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具有定制周期性和层状表皮结构的自组装、彩虹色、仿甲壳动物的纳米复合材料。

Self-Assembled, Iridescent, Crustacean-Mimetic Nanocomposites with Tailored Periodicity and Layered Cuticular Structure.

机构信息

DWI - Leibniz Institute for Interactive Materials , Forckenbeckstr. 50, 52056 Aachen, Germany.

出版信息

ACS Nano. 2015 Nov 24;9(11):10637-46. doi: 10.1021/acsnano.5b05074. Epub 2015 Sep 21.

Abstract

Natural high-performance materials inspire the pursuit of ordered hard/soft nanocomposite structures at high fractions of reinforcements and with balanced molecular interactions. Herein, we develop a facile, waterborne self-assembly pathway to mimic the multiscale cuticle structure of the crustacean armor by combining hard reinforcing cellulose nanocrystals (CNCs) with soft poly(vinyl alcohol) (PVA). We show iridescent CNC nanocomposites with cholesteric liquid-crystal structure, in which different helical pitches and photonic band gaps can be realized by varying the CNC/PVA ratio. We further show that multilayered crustacean-mimetic materials with tailored periodicity and layered cuticular structure can be obtained by sequential preparation pathways. The transition from a cholesteric to a disordered structure occurs for a critical polymer concentration. Correspondingly, we find a transition from stiff and strong mechanical behavior to materials with increasing ductility. Crack propagation studies using scanning electron microscopy visualize the different crack growth and toughening mechanisms inside cholesteric nanocomposites as a function of the interstitial polymer content for the first time. Different extents of crack deflection, layered delamination, ligament bridging, and constrained microcracking can be observed. Drawing of highly plasticized films sheds light on the mechanistic details of the transition from a cholesteric/chiral nematic to a nematic structure. The study demonstrates how self-assembly of biobased CNCs in combination with suitable polymers can be used to replicate a hierarchical biological structure and how future design of these ordered multifunctional nanocomposites can be optimized by understanding mechanistic details of deformation and fracture.

摘要

天然高性能材料激发了人们对高含量增强体和平衡分子相互作用的有序硬/软纳米复合材料结构的追求。在此,我们开发了一种简便的水分散体自组装方法,通过将硬增强纤维素纳米晶体 (CNC) 与软聚(乙烯醇) (PVA) 结合,模拟甲壳类动物盔甲的多尺度表皮结构。我们展示了具有胆甾相液晶结构的彩虹色 CNC 纳米复合材料,其中通过改变 CNC/PVA 比可以实现不同的螺旋节距和光子带隙。我们进一步表明,可以通过顺序制备途径获得具有定制周期性和分层表皮结构的多层甲壳类仿生材料。从胆甾相向无序结构的转变发生在聚合物浓度达到临界值时。相应地,我们发现机械性能从刚性和强性转变为具有更高延展性的材料。使用扫描电子显微镜进行的裂纹扩展研究首次可视化了不同的裂纹增长和增韧机制,这取决于胆甾相纳米复合材料中聚合物的间隔含量。可以观察到不同程度的裂纹偏转、分层分层、韧带桥接和约束微裂纹。高增塑薄膜的拉伸揭示了从胆甾相/手性向列相到向列相结构转变的力学细节。该研究表明,如何通过将生物基 CNC 自组装与合适的聚合物结合来复制分层生物结构,以及如何通过了解变形和断裂的力学细节来优化这些有序多功能纳米复合材料的未来设计。

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