Molecular Additives as Competitive Binding Agents to Control Supramolecular-Driven Nanoparticle Assembly

Colloidal nanoparticle assembly methods can produce intricate superlattice structures and often use knowledge of atomic crystallization behaviors to guide their design. While this analogy has enabled multiple routes to programming colloidal crystallization thermodynamics, fewer tools or strategies exist to manipulate nanoparticle superlattice growth kinetics in a controlled manner. Here we investigate how small-molecule additives can be used to modulate the thermodynamics and kinetics of supramolecular-chemistry-driven nanoparticle assembly. Specifically, we introduce monovalent binding agents into the superlattice growth solution that compete with the multivalent interparticle bonding interactions driving particle assembly, thereby altering interparticle bond strength by reducing the number of bridging complexes formed between particles. In this manner, the assemblies can be steered to avoid kinetic traps and crystallize into faceted single crystals under isothermal conditions, alleviating the need for precise thermal control that has conventionally been required to produce large, faceted crystals in prior assembly methods.

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Publication Details

Journal
ACS Nanoscience Au
Published
2024-10-31
DOI
https://doi.org/10.1021/acsnanoscienceau.4c00062
Citations
3
Primary Topic
Pickering emulsions and particle stabilization
Type
article
Field-Weighted Citation Impact
0.35

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article

Molecular Additives as Competitive Binding Agents to Control Supramolecular-Driven Nanoparticle Assembly

Matthew Ye, Nicholas Sbalbi, Rebecca L. Li, Robert J. Macfarlane
3 citations
ACS Nanoscience Au
Pickering emulsions and particle stabilization
0.35
article

Molecular Additives as Competitive Binding Agents to Control Supramolecular-Driven Nanoparticle Assembly

Matthew Ye, Nicholas Sbalbi, Rebecca L. Li, Robert J. Macfarlane
article en
3 citations

Abstract

Colloidal nanoparticle assembly methods can produce intricate superlattice structures and often use knowledge of atomic crystallization behaviors to guide their design. While this analogy has enabled multiple routes to programming colloidal crystallization thermodynamics, fewer tools or strategies exist to manipulate nanoparticle superlattice growth kinetics in a controlled manner. Here we investigate how small-molecule additives can be used to modulate the thermodynamics and kinetics of supramolecular-chemistry-driven nanoparticle assembly. Specifically, we introduce monovalent binding agents into the superlattice growth solution that compete with the multivalent interparticle bonding interactions driving particle assembly, thereby altering interparticle bond strength by reducing the number of bridging complexes formed between particles. In this manner, the assemblies can be steered to avoid kinetic traps and crystallize into faceted single crystals under isothermal conditions, alleviating the need for precise thermal control that has conventionally been required to produce large, faceted crystals in prior assembly methods.

ACS Nanoscience AuVol. 4(6)
Massachusetts Institute of Technology (US)
National Science Foundation, U.S. Department of Energy, American Society for Engineering Education, Office of Science, Materials Research Science and Engineering Center, Harvard University, Division of Chemistry, Army Research Office, Argonne National Laboratory, Army Research Laboratory
Openalex Percentile: Top 43%
Pickering emulsions and particle stabilization
0.35
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