Photomotility of polymers

被引:218
作者
Wie, Jeong Jae [1 ,2 ,3 ]
Shankar, M. Ravi [4 ]
White, Timothy J. [1 ]
机构
[1] Air Force Res Lab, Mat & Mfg Directorate, Wright Patterson AFB, OH 45433 USA
[2] Azimuth Corp, Dayton, OH 45432 USA
[3] Inha Univ, Dept Polymer Sci & Engn, Inchon 22212, South Korea
[4] Univ Pittsburgh, Dept Ind Engn, Pittsburgh, PA 15261 USA
关键词
MOLECULAR-CRYSTALS; SOFT ROBOT; NETWORKS; MOTION; GLASSY; LIGHT; ACTUATORS; SURFACE; MECHANICS;
D O I
10.1038/ncomms13260
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Light is distinguished as a contactless energy source for microscale devices as it can be directed from remote distances, rapidly turned on or off, spatially modulated across length scales, polarized, or varied in intensity. Motivated in part by these nascent properties of light, transducing photonic stimuli into macroscopic deformation of materials systems has been examined in the last half-century. Here we report photoinduced motion (photomotility) in monolithic polymer films prepared from azobenzene-functionalized liquid crystalline polymer networks (azo-LCNs). Leveraging the twisted-nematic orientation, irradiation with broad spectrum ultraviolet-visible light (320-500 nm) transforms the films from flat sheets to spiral ribbons, which subsequently translate large distances with continuous irradiation on an arbitrary surface. The motion results from a complex interplay of photochemistry and mechanics. We demonstrate directional control, as well as climbing.
引用
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页数:8
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