Is the active suspension in a complex viscoelastic fluid more chaotic or more ordered?
Yuan Zhou, Qingzhi Zou, Ignacio Pagonabarraga, Kaihuan Zhang, Kai Qi
TL;DR
The paper investigates how a viscoelastic polymeric medium influences collective motion of microswimmers (squirmers) using lattice Boltzmann simulations. It reports a pronounced increase in orientational polarization in polymer solutions at intermediate swimmer concentrations, up to factors of $26$ for neutral squirmers and $5$ for pullers, compared with Newtonian fluids. The authors identify a hydrodynamic feedback mechanism: squirmer flows stretch polymers, which align with the swimmers and act as soft confinements, reinforcing swimmer orientation and polarization via hydrodynamic and steric interactions. They validate this by a strong correlation between polarization and a polymer–swimmer alignment parameter, and show that neither squirmer–polymer entanglement nor polymer–polymer entanglement explains the enhancement. These findings provide a framework for controlling active matter via polymer-mediated interactions and highlight the role of polymer deformation in complex fluids.
Abstract
The habitat of microorganisms is typically complex and viscoelastic. A natural question arises: Do polymers in a suspension of active swimmers enhance chaotic motion or promote orientational order? We address this issue by performing lattice Boltzmann simulations of squirmer suspensions in polymer solutions. At intermediate swimmer volume fractions, comparing to the Newtonian counterpart, polymers enhance polarization by up to a factor of 26 for neutral squirmers and 5 for pullers, thereby notably increasing orientational order. This effect arises from hydrodynamic feedback mechanism: squirmers stretch and align polymers, which in turn reinforce swimmer orientation and enhance polarization via hydrodynamic and steric interactions. The mechanism is validated by a positive correlation between polarization and a defined polymer-swimmer alignment parameter. Our findings establish a framework for understanding collective motion in complex fluids and suggest strategies for controlling active systems via polymer-mediated interactions.
