Investigating the electrochemical properties of poly(vinylidene fluoride)/polyaniline blends doped with lithium-based salt.

Conductive polymers have attracted much attention in various applications, owing to their excellent chemical, thermal, and oxidative stability. However, they have low dielectric constant, which limits their performance in electrochemical devices. To overcome this drawback, blending with other polymers helps improving their electrochemical properties. Herein, we investigate structural and electrochemical properties of poly (vinylidene fluoride) (PVDF)/polyaniline (PANI) blends doped with lithium-based salt. Results showed that the blends exhibit phase separation of PANI and PVDF, which is confirmed by the thermodynamic interaction parameter. We found that the interaction between the two polymers enhanced the ionic conductivity from 4.9 × 10-5 S cm-1 for neat PVDF to 5.3 × 10-4 S cm-1 for composition of 50:50 (PANI50), whereas the ionic conductivity was inversely proportional to the temperature. Moreover, by adding lithium salt to the blend, the thermal stability increased from 376.6 to 478.5 °C for PANI50. The ionic conductivity of the blends depends on the PVDF content, which affects the interaction between the two polymers.

The many facets of RuII(dppe)2 acetylide compounds.

In this contribution, we describe the various research domains in which RuII alkynyl derivatives are involved. Their peculiar molecular properties stem from a strong and intimate overlap between the metal centered d orbitals and the p system of the acetylide ligands, resulting in plethora of fascinating properties such as strong and tunable visible light absorption with a strong MLCT character  essential for sensing, photovoltaics, light-harvesting applications or non-linear optical properties. Likewise, the d/p mixing results in tunable redox properties at low potential due to the raising of the HOMO level, and making those compounds particularly suited to achieve redox switching of various properties associated to the acetylide conjugated ligand, such as photochromism, luminescence or magnetism, for charge transport at the molecular level and in field effect transistor devices, or charge storage for memory devices. Altogether, we show in this review the potential of RuII acetylide compounds, insisting on the molecular design and suggesting further research developments for this class of organometallic dyes, including supramolecular chemistry.

The electrochemical properties of bimetallic silver-gold nanoparticles nano film's.

Electrode modification has been one of the most active areas of interest in electrochemistry research. Hence, the investigation of the effects of chemically and electrochemically modified GCE nano-films on the NPs electrochemical properties. The electrochemistry of nano-films of Ag NPs, Au NPs and bimetallic Ag-Au (1:2) NPs of chemical citrate reduction synthesis drop coated (DCT) and electro-deposition method (EDP) are reported. The Chemically synthesized NPs were confirmed through FT-IR, UV-visible, XRD and SEM techniques while electro-deposited NPs were ascertained by double-pulsed chrono-amperometry and electrochemical impedance spectroscopy (EIS). The nano films; GCE/Ag NPs, GCE/Au NPs and GCE/Ag-Ag (1:2) NPs in 0.1 M HCl supporting electrolyte were studied via Cyclic Voltammetry (CV) and Differential Pulse Voltammetry (DPV) techniques. Generally the DCT nano films were electrochemically superior to the EDP film in terms of current intensities and GCE/Ag-Au (1:2) NPs showed enhanced α (0.019), k s (0.01 s-1), Q (3.6 × 10-9 C), Γ (5.3 × 10-13molescm-2) and D (1.31 × 10-1 cm2s-1), indicating better physicochemical properties for possible sensing applications compared to electro-deposited GCE nano-films.

Enhanced Electrochemical Performance of Tin Oxide Quantum Dots on Reduced Graphene Oxide under Light.

The study utilized a simple and cost-effective approach to improve the photoelectrochemical (PEC) water-splitting performance of various materials, including reduced graphene oxide (rGO), tin oxide nanostructures (SnO2), and rGO/SnO2 composites. The composites examined were rS15, containing 15 mg of rGO and 45 mg of SnO2, and rS5, with 5 mg of rGO and 50 mg of SnO2, tested in a sodium hydroxide (NaOH) electrolyte. Notably, the rS5 electrode showed a significant increase in PEC efficiency in 0.1 M NaOH, achieving a peak photocurrent density of 13.24 mA cm-2 under illumination, which was seven times higher than that of pristine rGO nanostructures. This enhancement was attributed to the synergistic effects of the heterostructure, which reduced resistance and minimized charge recombination, thereby maximizing the catalytic activity across the various electrochemical applications. Furthermore, the rS5 anode demonstrated improved Tafel parameters, indicating faster reaction kinetics and lower overpotential for efficient current generation. These results highlight the potential for optimizing nanostructures to significantly enhance PEC performance, paving the way for advancements in sustainable water-splitting technologies.

