Disposable-micropipette tip supported electrified liquid-organogel interface as a platform for sensing acetylcholine.

Sensing acetylcholine has been predominantly based on enzymatic strategies using acetylcholine esterase and choline oxidase because of its electrochemical inertness. Electrified liquid-liquid interfaces are not limited to oxidation/reduction processes, and can be utilized to detect non-redox molecules which cannot be detected using conventional solid electrodes. In this study, a disposable micropipette tip based liquid-organogel interface, in the presence/absence of calixarene has been developed as a platform for sensing acetylcholine.

Synthesis and Optoelectronic Features of Rhodamine-Triazole Dyads as Metallochromic Probes for Copper-Selective Chemosensing.

Rhodamine-based chromic materials have attracted significant interest owing to their cation recognition ability with high sensitivity. However, rhodamine chromophores with controllable sensing selectivity towards transition metal species are only at the advent. Herein, three triazole-conjugated rhodamine dyads with different peripheral substituents were synthesized.

Determination of urinary spermine using controlled dissolution of polysulfide modified gold electrode.

Spermine (SPM) is considered a biomarker for prostate cancer and detecting it becomes highly challenging due to its electro- and optical-inactive nature. SPM has a tendency to interact with groups such as phosphates and sulfides to form macrocyclic arrangements known as nuclear aggregates of polyamines. Using this tendency, an electrochemical sensor has been developed using a polysulfide (PS) modified Au electrode (PS@Au electrode).

Morphology-Dependent Electrocatalytic Behavior of Cobalt Chromite toward the Oxygen Evolution Reaction in Acidic and Alkaline Medium.

Exploiting an affordable, durable, and high-performance electrocatalyst for the oxygen evolution reaction (OER) under lower pH condition (acidic) is highly challengeable and much attractive toward the hydrogen-based energy technologies. A spinel CoCrO is observed as a potential noble-metal-free candidate for OER in alkaline medium. The presence of Cr further leads to electronic structure modulation of CoO and thereby greatly increases the corrosive resistance toward OER in acidic environment.

Precision Nanocluster-Based Toroidal and Supertoroidal Frameworks Using Photocycloaddition-Assisted Dynamic Covalent Chemistry.

Atomically precise nanoclusters (NCs) have recently emerged as ideal building blocks for constructing self-assembled multifunctional superstructures. The existing structures are based on various non-covalent interactions of the ligands on the NC surface, resulting in inter-NC interactions. Despite recent demonstrations on light-induced reversible self-assembly, long-range reversible self-assembly based on dynamic covalent chemistry on the NC surface has yet to be investigated.

Engineered Two-Dimensional Nanostructures as SERS Substrates for Biomolecule Sensing: A Review.

Two-dimensional nanostructures (2DNS) attract tremendous interest and have emerged as potential materials for a variety of applications, including biomolecule sensing, due to their high surface-to-volume ratio, tuneable optical and electronic properties. Advancements in the engineering of 2DNS and associated technologies have opened up new opportunities. Surface-enhanced Raman scattering (SERS) is a rapid, highly sensitive, non-destructive analytical technique with exceptional signal amplification potential.

Bioadhesive Gauze Embedded with Chitosan-Butein Bioconjugate: A Redox-Active pH Sensor Platform.

With the ever-growing global wound care market, demand for robust redox-active healthcare material is obvious for the construction of wearable sensor platforms. Surface reactive functional group-rich material like chitosan holds huge potential for electrochemical biosensor application. Herein, a metal-free redox-active chitosan-butein (CSB) bioconjugate is processed into epidermal bioadhesive electrode material useful for pH sensors promising toward wound site analysis.

Electrochromic Performance of Sputtered NbTi-Based Mixed Metal Oxide Thin Films with a Metallic Seed Layer.

An attempt has been made to promote the efficiency of the electrochromic (EC) windows to perform at a faster switching rate with good coloration and easy recyclability. In this work, ion-assisted pulsed DC unbalanced confocal magnetron sputtering is used to fabricate mixed metal oxide thin films of Nb and Ti (which are termed as NTO) for EC applications. Further, to increase the EC efficiency of this film, a very thin metallic seed layer is incorporated between the substrate and the film using the layer-by-layer (LBL) coating strategy.

Ultrasensitive detection of SARS-CoV-2 S protein with aptamers biosensor based on surface-enhanced Raman scattering.

