Sodium-Vanadium Bronze Na9V14O35: An Electrode Material for Na-Ion Batteries

Na9V14O35 (η-NaxV2O5) has been synthesized via solid-state reaction in an evacuated sealed silica ampoule and tested as electroactive material for Na-ion batteries. According to powder X-ray diffraction, electron diffraction and atomic resolution scanning transmission electron microscopy, Na9V14O35 adopts a monoclinic structure consisting of layers of corner- and edge-sharing VO5 tetragonal pyramids and VO4 tetrahedra with Na cations positioned between the layers, and can be considered as sodium vanadium(IV,V) oxovanadate Na9V104.1+O19(V5+O4)4. Behavior of Na9V14O35 as a positive and negative electrode in Na half-cells was investigated by galvanostatic cycling against metallic Na, synchrotron powder X-ray diffraction and electron energy loss spectroscopy. Being charged to 4.6 V vs. Na+/Na, almost 3 Na can be extracted per Na9V14O35 formula, resulting in electrochemical capacity of ~60 mAh g−1. Upon discharge below 1 V, Na9V14O35 uptakes sodium up to Na:V = 1:1 ratio that is accompanied by drastic elongation of the separation between the layers of the VO4 tetrahedra and VO5 tetragonal pyramids and volume increase of about 31%. Below 0.25 V, the ordered layered Na9V14O35 structure transforms into a rock-salt type disordered structure and ultimately into amorphous products of a conversion reaction at 0.1 V. The discharge capacity of 490 mAh g−1 delivered at first cycle due to the conversion reaction fades with the number of charge-discharge cycles.

New Construction of Functionalized CuO/Al2O3 Nanocomposite-Based Polymeric Sensor for Potentiometric Estimation of Naltrexone Hydrochloride in Commercial Formulations

Electrically conductive polymeric nanocomposites with nanoparticles are adaptable types of nanomaterials that are prospective for various applications. The extraordinary features of copper oxide (CuO) and aluminium oxide (Al2O3) nanostructures, encourages extensive studies to prospect these metal oxide nanocomposites as potential electroactive materials in sensing and biosensing applications. This study suggested a new CuO/Al2O3 nanocomposite-based polymeric coated wire membrane sensor for estimating naltrexone hydrochloride (NTX) in commercial formulations. Naltrexone hydrochloride and sodium tetraphenylborate (Na-TPB) were incorporated in the presence of polymeric polyvinyl chloride (PVC) and solvent mediator o-nitrophenyloctyl ether (o-NPOE) to form naltrexone tetraphenylborate (NTX-TPB) as an electroactive material. The modified sensor using NTX-TPB-CuO/Al2O3 nanocomposite displayed high selectivity and sensitivity for the discrimination and quantification of NTX with a linearity range 1.0 × 10−9–1.0 × 10−2 mol L−1 and a regression equation EmV = (58.25 ± 0.3) log [NTX] + 754.25. Contrarily, the unmodified coated wire sensor of NTX-TPB exhibited a Nernstian response at 1.0 × 10−5–1.0 × 10−2 mol L−1 and a regression equation EmV = (52.1 ± 0.2) log [NTX] + 406.6. The suggested modified potentiometric system was validated with respect to various criteria using the methodology recommended guidelines.

Ion-selective Electrodes Based on PVC Membranes for Potentiometric Sensor Applications: A Review

Ion-selective electrodes (ISEs) are potentiometric sensors used to measure some of the most critical analytes in environmental laboratory. Recently ion sensors are taking place of various analytical techniques, as they provide a convenient and fast method of electroanalysis. Ion-selective electrodes are simple, relatively inexpensive, robust, durable, and ideal to be used for the detection of heavy metal ions. Important characterisctics of ISEs are selectivity, response time, detection limit, working range, effect of pH etc. Lot of research work is being done for the formation of ISEs by using polymeric membrane incorporated with ionophores or electroactive material. Various types of Schiff bases, macromolecules and metal complexes may be used as ionophores along with plasticizer, ion-excluder for the membrane preparation. Ion-selective electrodes will be optimized for pH range, selectivity, sensitivity, working concentration range and lifetime before their use as sensor electrode for determining the concentration of ions in solution. Various researchers are working in the field to develop Ion-selective electrodes which shows better selectivity and sensitivity than the previously reported electrodes and can be used as electrocatalysts. These ISEs can be used as electrochemical sensors for the analysis of food products, drinking water, beverages, fertilizers, and for the analysis of sample containing toxic substances.

