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自推进双嵌段共聚物链的构型与动力学

Configuration and dynamics of a self-propelled diblock copolymer chain.

作者信息

Jiao Yang, Wang Jing, Tian Wen-de, Chen Kang

机构信息

Center for Soft Condensed Matter Physics & Interdisciplinary Research, School of Physical Science and Technology, Soochow University, Suzhou 215006, China.

School of Physics and Information Engineering, Shanxi Normal University, Linfen 041004, China.

出版信息

Soft Matter. 2023 Jul 26;19(29):5468-5476. doi: 10.1039/d3sm00596h.

Abstract

Active polymers are slender or chain-like self-propelled objects. Synthetic chains of self-propelled colloidal particles are one of the examples, which provide a potential way to develop varied active polymers. Here, we study the configuration and dynamics of an active diblock copolymer chain. Our focus is on the competition and the cooperation between the equilibrium self-assembly due to chain heterogeneity and the dynamic self-assembly due to propulsion. Simulations show that an active diblock copolymer chain can form the spiral(+)/tadpole(+) states under forward propulsion and the spiral(-)/tadpole(-)/bean states under backward propulsion. Interestingly, it is easier for the backward-propelled chain to form a spiral. The transitions between the states can be analyzed in terms of work and energy. For forward propulsion, we found a key quantity, the chirality of the packed self-attractive A block, which determines the configuration of the whole chain and the dynamics. However, no such quantity is found for the backward propulsion. Our results set the foundation for further study of the self-assembly of multiple active copolymer chains and provide a reference for the design and application of polymeric active materials.

摘要

活性聚合物是细长的或链状的自推进物体。自推进胶体颗粒的合成链就是其中一个例子,它为开发各种活性聚合物提供了一种潜在途径。在此,我们研究活性双嵌段共聚物链的构型和动力学。我们关注的是由于链的不均匀性导致的平衡自组装与由于推进作用导致的动态自组装之间的竞争与合作。模拟表明,活性双嵌段共聚物链在向前推进时可形成螺旋(+)/蝌蚪(+)态,在向后推进时可形成螺旋(-)/蝌蚪(-)/豆状态。有趣的是,向后推进的链更容易形成螺旋。这些状态之间的转变可以从功和能量的角度进行分析。对于向前推进,我们发现了一个关键量,即紧密堆积的自吸引A嵌段的手性,它决定了整个链的构型和动力学。然而,对于向后推进未发现这样的量。我们的结果为进一步研究多个活性共聚物链的自组装奠定了基础,并为聚合物活性材料的设计和应用提供了参考。

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