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Verfasst von:Hsu, Li-Yun [VerfasserIn]   i
 Gomez Melo, Santiago [VerfasserIn]   i
 Vázquez-Martel, Clara [VerfasserIn]   i
 Spiegel, Christoph A. [VerfasserIn]   i
 Ziebert, Falko [VerfasserIn]   i
 Schwarz, Ulrich S. [VerfasserIn]   i
 Blasco, Eva [VerfasserIn]   i
Titel:Alignment and actuation of liquid crystals via 3D confinement and two-photon laser printing [data]
Verf.angabe:Li-Yun Hsu, Santiago Gomez Melo, Clara Vazquez-Martel, Christoph A. Spiegel, Falko Ziebert, Ulrich S. Schwarz, Eva Blasco
Verlagsort:Heidelberg
Verlag:Universität
E-Jahr:2024
Jahr:2024-07-02
Umfang:1 Online-Ressource (8 Files)
Fussnoten:Gefördert durch: Deutsche Forschungsgemeinschaft: Excellence Cluster “3D Matter Made to Order” EXC-2082/1-390761711; Carl Zeiss Foundation: Carl-Zeiss-Foundation-FocusHEiKA; Fonds der Chemischen Industrie: Kekulé Fellowship ; Gesehen am 01.08.2024
Abstract:Liquid crystalline (LC) materials are especially suited for the preparation of active 3D/4D microstructures using two-photon laser printing. To achieve the desired actuation, the alignment of the LCs has to be controlled during the printing process. In most cases studied to date, the alignment relied on surface modifications and therefore, complex alignment patterns and concomitant actuation were not possible. Here, we introduce a strategy for spatially aligning LC domains in three-dimensional space by utilizing 3D-printed polydimethylsiloxane-based microscaffolds as confinement barriers, which induce the desired director field. The director field resulting from the boundary conditions is calculated with Landau de Gennes theory and validated by comparing experimentally measured and theoretically predicted birefringence patterns. We demonstrate our procedures for structures of varying complexity and then employed to fabricate 4D microstructures that show the desired actuation. Overall, we obtain excellent agreement between theory and experiment. This opens the door for rational design of functional materials for 4D (micro)printing in the future.
DOI:doi:10.11588/data/CHNSX7
URL:kostenfrei: Volltext: https://doi.org/10.11588/data/CHNSX7
 kostenfrei: Volltext: https://heidata.uni-heidelberg.de/dataset.xhtml?persistentId=doi:10.11588/data/CHNSX7
 DOI: https://doi.org/10.11588/data/CHNSX7
Datenträger:Online-Ressource
Dokumenttyp:Forschungsdaten
 Datenbank
Sprache:eng
Sonstige Nr.:Grant number: DFG EXC-2082/1-390761711
Sach-SW:Chemistry
K10plus-PPN:1897343361
 
 
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