The interplay between activity and confinement leads to unexpected features in suspensions of active polymer chains and rings
ORAL · Invited
Abstract
In two dimensions [2], active filaments can either be in an open chain state (at low activity) or form spirals (at high activity), independently on their bending rigidity and the model used to implement activity along the chain. When considering length polydispersity, filament length is the control parameter for hierarchical self-assembly [3,4], displaying a collective wrapping mechanism absent in length monodisperse filaments.
Active filaments confined in a cylindrical channel show anomalous behaviours under different confinement and activity: the ratio between the end-to-end distance of passive polymer chains in channels and in bulk is broken by activity [5].
While passive polymers confined in corrugated channels display multiple dynamical features upon increasing their degree of polymerization. Such behaviour can be described via a Fick-Jacobs approach which can be used to design porous filters capable of separating polymers by their size [6].
The interplay between activity, topology, and confinement can lead to a spontaneous segregation from an initially one-component solution. In a suspension of active polymer rings confined between two parallel plates, a self-organized dynamical state emerges, characterized by the coexistence of slowly diffusing clusters of rotating disks and faster rings moving in between them [7]. This self-organization displays a non-monotonic dependence on the activity-induced entanglement, since increasing entanglement interferes with the planar conformations required to form aligned stacks [8].
*C.V. acknowledges fundings IHRC22/00002 and Proyecto PID2022-140407NB-C21 funded by MCIN/AEI /10.13039/501100011033 and FEDER, UE.
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Publication: [1] "Coil-to-globule collapse of active polymers: a Rouse perspective"
P Malgaretti, E. Locatelli and C.Valeriani
Molecular Physics, 123 "Giovanni Ciccotti: A Renaissance Physicist", Issue 7-8 (2025)
[2] "Exploring active polymer behavior: tangential versus push-pull models in two dimensions"
G Janzen, J P Miranda, J Martin-Roca, C Valeriani and D.Matoz Fernandez
J. Chem. Phys. 162, 114905 (2025)
[3] "Active bivalent patchy colloids"
C. Landi, J. Russo, F. Sciortino and C Valeriani
Soft Matter, 2025,21, 45-54
[4] "Collective filament wrapping and nested spiral formation in active polydisperse systems
"C Landi, G Janzen, F Sciortino, J Russo, C Valeriani and D Matoz-Fernandez
Soft Matter, accepted (2025)
[5]"Tangentially Active Polymers in Cylindrical Channels"
J Martín-Roca, E Locatelli, V Bianco, P Malgaretti and C Valeriani
SciPost Phys. 17, 107 (2024)
[6]"Nonmonotonous Translocation Time of Polymers across Pores",
E Locatelli, V Bianco, C Valeriani and P Malgaretti,
Phys. Rev. Lett. 131, 048101 (2023)
[7]Self-organized states of solutions of active ring polymers in bulk and under confinement
J Miranda, E. Locatelli and C.Valeriani
J. Chem. Theory Comput. 2024, 20, 4, 1636–1645
[8]Geometrical entanglement and alignment regulate self-prganization in active ring polymer suspensions,
J P Miranda, E Locatelli, C Micheletti, D Levis and C Valeriani
J Chem Theory Computation in press (2025)
Presenters
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Chantal Valeriani
- Universidad Complutense de Madrid