SARS-CoV-2-on-Chip for Long COVID Management.

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has become a "wicked evil" in this century due to its extended progression and huge human mortalities. Although the diagnosis of SARS-CoV-2 viral infection is made simple and practical by employing reverse transcription polymerase chain reaction (RT-PCR) investigation, the process is costly, complex, time-consuming, and requires experts for testing and the constraints of a laboratory. Therefore, these challenges have raised the paradigm of on-site portable biosensors on a single chip, which reduces human resources and enables remote access to minimize the overwhelming burden on the existing global healthcare sector. This article reviews the recent advancements in biosensors for long coronavirus disease (COVID) management using a multitude of devices, such as point-of-care biosensors and lab-on-chip biosensors. Furthermore, it details the shift in the paradigm of SARS-CoV-2-on-chip biosensors from the laboratory to on-site detection with intelligent and economical operation, representing near-future diagnostic technologies for public health emergency management.

Flexible supercapacitor electrodes using metal-organic frameworks.

Advancements in the field of flexible and wearable devices require flexible energy storage devices to cater their power demands. Metal-ion batteries (such as lithium-ion batteries, sodium-ion batteries, etc.) and electrochemical capacitors (also called supercapacitors or ultracapacitors) have achieved great interest in the recent past due to their superior energy storage characteristics like high power density and long cycle life. A major bottleneck of using metal-ion batteries in wearable devices is their lack of flexibility. Low power density, toxicity and flammability due to organic electrolytes inhibit them from safe on-body device applications. On the other hand, supercapacitors can be made with aqueous electrolytes, making them a safer alternative for wearable applications. Metal-organic frameworks (MOFs) are novel candidates as electrode materials due to their salient features such as large surface area, three-dimensional porous architecture, permeability to foreign entities, structural tailorability, etc. Though pristine MOFs suffer from poor intrinsic conductivity, this can be rectified by preparing composites with other electronically conducting materials. MOF-based electrodes are highly promising for flexible and wearable supercapacitors since they exhibit good energy and power densities. This review focuses on the new developments in the field of MOF-based composite electrodes for developing flexible supercapacitors.

New Method for the Synthesis of 2D Vanadium Nitride (MXene) and Its Application as a Supercapacitor Electrode.

MXenes are the class of two-dimensional transition metal carbides and nitrides that exhibit unique properties and are used in a multitude of applications such as biosensors, water purification, electromagnetic interference shielding, electrocatalysis, supercapacitors, and so forth. Carbide-based MXenes are being widely explored, whereas investigations on nitride-based ones are seldom. Among the nitride-based MXenes obtained from their MAX phases, only Ti4N3 and Ti2N are reported so far. Herein, we report a novel synthesis of V2NT x (T x is the surface termination) obtained by the selective removal of "Al" from V2AlN by immersing powders of V2AlN in the LiF-HCl mixture (salt-acid etching) followed by sonication to obtain V2NT x (T x = -F, -O) MXene which is then delaminated using the dimethyl sulfoxide solvent. The V2NT x MXene is characterized by X-ray diffraction studies, field emission scanning electron microscope imaging, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and high-resolution transmission electron microscope imaging. Supercapacitor electrodes are prepared using V2NT x MXenes and their electrochemical performances are examined by cyclic voltammetry, galvanostatic charge/discharge measurement, and electrochemical impedance spectroscopy. The V2NT x MXene electrode exhibits a specific capacitance of 112.8 F/g at a current density of 1.85 mA/cm2 with an energy and power density of 15.66 W h/kg and 3748.4 W/kg, respectively, in 3.5 M KOH aqueous electrolyte. The electrode exhibits an excellent capacitance retention of 96% even after 10,000 charge/discharge cycles. An asymmetric supercapacitor fabricated with V2NT x as a negative electrode and Mn3O4 nanowalls as a positive electrode helps obtain a cell voltage of 1.8 V in aqueous KOH electrolyte.

Synthesis of air-stable two-dimensional nanoplatelets of Ruddlesden-Popper organic-inorganic hybrid perovskites.

