期刊
ADVANCED MATERIALS
卷 34, 期 12, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202106535
关键词
3D printing; liquid crystals; materials computation; polymerization; unconventional triggers
类别
资金
- Army Research Office [W911NF-15-1-0568, W911NF-17-1-0575]
This study presents a chemically triggered polymerization method based on a liquid crystal printhead, which allows for spatial and temporal control. By designing different geometries of the liquid crystal printhead, various polymerization reactions can be achieved: bulk solution polymerization, synthesis of thin surface-confined polymeric coatings, polymerization-induced self-assembly of block copolymers to form different nanostructures, and 3D printing of polymeric structures based on local solution conditions. The approach utilizes amphiphiles, multivalent ions, and biomolecules as stimuli.
Polymerization reactions triggered by stimuli play a pivotal role in materials science, with applications ranging from lithography to biomedicine to adaptive materials. However, the development of chemically triggered, stimuli-responsive systems that can confer spatial and temporal control on polymerization remains a challenge. Herein, chemical-stimuli-induced polymerization based on a liquid crystal (LC) printhead is presented. The LC responds to a local chemical stimulus at its aqueous interface, resulting in the ejection of initiator into the solution to trigger polymerization. Various LC printhead geometries are designed, allowing programming of: i) bulk solution polymerization, ii) synthesis of a thin surface-confined polymeric coating, iii) polymerization-induced self-assembly of block copolymers to form various nanostructures (sphere, worm-like, and vesicles), and iv) 3D polymeric structures printed according to local solution conditions. The approach is demonstrated using amphiphiles, multivalent ions, and biomolecules as stimuli.
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