High entropy alloying strategy for accomplishing quintuple-nanoparticles grafted carbon towards exceptional high-performance overall seawater splitting.

High entropy alloys (HEAs), a novel class of material, have been explored in terms of their excellent mechanical properties. Seawater electrolysis is a step towards sustainable production of carbon-neutral fuels such as H2, O2, and industrially demanding Cl2. Herein, we report a practically viable FeCoNiMnCr HEA nanoparticles system grafted on a conductive carbon matrix for promising seawater electrolysis. The comprehensive kinetics analysis of the hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and chlorine evolution reaction (CER) confirms the effectiveness of our system. As an electrocatalyst, HEAs grafted on carbon black show trifunctionality with promising kinetics, selectivity and enduring performance, towards seawater splitting. We optimize high entropy alloy decorated/grafted carbon black (HEACB) catalysts, studying their synthesis temperature to scrutinize the effect of alloy formation variation on the catalysis efficacy. During the catalysis, selectivity between two mutually competing reactions, CER and OER, in the electrochemical catalysis of seawater is controlled by the reaction media pH. We employ Mott-Schottky measurements to probe the band structure of the intrinsically induced metal-semiconductor junction in the HEACB catalyst, where the carrier density and flat band potential are optimized. The HEACB sample provides promising results towards overall seawater electrolysis with a net half-cell potential of about 1.65 V with good stability, which strongly implies its broad practical applicability.

Understanding the endocrine disruptor and determination of bisphenol A by functional Cu-BTABB-MOF/rGO composite as facile rapid electrochemical sensor: an experimental and DFT investigation.

A pioneering CuBTABB-MOF/rGO composite customized electrode is fabricated and utilized as a sensor towards identifying bisphenol A (BPA) in a phosphate buffer solution of pH 7.0. The composite is characterized by FTIR, Raman spectroscopy, XRD, SEM, EDX, HRTEM, and XPS to study its structural and morphological properties. Compared with Cu-BTABB-MOF and Cu-BTABB-MOF@GO, the Cu-BTABB-MOF@rGO modified electrode is more sensitive and selective to BPA due to a strong interaction between them. The developed Cu-BTABB-MOF@rGO modified electrode exhibits good sensitivity (6.95 × 10-5 A mol-1 L-1) for BPA having a wide linear range of 0-100 µmol L-1 with the LOD of 2.08 × 10-5 mol L-1, reproducibility of 4.35%, and relative standard deviation (RSD) and stability of 90% for thirty days. In addition, the developed electrocatalyst remained unoccupied from interfering substances and consequently provided an encouraging platform for swift detection of BPA in real samples such as pond water and packed water bottles. Additionally, we utilized DFT (density functional theory) to model GO and Cu-BTABB-MOF structures for detecting BPA molecules.

Review on recent progress in metal-organic framework-based materials for fabricating electrochemical glucose sensors.

Diabetes is a type of disease that threatens human health, which can be diagnosed based on the level of glucose in the blood. Recently, various MOF-based materials have been developed as efficient electrochemical glucose sensors because of their tunable pore channels, large specific surface area well dispersed metallic active sites, etc. In this review, the significance of glucose detection and the advantages of MOF-based materials for this application are primarily discussed. Then, the application of MOF-based materials can be categorized into two types of glucose sensors: enzymatic biosensors and non-enzymatic sensors. Finally, insights into the current research challenges and future breakthrough possibilities regarding electrochemical glucose sensors are considered.

Improved performance of lithium-sulfur batteries by employing a sulfonated carbon nanoparticle-modified glass fiber separator.

Some of the most promising alternatives in the energy storage sector are lithium-sulfur batteries, which have a high energy density and theoretical capacity. However, the low electrical conductivity of sulfur and the shuttle effect of polysulfides remain important technical obstacles in the practical use of lithium-sulfur batteries (LSBs). This work employed a glass fiber separator with sulfonated carbon nanoparticles (SCNPs) to reduce the shuttle effect. The negatively charged sulfonic groups in SCNPs might prevent polysulfide migration and anchor lithium polysulfides. By using carbon-based interlayers, this method improves ion conductivity. Furthermore, the equally scattered sulfonic groups serve as active sites, causing sulfur to be distributed consistently and limiting sulfur growth while enhancing active sulfur utilization. After 200 cycles at 1C, the SCNP separator-containing cell showed a specific capacity of 1080 mA h g-1. After 200 cycles, the cell with a CNP separator only showed a specific capacity of 854 mA h g-1, demonstrating that CNPs' polysulfide diffusion suppression was ineffective. The cell with the SCNP separator still showed a high capacity of 901 mA h g-1 after 500 cycles, with an average coulombic efficiency of almost 98%.

Solid-state thermal exfoliation of graphite nano-fibers to edge-nitrogenized graphene nanosheets for oxygen reduction reaction.

We demonstrate a simple, single-step and scalable synthesis of edge-nitrogenated graphene nanosheets (E-N-GNS) through thermal exfoliation of graphite platelet nanofibers (GPNF) in the presence of melamine. This material was characterized using different physical characterization techniques which divulges that, the edges are selectively functionalised with pyridinic and pyrrolic type nitrogens leading to the formation of E-N-GNS. Further, the electrocatalytic activity of E-N-GNS towards oxygen reduction reaction (ORR) in alkaline medium was studied using electrochemical techniques to reveal superior electrocatalytic activity of E-N-GNS towards ORR than that of GPNF, perhaps due to the incorporation of N at the edges. The cyclic voltammetry (CV), however, shows a 50 mV and 71 mV positive shift in the onset and peak potentials respectively, which in combination with the rotating ring disk electrode (RRDE) results suggest that ORR follows a direct four electron transfer path on E-N-GNS in comparison with a two electron path on GPNF modified electrodes. This E-N-GNS also shows superior stability for 5000 cycles along with a high methanol-tolerance and durability than that of benchmark ORR electrocatalyst Pt/C (20%) to suggest its potential applications in fuel cells and metal-air batteries.