The Use of an Acylhydrazone-Based Metal-Organic Framework in Solid-Contact Potassium-Selective Electrode for Water Analysis

A solid-contact ion-selective electrode was developed for detecting potassium in environmental water. Two versions of a stable cadmium acylhydrazone-based metal organic framework, i.e., JUK-13 and JUK-13_H2O, were used for the construction of the mediation layer. The potentiometric and electrochemical characterizations of the proposed electrodes were carried out. The implementation of the JUK-13_H2O interlayer is shown to improve the potentiometric response and stability of measured potential. The electrode exhibits a good Nernstian slope (56.30 mV/decade) in the concentration range from 10−5 to 10−1 mol L−1 with a detection limit of 2.1 µmol L−1. The long-term potential stability shows a small drift of 0.32 mV h−1 over 67 h. The electrode displays a good selectivity comparable to ion-selective electrodes with the same membrane. The K-JUK-13_H2O-ISE was successfully applied for the determination of potassium in three certified reference materials of environmental water with great precision (RSD < 3.00%) and accuracy (RE < 3.00%).

Effect of the supergravity on the formation and cycle life of non-aqueous lithium metal batteries

Extra-terrestrial explorations require electrochemical energy storage devices able to operate in gravity conditions different from those of planet earth. In this context, lithium (Li)-based batteries have not been fully investigated, especially cell formation and cycling performances under supergravity (i.e., gravity > 9.8 m s−2) conditions. To shed some light on these aspects, here, we investigate the behavior of non-aqueous Li metal cells under supergravity conditions. The physicochemical and electrochemical characterizations reveal that, distinctly from earth gravity conditions, smooth and dense Li metal depositions are obtained under supergravity during Li metal deposition on a Cu substrate. Moreover, supergravity allows the formation of an inorganic-rich solid electrolyte interphase (SEI) due to the strong interactions between Li+ and salt anions, which promote significant decomposition of the anions on the negative electrode surface. Tests in full Li metal pouch cell configuration (using LiNi0.8Co0.1Mn0.1O2-based positive electrode and LiFSI-based electrolyte solution) also demonstrate the favorable effect of the supergravity in terms of deposition morphology and SEI composition and ability to carry out 200 cycles at 2 C (400 mA g−1) rate with a capacity retention of 96%.

Machine-Learning Assisted Exploration: Toward the Next-Generation Catalyst for Hydrogen Evolution Reaction

The development of active catalysts for hydrogen evolution reaction (HER) made from low-cost materials constitutes a crucial challenge in the utilization of hydrogen energy. Earth-abundant molybdenum disulfide (MoS2) has been discovered recently with good activity and stability for HER. In this report, we employ a hydrothermal technique for MoS2 synthesis which is a cost-effective and environmentally friendly approach and has the potential for future mass production. Machine-learning (ML) techniques are built and subsequently used within a Bayesian Optimization framework to validate the optimal parameter combinations for synthesizing high-quality MoS2 catalyst within the limited parameter space. Compared with the heavy-labor and time-consuming trial-and-error approach, the ML techniques provide a more efficient toolkit to assist exploration of the most effective HER catalyst in hydrothermal synthesis. To investigate the structure-property relationship, scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), and various electrochemical characterizations have been conducted to investigate the superiority of the ML validated optimized sample. A strong correlation between the material structure and the HER performance has been observed for the optimized MoS2 catalyst.

Nanofibrous PEDOT-Carbon Composite on Flexible Probes for Soft Neural Interfacing

In this study, we report a flexible implantable 4-channel microelectrode probe coated with highly porous and robust nanocomposite of poly (3,4-ethylenedioxythiophene) (PEDOT) and carbon nanofiber (CNF) as a solid doping template for high-performance in vivo neuronal recording and stimulation. A simple yet well-controlled deposition strategy was developed via in situ electrochemical polymerization technique to create a porous network of PEDOT and CNFs on a flexible 4-channel gold microelectrode probe. Different morphological and electrochemical characterizations showed that they exhibit remarkable and superior electrochemical properties, yielding microelectrodes combining high surface area, low impedance (16.8 ± 2 MΩ µm2 at 1 kHz) and elevated charge injection capabilities (7.6 ± 1.3 mC/cm2) that exceed those of pure and composite PEDOT layers. In addition, the PEDOT-CNF composite electrode exhibited extended biphasic charge cycle endurance and excellent performance under accelerated lifetime testing, resulting in a negligible physical delamination and/or degradation for long periods of electrical stimulation. In vitro testing on mouse brain slices showed that they can record spontaneous oscillatory field potentials as well as single-unit action potentials and allow to safely deliver electrical stimulation for evoking field potentials. The combined superior electrical properties, durability and 3D microstructure topology of the PEDOT-CNF composite electrodes demonstrate outstanding potential for developing future neural surface interfacing applications.

