| 1. |
- Alkadir Abdulahi, Birhan, 1985, et al.
(författare)
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Open-Circuit Voltage Modulations on All-Polymer Solar Cells by Side Chain Engineering on 4,8-Di(thiophen-2-yl)benzo[1,2- b:4,5- b′]dithiophene-Based Donor Polymers
- 2018
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Ingår i: ACS Applied Energy Materials. - : American Chemical Society (ACS). - 2574-0962. ; 1:6, s. 2918-2926
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Tidskriftsartikel (refereegranskat)abstract
- In recent years, all-polymer solar cells (all-PSCs), incorporating active layers based on blends of electron-donor (D) and acceptor (A) polymers, have drawn attention because of the advantages they hold in the flexibility of choosing the D:A combinations to modulate their energy levels and to improve their overall open-circuit voltages (V oc ) and power conversion efficiencies (PCE)s. V oc is one of the key parameters for the determination of the PCEs of PSCs. In this work, we synthesized six donor polymers with three different side chains appended to the 4,8-di(thiophen-2-yl)benzo[1,2-b:4,5-b′]dithiophene (BDT) units. By substituting carbon with sulfur and silicon atoms at the 5-position of the thiophenes attached to the BDT units, the highest occupied molecular orbital (HOMO) levels of the donor polymers could be successfully lowered. As anticipated, the V oc values of the resulting all-PSCs increased along with the lowering of the HOMO levels of the donor polymers. Among the six all-PSCs, the PBDT-BDD:PNDI-T10 all-PSC realized a balance between the photovoltage and photocurrent, where a decent PCE of 5.6% was obtained with a V oc of 0.9 V and a photocurrent of 10.5 mA/cm 2 .
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| 2. |
- Benavides, Cindy Montenegro, et al.
(författare)
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High-Performance Organic Photodetectors from a High-Bandgap Indacenodithiophene-Based π-Conjugated Donor-Acceptor Polymer
- 2018
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Ingår i: ACS Applied Materials & Interfaces. - : American Chemical Society (ACS). - 1944-8252 .- 1944-8244. ; 10:15, s. 12937-12946
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Tidskriftsartikel (refereegranskat)abstract
- A conjugated donor-acceptor polymer, poly[4,4,9,9-tetrakis(4-hexylphenyl)-4,9-dihydro-s-indaceno[1,2-b:5,6-b′]dithiophene-2,7-diyl-alt-5-(2-ethylhexyl)-4H-thieno[3,4-c] pyrrole-4,6(5H)-dione-1,3-diyl] (PIDT-TPD), is blended with the fullerene derivative [6,6] phenyl-C61-butyric acid methyl ester (PC 61 BM) for the fabrication of thin and solution-processed organic photodetectors (OPDs). Systematic screening of the concentration ratio of the blend and the molecular weight of the polymer is performed to optimize the active layer morphology and the OPD performance. The device comprising a medium molecular weight polymer (27.0 kg/mol) in a PIDT-TPD:PC 61 BM 1:1 ratio exhibits an external quantum efficiency of 52% at 610 nm, a dark current density of 1 nA/cm 2 , a detectivity of 1.44 × 10 13 Jones, and a maximum 3 dB cutoff frequency of 100 kHz at -5 V bias. These results are remarkable among the state-of-the-art red photodetectors based on conjugated polymers. As such, this work presents a functional organic active material for high-speed OPDs with a linear photoresponse at different light intensities.
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| 3. |
- Murto, Petri Henrik, 1984, et al.
(författare)
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High performance all-polymer photodetector comprising a donor-Acceptor-Acceptor structured indacenodithiophene-bithieno[3,4-c] pyrroletetrone copolymer
- 2018
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Ingår i: ACS Macro Letters. - : American Chemical Society (ACS). - 2161-1653. ; 7:4, s. 395-400
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Tidskriftsartikel (refereegranskat)abstract
- The synthesis of an acceptor polymer PIDT-2TPD, comprising indacenodithiophene (IDT) as the electron-rich unit and an interconnected bithieno[3,4-c]pyrrole-4,4′,6,6′-Tetrone (2TPD) as the electron-deficient unit, and its application for all-polymer photodetectors is reported. The optical, electrochemical, charge transport, and device properties of a blend of poly(3-hexylthiophene) and PIDT-2TPD are studied. The blend shows strong complementary absorption and balanced electron and hole mobility, which are desired properties for a photoactive layer. The device exhibits dark current density in the order of 10 -5 mA/cm 2 , external quantum efficiency broadly above 30%, and nearly planar detectivity over the entire visible spectral range (maximum of 1.1 × 10 12 Jones at 610 nm) under-5 V bias. These results indicate that PIDT-2TPD is a highly functional new type of acceptor and further motivate the use of 2TPD as a building block for other n-Type materials.
