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 (2/2 displayed)

  • 2010Controlling morphology and photovoltaic properties by chemical structure in copolymers of cyclopentadithiophene and thiophene segments3citations
  • 2008The synthesis and photovoltaic performance of regioregular poly[3-(n-butoxymethyl)thiophene]7citations

Places of action

Chart of shared publication
Wienk, M. M.
2 / 54 shared
Bijleveld, J. C.
1 / 8 shared
Janssen, René A. J.
2 / 151 shared
Leenen, M. A. M.
1 / 3 shared
Zoombelt, A. P.
1 / 6 shared
Chart of publication period
2010
2008

Co-Authors (by relevance)

  • Wienk, M. M.
  • Bijleveld, J. C.
  • Janssen, René A. J.
  • Leenen, M. A. M.
  • Zoombelt, A. P.
OrganizationsLocationPeople

article

Controlling morphology and photovoltaic properties by chemical structure in copolymers of cyclopentadithiophene and thiophene segments

  • Wienk, M. M.
  • Turon, M. Fonrodona
  • Bijleveld, J. C.
  • Janssen, René A. J.
Abstract

A series of polythiophenes (PTn) based on dialkyl-cyclopentadithiophene (CPDT) units alternating with short un-substituted thiophene segments of length n (n being the number of thiophenes) along the chain has been synthesized to control the morphology of PTn:PCBM blends for solar cell applications via the chemical structure of the polymer rather than via (post) processing conditions. The degree of phase separation in PTn:PCBM blends can be controlled via n, because with increase in n the number of solublizing side chains per thiophene is reduced. For the most soluble derivative, PT0, we find that PCBM crystallizes first, while for the least soluble version, PT3, polymer aggregation prevails. The most intimately mixed morphology and best solar cells were obtained for PT2, which exhibits a power conversion efficiency (PCE) of about 1.5% under AM1.5G conditions when mixed with PCBM. Although the final PCE is moderate, the study represents an example of a rational approach towards morphology control via chemical structure, rather than via processing

Topics
  • impedance spectroscopy
  • morphology
  • phase
  • copolymer
  • power conversion efficiency