Tokyo Institute of Technology, Meguro-ku, Tokyo, 152-8550, Japan.
Nanotechnology facility, Center for Micro-Photonics, Swinburne University of Technology, John st., Hawthorn, Victoria, 3122, Australia.
Sci Rep. 2017 Aug 7;7(1):7419. doi: 10.1038/s41598-017-07502-3.
Molecular alignment underpins optical, mechanical, and thermal properties of materials, however, its direct measurement from volumes with micrometer dimensions is not accessible, especially, for structurally complex bio-materials. How the molecular alignment is linked to extraordinary properties of silk and its amorphous-crystalline composition has to be accessed by a direct measurement from a single silk fiber. Here, we show orientation mapping of the internal silk fiber structure via polarisation-dependent IR absorbance at high spatial resolution of 4.2 μm and 1.9 μm in a hyper-spectral IR imaging by attenuated total reflection using synchrotron radiation in the spectral fingerprint region around 6 μm wavelength. Free-standing longitudinal micro-slices of silk fibers, thinner than the fiber cross section, were prepared by microtome for the four polarization method to directly measure the orientational sensitivity of absorbance in the molecular fingerprint spectral window of the amide bands of β-sheet polypeptides of silk. Microtomed lateral slices of silk fibers, which may avoid possible artefacts that affect spectroscopic measurements with fibers of an elliptical cross sections were used in the study. Amorphisation of silk by ultra-short laser single-pulse exposure is demonstrated.
分子取向是材料光学、力学和热学性能的基础,但对于具有微米尺寸体积的材料,其直接测量是不可行的,尤其是对于结构复杂的生物材料。蚕丝的分子取向与其非晶-晶态组成之间的关系,需要通过对单根蚕丝纤维进行直接测量来确定。在这里,我们通过使用同步辐射在大约 6 微米波长的光谱指纹区域中的衰减全反射,以高空间分辨率(4.2μm 和 1.9μm),在超光谱红外成像中展示了内部蚕丝纤维结构的偏振相关红外吸收的取向映射。通过使用微切片机制备的比纤维横截面更薄的自由立体重叠微切片,进行四偏振法测量,以直接测量蚕丝中β-折叠多肽酰胺带的分子指纹光谱窗口中吸收的各向异性灵敏度。在这项研究中,使用了丝绸纤维的横向切片,以避免可能影响具有椭圆形横截面的纤维的光谱测量的人为因素。通过超短激光单脉冲曝光实现了蚕丝的非晶化。