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| 4. |
- Murto, Petri Henrik, 1984, et al.
(författare)
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Incorporation of Designed Donor−Acceptor−Donor Segments in a Host Polymer for Strong Near-Infrared Emission from a Large-Area Light-Emitting Electrochemical Cell
- 2018
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Ingår i: ACS Applied Energy Materials. - : American Chemical Society (ACS). - 2574-0962. ; 1:4, s. 1753-1761
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Tidskriftsartikel (refereegranskat)abstract
- Cost-efficient thin-film devices that emit in the nearinfrared (NIR) range promise a wide range of important applications. Here, the synthesis and NIR application of a series of copolymers comprising poly[indacenodithieno[3,2- b ]thiophene-2,8-diyl] (PIDTT) as the host and different donor−acceptor−donor (DAD) segments as the guest are reported. We find that a key design criterion for efficient solid-state host-to-guest energy transfer is that the DAD conformation is compatible with the conformation of the host. Such host−guest copolymers are evaluated as the emitter in light-emitting electrochemical cells (LECs) and organic light-emitting diodes, and the best performance is invariably attained from the LEC devices because of the observed balanced electrochemical doping that alleviates issues with a noncentered emission zone. An LEC device comprising a host−guest copolymer with 4,4-bis(2-ethylhexyl)-4 H -silolo[3,2- b :4,5- b′ ]dithiophene as the donor and benzo[ c ][1,2,5]thiadiazole as the acceptor delivers an impressive near-infrared (NIR) performance in the form of a high radiance of 1458 μ W/cm2 at a peak wavelength of 725 nm when driven by a current density of 500 mA/cm2, a second-fast turn-on, and a good stress stability as manifested in a constant radiance output during 3 days of uninterrupted operation. The high-molecular-weight copolymer features excellent processability, and the potential for low-cost and scalable NIR applications is verified through a spray-coating fabrication of a >40 cm2 large-area device, which emits intense and uniform NIR light at a low drive voltage of 4.5 V.
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| 5. |
- Murto, Petri Henrik, 1984, et al.
(författare)
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Triazolobenzothiadiazole-Based Copolymers for Polymer Light-Emitting Diodes: Pure Near-Infrared Emission via Optimized Energy and Charge Transfer
- 2016
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Ingår i: Advanced Optical Materials. - : Wiley. - 2195-1071. ; 4:12, s. 2068-2076
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Tidskriftsartikel (refereegranskat)abstract
- © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.A series of new near-infrared (NIR) emitting copolymers, based on a low band gap 6-(2-butyloctyl)-4,8-di(thiophen-2-yl)-[1,2,3]triazolo[4',5':4,5]benzo[1,2-c]-[1,2,5]thiadiazole (TBTTT) fluorophore copolymerized into a high band gap poly[3,3'-ditetradecyl-2,2'-bithiophene-5,5'-diyl-alt-5-(2-ethylhexyl)-4H-thieno[3,4-c]pyrrole-4,6(5H)-dione-1,3-diyl] (P2TTPD) host backbone, for polymer light-emitting diode (PLED) applications is reported. PLEDs fabricated from the host polymer (P2TTPD-0) show external quantum efficiencies (EQEs) up to 0.49% at 690 nm, with turn-on voltage (Von) at only 2.4 V. By incorporating the TBTTT segments into the host polymer backbone, pure NIR emission peaking at ca. 900 nm is obtained with Von remaining below 5 V. This work demonstrates that such a low Von can be attributed to efficient intrachain energy and/or charge transfer to the TBTTT sites. When the NIR emitting copolymer (P2TTPD-10) is blended with P2TTPD-0, the TBTTT are confined to well-separated polymer chains. As a result, the EQE from the blend is lower and the Von higher than that obtained from the pure copolymer (P2TTPD-1.0) with equal content of TBTTT. An analogous copolymer (P4T-1.0), consisting of poly[3,3'-ditetradecyl-2,2':5',2'':5'',2'''-quaterthiophene-5,5'''-diyl] (P4T) as the host and 1% TBTTT as the NIR emitter, further demonstrates that pure NIR emission can be obtained only through optimized molecular orbital energy levels, as in P2TTPD-1.0, which minimizes chances for either charge trapping or exciton splitting.
