New solution processed bulk-heterojunction organic solar cells based on a triazine-bridged porphyrin dyad as electron donor

RSC Advances ◽  
2014 ◽  
Vol 4 (92) ◽  
pp. 50819-50827 ◽  
Author(s):  
Ganesh D. Sharma ◽  
Galateia E. Zervaki ◽  
Panagiotis Angaridis ◽  
Athanassios G. Coutsolelos
Keyword(s):  
Solar Cells ◽  
Active Layer ◽  
Electron Donor ◽  
Organic Solar Cells ◽  
Bulk Heterojunction ◽  
Solution Processed ◽  
Zinc Porphyrin ◽  
Donor And Acceptor ◽  
Electron Donor And Acceptor ◽  
Covalently Linked

An unsymmetrical porphyrin dyad (ZnP)-[triazine-Npip]-(ZnPCOOH) consisting of two zinc-porphyrin units covalently linked to a peridine-containing triazine group has been used with PC71BM as electron donor and acceptor, respectively, for the active layer of solution-processed BHJ organic solar cells.

Study Phase Separation of Donor: Acceptor in Inkjet Printed Thin Films of Bulk Heterojunction Organic Solar Cells Using AFM Phase Imaging

2011 ◽  
Vol 364 ◽  
pp. 465-469 ◽  
Author(s):  
Vivi Fauzia ◽  
Akrajas Ali Umar ◽  
Muhamad Mat Salleh ◽  
Muhammad Yahaya
Keyword(s):  
Thin Films ◽  
Solar Cells ◽  
Phase Separation ◽  
Electron Donor ◽  
Organic Solar Cells ◽  
Bulk Heterojunction ◽  
Study Phase ◽  
Phase Imaging ◽  
Donor And Acceptor ◽  
Electron Donor And Acceptor

This paper reports an application of Atomic Force Microscopy (AFM) phase imaging to observe the phase separation between electron donor and acceptor materials in bulk heterojunction organic solar cells. The solar cells were fabricated using inkjet printed thin films of blended poly (3-octylthiophene-2,5-diyl)(P3OT) and (6,6)-phenyl C71 butyric acid methyl ester (PC71BM) as donor and acceptor materials respectively. The content PC71BM in the blended was varying from 25, 50 and 75 wt %. The AFM phase images of the thin film which contains 25 wt % PC71BM indicated that the acceptor molecules, PC71BM, are well distributed in the polymer chain of donor material, P3OT. The solar cell contains this film has the highest generated photocurrent. Hence, the phase separation between electron donor and acceptor materials in bulk heterojunction organic solar cells is one essential aspect that influences generation of photocurrent.

scholarly journals Optimization of solution-processed oligothiophene:fullerene based organic solar cells by using solvent additives

2013 ◽  
Vol 4 ◽  
pp. 680-689 ◽  
Author(s):  
Gisela L Schulz ◽  
Marta Urdanpilleta ◽  
Roland Fitzner ◽  
Eduard Brier ◽  
Elena Mena-Osteritz ◽  
...  
Keyword(s):  
Solar Cells ◽  
Organic Solar Cells ◽  
Bulk Heterojunction ◽  
Solution Processed ◽  
Heterojunction Solar Cells ◽  
Force Microscopy ◽  
Vacuum Technology ◽  
Atomic Force ◽  
Donor And Acceptor ◽  
Conversion Efficiencies

The optimization of solution-processed organic bulk-heterojunction solar cells with the acceptor-substituted quinquethiophene DCV5T-Bu 4 as donor in conjunction with PC61BM as acceptor is described. Power conversion efficiencies up to 3.0% and external quantum efficiencies up to 40% were obtained through the use of 1-chloronaphthalene as solvent additive in the fabrication of the photovoltaic devices. Furthermore, atomic force microscopy investigations of the photoactive layer gave insight into the distribution of donor and acceptor within the blend. The unique combination of solubility and thermal stability of DCV5T-Bu 4 also allows for fabrication of organic solar cells by vacuum deposition. Thus, we were able to perform a rare comparison of the device characteristics of the solution-processed DCV5T-Bu 4 :PC61BM solar cell with its vacuum-processed DCV5T-Bu 4 :C60 counterpart. Interestingly in this case, the efficiencies of the small-molecule organic solar cells prepared by using solution techniques are approaching those fabricated by using vacuum technology. This result is significant as vacuum-processed devices typically display much better performances in photovoltaic cells.

High photocurrent in oligo-thienylenevinylene-based small molecule solar cells with 4.9% solar-to-electrical energy conversion

2015 ◽  
Vol 3 (21) ◽  
pp. 11340-11348 ◽  
Author(s):  
Núria F. Montcada ◽  
Rocío Domínguez ◽  
Beatriz Pelado ◽  
Pilar de la Cruz ◽  
Emilio Palomares ◽  
...  
Keyword(s):  
Solar Cells ◽  
Energy Conversion ◽  
Small Molecule ◽  
Electron Donor ◽  
Electron Acceptor ◽  
Organic Solar Cells ◽  
Organic Molecules ◽  
Bulk Heterojunction ◽  
Electrical Energy ◽  
Solution Processed

A set of five novel oligo-thienylenevinylene organic molecules have been synthesized and characterized for use as electron donor moieties in bulk-heterojunction solution-processed organic solar cells combined with PC71BM as an electron acceptor.

