ◽  
Author(s):  
Karin Van De Wetering ◽  
Cyril Brochon ◽  
Chheng Ngov ◽  
Georges Hadziioannou

RSC Advances ◽  
2016 ◽  
Vol 6 (18) ◽  
pp. 14893-14908 ◽  
Author(s):  
M. L. Keshtov ◽  
S. A. Kuklin ◽  
N. A. Radychev ◽  
A. Yu. Nikolaev ◽  
E. N. Koukaras ◽  
...  

Two D–A copolymers, F1 and F2, with fluorene and thiazole units were substituted, respectively, on a thiadiazoloquinoxaline (TDQ) unit to enhance the electron-accepting strength of TDQ.


2015 ◽  
Vol 53 (10) ◽  
pp. 1287-1295 ◽  
Author(s):  
Jonathan Zhaozhi Low ◽  
Wei Teng Neo ◽  
Qun Ye ◽  
Wen Jie Ong ◽  
Ivy Hoi Ka Wong ◽  
...  

RSC Advances ◽  
2018 ◽  
Vol 8 (53) ◽  
pp. 30468-30480 ◽  
Author(s):  
Savita Meena ◽  
Tauheed Mohammad ◽  
Viresh Dutta ◽  
Josemon Jacob

Newly designed N-substituted perylene diimide based acceptor copolymers have been characterized and tested for organic solar cells with P3HT in different weight ratios.


2018 ◽  
Vol 5 (5) ◽  
pp. 777-787 ◽  
Author(s):  
Abbasriyaludeen Abdul Raheem ◽  
Santhosh Kamaraj ◽  
Veeman Sannasi ◽  
Chandrasekar Praveen

Low band gap molecular semiconductors based on push–pull systems with appropriate HOMO–LUMO energy levels for organic photovoltaic applications were accomplished.


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.


2015 ◽  
Vol 23 ◽  
pp. 171-178 ◽  
Author(s):  
Olzhas A. Ibraikulov ◽  
Rony Bechara ◽  
Patricia Chavez ◽  
Ibrahim Bulut ◽  
Dias Tastanbekov ◽  
...  

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