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| 6. |
- Tang, Shi, et al.
(författare)
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Intense and Stable Near-Infrared Emission from Light-Emitting Electrochemical Cells Comprising a Metal-Free Indacenodithieno[3,2-b]thiophene-Based Copolymer as the Single Emitter
- 2017
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Ingår i: Chemistry of Materials. - : American Chemical Society (ACS). - 1520-5002 .- 0897-4756. ; 29:18, s. 7750-7759
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Tidskriftsartikel (refereegranskat)abstract
- We report on the synthesis, characterization, and application of a series of metal-free near-infrared (NIR) emitting alternating donor/acceptor copolymers based on indacenodithieno[3,2-b]thiophene (IDTT) as the donor unit. A light-emitting electrochemical cell (LEC), comprising a blend of the copolymer poly[indacenodithieno[3,2-b]thiophene-2,8-diyl-alt-2,3-diphenyl-5,8-di(thiophen-2-y1)- quinoxaline-5,5'-diy1] and an ionic liquid as the single-layer active material sandwiched between two air-stable electrodes, delivered NIR emission (lambda(peak) = 705 nm) with a high radiance of 129 mu W/cm(2) when driven by a low voltage of 3.4 V. The NIR-LEC also featured good stress stability, as manifested in that the peak NIR output from a nonencapsulated device after 24 h of continuous operation only had dropped by 3% under N-2 atmosphere and by 27% under ambient air. This work accordingly introduces IDTT-based donor/acceptor copolymers as functional metal-free electroluminescent materials in NIR-emitting devices and also provides guidelines for how future NIR emitters should be designed for further improved performance.
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| 7. |
- Tao, Qiang, 1987, et al.
(författare)
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D-A(1)-D-A(2) Copolymers with Extended Donor Segments for Efficient Polymer Solar Cells
- 2015
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Ingår i: Macromolecules. - : American Chemical Society (ACS). - 1520-5835 .- 0024-9297. ; 48:4, s. 1009-1016
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Tidskriftsartikel (refereegranskat)abstract
- Typically a donor-acceptor (D-A) design strategy is used for engineering the bandgap of polymers for solar cells. However, in this work, a series of alternating D-A(1-)D-A(2) copolymers PnTQTI(F) were synthesized and characterized with oligothiophenes (nT, n = 1, 2, 3) as the donor and two electron-deficient moieties, quinoxaline and isoindigo, as the acceptors in the repeating unit. We have studied the influence of the donor segments with different numbers of thiophene units and the effect of the addition of fluorine to the quinoxaline unit of the D-A(1)-D-A(2) polymers. The photophysical, electrochemical, and photovoltaic properties of the polymers were examined via a range of techniques and related to theoretical simulations. On increasing the length of the donor thiophene units, broader absorption spectra were observed in addition to a sequential increase in HOMO levels, while the LUMO levels displayed very small variations. The addition of fluorine to the quinoxaline unit not only decreased the HOMO levels of the resulting polymers but also enhanced the absorption coefficients. A superior photovoltaic performance was observed for the P3TQTI-F-based device with a power conversion efficiency (PCE) of 7.0%, which is the highest efficiency for alternating D-A(1)-D-A(2) polymers reported to date. The structureproperty correlations of the PnTQTI(F) polymers demonstrate that varying of the length of the donor segments is a valuable method for designing high-performance D-A(1)-D-A(2) copolymers and highlight the promising nature of D-A(1)-D-A(2) copolymers for efficient bulk-heterojunction solar cells.
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| 8. |
- Xu, Xiaofeng, 1984, et al.
