Abstract:Fiber-shaped supercapacitors have drawn much attention for their great potential application in future portable and wearable electronics because of their outstanding flexibility, tiny volume, and good deformability. In this work, commercial poly(ethylene terephthalate) (PET) thread was successfully converted into an electrically conductive and electrochemically active thread by introducing copper sulfide (CuS) and polyaniline (PANI) via simple chemical bath deposition and electrochemical deposition. The obtain… Show more
“…This is proven by plotting the square root of the scan rage against the peak currents of the anodic and cathodic process of the redox transition ( Figure 5 b). The linear relationship implies that the redox reaction is diffusion controlled within the range of 20–300 mVs −1 , suggesting the good rate capability of the electrode [ 57 ].…”
The major drawbacks of the conventional methods for preparing polyaniline (PANI) are the large consumptions of toxic chemicals and long process durations. This paper presents a remarkably simple and green route for the chemical oxidative synthesis of PANI nanofibers, utilizing sodium phytate as a novel and environmentally friendly plant derived dopant. The process shows a remarkable reduction in the synthesis time and usage of toxic chemicals with good dispersibility and exceedingly high conductivity up to 10 S cm−1 of the resulting PANI at the same time. A detailed characterization of the PANI samples has been made showing excellent relationships between their structure and properties. Particularly, the electrochemical properties of the synthesized PANI as electrode material for supercapacitors were analyzed. The PANI sample, synthesized at pre-optimized conditions, exhibited impressive supercapacitor performance having a high specific capacitance (Csp) (832.5 Fg−1 and 528 Fg−1 at 1 Ag−1 and 40 Ag−1, respectively) as calculated from galvanostatic charge/discharge (GCD) curves. A good rate capability with a capacitance retention of 67.6% of its initial value was observed. The quite low solution resistance (Rs) value of 281.0 × 10−3 Ohm and charge transfer resistance value (Rct) of 7.44 Ohm represents the excellence of the material. Further, a retention of 95.3% in coulombic efficiency after 1000 charge discharge cycles, without showing any significant degradation of the material, was also exhibited.
“…This is proven by plotting the square root of the scan rage against the peak currents of the anodic and cathodic process of the redox transition ( Figure 5 b). The linear relationship implies that the redox reaction is diffusion controlled within the range of 20–300 mVs −1 , suggesting the good rate capability of the electrode [ 57 ].…”
The major drawbacks of the conventional methods for preparing polyaniline (PANI) are the large consumptions of toxic chemicals and long process durations. This paper presents a remarkably simple and green route for the chemical oxidative synthesis of PANI nanofibers, utilizing sodium phytate as a novel and environmentally friendly plant derived dopant. The process shows a remarkable reduction in the synthesis time and usage of toxic chemicals with good dispersibility and exceedingly high conductivity up to 10 S cm−1 of the resulting PANI at the same time. A detailed characterization of the PANI samples has been made showing excellent relationships between their structure and properties. Particularly, the electrochemical properties of the synthesized PANI as electrode material for supercapacitors were analyzed. The PANI sample, synthesized at pre-optimized conditions, exhibited impressive supercapacitor performance having a high specific capacitance (Csp) (832.5 Fg−1 and 528 Fg−1 at 1 Ag−1 and 40 Ag−1, respectively) as calculated from galvanostatic charge/discharge (GCD) curves. A good rate capability with a capacitance retention of 67.6% of its initial value was observed. The quite low solution resistance (Rs) value of 281.0 × 10−3 Ohm and charge transfer resistance value (Rct) of 7.44 Ohm represents the excellence of the material. Further, a retention of 95.3% in coulombic efficiency after 1000 charge discharge cycles, without showing any significant degradation of the material, was also exhibited.
“…[1][2][3][4][5] The general strategy to achieve structures having satisfactory both mechanical and electrochemical properties combines the elastic matrix (such as carbon clothes, elastoplastic films, cotton, cellulosic, and silk fibers) with fillers (carbon derivatives, conducting polymers, and metal oxide nanoparticles). 3,[6][7][8] However, the combination of different materials for use as flexible substrates (such as carbon paper 9 and cotton-based fibers 7,[10][11][12] ) introduces drawbacks under severe mechanical deformations, such as delamination and fast degradation. The development of all-gel-state supercapacitors is a possibility to avoid these processes because of the minimal interface between distinct materials applied in the assembly of devices.…”
The development of supramolecular structures (conducting hydrogels) obtained from the charge–charge interaction of sodium dodecyl sulfate micelles and oppositely charged polypyrrole chains represents an important step to obtain self‐supported and flexible electrodes for supercapacitors. Herein, the energy density of polypyrrole hydrogel‐based supercapacitors is enhanced by the incorporation of graphene nanoplatelets that introduced the electrical double capacitance contribution to the overall response. The electrochemical performance of synthesized electrodes was optimized from the relative variation in the concentration of supramolecular arrangements (micelles of sodium dodecyl sulfate), pyrrole, and graphene nanoplatelets. As result, higher capacitive retention is observed for modified electrodes (with the incorporation of graphene) – in order of 90% after 1000 cycles of use, preserving the high conductivity and intrinsic mechanical properties (flexibility and stretchability) reaching an areal capacitance of 210.7 mFcm−2.
“…utilized commercial polyethylene terephthalate (PET) thread as template to coat CuS followed by PANI via chemical bath deposition and electrodeposition. [ 178 ] The cost‐effectiveness, chemical inertness, high mechanical strength, and abundance of PET has caught the attention of research groups working in the field of FSCs. [ 179 ] The fabricated PANI/CuS/PET electrodes twisted together to form a symmetric TFSC and this device delivered a high specific capacitance of 29 mF cm −2 and 93.1% capacitance retention after 1000 cycles in PVA–H 3 PO 4 electrolyte.…”
Section: Fiber‐shaped Energy Storage Devicesmentioning
confidence: 99%
“…[ 179 ] The fabricated PANI/CuS/PET electrodes twisted together to form a symmetric TFSC and this device delivered a high specific capacitance of 29 mF cm −2 and 93.1% capacitance retention after 1000 cycles in PVA–H 3 PO 4 electrolyte. [ 178 ] The high electrical conductivity of PANI is favorable in aiding high specific capacitance to the electrode. In another attempt, a core–sheath porous structure that consisted of 1D PANI nanorods, which relieved the volume expansion during the charge–discharge process offered good stability to the electrode [ 180 ] ( Figure 19 ).…”
Section: Fiber‐shaped Energy Storage Devicesmentioning
Textile electronics embedded in clothing represent an exciting new frontier for modern healthcare and communication systems. Fundamental to the development of these textile electronics is the development of the fibers forming the cloths into electronic devices. An electronic fiber must undergo diverse scrutiny for its selection for a multifunctional textile, viz., from the material selection to the device architecture, from the wearability to mechanical stresses, and from the environmental compatibility to the end‐use management. Herein, the performance requirements of fiber‐shaped electronics are reviewed considering the characteristics of single electronic fibers and their assemblies in smart clothing. Broadly, this article includes i) processing strategies of electronic fibers with required properties from precursor to material, ii) the state‐of‐art of current fiber‐shaped electronics emphasizing light‐emitting devices, solar cells, sensors, nanogenerators, supercapacitors storage, and chromatic devices, iii) mechanisms involved in the operation of the above devices, iv) limitations of the current materials and device manufacturing techniques to achieve the target performance, and v) the knowledge gap that must be minimized prior to their deployment. Lessons learned from this review with regard to the challenges and prospects for developing fiber‐shaped electronic components are presented as directions for future research on wearable electronics.
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