Department of Polymer Science & Engineering, University of Massachusetts, Amherst, MA 01003 (USA).
Angew Chem Int Ed Engl. 2015 Apr 27;54(18):5434-7. doi: 10.1002/anie.201412160. Epub 2015 Mar 5.
Patterning deformation within the plane of thin elastic sheets represents a powerful tool for the definition of complex and stimuli-responsive 3D buckled shapes. Previous experimental methods, however, have focused on sheets that access a limited number of shapes pre-programmed into the sheet, restricting the degree of dynamic control. Here, we demonstrate on-demand reconfigurable buckling of poly(N-isopropylacrylamide-co-acrylic acid) (PNIPAM) hydrogel network films containing gold nanoparticles (AuNPs) by patterned photothermal deswelling. Predictable, easily controllable, and reversible transformations from a single flat gel sheet to numerous different three-dimensional forms are shown. Importantly, the response time is limited by poroelastic mass transport, rather than photochemical switching kinetics, enabling reconfiguration of shape on timescales of several seconds, with further increases in speed possible by reducing film thickness.
在薄弹性片平面内进行图案变形是定义复杂和响应刺激的 3D 弯曲形状的有力工具。然而,以前的实验方法主要集中在能够获取预先编程到片材中的有限数量形状的片材上,从而限制了动态控制的程度。在这里,我们通过图案化光热收缩证明了含有金纳米粒子(AuNPs)的聚(N-异丙基丙烯酰胺-共-丙烯酸)(PNIPAM)水凝胶网络膜的按需可重构弯曲。显示了从单个平凝胶片到许多不同三维形式的可预测、易于控制和可逆的转变。重要的是,响应时间受多孔弹性质量传输而不是光化学开关动力学的限制,从而能够在几秒钟的时间尺度内重新配置形状,通过减小膜厚度可以进一步提高速度。