scholarly journals Fullerene derivative induced morphology of bulk heterojunction blends: PIPCP:PC61BM

RSC Advances ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 4106-4112 ◽  
Author(s):  
Tzu-Yen Huang ◽  
Hongping Yan ◽  
Maged Abdelsamie ◽  
Victoria Savikhin ◽  
Sebastian A. Schneider ◽  
...  

The performance of organic solar cells depends on the morphology in bulk heterojunctions, including the polymer degree of crystallinity and the amount of each phase: aggregated donor, aggregated acceptor and molecularly mixed donor : acceptor phase.

2006 ◽  
Vol 974 ◽  
Author(s):  
Date J. D. Moet ◽  
Lenneke H. Slooff ◽  
Jan M. Kroon ◽  
Svetlana S. Chevtchenko ◽  
Joachim Loos ◽  
...  

ABSTRACTThis paper discusses the characterization and optimization of organic solar cells based on a bulk heterojunction consisting of an alternating copolymer, containing a fluorene and a benzathiadiazole unit with two neighboring thiophene rings, and a fullerene derivative (PCBM). The resulting power conversion efficiency amounts 3.9±0.2 % (AM1.5, 100 mW/cm2) and these polymer solar cells are therefore considered auspicious for further research.


2020 ◽  
Vol 181 ◽  
pp. 108523 ◽  
Author(s):  
Dmitry O. Balakirev ◽  
Yuriy N. Luponosov ◽  
Artur L. Mannanov ◽  
Petr S. Savchenko ◽  
Yury Minenkov ◽  
...  

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Ruimin Zhou ◽  
Zhaoyan Jiang ◽  
Chen Yang ◽  
Jianwei Yu ◽  
Jirui Feng ◽  
...  

AbstractThe high efficiency all-small-molecule organic solar cells (OSCs) normally require optimized morphology in their bulk heterojunction active layers. Herein, a small-molecule donor is designed and synthesized, and single-crystal structural analyses reveal its explicit molecular planarity and compact intermolecular packing. A promising narrow bandgap small-molecule with absorption edge of more than 930 nm along with our home-designed small molecule is selected as electron acceptors. To the best of our knowledge, the binary all-small-molecule OSCs achieve the highest efficiency of 14.34% by optimizing their hierarchical morphologies, in which the donor or acceptor rich domains with size up to ca. 70 nm, and the donor crystals of tens of nanometers, together with the donor-acceptor blending, are proved coexisting in the hierarchical large domain. All-small-molecule photovoltaic system shows its promising for high performance OSCs, and our study is likely to lead to insights in relations between bulk heterojunction structure and photovoltaic performance.


2017 ◽  
Vol 5 (44) ◽  
pp. 23067-23077 ◽  
Author(s):  
Keisuke Ogumi ◽  
Takafumi Nakagawa ◽  
Hiroshi Okada ◽  
Ryohei Sakai ◽  
Huan Wang ◽  
...  

Acceptor–donor–acceptor conjugated magnesium porphyrins showed a power conversion efficiency of 5.73%, high open-circuit voltage of 0.79 V, or an extended incident photon-to-current conversion efficiency spectrum to 1100 nm, depending on the substituents.


2017 ◽  
Vol 19 (31) ◽  
pp. 20974-20983 ◽  
Author(s):  
Tim Albes ◽  
Alessio Gagliardi

Gaining insight into the spatial charge carrier distribution and its relation to geminate and nongeminate recombination in bulk-heterojunction organic solar cells.


MRS Bulletin ◽  
2005 ◽  
Vol 30 (1) ◽  
pp. 33-36 ◽  
Author(s):  
René A. J. Janssen ◽  
Jan C. Hummelen ◽  
N. Serdar Sariciftci

AbstractNanostructured phase-separated blends, or bulk heterojunctions, of conjugated polymers and fullerene derivatives form a very attractive approach to large-area, solid-state organic solar cells. The key feature of these cells is that they combine easy processing from solution on a variety of substrates with good performance. Efficiencies of up to 5% in solar light have been achieved, and lifetimes are increasing to thousands of hours. Further improvements can be expected and some of the promising strategies towards that goal are presented in this article.


Molecules ◽  
2020 ◽  
Vol 25 (20) ◽  
pp. 4700
Author(s):  
Thu Trang Do ◽  
Meera Stephen ◽  
Khai Leok Chan ◽  
Sergei Manzhos ◽  
Paul L. Burn ◽  
...  

We introduce two novel solution-processable electron acceptors based on an isomeric core of the much explored diketopyrrolopyrrole (DPP) moiety, namely pyrrolo[3,2-b]pyrrole-1,4-dione (IsoDPP). The newly designed and synthesized compounds, 6,6′-[(1,4-bis{4-decylphenyl}-2,5-dioxo-1,2,4,5-tetrahydropyrrolo[3,2-b]pyrrole-3,6-diyl)bis(thiophene-5,2-diyl)]bis[2-(2-butyloctyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione] (NAI-IsoDPP-NAI) and 5,5′-[(1,4-bis{4-decylphenyl}-2,5-dioxo-1,2,4,5-tetrahydropyrrolo[3,2-b]pyrrole-3,6-diyl)bis(thiophene-5,2-diyl)]bis[2-(2-butyloctyl)isoindoline-1,3-dione] (PI-IsoDPP-PI) have been synthesized via Suzuki couplings using IsoDPP as a central building block and napthalimide or phthalimide as end-capping groups. The materials both exhibit good solubility in a wide range of organic solvents including chloroform (CF), dichloromethane (DCM), and tetrahydrofuran (THF), and have a high thermal stability. The new materials absorb in the wavelength range of 300–600 nm and both compounds have similar electron affinities, with the electron affinities that are compatible with their use as acceptors in donor-acceptor bulk heterojunction (BHJ) organic solar cells. BHJ devices comprising the NAI-IsoDPP-NAI acceptor with poly(3-n-hexylthiophene) (P3HT) as the donor were found to have a better performance than the PI-IsoDPP-PI containing cells, with the best device having a VOC of 0.92 V, a JSC of 1.7 mAcm−2, a FF of 63%, and a PCE of 0.97%.


2015 ◽  
Vol 2015 (21) ◽  
pp. 4629-4634 ◽  
Author(s):  
Edison Castro ◽  
Andrea Cabrera-Espinoza ◽  
Eva Deemer ◽  
Luis Echegoyen

Sign in / Sign up

Export Citation Format

Share Document