Liu Mingzhu, Yang Shu
Key Laboratory of Bio-inspired Smart Interfacial Science and Technology of Ministry of Education, School of Chemistry, Beihang University, Beijing 100191, P. R. China.
Department of Materials Science and Engineering, University of Pennsylvania, 3231 Walnut Street, Philadelphia, Pennsylvania 19104, United States.
Acc Chem Res. 2024 Mar 5;57(5):739-750. doi: 10.1021/acs.accounts.3c00761. Epub 2024 Feb 25.
ConspectusThe intrinsic molecular order of liquid crystals (LCs) and liquid crystalline elastomers (LCEs) is the origin of their stimuli-responsive properties. The programmable responsiveness and functionality, such as shape morphing and color change under external stimuli, are the key features that attract interest in designing LC- and LCE-based intelligent material platforms. Methods such as mechanical stretching and shearing, surface alignment, and field-assisted alignment have been exploited to program the order of LC molecules for the desired responsiveness. However, the huge size mismatch between the nanometer-sized LC mesogens and the targeted macroscopic objects calls for questions about how to delicately control molecular order for desired performance. Microparticles that can be synthesized with intrinsic molecular order precisely controlled to micrometer size can be used as building blocks for bulk materials, thus offering opportunities to bridge the gap and transcend molecular orders across scales. By taking advantage of the interfacial anchoring effects, we can control and engineer the molecular orders inside the microdroplets, allowing for the realization of various responsive behaviors. Furthermore, designer LC microparticles with multiple responsiveness can be assembled and confined within a matrix, opening a new pathway to engineering LC-enabled intelligent materials.In this Account, we present our recent work on exploiting the molecular order inside microdroplets for the construction of intelligent materials. We briefly introduce the typical chemicals used in the synthesis and the methods developed to control LC molecular alignment within a microdroplets. We then present examples of microparticles synthesized from microdroplets that can transform into complex morphologies upon cooling from the isotropic to nematic phase or due to phase separation within the droplets coupled with the segregation of LC oligomers (LCOs) with polydisperse chain lengths. Furthermore, we show the synthesis of elliptical LCE microparticles and exploit their thermal and magnetic responsiveness to program shape-morphing behaviors and microarrays with switchable optical polarization. By mixing magnetic nanoparticles in cholesteric liquid crystals (CLCs) and silicone oils, we created Janus microparticles capable of color switching for camouflage and information encryption. Moreover, we can engineer complex molecular orders in LCE microparticles by mixing different surfactants, yielding microparticles of diverse anisotropic, temperature-responsive shapes after photopolymerization and extraction of the template LC molecules with different solvents. We conclude the Account with an outlook on the design of intelligent material systems via the design of unprecedented molecular ordering within the microparticles and their coupling with bulk materials.
综述
液晶(LC)和液晶弹性体(LCE)的固有分子排列是其刺激响应特性的起源。可编程的响应性和功能性,如在外部刺激下的形状变形和颜色变化,是吸引人们设计基于LC和LCE的智能材料平台的关键特性。诸如机械拉伸和剪切、表面取向以及场辅助取向等方法已被用于对LC分子的排列进行编程,以实现所需的响应性。然而,纳米尺寸的LC液晶元与目标宏观物体之间巨大的尺寸不匹配引发了关于如何精确控制分子排列以实现所需性能的问题。可以合成其固有分子排列被精确控制到微米尺寸的微粒,这些微粒可作为块状材料的构建单元,从而为弥合差距并跨越尺度超越分子排列提供了机会。通过利用界面锚定效应,我们可以控制和设计微滴内部的分子排列,从而实现各种响应行为。此外,具有多种响应性的定制LC微粒可以组装并限制在基质内,为工程化基于LC的智能材料开辟了一条新途径。
在本综述中,我们展示了我们最近关于利用微滴内部的分子排列来构建智能材料的工作。我们简要介绍了合成中使用的典型化学品以及为控制微滴内LC分子排列而开发的方法。然后,我们展示了由微滴合成的微粒的例子,这些微粒在从各向同性相冷却到向列相时或由于微滴内的相分离以及具有多分散链长的LC低聚物(LCO)的分离而转变为复杂形态。此外,我们展示了椭圆形LCE微粒的合成,并利用它们的热响应性和磁响应性来编程形状变形行为以及具有可切换光学偏振的微阵列。通过将磁性纳米颗粒与胆甾相液晶(CLC)和硅油混合,我们制备了能够进行颜色切换以用于伪装和信息加密的Janus微粒。此外,我们可以通过混合不同的表面活性剂来设计LCE微粒中的复杂分子排列,在光聚合并用不同溶剂萃取模板LC分子后,得到具有各种各向异性、温度响应形状的微粒。我们在本综述结尾展望了通过设计微粒内前所未有的分子排列及其与块状材料的耦合来设计智能材料系统。