<?xml version="1.0" encoding="UTF-8"?>
<rss xmlns:dc="http://purl.org/dc/elements/1.1/" version="2.0">
  <channel>
    <title>Repository Collection: null</title>
    <link>https://scholar.dgist.ac.kr/handle/20.500.11750/60679</link>
    <description />
    <pubDate>Thu, 05 Nov 2026 04:48:21 GMT</pubDate>
    <dc:date>2026-11-05T04:48:21Z</dc:date>
    <item>
      <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>
      <pubDate>Mon, 31 Aug 2026 15:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://scholar.dgist.ac.kr/handle/20.500.11750/60951</guid>
      <dc:date>2026-08-31T15:00:00Z</dc:date>
    </item>
  </channel>
</rss>

