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Structural Colored Fabric Based on Monodisperse Cu2O Microspheres
Xiaowen Li1, Zhen Yin2, Zhanghan She1
1Key Laboratory of Advanced Textile Materials and Manufacturing Technology, Ministry of Education, Zhejiang Sci-Tech University, Hangzhou 310018, China.
Materials (Basel, Switzerland)
|July 13, 2024
Summary
Researchers developed eco-friendly, dyeless structural colors using tunable copper oxide (Cu2O) microspheres. Adjusting microsphere size created different colors, with poly(butyl acrylate) enhancing durability against friction and bending.
Area of Science:
- Materials Science
- Nanotechnology
- Optics
Background:
- Structural-colored fabrics offer eco-friendly, dyeless alternatives with anti-fading properties.
- High refractive index materials like metal, metal oxide, and semiconductor microspheres are key for photonic crystals and structural colors.
Purpose of the Study:
- To synthesize tunable copper(I) oxide (Cu2O) microspheres for structural coloration.
- To investigate the influence of microsphere size and concentration on fabric color.
- To assess the durability of the resulting structural colors.
Main Methods:
- Two-step reduction method at room temperature to synthesize Cu2O microspheres.
- Controlled microsphere size (275 nm to 190 nm) by adjusting the citrate to Cu2+ molar ratio.
- Preparation of monodisperse Cu2O microsphere dispersions and evaluation of structural color with poly(butyl acrylate).
Main Results:
- Achieved tunable structural colors in fabrics by precisely controlling Cu2O microsphere size.
- Demonstrated improved color fastness against friction and bending using poly(butyl acrylate) as an adhesive.
- Established a method for creating vibrant, durable, and eco-friendly colored fabrics.
Conclusions:
- Cu2O microspheres are effective for creating tunable structural colors in textiles.
- Poly(butyl acrylate) significantly enhances the stability and durability of these structural colors.
- This approach offers a promising, environmentally friendly alternative to traditional dyeing methods.