The electrochemical mechanism of biochar for mediating the product ratio of N2O/(N2O + N2) in the denitrification process.

The biochar electrochemical properties and surface functional groups significantly impact N2O production and reduction during denitrification process. However, its effects on N2O emissions during the denitrification process and its electrochemical mechanisms remain unclear. The study examined the impact of pristine and oxidized biochar combined with two types of nitrogen fertilizers on the N2O/(N2O + N2) ratio and N2O emissions in an incubation experiment with seven treatments: (1) CK (no application of chemical fertilizer); (2) N1 (applying (NH4)2SO4); (3) N1B ((NH4)2SO4 + pristine biochar); (4) N1BO ((NH4)2SO4 + oxidized biochar); (5) N2 (applying KNO3); (6) N2B (KNO3 + pristine biochar); (7) N2BO (KNO3 + oxidized biochar). The study found that in comparison with applying nitrogen fertilizer alone, combining pristine biochar decreased soil N2O concentration by 7.1 %-85.8 %, while combining oxidized biochar increased it by 15.7 %-125.6 %. Applying pristine biochar reduced N2O/(N2O + N2) ratio by 10.4 %-86.2 %, whereas applying oxidized biochar increased it by 12.9 %-121.6 %. The application of pristine biochar increased the nosZ gene abundance and decreased the (nirS + nirK)/nosZ ratio, which contributed to reducing N2O to N2. Compared with oxidized biochar, the oxygen-containing functional groups of pristine biochar decreased by 46.6 %, and it possessed a higher specific surface area (23.01 m2 g-1) and electrical conductivity (0.003 mS cm-1). The correlation analysis showed that DOC and inorganic nitrogen were the key environmental factors affecting N2O emissions. Additionally, the electrical conductivity, specific capacitance, and oxygen-containing functional groups of the biochar were identified as the main factors driving N2O emissions. The SEM analysis suggested that the indirect influence of biochar electrochemical properties on N2O emissions was greater than its direct influence. Our work provides fresh perspectives on reducing soil N2O emissions and establishes a theoretical foundation for the subsequent preparation of biochar materials with enhanced N2O reduction capabilities.

Enhanced Electrochemical Performance and Cycling Stability of the (NH4)8[VIV12VV7O41(OH)9]·11H2O Cathode in Aqueous Zinc Ion Batteries.

Although vanadium-based compounds possess several advantageous characteristics, such as multivalency, open structure, and high theoretical specific capacity, which render them highly promising candidates for cathode materials in aqueous zinc ion batteries (AZIBs), their large-scale application still necessitates addressing the challenges posed by slow kinetics resulting from low conductivity and capacity degradation caused by material dissolution. Therefore, we have successfully synthesized high-purity mixed multivalent (NH4)8[VIV12VV7O41(OH)9]·11H2O (NVO) crystalline materials via a liquid-phase precipitation modulation method and employed it as an innovative AZIB cathode material for the first time. It exhibits a remarkable reversible specific capacity of 240 and 102.2 mAh g-1 after undergoing 1000 cycles at current densities of 1 and 5 A g-1, respectively, highlighting its exceptional cycling stability and electrochemical performance. The results from cyclic voltammetry (CV) and GITT tests demonstrate that the dominant factor influencing the charge storage is the pseudocapacitive behavior, which is accompanied by an exceptionally high diffusion coefficient of Zn2+ at a rate of 10-10 cm2 s-1. The highly reversible intercalation-deintercalation of Zn2+ in NVO/Zn cells is demonstrated through ex-situ TEM, XRD, and XPS analyses. This work provides a benchmark for the development of high-performance POV electrode materials.