A rapid and accurate diagnostic modality is essential to prevent the spread of SARS-CoV-2. In this study, we proposed a SARS-CoV-2 detection sensor based on surface-enhanced Raman scattering (SERS) to achieve rapid and ultrasensitive detection. The sensor utilized spike protein deoxyribonucleic acid aptamers with strong affinity as the recognition entity to achieve high specificity.

Morphology Tuning via Linker Modulation: Metal-Free Covalent Organic Nanostructures with Exceptional Chemical Stability for Electrocatalytic Water Splitting.

The development of synthetic routes for the formation of robust porous organic polymers (POPs) with well-defined nanoscale morphology is fundamentally significant for their practical applications. The thermodynamic characteristics that arise from reversible covalent bonding impart intrinsic chemical instability in the polymers, thereby impeding their overall potential. Herein, a unique strategy is reported to overcome the stability issue by designing robust imidazole-linked POPs via tandem reversible/irreversible bond formation.

Tailoring of 1T Phase-Domain MoS Active Sites with Bridging S/Apical S Phase-Selective Precursor Modulation for Enriched HER Kinetics.

Molybdenum disulfide (MoS) is a promising alternative electrocatalyst for hydrogen evolution reaction (HER) due to its relatively near zero hydrogen adsorption free energy (Δ = 0.08) and availability as a metallic (1T) phase. The superior catalytic activity of the 1T phase over 2H is owing to the availability of dense active sites, 10 fold higher conductivity, and greater hydrophilicity.

Mechanosynthesis of Triazolyl-bis(indolyl)methane Pharmacophores via Gold Catalysis: A Prelude to Their Molecular Electronic Properties and Biological Potency.

Chemical structures possessing both 1,2,3-triazole and bis(indolyl)methane fragments gained considerable interest in drug synthesis owing to their established biological efficacies. However, 1,2,3-triazoles linked at the bridging position of bis(indolyl)methane is a logical and unexplored design approach. In this regard, nine new triazolyl-bis(indolyl)methane conjugates under AuCl catalyzed ball-milling conditions were accomplished.

Modulating the Surface Electronic Structure of Active Ni Sites by Engineering Hierarchical NiFe-LDH/CuS over Cu Foam as an Efficient Electrocatalyst for Water Splitting.

Water electrolysis encounters a challenging problem in designing a highly efficient, long durable, non-noble metal-free electrocatalyst for both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). Here, in our work, a two-step hydrothermal reaction was performed to construct a hierarchal NiFe-layer double hydroxide (LDH)/CuS over copper foam for the overall water splitting reaction. While employed the same as an anode material, the designed heterostructure electrode NiFe-LDH/CuS/Cu exhibits excellent OER performance and it demands 249 mV overpotential to reach a current density of 50 mA cm with a lower Tafel slope value of 81.

Peptide-based direct electrochemical detection of receptor binding domains of SARS-CoV-2 spike protein in pristine samples.

RNA isolation and amplification-free user-friendly detection of SARS-CoV-2 is the need of hour especially at resource limited settings. Herein, we devised the peptides of human angiotensin converting enzyme-2 (ACE-2) as bioreceptor at electrode interface for selective targeting of receptor binding domains (RBD) of SARS-CoV-2 spike protein (SP). Disposable carbon-screen printed electrode modified with methylene blue (MB) electroadsorbed graphene oxide (GO) has been constructed as cost-efficient and scalable platform for ACE-2 peptide-based SARS-CoV-2 detection.

Stabilization of Ru NPs over 3D LaCrO Nanostructures for High-Performance HER Catalysts in Acidic Media.

Hydrogen is considered as one of the best alternatives to carbon-based fossil fuels as energy sources. Electrocatalytic water splitting is one of the finest and eco-friendly methods for the production of hydrogen as compared to all other methods such as stream reforming carbon, hydrolysis of metal hydrides, etc. However, the sluggish kinetics on both the half-cell reactions limits the large-scale production of hydrogen.

Catalytically active silver nanoparticles stabilized on a thiol-functionalized metal-organic framework for an efficient hydrogen evolution reaction.

A post-synthetic technique, Solvent Assisted Ligand Incorporation (SALI), was used for thiol functionalization in the zirconium-based metal-organic framework NU-1000. This thiol-functionalized MOF was employed as a support for the growth of silver nanoparticles (Ag NPs) through coordination of a Ag(I) complex with a node-anchored thiol-ligand, followed by the reduction of Ag(I) to Ag(0). X-ray photoelectron spectroscopy revealed that the ratio of Ag(0) to Ag(I) proportionally increased with the loading of silver ions.

Bifunctional g-CN/carbon nanotubes/WO ternary nanohybrids for photocatalytic energy and environmental applications.

