Early Formation Pathways of Surfactant Micelle Directed Ultrasmall Silica Ring and Cage Structures

Journal Article (2018)
Authors

Kai Ma (Cornell University)

Katherine A. Spoth (Cornell University)

Ying Cong (Cornell University)

Duhan Zhang (Cornell University)

Tangi Aubert (Universiteit Gent, Cornell University)

Melik Z. Turker (Cornell University)

Lena F. Kourkoutis (Cornell University)

E Mendes (TU Delft - ChemE/Advanced Soft Matter)

Ulrich Wiesner (Cornell University)

Research Group
ChemE/Advanced Soft Matter
To reference this document use:
https://doi.org/10.1021/jacs.8b08802
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Publication Year
2018
Language
English
Research Group
ChemE/Advanced Soft Matter
DOI:
https://doi.org/10.1021/jacs.8b08802

Abstract

By combining a surfactant, an organic pore expander, a silane, and poly(ethylene glycol) (PEG), we have observed the formation of a previously unknown set of ultrasmall silica structures in aqueous solutions. At appropriate concentrations of reagents, â2 nm primary silica clusters arrange around surfactant micelles to form ultrasmall silica rings, which can further evolve into cage-like structures. With increasing concentration, these rings line up into segmented worm-like one-dimensional (1D) structures, an effect that can be dramatically enhanced by PEG addition. PEG adsorbed 1D striped cylinders further arrange into higher order assemblies in the form of two-dimensional (2D) sheets or three-dimensional (3D) helical structures. Results provide insights into synergies between deformable noncovalent organic molecule assemblies and covalent inorganic network formation as well as early transformation pathways from spherical soft materials into 1D, 2D, and 3D silica solution structures, hallmarks of mesoporous silica materials formation. The ultrasmall silica ring and cage structures may prove useful in nanomedicine and other nanotechnology based applications.

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