Inverted P3HT:PC61BM organic solar cells incorporating a π-extended squaraine dye with H- and (or) J-aggregation

2018 ◽  
Vol 96 (7) ◽  
pp. 703-711 ◽  
Author(s):  
Sergey V. Dayneko ◽  
Abby-Jo Payne ◽  
Gregory C. Welch

In this report, we investigated the impact of adding a large π-extended squaraine dye to the classic bulk heterojunction P3HT:PC61BM system. The compound, SQIQ-A, is a bis-indole squaraine dye appended with acetylene-indoloquinoxaline end-capping units that exhibits strong optical absorption in thin film from 650 to 750 nm, beyond the absorption wavelength cut-off for P3HT:PC61BM films (ca. ∼650 nm). The dye SQIQ-A can form H- or J-aggregates (blue or red shifting the optical absorption profiles) via solvent vapour annealing with CHCl3 or THF, respectively, thus providing a simple method to control the morphology and optical properties of the molecule. Ternary blended films composed of P3HT:PC61BM:SQIQ-A (1:1:0.3 mass ratio) were investigated as-cast, after solvent vapour annealing, and after thermal annealing. Films were characterized using optical absorption spectroscopy, X-ray diffraction, atomic force microscopy, and polarized light microscopy. Solar cells were fabricated using an inverted architecture in air and analysed using current–voltage and external quantum efficiency measurements. It was found that solar cells thermally annealed at 130 °C for 10 min gave good power conversion efficiencies of 3%, similar to the control P3HT:PC61BM but with improved fill factors and noticeable photocurrent generation from 650 to 760 nm where the SQIQ-A molecule absorbs. Exposure to solvent vapour (CHCl3 or THF) results in aggregation of all components but specifically leads to the formation of micron-sized domains, lowering the overall photovoltaic performance.

2016 ◽  
Vol 700 ◽  
pp. 012052
Author(s):  
D Stoyanova ◽  
S Kitova ◽  
J Dikova ◽  
M Kandinska ◽  
A Vasilev ◽  
...  

Materials ◽  
2020 ◽  
Vol 13 (6) ◽  
pp. 1267 ◽  
Author(s):  
Hugo Gaspar ◽  
Flávio Figueira ◽  
Karol Strutyński ◽  
Manuel Melle-Franco ◽  
Dzmitry Ivanou ◽  
...  

The impact of fullerene side chain functionalization with thiophene and carbazole groups on the device properties of bulk-heterojunction polymer:fullerene solar cells is discussed through a systematic investigation of material blends consisting of the conjugated polymer poly[(5,6-difluoro-2,1,3-benzothiadiazol-4,7-diyl)-alt-(3,3‴-di(2-octyldodecyl)-2,2′;5′,2″;5″,2‴-quaterthiophen-5,5‴-diyl)] (PffBT4T-2OD) as donor and C60 or C70 fulleropyrrolidines as acceptors. The photovoltaic performance clearly depended on the molecular structure of the fulleropyrrolidine substituents although no direct correlation with the surface morphology of the photoactive layer, as determined by atomic force microscopy, could be established. Although some fulleropyrrolidines possess favorable lowest unoccupied molecular orbital levels, when compared to the standard PC71BM, they originated OPV cells with inferior efficiencies than PC71BM-based reference cells. Fulleropyrrolidines based on C60 produced, in general, better devices than those based on C70, and we attribute this observation to the detrimental effect of the structural and energetic disorder that is present in the regioisomer mixtures of C70-based fullerenes, but absent in the C60-based fullerenes. These results provide new additional knowledge on the effect of the fullerene functionalization on the efficiency of organic solar cells.


2019 ◽  
Vol 01 (01) ◽  
pp. 071-077
Author(s):  
Di Zhou ◽  
Zhilin Liu ◽  
Dangqiang Zhu ◽  
Xiyue Yuan ◽  
Xichang Bao ◽  
...  

How to broaden the optical absorption of photovoltaic materials is one of the key issues in the design of high-performance organic solar cells. Nowadays, the sunlight of 400–550 nm wavelength range is not effectively utilized for most small-molecule nonfullerene acceptors. In this work, we proposed the “spliced” strategy of combining the acceptor–donor–acceptor type narrow band-gap small molecules and wide-band-gap perylene diimide (PDI) moieties via a flexible alkyl chain linkage, which could give the superposition effect of the absorption spectra, and three small-molecule acceptors (S1, S2, and S3) were designed based on various end-capping groups with different electron withdrawing abilities. Encouragingly, the as-constructed molecules can well make use of 400–550 nm sunlight with two independent absorption regions. Meanwhile, the aggregation of S1 with a highly planar end-capping group was dominated by both the PDI unit and main skeleton, while S2 and S3 exhibited PDI-controlled aggregation. When fabricated into organic solar cells, S1-based devices achieved a superior efficiency of 3.41% in comparison with those of the other two. The poor photovoltaic performance could be attributed to severe PDI aggregation, which can hinder the charge transfer through the main skeletons. This work could provide a new perspective to modulate optical absorption through the spliced strategy.


2011 ◽  
Vol 1 (2) ◽  
pp. 137-137 ◽  
Author(s):  
Valentin Kamm ◽  
Glauco Battagliarin ◽  
Ian A. Howard ◽  
Wojciech Pisula ◽  
Alexey Mavrinskiy ◽  
...  

2015 ◽  
Vol 5 (20) ◽  
pp. n/a-n/a ◽  
Author(s):  
Jens Adams ◽  
Michael Salvador ◽  
Luca Lucera ◽  
Stefan Langner ◽  
George D. Spyropoulos ◽  
...  

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