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Liquid phase fast electron tomography unravels the true 3D structure of colloidal assemblies

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Academic paper
1

Academic Paper attributes

arXiv ID
2311.053091
arXiv Classification
Physics
Physics
1
Publication URL
arxiv.org/pdf/2311.0...09.pdf1
Publisher
ArXiv
ArXiv
1
DOI
doi.org/10.48550/ar...11.053091
Paid/Free
Free1
Academic Discipline
Physics
Physics
1
Condensed matter physics
Condensed matter physics
1
Materials science
Materials science
1
Chemical physics
Chemical physics
1
Computer science
Computer science
1
Soft matter
Soft matter
1
Submission Date
November 9, 2023
1
November 23, 2023
1
Author Names
Luis M. Liz-Marzán1
Stavros Nicolopoulos1
Sara Bals1
Jesus Gonzalez Casablanca1
Noa Olluyn1
Ajinkya Kadu1
Alejandro Gomez Perez1
Ana Sánchez Iglesias1
...
Paper abstract

Electron tomography has become a commonly used tool to investigate the three-dimensional (3D) structure of nanomaterials, including colloidal nanoparticle assemblies. However, the nature of the electron microscopy technique typically requires such characterization to be carried out under high vacuum. Therefore, pre-treatment sample preparation is needed for assemblies prepared by (wet) colloid chemistry methods, including solvent evaporation and deposition on a solid substrate (TEM grid). As a result, changes are consistently imposed on the actual nanoparticle organization, which is largely responsible for the nanomaterial properties. Therefore, we propose herein the application of (fast) electron tomography of nanoparticle assemblies while in their original colloidal environment. To address the challenges related to electron tomography in liquid, we devised a method that combines fast data acquisition in a commercial liquid in situ TEM cell with a dedicated reconstruction workflow. We present the application of this method to two different systems, which exemplify the effects of drying and vacuum, depending on the nature of the protecting ligands. 3D reconstructions of assemblies comprising polystyrene-capped Au nanoparticles encapsulated in polymeric shells revealed less compact and more distorted configurations for experiments performed in a liquid medium compared to their dried counterparts. On the other hand, quantitative analysis of the interparticle distance of self-assembled Au nanorods in water agrees with the previously reported dimensions of the ligand layers surrounding the nanorods, whereas the nanorods are in much closer contact in similar dried assemblies. This study, therefore, emphasizes the importance of developing high-resolution characterization tools that preserve the native environment of colloidal nanostructures.

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