Ternary nanohybrids based on mesoporous graphitic carbon nitride (g-CN) were synthesized and presented for developing stable and efficient Hydrogen (H) production system. Based on photocatalytic activity, optimization was performed in three different stages to develop carbon nanotubes (CNTs) and WO loaded g-CN (CWG-3). Initially, the effect of exfoliation was investigated, and a maximum specific surface area of 100.

electrochemical transformation of Ni to NiOOH as an effective electrode for water oxidation reaction.

The poor kinetic background with the four-electron transfer of the oxygen evolution reaction (OER) was eradicated using a nickel-based catalyst, which was identified as an alternative to noble-metal catalysts. Here, we report the simple formation of an earth-abundant nickel oxyhydroxide (NiOOH) electrocatalyst for efficient OER in an alkaline medium. Electroless material preparation, namely, the direct modification of a gas diffusion layer (GDL) with a nickel salt, was studied, and the layered oxyhydroxide phase was found to influence the rate of the OER.

A converged approach of electro-biological process for decolorization and degradation of toxic synthetic dyes.

Being one of the leading industries worldwide, the textile industry has been consuming large quantities of groundwater and discharging huge volumes of dye-contaminated effluents into our aquatic environment. Augmentation of water sources via reuse of treated effluents is therefore highly necessary. In the present study, the decolorization and degradation of synthetic toxic dye from an aqueous solution were investigated through an electro-biological route.

Accelerating the Electrocatalytic Performance of NiFe-LDH via Sn Doping toward the Water Oxidation Reaction under Alkaline Condition.

To generate green hydrogen by water electrolysis, it is vital to develop highly efficient electrocatalysts for the oxygen evolution reaction (OER). The utilization of various 3d transition metal-based layered double hydroxides (LDHs), especially NiFe-LDH, has gained vast attention for OER under alkaline conditions. However, the lack of a proper electronic structure of the NiFe-LDH and low stability under high-pH conditions limit its large-scale application.

Iminium-Bridged Resorcinol-Silane Networks and Their Pyrolyzed Derivatives as Electrode Materials for the Electrocatalytic Oxygen Reduction Reaction and Supercapacitors.

We report the synthesis of iminium-bridged resorcinol-silane (I-R-S) gel networks through the reaction of resorcinol with 3-aminopropyl triethoxysilane (APTES) in the presence of acetone under ambient conditions. Ambient pressure drying leads to monolithic gels with minimal shrinkage and cracks, eliminating the use of conventional supercritical drying. The gels were found to have bulk and skeletal densities of 0.

First principles study on thickness dependent structural and electronic properties unveiling the growth and stability of 2D layered II-VI semiconducting compounds.

By employing first principles density functional theory calculations on thickness dependent structural and electronic properties of (0001) surface slabs of wurtzite MX compounds, our study demonstrated the possibility of the existence of 2D layered materials from II-VI group traditional semiconducting compounds that are widely used in various fields. Our calculations revealed that (0001) surface slabs of wurtzite ZnO and CdO compounds prefer to stabilize as sp hybridized - atomically thin graphitic layers as observed in earlier work, which are separated by van der Waals distances, when compared to the respective wurtzite slabs. On the other hand, for surface slabs of other ZnX and CdX (X = S, Se, Te) compounds, sp hybridized bilayers, which comprise an X-Zn(Cd)-Zn(Cd)-X structural arrangement, are energetically stable until certain thicknesses of the slabs.

Anion Exchange Membranes for Alkaline Polymer Electrolyte Fuel Cells-A Concise Review.

Solid anion exchange membrane (AEM) electrolytes are an essential commodity considering their importance as separators in alkaline polymer electrolyte fuel cells (APEFC). Mechanical and thermal stability are distinguished by polymer matrix characteristics, whereas anion exchange capacity, transport number, and conductivities are governed by the anionic group. The physico-chemical stability is regulated mostly by the polymer matrix and, to a lesser extent, the cationic head framework.

Exploring the Defect Sites in UiO-66 by Decorating Platinum Nanoparticles for an Efficient Hydrogen Evolution Reaction.

UiO-66 has been tailored using defect engineering methodology to introduce thiol functionalities into the MOF skeletal structure. The thiolated UiO-66 serves as a scaffold to support the platinum nanoparticles with a size of ∼2 nm through a soft-soft interaction. This Pt@UiO-66-SH, utilized as an HER catalyst, exhibited an overpotential of 57 mV at a current density of 10 mA cm in an acidic medium with a Tafel slope of 75 mV/dec and a high TOF value (389.