Principal Investigator

Prof. Dr. Kurt Kremer
Prof. Dr. Kurt Kremer
Scientific member (Director)
Phone:06131 - 379 141


Project Coordinator

Dr. Kostas Daoulas
Dr. Kostas Daoulas
Project Leader
Phone:+49 6131 379 218

Researcher-ID: L-8771-2013

Recent Publications

A coarse-grained polymer model for studying the glass transition, Hsiao-Ping Hsu, Kurt Kremer, J. Chem. Phys. 150, 091101 (2019) [pdf]

Threading of unconcatenated ring polymers at high concentrations: double-folded vs. time-equilibrated structures, Jan Smrek, Kurt Kremer, Angelo Rosa, ACS Macro Lett., Accepted Article (2018) [pdf]

Hierarchical modelling of polystyrene melts: from soft blobs to atomistic resolution, Guojie Zhang, Anthony Chazirakis, Vagelis A. Harmandaris, Torsten Stuehn, Kostas Ch. Daoulas, Kurt Kremer, Soft Matter 15, 289-302 (2019) [pdf]


Structure-Process-Property Relations in Soft Matter – a Computational Physics Approach      


Principal Investigator:
Prof. Dr. Kurt Kremer

Project Coordinator:
Dr. Kostas Daoulas

Duration: 5 years
Starting date: February 2014

From cell biology to polymer photovoltaics, (self-)assembly processes that give rise to morphology and functionality result from non-equilibrium processes, which are driven by both, external forces, such as flow due to pressure gradients, inserting energy, or manipulation on a local molecular level, or internal forces, such as relaxation into a state of lower free energy. The resulting material is arrested in a metastable state. Most previous work has focused on the relationship between structure and properties, while insight into the guiding principles governing the formation of a (new) material, has been lacking. However, a comprehensive molecular level understanding of non-equilibrium assembly would allow for control and manipulation of material processes and their resulting properties. This lag of knowledge can be traced to the formidable challenge in obtaining a molecular picture of non-equilibrium assembly. Non-equilibrium processes have been studied extensively on a macroscopic level by non-equilibrium thermodynamics. We take a novel route approaching the challenge from a molecular point of view. Recent advances in experimental, but especially computational modeling, now allow to follow (supra-) molecular structural evolution across the range of length and time scales necessary to comprehend, and ultimately control and manipulate macroscopic functional properties of soft matter at the molecular level. Soft matter is particularly suited for that approach, as it is “slow” and easy to manipulate. We take the computational physics route, based on simulations on different levels of resolution (all atom, coarse grained, continuum) in combination with recent multiscale and adaptive resolution techniques. This work will initiate the way towards a paradigm change from conventional Structure Property Relations (SPR) to molecularly based Structure Process Property Relations (SPPR).

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