| 1. |
- De, Swati, et al.
(författare)
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Geminate charge recombination in alternating polyfluorene copolymer/fullerene blends
- 2007
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Ingår i: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 0002-7863 .- 1520-5126. ; 129:27, s. 8466-8472
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Tidskriftsartikel (refereegranskat)abstract
- By measuring excited state and charge dynamics in blends of an alternating polyfluorene copolymer and fullerene derivative over nine orders in time and two orders in light intensity, we have monitored the light-induced processes from ultrafast charge photogeneration to much slower decay of charges by recombination. We find that at low light intensities relevant to solar cell operation relatively fast (∼30 ns) geminate recombination is the dominating charge decay process, while nongeminate recombination has a negligible contribution. The conclusion of our work is that under solar illumination conditions geminate recombination of charges may be directly competing with efficient charge collection in polymer/fullerene solar cells. © 2007 American Chemical Society.
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| 2. |
- Jespersen, Kim, et al.
(författare)
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Charge formation and transport in bulk-heterojunction solar cells based on alternating polyfluorene copolymers blended with fullerenes
- 2006
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Ingår i: Organic Electronics. - : Elsevier BV. - 1566-1199 .- 1878-5530. ; 7:4, s. 235-242
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Tidskriftsartikel (refereegranskat)abstract
- We investigate charge formation in bulk-heterojunction solar cells based on conjugated polymers in the form of alternating polyfluorene copolymers and the methanofullerene PCBM. Using transient absorption spectroscopy we show that optimal charge formation is obtained with 20-50 wt% PCBM. This is in contrast to the maximum short circuit current density obtained at similar to 80 wt% PCBM as determined by steady state current density-voltage characterization. Hence, we show explicitly that the solar cell performance of these interpenetrating polymer networks containing PCBM is limited by charge transport rather than by formation of charges. (c) 2006 Elsevier B.V. All rights reserved.
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| 3. |
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| 4. |
- Jespersen, Kim, et al.
(författare)
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Excited state dynamics in alternating polyfluorene copolymers
- 2005
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Ingår i: Synthetic Metals. - : Elsevier BV. - 0379-6779. ; 155:2, s. 262-265
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Tidskriftsartikel (refereegranskat)abstract
- We present the excited state dynamics of the low band gap alternating polyfluorene copolymer, DiO-PFDTBT. The copolymer structure is an alternating sequence of donor and acceptor units consisting of 9,9-dioctyl-9H-fluorene and 4,7-di-thiophen-2-yl-benzo[1,2,5]thiadiazolyl units. Calculations have predicted that the first excited state has charge transfer character, while the second strongly allowed excited state is a delocalized π-conjugated state. We show that the excited state dynamics involves internal conversion (IC) from the second strongly allowed excited state to the first excited state. Furthermore, excitation energy transfer (EET) on the 1–10 ps time scale is observed as well as a subsequent formation of a stabilized long-lived emissive state, which has a decay time of 3.25 ns. The origin of this stabilized state is discussed in relation to the intrinsic charge transfer nature of the DiO-PFDTBT.
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| 5. |
- Jespersen, Kim, et al.
(författare)
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The electronic states of polyfluorene copolymers with alternating donor-acceptor units
- 2004
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Ingår i: Journal of Chemical Physics. - : AIP Publishing. - 0021-9606. ; 121:24, s. 12613-12617
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Tidskriftsartikel (refereegranskat)abstract
- We calculate the electronic states of the low bandgap polyfluorene-based copolymer DiO-PFDTBT, which consists of alternating 9,9-dioctyl-9H-fluorene and 4,7-di-thiophen-2-ylbenzo[1,2,5]thiadiazole (TBT) units, and compare with the steady-state absorption, emission, and excitation spectrum. Using the semiempirical quantum-chemical (ZINDO) method we can assign the characteristic bands of the "camel-back" absorption spectrum to one charge transfer state at lower energy localized on the TBT unit, and one delocalized excitonic state at higher energy corresponding to the -conjugated electron system. Additional "dark" charge transfer states in the gap between these bands have been revealed. Calculations are also made on the red light emitting polyfluorene-based copolymer poly(fluorene-co-benzothiadiazole) (F8BT), which contains benzo[1,2,5]thiadiazole instead of TBT. The nature of the electronic states in F8BT and DiO-PFDTBT are found to be qualitatively the same. ©2004 American Institute of Physics.
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| 6. |
- Kattge, Jens, et al.
(författare)
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TRY plant trait database - enhanced coverage and open access
- 2020
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Ingår i: Global Change Biology. - : Wiley-Blackwell. - 1354-1013 .- 1365-2486. ; 26:1, s. 119-188
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Tidskriftsartikel (refereegranskat)abstract
- Plant traits-the morphological, anatomical, physiological, biochemical and phenological characteristics of plants-determine how plants respond to environmental factors, affect other trophic levels, and influence ecosystem properties and their benefits and detriments to people. Plant trait data thus represent the basis for a vast area of research spanning from evolutionary biology, community and functional ecology, to biodiversity conservation, ecosystem and landscape management, restoration, biogeography and earth system modelling. Since its foundation in 2007, the TRY database of plant traits has grown continuously. It now provides unprecedented data coverage under an open access data policy and is the main plant trait database used by the research community worldwide. Increasingly, the TRY database also supports new frontiers of trait-based plant research, including the identification of data gaps and the subsequent mobilization or measurement of new data. To support this development, in this article we evaluate the extent of the trait data compiled in TRY and analyse emerging patterns of data coverage and representativeness. Best species coverage is achieved for categorical traits-almost complete coverage for 'plant growth form'. However, most traits relevant for ecology and vegetation modelling are characterized by continuous intraspecific variation and trait-environmental relationships. These traits have to be measured on individual plants in their respective environment. Despite unprecedented data coverage, we observe a humbling lack of completeness and representativeness of these continuous traits in many aspects. We, therefore, conclude that reducing data gaps and biases in the TRY database remains a key challenge and requires a coordinated approach to data mobilization and trait measurements. This can only be achieved in collaboration with other initiatives.
