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Pseudomorphic amorphization of three-dimensional superlattices through morphological transformation of nanocrystal building blocks
Nanocrystal (NC) superlattices (SLs) have been widely studied as a new class of functional mesoscopic materials with collective physical properties. The arrangement of NCs in SLs governs the collective properties of SLs, and thus investigations of phenomena that can change the assembly of NC constit...
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Published in: | Chemical science (Cambridge) 2024-02, Vol.15 (7), p.2425-2432 |
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Main Authors: | , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | Nanocrystal (NC) superlattices (SLs) have been widely studied as a new class of functional mesoscopic materials with collective physical properties. The arrangement of NCs in SLs governs the collective properties of SLs, and thus investigations of phenomena that can change the assembly of NC constituents are important. In this study, we investigated the dynamic evolution of NC arrangements in three-dimensional (3D) SLs, specifically the morphological transformation of NC constituents during the direct liquid-phase synthesis of 3D NC SLs. Electron microscopy and synchrotron-based
in situ
small angle X-ray scattering experiments revealed that the transformation of spherical Cu
2
S NCs in face-centred-cubic 3D NC SLs into anisotropic disk-shaped NCs collapsed the original ordered close-packed structure. The random crystallographic orientation of spherical Cu
2
S NCs in starting SLs also contributed to the complete disordering of the NC array
via
random-direction anisotropic growth of NCs. This work demonstrates that an understanding of the anisotropic growth kinetics of NCs in the post-synthesis modulation of NC SLs is important for tuning NC array structures.
The dynamic order-to-disorder transition of nanocrystal arrangements in three-dimensional superlattices is caused by the morphological transformation of nanocrystal constituents during the direct liquid-phase synthesis of superlattices. |
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ISSN: | 2041-6520 2041-6539 |
DOI: | 10.1039/d3sc05085h |