Advancing Metallic Lithium Anodes: A Review of Interface Design, Electrolyte Innovation, and Performance Enhancement Strategies.

Lithium (Li) metal is one of the most promising anode materials for next-generation, high-energy, Li-based batteries due to its exceptionally high specific capacity and low reduction potential. Nonetheless, intrinsic challenges such as detrimental interfacial reactions, significant volume expansion, and dendritic growth present considerable obstacles to its practical application. This review comprehensively summarizes various recent strategies for the modification and protection of metallic lithium anodes, offering insight into the latest advancements in electrode enhancement, electrolyte innovation, and interfacial design, as well as theoretical simulations related to the above. One notable trend is the optimization of electrolytes to suppress dendrite formation and enhance the stability of the electrode-electrolyte interface. This has been achieved through the development of new electrolytes with higher ionic conductivity and better compatibility with Li metal. Furthermore, significant progress has been made in the design and synthesis of novel Li metal composite anodes. These composite anodes, incorporating various additives such as polymers, ceramic particles, and carbon nanotubes, exhibit improved cycling stability and safety compared to pure Li metal. Research has used simulation computing, machine learning, and other methods to achieve electrochemical mechanics modeling and multi-field simulation in order to analyze and predict non-uniform lithium deposition processes and control factors. In-depth investigations into the electrochemical reactions, interfacial chemistry, and physical properties of these electrodes have provided valuable insights into their design and optimization. It systematically encapsulates the state-of-the-art developments in anode protection and delineates prospective trajectories for the technology's industrial evolution. This review aims to provide a detailed overview of the latest strategies for enhancing metallic lithium anodes in lithium-ion batteries, addressing the primary challenges and suggesting future directions for industrial advancement.

Self-Healable, High-Stability Anode for Rechargeable Magnesium Batteries Realized by Graphene-Confined Gallium Metal.

In this work, a self-healable, high-stability anode material for rechargeable magnesium batteries (RMBs) has been developed by introducing a core-shell structure of Ga confined by reduced graphene oxide (Ga@rGO). Via this Ga@rGO anode, a specific capacity of 150 mAh g-1 at a current of 0.5 A g-1 stable up to 1200 cycles at room temperature and a specific capacity of 100 mAh g-1 under an ultrahigh current of 1 A g-1 stable up to 700 cycles at a slightly elevated temperature of 40 °C have been achieved. Additionally, the ultrahigh rate, high-cycling stability, and long-cycle life of the anode are attributed to the stabilized structure; such a low-cost, simple, and environmentally friendly direct drop coating (DDC) method is developed to maximize the original state of the active materials. Remarkably, the self-healing ability of anodes is still presented under the ultrahigh charging current. This anode is promising for the development of high rate and high stability RMBs.

Mo modulating the structure of monoclinic vanadium dioxide boosting the aqueous ammonium-ion storage for high-performance supercapacitor.

Supercapacitors (SCs) using ammonium-ion (NH4+) as the charge carrier (NH4+-SCs) have attracted continuous attention and vanadium-based materials are proved to have high-efficient NH4+-storage properties. Monoclinic vanadium dioxide, VO2(B), as an anode material applied to SCs has been rarely reported and modulating its electronic structure for boosted NH4+-storage is full of challenge. In this work, molybdenum-doped VO2(B) (Mo-doped VO2(B)) is designed and synthesize to enhance its NH4+-storage. The introduction of Mo atom into the crystal structure of VO2(B) can modulate its crystal structure and bring in some defects. Experimental results manifest that Mo-doped VO2(B) with 2 % Mo-doping shows the best electrochemical properties. Mo-doped VO2(B) achieves the specific capacitance of 1403 F g-1 (390 mAh g-1) at 0.1 A g-1 and the capacitance retention of about 98 % after 5000 cycle, superior to that of VO2(B) (893 F g-1, 248 mAh g-1 at 0.1 A g-1 and 60 % capacitance retention. The hybrid supercapacitor (HSC) assembled by Mo-doped VO2(B) and active carbon delivers good electrochemical performance with the energy density of 38.6 Wh kg-1 at power density of 208.3 W kg-1. This work proves that the Mo-doping is an efficient strategy for boosted NH4+-storage of VO2(B) and this strategy is like a Chinese idiom "like adding wings to a tiger" to guide the design of electrode materials for high-efficient NH4+-storage.

