MWCNT/Ruthenium hydroxide aerogel supercapacitor production and investigation of electrochemical performances.
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ABSTRACT:
SUBMITTER: Korkmaz S
PROVIDER: S-EPMC9329456 | biostudies-literature |
REPOSITORIES: biostudies-literature
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Project description:High-quality ultrathin two-dimensional nanosheets of ?-Ni(OH)2 are synthesized at large scale via microwave-assisted liquid-phase growth under low-temperature atmospheric conditions. After heat treatment, non-layered NiO nanosheets are obtained while maintaining their original frame structure. The well-defined and freestanding nanosheets exhibit a micron-sized planar area and ultrathin thickness (<2 nm), suggesting an ultrahigh surface atom ratio with unique surface and electronic structure. The ultrathin 2D nanostructure can make most atoms exposed outside with high activity thus facilitate the surface-dependent electrochemical reaction processes. The ultrathin ?-Ni(OH)2 and NiO nanosheets exhibit enhanced supercapacitor performances. Particularly, the ?-Ni(OH)2 nanosheets exhibit a maximum specific capacitance of 4172.5 F g(-1) at a current density of 1 A g(-1). Even at higher rate of 16 A g(-1), the specific capacitance is still maintained at 2680 F g(-1) with 98.5% retention after 2000 cycles. Even more important, we develop a facile and scalable method to produce high-quality ultrathin transition metal hydroxide and oxide nanosheets and make a possibility in commercial applications.
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Project description:A novel electroactive polypyrrole/graphene oxide@graphene aerogel (PGO@GA) was synthesized for the first time by pulse electropolymerization. The off-time in this technique allows polypyrrole (PPy) to go through a more stable structural arrangement, meanwhile its electronic transmission performance is enhanced by immobilizing graphene oxide between PPy chains. Moreover, graphene aerogel provides a three-dimensional structure with high conductivity to protect PPy from swelling and shrinking during the capacitive testing. Under these synergistic effects, PGO@GA presents exceptional capacitive performances including high specific capacitance (625 F g-1 at 1 A g-1), excellent rate capability (keeping 478 F g-1 at 15 A g-1 with retention rate of 76.5%), and excellent cycling life (retaining 85.7% of its initial value when cycling 5000 times at 10 A g-1). Therefore, the strategy adopted by this research provides a good reference for preparing other PPy-based electrode materials applied in the fields of catalysis, sensing, adsorption and energy storage.
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Project description:In this study, we examine the electrochemical performance of supercapacitor (SC) electrodes made from 3D-printed nanocomposites. These composites consist of multiwalled carbon nanotubes (MWCNTs) and polyether ether ketone (PEEK), coated with poly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS). The electrochemical performance of a 3D-printed PEEK/MWCNT solid electrode with a surface area density of 1.2 mm-1 is compared to two distinct periodically porous PEEK/MWCNT electrodes with surface area densities of 7.3 and 7.1 mm-1. To enhance SC performance, the 3D-printed electrodes are coated with a conductive polymer, PEDOT:PSS. The architected cellular electrodes exhibit significantly improved capacitive properties, with the cellular electrode (7.1 mm-1) displaying a capacitance nearly four times greater than that of the solid 3D-printed electrode-based SCs. Moreover, the PEDOT:PSS-coated cellular electrode (7.1 mm-1) demonstrates a high specific capacitance of 12.55 mF·cm-3 at 50 mV·s-1, contrasting to SCs based on 3D-printed cellular electrodes (4.09 mF·cm-3 at 50 mV·s-1) without the coating. The conductive PEDOT:PSS coating proves effective in reducing surface resistance, resulting in a decreased voltage drop during the SCs' charging and discharging processes. Ultimately, the 3D-printed cellular nanocomposite electrode with the conductive polymer coating achieves an energy density of 1.98 μW h·cm-3 at a current of 70 μA. This study underscores how the combined effect of the surface area density of porous electrodes enabled by 3D printing, along with the conductivity imparted by the polymer coating, synergistically improves the energy storage performance.
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Project description:The NiO-CNT and NiO-Fe-CNT composites that have been prepared from waste high density polyethylene plastic and their carbon nanotube (CNT) quality-dependent supercapacitance tuning have been reported here. Multiwalled CNT (MWCNT) formation has been confirmed from TEM and Raman spectra with an ID/IG ratio of 0.77, which stands for high graphitization. The specific surface area (SSA) of MWCNTs in the NiO-Fe-CNT composite was 87.8 m2/g, while in the NiO-CNT composite, it was 25 m2/g. NiO-Fe-CNT displayed higher specific capacitance and energy density (1360 Fg-1 and 1180 W h kg-1) than NiO-CNT (1250 Fg-1 and 1000 W h kg-1), which may be due to the presence of higher-quality MWCNTs in the NiO-Fe-CNT composite. NiO-Fe-CNT displayed higher contributions of electric double-layer capacitor (59%) behavior compared to NiO-CNT (38%) and represented a hybrid supercapacitor. NiO-Fe-CNT also displayed a capacitive retention of 96% after 1000 charge-discharge cycles. Furthermore, studies in acidic electrolytes revealed higher performance of NiO-Fe-CNT than NiO-CNT, displaying specific capacitances of NiO-Fe-CNT to be 1147 Fg-1 in 2 M H2SO4 and 943 Fg-1 in 2 M HCl. It has been qualitatively explored that the quality of CNTs, SSA, and quantum confinement effects in the composites may be the factors responsible for the performance difference in NiO-Fe-CNT and NiO-CNT. The present work is geared toward the low-cost fabrication of high-quality CNT composites for supercapacitors and energy storage applications. The present work also contributes quantitatively to the understanding of CNT quality as an important parameter for the performance of CNT-composite-based supercapacitors.