We present a simple and facile method to synthesize nanoplatelets of 2D Ruddlesden-Popper (RP) perovskites of the type (CH3(CH2)3NH3)2(CH3NH3)Pb2I7 where n = 2. The 2D RP nanoplatelets are synthesized from bulk 2D RP crystals via a reflux pre-treatment mediated-ultrasonication method. The as-synthesized 2D RP nanoplatelets are highly air-stable even after two months of storage under an ambient atmosphere. The bulk 2D RP crystals and 2D RP nanoplatelets are characterized using X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Kelvin probe force microscopy, UV-visible spectroscopy, X-ray photoelectron spectroscopy (XPS), photoluminescence, time correlated single photon counting measurement, etc. A significant blue shift in the ultraviolet-visible absorption spectrum, high photoluminescence in the UV region, and the modified work function of the nanoplatelets indicate a strong quantum confinement effect. The quantum confinement in the nanoplatelets is further confirmed using XPS. A photodetector fabricated using these 2D RP nanoplatelets exhibits a high photodetectivity of 3.09 × 1010 Jones.

Ultrasensitive and ultrathin phototransistors and photonic synapses using perovskite quantum dots grown from graphene lattice.

Organic-inorganic halide perovskite quantum dots (PQDs) constitute an attractive class of materials for many optoelectronic applications. However, their charge transport properties are inferior to materials like graphene. On the other hand, the charge generation efficiency of graphene is too low to be used in many optoelectronic applications. Here, we demonstrate the development of ultrathin phototransistors and photonic synapses using a graphene-PQD (G-PQD) superstructure prepared by growing PQDs directly from a graphene lattice. We show that the G-PQDs superstructure synchronizes efficient charge generation and transport on a single platform. G-PQD phototransistors exhibit excellent responsivity of 1.4 × 108 AW-1 and specific detectivity of 4.72 × 1015 Jones at 430 nm. Moreover, the light-assisted memory effect of these superstructures enables photonic synaptic behavior, where neuromorphic computing is demonstrated by facial recognition with the assistance of machine learning. We anticipate that the G-PQD superstructures will bolster new directions in the development of highly efficient optoelectronic devices.

Vertically Aligned Graphene-Carbon Fiber Hybrid Electrodes with Superlong Cycling Stability for Flexible Supercapacitors.

Graphene electrode-based supercapacitors are in high demand due to their superior electrochemical characteristics. A major bottleneck of using the supercapacitors for commercial applications lies in their inferior electrode cycle life. Herein, a simple and facile method to fabricate highly efficient supercapacitor electrodes using pristine graphene sheets vertically stacked and electrically connected to the carbon fibers which can result in vertically aligned graphene-carbon fiber nanostructure is developed. The vertically aligned graphene-carbon fiber electrode prepared by electrophoretic deposition possesses a mesoporous 3D architecture which enabled faster and efficient electrolyte-ion diffusion with a gravimetric capacitance of 333.3 F g-1 and an areal capacitance of 166 mF cm-2 . The electrodes displayed superlong electrochemical cycling stability of more than 100 000 cycles with 100% capacitance retention hence promising for long-lasting supercapacitors. Apart from the electrochemical double layer charge storage, the oxygen-containing surface moieties and α-Ni(OH)2 present on the graphene sheets enhance the charge storage by faradaic reactions. This enables the assembled device to provide an excellent gravimetric energy density of 76 W h kg-1 with a 100% capacitance retention even after 1000 bending cycles. This study opens the door for developing high-performing flexible graphene electrodes for wearable energy storage applications.

Two-Dimensional Mn3O4 Nanowalls Grown on Carbon Fibers as Electrodes for Flexible Supercapacitors.

