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Conformation and dynamics of wet tangentially-driven active filaments
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We explore the impact of hydrodynamic interactions on the conformational and dynamical properties of wet tangentially-driven active polymers using multiparticle collision dynamics simulations. By analyzing active filaments with varying degrees of flexibility, we find that fluid-mediated interactions significantly influence both their conformation and dynamics. These interactions cause polymer conformations to shrink relative to their dry counterparts, especially for semiflexible polymers at high activity levels, where the average size of wet chains becomes nearly three times smaller, due to local buckling of wet polymers. This hydrodynamic-induced shrinkage is a hallmark of active polymers, as fluid-mediated interactions do not affect conformational properties of passive polymers. Furthermore, for tangentially-driven polymers where activity and conformation are coupled, hydrodynamic interactions significantly enhance the orientational and translational dynamics compared to their dry counterparts.
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Cited by 2 Pith papers
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Computational study of active polar polymer melts: from active reptation to activity induced local alignment
In simulated polymer melts with tangential self-propulsion, chain diffusion becomes independent of molecular weight at low activity, and at higher activity chains develop stretched tubes and dynamic local alignment.
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Locally tuned hydrodynamics of active polymer chains
Simulations show that the location of the counterforce on the fluid, not just the active monomer, determines whether an active polymer creates pusher or puller flow fields, and that stiff chains transmit forces in a w...
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