S. Chandra Sekhar

Wearable Fabrics with Self-Branched Bimetallic Layered Double Hydroxide Coaxial Nanostructures for Hybrid Supercapacitors

We report a flexible battery-type electrode based on binder-free nickel cobalt layered double hydroxide nanosheets adhered to nickel cobalt layered double hydroxide nanoflake arrays on nickel fabric (NC LDH NFAs@NSs/Ni fabric) using facile and eco-friendly synthesis methods. Herein, we utilized discarded polyester fabric as a cost-effective substrate for in situ electroless deposition of Ni, which exhibited good flexibility, light weight, and high conductivity. Subsequently, the vertically aligned NC LDH NFAs were grown on Ni fabric by means of a hot-air oven-based method, and fluffy-like NC LDH NS branches are further decorated on NC LDH NFAs by a simple electrochemical deposition method. The as-prepared core-shell-like nanoarchitectures improve the specific surface area and electrochemical activity, which provides the ideal pathways for electrolyte diffusion and charge transportation. When the electrochemical performance was tested in 1 M KOH aqueous solution, the core-shell-like NC LDH NFAs@NSs/Ni fabric electrode liberated a maximum areal capacity of 536.96 μAh/cm2 at a current density of 2 mA/cm2 and excellent rate capability of 78.3% at 30 mA/cm2 (420.5 μAh/cm2) with a good cycling stability. Moreover, a fabric-based hybrid supercapacitor (SC) was assembled, which achieves a stable operational potential window of 1.6 V, a large areal capacitance of 1147.23 mF/cm2 at 3 mA/cm2, and a high energy density of 0.392 mWh/cm2 at a power density of 2.353 mW/cm2. Utilizing such high energy storage abilities and flexible properties, the fabricated hybrid SC operated the wearable digital watch and electric motor fan for real-time applications.

Designed construction of yolk–shell structured trimanganese tetraoxide nanospheres via polar solvent-assisted etching and biomass-derived activated porous carbon materials for high-performance asymmetric supercapacitors

Recently, yolk–shell structured electrode materials have attracted increasing interest in supercapacitors (SCs) due to their high surface area, good electrochemical activity and excellent mechanical stability towards superior energy storage performance. However, the synthesis strategies to prepare such yolk–shell structured materials without using chemical surfactants/solid templates are still inferior. Herein, a facile and cost-effective strategy to design yolk–shell structured trimanganese tetraoxide nanospheres (Mn3O4 NSs) with a distinctive core–void–shell configuration to use as an efficient positive electrode material in asymmetric SCs is demonstrated. Specifically, the yolk–shell structured Mn3O4 NSs were prepared by the inclusion of water droplets to the manganese precursor–isopropyl alcohol system, which facilitates the inside-out Ostwald ripening process to construct a yolk–shell-like configuration with porous properties. In aqueous electrolyte solution, the corresponding material exhibited a high specific capacitance (211.36 F g−1 at a current density of 0.5 A g−1), a good rate capability (79.4% at 10 A g−1) and an excellent cycling stability (92% after 2000 cycles) compared to its solid counterparts. Meanwhile, a low-cost material based on biomass-derived activated carbon with a honeycomb-like structure is also prepared using waste corrugated boxes, which exhibits a reliable electrochemical performance for use as a negative electrode material. Moreover, the fabricated asymmetric SC using both electrode materials offers a maximum potential window of 2 V with higher energy density (19.47 W h kg−1) and power density (2263.89 W kg−1) values, which can effectively power up commercial light-emitting diodes for practical applications.

Birnessite-type MnO2 nanosheet arrays with interwoven arrangements on vapor grown carbon fibers as hybrid nanocomposites for pseudocapacitors

Manganese dioxide nanosheet arrays with interconnected arrangements are easily synthesized on vapor grown carbon fibers (MnO2 NSAs@VCFs) by a simple wet-chemical method at low temperature. The conductive nature of the VCFs serves as a scaffold and easily reduces potassium permanganate species for the formation of hierarchical MnO2 NSAs@VCFs. When utilized as an electroactive material for pseudocapacitors, the sophisticated configuration of the nanocomposite provides an effective electrochemical activity and an electron pathway for higher electrochemical performance in 1 M Na2SO4 aqueous solution. The hierarchical MnO2 NSAs@VCFs exhibit a maximum specific capacitance of 115.3 F g-1 at a current density of 0.5 A g-1 with an excellent cycling stability of 85.6% after 2000 cycles at a current density of 5 A g-1. Such facile and cost-effective fabrication of a metal oxide nanocomposite with improved electrochemical performance allows it to be considered as a promising electroactive material for energy storage devices.

