Parasitic crystallization of colloidal electrolytes: growing a metastable crystal from the nucleus of a stable phase. Issue 3 (21st December 2020)

• Record Type: Journal Article
• Authors: Sanchez-Burgos, Ignacio; Garaizar, Adiran; Vega, Carlos; Sanz, Eduardo; Espinosa, Jorge R.
• Is Part Of: Soft matter. Volume 17:Issue 3(2021)
• Page Start: 489
• Page End: 505
• Publication Date: 2020-12-21
• Subjects: Soft condensed matter -- Periodicals; 530.413
• DOI: 10.1039/d0sm01680b
• Languages: English
• ISSNs: 1744-683X

Abstract

Abstract : Despite its lower stability and higher nucleation barrier, a metastable charge-disordered colloidal phase manages to parasitically crystallize from nuclei of the stable charge-ordered phase due to its enhanced kinetic crystal growth. Abstract : Colloidal particles have been extensively used to comprehend the main principles governing liquid-crystal nucleation. Multiple mechanisms and frameworks have been proposed, through either experiments or computational approaches, to rationalise the ubiquitous formation of colloidal crystals. In this work, we elucidate the nucleation scenario behind the crystallization of oppositely charged colloids. By performing molecular dynamics simulations of colloidal electrolytes in combination with the Seeding technique, we evaluate the fundamental factors, such as the nucleation rate, free energy barrier, surface tension and kinetic pre-factor, that determine the liquid-to-solid transition of several crystalline polymorphs. Our results show that at a high packing fraction, there is a cross-over between the nucleation of the CsCl structure and that of a substitutionally disordered fcc phase, despite the CuAu crystal being the most stable phase. We demonstrate that the crucial factor in determining which phase nucleates the fastest is the free energy cost of the cluster formation rather than their kinetic ability to grow from the liquid. While at a low packing fraction, the stable phase, CsCl, is the one that nucleates and subsequently grows, we show how at moderate and high packing fractions, a disordered fcc phase subsequently grows regardless of the nature of the nucleating phase, termed parasitic crystallization. Taken together, our results provide a panoramic perspective of the complex nucleation scenario of oppositely charged colloids at moderate temperature and rationalise the different thermodynamic and kinetic aspects behind it.