Dynamical networking of polymer networks with dedicated cross-linker particles

This paper extends a field-theoretical dynamical networking formalism for mesoscopic polymer dynamics to explicitly include dedicated cross-linker particles. Cross-linkers are represented within a Martin-Siggia-Rose generating functional and reversibly coupled to polymers through Gaussian networking fields, enabling an approximation scheme that reduces their degrees of freedom while remaining compatible with polymer dynamics. The framework is applied to a two-species polymer system in which intra- and inter-species cross-linking are assigned different statistical advantages. Effective networking potentials are derived and used to calculate correlation functions and dynamic structure factors. To validate these results, molecular dynamics simulations of semi-flexible polymers with reversible intra- and inter-species cross-linking are performed. Simulations show that cross-linking decreases polymer persistence lengths and local alignment, and the resulting trajectories yield dynamic structure factors consistent with theoretical predictions. Qualitative comparison reveals that in both approaches, cross-linking broadens the diffusive peaks and enhances the high-frequency tails of the structure factors. Together, theory and simulation provide complementary insights into the dynamics of cross-linked polymers, establishing a tractable framework that captures essential features observed in experiments and offering a basis for exploring more complex synthetic and biological networks.

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Publication Details

Journal
The European Physical Journal E
Published
2026-04-01
DOI
https://doi.org/10.1140/epje/s10189-026-00568-w
Primary Topic
Block Copolymer Self-Assembly
Type
article
Field-Weighted Citation Impact
0.00

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article

Dynamical networking of polymer networks with dedicated cross-linker particles

K.K. Müller-Nedebock, Giuseppe Pellicane, Nadine du Toit
The European Physical Journal E
Block Copolymer Self-Assembly
article

Dynamical networking of polymer networks with dedicated cross-linker particles

K.K. Müller-Nedebock, Giuseppe Pellicane, Nadine du Toit
article en

Abstract

This paper extends a field-theoretical dynamical networking formalism for mesoscopic polymer dynamics to explicitly include dedicated cross-linker particles. Cross-linkers are represented within a Martin-Siggia-Rose generating functional and reversibly coupled to polymers through Gaussian networking fields, enabling an approximation scheme that reduces their degrees of freedom while remaining compatible with polymer dynamics. The framework is applied to a two-species polymer system in which intra- and inter-species cross-linking are assigned different statistical advantages. Effective networking potentials are derived and used to calculate correlation functions and dynamic structure factors. To validate these results, molecular dynamics simulations of semi-flexible polymers with reversible intra- and inter-species cross-linking are performed. Simulations show that cross-linking decreases polymer persistence lengths and local alignment, and the resulting trajectories yield dynamic structure factors consistent with theoretical predictions. Qualitative comparison reveals that in both approaches, cross-linking broadens the diffusive peaks and enhances the high-frequency tails of the structure factors. Together, theory and simulation provide complementary insights into the dynamics of cross-linked polymers, establishing a tractable framework that captures essential features observed in experiments and offering a basis for exploring more complex synthetic and biological networks.

The European Physical Journal EVol. 49(4)
University of Messina (IT), Stellenbosch University (ZA), National Institute for Theoretical Physics (ZA), University of KwaZulu-Natal (ZA)
National Research Foundation, Universiteit Stellenbosch, Center for High Performance Computing, Engineering and Physical Sciences Research Council, Division of Mathematical Sciences
Peace, Justice and strong institutions
Openalex Percentile: Top 28%
Block Copolymer Self-Assembly
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