A facile drop-casting approach to nanostructured copper oxide-painted conductive woven textile as binder-free electrode for improved energy storage performance in redox-additive electrolyte

Hierarchical copper oxide (CuO) nanostructures (NSs) with caterpillar-like morphologies were facilely integrated onto a highly flexible conductive woven textile substrate (CWTs) by a drop-casting approach. Initially, the CuO NSs were synthesized via a simple and green wet-chemical method in 30 min and the obtained colloidal solution of CuO was easily dropped onto well-cleaned CWTs. By virtue of their interesting structural features, the caterpillar-like CuO NSs on CWTs were employed as binder-free electrodes for supercapacitors and their electrochemical properties were investigated in 1 M KOH solution. Additionally, a small portion of redox-additive potassium ferricyanide (K3Fe(CN)6) was added to the 1 M KOH solution, which led to efficient enhancement of energy storage performance with superior cycling stability for the caterpillar-like CuO NSs on CWTs. Furthermore, the fabricated asymmetric supercapacitor (SC) with CuO NSs on CWTs and activated carbon with an operating potential window of 1.5 V simultaneously exhibited excellent energy density and power density values. Such a simple and low-cost approach to easily construct metal oxide nanomaterials on flexible textiles with redox-additive electrolyte may be useful for several potential applications in high-performance energy storage devices.

Rational design of forest-like nickel sulfide hierarchical architectures with ultrahigh areal capacity as a binder-free cathode material for hybrid supercapacitors

Evolution of a simple, efficient and reproducible strategy for the rational design of hierarchically structured metal chalcogenide-based supercapacitors has attracted considerable research interest in recent years. Herein, a facile wet-chemistry approach is employed to design three-dimensional forest-like porous nickel sulfide nanotrees on nickel foam (NiS NTs/Ni foam) for use as a cathode material in hybrid supercapacitors. The growth time plays a crucial role in controlling the surface morphology, and the optimal growth conditions (3 h at 85 °C) led to the growth of forest-like NiS NTs/Ni foam with reliable adherence. The forest-like NiS NTs/Ni foam shows maximum areal and specific capacities of 752.71 μA h cm−2 and 342.1 mA h g−1 at a current density of 4 mA cm−2, with an excellent cycling stability of 89.4%. This result is primarily due to the availability of more surface-active sites in the well-defined hierarchical architecture, which allow the rapid diffusion of electrolyte ions and minimize the electron transport limitation. Utilizing the hierarchical NiS NTs/Ni foam as a cathode and activated carbon-based anode, we further fabricated a hybrid supercapacitor, which demonstrates a wide potential window of 1.6 V with high areal energy and power densities of 0.472 mW h cm−2 and 21.5 mW cm−2, respectively. The fabricated hybrid supercapacitor is successfully utilized to drive various electronic gadgets for real-life applications. The electrochemical performance of a hierarchically structured NiS-based binder-free electrode with our facile approach paves a new pathway for the development of novel metal chalcogenides for high-performance hybrid supercapacitors.

