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    <title>Repository Collection: null</title>
    <link>https://scholar.dgist.ac.kr/handle/20.500.11750/60679</link>
    <description />
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        <rdf:li rdf:resource="https://scholar.dgist.ac.kr/handle/20.500.11750/60951" />
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    <dc:date>2026-11-05T04:49:23Z</dc:date>
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  <item rdf:about="https://scholar.dgist.ac.kr/handle/20.500.11750/60951">
    <title>Meniscus-Guided Soft-Lithographic Assembly of Grid-Type Molecular Martensite Films for Single-Crystal-Like Actuation</title>
    <link>https://scholar.dgist.ac.kr/handle/20.500.11750/60951</link>
    <description>Title: Meniscus-Guided Soft-Lithographic Assembly of Grid-Type Molecular Martensite Films for Single-Crystal-Like Actuation
Author(s): Ra, Sooyeon; Jagdale, Sourabh R.; Jang, Jin Hyeok; Jang, Minwoo; Hwang, Kyoungtae; Lee, Taewoo; Jeong, Eun Hui; Yoon, Soon Ho; Moon, Byung Joon; Son, Jangyup; Lee, Dong-Su; Bae, Sukang; Park, Jun Dong; Kim, Tae-Wook; An, Sangmin; Park, Sang Kyu
Abstract: Dynamic molecular martensites exhibit large, reversible deformations and high force densities. However, device integration has been limited by the brittleness and poor formability of single crystals. Here, we report a thin-film route that translates molecular cooperativity into processable actuator architectures while preserving directional deformation. Meniscus-guided printing is combined with microtransfer molding to fabricate two-dimensional grid actuators of 6,13-bis(triisopropylsilylethynyl)pentacene. A partial drag-out regime in microchannel molds delays crystallization and enables seed-mediated sequential growth across intersections between horizontal and vertical microchannels. This mechanism produces a preferred b-axis-correlated preferential texture across the grid, with the crystallographic b-axis nearly aligned with the printing direction while allowing a small in-plane offset in twin-related variants. This texture provides the structural basis for predictable deformation comparable to that in single crystals. The resulting films are ultrathin, transferable over centimeter-scale areas, and mechanically robust, reproducing large thermoelastic strain and withstanding repeated actuation cycles without loss of performance. Beyond simple elongation, multi-unit assemblies can be constructed to achieve compression, demonstrating how different spatial arrangements enable various modes of actuation. Thus, this study bridges molecular-scale cooperativity and thin-film manufacturability, and provides an extendable strategy for translating thermally stable, solution-processable dynamic crystalline materials into functional, transferable, and microstructured actuator platforms.</description>
    <dc:date>2026-08-31T15:00:00Z</dc:date>
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