Zhang Yang, Zhan Qi, Wang Changrui, Gao Jie, Zhou Guofu, Zhao Wei, Chen Jiawen
South China Academy of Advanced Optoelectronics, South China Normal University, Guangzhou 510006, China.
SCNU-TUE Joint Lab of Device Integrated Responsive Materials (DIRM), National Center for International Research on Green Optoelectronics, South China Normal University, Guangzhou 510006, China.
ACS Appl Mater Interfaces. 2023 Oct 24. doi: 10.1021/acsami.3c12732.
Polymer-stabilized liquid crystals (PSLCs) are important electrically switchable materials due to their superior electro-optical properties. Nevertheless, it remains a formidable challenge to balance PSLCs' instant electro-optical performance and long-term durability due to their relatively low polymer content and the related sensitivity to external force. Herein, we demonstrate the possibility of regulating the polymer network structure in PSLCs via reversible addition-fragmentation chain transfer (RAFT) polymerization reactions of acrylate monomers with a chain transfer agent (CTA). By controlling the concentration of CTA and conditions of photopolymerization, the kinetics of the polymerization reaction can be modified. Compared to conventional free-radical (FR) polymerization, the reduced chain growth rate leads to sufficient chain relaxation, reorientation of liquid crystal (LC) directors, and alleviation of shrinkage stresses in the RAFT polymerization process. This in turn produces an ordered polymer network structure in the vertical direction and a uniform distribution in the horizontal plane. As a result, the PSLC network presents increased elasticity with a lower hysteresis effect and greatly improved durability. Our research offers insightful guidance for the fine-tuning of polymer network structures to prepare advanced LC/polymer composite structures with outstanding performances.
聚合物稳定液晶(PSLCs)因其优异的电光性能而成为重要的电可切换材料。然而,由于其聚合物含量相对较低以及对外力的相关敏感性,要平衡PSLCs的即时电光性能和长期耐久性仍然是一项艰巨的挑战。在此,我们展示了通过丙烯酸酯单体与链转移剂(CTA)的可逆加成-断裂链转移(RAFT)聚合反应来调节PSLCs中聚合物网络结构的可能性。通过控制CTA的浓度和光聚合条件,可以改变聚合反应的动力学。与传统自由基(FR)聚合相比,链增长速率降低导致链充分松弛、液晶(LC)指向矢重新取向,并减轻了RAFT聚合过程中的收缩应力。这反过来在垂直方向上产生有序的聚合物网络结构,在水平面上产生均匀分布。结果,PSLC网络呈现出更高的弹性,滞后效应更低,耐久性大大提高。我们的研究为微调聚合物网络结构以制备具有优异性能的先进LC/聚合物复合结构提供了有见地的指导。