The Continuous Exudation of Micro‐Meniscus Capsules by Polymer Perspiration

Perspiration is a common phenomenon in many natural creatures in order to maintain their steady state. Here, through the facile use of a linear polymer of polymethylmethacrylate (PMMA) and an incompatible polymer of cross‐linked polydimethylsiloxane (PDMS) under an organic‐solvent atmosphere, the polymer system undergoes an analogous perspiration phenomenon as a result of the macroscopic phase separation between the two polymers. The resulting “sweat,” consisting of PMMA and solvent, are solidified into extraordinary micro‐meniscus capsules on the PDMS surface, which does not rely on the shape and topography of the PDMS substrates. Perspiration continues until the sweat of PMMA is exhausted, enabling the production of recoverable microstructures without complicated manufacturing processes. A thorough assessment of the influencing factors for the perspiration reveals that the formation of micro‐meniscus capsules follows a process of protrusion, ripening, and solidification. The micro‐meniscus capsules are primarily evaluated for applications in light scattering, in organic‐vapor sensing, and in bio‐macromolecular immobilization.     

热致型形状记忆高分子材料的研究进展

从记忆机理、制备技术等方面总结了热致型形状记忆高分子材料的最新发展并简述了当前几种重要的材料类型,特别是对近期发展的超分子形状记忆材料和可生物降解材料进行了重点描述,对未来热致型形状记忆高分子材料的发展方向进行了展望和评述.     

Magnetically Addressable Shape‐Memory and Stiffening in a Composite Elastomer

With a specific stimulus, shape‐memory materials can assume a temporary shape and subsequently recover their original shape, a functionality that renders them relevant for applications in fields such as biomedicine, aerospace, and wearable electronics. Shape‐memory in polymers and composites is usually achieved by exploiting a thermal transition to program a temporary shape and subsequently recover the original shape. This may be problematic for heat‐sensitive environments, and when rapid and uniform heating is required. In this work, a soft magnetic shape‐memory composite is produced by encasing liquid droplets of magneto‐rheological fluid into a poly(dimethylsiloxane) matrix. Under the influence of a magnetic field, this material undergoes an exceptional stiffening transition, with an almost 30‐fold increase in shear modulus. Exploiting this transition, fast and fully reversible magnetic shape‐memory is demonstrated in three ways, by embossing, by simple shear, and by unconstrained 3D deformation. Using advanced synchrotron X‐ray tomography techniques, the internal structure of the material is revealed, which can be correlated with the composite stiffening and shape‐memory mechanism. This material concept, based on a simple emulsion process, can be extended to different fluids and elastomers, and can be manufactured with a wide range of methods.     

形状记忆材料研究综述

综述了镍钛、铜基、铁基形状记忆合金,热致型、光致型、电致型、磁致型、化学感应型形状记忆高分子,以及形状记忆陶瓷的形状记忆机理、特性及其应用现状,并提出形状记忆材料的研究方向为：加强形状记忆合金的抗疲劳性能研究,建立一套统一的研究方法和合理的评价体系;加强形状记忆高分子材料的结构设计研究;改善陶瓷的形状记忆性能,以拓展形状记忆陶瓷的应用领域。     

3D Printed Photoresponsive Devices Based on Shape Memory Composites

Compared with traditional stimuli‐responsive devices with simple planar or tubular geometries, 3D printed stimuli‐responsive devices not only intimately meet the requirement of complicated shapes at macrolevel but also satisfy various conformation changes triggered by external stimuli at the microscopic scale. However, their development is limited by the lack of 3D printing functional materials. This paper demonstrates the 3D printing of photoresponsive shape memory devices through combining fused deposition modeling printing technology and photoresponsive shape memory composites based on shape memory polymers and carbon black with high photothermal conversion efficiency. External illumination triggers the shape recovery of 3D printed devices from the temporary shape to the original shape. The effect of materials thickness and light density on the shape memory behavior of 3D printed devices is quantified and calculated. Remarkably, sunlight also triggers the shape memory behavior of these 3D printed devices. This facile printing strategy would provide tremendous opportunities for the design and fabrication of biomimetic smart devices and soft robotics.     

