On the Formation of Equilibrium Gels via a Macroscopic Bond Limitation
arXiv:1605.07572 · doi:10.1063/1.4960773
Abstract
Restricting the number of attractive physical "bonds" that can form between particles in a fluid suppresses the usual demixing phase transition to very low particle concentrations, allowing for the formation of open, percolated, and homogeneous states, aptly called equilibrium or "empty" gels. Most demonstrations of this concept have directly limited the microscopic particle valence via anisotropic (patchy) attractions; however, an alternative macroscopic valence limitation would be desirable for greater experimental tunability and responsiveness. One possibility, explored in this paper, is to employ primary particles with attractions mediated via a secondary species of linking particles. In such a system, the linker-to-primary particle ratio serves as a macroscopic control parameter for the average microscopic valence. We show that the phase behavior of such a system predicted by Wertheim's first order perturbation theory is consistent with equilibrium gel formation: the primary particle concentrations corresponding to the two-phase demixing transition are significantly suppressed at both low and high linker-to-primary particle ratios. Extensive molecular dynamics simulations validate these theoretical predictions but also reveal the presence of loops of bonded particles, which are neglected in the theory. Such loops cause densification and inhibit percolation, and hence the range of viable empty gel state conditions is somewhat reduced relative to the Wertheim theory predictions.
13 pages, 8 figures
References in corpus (10)
- Phase diagram of patchy colloids: towards empty liquids
- Colloidal systems with competing interactions: from an arrested repulsive cluster phase to a gel
- Gelation as arrested phase separation in short-ranged attractive colloid-polymer mixtures
- Mobile linkers on DNA-coated colloids: valency without patches
- Phase diagrams of binary mixtures of patchy colloids with distinct numbers of patches: The network fluid regime
- Accurate phase diagram of tetravalent DNA nanostars
- Self-assembly in chains, rings and branches: a single component system with two critical points
- Resummed thermodynamic perturbation theory for bond cooperativity in associating fluids
- Accurate simulation estimates of cloud points of polydisperse fluids
- Wertheim perturbation theory: thermodynamics and structure of patchy colloids
Cited by in corpus (20)
- Equilibrium gels of limited valence colloids
- Assembling Inorganic Nanocrystal Gels
- Unsupervised machine learning for detection of phase transitions in off-lattice systems I. Foundations
- Gelation of Plasmonic Metal Oxide Nanocrystals by Polymer-Induced Depletion-Attractions
- Structure and phase behavior of polymer-linked colloidal gels
- Unsupervised machine learning for detection of phase transitions in off-lattice systems II. Applications
- Simulating the chromatin mediated phase separation of model proteins with multiple domains
- Noether-Constrained Correlations in Equilibrium Liquids
- Assembly of particle strings via isotropic potentials
- Universal Gelation of Metal Oxide Nanocrystals via Depletion Attractions
- Effects of linker flexibility on phase behavior and structure of linked colloidal gels
- Optimization of Non-Equilibrium Self-Assembly Protocols Using Markov State Models
- Binding branched and linear DNA structures: from isolated clusters to fully bonded gels
- Percolation in binary mixtures of linkers and particles: chaining {\it {vs}} branching
- Wertheim's thermodynamic perturbation theory with double-bond association and its application to colloid-linker mixtures
- Inhomogeneous steady shear dynamics of a three-body colloidal gel former
- Dynamics of equilibrium linked colloidal gels
- The ion activated attractive patchy particles model and its application to the liquid-vapour phase transitions
- Postponing the dynamical transition density using competing interactions
- Effects of Ligand vs. Linker on Phase Behavior and Mechanical Properties of Nanoparticle Gels