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Hierarchical supercrystalline nanocomposites through the self-assembly of organically-modified ceramic nanoparticles
Citation Link: https://doi.org/10.15480/882.2161
Publikationstyp
Journal Article
Date Issued
2019-03-05
Sprache
English
TORE-DOI
TORE-URI
Journal
Volume
9
Issue
1
Start Page
Art.-Nr. 3435
Citation
Scientific reports 1 (9): 3435 (2019)
Publisher DOI
Scopus ID
Biomaterials often display outstanding combinations of mechanical properties thanks to their hierarchical structuring, which occurs through a dynamically and biologically controlled growth and self-assembly of their main constituents, typically mineral and protein. However, it is still challenging to obtain this ordered multiscale structural organization in synthetic 3D-nanocomposite materials. Herein, we report a new bottom-up approach for the synthesis of macroscale hierarchical nanocomposite materials in a single step. By controlling the content of organic phase during the self-assembly of monodisperse organically-modified nanoparticles (iron oxide with oleyl phosphate), either purely supercrystalline or hierarchically structured supercrystalline nanocomposite materials are obtained. Beyond a critical concentration of organic phase, a hierarchical material is consistently formed. In such a hierarchical material, individual organically-modified ceramic nanoparticles (Level 0) self-assemble into supercrystals in face-centered cubic superlattices (Level 1), which in turn form granules of up to hundreds of micrometers (Level 2). These micrometric granules are the constituents of the final mm-sized material. This approach demonstrates that the local concentration of organic phase and nano-building blocks during self-assembly controls the final material's microstructure, and thus enables the fine-tuning of inorganic-organic nanocomposites' mechanical behavior, paving the way towards the design of novel high-performance structural materials.
DDC Class
600: Technik
620: Ingenieurwissenschaften
More Funding Information
The authors gratefully acknowledge the financial support from the German Research Foundation (DFG) via the SFB 986-M3, projects A1, A6, Z2, and Z3. We thank Dr. F. Beckmann (Helmholtz-Zentrum Geesthacht, Geesthacht, Germany) for scanning the sample with the technique SRµCT and for reconstructing the slices, and Dr. I. Greving (Helmholtz-Zentrum Geesthacht, Geesthacht, Germany) for her inputs on SRµCT. Dr. F. Brun (National Institute of Nuclear Physics, Trieste, Italy) is acknowledged for the discussion regarding quantitative analysis using Pore3d.
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