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Title: Switching Binary States of NanoparticleSuperlattices and Dimer Clusters by DNA Strands

Journal Article · · Nature Nanotechnology
OSTI ID:983860

Nanoscale components can be self-assembled into static three-dimensional structures1-6, arrays7-9 and clusters10-13 using biomolecularmotifs. The structural plasticity of biomolecules and the reversibility of their interactions can also be used to make nanostructures that are dynamic, reconfigurable and responsive. DNA has emerged as an ideal biomolecular motif for making such nanostructures, partly because its versatile morphology permits in situ conformational changes using molecular stimuli12,14-22. This has allowed DNA nanostructures to exhibit reconfigurable topologies and mechanical movement17,18. Recently, researchers have begun to translate this approach to nanoparticle interfaces18,23,24, where, for example, the distances between nanoparticles can be modulated, resulting in a distance-dependent plasmonic response18,23,25. Here, we report the assembly of nanoparticles into three-dimensional superlattices and dimer clusters, using a reconfigurable DNA device that acts as an interparticle linkage. The interparticle distances in the superlattices and clusters can be modified, while preserving structural integrity, by adding molecular stimuli (simple DNA strands) after the self-assembly processes has been completed. Both systems were found to switch between two distinct rigid states, but atransition to a flexible device configuration within a superlattice showed a significant hysteresis.

Research Organization:
Brookhaven National Lab. (BNL), Upton, NY (United States). Center for Functional Nanomaterials (CFN)
Sponsoring Organization:
Doe - Office Of Science
DOE Contract Number:
DE-AC02-98CH10886
OSTI ID:
983860
Report Number(s):
BNL-93658-2010-JA; R&D Project: NC-001; TRN: US201014%%1852
Journal Information:
Nature Nanotechnology, Vol. 5, Issue 2
Country of Publication:
United States
Language:
English