Electrostatically Assembled Open Square and Checkerboard Superlattices

Programmable assembly of nanoparticles into structures other than hexagonal lattices remains challenging. Assembling an open checkerboard or square lattice is harder to achieve compared to a close-packed hexagonal structure. Here, we introduce a unified, robust approach to assemble nanoparticles into a diverse family of two-dimensional superlattices at the liquid-air interface. Gold nanoparticles are grafted with pH-responsive, water-soluble poly(ethylene glycol) chains terminating in -COOH or -NH2 end groups, enabling control over interparticle interactions, while the grafted polymer's molecular weight dictates its conformation. This combined control crystallizes checkerboard, simple-square, and body-centered honeycomb superlattices. We find that even for identical nanoparticle core sizes, the polymer's molecular weight dictates superlattice symmetry and stability. Furthermore, tuning pH induces structural transitions between different lattice types. This method opens new avenues for the programmable fabrication of colloidal superstructures with tailored architectures.

Publication Details

Journal
arXiv (Cornell University)
Published
2025-07-11
Primary Topic
Pickering emulsions and particle stabilization
Type
article
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article

Electrostatically Assembled Open Square and Checkerboard Superlattices

arXiv (Cornell University)
Pickering emulsions and particle stabilization
article

Electrostatically Assembled Open Square and Checkerboard Superlattices

article en

Abstract

Programmable assembly of nanoparticles into structures other than hexagonal lattices remains challenging. Assembling an open checkerboard or square lattice is harder to achieve compared to a close-packed hexagonal structure. Here, we introduce a unified, robust approach to assemble nanoparticles into a diverse family of two-dimensional superlattices at the liquid-air interface. Gold nanoparticles are grafted with pH-responsive, water-soluble poly(ethylene glycol) chains terminating in -COOH or -NH2 end groups, enabling control over interparticle interactions, while the grafted polymer's molecular weight dictates its conformation. This combined control crystallizes checkerboard, simple-square, and body-centered honeycomb superlattices. We find that even for identical nanoparticle core sizes, the polymer's molecular weight dictates superlattice symmetry and stability. Furthermore, tuning pH induces structural transitions between different lattice types. This method opens new avenues for the programmable fabrication of colloidal superstructures with tailored architectures.

arXiv (Cornell University)
Openalex Percentile: Top 60%
Pickering emulsions and particle stabilization
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Electrostatically Assembled Open Square and Checkerboard Superlattices · arXiv (Cornell University) (2025) | TGRS Research Map | TGRS