Amrita De Adhikari

A V2O5 nanorod decorated graphene/polypyrrole hybrid electrode: a potential candidate for supercapacitors

Vanadium pentoxide (V2O5) nanorod decorated graphene polypyrrole nanocomposites have been synthesized successfully by a facile hydrothermal process for supercapacitor (SC) applications. The morphological study revealed the successful decoration of V2O5 nanorods and polypyrrole (PPy) within the intergallery of graphitic materials due to their high degree of propensity for intercalation which leads to the formation of mesoporous 3D nanostructures. These mesoporous structures can efficiently allow fast diffusion and ion transport at the electrode–electrolyte interface towards high electrochemical utilization and superior performance. Here, decoration of V2O5 within a polymer matrix along with a graphitic material renders different electrical profiles by virtue of their electron hopping within nanocomposites. Galvanostatic charging discharging revealed that VGP was found to be superior with a maximum specific capacitance of 787 F g−1 at a current density of 1 A g−1 using KCl as an electrolyte. These observations were also confirmed by electrochemical measurements through CV and EIS studies. Furthermore, cyclic stability performed for 5000 consecutive cycles also substantiate their high durability and high power delivery uptake. Thus, considering all such key features, V2O5 based nanocomposites can be suitable for SC applications.

Hierarchical self-assembled nanoclay derived mesoporous CNT/polyindole electrode for supercapacitors

A series of self-assembled and open interconnected mesoporous CNT/polyindole (Pind) electrodes were synthesized by a facile in situ & ex situ approach in the presence of layered silicate material. In the present study, the presence of nanoclay and its electrochemical performance is explored on the imparted hierarchical structure of CNT/Pind (CI) system. The microstructural evolution and coating of Pind on CNT and the nanoclay sheet revealed the formation of a high surface area interconnected mesoporous structure which can efficiently allow easy penetration and rapid transport of electrolyte ions for an improved electrochemical performance. Cyclic voltammetry (CV) analysis at 10 mV s−1 revealed the in situ and ex situ incorporation of the nanoclay to the CNT/Pind system exhibited a 258% and 136% increase in the specific capacitance of the ternary nanocomposite, respectively. These observations were very consistent with the 148% increased specific capacitance of NI (nanoclay/Pind) as compared to Pind. Galvanostatic charging–discharging (GCD) and electrochemical impedance spectroscopy (EIS) also confirmed the improved electronic conductivity and cyclic stability of electrode material. In situ CNI (i.e. CNT/nanoclay/Pind) displayed a better electrochemical performance than ex situ CIN (i.e. CNT/Pind/nanoclay) and other related systems. That the electrode exhibited 96% of the initial specific capacitance retention after 2000 cycles also suggests a high cyclic stability and power delivery uptake of electrode material. It is believed that a nanoclay tailored CNT/Pind nanocomposite can effectively promote their high utilization for SC application.

Zn-doped SnO2 nano-urchin-enriched 3D carbonaceous framework for supercapacitor application

Hierarchical Zn-doped SnO2 nano-urchins decorated on RGO nanosheets were fabricated for supercapacitor applications. In this study, SnO2 nanospheres were doped with Zn2+ to tailor their electrical and morphological properties. Zn2+ doping of the SnO2 nanospheres prevented Sn clustering and thereby reduced the particle size leading to the formation of urchin-like nanostructures. These urchins with a high surface area and short transport paths can offer high capacitive performance by assembling with RGO nanosheets. The X-ray photoelectron spectroscopy and X-ray diffraction analyses confirmed the presence of SnO2 crystal planes and successful doping of the Zn2+. The incorporation of the RGO nanosheets augmented the coulombic efficiency, specific capacitance, and cycling performance. The enhancement of the capacitive behavior resulted from the synergistic effects owing to the combined properties of pseudocapacitance and double layer capacitance. The composite electrode material offered a specific capacitance of 635 F g−1 at a current density of 1 A g−1 and has a high cycling stability up to 5000 cycles with a capacitance retention of 78.4%.

Polyaniline-Stabilized Intertwined Network-like Ferrocene/Graphene Nanoarchitecture for Supercapacitor Application

The present work highlights the effective H-π interaction between metallocenes (ferrocene; Fc) and graphene and their stabilization in the presence of polyaniline (PANI) through π-π interactions. The PANI-stabilized Fc@graphene nanocomposite (FcGA) resembled an intertwined network-like morphology with high surface area and porosity, which could make it a potential candidate for energy-storage applications. The relative interactions between the components were assessed through theoretical (DFT) calculations. The specific capacitance calculated from galvanostatic charging/discharging indicated that the PANI-stabilized ternary nanocomposite exhibited a maximum specific capacitance of 960 F g- at an energy density of 85 Wh Kg-1 and a current density of 1 A g- . Furthermore, electrochemical impedance spectroscopy (EIS) analysis confirmed the low internal resistance of the as-prepared nanocomposites, which showed improved charge-transfer properties of graphene after incorporation of Fc and stabilization with PANI. Additionally, all electrodes were found to be stable up to 5000 cycles with a specific capacitance retention of 86 %, thus demonstrating the good reversibility and durability of the electrode material.