Influence of Synthesis Approach on Controlled Microstructures and Photocatalytic Properties of Ag/AgBr-Activated Carbon Composites on Visible Light Degradation of Tetracycline

The influence of the synthesis approach (thermal polyol and deposition–precipitation) regarding the dispersion of Ag/AgBr nanoparticles dispersed on activated carbon prepared from chemical impregnated pinecone (TP-AABR-ACK, and DP-AABR-ACK) was studied, to increase their photocatalytic efficiency on the degradation of tetracycline (TC). The physicochemical characterization evidenced the significance of the ACK catalyst promoter in enhancing controlled microstructures (morphologies and particle size distributions), synergistic interface interaction between AABR NPs and the carbonaceous support, and efficient photogenerated charge carriers separation within TP-AABR-ACK, and DP-AABR-ACK composites. The results revealed 92% removal of TC within 180 min under the LED visible light irradiation, which was achieved using TP-AABR-ACK when compared to DP-AABR-ACK composite and other catalysts in this study. Such superior results achieved with TP-AABR-ACK composite were attributed to controlled morphologies, reduced particle size and agglomeration, improved absorptivity, and superior cooperative effect between the AABR and ACK catalyst promoter as evidenced from SEM, EDX, TEM, UV-DRS, and electrochemical characterizations, respectively. Furthermore, enhanced TOC removal and abundance of reactive superoxide anion generation were achieved with the TP-AABR-ACK composite in this study.

Electrode Material as Anode for Improving the Electrochemical Performance of Microbial Fuel Cells

The energy generation without causing environmental pollution is a unique idea to make a better survival for human beings. In this regard, microbial fuel cells (MFCs) have been considered to be eco-friendly and efficient technology to produce renewable energy. The operations and functioning of MFCs technology were affected by many factors but the electrodes are the most essential and significant aspects in MFCs. Moreover, a wide variety of electrodes and MFCs configurations have been developed to enhance the electrochemical performance of MFCs. The carbon materials (graphite, graphene etc.) were commonly used for the electrode fabrication, due to some unique properties such as high conductivity, good thermal stability, high surface area, good mechanical power etc. In this chapter, different electrode materials, used for anode fabrication were summarized to reveal the performance/efficiency toward the generation of electricity. Finally, the electrochemical characterizations tool, current challenges, and future perspectives of the electrode in MFCs were discussed briefly.

Complex Activity and Sensor Potential toward Metal Ions in Environmental Water Samples of N-Phthalimide Azo-Azomethine Dyes

Herein, the spectral and electrochemical characterizations of three different substituted N-phthalimide azo-azomethine (NAA) dyes (L) containing an o-hydroxy group and their NAA-M(II) chelates [M(II): Cu, Ni, Co, Pb] were reported by using UV–Vis and fluorescence spectroscopy and potentiometric and voltamperometric techniques. The pK value of the dyes as well as the stoichiometry and stability of the NAA-metal chelates were studied, and the stoichiometry was found to be mostly 1:2 (ML2) with high complex stability constant values. The sensor activity of N-phthalimide azo-azomethine derivatives toward pH and metal ions has been also investigated and tested for indicator application in acid–base analysis and detection of Cu(II) ions in real samples of surface river water using voltamperometric detection. The results showed that one of the ligands possesses the highest electrochemical response upon binding to copper ions and could be successfully used in the analysis of copper in water at a concentration range of the analyte from 3.7 × 10−7 to 5.0 × 10−6 mol L−1, with analytical characteristics of the method being Sr = 1.5%, LOD = 3.58 µg L−1 and LOQ =11.9 µg L−1

Effect of Ag alloying and trace precipitation on corrosion resistance of Ti-Ta-Ag ternary alloy

This work systematically analysed the electrochemical and corrosion behaviour of Ti-Ta-Ag ternary alloy samples in Hank's solution. For the samples with 1.5% and 3% Ag content, the sintering temperature increased from 750 to 950°C, and the corresponding corrosion resistance increased by 100 times due to the increased alloying of Ag; meanwhile for the sample with 4.5% Ag content, the sintering temperature increased from 750 to 950°C, and the corresponding corrosion resistance decreased by six times due to the increased precipitation of Ag. These tests prove that the Ag alloying is beneficial to the enhancement of the corrosion resistance of Ti-Ta-Ag ternary alloy, but the Ag trace precipitation has the opposite effect. A series of electrochemical characterizations and density functional theory calculations explain the mechanism of the above phenomenon. Ag alloying can promote the formation of uniform, complete, dense, stable and thick passivation layer on the surface of Ti-Ta-Ag ternary alloy, which makes Ti-Ta-Ag ternary alloy uniformly corroded without pitting. In addition, Ag alloying can effectively reduce the contact resistance of the solid–liquid interface. However, the trace precipitation of Ag plays the opposite role to the above effect.

The role of oxygen-permeable ionomer for polymer electrolyte fuel cells

In recent years, considerable research and development efforts are devoted to improving the performance of polymer electrolyte fuel cells. However, the power density and catalytic activities of these energy conversion devices are still far from being satisfactory for large-scale operation. Here we report performance enhancement via incorporation, in the cathode catalyst layers, of a ring-structured backbone matrix into ionomers. Electrochemical characterizations of single cells and microelectrodes reveal that high power density is obtained using an ionomer with high oxygen solubility. The high solubility allows oxygen to permeate the ionomer/catalyst interface and react with protons and electrons on the catalyst surfaces. Furthermore, characterizations of single cells and single-crystal surfaces reveal that the oxygen reduction reaction activity is enhanced owing to the mitigation of catalyst poisoning by sulfonate anion groups. Molecular dynamics simulations indicate that both the high permeation and poisoning mitigation are due to the suppression of densely layered folding of polymer backbones near the catalyst surfaces by the incorporated ring-structured matrix. These experimental and theoretical observations demonstrate that ionomer’s tailored molecular design promotes local oxygen transport and catalytic reactions.