Facile Fabrication of Large-Area CuO Flakes for Sodium-Ion Energy Storage Applications.

CuO is recognized as a promising anode material for sodium-ion batteries because of its impressive theoretical capacity of 674 mAh g-1, derived from its multiple electron transfer capabilities. However, its practical application is hindered by slow reaction kinetics and rapid capacity loss caused by side reactions during discharge/charge cycles. In this work, we introduce an innovative approach to fabricating large-area CuO and CuO@Al2O3 flakes through a combination of magnetron sputtering, thermal oxidation, and atomic layer deposition techniques. The resultant 2D CuO flakes demonstrate excellent electrochemical properties with a high initial reversible specific capacity of 487 mAh g-1 and good cycling stability, which are attributable to their unique architectures and superior structural durability. Furthermore, when these CuO flakes are coated with an ultrathin Al2O3 layer, the integration of the 2D structures with outer nanocoating leads to significantly enhanced electrochemical properties. Notably, even after 70 rate testing cycles, the CuO@Al2O3 materials maintain a high capacity of 525 mAh g-1 at a current density of 50 mA g-1. Remarkably, at a higher current density of 2000 mA g-1, these materials still achieve a capacity of 220 mAh g-1. Moreover, after 200 cycles at a current density of 200 mA g-1, a high charge capacity of 319 mAh g-1 is sustained. In addition, a full cell consisting of a CuO@Al2O3 anode and a NaNi1/3Fe1/3Mn1/3O2 cathode is investigated, showcasing remarkable cycling performance. Our findings underscore the potential of these innovative flake-like architectures as electrode materials in high-performance sodium-ion batteries, paving the way for advancements in energy storage technologies.

Core-Double-Shell TiO2@Fe3O4@C Microspheres with Enhanced Cycling Performance as Anode Materials for Lithium-Ion Batteries.

Due to the volume expansion effect during charge and discharge processes, the application of transition metal oxide anode materials in lithium-ion batteries is limited. Composite materials and carbon coating are often considered feasible improvement methods. In this study, three types of TiO2@Fe3O4@C microspheres with a core-double-shell structure, namely TFCS (TiO2@Fe3O4@C with 0.0119 g PVP), TFCM (TiO2@Fe3O4@C with 0.0238 g PVP), and TFCL (TiO2@Fe3O4@C with 0.0476 g PVP), were prepared using PVP (polyvinylpyrrolidone) as the carbon source through homogeneous precipitation and high-temperature carbonization methods. After 500 cycles at a current density of 2 C, the specific capacities of these three microspheres are all higher than that of TiO2@Fe2O3 with significantly improved cycling stability. Among them, TFCM exhibits the highest specific capacity of 328.3 mAh·g-1, which was attributed to the amorphous carbon layer effectively mitigating the capacity decay caused by the volume expansion of iron oxide during charge and discharge processes. Additionally, the carbon coating layer enhances the electrical conductivity of the TiO2@Fe3O4@C materials, thereby improving their rate performance. Within the range of 100 to 1600 mA·g-1, the capacity retention rates for TiO2@Fe2O3, TFCS, TFCM, and TFCL are 27.2%, 35.2%, 35.9%, and 36.9%, respectively. This study provides insights into the development of new lithium-ion battery anode materials based on Ti and Fe oxides with the abundance and environmental friendliness of iron, titanium, and carbon resources in TiO2@Fe3O4@C microsphere anode materials, making this strategy potentially applicable.

Structure engineering of nickel silicate/carbon composite with boosted electrochemical performances for hybrid supercapacitors.

