Tunable Anisotropy in Inverse Opals and Emerging Optical Properties
Author(s) -
Katherine R. Phillips,
Nicolas Vogel,
Yuhang Hu,
Mathias Kolle,
Carole C. Perry,
Joanna Aizenberg
Publication year - 2014
Publication title -
chemistry of materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.741
H-Index - 375
eISSN - 1520-5002
pISSN - 0897-4756
DOI - 10.1021/cm403812y
Subject(s) - anisotropy , materials science , isotropy , condensation , nanomaterials , inverse , shrinkage , spectroscopy , self assembly , nanotechnology , chemical physics , optics , composite material , geometry , physics , mathematics , quantum mechanics , thermodynamics
Using self-assembly, nanoscale materials can be fabricated from the bottom up. Opals and inverse opals are examples of self-assembled nanomaterials made from crystallizing colloidal particles. As self-assembly requires a high level of control, it is challenging to use building blocks with anisotropic geometry to form complex opals, which limits the possible structures. Typically, spherical colloids are employed as building blocks, leading to symmetric, isotropic superstructures. However, a significantly richer palette of directionally dependent properties are expected if less symmetric, anisotropic structures can be created, especially originating from the assembly of regular, spherical particles. Here we show a simple method for introducing anisotropy into inverse opals by subjecting them to a post-assembly thermal treatment that results in directional shrinkage of the silica matrix caused by condensation of partially hydrated sol–gel silica structures. In this way, we can tailor the shape of the pores, ...
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