Emerging flexible and wearable electronic devices necessitates the development of fiber-type energy storage devices to power them. Supercapacitors received great attention for applications in flexible and wearable devices due to their scalability, safety, and miniature size. Herein, we report the fabrication of a flexible supercapacitor using manganese(II,III) oxide (Mn3O4) nanowalls (NWs) grown by electrochemical deposition on carbon fiber (CF) as electrode-active material. Here, CF serves as both a substrate for the growth of Mn3O4 NWs and a current collector for making a lightweight supercapacitor. Two-dimensional Mn3O4 NWs were uniformly grown on CF with high surface coverage. A three-dimensional nanostructured electrode is obtained using these individual two-dimensional Mn3O4 NWs. The Mn3O4 NWs grown on CF are characterized by scanning electron microscopy, energy-dispersive X-ray spectroscopy, X-ray diffraction, and Raman spectroscopy. A symmetric sandwich-type supercapacitor is fabricated using two-dimensional Mn3O4 NW electrodes in an aqueous 1 M Na2SO4 electrolyte. The Mn3O4 NW supercapacitor electrode exhibits a specific capacitance of 300.7 F g-1 at a scan rate of 5 mV s-1. The assembled symmetric sandwich-type supercapacitor displayed high flexibility even at a bending angle of 180° without altering its performance. The Mn3O4 NW supercapacitor also displayed a long cycle life of 7500 cycles with 100% capacitance retention.

Novel mesoporous electrode materials for symmetric, asymmetric and hybrid supercapacitors.

Electrochemical capacitors or supercapacitors have achieved great interest in the recent past due to their potential applications ranging from microelectronic devices to hybrid electric vehicles. Supercapacitors can provide high power densities but their inherently low energy density remains a great challenge. The high-performance supercapacitors utilize large electrode surface area for electrochemical double-layer capacitance and/or pseudocapacitance. To enhance the performance of supercapacitors, various strategies have been adopted such as electrode nanostructuring, hybrid electrode designs using nanocomposite electrodes and hybrid supercapacitor (HSC) configurations. Nanoarchitecturing of electrode-active materials is an effective way of enhancing the performance of supercapacitors as it increases the effective electrode surface area for enhanced electrode/electrolyte interaction. In this review, we focus on the recent developments in the novel electrode materials and various hybrid designs used in supercapacitors for obtaining high specific capacitance and energy density. A family of electrode-active materials including carbon nanomaterials, transition metal-oxides, transition metal-nitrides, transition metal-hydroxides, electronically conducting polymers, and their nanocomposites are discussed in detail. The HSC configurations for attaining enhanced supercapacitor performance as well as strategies to integrate with other microelectronic devices/wearable fabrics are also included.

Hierarchical carbon nanopetal/polypyrrole nanocomposite electrodes with brush-like architecture for supercapacitors.

Hierarchical 3D nanocomposite electrodes with tube brush-like morphology are synthesized by electrochemically depositing polypyrrole (PPY) on carbon nanopetal (CNP) coated carbon fibers (CFs). Initially CNPs are synthesized on CF substrate by chemical vapour deposition. The CNPs synthesized on CF (CNPCF) are further used as an electrically conducting large surface area bearing template for the electropolymerization of PPY in order to fabricate CNPCF-PPY nanocomposite electrodes for supercapacitors (SCs). The CF in CNPCF-PPY nanocomposite functions as (i) a mechanical support for the CNPs, (ii) a current collector for the SC cell and also (iii) to prevent the agglomeration of CNPs within the CNPCF-PPY nanocomposite. Transmission electron microscopy and scanning electron microscopy are used to examine the surface morphology of CNPCF-PPY nanocomposites. The chemical structure of the nanocomposites is analysed by Fourier transform infrared spectroscopy. X-Ray photoelectron spectroscopy has been used to understand the chemical bonding states of the hierarchical CNPCF-PPY nanocomposites. The electrochemical properties of symmetric type CNPCF-PPY SC cells are examined by electrochemical impedance spectroscopy, cyclic voltammetry and galvanostatic charge-discharge measurements. The hierarchical CNPCF-PPY SC exhibits a maximum gravimetric capacitance of 280.4 F g(-1) and an area specific capacitance of 210.3 mF cm(-2) at a current density of 0.42 mA cm(-2). The CNPCF-PPY SC cell exhibits good cycling stability of more than 5000 cycles. The present study proclaims the development of a novel lightweight SC with high-performance.