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Project description:Hybrid electric storage systems that combine capacitive and faradaic materials need to be well designed to benefit from the advantages of batteries and supercapacitors. The ultimate capacitive material is graphite (GR), yet high capacitance is usually not achieved due to restacking of its sheets. Therefore, an appealing approach to achieve high power and energy systems is to embed a faradaic 2D material in between the graphite sheets. Here, a simple one-step approach was developed, whereby a faradaic material [layered double hydroxide (LDH)] was electrochemically formed inside electrochemically exfoliated graphite. Specifically, GR was exfoliated under negative potentials by CoII and, in the presence of MnII , formed GR-CoMn-LDH, which exhibited a high areal capacitance and energy density. The high areal capacitance was attributed to the exfoliation of the graphite at very negative potentials to form a 3D foam-like structure driven by hydrogen evolution as well as the deposition of CoMn-LDH due to hydroxide ion generation inside the GR sheets. The ratio between the CoII and MnII in the CoMn-LDH was optimized and analyzed, and the electrochemical performance was studied. Analysis of a cross-section of the GR-CoMn-LDH confirmed the deposition of LDH inside the GR layers. The areal capacitance of the electrode was 186 mF cm-2 at a scan rate of 2 mV s-1 . Finally, an asymmetric supercapacitor was assembled with GR-CoMn-LDH and exfoliated graphite as the positive and negative electrodes, respectively, yielding an energy density of 96.1 μWh cm-3 and a power density of 5 mW cm-3 .
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Project description:In the context of recent progress in designing metal-organic framework (MOF)-based supercapacitor electrodes, we report herein the successful growth of two different crystal morphologies of a cerium-based MOF, octahedral crystals named IRH-2-O and elongated square-bipyramidal crystals named IRH-2-ESBP (IRH = Institute de Recherche sur l'Hydrogène). The identical crystal structure of both materials was confirmed by powder X-ray diffraction (PXRD). Furthermore, scanning electron microscopy and energy-dispersive X-ray mapping analysis corroborated this fact and showed the crystal shape variation versus the surface composition of synthesized materials. Fourier transform infrared spectroscopy, UV-vis spectroscopy, and PXRD were used to confirm the purity of pristine MOFs as well as desired MOF//PANI composites. Cyclic voltammetry and electrochemical impedance spectroscopy highlighted the effect of crystal shape on the electrochemical performance of IRH-2 MOFs; the specific capacitance tripled from 43.1 F·g-1 for IRH-2-O to 125.57 F·g-1 for IRH-2-ESBP at 5 mV·s-1. The cycling stability was notably ameliorated from 7 K for IRH-2-O to 20 K for IRH-2-ESBP. Regarding the composites, the cell voltage was notably ameliorated from 1.8 to 1.95 V. However, the electrochemical performance of IRH-2/PANI composites was drastically decreased due to instability in the acidic media. To the best of our knowledge, our work is the first work that related the MOF crystal shape and the electrochemical performance.
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Project description:Three-dimensional (3D) nanostructures have attracted considerable attention because of their high surface areas and unique properties which gives outstanding performance in catalysis and energy storage applications. This paper proposes the growth mechanism of 3D flower-like β-Ni(OH)2 constructed through a two dimensional sheet framework using a one-step oleylamine-assisted solvothermal approach, where oleylamine acts as the surfactant, co-solvent, stabilizer, and reducing agent. A detailed examination of the product morphology after various reaction times suggested that the self-assembly of flower occurs through a mechanism involving nucleation, Ostwald ripening, and recrystallization. The associated characterization revealed it to be pure β-Ni(OH)2 without any sign of contamination. The effect of the morphology (sheet to 3D flower-like β-Ni(OH)2) on the electrochemical supercapacitive behavior was assessed by cyclic voltammetry and galvanostatic charge-discharge tests. The results showed that 3D flower-like β-Ni(OH)2 exhibited better specific capacitance of ~1567 F g(-1) at a current density of 1 A g(-1) and retained ~25% capacitance at a high current density of 10 A g(-1) compared to the other reference materials. The superior electrochemical properties of the 3D flower-like β-Ni(OH)2 originate from their large specific surface area and unique structure.
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