NiVCe-Layered Double Hydroxide as Multifunctional Nanomaterials for Energy and Sensor Applications

Multifunctional nanomaterials have been attracting increasing attention as solutions to the existing challenges in energy systems and sensing technologies. In this regard, multifunctional NiVCe-layered double hydroxide (NiVCe-LDH) nanoparticles were synthesized by the modified sol-gel method. The analysis of this material demonstrated excellent potential for its utilization as electrode materials for hybrid supercapacitor, oxygen evolution reaction (OER), and sensor applications. The NiVCe-LDH nanoparticles delivered a specific charge of 740 C g−1 at 10 A g−1 and decent rate performance (charge retention of 68.7% at 100 A g−1), showing excellent prospects as electrode material for hybrid energy storage devices. In addition, NiVCe-LDH nanoparticles have also been successfully applied as a proof-of-concept for OER, as confirmed by their low Tafel slope of 47 mV dec−1. Finally, trimetallic NiVCe-LDH-based screen-printed electrodes were developed for the sensing of hydrogen peroxide directly in a real complex mouthwash sample, achieving a satisfactory recovery value of around 98% using a fast and simple batch injection analysis procedure. These results allow us to predict the great potential of this trimetallic hydroxide for building electrochemical sensors with good perspectives as electroactive material for OER processes and energy storage technologies.

X-ray fluorescence mapping: Insights into mesoscale structure impact on battery functional electrochemistry

Electron transfer and ion transport occurs over multiple-length scales ranging from the atomic to mesoscale within battery materials and electrodes. Micro-X-ray fluorescence (µ-XRF) is an important characterization tool as it can resolve structural, compositional, and redox information while providing insight into the spatial distribution of an electroactive material. In this work, µ-XRF mapping is used to probe the distribution of iron within thin planar slurry-based and thick porous carbon nanotube (CNT)-based magnetite (Fe3O4) electrodes. Notably, the porous CNT-based electrode showed homogenous distribution of Fe within the electrode whereas the planar electrode demonstrated distinct Fe aggregates. This information was used to rationalize the electrochemistry observed by cyclic voltammetry and galvanostatic cycling. The thick porous electrode delivered 215% more capacity per gram of magnetite during the first discharge, consistent with increased electrode homogeneity enabling effective ion access and electron transfer. Graphical Abstract

Enhanced Chemical and Electrochemical Stability of Polyaniline-Based Layer-by-Layer Films

Polyaniline (PANI) has been widely used as an electroactive material in various applications including sensors, electrochromic devices, solar cells, electroluminescence, and electrochemical energy storage, owing to PANI’s unique redox properties. However, the chemical and electrochemical stability of PANI-based materials is not sufficiently high to maintain the performance of devices under many practical applications. Herein, we report a route to enhancing the chemical and electrochemical stability of PANI through layer-by-layer (LbL) assembly. PANI was assembled with different types of polyelectrolytes, and a comparative study between three different PANI-based layer-by-layer (LbL) films is presented here. Polyacids of different acidity and molecular structure, i.e., poly(acrylic acid) (PAA), polystyrene sulfonate (PSS), and tannic acid (TA), were used. The effect of polyacids’ acidity on film growth, conductivity, and chemical and electrochemical stability of PANI was investigated. The results showed that the film growth of the LbL system depended on the acidic strength of the polyacids. All LbL films exhibited improved chemical and electrochemical stability compared to PANI films. The doping level of PANI was strongly affected by the type of dopants, resulting in different chemical and electrochemical properties; the strongest polyacid (PSS) can provide the highest conductivity and chemical stability of conductive PANI. However, the electrochemical stability of PANI/PAA was found to be better than all the other films.

Microwave Synthesis of MnO2-Lignin Composite Electrodes for Supercapacitors

The demand for energy storage devices made from biodegradable materials has increased significantly due to sustainability. Currently, such devices possess vital issues, such as high manufacturing costs and toxicity, low reliability, as well as poor electrochemical performance. In this research, microwave synthesis was conducted to fabricate a low-cost, high-performing, plant-based electroactive material. MnO2 microparticles fabricated via microwave irradiation were deposited on two plant-based materials as substrates made of Al/lignin and Al/AC/lignin. The quasi-solid-state supercapacitors were assembled using a polymeric gel electrolyte of PVA/H3PO4. Scanning electron microscopy was performed to examine the polydispersity, morphology, and porosity of the micro-MnO2 deposited materials. FTIR and UV-vis spectroscopy were performed to study the composition and verify deposition of micro-MnO2 on the lignin-based matrixes. Cyclic voltammetry (CV) was employed to study the polarization resistance of the system. The cyclic charge-discharge (CCD) and electrochemical impedance spectroscopy (EIS) were performed to observe cyclic performance and interfacial resistances. Electrochemical tests showed that after 700 cycles of charge-discharge, both the supercapacitors exhibited high capacitance retention above 90%. Compared to the existing technology, this method enables consistent material structurization with tunable properties due to the controlled heating time and exposure to radiation with minimal waste. This work provides an alternative approach to synthesize low-cost and scalable green composite electrodes for flexible supercapacitors.