Self‐Healing of Polarizing Films via the Synergy between Gold Nanorods and Vitrimer

Conventional self‐healing is about the recovery of shape and mechanical properties. In contrast, recovery of functional properties is still a great challenge, especially for optical functional materials, as the known self‐healing methods are incompatible with optical properties. By utilizing the synergistic effect between Au nanorods and vitrimer, the alignment of Au nanorods can be achieved in the crosslinked polymer. The optical properties of the resulting polarizing film, such as light transmittance and polarization degree, can be fully recovered without an external repair agent. With simple laser irradiation to induce the photothermal effect of Au nanorods, the shape‐memory effect of vitrimer returns the Au nanorods to their initial orientation, and the plasticity achieves in situ self‐healing of the cutting area. The self‐healing of polarizing film provides a new research direction and reference for the application of self‐healing systems in functional materials.     

A finite element method for light activated shape‐memory polymers

Shape‐memory polymers (SMPs) belong to a class of smart materials that have shown promise for a wide range of applications. They are characterized by their ability to maintain a temporary deformed shape and return to an original parent permanent shape. In this paper, we consider the coupled photomechanical behavior of light activated shape‐memory polymers (LASMPs), focusing on the numerical aspects for finite element simulations at the engineering scale. The photomechanical continuum framework is summarized, and some specific constitutive equations for LASMPs are described. Numerical implementation of the multiphysics governing partial differential equations takes the form of a user defined element subroutine within the commercial software package ABAQUS . We verify our two‐dimensional and three‐dimensional finite element procedure for multiple analytically tractable cases. To show the robustness of the numerical implementation, simulations are performed under various geometries and complex photomechanical loading. Copyright © 2016 John Wiley & Sons, Ltd.     

Highly Stretchable,Shape Memory Organohydrogels Using Phase‐Transition Microinclusions

Shape memory effect in polymer materials has attracted considerable attention due to its promising applications in a variety of fields. However, shape memory polymers prepared by conventional strategy suffer from a common problem, in which high strain capacity and excellent shape memory behavior cannot be simultaneously achieved. This study reports a general and synergistic strategy to fabricate high‐strain and tough shape memory organohydrogels that feature binary cooperative phase. The phase‐ transition micro‐organogels and elastic hydrogel framework act synergistically to provide excellent thermomechanical performance and shape memory effect. During shape memory process, the organohydrogels exhibit high strain capacity, featuring fully recoverable stretching deformation by up to 2600% and compression by up to 85% beneath a load ≈20 times the organohydrogel's weight. Furthermore, owing to the micro‐organogel and hydrogel heterostructures, the interfacial tension derived from heterophases dominates the shape recovery of the organohydrogel material. Simple processing and smart surface patterning of the shape memory behavior and multiple shape memory effects can also be realized. Meanwhile, these organohydrogels are also nonswellable in water and oil, which is important for multimedia applications.     

n‐Type Doped Conjugated Polymer for Nonvolatile Memory

This study demonstrates a facile way to efficiently induce strong memory behavior from common p‐type conjugated polymers by adding n‐type dopant 2‐(2‐methoxyphenyl)‐1,3‐dimethyl‐2,3‐dihydro‐1H‐benzoimidazole. The n‐type doped p‐channel conjugated polymers not only enhance n‐type charge transport characteristics of the polymers, but also facilitate to storage charges and cause reversible bistable (ON and OFF states) switching upon application of gate bias. The n‐type doped memory shows a large memory window of up to 47 V with an on/off current ratio larger than 10 000. The charge retention time can maintain over 100 000 s. Similar memory behaviors are also observed in other common semiconducting polymers such as poly(3‐hexyl thiophene) and poly[2,5‐bis(3‐tetradecylthiophen‐2‐yl)thieno[3,2‐b]thiophene], and a high mobility donor–acceptor polymer, poly(isoindigo‐bithiophene). In summary, these observations suggest that this approach is a general method to induce memory behavior in conjugated polymers. To the best of the knowledge, this is the first report for p‐type polymer memory achieved using n‐type charge‐transfer doping.     

Shape Memory Materials for Biomedical Applications

Shape memory properties provide a very attractive insight into materials science, opening unexplored horizons and giving access to unconventional functions in every material class (metals, polymers, and ceramics). In this regard, the biomedical field, forever in search of materials that display unconventional properties able to satisfy the severe specifications required by their implantation, is now showing great interest in shape memory materials, whose mechanical properties make them extremely attractive for many biomedical applications. However, their biocompatibility, particularly for long‐term and permanent applications, has not yet been fully established and is therefore the object of controversy. On the other hand, shape memory polymers (SMPs) show promise, although thus far, their biomedical applications have been limited to the exploration. This paper will first review the most common biomedical applications of shape memory alloys and SMPs and address their critical biocompatibility concerns. Finally, some engineering implications of their use as biomaterials will be examined.     