Fallen leaves derived honeycomb-like porous carbon as a metal-free and low-cost counter electrode for dye-sensitized solar cells with excellent tri-iodide reduction

Utilizing carbon-based counter electrodes (CEs) in dye-sensitized solar cells (DSSCs) have received much attention in recent times, owing to their low cost, good electrochemical activity, natural abundance and eco-friendly nature. Herein, we have facilely prepared quince leaves derived porous carbon (QLPC) using fallen quince leaves (QLs) and it was used as a cost-effective CE for the fabrication of DSSCs. By means of alkali treatment and pyrolysis process (at different temperatures of 700, 800 and 900 °C), the QLs powder undergoes chemical activation and carbonization, which results in a honeycomb-like QLPC with abundant micro/mesopores and large surface area. Simple and straightforward coating of QLPC samples onto fluorine doped tin oxide glass substrates led to improved electrocatalytic activity and good tri-iodide reduction in DSSCs. When the DSSCs were illuminated under 1 sun condition (AM 1.5; 100 mW cm-2), the device assembled with QLPC-based CE (prepared at 800 °C) showed a higher current density of ∼14.99 mA/cm2 and power conversion efficiency of ∼5.52% among the other QLPC-based CEs, which are comparable with the platinum-based CE in DSSCs. This facile process for the preparation of biomass derived carbon-based CE provides an alternative to the noble metal-free CE in DSSCs.

Achieving a High Areal Capacity with a Binder-Free Copper Molybdate Nanocone Array-Based Positive Electrode for Hybrid Supercapacitors

Herein, we develop a binder-free copper molybdate nanocone array with a prism-like morphology on nickel foam (Cu3Mo2O9 NCAs/Ni foam) using a single-step hydrothermal method. With an optimal growth time (10 h) under hydrothermal conditions, the prism-like Cu3Mo2O9 NCAs are uniformly decorated on Ni foam with good adhesion and crystallinity. The prepared Cu3Mo2O9 NCAs/Ni foam has been directly used as a binder-free electrode to examine its suitability as a positive electrode in hybrid supercapacitors. In an aqueous 1 M KOH electrolyte, the binder-free Cu3Mo2O9 NCAs/Ni foam showed battery-type behavior with a high areal capacity of 449.5 μAh cm-2 at a discharge current density of 2 mA cm-2 and also exhibited a good cycling stability. In addition, the pouch-type hybrid supercapacitor is assembled using the prism-like Cu3Mo2O9 NCAs/Ni foam as a positive electrode and the activated carbon as a negative electrode in a 1 M KOH electrolyte. The hybrid supercapacitor achieves a maximum cell potential of 1.6 V with superior energy storage properties, including a high areal capacitance of 609.7 mF cm-2 at 3.5 mA cm-2, a high areal energy (0.21 mWh cm-2), and a high power density (2.73 mW cm-2). The obtained results suggest that the facilely synthesized Cu3Mo2O9 NCAs/Ni foam electrode has great potential in high-performance energy storage devices.

Hierarchically Designed Ag@Ce6Mo10O39 Marigold Flower-Like Architectures: An Efficient Electrode Material for Hybrid Supercapacitors

We facilely prepared silver nanoparticle-decorated Ce6Mo10O39 marigold flower-like structures (Ag NPs@CM MFs) for use as an effective positive material in hybrid supercapacitors (HSCs). With the aid of ethylenediaminetetraacetic acid (EDTA) as a chelating agent, self-assembled CM MFs were synthesized by a single-step hydrothermal method. When the electrochemical properties were tested in an aqueous alkaline electrolyte, the synthesized CM MFs with 0.15 g of EDTA exhibited a relatively high charge storage property (55.3 μA h/cm2 at 2 mA/cm2) with a battery-type redox behavior. The high capacity performance is mainly because of the large surface area of the CM MFs, and the hierarchically connected nanoflakes provide wide open wells for rapid accessibility of electrolyte ions and enable fast transportation of electrons. A further improvement in electrochemical performance was achieved (62 μA h/cm2 at 2 mA/cm2) by decorating Ag NPs on the surface of the CM MFs (i.e., Ag NPs@CM MFs), which is attributed to the increased electric conductivity. Considering the synergistic effect and the high electrochemical activity, Ag NPs@CM MFs were further employed as an effective positive electrode for the fabrication of pouch-type HSC with porous carbon (negative electrode) in an alkaline electrolyte. The HSC exhibited a high cell potential (1.5 V) with maximum energy and power densities of 0.0183 mW h/cm2 and 10.237 mW/cm2, respectively. The potency of HSC in practical applications was also demonstrated by energizing red and yellow light-emitting diodes as well as a three-point pattern torch light.