Engineering Entropy for the Inverse Design of Colloidal Crystals from Hard Shapes
arXiv:1712.02471 · doi:10.1126/sciadv.aaw0514
Abstract
Throughout the physical sciences, entropy stands out as a pivotal but enigmatic concept that, in materials design, often takes a backseat to energy. Here, we demonstrate how to precisely engineer entropy to achieve desired colloidal crystals. We demonstrate the inverse design of hard particles that assemble six different target colloidal crystals due solely to entropy maximization. Our approach efficiently samples particle shapes from 88- and 192-dimensional design spaces to discover thermodynamically optimal shapes. We design particle shapes that self assemble known crystals with optimized thermodynamic stability, as well as new crystal structures with no known atomic or other equivalent.
6 pages
References in corpus (1)
Cited by in corpus (14)
- Inverse methods for design of soft materials
- Programming patchy particles to form complex periodic structures
- Programmable patchy particles for materials design
- FCC-to-BCC phase transitions in convex and concave hard particle systems
- Chiral Skyrmions Interacting with Chiral Flowers
- Soft matter crystallography -- complex, diverse, and new crystal structures in condensed materials on the mesoscale
- Shape and Interaction Decoupling for Colloidal Pre-Assembly
- Inverse design of two-dimensional structure by self-assembly of patchy particles
- Self-assembly and entropic effects in pear-shaped colloid systems: II. Depletion attraction of pear-shaped particles in a hard sphere solvent
- Robust Design from Systems Physics
- The Excluded Area of Superellipse Sector Particles
- Designing binary mixtures of colloidal particles with simple interactions that assemble complex crystals
- relentless: Transparent, reproducible molecular dynamics simulations for optimization
- Tuning Stoichiometry to Promote Formation of Binary Colloidal Superlattices