No abstract
The aim of this article is to investigate the origin of the open circuit voltage ͑V oc ͒ in organic heterojunction solar cells. The studied devices consist of buckminsterfullerene C 60 as acceptor material and an oligophenyl-derivative 4 , 4Ј-bis-͑N , N-diphenylamino͒quaterphenyl ͑4P-TPD͒ as donor material. These photoactive materials are sandwiched between indium tin oxide and p-doped hole transport layers. Using two different p-doped hole transport layers, the built-in voltage of the solar cells is independently changed from the metal contacts. The influence of the built-in voltage on the V oc is investigated in bulk and planar heterojunctions. In bulk heterojunctions, in which doped transport layers border directly on the photoactive blend layer, V oc cannot exceed the built-in voltage significantly. Though, in planar heterojunctions, V oc is identical with the splitting of quasi-Fermi levels at the donor-acceptor interface and is thus primarily determined by the difference of the lowest unoccupied molecular orbital of C 60 and the highest occupied molecular orbital of 4P-TPD. In planar heterojunctions, the open circuit voltage can exceed the built-in voltage. Furthermore, the investigations show that the efficiency of organic solar cells can be improved by using p-doped charge transport layers with optimized energy level alignment to the active materials. The optimized planar heterojunction shows a fill factor of up to 65.5% and a V oc of 0.95 V. For solar cells with insufficient energy level alignment between the photoactive layer system and the hole transport layer, a reduced V oc in bulk heterojunction cells and a characteristic S shape of the I-V characteristics in planar heterojunction cells are observed.
We present highly efficient, semitransparent small molecule organic solar cells. The devices employ an indium tin oxide-free top contact, consisting of thin metal films. An additional organic layer is used to enhance light outcoupling. The solar cell incorporates two stacked subcells, each containing a donor:acceptor bulk heterojunction. The two subcells have complementary absorbers, with separate blue (C60), red (fluorinated zinc phthalocyanine), and green (dicyanovinyl oligothiophene derivative) absorbing molecules. A power conversion efficiency of 4.9 ± 0.2% is obtained for the device having an average transmission of 24% in the visible range.
Penetrating, high-energy synchrotron X-rays are in strong demand, particularly for high-pressure research in physics, chemistry and geosciences, and for materials engineering research under less extreme conditions. A new high-energy wiggler beamline P61 has been constructed to meet this need at PETRA III in Hamburg, Germany. The first part of the paper offers an overview of the beamline front-end components and beam characteristics. The second part describes the performance of the instrumentation and the latest developments at the P61B endstation. Particular attention is given to the unprecedented high-energy photon flux delivered by the ten wigglers of the PETRA III storage ring and the challenges faced in harnessing this amount of flux and heat load in the beam. Furthermore, the distinctiveness of the world's first six-ram Hall-type large-volume press, Aster-15, at a synchrotron facility is described for research with synchrotron X-rays. Additionally, detection schemes, experimental strategies and preliminary data acquired using energy-dispersive X-ray diffraction and radiography techniques are presented.
We present semitransparent small-molecule organic solar cells (OSC) deposited by thermal evaporation onto indium tin oxide (ITO)-coated glass substrates. The devices employ ITO-free ultrathin metal layers as top electrodes, containing 1nm metal surfactant interlayer for improved morphology. Using a bulk heterojunction of zinc phthalocyanine and C60, sandwiched in between doped dedicated transport layers for efficient charge carrier extraction, power conversion efficiencies comparable to conventional OSC with an intransparent thick back electrode and similar device layout are achieved: the semitransparent OSC yield power conversion efficiencies well above 2% with external quantum efficiencies above 30%–40%. Organic light incoupling layers improve the transmission to up to 50% in the visible part of the optical spectrum.
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