In the wake of the carbon-neutral era, the exploration of innovative materials for energy storage and conversion has garnered increasing attention. While nickel silicates have been a focal point in energy storage research, their application in supercapacitors (SCs) has been relatively underreported due to poor conductivity. A newly designed architecture, designated as rGO@NiSiO@NiO/C (abbreviated for reduced graphene oxide (rGO), nickel silicate (NiSiO), nickel oxide/carbon (NiO/C)), has been developed to enhance the electrochemical performance of NiSiO. The incorporation of inner rGO provides structural support for NiSiO, enhancing conductivity, while the outer NiO/C layer not only boosts conductivity but also safeguards NiSiO from structural degradation and electrolyte dissolution. This architecture eliminates multi-phase mixtures, facilitating rapid electron/mass transfer kinetics and accelerating electrochemical reactions, resulting in exceptional electrochemical properties. The rGO@NiSiO@NiO/C architecture achieves a specific capacitance of 324F·g-1 at 0.5 A·g-1, with a superb cycle performance of âˆ¼ 91 % after 10,000 cycles, surpassing state-of-the-art nickel silicates. Furthermore, the hybrid supercapacitor (HSC) device incorporating the rGO@NiSiO@NiO/C electrode attains an areal capacitance of 159 mF·cm-2 at 2.5 mA·cm-2, a retention ratio of âˆ¼ 98 % after 10,000 cycles, and an energy density of 0.68 Wh·m-2 (26.7 Wh·kg-1) at 3.4 W·m-2 (343.8 W·kg-1). This study presents a layer-by-layer approach for constructing transition metal silicates/C architectures to enhance their electrochemical performance.

Fabrication of Microgel-Modified Hydrogel Flexible Strain Sensors Using Electrohydrodynamic Direct Printing Method.

Hydrogel flexible strain sensors, renowned for their high stretchability, flexibility, and wearable comfort, have been employed in various applications in the field of human motion monitoring. However, the predominant method for fabricating hydrogels is the template method, which is particularly inefficient and costly for hydrogels with complex structural requirements, thereby limiting the development of flexible hydrogel electronic devices. Herein, we propose a novel method that involves using microgels to modify a hydrogel solution, printing the hydrogel ink using an electrohydrodynamic printing device, and subsequently forming the hydrogel under UV illumination. The resulting hydrogel exhibited a high tensile ratio (639.73%), high tensile strength (0.4243 MPa), and an ionic conductivity of 0.2256 S/m, along with excellent electrochemical properties. Moreover, its high linearity and sensitivity enabled the monitoring of a wide range of subtle changes in human movement. This novel approach offers a promising pathway for the development of high-performance, complexly structured hydrogel flexible sensors.

Tailoring of High-Valent Sn-Doped Porous Na3V2(PO4)3/C Nanoarchitechtonics: An Ultra High-Rate Cathode for Sodium-Ion Batteries.

NASICON structured Na3V2(PO4)3 (NVP) has captured enormous attention as a potential cathode for next-generation sodium-ion batteries (SIBs), owing to its sturdy crystal structure and high theoretical capacity. Nonetheless, its poor intrinsic electronic conductivity has led to inferior electrochemical performance in terms of rate capability and long cycling performance. To address this problem, a combined strategy is adopted, such as (1) carbon coating and (2) high valent Sn4+ ion doping in the lattice site of vanadium in the NVP cathode. Carbon coating can effectively enhance the surface electronic conductivity, wherein high-valent Sn4+ improves the bulk intrinsic electronic conductivity of the materials. Moreover, Sn is a well-known alloying/dealloying type anode for SIBs; thus, doping of such metal in cathode materials will assume the role of structure stabilizing pillars and establishing high-performing cathode materials. Herein, Na3V2-xSnx(PO4)3/C (denoted as Sn(x)-NVP/C, where x = 0.00, 0.03, 0.05, 0.07, 0.1) were synthesized via sol-gel route, followed by calcination at 800 °C. XRD, Raman, XPS, and electron microscopy data confirmed the high purity of the synthesized cathode. The optimized Sn(0.07)-NVP/C exhibited excellent electrochemical performance in terms of high rate capability and long cycling performance, a high appreciable capacity of 98 mAh g-1 with capacity retention of 85% after 500 cycles. Similarly, at a high current of 20C, it is still able to deliver a stable capacity of 76 mAh g-1 with 85% capacity retention after 3000 cycles. The rate capability study indicates the high current tolerance of Sn(0.07)-NVP/C up to 70 C with a capacity delivery of 55 mAh g-1. It is worth mentioning that CV and EIS analysis for Sn(0.07)-NVP/C cathode displayed minimum voltage polarization and enhanced diffusion coefficient. Moreover, DFT calculation also proved that the electronic and ionic conductivity of NVP is promoted by Sn doping. Hence, the present results demonstrated that Sn(0.07)-NVP/C is considered a promising cathode for sodium-ion battery application.