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| 7. |
- Westerling, M., et al.
(författare)
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Photoexcitation dynamics in an alternating polyfluorene copolymer
- 2007
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Ingår i: Phys. Rev. B: Condens. Matter Mater. Phys. FIELD Full Journal Title:Physical Review B: Condensed Matter and Materials Physics. ; 75:22
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Tidskriftsartikel (refereegranskat)abstract
- The authors used transient photoinduced absorption on femtosecond to nanosecond time scales as well as delayed fluorescence up to microseconds to study the photogeneration and recombination of charges in thin films of the alternating polyfluorene copolymer poly[2,7-(9,9-dioctylfluorene)-alt-5,5-(4',7'-di-2-thienyl-2',1',3'-benzothiadiazole)]. The authors interpret the results using a coupled rate equation model and find that the authors can fit all exptl. results with a single set of parameters. The model includes prompt (
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| 8. |
- Zaushitsyn, Yuri, et al.
(författare)
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Ultrafast dynamics of singlet-singlet and singlet-triplet exciton annihilation in poly(3-2 '-methoxy-5 '-octylphenyl)thiophene films
- 2007
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Ingår i: Physical Review B (Condensed Matter and Materials Physics). - 1098-0121. ; 75:19
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Tidskriftsartikel (refereegranskat)abstract
- Singlet-singlet (S-S) and singlet-triplet (S-T) exciton annihilation was studied in poly(3-2(')-methoxy-5(')octylphenyl)thiophene films. For the S-S exciton annihilation studies, transient absorption spectroscopy at excitation laser pulse fluences of 1.2x10(13)-4.4x10(14) photons/cm(2) and 2.5 kHz pulse repetition rate was applied. The obtained kinetics demonstrate a typical nonexponential character with intensity-dependent amplitudes and lifetimes. In time-resolved fluorescence experiments, low excitation pulse fluences of 1.6x10(9)-2.2x10(12) photons/cm(2) at high repetition rates of 0.4, 0.8, 4, and 81 MHz lead to S-T exciton annihilation as a result of triplet exciton accumulation. S-T annihilation kinetics results in monoexponential decay of the fluorescence kinetics and manifests itself as a decrease of the singlet exciton lifetime. The calculated time-independent S-S and S-T exciton annihilation rates strongly support the conclusion that the processes are controlled by the interchain diffusion of singlet excitons. Despite the low efficiency of S-T annihilation compared to that of S-S annihilation, it has a substantial effect on the singlet exciton lifetime due to a relatively long triplet lifetime (60 mu s). Thus, even optical excitation with low fluence at high pulse repetition rate creates a significant concentration of triplet states that efficiently quenches singlet excitons.
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| 9. |
- Zhang, Fengling, et al.
(författare)
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Influence of solvent mixing on the morphology and performance of solar cells based on polyfluorene copolymer/fullerene blends
- 2006
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Ingår i: Advanced Functional Materials. - : Wiley. - 1616-3028 .- 1616-301X. ; 16:5, s. 667-674
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Tidskriftsartikel (refereegranskat)abstract
- The influence of the solvent on the morphol. and performance of polymer solar cells was studied in devices based on blends of the polyfluorene copolymer, poly(2,7-(9,9-dioctyl-fluorene)-alt-5,5-(4',7'-di-2-thienyl-2', 1',3'-benzothiadiazole)), and [6,6]-phenyl-C61-butyric acid Me ester. The blends are spin-coated from CHCl3 or from CHCl3 mixed with small amts. of xylene, toluene, or chlorobenzene. The devices are characterized under monochromatic light and AM1.5 solar illumination. An enhancement of the photocurrent d. was obsd. in diodes made from CHCl3 mixed with chlorobenzene, and a decreased photocurrent d. is obsd. in diodes made from CHCl3 mixed with xylene or toluene, compared to diodes made from neat CHCl3. The open-circuit voltages are almost the same for all diodes. The surfaces of the active layers were imaged with AFM. Height images indicate that a finer and more uniform distribution of domains corresponds to the diodes with enhanced photocurrent that are made from CHCl3 mixed with chlorobenzene, while a structure with larger domains is assocd. with the lower photocurrents in the diodes made from CHCl3 mixed with xylene or toluene. The influence of the morphol. on the excited-state dynamics and charge generation was studied using time-resolved spectroscopy. Fast formation of bound charge pairs followed by their conversion into free charge carriers was resolved, and excitation-intensity-dependent non-geminate recombination of free charges was obsd. A significant enhancement in free-charge-carrier generation was obsd. on introducing chlorobenzene into CHCl3. Imaging photocurrent generation from the solar cells with a light-pulse technique shows an inhomogeneous photocurrent distribution, which is related to the undulations in the thickness of the active layer. Thicker parts of the diodes yield higher photocurrent values. [on SciFinder (R)]
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