(författare)
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Effects of side chain isomerism on the physical and photovoltaic properties of indacenodithieno[3,2-b]thiophene–quinoxaline copolymers: toward a side chain design for enhanced photovoltaic performance
- 2014
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Ingår i: Journal of Materials Chemistry. - 1364-5501 .- 0959-9428. ; 2:44, s. 18988-18997
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Tidskriftsartikel (refereegranskat)abstract
- Four new D–A polymers PIDTT-Q-p, PIDTT-Q-m, PIDTT-QF-p and PIDTT-QF-m, using indacenodithieno[3,2-b]thiophene (IDTT) as an electron-rich unit and quinoxaline (Q) as an electron-deficient unit, were synthesized via a Pd-catalyzed Stille polymerization. The side chains on the pendant phenyl rings of IDTT were varied from the para- to the meta-position, and the effect of the inclusion of fluorine on the quinoxaline unit was simultaneously investigated. The influence on the optical and electrochemical properties, film topography and photovoltaic properties of the four copolymers were thoroughly examined via a range of techniques. The inductively electron-withdrawing properties of the fluorine atoms result in a decrease of the highest occupied molecular orbital (HOMO) energy levels. The effect of meta-substitution on the PIDTT-Q-m polymer leads to good solubility and in turn higher molecular weight. More importantly, it exhibits optimal morphological properties in the PIDTT-Q-m/PC71BM blends. As a result, the corresponding solar cells (ITO/PEDOT:PSS/polymer:PC71BM/LiF/Al) attain the best power conversion efficiency (PCE) of 6.8%. The structure–property correlations demonstrate that the meta-alkyl-phenyl substituted IDTT unit is a promising building block for efficient organic photovoltaic materials. This result also extends our strategy with regards to side chain isomerism of IDTT-based copolymers for enhanced photovoltaic performance.
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| 9. |
- Xu, Xiaofeng, 1984, et al.
(författare)
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Pyrrolo[3,4-g]quinoxaline-6,8-dione-based conjugated copolymers for bulk heterojunction solar cells with high photovoltages
- 2015
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Ingår i: Polymer Chemistry. - : ROYAL SOC CHEMISTRY. - 1759-9954 .- 1759-9962. ; 6:25, s. 4624-4633
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Tidskriftsartikel (refereegranskat)abstract
- A new electron-deficient building block 5,9-di(thiophen-2-yl)-6H-pyrrolo[3,4-g]quinoxaline-6,8(7H)-dione (PQD) was synthesized via functionalizing the 6- and 7-positions of quinoxaline (Qx) with a dicarboxylic imide moiety. Side chain substitution on the PQD unit leads to good solubility which enables very high molecular weight copolymers to be attained. The fusion of two strong electron-withdrawing groups (Qx and dicarboxylic imide) makes the PQD unit a stronger electron-deficient moiety than if the unit had just one electron-withdrawing group, thus enhancing the intramolecular charge transfer between electron-rich and deficient units of the copolymer. Four PQD-based polymers were synthesized which feature deep-lying highest occupied molecular orbital (HOMO) levels and bathochromic absorption spectra when compared to PBDT-Qx and PBDT-TPD analogues. The copolymers incorporated with benzo[1,2-b:4,5-b]dithiophene (BDT) units show that the 1D and 2D structural variations of the side groups on the BDT unit are correlated with the device performance. As a result, the corresponding solar cells (ITO/PEDOT:PSS/polymer: PC71BM/LiF/Al) based on the four copolymers feature very high open-circuit voltages (V-oc) of around 1.0 V. The copolymer PBDT-PQD1 attains the best power conversion efficiency of 4.9%, owing to its relatively high absorption intensity and suitable film morphology. The structure-property correlation demonstrates that the new PQD unit is a promising electron-deficient building block for efficient photovoltaic materials with high V-oc.
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| 10. |
- Bergenti, Ilaria, et al.
(författare)
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Highly Ordered Organic Ferroelectric DIPAB-Patterned Thin Films
- 2017
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Ingår i: Langmuir. - : American Chemical Society (ACS). - 1520-5827 .- 0743-7463. ; 33:45, s. 12859-12864
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Tidskriftsartikel (refereegranskat)abstract
- Ferroelectric molecular compounds present great advantages for application in electronics because they combine high polarization values, comparable to those of inorganic materials, with the flexibility and low-cost properties of organic ones. However, some limitations to their applicability are related to the high crystallinity required to deploy ferroelectricity. In this article, highly ordered ferroelectric patterned thin films of diisopropylammonium bromide have been successfully fabricated by a lithographically controlled wetting technique. Confinement favors the self-organization of ferroelectric crystals, avoiding the formation of polymorphs and promoting the long-range orientation of crystallographic axes. Patterned structures present high stability, and the polarization can be switched to be arranged in stable domain pattern for application in devices.
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