| 1. |
- Yuan, Jun, et al.
(författare)
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Understanding energetic disorder in electron-deficient-core-based non-fullerene solar cells
- 2020
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Ingår i: Science in China Series B. - : SCIENCE PRESS. - 1674-7291 .- 1869-1870. ; 63:8, s. 1159-1168
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Tidskriftsartikel (refereegranskat)abstract
- Recent advances in material design for organic solar cells (OSCs) are primarily focused on developing near-infrared non-fullerene acceptors, typically A-DA D-A type acceptors (where A abbreviates an electron-withdrawing moiety and D, an electron-donor moiety), to achieve high external quantum efficiency while maintaining low voltage loss. However, the charge transport is still constrained by unfavorable molecular conformations, resulting in high energetic disorder and limiting the device performance. Here, a facile design strategy is reported by introducing the "wing" (alkyl chains) at the terminal of the DA D central core of the A-DA D-A type acceptor to achieve a favorable and ordered molecular orientation and therefore facilitate charge carrier transport. Benefitting from the reduced disorder, the electron mobilities could be significantly enhanced for the "wing"-containing molecules. By carefully changing the length of alkyl chains, the mobility of acceptor has been tuned to match with that of donor, leading to a minimized charge imbalance factor and a high fill factor (FF). We further provide useful design strategies for highly efficient OSCs with high FF.
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| 2. |
- Cai, Yunhao, et al.
(författare)
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Effect of the Energy Offset on the Charge Dynamics in Nonfullerene Organic Solar Cells
- 2020
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Ingår i: ACS Applied Materials and Interfaces. - : AMER CHEMICAL SOC. - 1944-8244 .- 1944-8252. ; 12:39, s. 43984-43991
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Tidskriftsartikel (refereegranskat)abstract
- The energy offset, considered as the driving force for charge transfer between organic molecules, has significant effects on both charge separation and charge recombination in organic solar cells. Herein, we designed material systems with gradually shifting energy offsets, including both positive and negative values. Time-resolved spectroscopy was used to monitor the charge dynamics within the bulk heterojunction. It is striking to find that there is still charge transfer and charge generation when the energy offset reached -0.10 eV (ultraviolet photoelectron spectroscopy data). This work not only indicates the feasibility of the free carrier generation and the following charge separation under the condition of a negative offset but also elucidates the relationship between the charge transfer and the energy offset in the case of polymer chlorination.
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| 3. |
- Ma, Qing, et al.
(författare)
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Promoting charge separation resulting in ternary organic solar cells efficiency over 17.5%
- 2020
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Ingår i: Nano Energy. - : ELSEVIER. - 2211-2855 .- 2211-3282. ; 78
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Tidskriftsartikel (refereegranskat)abstract
- Ternary blend has been an effective strategy for achieving high efficiency in organic solar cells (OSCs). Herein, a non-fullerene small molecule acceptor (C8-DTC) was synthesized and added to the PM6: Y6 system as a third component. By adding 10% of C8-DTC as the second acceptor in the PM6:Y6 system, an impressive power conversion efficiency of 17.52% was achieved with simultaneously increased open-circuit voltage, short-circuit current-density, and fill factor. The reduced voltage loss was due to the lowered non-radiative recombination loss in comparison with the binary device. It was also found that a small amount of C8-DTC in the PM6:Y6 blend resulted in enhanced charge separation and charge transport by providing possible extra channels of hole extraction. And the ternary system formed a good phase separation and favored bi-continuous transport network, which is more conducive to balance the electron and hole transport. The results indicate that the ternary system formed by C8-DTC as the third component is an effective method to improve the performance of the PM6:Y6 based OSCs.
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| 4. |
- Yuan, Jun, et al.
(författare)
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Reducing Voltage Losses in the A-DAD-A Acceptor-Based Organic Solar Cells
- 2020
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Ingår i: Chem. - : CELL PRESS. - 2451-9308 .- 2451-9294. ; 6:9, s. 2147-2161
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Tidskriftsartikel (refereegranskat)abstract
- Power conversion efficiencies (PCEs) of solution-processed organic solar cells (OSCs) have recently reached 17.4% (certified) for single-junction devices. Crucial to this advancement is the development of non-fullerene acceptors (NFAs) since 2015. The recent A-DAD-A NFAs have attracted widespread attention because of their ladder-type electron-deficient-core-based central fused ring with improved transport properties and optimum energy levels. With the synergistic effect of electron-deficient-core and specific molecular geometry, the A-DADA molecules could achieve low voltage losses and high current generation at the same time, reaching new regimes of device physics and photophysics. This perspective will discuss the voltage losses in state-of-the-art A-DAD-A NFA-based OSCs and propose new molecular design strategies to achieve PCEs over 20% in OSCs based on these new acceptors by further decreasing their total voltage losses.
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| 5. |
- Zhao, Fuwen, et al.
(författare)
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Emerging Approaches in Enhancing the Efficiency and Stability in Non-Fullerene Organic Solar Cells
- 2020
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Ingår i: Advanced Energy Materials. - : WILEY-V C H VERLAG GMBH. - 1614-6832 .- 1614-6840.
