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Journal of materials chemistry. A, Materials for energy and sustainability, 2018, Vol.6 (45), p.22889-22898
2018
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Autor(en) / Beteiligte
Titel
Effects of end-on oriented polymer chains at the donor/acceptor interface in organic solar cells
Ist Teil von
  • Journal of materials chemistry. A, Materials for energy and sustainability, 2018, Vol.6 (45), p.22889-22898
Ort / Verlag
Cambridge: Royal Society of Chemistry
Erscheinungsjahr
2018
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
  • Molecular alignment at the interface between the electron donor and acceptor (D/A) materials in thin films may have a large effect on the charge generation process in organic solar cells (OSCs). In this study, the effects of the polymer chain orientations at the D/A interface were investigated in OSCs with planar heterojunction (PHJ) structures. Poly(3-alkylthiophene) films with edge-on (main chain parallel to the interface) and end-on (main chain vertical to the interface) orientations at the surface were used to construct PHJs with a fullerene derivative. Ultraviolet photoelectron spectroscopy and low-energy inverse photoelectron spectroscopy revealed that the difference in polarization energy through the charge-permanent quadrupole interaction causes a rigid energy shift of 0.5 eV between the two orientations. The PHJ device with the end-on oriented polymer chains at the D/A interface showed a smaller photovoltage loss expected from the energy structure and a more efficient charge separation than the device with the edge-on oriented polymer chains. These improvements were attributed to charge delocalization along the end-on oriented polymer chains normal to the D/A interface, through which the effective binding energy of the charge pairs in the interfacial charge-transfer state was reduced. These results provide important information about molecular arrangements at the D/A interface that may enable further improvements in OSC performance.
Sprache
Englisch
Identifikatoren
ISSN: 2050-7488
eISSN: 2050-7496
DOI: 10.1039/C8TA09307E
Titel-ID: cdi_proquest_journals_2135780711

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