One-step hydrothermal synthesis of vanadium dioxide/carbon core-shell composite with improved ammonium ion storage for aqueous ammonium-ion battery.

Aqueous nonmetallic ion batteries have garnered significant interest due to their cost-effectiveness, environmental sustainability, and inherent safety features. Specifically, ammonium ion (NH4+) as a charge carrier has garnered more and more attention recently. However, one of the persistent challenges is enhancing the electrochemical properties of vanadium dioxide (VO2) with a tunnel structure, which serves as a highly efficient NH4+ (de)intercalation host material. Herein, a novel architecture, wherein carbon-coated VO2 nanobelts (VO2@C) with a core-shell structure are engineered to augment NH4+ storage capabilities of VO2. In detail, VO2@C is synthesized via the glucose reduction of vanadium pentoxide under hydrothermal conditions. Experimental results manifest that the introduction of the carbon layer on VO2 nanobelts can enhance mass transfer, ion transport and electrochemical kinetics, thereby culminating in the improved NH4+ storage efficiency. VO2@C core-shell composite exhibits a remarkable specific capacity of ∼300 mAh/g at 0.1 A/g, which is superior to that of VO2 (∼238 mAh/g) and various other electrode materials used for NH4+ storage. The NH4+ storage mechanism can be elucidated by the reversible NH4+ (de)intercalation within the tunnel of VO2, facilitated by the dynamic formation and dissociation of hydrogen bonds. Furthermore, when integrated into a full battery with polyaniline (PANI) cathode, the VO2@C//PANI full battery demonstrates robust electrochemical performances, including a specific capacity of ∼185 mAh·g-1 at 0.2 A·g-1, remarkable durability of 93 % retention after 1500 cycles, as well as high energy density of 58 Wh·kg-1 at 5354 W·kg-1. This work provides a pioneering approach to design and explore composite materials for efficient NH4+ storage, offering significant implications for future battery technology enhancements.

Thixotropic Composite Hydrogel Electrode Composed of a Polymer Hydrogelator and Water-Dispersive Tungsten Oxide Flat Microparticles.

Here, we introduce an organic/inorganic composite hydrogel as a versatile gel electrode material. This composite hydrogel was formed by simply mixing an aqueous solution of flat microparticles of tungsten oxide, exhibiting superior water dispersibility, with a hydrogel composed of a water-soluble polyaramide-based polymer hydrogelator. The resulting composite hydrogel exhibited uniform dispersion of tungsten oxide flat particles throughout the hydrogel matrix, supplementing the structure formed by the polymer hydrogelator. It maintained the gel-forming capability and thixotropic behavior inherent to the polymer hydrogelator while showcasing the electrochemical characteristics of tungsten oxide. With its spreadability and applicability to various electrode shapes, a composite hydrogel is presented as a potential spreadable gel electrode material.

Influence of Li concentration on structural, morphological and electrochemical properties of anatase-TiO2 nanoparticles.

Lithium-doped anatase-TiO2 nanoparticles (LixTi1-xO2 NPs, x = 0, 0.05, 0.10, 0.15 and 0.20) could be synthesized by a simple sol-gel process. X-ray diffraction (XRD) results displayed the tetragonal (space group: I41/amd) of polycrystalline TiO2 anatase phase. The spectroscopy results of Raman and FT-IR confirmed the anatase phase of TiO2 through the specific modes of metal oxides vibration in the crystalline TiO2. Surfaces micrographs by scanning electron microscope (SEM) of agglomerated LixTi1-xO2 NPs showed a spongy like morphology. Transmission electron microscope (TEM) illustrated a cuboidal shape of dispersed NPs with particle size distributed in a narrow range 5-10 nm. Bruanauer Emmett-Teller (BET) results showed the increased surface area of LixTi1-xO2 NPs with increasing Li content. LixTi1-xO2 NPs (x = 0.05-0.20) working electrodes illustrated a pseudocapacitive behavior with excellent electrochemical properties through the whole cycles of GCD test. Interestingly, Li0.1Ti0.9O2 NPs electrode illustrated a high performance in terms of maximum specific capacitance 822 F g-1 at 1.5 A g-1 in 0.5 M Li2SO4 electrolyte, with excellent capacitive retention 92.6% after 5000 cycles GCD test.

