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Autor(en) / Beteiligte
Titel
Intermolecular Interactions, Morphology, and Photovoltaic Patterns in p–i–n Heterojunction Solar Cells With Fluorine‐Substituted Organic Photovoltaic Materials
Ist Teil von
  • Small (Weinheim an der Bergstrasse, Germany), 2024-03, Vol.20 (13), p.e2308165-n/a
Ort / Verlag
Germany: Wiley Subscription Services, Inc
Erscheinungsjahr
2024
Link zum Volltext
Quelle
Wiley Online Library Journals Frontfile Complete
Beschreibungen/Notizen
  • During the layer‐by‐layer (LBL) processing of polymer solar cells (PSCs), the swelling and molecule interdiffusion are essential for achieving precise, controllable vertical morphology, and thus efficient PSCs. However, the influencing mechanism of material properties on morphology and correlated device performance has not been paid much attention. Herein, a series of fluorinated/non‐fluorinated polymer donors (PBDB‐T and PBDB‐TF) and non‐fullerene acceptors (ITIC, IT‐2F, and IT‐4F) are employed to investigate the performance of LBL devices. The impacts of fluorine substitution on the repulsion and miscibility between the donor and acceptor, as well as the molecular arrangement of the donor/acceptor and the vertical distribution of the LBL devices are systematically explored by the measurement of donor/acceptor Flory–Huggins interaction parameters, spectroscopic ellipsometry, and neutron reflectivity, respectively. With efficient charge transfer due to the ideal vertical and horizon morphology properties, devices based on PBDB‐TF/IT‐4F exhibit the highest fill factors (FFs) as well as champion power conversion efficiencies (PCEs). With this guidance, high‐performance LBL devices with PCE of 17.2%, 18.5%, and 19.1% are obtained by the fluorinated blend of PBDB‐TF/Y6, PBDB‐TF/L8‐BO, and D18/L8‐BO respectively. It is identified that intermolecular interactions, and morphology of layer‐by‐layer (LBL) processed solar cells can be rational designed by fluorine‐substitution. The relationship between the characteristics of the material itself and the morphological evolution rules of LBL‐processed films are elucidated.

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