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The self-assembly of nanoparticles has attracted a vast amount of attention due to the ability of the nanostructure to control light at the sub-wavelength scale, along with consequent strong electromagnetic field enhancement. However, most approaches developed for the formation of discrete assemblies are limited to a single and homogeneous system, and incorporation of larger or asymmetrical nanoparticles into assemblies with high purity remains a key challenge. Here, a simple and versatile approach to assemble nanoparticles of different sizes, shapes, and materials into various discrete homo- or hetero-structures using only two complementary deoxyribonucleic acid (DNA) strands is presented. First, surface functionalisation using DNA and alkyl-polyethylene glycol (PEG) enables transformation of as-synthesised nanoparticles into readily usable plasmonic building blocks for self-assembly. Optimisation of the DNA coverage enables the production of different assembly types, such as homo- and hetero-dimers, trimers and tetramers and core-satellite structures, which are produced in high purity using electrophoresis purification. The approach is extended from purely plasmonic structures to incorporate (luminescent) semiconductor nanoparticles for formation of hybrid assemblies. The deposited assemblies form a high yield of specific geometrical arrangements, attributed to the van der Waals attraction between particles. This method will enable the development of new complex colloidal nanoassemblies for biological and optical applications.


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Flexible synthesis of high-purity plasmonic assemblies

Show Author's information Laurent LermusiauxAnum NisarAlison M. Funston( )
ARC Centre of Excellence in Exciton Science and School of Chemistry, Monash University, Clayton, VIC 3800, Australia

Present address: Université de Bordeaux, CNRS, ICMCB, UMR 5026, Pessac 33600, France

Abstract

The self-assembly of nanoparticles has attracted a vast amount of attention due to the ability of the nanostructure to control light at the sub-wavelength scale, along with consequent strong electromagnetic field enhancement. However, most approaches developed for the formation of discrete assemblies are limited to a single and homogeneous system, and incorporation of larger or asymmetrical nanoparticles into assemblies with high purity remains a key challenge. Here, a simple and versatile approach to assemble nanoparticles of different sizes, shapes, and materials into various discrete homo- or hetero-structures using only two complementary deoxyribonucleic acid (DNA) strands is presented. First, surface functionalisation using DNA and alkyl-polyethylene glycol (PEG) enables transformation of as-synthesised nanoparticles into readily usable plasmonic building blocks for self-assembly. Optimisation of the DNA coverage enables the production of different assembly types, such as homo- and hetero-dimers, trimers and tetramers and core-satellite structures, which are produced in high purity using electrophoresis purification. The approach is extended from purely plasmonic structures to incorporate (luminescent) semiconductor nanoparticles for formation of hybrid assemblies. The deposited assemblies form a high yield of specific geometrical arrangements, attributed to the van der Waals attraction between particles. This method will enable the development of new complex colloidal nanoassemblies for biological and optical applications.

Keywords: deoxyribonucleic acid (DNA) self-assembly, electrophoretic purification, nanoparticle assemblies, colloidal stability

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Publication history
Copyright
Acknowledgements

Publication history

Received: 13 May 2020
Revised: 01 September 2020
Accepted: 02 September 2020
Published: 01 March 2021
Issue date: March 2021

Copyright

© Tsinghua University Press and Springer-Verlag GmbH Germany, part of Springer Nature

Acknowledgements

This work was supported by the Australian Research Council (ARC) Grants for the ARC Centre of Excellence in Exciton Science, CE170100026 and DP140103011. The authors acknowledge use of facilities within the Monash Centre for Electron Microscopy (MCEM).

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