Chemically symmetric and asymmetric self-driven rigid dumbbells in 2D polymer gel

Abstract

We employ computer simulations to unveil the translational and rotational dynamics of the self-driven chemically symmetric and asymmetric rigid dumbbells in two-dimensional polymer gel. Our results show that activity or the self-propulsion always enhances the dynamics of the dumbbells. Making the self-propelled dumbbell chemically asymmetric leads to further enhancement in dynamics. Additionally, the direction of self-propulsion is a key factor for the chemically asymmetric dumbbells, where self-propulsion towards the non-sticky half of the dumbbell results in faster translational and rotational dynamics compare to the case with the self-propulsion towards the sticky half of the dumbbell. Our analyses show that both the symmetric and asymmetric passive rigid dumbbells get trapped inside the mesh of the polymer gel, but the chemical asymmetry always facilitates mesh to mesh motion of the dumbbell and it is even more pronounced when the dumbbell is self-propelled. This results multiple peaks in the van Hove function with increasing self-propulsion. In a nutshell, we believe that our in silico study can guide the researchers design efficient artificial microswimmers possessing potential applications in site-specific delivery.

Small changes in the title, texts, new references added, to appear in Soft Matter

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Cited by in corpus (2)

• Dynamics of self-propelled tracer particles inside a polymer network
• Escape dynamics of a self-propelled nanorod from circular confinements with narrow openings