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 (3/3 displayed)

  • 2020Order and Disorder in ABCA′ Tetrablock Terpolymers8citations
  • 2017Thermal processing of diblock copolymer melts mimics metallurgy261citations
  • 2016Cornucopia of Nanoscale Ordered Phases in Sphere-Forming Tetrablock Terpolymers98citations

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Matta, Megan E.
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Dorfman, Kevin D.
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Bates, Frank S.
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Radlauer, Madalyn R.
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Schulze, Morgan W.
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Lewis, Ronald M.
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Chanpuriya, Siddharth
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Lee, Sangwoo
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Fredrickson, Glenn H.
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Delaney, Kris T.
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2020
2017
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Co-Authors (by relevance)

  • Matta, Megan E.
  • Dorfman, Kevin D.
  • Bates, Frank S.
  • Radlauer, Madalyn R.
  • Schulze, Morgan W.
  • Lewis, Ronald M.
  • Chanpuriya, Siddharth
  • Lee, Sangwoo
  • Zhang, Jingwen
  • Fredrickson, Glenn H.
  • Delaney, Kris T.
OrganizationsLocationPeople

article

Order and Disorder in ABCA′ Tetrablock Terpolymers

  • Matta, Megan E.
  • Dorfman, Kevin D.
  • Bates, Frank S.
  • Arora, Akash
  • Radlauer, Madalyn R.
Abstract

<p>Self-assembly of poly(styrene)-block-poly(isoprene)-block-poly(lactide)-block-poly(styrene) (PS-PI-PLA-PS′ or SILS′) tetrablock terpolymers, where the volume fractions of the first three blocks are nearly equivalent, was studied both experimentally and using the self-consistent field theory (SCFT). SCFT indicates that addition of the terminal PS′ chain to a low-molecular-mass, hexagonally packed cylinders forming, SIL precursor can produce a disordered state due to preferential mixing of the polystyrene end-blocks with the PI and PLA midblocks in the SILS′ tetrablock, alleviating the unfavorable contact between the highly incompatible PI and PLA segments. In contrast, SCFT predicts that higher-molar-mass triblock precursors will maintain an ordered morphology upon addition of the terminal PS′ block due to stronger overall segregation strengths. These predictions were tested using three sets of SILS′ polymers that were synthesized based on three precursor SIL triblock polymers differing in total molar mass (14, 30, and 47 kg mol-1) and varying the length of the terminal PS′ chain. In the lowest-molar-mass set of tetrablock polymers, the shift from order to disorder was observed in the materials at ambient temperature as the molar mass of the terminal PS′ block was increased, consistent with SCFT calculations. Disorder with longer S′ chain lengths was not found in the two higher-molar-mass polymer sets; the medium-molar-mass set showed both microphase separation and long-range order based on transmission electron microscopy (TEM) and small-angle X-ray scattering (SAXS), while the largest of these block polymers microphase separated but showed limited long-range order. The combination of the experimental and theoretical results presented in this work provides insights into the self-assembly of ABCA′-type polymers and highlights potential complications that arise from frustration in accessing well-ordered materials.</p>

Topics
  • morphology
  • polymer
  • theory
  • strength
  • transmission electron microscopy
  • forming
  • small angle x-ray scattering
  • self-assembly