Structural, Electrical and Corrosion Properties of Bulk Ti-Cu Alloys Produced by Mechanical Alloying and Powder Metallurgy.

Binary Ti100-x-Cux (x = 1.6 and 3.0 wt.%) alloys were produced by the application of mechanical alloying and powder metallurgy processes. The influence of the copper concentration in titanium on the microstructure and properties of bulk alloys was investigated. The synthesized materials were characterized by an X-ray diffraction technique, scanning electron microscopy, and chemical composition determination. The electrochemical and corrosion properties were also investigated. Cold compaction and sintering reduced the content of α-Ti content in Ti98.4-Cu1.6 and Ti97-Cu3 alloys to 92.4% and 83.7%, respectively. Open Circuit Potential measurements showed a positive shift after the addition of copper, suggesting a potential deterioration in the corrosion resistance of the Ti-Cu alloys compared to pure Ti. Electrochemical Impedance Spectroscopy analysis revealed significant improvement in electrical conductivity after the addition of copper. Corrosion testing results demonstrated compromised corrosion resistance of Ti-Cu alloys compared to pure Ti. In summary, the comprehensive investigation of Ti100-x-Cux alloys provides valuable insights for potential applications in biosensing.

Application of a Carbon Fiber Microelectrode as a Sensor for Apocynin Electroanalysis.

In this study, a carbon fiber microelectrode (CF) was applied for the investigation of the electrochemical behavior of the natural antioxidant, apocynin (APO). Given the limited solubility of APO in water, a mixture of anhydrous acetic acid (AcH) with 20%, v/v acetonitrile (AN) and 0.1 mol L-1 sodium acetate (AcNa) was used. The electrochemical properties of APO were examined through linear sweep voltammetry (LSV), differential pulse voltammetry (DPV), and cyclic voltammetry (CV). The anodic oxidation of APO, which is the basis of the method used, proved to be diffusion-controlled and proceeded with a two-electron and one proton exchange. Both radicals and radical cations, arising from the first and second step of electrode reactions, respectively, underwent subsequent chemical transformations to yield more stable final products (EqCiEiCi mechanism). Using optimized DPV conditions, the anodic peak current of APO at a potential of 0.925 V vs. Ag/AgCl showed a good linear response within the concentration range of 2.7 × 10-6-2.6 × 10-4 mol L-1. The detection and quantification limits were determined as 8.9 × 10-7 and 2.7 × 10-6 mol L-1, respectively. The developed DPV method enabled the successful determination of APO in herbal extracts and in dietary supplements. It should be noted that this is the first method to be used for voltammetric determination of APO.

A data-driven approach for revealing the linkages between differences in electrochemical properties of biochar during anaerobic digestion using automated machine learning.

Biochar is commonly used to enhance the anaerobic digestion of organic waste solids and wastewater, due to its electrochemical properties, which intensify the electron transfer of microorganisms attached to its large surface area. However, it is difficult to create biochar with both high conductivity and high capacitance, which makes selecting the right biochar for engineering applications challenging. To address this issue, two Auto algorithms (TPOT and H2O) were applied to model the effects of different biochar properties on anaerobic digestion processes. The results showed that the gradient boosting machine had the highest predictive accuracy (R2 = 0.96). Feature importance analysis showed that feedstock concentration, digestion time, capacitance, and conductivity of biochar were the main factors affecting methane yield. According to the two-dimensional (2D) partial dependence plots, high-capacitance biochar (0.27-0.29 V·mA) is favorable for substrates with low-solid content (< 19.6 TS%), while the high-conductivity biochar (80.82-170.58 mS/cm) is suitable for high-solids substrates (> 20.1 TS%). The software, based on the optimal model, can be used to obtain the ideal range of biochar for AD trials, aiding researchers in practical applications prior to implementation.