光子学
材料科学
光掩模
纳米技术
光学工程
聚合物
光子晶体
仿生学
光致聚合物
液晶
结构着色
光电子学
纳米光刻
屈曲
光学现象
光子超材料
分子工程
光纤
3D打印
组织工程
纤维素
应变工程
光学
自组装
超材料
集成光学
作者
Jiemin Qiu,Jie Li,Rui Xiong
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-11-02
卷期号:26 (44): 15368-15377
标识
DOI:10.1021/acs.nanolett.6c04143
摘要
Natural structural colors often emerge from interactions between chiral lattices and three-dimensional (3D) microstructures, yet integrating surface topography with structural order in artificial photonic materials remains challenging. Here, we develop a light-driven self-growth strategy for programmable 3D photonic structures by engineering through-thickness gradients in a preassembled chiral nematic cellulose scaffold. Confined UV photopolymerization drives localized reactions and directional mass transport, creating coupled gradients in cross-linking density, polymer concentration, and helical pitch. These gradients enable continuous structural-color tuning from blue to red, while differential swelling-induced buckling produces patterned protrusions with programmable heights. The resulting interpenetrating network provides structural integrity and mechanical robustness. Combined with photomask lithography, this approach yields spatially resolved multicolor architectures featuring programmable 3D topographies, angle-dependent optical responses, and self-cleaning properties. It further enables four-channel optical encryption integrating polarization, multipeak reflection, 3D topography, and photoluminescence, demonstrating gradient engineering as a versatile route to advanced multifunctional bioinspired photonic material design.
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