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      Self-healable electroluminescent devices

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          Abstract

          Electroluminescent (EL) devices have been extensively integrated into multi-functionalized electronic systems in the role of the vitally constituent light-emitting part. However, the lifetime and reliability of EL devices are often severely restricted by concomitant damage, especially when the strain exceeds the mechanical withstanding limit. We report a self-healable EL device by adopting a modified self-healable polyacrylic acid hydrogel as the electrode and a self-healable polyurethane as a phosphor host to realize the first omni-layer-healable light-emitting device. The physicochemical properties of each functionalized layer can be efficiently restored after experiencing substantial catastrophic damage. As a result, the luminescent performance of the self-healable EL devices is well recovered with a high healing efficiency (83.2% for 10 healing cycles at unfixed spots, and 57.7% for 20 healing cycles at a fixed spot). In addition, inter-device healing has also been developed to realize a conceptual “LEGO”-like assembly process at the device level for light-emitting devices. The design and realization of the self-healable EL devices may revive their performance and expand their lifetime even after undergoing a deadly cut. Our self-healable EL devices may serve as model systems for electroluminescent applications of the recently developed ionically conductive healable hydrogels and dielectric polymers.

          Electroluminescence: Self-healing electroluminescent devices

          Inspired by the self-healing abilities of biological systems, scientists have developed an electroluminescent (EL) device that heals itself after being damaged, paving the way for a range of new applications. Although EL devices are used in a wide range of electronic applications, including backlights for the control panels, digital displays, and wearable electronics, they are prone to damage, which restricts their working life and reliability, limiting their applications. Now, Chunyi Zhi and colleagues from the City University of Hong Kong have developed the first self-healing EL device by using a modified self-healable polyacrylic acid hydrogel for electrodes and self-healable polyurethane as a phosphor host. Even after experiencing dozens of catastrophic damages, the physiochemical properties of the device can be restored and could be used in new applications, such as healable hydrogels and dielectric polymers.

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          Most cited references26

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          An electrically and mechanically self-healing composite with pressure- and flexion-sensitive properties for electronic skin applications.

          Pressure sensitivity and mechanical self-healing are two vital functions of the human skin. A flexible and electrically conducting material that can sense mechanical forces and yet be able to self-heal repeatably can be of use in emerging fields such as soft robotics and biomimetic prostheses, but combining all these properties together remains a challenging task. Here, we describe a composite material composed of a supramolecular organic polymer with embedded nickel nanostructured microparticles, which shows mechanical and electrical self-healing properties at ambient conditions. We also show that our material is pressure- and flexion-sensitive, and therefore suitable for electronic skin applications. The electrical conductivity can be tuned by varying the amount of nickel particles and can reach values as high as 40 S cm(-1). On rupture, the initial conductivity is repeatably restored with ∼90% efficiency after 15 s healing time, and the mechanical properties are completely restored after ∼10 min. The composite resistance varies inversely with applied flexion and tactile forces. These results demonstrate that natural skin's repeatable self-healing capability can be mimicked in conductive and piezoresistive materials, thus potentially expanding the scope of applications of current electronic skin systems.
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            Hydraulically amplified self-healing electrostatic actuators with muscle-like performance.

            Existing soft actuators have persistent challenges that restrain the potential of soft robotics, highlighting a need for soft transducers that are powerful, high-speed, efficient, and robust. We describe a class of soft actuators, termed hydraulically amplified self-healing electrostatic (HASEL) actuators, which harness a mechanism that couples electrostatic and hydraulic forces to achieve a variety of actuation modes. We introduce prototypical designs of HASEL actuators and demonstrate their robust, muscle-like performance as well as their ability to repeatedly self-heal after dielectric breakdown-all using widely available materials and common fabrication techniques. A soft gripper handling delicate objects and a self-sensing artificial muscle powering a robotic arm illustrate the wide potential of HASEL actuators for next-generation soft robotic devices.
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              A self-healable and highly stretchable supercapacitor based on a dual crosslinked polyelectrolyte

              Superior self-healability and stretchability are critical elements for the practical wide-scale adoption of personalized electronics such as portable and wearable energy storage devices. However, the low healing efficiency of self-healable supercapacitors and the small strain of stretchable supercapacitors are fundamentally limited by conventional polyvinyl alcohol-based acidic electrolytes, which are intrinsically neither self-healable nor highly stretchable. Here we report an electrolyte comprising polyacrylic acid dual crosslinked by hydrogen bonding and vinyl hybrid silica nanoparticles, which displays all superior functions and provides a solution to the intrinsic self-healability and high stretchability problems of a supercapacitor. Supercapacitors with this electrolyte are non-autonomic self-healable, retaining the capacitance completely even after 20 cycles of breaking/healing. These supercapacitors are stretched up to 600% strain with enhanced performance using a designed facile electrode fabrication procedure.
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                Author and article information

                Contributors
                junfan@cityu.edu.hk
                852-34427891 , cy.zhi@cityu.edu.hk
                Journal
                Light Sci Appl
                Light Sci Appl
                Light, Science & Applications
                Nature Publishing Group UK (London )
                2095-5545
                2047-7538
                5 December 2018
                5 December 2018
                2018
                : 7
                : 102
                Affiliations
                [1 ]ISNI 0000 0004 1792 6846, GRID grid.35030.35, Department of Materials Science and Engineering, , City University of Hong Kong, ; 83 Tat Chee Avenue, Kowloon, China
                [2 ]ISNI 0000 0004 1792 6846, GRID grid.35030.35, Shenzhen Research Institute, , City University of Hong Kong, ; High-Tech Zone, Nanshan District Shenzhen, 518057 China
                Article
                96
                10.1038/s41377-018-0096-8
                6281662
                76fef794-51b7-41c7-b645-eba853a1cf99
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 11 June 2018
                : 30 October 2018
                : 4 November 2018
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