Unraveling CoNiP-CoP2 3D-on-1D Hybrid Nanoarchitecture for Long-Lasting Electrochemical Hybrid Cells and Oxygen Evolution Reaction.

Evolving cost-effective transition metal phosphides (TMPs) using general approaches for energy storage is pivotal but challenging. Besides, the absence of noble metals and high electrocatalytic activity of TMPs allow their applicability as catalysts in oxygen evolution reaction (OER). Herein, CoNiP-CoP2 (CNP-CP) composite is in situ deposited on carbon fabric by a one-step hydrothermal technique. The CNP-CP reveals hybrid nanoarchitecture (3D-on-1D HNA), i.e., cashew fruit-like nanostructures and nanocones. The CNP-CP HNA electrode delivers higher areal capacity (82.8 µAh cm-2 ) than the other electrodes. Furthermore, a hybrid cell assembled with CNP-CP HNA shows maximum energy and power densities of 31 µWh cm-2 and 10.9 mW cm-2 , respectively. Exclusively, the hybrid cell demonstrates remarkable durability over 30 000 cycles. In situ/operando X-ray absorption near-edge structure analysis confirms the reversible changes in valency of Co and Ni elements in CNP-CP material during real-time electrochemical reactions.  Besides, a quasi-solid-state device unveils its practicability by powering electronic components. Meanwhile, the CNP-CP HNA verifies its higher OER activity than the other catalysts by revealing lower overpotential (230 mV). Also, it exhibits relatively small Tafel slope (38 mV dec-1 ) and stable OER activity over 24 h. This preparation strategy may initiate the design of advanced TMP-based materials for multifunctional applications.

One-Pot Hydrothermal-Derived NiS2 -CoMo2 S4 with Vertically Aligned Nanorods as a Binder-Free Electrode for Coin-Cell-Type Hybrid Supercapacitor.

Transition bimetallic sulfides are exploited as high-capacity electrode materials in energy storage devices owing to their abundant electroactive sites and relatively high electrical conductivity compared with metal oxides. Here, an in situ conversion of metal ions into NiS2 -CoMo2 S4 vertically aligned nanorod arrays on nickel foam (NS-CMS NRAs@NF) using a one-step hydrothermal technique to address the "dead-mass" limitation and multi-step preparation methods is reported. An in situ-converted NS-CMS NRAs obtained for 12 h of reaction time (NS-CMS NRAs-12 h@NF) delivers a superior areal capacity of 780 µAh cm-2 to the other NS-CMS electrodes synthesized for 6 h (543.1 µAh cm-2 ) and 18 h (636.7 µAh cm-2 ) at 7 mA cm-2 . A coin-cell-type hybrid supercapacitor (HSC) is also fabricated to unveil the practical adaptability of NS-CMS NRAs-12 h@NF electrode. Utilizing its structural and active material intriguing features, assembled coin-cell-type HSC achieves a high areal capacitance of 246.2 mF cm-2 (5 mA cm-2 ) along with maximum areal energy density (147 µWh cm-2 ) and power density (21.3 mW cm-2 ), respectively. Furthermore, the capability of coin-cell-type HSC in real-time applications is also inspected. This work promotes in situ deposition strategy to fabricate metal sulfide-based nanostructures for high-performance electrochemical capacitors.

Nanosilver-Particles Integrated Ni3 Sn2 S2 -CoS Composite as an Advanced Electrode for High Energy Density Hybrid Cell.

An ion-exchange process is a promising approach to design advanced electrode materials for high-performance energy storage devices. Herein, a nanostructured Ni3 Sn2 S2 -CoS (NSS-CS) composite is fabricated by successive hydrothermal and ion-exchange processes. Since the incorporation of redox-rich cobalt element enables the NSS-CS composite to be more electrochemically active, its impact on the electrochemical performance is therefore extensively studied. Particularly, the NSS-CS-0.2 g electrode material delivered a high areal capacity of 830.4 µAh cm-2 at 5 mA cm-2 . Additionally, a room-temperature wet-chemical approach is employed to anchor nanosilver (nAg)-particles on the NSS-CS-0.2 g (nAg@NSS-CS-0.2 g) to further exalt its electrokinetics. Consequently, the nAg@NSS-CS-0.2 g electrode shows a higher areal capacity of 948.5 µAh cm-2 (193.5 mAh g-1 ) than that of the NSS-CS-0.2 g. Furthermore, its practicability is also examined by assembling a hybrid cell. The assembled hybrid cell delivers a high areal capacity of 969.2 µAh cm-2 (49.2 mAh g-1 ) at 7 mA cm-2 and maximum areal energies and power densities of 0.784 mWh cm-2 (40.8 Wh kg-1 ) and 45 mW cm-2 (2347.4 W kg-1 ), respectively. The efficiency of the hybrid cells is also tested by harvesting solar energy, followed by energizing electronic components. This work can pave the way for significant attraction in designing advanced electrodes for energy-related fields.

