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Reversible microscale assembly of nanoparticles driven by the phase transition of a thermotropic liquid crystal

Abstract:
The arrangement of nanoscale building blocks into patterns with microscale periodicity is challenging to achieve via self-assembly processes. Here, we report on the phase-transition-driven collective assembly of gold nanoparticles in a thermotropic liquid crystal. A temperature-induced transition from the isotropic to the nematic phase under anchoring-driven planar alignment leads to the assembly of individual nanometer-sized particles into arrays of micrometer-sized agglomerates, whose size and characteristic spacing can be tuned by varying the cooling rate. Phase field simulations coupling the conserved and nonconserved order parameters exhibit a similar evolution of the morphology as the experimental observations. This fully reversible process offers control over structural order on the microscopic level and is an interesting model system for the programmable and reconfigurable patterning of nanocomposites with access to micrometer-sized periodicities.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1021/acsnano.2c09203

Authors


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Role:
Author
ORCID:
0000-0001-8459-9994
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Role:
Author
ORCID:
0000-0002-6371-3089
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Role:
Author
ORCID:
0000-0002-8602-012X
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Role:
Author
ORCID:
0000-0001-9344-9349
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Institution:
University of Oxford
Division:
MPLS
Department:
Engineering Science
Oxford college:
St Catherine's College
Role:
Author
ORCID:
0000-0002-5229-8991


Publisher:
American Chemical Society
Journal:
ACS Nano More from this journal
Volume:
17
Issue:
11
Pages:
9906-9918
Place of publication:
United States
Publication date:
2023-05-24
Acceptance date:
2023-05-15
DOI:
EISSN:
1936-086X
ISSN:
1936-0851
Pmid:
37222568


Language:
English
Keywords:
Pubs id:
1489840
Local pid:
pubs:1489840
Deposit date:
2023-11-10

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