文献类型：期刊文献

英文题名：Organic Molecule-Driven Polymeric Actuators

作者：Lin, Huijuan[1,2];Zhang, Suyun[3];Xiao, Yan[4];Zhang, Chenjun[1,2];Zhu, Jixin[1,2];Dunlop, John W. C.[5];Yuan, Jiayin[6]

机构：[1]Nanjing Tech Univ, Key Lab Flexible Elect, Jiangsu Natl Synerget Innovat Ctr Adv Mat, Nanjing 210009, Jiangsu, Peoples R China;[2]Nanjing Tech Univ, Inst Adv Mat, Jiangsu Natl Synerget Innovat Ctr Adv Mat, Nanjing 210009, Jiangsu, Peoples R China;[3]Chinese Acad Sci, State Key Lab Struct Chem, Fujian Inst Res Struct Matter, Fuzhou 350002, Fujian, Peoples R China;[4]East China Univ Sci & Technol, Key Lab Ultrafine Mat, Minist Educ, Sch Mat Sci & Engn, Shanghai 200237, Peoples R China;[5]Paris Lodron Univ Salzburg, Morphophys Grp, Dept Chem & Phys Mat, A-5020 Salzburg, Austria;[6]Stockholm Univ, Dept Mat & Environm Chem, Arrhenius Lab, S-10691 Stockholm, Sweden

年份：2019

卷号：40

期号：7

外文期刊名：MACROMOLECULAR RAPID COMMUNICATIONS

收录：;EI(收录号：20191006590576);WOS:【SCI-EXPANDED(收录号:WOS:000467997700009)】；

基金：H.L. and S.Z. equally contributed to this work. This work was financially supported by the National Natural Science Foundation of China (21403234), the Natural Science Foundation of Shanghai (18ZR1410200), the Jiangsu Provincial Foundation for Distinguished Young Scholar (BK20170045), start-up fund at Nanjing Tech University (3827400203), and National Key Basic Research Program of China (973) (2015CB932200). J.Y. acknowledges financial support from the European Research Council (ERC) Starting Grant (No. 639720-NAPOLI), the Wallenberg Academy Fellow program (No. KAW2017.0166) from the Knut and Alice Wallenberg Foundation in Sweden, and the Strategic Fund from Stockholm University (Contract number: SU FV-2.1.1-005).

语种：英文

外文关键词：bilayer structures; gradient type; organic molecule-driven motions; polymeric actuators

摘要：Inspired by the motions of plant tissues in response to external stimuli, significant attention has been devoted to the development of actuating polymeric materials. In particular, polymeric actuators driven by organic molecules have been designed due to their combined superiorities of tunable functional monomers, designable chemical structures, and variable structural anisotropy. Here, the recent progress is summarized in terms of material synthesis, structure design, polymer-solvent interaction, and actuating performance. In addition, various possibilities for practical applications, including the ability to sense chemical vapors and solvent isomers, and future directions to satisfy the requirement of sensing and smart systems are also highlighted.