Solid state nanofibers based on self-assemblies: from cleaving from self-assemblies to multilevel hierarchical constructs

Scientific publication - Journal Article uoadl:2959224 45 Read counter

Unit:
Department of Chemistry
Title:
Solid state nanofibers based on self-assemblies: from cleaving from self-assemblies to multilevel hierarchical constructs
Languages of Item:
English
Abstract:
Self-assemblies and their hierarchies are useful to construct soft materials with structures at different length scales and to tune the materials properties for various functions. Here we address routes for solid nanofibers based on different forms of self-assemblies. On the other hand, we discuss rational "bottom-up" routes for multi-level hierarchical self-assembled constructs, with the aim of learning more about design principles for competing interactions and packing frustrations. Here we use the triblock copolypeptide poly(l-lysine)-b-poly(γ-benzyl-l-glutamate)-b-poly(l-lysine) complexed with 2′-deoxyguanosine 5′-monophosphate. Supramolecular disks (G-quartets) stabilized by metal cations are formed and their columnar assembly leads to a packing frustration with the cylindrical packing of helical poly(γ-benzyl-l-glutamate), which we suggest is important in controlling the lateral dimensions of the nanofibers. We foresee routes for functionalities by selecting different metal cations within the G-quartets. On the other hand, we discuss nanofibers that are cleaved from bulk self-assemblies in a "top-down" manner. After a short introduction based on cleaving nanofibers from diblock copolymeric self-assemblies, we focus on native cellulose nanofibers, as cleaved from plant cell wall fibers, which are expected to have feasible mechanical properties and to be templates for functional nanomaterials. Long nanofibers with 5-20 nm lateral dimensions can be cleaved within an aqueous medium to allow hydrogels and water can be removed to allow highly porous, lightweight, and flexible aerogels. We further describe inorganic/organic hybrids as prepared by chemical vapour deposition and atomic layer deposition of the different nanofibers. We foresee functional materials by selecting inorganic coatings. Finally we briefly discuss how the organic template can be removed e.g., by thermal treatments to allow completely inorganic hollow nanofibrillar structures. © 2009 The Royal Society of Chemistry.
Publication year:
2009
Authors:
Olli Ikkala
Robin H. A. Ras
Nikolay Houbenov
Janne Ruokolainen
Marjo Pääkkö
Janne Laine
Markku Leskelä
Lars A. Berglund
Tom Lindström
Gerrit ten Brinke
Hermis Iatrou
Nikos Hadjichristidis
Charl F. J. Faul
Journal:
Faraday Discussions
Publisher:
Royal Society of Chemistry (RSC)
Volume:
143
Pages:
95
Keywords:
nanomaterial, article; chemistry; conformation; crystallization; macromolecule; materials testing; methodology; nanotechnology; particle size; phase transition; surface property; ultrastructure, Crystallization; Macromolecular Substances; Materials Testing; Molecular Conformation; Nanostructures; Nanotechnology; Particle Size; Phase Transition; Surface Properties
Main subject category:
Science
Official URL (Publisher):
DOI:
10.1039/b905204f
The digital material of the item is not available.