Wertheim's thermodynamic perturbation theory with double-bond association and its application to colloid-linker mixtures

Abstract

We extend Wertheim's thermodynamic perturbation theory to derive the association free energy of a multicomponent mixture for which double bonds can form between any two pairs of the molecules' arbitrary number of bonding sites. This generalization reduces in limiting cases to prior theories that restrict double bonding to at most one pair of sites per molecule. We apply the new theory to an associating mixture of colloidal particles ("colloids") and flexible chain molecules ("linkers"). The linkers have two functional end groups, each of which may bond to one of several sites on the colloids. Due to their flexibility, a significant fraction of linkers can "loop" with both ends bonding to sites on the same colloid instead of bridging sites on different colloids. We use the theory to show that the fraction of linkers in loops depends sensitively on the linker end-to-end distance relative to the colloid bonding-site distance, which suggests strategies for mitigating the loop formation that may otherwise hinder linker-mediated colloidal assembly.

The physics of empty liquids: from patchy particles to water

“…We note for completeness that recently there have been attempt to extend the Wertheim theory to relax the assumption of single bond per patch conditions and multiple inter-particle bondings [99][100][101][102][103].…”

The physics of Empty Liquids: from Patchy particles to Water

“…We note for completeness that recently there have been attempt to extend the Wertheim theory to relax the assumption of single bond per patch conditions and multiple inter-particle bondings [89][90][91][92][93].…”