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      From nature to synthetic systems: shape transformation in soft materials

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      J. Mater. Chem. B
      Royal Society of Chemistry (RSC)

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          Abstract

          This review summarizes the latest developments in the shape transformation of thin, sheet-like soft materials.

          Nature offers a plethora of astonishing examples of shapes and functions from the aspects of both simplicity and complexity. The creation of synthetic systems that can morph in a controlled manner as seen in nature is of paramount importance in many fields of fundamental and applied sciences. The tremendous interest in self-shaping materials stems from a wide range of applications for these materials, ranging from biomedical devices to aircraft design. This review article highlights recent advances in understanding and designing thin, sheet-like soft materials that can transform into complex three-dimensional structures in a controlled manner by modulating the internal stresses. We review the general principles underlying shape transformation phenomena in natural and synthetic systems, and the significant achievements in fabricating self-shaping of soft materials via representative examples. We conclude with a discussion on the challenges facing the field, and future directions from the perspective of theoretical and experimental methodology and interdisciplinary applications.

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          Most cited references73

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          Fabrication of novel biomaterials through molecular self-assembly.

          Two complementary strategies can be used in the fabrication of molecular biomaterials. In the 'top-down' approach, biomaterials are generated by stripping down a complex entity into its component parts (for example, paring a virus particle down to its capsid to form a viral cage). This contrasts with the 'bottom-up' approach, in which materials are assembled molecule by molecule (and in some cases even atom by atom) to produce novel supramolecular architectures. The latter approach is likely to become an integral part of nanomaterials manufacture and requires a deep understanding of individual molecular building blocks and their structures, assembly properties and dynamic behaviors. Two key elements in molecular fabrication are chemical complementarity and structural compatibility, both of which confer the weak and noncovalent interactions that bind building blocks together during self-assembly. Using natural processes as a guide, substantial advances have been achieved at the interface of nanomaterials and biology, including the fabrication of nanofiber materials for three-dimensional cell culture and tissue engineering, the assembly of peptide or protein nanotubes and helical ribbons, the creation of living microlenses, the synthesis of metal nanowires on DNA templates, the fabrication of peptide, protein and lipid scaffolds, the assembly of electronic materials by bacterial phage selection, and the use of radiofrequency to regulate molecular behaviors.
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            How the Venus flytrap snaps.

            The rapid closure of the Venus flytrap (Dionaea muscipula) leaf in about 100 ms is one of the fastest movements in the plant kingdom. This led Darwin to describe the plant as "one of the most wonderful in the world". The trap closure is initiated by the mechanical stimulation of trigger hairs. Previous studies have focused on the biochemical response of the trigger hairs to stimuli and quantified the propagation of action potentials in the leaves. Here we complement these studies by considering the post-stimulation mechanical aspects of Venus flytrap closure. Using high-speed video imaging, non-invasive microscopy techniques and a simple theoretical model, we show that the fast closure of the trap results from a snap-buckling instability, the onset of which is controlled actively by the plant. Our study identifies an ingenious solution to scaling up movements in non-muscular engines and provides a general framework for understanding nastic motion in plants.
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              Soft robotics for chemists.

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                Author and article information

                Journal
                JMCBDV
                J. Mater. Chem. B
                J. Mater. Chem. B
                Royal Society of Chemistry (RSC)
                2050-750X
                2050-7518
                2014
                2014
                : 2
                : 17
                : 2357-2368
                Article
                10.1039/C3TB21462A
                32261408
                b3258d68-33cc-4590-beb4-b8eee5b543af
                © 2014
                History

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