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Electron microscopy of nanoparticle superlattice formation at a solid-liquid interface in nonpolar liquids
Nanoparticle superlattice films form at the solid-liquid interface and are important for mesoscale materials, but are notoriously difficult to analyze before they are fully dried. Here, the early stages of nanoparticle assembly were studied at solid-liquid interfaces using liquid-phase electron micr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220325/ https://www.ncbi.nlm.nih.gov/pubmed/32426507 http://dx.doi.org/10.1126/sciadv.aba1404 |
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author | Cepeda-Perez, E. Doblas, D. Kraus, T. de Jonge, N. |
author_facet | Cepeda-Perez, E. Doblas, D. Kraus, T. de Jonge, N. |
author_sort | Cepeda-Perez, E. |
collection | PubMed |
description | Nanoparticle superlattice films form at the solid-liquid interface and are important for mesoscale materials, but are notoriously difficult to analyze before they are fully dried. Here, the early stages of nanoparticle assembly were studied at solid-liquid interfaces using liquid-phase electron microscopy. Oleylamine-stabilized gold nanoparticles spontaneously formed thin layers on a silicon nitride (SiN) membrane window of the liquid enclosure. Dense packings of hexagonal symmetry were obtained for the first monolayer independent of the nonpolar solvent type. The second layer, however, exhibited geometries ranging from dense packing in a hexagonal honeycomb structure to quasi-crystalline particle arrangements depending on the dielectric constant of the liquid. The complex structures formed by the weaker interactions in the second particle layer were preserved, while the surface remained immersed in liquid. Fine-tuning the properties of the involved materials can thus be used to control the three-dimensional geometry of a superlattice including quasi-crystals. |
format | Online Article Text |
id | pubmed-7220325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-72203252020-05-18 Electron microscopy of nanoparticle superlattice formation at a solid-liquid interface in nonpolar liquids Cepeda-Perez, E. Doblas, D. Kraus, T. de Jonge, N. Sci Adv Research Articles Nanoparticle superlattice films form at the solid-liquid interface and are important for mesoscale materials, but are notoriously difficult to analyze before they are fully dried. Here, the early stages of nanoparticle assembly were studied at solid-liquid interfaces using liquid-phase electron microscopy. Oleylamine-stabilized gold nanoparticles spontaneously formed thin layers on a silicon nitride (SiN) membrane window of the liquid enclosure. Dense packings of hexagonal symmetry were obtained for the first monolayer independent of the nonpolar solvent type. The second layer, however, exhibited geometries ranging from dense packing in a hexagonal honeycomb structure to quasi-crystalline particle arrangements depending on the dielectric constant of the liquid. The complex structures formed by the weaker interactions in the second particle layer were preserved, while the surface remained immersed in liquid. Fine-tuning the properties of the involved materials can thus be used to control the three-dimensional geometry of a superlattice including quasi-crystals. American Association for the Advancement of Science 2020-05-13 /pmc/articles/PMC7220325/ /pubmed/32426507 http://dx.doi.org/10.1126/sciadv.aba1404 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Research Articles Cepeda-Perez, E. Doblas, D. Kraus, T. de Jonge, N. Electron microscopy of nanoparticle superlattice formation at a solid-liquid interface in nonpolar liquids |
title | Electron microscopy of nanoparticle superlattice formation at a solid-liquid interface in nonpolar liquids |
title_full | Electron microscopy of nanoparticle superlattice formation at a solid-liquid interface in nonpolar liquids |
title_fullStr | Electron microscopy of nanoparticle superlattice formation at a solid-liquid interface in nonpolar liquids |
title_full_unstemmed | Electron microscopy of nanoparticle superlattice formation at a solid-liquid interface in nonpolar liquids |
title_short | Electron microscopy of nanoparticle superlattice formation at a solid-liquid interface in nonpolar liquids |
title_sort | electron microscopy of nanoparticle superlattice formation at a solid-liquid interface in nonpolar liquids |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220325/ https://www.ncbi.nlm.nih.gov/pubmed/32426507 http://dx.doi.org/10.1126/sciadv.aba1404 |
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