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      Electropolymerized Poly(3,4-ethylenedioxythiophene)/Screen-Printed Reduced Graphene Oxide–Chitosan Bilayer Electrodes for Flexible Supercapacitors

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          Abstract

          An electropolymerized poly(3,4-ethylenedioxythiophene) (PEDOT)/screen-printed reduced graphene oxide (rGO)–chitosan (CS) bilayer material was coated on carbon cloth to form electrodes for gel-electrolyte flexible supercapacitors. The conductive polymer and carbon-based materials mainly contribute pseudocapacitance (PC) and electrical double-layer capacitance (EDLC), respectively. The high porosity and hydrophilicity of the PEDOT/rGO–CS bilayer material offers a large contact area and improves the contact quality for the gel electrolyte, thereby enhancing the capacitive performance. Cyclic voltammetry (CV) under a potential scan rate of 2 mV/s revealed that a maximum areal capacitance of 1073.67 mF/cm 2 was achieved. The capacitance contribution ratio PC/EDLC was evaluated to be ∼67/33 by the Trasatti method. A 10,000-cycle CV test showed a capacitance retention rate of 99.3% under a potential scan rate of 200 mV/s, indicating good stability. The areal capacitance remains similar under bending with a bending curvature of up to 1.5 cm –1.

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          Highly flexible and all-solid-state paperlike polymer supercapacitors.

          In recent years, much effort have been dedicated to achieve thin, lightweight and even flexible energy-storage devices for wearable electronics. Here we demonstrate a novel kind of ultrathin all-solid-state supercapacitor configuration with an extremely simple process using two slightly separated polyaniline-based electrodes well solidified in the H(2)SO(4)-polyvinyl alcohol gel electrolyte. The thickness of the entire device is much comparable to that of a piece of commercial standard A4 print paper. Under its highly flexible (twisting) state, the integrate device shows a high specific capacitance of 350 F/g for the electrode materials, well cycle stability after 1000 cycles and a leakage current of as small as 17.2 μA. Furthermore, due to its polymer-based component structure, it has a specific capacitance of as high as 31.4 F/g for the entire device, which is more than 6 times that of current high-level commercial supercapacitor products. These highly flexible and all-solid-state paperlike polymer supercapacitors may bring new design opportunities of device configuration for energy-storage devices in the future wearable electronic area.
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            “Inner” and “outer” active surface of RuO2 electrodes

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              Wearable Self-Charging Power Textile Based on Flexible Yarn Supercapacitors and Fabric Nanogenerators.

              A novel and scalable self-charging power textile is realized by combining yarn supercapacitors and fabric triboelectric nanogenerators as energy-harvesting devices.
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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                21 June 2021
                29 June 2021
                : 6
                : 25
                : 16455-16464
                Affiliations
                []Graduate Institute of Applied Mechanics, National Taiwan University , Taipei City 106319, Taiwan
                []Department of Materials Science and Engineering, National Taiwan University , Taipei City 106319, Taiwan
                [§ ]Department of Mechanical Engineering, National Taiwan University , Taipei City 106319, Taiwan
                []Graduate Institute of Photonics and Optoelectronics & Department of Electrical Engineering, National Taiwan University , Taipei City 106319, Taiwan
                []Advanced Research Center for Green Materials Science and Technology, National Taiwan University , Taipei City 106319, Taiwan
                Author notes
                Author information
                https://orcid.org/0000-0003-3972-1086
                https://orcid.org/0000-0003-2209-3298
                https://orcid.org/0000-0002-1071-2234
                Article
                10.1021/acsomega.1c01601
                8246451
                34235317
                0350869e-e288-4265-85fd-83c930031ea2
                © 2021 The Authors. Published by American Chemical Society

                Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works ( https://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 25 March 2021
                : 10 June 2021
                Funding
                Funded by: Ministry of Education, doi 10.13039/501100002701;
                Award ID: 110L9006
                Funded by: Ministry of Science and Technology, Taiwan, doi 10.13039/501100004663;
                Award ID: MOST 110-2634-F-002-043
                Funded by: Ministry of Science and Technology, Taiwan, doi 10.13039/501100004663;
                Award ID: MOST 108-2221-E-002-088-MY3
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                Article
                Custom metadata
                ao1c01601
                ao1c01601

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