New Triblock Copolymer Templates,PEO‐PB‐PEO,for the Synthesis of Titania Films with Controlled Mesopore Size,Wall Thickness,and Bimodal Porosity

The synthesis and properties of a series of new structure‐directing triblock copolymers with PEO‐PB‐PEO structure (PEO = poly(ethylene oxide) and PB = polybutadiene) and their application as superior pore‐templates for the preparation of mesoporous titania coatings are reported. Starting from either TiCl₄ or from preformed TiO₂ nanocrystalline building blocks, mesoporous crystalline titanium oxide films with a significant degree of mesoscopic ordered pores are derived, and the pore size can be controlled by the molecular mass of the template polymer. Moreover, the triblock copolymers form stable micelles already at very low concentration, i.e., prior to solvent evaporation during the evaporation‐induced self‐assembly process (EISA). Consequently, the thickness of pore walls can be controlled independently of pore size by changing the polymer‐to‐precursor ratio. Thus, unprecedented control of wall thickness in the structure of mesoporous oxide coatings is achieved. In addition, the micelle formation of the new template polymers is sufficiently distinct from that of typical commercial PPO‐PEO‐PPO polymers (Pluronics; PPO = poly(propylene oxide)), so that a combination of both polymers facilitates bimodal porosity via dual micelle templating.     

The recovery properties under load of a shape memory polymer composite material

In many applications, shape memory alloys are being replaced by shape memory polymers as they have some better properties than shape memory alloys. Nevertheless, shape memory alloys can recover under load which shape memory polymers cannot. Shape memory polymers are not capable of giving full recovery even lifting a tiny load. The melting temperature or the glass transition temperature is the transition temperatures to which shape memory polymers are closely heated. Then a deforming force up to a certain position is applied to the heated shape memory polymers. After that shape memory polymer is permitted to cool while keeping it deformed. After the cooling, shape memory polymer obtains the temporary shape which can be recovered by reheating it at the similar transition temperature (glass transition or melting). Consequently, it recovers at its initial state. Shape memory polymer can achieve constrained recovery and unconstrained recovery, nonetheless; under stress, it is partly recovered. In current work, recovery under load has been investigated of an asymmetrical shape memory composite. It is established that it is capable to recover under various loads. Under various loads, it shows full recovery in reference to initial state. The ability to recover under load can be potentially used in diverse applications.     

A review of shape memory polymer composites and blends

Shape memory polymers (SMPs) are a kind of very important smart polymers. In order to improve the properties or obtain new functions of SMPs, SMP composites and blends are prepared. We thoroughly examine the research in SMP composites and blends achieved by numerous research groups around the world. The preparation of SMPs composites and blends is mainly for five aims: (1) to improve shape recovery stress and mechanical properties; (2) to decrease shape recovery induction time by increasing thermal conductivity; (3) to create new polymer/polymer blends with shape-memory effect (SME); (4) to tune switch temperature, mechanical properties, and biomedical properties of SMPs; (5) to fabricate shape memory materials sensitive to electricity, magnetic, light and moisture. The trend of SMP composite development is discussed. SMP composites and blends exhibit novel properties that are different from the conventional SMPs and thus can be utilized in various applications.     

Shape Memory Polymers for Body Motion Energy Harvesting and Self‐Powered Mechanosensing

Growing demand in portable electronics raises a requirement to electronic devices being stretchable, deformable, and durable, for which functional polymers are ideal choices of materials. Here, the first transformable smart energy harvester and self‐powered mechanosensation sensor using shape memory polymers is demonstrated. The device is based on the mechanism of a flexible triboelectric nanogenerator using the thermally triggered shape transformation of organic materials for effectively harvesting mechanical energy. This work paves a new direction for functional polymers, especially in the field of mechanosensation for potential applications in areas such as soft robotics, biomedical devices, and wearable electronics.     

