Department of Polymer Science and Engineering, University of Massachusetts Amherst , Amherst, Massachusetts 01003, United States.
Acc Chem Res. 2017 Feb 21;50(2):161-169. doi: 10.1021/acs.accounts.6b00570. Epub 2017 Feb 9.
The formation of well-defined and functional three-dimensional (3D) structures by buckling of thin sheets subjected to spatially nonuniform stresses is common in biological morphogenesis and has become a subject of great interest in synthetic systems, as such programmable shape-morphing materials hold promise in areas including drug delivery, biomedical devices, soft robotics, and biomimetic systems. Given their ability to undergo large changes in swelling in response to a wide variety of stimuli, hydrogels have naturally emerged as a key type of material in this field. Of particular interest are hybrid systems containing rigid inclusions that can define both the anisotropy and spatial nonuniformity of swelling as well as nanoparticulate additives that can enhance the responsiveness and functionality of the material. In this Account, we discuss recent progress in approaches to achieve well-defined shape morphing in hydrogel hybrids. First, we provide an overview of materials and methods that facilitate fabrication of such systems and outline the geometry and mechanics behind shape morphing of thin sheets. We then discuss how patterning of stiff inclusions within soft responsive hydrogels can be used to program both bending and swelling, thereby providing access to a wide array of complex 3D forms. The use of discretely patterned stiff regions to provide an effective composite response offers distinct advantages in terms of scalability and ease of fabrication compared with approaches based on smooth gradients within a single layer of responsive material. We discuss a number of recent advances wherein control of the mechanical properties and geometric characteristics of patterned stiff elements enables the formation of 3D shapes, including origami-inspired structures, concatenated helical frameworks, and surfaces with nonzero Gaussian curvature. Next, we outline how the inclusion of functional elements such as nanoparticles can enable unique pathways to programmable and even reprogrammable shape-morphing materials. We focus to a large extent on photothermally reprogrammable systems that include one of a variety of additives that serve to efficiently absorb light and convert it into heat, thereby driving the response of a temperature-sensitive hydrogel. Such systems are advantageous in that patterns of light can be defined with very high spatial and temporal resolution in addition to offering the potential for wavelength-selective addressability of multiple different inclusions. We highlight recent advances in the preparation of light-responsive hybrid systems capable of undergoing reprogrammable bending and buckling into well-defined 3D shapes. In addition, we describe several examples where shape tuning of hybrid systems enables control over the motion of responsive hydrogel-based materials. Finally, we offer our perspective on open challenges and future areas of interest for the field.
薄片状物体在受到空间非均匀应力时发生的弯曲可形成具有明确和功能的三维(3D)结构,这种现象在生物形态发生中很常见,并且在合成系统中也成为了一个备受关注的主题,因为这种可编程形状变形材料在药物输送、生物医学设备、软机器人和仿生系统等领域具有广阔的应用前景。由于水凝胶能够对各种刺激产生大的溶胀变化,因此它们自然而然地成为该领域的关键材料类型。特别有趣的是包含刚性内含物的混合系统,这些刚性内含物可以定义溶胀的各向异性和空间非均匀性,以及纳米颗粒添加剂可以增强材料的响应能力和功能性。在本综述中,我们讨论了实现水凝胶混合体中明确形状变形的最新进展。首先,我们提供了促进此类系统制造的材料和方法概述,并概述了薄片状物体形状变形背后的几何形状和力学原理。然后,我们讨论了如何在软响应水凝胶中对刚性内含物进行图案化以编程弯曲和溶胀,从而获得广泛的复杂 3D 形状。与基于单层响应材料中的平滑梯度的方法相比,使用离散图案化的刚性区域提供有效复合材料响应具有明显的优势,在可扩展性和制造便利性方面都是如此。我们讨论了一些最新进展,其中图案化的刚性元素的机械性能和几何特征的控制能够形成 3D 形状,包括折纸启发的结构、串联的螺旋框架和具有非零高斯曲率的表面。接下来,我们概述了如何将功能元素(例如纳米颗粒)包含在内,从而能够实现可编程甚至可重编程的形状变形材料的独特途径。我们主要关注包括各种添加剂在内的光热可重编程系统,这些添加剂用于高效地吸收光并将其转化为热,从而驱动热敏水凝胶的响应。此类系统具有以下优势:除了能够对多个不同内含物进行波长选择性寻址之外,还可以非常高的空间和时间分辨率定义光图案。我们重点介绍了能够经历可重编程弯曲和弯曲以形成明确 3D 形状的光响应混合系统的最新进展。此外,我们描述了几个示例,其中混合系统的形状调整能够控制基于响应性水凝胶的材料的运动。最后,我们提供了对该领域的开放挑战和未来关注领域的看法。