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      Photocontrollable liquid-crystalline block copolymers: design, photo-directed self-assembly and applications

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          Abstract

          Recent progress in various photocontrollable liquid-crystalline block copolymers, including their photoresponsive mechanisms, alignment techniques of microphase-separated nanodomains, outstanding properties and applications is shown.

          Abstract

          Photocontrollable liquid-crystalline block copolymers have exhibited remarkable light-response properties, due to their unique features elegantly combining mesogenic ordering with microphase-separated nanostructures. Their exceptional optical characteristics make them excellent candidates for ever-increasingly widespread applications, especially, in the area which is utilized for nanopatterns. However, their unsatisfactory structure design and performance have limited their further potential in those applications. In the last few years, tremendous efforts have been made to improve their capability and performance by elaborating the structural design strategy. Here, we summarize recent progress in various photocontrollable liquid-crystalline block copolymers, including their photoresponsive mechanisms, alignment techniques of microphase-separated nanodomains, and intriguing properties. Critical discussions are given in directed self-assembly, which is a novel bottom-up lithography technology that can be manipulated by actinic light. Additionally, their potential applications in energy storage, holographic gratings, photo-driven actuators, nanotemplates and information storage are comprehensively summarized. Finally, the existing challenges and prospects in this field are discussed.

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          Most cited references131

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          Block Copolymers—Designer Soft Materials

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            Epitaxial self-assembly of block copolymers on lithographically defined nanopatterned substrates.

            Parallel processes for patterning densely packed nanometre-scale structures are critical for many diverse areas of nanotechnology. Thin films of diblock copolymers can self-assemble into ordered periodic structures at the molecular scale (approximately 5 to 50 nm), and have been used as templates to fabricate quantum dots, nanowires, magnetic storage media, nanopores and silicon capacitors. Unfortunately, perfect periodic domain ordering can only be achieved over micrometre-scale areas at best and defects exist at the edges of grain boundaries. These limitations preclude the use of block-copolymer lithography for many advanced applications. Graphoepitaxy, in-plane electric fields, temperature gradients, and directional solidification have also been demonstrated to induce orientation or long-range order with varying degrees of success. Here we demonstrate the integration of thin films of block copolymer with advanced lithographic techniques to induce epitaxial self-assembly of domains. The resulting patterns are defect-free, are oriented and registered with the underlying substrate and can be created over arbitrarily large areas. These structures are determined by the size and quality of the lithographically defined surface pattern rather than by the inherent limitations of the self-assembly process. Our results illustrate how hybrid strategies to nanofabrication allow for molecular level control in existing manufacturing processes.
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              Photocontrol of fluid slugs in liquid crystal polymer microactuators

              The manipulation of small amounts of liquids has applications ranging from biomedical devices to liquid transfer. Direct light-driven manipulation of liquids, especially when triggered by light-induced capillary forces, is of particular interest because light can provide contactless spatial and temporal control. However, existing light-driven technologies suffer from an inherent limitation in that liquid motion is strongly resisted by the effect of contact-line pinning. Here we report a strategy to manipulate fluid slugs by photo-induced asymmetric deformation of tubular microactuators, which induces capillary forces for liquid propulsion. Microactuators with various shapes (straight, 'Y'-shaped, serpentine and helical) are fabricated from a mechanically robust linear liquid crystal polymer. These microactuators are able to exert photocontrol of a wide diversity of liquids over a long distance with controllable velocity and direction, and hence to mix multiphase liquids, to combine liquids and even to make liquids run uphill. We anticipate that this photodeformable microactuator will find use in micro-reactors, in laboratory-on-a-chip settings and in micro-optomechanical systems.
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                Author and article information

                Contributors
                Journal
                JMCCCX
                Journal of Materials Chemistry C
                J. Mater. Chem. C
                Royal Society of Chemistry (RSC)
                2050-7526
                2050-7534
                March 03 2023
                2023
                : 11
                : 9
                : 3180-3196
                Affiliations
                [1 ]School of Material Science and Engineering, Key Laboratory of Polymer Chemistry and Physics of Ministry of Education, Peking University, Beijing, 100871, China
                [2 ]College of Chemistry, Zhengzhou University, Zhengzhou, Henan 450001, People's Republic of China
                [3 ]Macao Institute of Materials Science and Engineering, Zhuhai MUST Science and Technology Research Institute, Faculty of Innovation Engineering, Macau University of Science and Technology, Taipa, 999078, Macao, China
                Article
                10.1039/D2TC05134F
                8b547c76-4c3a-4324-81af-2180d841795e
                © 2023

                http://rsc.li/journals-terms-of-use

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