| 1. |
- Admassie, Shimelis, et al.
(author)
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Electrochemical and optical studies of the band gaps of alternating polyfluorene copolymers
- 2006
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In: Synthetic Metals. ; 156:7-8, s. 614-623
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Journal article (peer-reviewed)abstract
- The electrochem. and optical properties of alternating polyfluorene copolymers with low band gaps were detd. These polymers incorporated fluorene units alternating with groups including electron-withdrawing (A) and electron-donating (D) groups in donor-acceptor-donor (DAD) sequence to achieve the lowering of band gaps. The polymers were solvent-casted on Pt disk electrode and the band gaps were estd. from cyclic voltammetry (CV). These values were compared with values obtained from optical absorption measurements. Although the electrochem. detd. band gaps are slightly higher than the optical band gap in most cases, values are well correlated. The values of the band gaps detd. range from 2.1 to 1.3 eV. [on SciFinder (R)]
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| 2. |
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| 3. |
- Gadisa, Abay, et al.
(author)
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A new donor-acceptor-donor polyfluorene copolymer with balanced electron and hole mobility
- 2007
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In: Adv. Funct. Mater. FIELD Full Journal Title:Advanced Functional Materials. ; 17:18, s. 3836-3842
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Journal article (peer-reviewed)abstract
- A new alternating polyfluorene copolymer poly[2,7-(9,9-dioctylfluoren)-alt-5,5-(5',8'-di-2-thienyl-(2',3'-bis-(3''-octyloxyphenyl)-quinoxaline))] (APFO-15), which has electron donor-acceptor-donor units in between the fluorene units, is synthesized and characterized. This polymer has a strong absorption and emission in the visible range of the solar spectrum. Its electroluminescence and photolumin escence emissions extend from about 560 to 900 nm. Moreover, solar cells with efficiencies in excess of 3.5 % have been realized from blends of APFO-15 and an electron acceptor mol., a mathanofullerene [6,6]-phenyl-C61-butyric acid Me ester (PCBM). It has also been obsd. that electron and hole transport is balanced both in the pure polymer phase and in polymer/PCBM bulk heterojunction films, which makes this material quite attractive for applications in opto-electronic devices. [on SciFinder (R)]
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| 4. |
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| 5. |
- Gedefaw, Desta Antenehe, 1971, et al.
(author)
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Conjugated polymers with polar side chains in bulk heterojunction solar cell devices
- 2014
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In: Polymer International. - : Wiley. - 1097-0126 .- 0959-8103. ; 63:1, s. 22-30
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Journal article (peer-reviewed)abstract
- Two polymers with polar side chains, namely poly[2,7-(9,9-dioctylfluorene)-alt-5,5-(5',8'-di-2-thienyl-(2',3'-bis(3''-(2-(2-methoxyethoxy)ethoxy)phenyl)quinoxaline))] (P1) and poly[2,7-(9,9-bis(2-(2-methoxyethoxy)ethyl)fluorene)-alt-5,5-(5',8'-di-2-thienyl-(2',3'-bis(3''-(2-(2-methoxyethoxy)-ethoxy)phenyl)quinoxaline))] (P2), were synthesized for solar cell application. A series of bulk heterojunction solar cells were systematically fabricated and characterized by varying the electron-acceptor materials, processing solvents and thickness of the active layer. The results show that P1, with a higher molecular weight and good film-forming properties, performed better. The best device showed an open circuit voltage of 0.87 V, a short circuit current of 6.81 mA cm(-2) and a power conversion efficiency of 2.74% with 1:4 polymer:[6,6]-phenyl-C71-butyric acid methyl ester (PCBM[70]) mixture using o-dichlorobenzene (o-DCB) as processing solvent. P2 on the other hand showed a poorer performance with chlorobenzene as processing solvent, but a much improved performance was obtained using o-DCB instead. Thus, an open circuit voltage of 0.80 V, short circuit current of 6.21 mA cm(-2) and an overall power conversion efficiency of 2.22% were recorded for a polymer:PCBM[70] mixing ratio of 1:4. This is presumably due to the improvement of the morphology of the active layer using o-DCB as processing solvent. (c) 2013 Society of Chemical Industry
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| 6. |
- Gedefaw, Desta Antenehe, 1971, et al.