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Forskningsöversikt (refereegranskat)abstract
- The past three years have witnessed rapid growth in the field of organic solar cells (OSCs) based on non-fullerene acceptors (NFAs), with intensive efforts being devoted to material development, device engineering, and understanding of device physics. The power conversion efficiency of single-junction OSCs has now reached high values of over 18%. The boost in efficiency results from a combination of promising features in NFA OSCs, including efficient charge generation, good charge transport, and small voltage losses. In addition to efficiency, stability, which is another critical parameter for the commercialization of NFA OSCs, has also been investigated. This review summarizes recent advances in the field, highlights approaches for enhancing the efficiency and stability of NFA OSCs, and discusses possible strategies for further advances of NFA OSCs.
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| 6. |
- Jasiunas, Rokas, et al.
(författare)
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From Generation to Extraction: A Time-Resolved Investigation of Photophysical Processes in Non-fullerene Organic Solar Cells
- 2020
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Ingår i: The Journal of Physical Chemistry C. - : AMER CHEMICAL SOC. - 1932-7447 .- 1932-7455. ; 124:39, s. 21283-21292
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Tidskriftsartikel (refereegranskat)abstract
- Non-fullerene organic solar cells (NFOSCs) demonstrate record efficiencies exceeding 16%. In comparison with cells with the fullerene-based acceptor, the NFOSCs benefit from a longer wavelength absorption, which leads to a small highest occupied molecular orbital (HOMO) level offset. Here, we use several advanced transient investigation techniques, covering timescale from sub-ps to mu s, to address all sequence of processes starting from photoexcitation of donors or acceptors to carrier extraction in several NFOSCs and cells with phenyl-C71-butyric acid methyl ester (PCBM). Though small offsets result in higher open-circuit voltage, we show that at the same time, it limits cell performance because of inefficient hole transfer from excited acceptors to donors and enhanced geminate recombination. We demonstrate that 100 meV HOMO level offset and proper acceptor molecule structures are sufficient for efficient hole transfer (>70%) and for reduction of the geminate recombination losses down to about 20%. Subsequent extraction of unbound charge carriers in all NFOSCs is slightly faster than in cells with PCBM, while non-geminate carrier recombination causing additional losses is slightly slower in the best performing NFOSCs than in cells with PCBM.
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| 7. |
- Perdigon-Toro, Lorena, et al.
(författare)
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Barrierless Free Charge Generation in the High-Performance PM6:Y6 Bulk Heterojunction Non-Fullerene Solar Cell
- 2020
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Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 32
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Tidskriftsartikel (refereegranskat)abstract
- Organic solar cells are currently experiencing a second golden age thanks to the development of novel non-fullerene acceptors (NFAs). Surprisingly, some of these blends exhibit high efficiencies despite a low energy offset at the heterojunction. Herein, free charge generation in the high-performance blend of the donor polymer PM6 with the NFA Y6 is thoroughly investigated as a function of internal field, temperature and excitation energy. Results show that photocurrent generation is essentially barrierless with near-unity efficiency, regardless of excitation energy. Efficient charge separation is maintained over a wide temperature range, down to 100 K, despite the small driving force for charge generation. Studies on a blend with a low concentration of the NFA, measurements of the energetic disorder, and theoretical modeling suggest that CT state dissociation is assisted by the electrostatic interfacial field which for Y6 is large enough to compensate the Coulomb dissociation barrier.
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| 8. |
- Zhu, Can, et al.
(författare)
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Tuning the electron-deficient core of a non-fullerene acceptor to achieve over 17% efficiency in a single-junction organic solar cell
- 2020
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Ingår i: Energy & Environmental Science. - : ROYAL SOC CHEMISTRY. - 1754-5692 .- 1754-5706. ; 13:8, s. 2459-2466
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Tidskriftsartikel (refereegranskat)abstract
- Finding effective molecular design strategies to enable efficient charge generation and small energy loss is among the long-standing challenges in developing high performance non-fullerene organic solar cells (OSCs). Recently, we reported Y-series non-fullerene acceptors with an electron-deficient-core-based fused structure (typically Y6), opening a new door to achieve high external quantum efficiency (∼80%) while maintaining low energy loss (∼0.57 eV). On this basis, further reducing the energy losses and ultimately improving the performance of OSCs has become a research hotspot. In this paper, we design and synthesize a new member of the Y-series acceptor family, Y18, which adopts a fused benzotriazole segment with unique luminescence properties as its electron-deficient core. Compared to Y6, the benzotriazole-based acceptor Y18 exhibits extended optical absorption and higher voltage. Consequently, the device delivers a promising power conversion efficiency of 16.52% with a very low energy loss of 0.53 eV. Further device optimization by exploiting a ternary blend strategy allowed us to achieve a high efficiency of 17.11% (certified as 16.76% by NREL). Y18 may become one of the most important candidate materials for its broader absorption spectra and higher voltage of Y18 (compared to Y6) in the OSCs field.
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