Chemically Controlled Bending of Compositionally Anisotropic Microcylinders
Chemically Controlled Bending of Compositionally Anisotropic Microcylinders
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DOI:
10.1002/anie.201105387
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发表时间:
2012-01-01
影响因子:
16.6
通讯作者:
Lahann, Joerg
中科院分区:
文献类型:
--
作者:
Saha, Sampa;Copic, Davor;Lahann, Joerg
Soft materials that can undergo mechanical actuation in response to external stimuli,[1–7] such as changes in temperature, light, pHvalue, or ionic strength, have attracted increasing attention because of their potential use as thinfilm actuators,[8–10] smart sutures,[11, 12] and soft robots.[13, 14] These materials typically require specialty polymers, such as shape-memory polymers [15] or use macroscopically layered films.[16, 17] In layered films, the anisotropic distribution of two polymers, or a polymer and a metal, is essential. This creates a mismatch in mechanical properties that gives rise to a defined bending. In principle, this concept is not limited to macroscopic multilayer films, but can be achieved with colloidal materials, as long as the required anisotropy can be realized and different parts of the colloidal object will respond differently to the external stimulus. In recent years, compositionally anisotropic micro-and nanoparticles have been devised using a range of different synthesis methods including microfluidic and lithographic techniques,[18] particle replication in low surface energy templates,[19] selective crosslinking of polybutadiene segments in terpolymers,[20] lithographic patterning of microspheres,[21] electrochemical [22] and photochemical [23] reduction, templating of porous membranes [24, 25] and nanotubes,[26] surfactant aided growth,[27] graft polymerization,[28–30] and processes based on controlled surface nucleation.[31] Alternatively, electrohydrodynamic co-jetting is a method to prepare particles and fibers with multiple compartments by transferring fluids through a set of capillaries that can process dissimilar materials.[32] In the past, electrohydrodynamic co-jetting has resulted in particles with multiple compartments that contain different polymer blends, dyes, low-molecular weight additives, reactive molecules and even inorganic nanoparticles.[33, 34] If a reactive additive, such as a functionalized polymer, is added to one of the compartments, selective surface modification is possible and can result in spatially controlled immobilization of proteins or peptides.[35–37]Because different compartments can be loaded with dissimilar materials, entirely new sets of functions can arise from unique synergistic effects,[36] not just from the addition of the properties of the individual compartments. Herein, we report a new type of compositionally anisotropic microcylinders, where defined compartments within the same microcylinder undergo differential expansion due to the site-selective growth of a surface layer. The asymmetric expansion creates surface stresses resulting in significant and controllable bending of the microcylinders, which depends on the particle geometry and the architecture of the surface layers. Using finite element simulations, we verify the observed bending trends and derive a family of performance curves that predict a wide-range tunability of the actuation stroke based on the cylinder geometry and the amount of swelling.