Metal-Organic Framework-Derived Co3 V2 O8 @CuV2 O6 Hybrid Architecture as a Multifunctional Binder-Free Electrode for Li-Ion Batteries and Hybrid Supercapacitors.

Metal-organic frameworks (MOFs) are promising materials in diverse fields because of their constructive traits of varied structural topologies, high porosity, and high surface area. MOFs are also an ideal precursor/template to derive porous and functional morphologies. Herein, Co3 V2 O8 nanohexagonal prisms are grafted on CuV2 O6 nanorod arrays (CuV-CoV)-grown copper foam (CF) using solution-processing methods, followed by thermal treatment. Direct preparation of active material on CF can potentially eliminate electrochemically inactive and non-conductive binders, leading to improved charge-transfer rate. Furthermore, solution-processing methods are simple and cost-effective. Owing to versatile valence states and good redox activity, the vanadium-incorporated mixed metal oxides (CuV-CoV) exhibited superior electrochemical performance in lithium (Li)-ion battery and supercapacitor (SC) studies. Furthermore, hollow carbon particles (HCPs) derived from MOF particles (MOF-HCPs) are used as the anode material in SCs. A hybrid SC (HSC) fabricated with CuV-CoV and MOF-HCP materials exhibited noteworthy electrochemical properties. Moreover, a solid-state HSC (SSHSC) is constructed and its real-time feasibility is investigated by harvesting the dynamic energy of a bicycle with the help of a direct current generator. The charged SSHSCs potentially powered various electronic components.

Ternary MOF-Based Redox Active Sites Enabled 3D-on-2D Nanoarchitectured Battery-Type Electrodes for High-Energy-Density Supercapatteries.

Designing rationally combined metal-organic frameworks (MOFs) with multifunctional nanogeometries is of significant research interest to enable the electrochemical properties in advanced energy storage devices. Herein, we explored a new class of binder-free dual-layered Ni-Co-Mn-based MOFs (NCM-based MOFs) with three-dimensional (3D)-on-2D nanoarchitectures through a polarity-induced solution-phase method for high-performance supercapatteries. The hierarchical NCM-based MOFs having grown on nickel foam exhibit a battery-type charge storage mechanism with superior areal capacity (1311.4 µAh cm-2 at 5 mA cm-2), good rate capability (61.8%; 811.67 µAh cm-2 at 50 mA cm-2), and an excellent cycling durability. The superior charge storage properties are ascribed to the synergistic features, higher accessible active sites of dual-layered nanogeometries, and exalted redox chemistry of multi metallic guest species, respectively. The bilayered NCM-based MOFs are further employed as a battery-type electrode for the fabrication of supercapattery paradigm with biomass-derived nitrogen/oxygen doped porous carbon as a negative electrode, which demonstrates excellent capacity of 1.6 mAh cm-2 along with high energy and power densities of 1.21 mWh cm-2 and 32.49 mW cm-2, respectively. Following, the MOF-based supercapattery was further assembled with a renewable solar power harvester to use as a self-charging station for various portable electronic applications.

An Integrated Approach Toward Renewable Energy Storage Using Rechargeable Ag@Ni0.67 Co0.33 S-Based Hybrid Supercapacitors.

Self-powered charging systems in conjunction with renewable energy conversion and storage devices have attracted promising attention in recent years. In this work, a prolific approach to design a wind/solar-powered rechargeable high-energy density pouch-type hybrid supercapacitor (HSC) is proposed. The pouch-type HSC is fabricated by engineering nature-inspired nanosliver (nano-Ag) decorated Ni0.67 Co0.33 S forest-like nanostructures on Ni foam (nano-Ag@NCS FNs/Ni foam) as a battery-type electrode and porous activated carbon as a capacitive-type electrode. Initially, the core-shell-like NCS FNs/Ni foam is prepared via a single-step wet-chemical method, followed by a light-induced growth of nano-Ag onto it for enhancing the conductivity of the composite. Utilizing the synergistic effects of forest-like nano-Ag@NCS FNs/Ni foam as a composite electrode, the fabricated device shows a maximum capacitance of 1104.14 mF cm-2 at a current density of 5 mA cm-2 and it stores superior energy and power densities of 0.36 mWh cm-2 and 27.22 mW cm-2 , respectively along with good cycling stability, which are higher than most of previous reports. The high-energy storage capability of HSCs is further connected to wind fans and solar cells to harvest renewable energy. The wind/solar charged HSCs can effectively operate various electronic devices for a long time, enlightening its potency for the development of sustainable energy systems.

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.

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.

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.

Complex ambiguity-free Fourier domain optical coherence tomography through transverse scanning.

We introduce a simple and cheap method for phase-shifting Fourier domain optical coherence tomography (FDOCT) that does not need additional devices and can easily be implemented. A small beam offset at the fast beam-scanning mirror introduces a causal phase shift, which can be used for B-scan-based complex image reconstruction. We derive the conditions for optimal conjugate suppression and demonstrate the method on human skin in vivo for spectrometer-based FDOCT operating at 1300 nm employing a handheld scanner.