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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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
693.932 People People

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (7/7 displayed)

  • 2020Spatial Control of the Self-assembled Block Copolymer Domain Orientation and Alignment on Photopatterned Surfaces8citations
  • 2020Unusual Thermal Properties of Certain Poly(3,5-disubstituted styrene)s3citations
  • 2018Shewanella oneidensis as a living electrode for controlled radical polymerization88citations
  • 2015A facile synthesis of catechol‐functionalized poly(ethylene oxide) block and random copolymers15citations
  • 2008Polydispersity and block copolymer self-assembly438citations
  • 2008Theory of polydisperse block copolymer melts77citations
  • 2005Influence of polydispersity on the self-assembly of diblock copolymers291citations

Places of action

Chart of shared publication
Cheng, Joy Y.
1 / 1 shared
Blachut, Gregory
1 / 7 shared
Asano, Yusuke
2 / 5 shared
Kline, R. Joseph
1 / 3 shared
Maher, Michael J.
2 / 12 shared
Sanders, Daniel P.
1 / 1 shared
Bates, Christopher M.
1 / 5 shared
Sunday, Daniel F.
1 / 1 shared
Carlson, Matthew C.
1 / 2 shared
Willson, C. Grant
2 / 8 shared
Callan, Devon H.
1 / 1 shared
Rettner, Charles T.
1 / 2 shared
Liu, Philip
1 / 1 shared
Baiz, Carlos R.
1 / 1 shared
Kim, Ji Yeon
1 / 2 shared
Zhu, Qingjun
1 / 3 shared
Mapesa, Emmanuel U.
1 / 1 shared
Sangoro, Joshua R.
1 / 3 shared
Ha, Heonjoo
1 / 6 shared
Cater, Henry L.
1 / 1 shared
Koh, Jai Hyun
1 / 2 shared
Kim, Sung Soo
1 / 4 shared
Dundas, Christopher M.
1 / 1 shared
Fan, Gang
1 / 1 shared
Keitz, Benjamin K.
1 / 1 shared
Graham, Austin J.
1 / 1 shared
Latimer, Allegra A.
1 / 3 shared
Mcgrath, Alaina J.
1 / 2 shared
Hawker, Craig J.
1 / 23 shared
Hudson, Zachary M.
1 / 3 shared
Lundberg, Pontus
1 / 1 shared
Mattson, Kaila M.
1 / 1 shared
Meuler, Adam J.
1 / 6 shared
Matsen, Mark W.
1 / 4 shared
Chart of publication period
2020
2018
2015
2008
2005

Co-Authors (by relevance)

  • Cheng, Joy Y.
  • Blachut, Gregory
  • Asano, Yusuke
  • Kline, R. Joseph
  • Maher, Michael J.
  • Sanders, Daniel P.
  • Bates, Christopher M.
  • Sunday, Daniel F.
  • Carlson, Matthew C.
  • Willson, C. Grant
  • Callan, Devon H.
  • Rettner, Charles T.
  • Liu, Philip
  • Baiz, Carlos R.
  • Kim, Ji Yeon
  • Zhu, Qingjun
  • Mapesa, Emmanuel U.
  • Sangoro, Joshua R.
  • Ha, Heonjoo
  • Cater, Henry L.
  • Koh, Jai Hyun
  • Kim, Sung Soo
  • Dundas, Christopher M.
  • Fan, Gang
  • Keitz, Benjamin K.
  • Graham, Austin J.
  • Latimer, Allegra A.
  • Mcgrath, Alaina J.
  • Hawker, Craig J.
  • Hudson, Zachary M.
  • Lundberg, Pontus
  • Mattson, Kaila M.
  • Meuler, Adam J.
  • Matsen, Mark W.
OrganizationsLocationPeople

article

Polydispersity and block copolymer self-assembly

  • Meuler, Adam J.
  • Lynd, Nathaniel A.
Abstract

<p>Block copolymers consist of two or more chemically distinct polymers that are covalently bound. These materials self-assemble into fascinating mesostructures with features on the nanometer length scale and have been the subject of intense research interest for about four decades. These efforts have generally focused on model block copolymer systems where the molecular weight distributions of all blocks are very narrow. Traditionally, many block copolymer systems have been prepared by living anionic polymerization and thus usually exhibit narrow molecular weight distributions in all blocks. Therefore, the assumption of monodisperse blocks that greatly simplifies theoretical work is on solid experimental ground. Preparation of block copolymers with relatively broad molecular weight distributions in one or more block has become increasingly common, however, as use of synthetic techniques such as controlled radical polymerization has proliferated. Advances in these techniques have increased the number of monomers readily incorporated into block copolymers and potentially will drive commercial costs down. These polymerization strategies often, however, result in broader molecular weight distributions than are typically obtained using living anionic, cationic, or metal-catalyzed techniques; understanding polydispersity effects should aid deployment of these block copolymers in advanced materials applications. This review describes both theoretical and experimental investigations of the effects of polydispersity on the melt-phase morphological behavior of block copolymers. The summary includes research efforts focused on both continuous molecular weight distributions and multicomponent blends. The review concludes with a summary and outlook on the potential utility of polydispersity as a tool to tune the morphological behavior of block copolymers.</p>

Topics
  • impedance spectroscopy
  • melt
  • molecular weight
  • copolymer
  • block copolymer
  • polydispersity
  • self-assembly