The recent rapid growth in graphene-based supercapacitors has reached the point where there is a need for solid-state devices with physical flexibility, which will be a crucial advantage in modern electronic devices. Herein, we summarize recent developments toward an all solidstate graphene-based flexible supercapacitor. The routes to produce graphene-based electrode materials, along with the typical fabrication techniques for flexible devices, are thoroughly discussed. Furthermore, the structural morphology of the electrode materials is closely related to the electrochemical performance, and the influence of the electrode components on the mechanical flexibility of the fabricated devices is examined. Lastly, a summary of the overall electrochemical properties and current development of the reported devices is presented progressively to predict the future trends toward the realization of an ultimate-performance graphene-based flexible supercapacitor.
17This paper essentially reviews the types of graphene-based nanofillers and the fabrication of 18 graphene/polymer nanocomposites. Routes to produce the graphene materials, along with the 19 methods and modifications used to efficiently disperse the graphene nanofillers within the 20 polymer matrices are discussed. In addition, the mechanical properties, morphological, 21 structural, electrical conductivities, electrochemical activities, thermal stabilities, and gas 22 barrier properties are evaluated, along with the direct relationships of these properties with 23 the graphene-polymer interaction and their dispersion in the polymer matrix. Finally, a brief 24 summary of the practical applications of polymeric-graphene materials along with the current 25
SUMMARYA flexible polypyrrole/graphene oxide/manganese oxide-based supercapacitor was prepared via an electrodeposition process. The polypyrrole, graphene oxide, and manganese oxide were deposited onto a flexible and highly porous nickel foam, which acted as a current collector to enhance the electrochemical performances. The good coverage of the polypyrrole, graphene oxide, and manganese oxide onto the scaffold of the nickel foam was evidenced using field emission scanning electron microscopy and X-ray diffraction. The manganese species, which were present in the oxidation states of Mn 3+ and Mn 4+ , were shown using X-ray photoelectron spectroscopy. The presence of Mn 2 O 3 and MnO 2 polymorphs was detected using Fourier transform infrared and Raman spectroscopies. The cyclic stability of the ternary supercapacitor was consistent regardless of its geometry and curvature. In contrast, an activated carbon supercapacitor possesses limited energy storage capability compared to a ternary supercapacitor, which suppresses the electrochemical performances of activated carbon. The ternary as-fabricated supercapacitor could retain a specific capacitance of 96.58% after 1000 cycles, and the as-synthesized energy storage device was able to light up a light emitting diode.
Poly(lactic acid) (PLA)/poly(ε-caprolactone) (PCL) blends were prepared via melt blending technique. Glycidyl methacrylate (GMA) was added as reactive compatibilizer to improve the interfacial adhesion between immiscible phases of PLA and PCL matrices. Tensile test revealed that optimum in elongation at break of approximately 327% achieved when GMA loading was up to 3wt%. Slight drop in tensile strength and tensile modulus at optimum ratio suggested that the blends were tuned to be deformable. Flexural studies showed slight drop in flexural strength and modulus when GMA wt% increases as a result of improved flexibility by finer dispersion of PCL in PLA matrix. Besides, incorporation of GMA in the blends remarkably improved the impact strength. Highest impact strength was achieved (160% compared to pure PLA/PCL blend) when GMA loading was up to 3 wt%. SEM analysis revealed improved interfacial adhesion between PLA/PCL blends in the presence of GMA. Finer dispersion and smooth surface of the specimens were noted as GMA loading increases, indicating that addition of GMA eventually improved the interfacial compatibility of the nonmiscible blend.
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