Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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Materials Map under construction

The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (8/8 displayed)

  • 2024Weak dispersion of exciton Landé factor with band gap energy in lead halide perovskites: approximate compensation of the electron and hole dependences12citations
  • 2024The strength of uncoated and coated ultra-thin flexible glass under cyclic load3citations
  • 2021Local Shielding Gas Supply in Remote Laser Beam Welding2citations
  • 2021Compression Fatigue Testing Setups for Composites—A Review19citations
  • 2019Favorable Mixing Thermodynamics in Ternary Polymer Blends for Realizing High Efficiency Plastic Solar Cells47citations
  • 2019Charge Carriers Are Not Affected by the Relatively Slow-Rotating Methylammonium Cations in Lead Halide Perovskite Thin Films19citations
  • 2019Charge Carriers Are Not Affected by the Relatively Slow-Rotating Methylammonium Cations in Lead Halide Perovskite Thin Films19citations
  • 2019Charge Carriers Are Not Affected by the Relatively Slow-Rotating Methylammonium Cations in Lead Halide Perovskite Thin Films.citations

Places of action

Chart of shared publication
Sapega, Victor F.
1 / 1 shared
Dirin, Dmitry N.
1 / 37 shared
Höcker, Julian
1 / 2 shared
Kirstein, Erik
1 / 5 shared
Kudlacik, Dennis
1 / 5 shared
Zhukov, Evgeny A.
1 / 4 shared
Yakovlev, Dmitri R.
1 / 10 shared
Kopteva, Natalia E.
1 / 2 shared
Hordiichuk, Oleh
1 / 6 shared
Kalitukha, Ina V.
1 / 1 shared
Crooker, Scott A.
1 / 2 shared
Kovalenko, Maksym V.
1 / 195 shared
Dyakonov, Vladimir
5 / 20 shared
Bayer, Manfred
1 / 15 shared
Preußner, Thomas
1 / 3 shared
Rädlein, Edda
1 / 8 shared
Langgemach, Wiebke
1 / 2 shared
Ehrhardt, Manuela
1 / 1 shared
Schricker, Klaus
1 / 16 shared
Bergmann, Jean Pierre
1 / 54 shared
Hausmann, Joachim
1 / 2 shared
Li, Ning
1 / 16 shared
Spiecker, Erdmann
1 / 70 shared
Ameri, Tayebeh
1 / 18 shared
Portale, Giuseppe, A.
1 / 57 shared
Perea, Jose Dario
1 / 1 shared
Sperlich, Andreas
1 / 3 shared
Loi, Maria Antonietta
1 / 73 shared
Salvador, Michael
1 / 4 shared
Kahmann, Simon
1 / 30 shared
Gasparini, Nicola
1 / 20 shared
Brabec, Cj
1 / 407 shared
Rechberger, Stefanie
1 / 5 shared
De Angelis, Filippo
2 / 32 shared
Caselli, V. M.
1 / 3 shared
Meggiolaro, Daniele
3 / 27 shared
Mosconi, Edoardo
3 / 34 shared
Stranks, Samuel D.
3 / 101 shared
Hutter, E. M.
1 / 5 shared
Savenije, T. J.
1 / 12 shared
Fischer, Mathias
3 / 5 shared
Savenije, Tom J.
2 / 36 shared
Angelis, Filippo De
1 / 30 shared
Hutter, Eline M.
2 / 33 shared
Caselli, Valentina M.
2 / 12 shared
Chart of publication period
2024
2021
2019

Co-Authors (by relevance)

  • Sapega, Victor F.
  • Dirin, Dmitry N.
  • Höcker, Julian
  • Kirstein, Erik
  • Kudlacik, Dennis
  • Zhukov, Evgeny A.
  • Yakovlev, Dmitri R.
  • Kopteva, Natalia E.
  • Hordiichuk, Oleh
  • Kalitukha, Ina V.
  • Crooker, Scott A.
  • Kovalenko, Maksym V.
  • Dyakonov, Vladimir
  • Bayer, Manfred
  • Preußner, Thomas
  • Rädlein, Edda
  • Langgemach, Wiebke
  • Ehrhardt, Manuela
  • Schricker, Klaus
  • Bergmann, Jean Pierre
  • Hausmann, Joachim
  • Li, Ning
  • Spiecker, Erdmann
  • Ameri, Tayebeh
  • Portale, Giuseppe, A.
  • Perea, Jose Dario
  • Sperlich, Andreas
  • Loi, Maria Antonietta
  • Salvador, Michael
  • Kahmann, Simon
  • Gasparini, Nicola
  • Brabec, Cj
  • Rechberger, Stefanie
  • De Angelis, Filippo
  • Caselli, V. M.
  • Meggiolaro, Daniele
  • Mosconi, Edoardo
  • Stranks, Samuel D.
  • Hutter, E. M.
  • Savenije, T. J.
  • Fischer, Mathias
  • Savenije, Tom J.
  • Angelis, Filippo De
  • Hutter, Eline M.
  • Caselli, Valentina M.
OrganizationsLocationPeople

article

Favorable Mixing Thermodynamics in Ternary Polymer Blends for Realizing High Efficiency Plastic Solar Cells

  • Li, Ning
  • Spiecker, Erdmann
  • Ameri, Tayebeh
  • Portale, Giuseppe, A.
  • Perea, Jose Dario
  • Sperlich, Andreas
  • Loi, Maria Antonietta
  • Salvador, Michael
  • Kahmann, Simon
  • Dyakonov, Vladimir
  • Gasparini, Nicola
  • Brabec, Cj
  • Rechberger, Stefanie
  • Baumann, Andreas
Abstract

Ternary blends with broad spectral absorption have the potential to increase charge generation in organic solar cells but feature additional complexity due to limited intermixing and electronic mismatch. Here, a model system comprising the polymers poly[5,5-bis(2-butyloctyl)-(2,2-bithiophene)-4,4-dicarboxylate-alt-5,5-2,2-bithiophene] (PDCBT) and PTB7-Th and PC70BM as an electron accepting unit is presented. The power conversion efficiency (PCE) of the ternary system clearly surpasses the performance of either of the binary systems. The photophysics is governed by a fast energy transfer process from PDCBT to PTB7-Th, followed by electron transfer at the PTB7-Th:fullerene interface. The morphological motif in the ternary blend is characterized by polymer fibers. Based on a combination of photophysical analysis, GIWAXS measurements and calculation of the intermolecular parameter, the latter indicating a very favorable molecular affinity between PDCBT and PTB7-Th, it is proposed that an efficient charge generation mechanism is possible because PTB7-Th predominantly orients around PDCBT filaments, allowing energy to be effectively relayed from PDCBT to PTB7-Th. Fullerene can be replaced by a nonfullerene acceptor without sacrifices in charge generation, achieving a PCE above 11%. These results support the idea that thermodynamic mixing and energetics of the polymer-polymer interface are critical design parameter for realizing highly efficient ternary solar cells with variable electron acceptors.

Topics
  • impedance spectroscopy
  • power conversion efficiency
  • polymer blend