An Tong, Jiang Xinyu, Gao Feng, Schäfer Christian, Qiu Junjun, Shi Nan, Song Xiaokun, Zhang Manyao, Finlayson Chris E, Zheng Xuezhi, Li Xiuhong, Tian Feng, Zhu Bin, Sui Tan, Han Xianhong, Baumberg Jeremy J, Fan Tongxiang, Zhao Qibin
State Key Lab of Metal Matrix Composites, School of Materials Science and Engineering, Shanghai Jiao Tong University, Shanghai, 200240, China.
BASF SE, Dispersions & Resins, Carl-Bosch-Strasse 38, Ludwigshafen/Rhein, 67056, Germany.
Nat Commun. 2024 Jun 18;15(1):5215. doi: 10.1038/s41467-024-49535-z.
Stretching elastic materials containing nanoparticle lattices is common in research and industrial settings, yet our knowledge of the deformation process remains limited. Understanding how such lattices reconfigure is critically important, as changes in microstructure lead to significant alterations in their performance. This understanding has been extremely difficult to achieve due to a lack of fundamental rules governing the rearrangements. Our study elucidates the physical processes and underlying mechanisms of three-dimensional lattice transformations in a polymeric photonic crystal from 0% to over 200% strain during uniaxial stretching. Corroborated by comprehensive experimental characterizations, we present analytical models that precisely predict both the three-dimensional lattice structures and the macroscale deformations throughout the stretching process. These models reveal how the nanoparticle lattice and matrix polymer jointly determine the resultant structures, which breaks the original structural symmetry and profoundly changes the dispersion of photonic bandgaps. Stretching induces shifting of the main pseudogap structure out from the 1st Brillouin zone and the merging of different symmetry points. Evolutions of multiple photonic bandgaps reveal potential optical singularities shifting with strain. This work sets a new benchmark for the reconfiguration of soft material structures and may lay the groundwork for the study of stretchable three-dimensional topological photonic crystals.
在研究和工业环境中,拉伸含有纳米颗粒晶格的弹性材料很常见,但我们对其变形过程的了解仍然有限。了解这些晶格如何重新配置至关重要,因为微观结构的变化会导致其性能发生重大改变。由于缺乏控制重排的基本规则,很难实现这种理解。我们的研究阐明了在单轴拉伸过程中,聚合物光子晶体中三维晶格从0%到超过200%应变的转变的物理过程和潜在机制。通过全面的实验表征得到证实,我们提出了分析模型,能够精确预测整个拉伸过程中的三维晶格结构和宏观变形。这些模型揭示了纳米颗粒晶格和基体聚合物如何共同决定最终结构,这打破了原始结构的对称性,并深刻改变了光子带隙的色散。拉伸导致主要赝隙结构从第一布里渊区移出,并使不同对称点合并。多个光子带隙的演变揭示了潜在的光学奇点随应变移动。这项工作为软材料结构的重新配置设定了新的基准,并可能为可拉伸三维拓扑光子晶体的研究奠定基础。