Delocalization Transition in Colloidal Crystals

Sublattice melting is the loss of order of one lattice component in binary or ternary ionic crystals upon increasing the temperature. A related transition has been predicted in colloidal crystals. To understand the nature of this transition, we study delocalization in self-assembled, size-asymmetric binary colloidal crystals using a generalized molecular dynamics model. Focusing on body-centered cubic (BCC) lattices, we observe a smooth change from localized-to-delocalized interstitial particles for a variety of interaction strengths. Thermodynamic arguments, mainly the absence of a discontinuity in the heat capacity, suggest that the passage from localization-to-delocalization is continuous and not a phase transition. This change is enhanced by lattice vibrations, and the temperature of the onset of delocalization can be tuned by the strength of the interaction between the colloid species. Therefore, the localized and delocalized regimes of the sublattice are dominated by enthalpic and entropic driving forces, respectively. This work sets the stage for future studies of sublattice melting in colloidal systems with different stoichiometries and lattice types and it provides insights into superionic materials, which have the potential for application in energy storage technologies.

Automated summary

The researchers studied sublattice melting in colloidal crystals using a molecular dynamics model, finding that the transition from localization to delocalization is continuous, mainly influenced by lattice vibrations and interaction strengths between colloid species, and driven by thermodynamic factors.