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)

  • 2021Multiscale modeling and applications of bioinspired materials with gyroid structures10citations
  • 2019Molecular dynamics study of the mechanical properties of polydisperse pressure-sensitive adhesives5citations

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Chart of shared publication
Buehler, Markus J.
2 / 9 shared
Martin-Martinez, Francisco J.
2 / 6 shared
Jung, Gang Seob
1 / 1 shared
Hamm, Marc
1 / 1 shared
Paul, Charles W.
1 / 1 shared
Barreiro, Diego López
1 / 1 shared
Jin, Kai
1 / 1 shared
Chart of publication period
2021
2019

Co-Authors (by relevance)

  • Buehler, Markus J.
  • Martin-Martinez, Francisco J.
  • Jung, Gang Seob
  • Hamm, Marc
  • Paul, Charles W.
  • Barreiro, Diego López
  • Jin, Kai
OrganizationsLocationPeople

article

Molecular dynamics study of the mechanical properties of polydisperse pressure-sensitive adhesives

  • Qin, Zhao
  • Hamm, Marc
  • Paul, Charles W.
  • Buehler, Markus J.
  • Barreiro, Diego López
  • Martin-Martinez, Francisco J.
  • Jin, Kai
Abstract

<p>Amorphous polymers are one of the primary materials used in pressure sensitive adhesives (PSAs). Their design can be aided by a better understanding of the mechanisms governing the molecular and mesoscopic scale behavior. This work presents a molecular dynamics study of the toughness and failure modes of a coarse-grained polydisperse PSA model in probe peel tests, achieved by varying the crosslinking density and locations. Generally, the toughness of polydisperse PSAs increases at a crosslinking density of 0.5%, compared to the non-crosslinked structure, and declines at higher crosslinking densities, which also changes the failure mode from cohesive to adhesive. The performance is affected by the length of the polymer chains that form crosslinks, although high crosslinking densities make the system less sensitive to effects related to its polydispersity. The results herewith presented display an optimal performance when 35–45% of the particles in the system belong to the giant component of the PSA network. This is achieved at crosslinking densities of 0.5–1.0%, depending on the length of the chains that are allowed to crosslink.</p>

Topics
  • density
  • impedance spectroscopy
  • polymer
  • amorphous
  • molecular dynamics
  • laser emission spectroscopy
  • polydispersity