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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1.080 Topics available

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693.932 PEOPLE
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Show results for 693.932 people that are selected by your search filters.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (4/4 displayed)

  • 2016Development of a high performance donor-acceptor conjugated polymer – synergy in materials and device optimization37citations
  • 2014Tailored donor-acceptor polymers with an A-D1-A-D2 structure: Controlling intermolecular interactions to enable enhanced polymer photovoltaic devices182citations
  • 2014Organic Solar Cells Using a High-Molecular-Weight Benzodithiophene–Benzothiadiazole Copolymer with an Efficiency of 9.4%citations
  • 2011Band-gap tuning of pendant polymers for organic light-emitting devices and photovoltaic applications24citations

Places of action

Chart of shared publication
Scholes, Fiona
2 / 6 shared
Qin, Tianshi
3 / 4 shared
Chen, Ming
3 / 28 shared
Jones, David J.
2 / 3 shared
Skidmore, Melissa
1 / 3 shared
Chen, Xiwen
2 / 2 shared
Geraghty, Paul
1 / 1 shared
Gao, Mei
3 / 20 shared
Subbiah, Jegadesan
1 / 5 shared
Watkins, Edward
1 / 1 shared
Purushothaman, Balaji
2 / 4 shared
Wong, Wallace
2 / 3 shared
Holmes, Andrew
2 / 2 shared
Pisula, Wojciech
1 / 11 shared
Mullen, Klaus
1 / 2 shared
Watkins, Scott
3 / 8 shared
Baumgarten, Martin
1 / 7 shared
Zajaczkowski, Wojciech
1 / 3 shared
Subbiah, Jeg
1 / 1 shared
Evans, Richard
1 / 3 shared
Gupta, Akhil
1 / 2 shared
Chart of publication period
2016
2014
2011

Co-Authors (by relevance)

  • Scholes, Fiona
  • Qin, Tianshi
  • Chen, Ming
  • Jones, David J.
  • Skidmore, Melissa
  • Chen, Xiwen
  • Geraghty, Paul
  • Gao, Mei
  • Subbiah, Jegadesan
  • Watkins, Edward
  • Purushothaman, Balaji
  • Wong, Wallace
  • Holmes, Andrew
  • Pisula, Wojciech
  • Mullen, Klaus
  • Watkins, Scott
  • Baumgarten, Martin
  • Zajaczkowski, Wojciech
  • Subbiah, Jeg
  • Evans, Richard
  • Gupta, Akhil
OrganizationsLocationPeople

article

Band-gap tuning of pendant polymers for organic light-emitting devices and photovoltaic applications

  • Watkins, Scott
  • Evans, Richard
  • Wilson, Gerry
  • Gupta, Akhil
Abstract

The preparation of a series of novel polymers comprising pendant electro-active “push-pull” chromophores and their performance in solution-processed organic electronic devices is described. The design of the electro-active pendant chromophores was based on the well-known motif of cyano-substituted poly(p-phenylenevinylene). Optical band-gap engineering within this series of polymers was achieved by varying the conjugation length and the electron donor/acceptor functionalities of the pendant chromophores. The introduction of a cyanoimmine group into the electro-active pendant module resulted in a marked narrowing of the optical band-gap compared with the other electro-active pendant chromophores investigated in this work. Bulk heterojunction solar cell devices comprising these polymers were prepared by solution processing blends of each polymer with [6,6]-phenyl-C61-butyric acid methyl ester, and their performance was evaluated by measuring power conversion efficiencies. The best-performing solar cell in this series exhibited a power conversion efficiency of 0.3% and a maximum incident photon-to-current conversion efficiency of 22% and was produced using the polymer in which the electro-active chromophore comprised the cyanoimmine group.

Topics
  • impedance spectroscopy
  • polymer
  • ester
  • power conversion efficiency
  • solution processing