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Träfflista för sökning "L773:2367 198X srt2:(2018)"

Sökning: L773:2367 198X > (2018)

  • Resultat 1-4 av 4
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1.
  • Bose, Sourav, et al. (författare)
  • Optical Lithography Patterning of SiO2 Layers for Interface Passivation of Thin Film Solar Cells
  • 2018
  • Ingår i: Solar RRL. - : Wiley. - 2367-198X. ; 2:12
  • Tidskriftsartikel (refereegranskat)abstract
    • Ultrathin Cu(In,Ga)Se-2 solar cells are a promising way to reduce costs and to increase the electrical performance of thin film solar cells. An optical lithography process that can produce sub-micrometer contacts in a SiO2 passivation layer at the CIGS rear contact is developed in this work. Furthermore, an optimization of the patterning dimensions reveals constrains over the features sizes. High passivation areas of the rear contact are needed to passivate the CIGS interface so that high performing solar cells can be obtained. However, these dimensions should not be achieved by using long distances between the contacts as they lead to poor electrical performance due to poor carrier extraction. This study expands the choice of passivation materials already known for ultrathin solar cells and its fabrication techniques.
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2.
  • Duan, Chunhui, et al. (författare)
  • Improving Performance of All-Polymer Solar Cells Through Backbone Engineering of Both Donors and Acceptors
  • 2018
  • Ingår i: Solar RRL. - : Wiley. - 2367-198X. ; 2:12
  • Tidskriftsartikel (refereegranskat)abstract
    • All-polymer solar cells (APSCs), composed of semiconducting donor and acceptor polymers, have attracted considerable attention due to their unique advantages compared to polymer-fullerene-based devices in terms of enhanced light absorption and morphological stability. To improve the performance of APSCs, the morphology of the active layer must be optimized. By employing a random copolymerization strategy to control the regularity of the backbone of the donor polymers (PTAZ-TPDx) and acceptor polymers (PNDI-Tx) the morphology can be systematically optimized by tuning the polymer packing and crystallinity. To minimize effects of molecular weight, both donor and acceptor polymers have number-average molecular weights in narrow ranges. Experimental and coarse-grained modeling results disclose that systematic backbone engineering greatly affects the polymer crystallinity and ultimately the phase separation and morphology of the all-polymer blends. Decreasing the backbone regularity of either the donor or the acceptor polymer reduces the local crystallinity of the individual phase in blend films, affording reduced short-circuit current densities and fill factors. This two-dimensional crystallinity optimization strategy locates a PCE maximum at highest crystallinity for both donor and acceptor polymers. Overall, this study demonstrates that proper control of both donor and acceptor polymer crystallinity simultaneously is essential to optimize APSC performance.
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3.
  • Hua, Yong, et al. (författare)
  • Composite Hole-Transport Materials Based on a Metal-Organic Copper Complex and Spiro-OMeTAD for Efficient Perovskite Solar Cells
  • 2018
  • Ingår i: Solar RRL. - : WILEY-V C H VERLAG GMBH. - 2367-198X. ; 2:5
  • Tidskriftsartikel (refereegranskat)abstract
    • Spiro-OMeTAD has been the most commonly used hole-transport material in perovskite solar cells. However, this material shows intrinisic drawbacks, such as low hole mobility and conductivity in its pristine form, as well as self-aggregation when deposited as thin film. These are not beneficial properties for efficient hole transport and extraction. In order to address these issues, we have designed a new type of composite hole-transport materials based on a new metal-organic copper complex (CuH) and Spiro-OMeTAD. The incorporation of the molecularly bulky HTM CuH into the Spiro-OMeTAD material efficiently improves the hole mobility and suppresses the aggregation in the Spiro-OMeTAD film. As a result, the conversion efficiencies obtained for perovskite solar cells based on the composite HTM system reached as high as 18.83%, which is superior to solar cells based on the individual hole-transport materials CuH (15.75%) or Spiro-OMeTAD (14.47%) under the same working conditions. These results show that composite HTM systems may constitute an effective strategy to further improve the efficiency of perovskite solar cells.
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4.
  • Wang, Chuanfei, 1986-, et al. (författare)
  • Relationship of Ionization Potential and Oxidation Potential of Organic Semiconductor Films Used in Photovoltaics
  • 2018
  • Ingår i: Solar RRL. - : Wiley-Blackwell. - 2367-198X. ; 2:9
  • Tidskriftsartikel (refereegranskat)abstract
    • Ultraviolet photoelectron spectroscopy (UPS) and cyclic voltammetry (CV) are employed to measure energy levels for charge transport in organic semiconductor films. A series of classical molecules/polymers used in organic bulk heterojunction solar cells are deposited on platinum substrates/electrodes to form thin films and a linear relationship of vertical ionization potential (IP) measured by UPS and relative oxidation potential (Eox) obtained by CV is found, with a slope equal to unity. The intercept varies with the different reference redox couples and repeated potential sweep numbers during experiment processes. The relationship provides for an easy conversion of values obtained by the two techniques and correlates well with device parameters. The precision in the CV-derived IP values is not sufficient, however, to enable precise design of energy level alignment at heterojunction and the approach does not improve upon the current ?best practice? for obtaining donor ionization potential?acceptor electron affinity gaps at heterojunctions.
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  • Resultat 1-4 av 4

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