(author)
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Random polyfluorene co-polymers designed for a better optical absorption coverage of the visible region of the electromagnetic spectrum
- 2014
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In: Bulletin of the Chemical Society of Ethiopia. - : African Journals Online (AJOL). - 1726-801X .- 1011-3924. ; 28:1, s. 121-130
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Journal article (peer-reviewed)abstract
- Two alternating polyfluorenes (APFO15-F8BT and APFO3-F8BT) with full absorption of the visible region of the electromagnetic radiation were designed and synthesized for bulk-heterojunction solar cell devices. The optical and electrochemical properties of the two polymers were studied. The two polymers exhibited strong absorption in the visible region with no significant valley over the visible region extending up to 650 nm. Deep HOMO and ideally situated LUMO energy levels were the characteristics of the two polymers as revealed from the square wave voltammogram study: desired properties for extracting high open circuit voltage and for a facile charge transfer to the acceptor component in devices to take place, respectively. Photovoltaic devices were fabricated by blending the two polymers with PCBM[70] and up to similar to 2% power conversion efficiency were obtained.
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| 7. |
- Inganaes, Olle, et al.
(author)
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Alternating fluorene copolymer-fullerene blend solar cells
- 2005
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In: Optical Science and Engineering. ; 99, s. 387-402
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Journal article (peer-reviewed)abstract
- We present a new class of alternating fluorene copolymers, which can be combined with a fullerene acceptor, to make polymer blends suitable for photovoltaic energy conversion. By choice of comonomers in the polymer, it is possible to engineer the optical absorption spectrum and to cover the wavelength range down to 900 nm. The transport properties of the polymers investigated so far are competitive with other polymers used in polymer solar cells and the mixing of polymers with acceptors in the form of fullerenes is extensive. These polymers are therefore of interest in the future developments of high-performance polymer solar cells. [on SciFinder (R)]
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| 8. |
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| 9. |
- Lindgren, Lars Johan, 1977, et al.
(author)
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Synthesis, Characterization, and Devices of a Series of Alternating Copolymers for Solar Cells
- 2009
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In: CHEMISTRY OF MATERIALS. - : American Chemical Society (ACS). - 0897-4756 .- 1520-5002. ; 21:15, s. 3491-3502
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Journal article (peer-reviewed)abstract
- In this study we report the synthesis, characterization. and photovoltaic properties of a series of six Conjugated polymers based on donor-acceptor-donor (DAD) structure. The polymers are obtained via Suzuki polymerization of different alkoxy-substituted DAD monomers together with a substituted fluorene or phenylene monomer. Application of polymers as light-harvesting and electron-donating materials in solar cells, in conjunction with both [60]PCBM and [70]PCBM as acceptors, show power-conversion efficiencies (PCEs) up to 2.9%, values obtained without extensive optimization work. Furthermore, atomic force microscopy and field-effect transistor (FET) mobility measurements of acceptor-polymer mixtures show that differences in substitution on the polymers affect morphology, mobility, and device performance. Within the series of polymers, all showing similar optical absorption and redox behavior, substituents play an important role in phase separation on a micrometer scale, which in turn has a large impact on device performance. The phase-separation behavior is clearly seen in [70]PCBM devices where the best-performing devices are obtained using the polymers with short alkoxy groups or no substituents together with a high speed of spin coating during device preparation.
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| 10. |
- Ma, Zaifei, et al.
(author)
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A Facile Method to Enhance Photovoltaic Performance of Benzodithiophene-Isoindigo Polymers by Inserting Bithiophene Spacer
- 2014
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In: Advanced Energy Materials. - : Wiley. - 1614-6840 .- 1614-6832. ; 4:6, s. Art. no. 1301455-
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Journal article (peer-reviewed)abstract
- This study describes the synthesis and characterization of four polymers based on benzo[1,2-b:4,5-b']dithiophene (BDT) and isoindigo with zero, one, two, and three thiophene spacer groups. Results have demonstrated that the use of bithiophene as a spacer unit improves the geometry of the polymer chain, making it planar, and hence, potentially enhanced π- π stacking occurs. Due to favorable interaction of the polymer chains, enhanced absorption coefficient, and optimal morphology, PBDT-BTI, which possesses bithiophene as a spacer, revealed high current and fill factor leading to a power conversion efficiency of 7.3% in devices, making this polymer the best performing isoindigo-based material in polymer solar cells (PSCs). Also, PBDT-BTI could still maintain efficiency of over 6% with the active layer thickness of 270 nm, making it a potential candidate for a material in printed PSCs. These results demonstrate that the use of thiophene spacers in D-A polymers could be an important design strategy to produce high-performance PSCs.
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