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  • Woo, Han Young  (3)
  • Zou, Yingping  (3)
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  • 1
    In: Solar RRL, Wiley, Vol. 5, No. 1 ( 2021-01)
    Abstract: The power conversion efficiency (PCE) of state‐of‐the‐art organic solar cells is still limited by significant open‐circuit voltage ( V OC ) losses, partly due to the excitonic nature of organic materials and partly due to ill‐designed architectures. Thus, quantifying different contributions of the V OC losses is of importance to enable further improvements in the performance of organic solar cells. Herein, the spectroscopic and semiconductor device physics approaches are combined to identify and quantify losses from surface recombination and bulk recombination. Several state‐of‐the‐art systems that demonstrate different V OC losses in their performance are presented. By evaluating the quasi‐Fermi level splitting (QFLS) and the V OC as a function of the excitation fluence in nonfullerene‐based PM6:Y6, PM6:Y11, and fullerene‐based PPDT2FBT:PCBM devices with different architectures, the voltage losses due to different recombination processes occurring in the active layers, the transport layers, and at the interfaces are assessed. It is found that surface recombination at interfaces in the studied solar cells is negligible, and thus, suppressing the non‐radiative recombination in the active layers is the key factor to enhance the PCE of these devices. This study provides a universal tool to explain and further improve the performance of recently demonstrated high‐open‐circuit‐voltage organic solar cells.
    Type of Medium: Online Resource
    ISSN: 2367-198X , 2367-198X
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2882014-9
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  • 2
    In: Advanced Energy Materials, Wiley, Vol. 11, No. 22 ( 2021-06)
    Abstract: Organic solar cells (OSC) nowadays match their inorganic competitors in terms of current production but lag behind with regards to their open‐circuit voltage loss and fill‐factor, with state‐of‐the‐art OSCs rarely displaying fill‐factor of 80% and above. The fill‐factor of transport‐limited solar cells, including organic photovoltaic devices, is affected by material and device‐specific parameters, whose combination is represented in terms of the established figures of merit, such as θ and α. Herein, it is demonstrated that these figures of merit are closely related to the long‐range carrier drift and diffusion lengths. Further, a simple approach is presented to devise these characteristic lengths using steady‐state photoconductance measurements. This yields a straightforward way of determining θ and α in complete cells and under operating conditions. This approach is applied to a variety of photovoltaic devices—including the high efficiency nonfullerene acceptor blends—and show that the diffusion length of the free carriers provides a good correlation with the fill‐factor. It is, finally, concluded that most state‐of‐the‐art organic solar cells exhibit a sufficiently large drift length to guarantee efficient charge extraction at short circuit, but that they still suffer from too small diffusion lengths of photogenerated carriers limiting their fill factor.
    Type of Medium: Online Resource
    ISSN: 1614-6832 , 1614-6840
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2594556-7
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  • 3
    In: Solar RRL, Wiley, Vol. 4, No. 11 ( 2020-11)
    Abstract: Increasing the active layer thickness without sacrificing the power conversion efficiency (PCE) is one of the great challenges faced by organic solar cells (OSCs) for commercialization. Recently, PM6:Y6 as an OSC based on a non‐fullerene acceptor (NFA) has excited the community because of its PCE reaching as high as 15.9%; however, by increasing the thickness, the PCE drops due to the reduction of the fill factor (FF). This drop is attributed to change in mobility ratio with increasing thickness. Furthermore, this work demonstrates that by regulating the packing and the crystallinity of the donor and the acceptor, through volumetric content of chloronaphthalene (CN) as a solvent additive, one can improve the FF of a thick PM6:Y6 device (≈400 nm) from 58% to 68% (PCE enhances from 12.2% to 14.4%). The data indicate that the origin of this enhancement is the reduction of the structural and energetic disorders in the thick device with 1.5% CN compared with 0.5% CN. This correlates with improved electron and hole mobilities and a 50% suppressed bimolecular recombination, such that the non‐Langevin reduction factor is 180 times. This work reveals the role of disorder on the charge extraction and bimolecular recombination of NFA‐based OSCs.
    Type of Medium: Online Resource
    ISSN: 2367-198X , 2367-198X
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 2882014-9
    Location Call Number Limitation Availability
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