Dibenzo[b,def]chrysene Derivatives: Solution-Processable Small Molecules that Deliver High Power-Conversion Efficiencies in Bulk Heterojunction Solar Cells

2009 ◽  
Vol 21 (24) ◽  
pp. 5701-5703 ◽  
Author(s):  
Kevin N. Winzenberg ◽  
Peter Kemppinen ◽  
Giovanni Fanchini ◽  
Mark Bown ◽  
Gavin E. Collis ◽  
...  
RSC Advances ◽  
2016 ◽  
Vol 6 (64) ◽  
pp. 59218-59225 ◽  
Author(s):  
Huadong Huang ◽  
Liangang Xiao ◽  
Binglin Yang ◽  
Tianqi Lai ◽  
Lin Zhang ◽  
...  

Facile preparation of solution-processable small molecules with only two step reactions for bulk heterojunction solar cells, exhibiting a power conversion efficiency as high as 4.64%.


2016 ◽  
Vol 7 (25) ◽  
pp. 4160-4175 ◽  
Author(s):  
F. Caffy ◽  
N. Delbosc ◽  
P. Chávez ◽  
P. Lévêque ◽  
J. Faure-Vincent ◽  
...  

Dibenzosilole and quinoxaline based copolymers were synthesized and tested in bulk-heterojunction solar cells showing power conversion efficiencies up to 5.14%.


2010 ◽  
Vol 3 (10) ◽  
pp. 1427 ◽  
Author(s):  
Yaowen Li ◽  
Qing Guo ◽  
Zaifang Li ◽  
Jianing Pei ◽  
Wenjing Tian

2017 ◽  
Vol 5 (38) ◽  
pp. 9920-9928 ◽  
Author(s):  
Duško Popović ◽  
Ibrahim Ata ◽  
Johannes Krantz ◽  
Sebastian Lucas ◽  
Mika Lindén ◽  
...  

A series of A–D–A type co-oligomers used as donors in organic solar cells are presented. Devices prepared exclusively from non-halogenated solvents via doctor-blading gave power conversion efficiencies of up to 7%.


2016 ◽  
Vol 4 (17) ◽  
pp. 3715-3725 ◽  
Author(s):  
Christoph Wetzel ◽  
Amaresh Mishra ◽  
Elena Mena-Osteritz ◽  
Karsten Walzer ◽  
Martin Pfeiffer ◽  
...  

A new class of A–D–A molecular donor materials based on planar S,N-heterohexacenes is developed for vacuum-processed planar and bulk-heterojunction solar cells providing promising power conversion efficiencies up to 7.1%.


2021 ◽  
Vol 03 (02) ◽  
pp. 168-173
Author(s):  
Lukas Ahrens ◽  
Yvonne J. Hofstetter ◽  
Baris Celik ◽  
Julian F. Butscher ◽  
Frank Rominger ◽  
...  

Two covalently linked triisopropylsilyl-ethynylated phenazinothiadiazoles were prepared through condensation of a spirocyclic and a bicyclic tetraketone with a 5,6-diaminobenzothiadiazole. The spirobisindene- and the ethanoanthracene-based linkers render the electron acceptors amorphous in thin films. The optoelectronic properties of the non-conjugated dimers are indistinguishable from that of the crystalline monomer. Bulk heterojunction solar cells were prepared with power conversion efficiencies peaking at 1.6%. The choice of linker neither influenced optical and electrochemical properties nor device performance.


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