Material properties depend critically on the packing and order of constituent units throughout length scales. Beyond classically explored molecular self-assembly, structure formation in the nanoparticle and colloidal length scales have recently been actively explored for new functions. Structure of colloidal assemblies depends strongly on the assembly process, and higher structural control can be reliably achieved only if the process is deterministic. Here we show that self-assembly of cationic spherical metal nanoparticles and anionic rod-like viruses yields well-defined binary superlattice wires. The superlattice structures are explained by a cooperative assembly pathway that proceeds in a zipper-like manner after nucleation. Curiously, the formed superstructure shows right-handed helical twisting due to the right-handed structure of the virus. This leads to structure-dependent chiral plasmonic function of the material. The work highlights the importance of well-defined colloidal units when pursuing unforeseen and complex assemblies. Colloidal self-assembly is a unique method to produce three-dimensional materials with well-defined hierarchical structures and functionalities. Liljeström et al. show controlled preparation of macroscopic chiral wires with helical plasmonic superlattice structure composed of metal nanoparticles and viruses.
Cooperative colloidal self-assembly of metal-protein superlattice wires
Ville Liljeström,A. Ora,J. Hassinen,H. Rekola,Nonappa,M. Heilala,V. Hynninen,J. Joensuu,Robin H. A. Ras,P. Törmä,O. Ikkala,M. Kostiainen
Published 2017 in Nature Communications
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- Publication year
2017
- Venue
Nature Communications
- Publication date
2017-09-22
- Fields of study
Physics, Medicine, Materials Science, Chemistry
- Identifiers
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- Source metadata
Semantic Scholar, PubMed
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