TY - JOUR
T1 - What dielectric spectroscopy can tell us about supramolecular networks⋆
AU - Tress, Martin
AU - Xing, Kunyue
AU - Ge, Sirui
AU - Cao, Pengfei
AU - Saito, Tomonori
AU - Sokolov, Alexei
N1 - Publisher Copyright:
© 2019, EDP Sciences, Società Italiana di Fisica and Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2019/10/1
Y1 - 2019/10/1
N2 - Abstract.: Polymers which can form supramolecular networks are a promising class of materials to provide highly sought-after properties such as self-healing, enhanced mechanical strength, super-stretchability as well as easy recyclability. However, due to the vast range of possible chemical structures it is very demanding to optimize these materials for the desired performance. Consequently, a detailed understanding of the molecular processes that govern the macroscopic properties is paramount to their technological application. Here we discuss some telechelic model systems with hydrogen-bonding end groups and how dielectric spectroscopy in combination with linear oscillatory shear rheology helped to understand the association mechanism on a molecular scale, and verify the model of bond-lifetime renormalization. Furthermore, we analyze a limitation of these H-bonding polymers, namely that there is a trade-off between high plateau modulus and long terminal relaxation time --both cannot be maximized at the same time. Finally, we show how more complex end groups phase separate from the main chain melt and thus lead to a more sophisticated rheological behavior which can overcome that limitation. Graphical abstract: [Figure not available: see fulltext.].
AB - Abstract.: Polymers which can form supramolecular networks are a promising class of materials to provide highly sought-after properties such as self-healing, enhanced mechanical strength, super-stretchability as well as easy recyclability. However, due to the vast range of possible chemical structures it is very demanding to optimize these materials for the desired performance. Consequently, a detailed understanding of the molecular processes that govern the macroscopic properties is paramount to their technological application. Here we discuss some telechelic model systems with hydrogen-bonding end groups and how dielectric spectroscopy in combination with linear oscillatory shear rheology helped to understand the association mechanism on a molecular scale, and verify the model of bond-lifetime renormalization. Furthermore, we analyze a limitation of these H-bonding polymers, namely that there is a trade-off between high plateau modulus and long terminal relaxation time --both cannot be maximized at the same time. Finally, we show how more complex end groups phase separate from the main chain melt and thus lead to a more sophisticated rheological behavior which can overcome that limitation. Graphical abstract: [Figure not available: see fulltext.].
KW - Topical issue: Dielectric Spectroscopy Applied to Soft Matter
UR - http://www.scopus.com/inward/record.url?scp=85073584809&partnerID=8YFLogxK
U2 - 10.1140/epje/i2019-11897-4
DO - 10.1140/epje/i2019-11897-4
M3 - Article
C2 - 31624934
AN - SCOPUS:85073584809
SN - 1292-8941
VL - 42
JO - European Physical Journal E
JF - European Physical Journal E
IS - 10
M1 - 133
ER -