A solution-processable bipolar diketopyrrolopyrrole molecule used as both electron donor and acceptor for efficient organic solar cells

2015 ◽  
Vol 3 (5) ◽  
pp. 1902-1905 ◽  
Author(s):  
Hangqi Shi ◽  
Weifei Fu ◽  
Minmin Shi ◽  
Jun Ling ◽  
Hongzheng Chen
Keyword(s):  
Solar Cells ◽  
Charge Transport ◽  
Transport Properties ◽  
Electron Donor ◽  
Organic Solar Cells ◽  
Energy Levels ◽  
Donor And Acceptor ◽  
Solution Processable ◽  
Electron Donor And Acceptor ◽  
Bipolar Charge

A DPP molecule has appropriate energy levels and bipolar charge-transport properties for both donor and acceptor in OSCs.

Influence of additives in bulk heterojunction solar cells using magnesium tetraethynylporphyrin with triisopropylsilyl and anthryl substituents

2014 ◽  
Vol 18 (08n09) ◽  
pp. 735-740 ◽  
Author(s):  
Takafumi Nakagawa ◽  
Junichi Hatano ◽  
Yutaka Matsuo
Keyword(s):  
Solar Cells ◽  
Power Conversion Efficiency ◽  
Conversion Efficiency ◽  
Electron Donor ◽  
Organic Solar Cells ◽  
Bulk Heterojunction ◽  
Power Conversion ◽  
Acid Methyl Ester ◽  
Heterojunction Solar Cells ◽  
Donor And Acceptor

We designed and synthesized anthryl-disubstituted magnesium tetraethynylporphyrin([{5,15-bis(anthracen-9′-yl)ethynyl}-10,20-bis{(triisopropylsilyl)ethynyl}porphyrinato] magnesium(II)), and applied it as an electron donor to solution-processed bulk heterojunction small molecule organic solar cells. The compound was characterized by single crystal X-ray crystallography as well as UV-vis light absorption spectrum showing the absorption maximum and onset at 700 and 740 nm, respectively. Organic solar cells using this compound and [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM) as electron donor and acceptor, respectively, showed power conversion efficiency of 1.31% at the donor and acceptor ratio of 1:3. The use of pyridine as a coordinating additive increased power conversion efficiency to 1.61%, which was the best among tested additives, THF, pyradine, dioxane, and 1,8-diiodooctane.

Porphyrin dimers as donors for solution-processed bulk heterojunction organic solar cells

RSC Advances ◽  
2016 ◽  
Vol 6 (65) ◽  
pp. 60626-60632 ◽  
Author(s):  
Fang-Chi Hsu ◽  
Ming-Kuang Hsieh ◽  
Chiranjeevulu Kashi ◽  
Chen-Yu Yeh ◽  
Tai-Yuan Lin ◽  
...  
Keyword(s):  
Solar Cells ◽  
Organic Solar Cells ◽  
Bulk Heterojunction ◽  
Electron Donors ◽  
Solution Processed ◽  
Covalently Linked ◽  
Porphyrin Dimers

We synthesize a novel class of porphyrin dimers consisting of two zinc-metalated porphyrin units covalently linked through ethynyl or butadiyne group as electron donors for the fabrication of organic bulk heterojunction (BHJ) solar cells.

Regulating the optoelectronic properties of small molecule donors with multiple alternative electron-donor and acceptor units for organic solar cells

2018 ◽  
Vol 6 (17) ◽  
pp. 8101-8108 ◽  
Author(s):  
Yuan Zhao ◽  
Huan Wang ◽  
Weixuan Zeng ◽  
Shengpeng Xia ◽  
Feng Zhou ◽  
...  
Keyword(s):  
Solar Cells ◽  
Small Molecule ◽  
Electron Donor ◽  
Organic Solar Cells ◽  
Optoelectronic Properties ◽  
Structure Property ◽  
Donor And Acceptor ◽  
Multiple Alternative ◽  
Electron Donor And Acceptor ◽  
Property Performance

Small molecule donors with multiple alternative electron-donor and acceptor units were synthesized via C–H functionalization with the structure–property–performance relationship investigated.

Furan-bridged thiazolo [5,4-d]thiazole based D–π–A–π–D type linear chromophore for solution-processed bulk-heterojunction organic solar cells

RSC Advances ◽  
2015 ◽  
Vol 5 (9) ◽  
pp. 6286-6293 ◽  
Author(s):  
M. Nazim ◽  
Sadia Ameen ◽  
M. Shaheer Akhtar ◽  
Hyung-Kee Seo ◽  
Hyung-Shik Shin
Keyword(s):  
Solar Cells ◽  
Small Molecule ◽  
Organic Solar Cells ◽  
Bulk Heterojunction ◽  
Solution Processed ◽  
Organic Chromophore

Novel furan-bridged thiazolo[5,4-d]thiazole based π-conjugated organic chromophore (RFTzR) was formulated and utilized for the fabrication of solution-processed small molecule organic solar cells (SMOSCs).

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