Mechanochromic Photonic Gels

Polymer gels are remarkable materials with physical structures that can adapt significantly and quite rapidly with changes in the local environment, such as temperature, light intensity, electrochemistry, and mechanical force. An interesting phenomenon observed in certain polymer gel systems is mechanochromism – a change in color due to a mechanical deformation. Mechanochromic photonic gels are periodically structured gels engineered with a photonic stopband that can be tuned by mechanical forces to reflect specific colors. These materials have potential as mechanochromic sensors because both the mechanical and optical properties are highly tailorable via incorporation of diluents, solvents, nanoparticles, or polymers, or the application of stimuli such as temperature, pH, or electric or strain fields. Recent advances in photonic gels that display strain‐dependent optical properties are discussed. In particular, this discussion focuses primarily on polymer‐based photonic gels that are directly or indirectly fabricated via self‐assembly, as these materials are promising soft material platforms for scalable mechanochromic sensors.     

Design of High‐Mobility Diketopyrrolopyrrole‐Based π‐Conjugated Copolymers for Organic Thin‐Film Transistors

Since the report of the first diketopyrrolopyrrole (DPP)‐based polymer semiconductor, such polymers have received considerable attention as a promising candidate for high‐performance polymer semiconductors in organic thin‐film transistors (OTFTs). This Progress Report summarizes the advances in the molecular design of high‐mobility DPP‐based polymers reported in the last few years, especially focusing on the molecular design of these polymers in respect of tuning the backbone and side chains, and discussing the influences of structural modification of the backbone and side chains on the properties and device performance of corresponding DPP‐based polymers. This provides insights for the development of new and high‐mobility polymer semiconductors.     

Two-way shape memory effect in polymer laminates

Novel polymer laminate exhibiting two-way shape memory effect has been prepared by layer technique with the shape memory polymer and elastic polymer. In this paper, we demonstrate the two-way shape memory behavior, i.e., bending on heating and reverse bending on cooling; describe the preparation procedure; and investigate its two-way shape memory mechanism. Finally, it suggests that the mechanism can be ascribed to the release of elastic strain of shape memory polymer layer upon heating, and the elastic strain recovery induced by the bending force of substrate layer upon cooling.     

Artificial Muscles: Mechanisms,Applications, and Challenges

The area of artificial muscle is a highly interdisciplinary field of research that has evolved rapidly in the last 30 years. Recent advances in nanomaterial fabrication and characterization, specifically carbon nanotubes and nanowires, have had major contributions in the development of artificial muscles. However, what can artificial muscles really do for humans? This question is considered here by first examining nature's solutions to this design problem and then discussing the structure, actuation mechanism, applications, and limitations of recently developed artificial muscles, including highly oriented semicrystalline polymer fibers; nanocomposite actuators; twisted nanofiber yarns; thermally activated shape‐memory alloys; ionic‐polymer/metal composites; dielectric‐elastomer actuators; conducting polymers; stimuli‐responsive gels; piezoelectric, electrostrictive, magnetostrictive, and photostrictive actuators; photoexcited actuators; electrostatic actuators; and pneumatic actuators.     

Surfactant‐Free Shape Control of Gold Nanoparticles Enabled by Unified Theoretical Framework of Nanocrystal Synthesis

Gold nanoparticles have unique properties that are highly dependent on their shape and size. Synthetic methods that enable precise control over nanoparticle morphology currently require shape‐directing agents such as surfactants or polymers that force growth in a particular direction by adsorbing to specific crystal facets. These auxiliary reagents passivate the nanoparticles' surface, and thus decrease their performance in applications like catalysis and surface‐enhanced Raman scattering. Here, a surfactant‐ and polymer‐free approach to achieving high‐performance gold nanoparticles is reported. A theoretical framework to elucidate the growth mechanism of nanoparticles in surfactant‐free media is developed and it is applied to identify strategies for shape‐controlled syntheses. Using the results of the analyses, a simple, green‐chemistry synthesis of the four most commonly used morphologies: nanostars, nanospheres, nanorods, and nanoplates is designed. The nanoparticles synthesized by this method outperform analogous particles with surfactant and polymer coatings in both catalysis and surface‐enhanced Raman scattering.     

增强形状记忆聚合物材料研究进展

本文介绍了增强形状记忆聚合物的最新研究进展,详细探讨了各种增强材料对形状记忆聚合物的形状记忆效应的影响,总结了增强形状记忆聚合物研究的若干热点问题.