Issue 9, 2017

Vivid structural colors with low angle dependence from long-range ordered photonic crystal films

Abstract

Structural colored materials have attracted increasing attention due to their vivid color effects and non-photobleaching characteristics. However, the angle dependence of these structural colors severely restricts their practical applications, for example, in display and sensing devices. Here, a new strategy for obtaining low angle dependent structural colors is demonstrated by fabricating long-range ordered photonic crystal films. By using spheres with high refractive indices as building blocks, the angle dependence of the obtained colors has been strongly suppressed. Green, golden yellow and red structural colored films with low angle dependence were obtained by using 145 nm, 165 nm and 187 nm Cu2O spheres as building blocks, respectively. SEM images confirmed the long-range highly ordered arrays of the Cu2O photonic crystal films. Reflectance spectra and digital photographs clearly demonstrate the low angle dependence of these structural colors, which is in sharp comparison with the case of polystyrene (PS) and SiO2 photonic crystal films. Furthermore, these structural colors are vivid with high color saturation, not only under black background, but also under white background and natural light without adding any light-absorbing agents. These low angle dependent structural colors endow Cu2O photonic crystal films with great potential in practical applications. Our findings may broaden the strategies for the design and fabrication of angle independent structural colored materials.

Graphical abstract: Vivid structural colors with low angle dependence from long-range ordered photonic crystal films

Supplementary files

Article information

Article type
Paper
Submitted
23 Sep 2016
Accepted
30 Nov 2016
First published
30 Nov 2016

Nanoscale, 2017,9, 3002-3009

Vivid structural colors with low angle dependence from long-range ordered photonic crystal films

X. Su, H. Xia, S. Zhang, B. Tang and S. Wu, Nanoscale, 2017, 9, 3002 DOI: 10.1039/C6NR07523A

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