Search Results (146)

The separation of particles smaller than 1 µm either by composition or by size is still a challenge. For the separation of SiO₂ and SnO₂, the creation of a selective separation feature and the specific adsorption of salts and surfactants were investigated. The adsorption of various salts, e.g., AlCl₃, ZnCl₂, MnCl₂ and MgCl₂ were therefore analyzed, and the necessary concentration for the charge reversal of the material was determined. It was noticed that the investigated materials differ in their isoelectric point (IEP) and therefore in their adsorption behavior because only ZnCl₂ and MgCl₂ are suitable for a charge reversal of both metal oxides. The phase transfer of the pure material at different pH values with ZnCl₂ or MgCl₂ and sodium dodecyl sulfate (SDS) revealed that the adsorption behavior of the particle has an influence on the phase transfer. As a result, the phase transfer of SiO₂ is pH dependent, whereas the phase transfer of SnO₂ operates over a wider pH range. This allowed the separation of SiO₂ and SnO₂ to be controlled by the salt and surfactant concentration as well as pH. The separation of SiO₂ and SnO₂ was investigated for various parameters such as salt and surfactant concentration, particle concentration and composition of the mixture. Also, pH 8, where a selective phase transfer for SiO₂ occurs, and pH 6, where the greatest difference between the materials exists, were also investigated. By comparing the parameters, it was found that the combination of ZnCl₂/SDS and MgCl₂/SDS enables a selective separation of the materials. Furthermore, it was also found that the concentration of SDS has a significant effect on the separation, as the formation of a bilayer structure is important for the separation, and therefore, higher SDS concentrations are required at higher particle concentrations to increase the separation efficiency. Full article

This study aims to explore a new concept for a Power to Heat (P2H) device and demonstrate its effectiveness compared to a thermal heating method. The proposed concept is a medium-temperature system where electro-thermal conversion occurs via the Joule effect in a metallic tube (resistive element). This tube also serves as a heat exchange surface between the heat transfer fluid and the thermal storage medium. The heat storage material here proposed consists of base concrete formulated on purpose to ensure its operation at high temperatures, good performance and prolongated thermal stability. The addition of 10%_wt phase change material (i.e., solar salts) stabilized in shape through a diatomite porous matrix allows the energy density stored in the medium itself to increase (hybrid sensible/latent system). Testing of the heat storage module has been conducted within a temperature range of 220–280 °C. An experimental comparison of charging times has demonstrated that electric heating exhibits faster dynamics compared to thermal heating. In both electrical and thermal heating methods, the concrete module has achieved 86% of its theoretical storage capacity, limited by thermal losses. In conclusion, this study successfully demonstrates the viability and efficiency of the proposed hybrid sensible/latent P2H system, highlighting the faster charging dynamics of direct electrical heating compared to conventional thermal methods, while achieving a comparable storage capacity despite thermal losses. Full article

This article proposes a 3D mathematical model of the influence of electrical heterogeneity of the ion exchange membrane surface on the processes of salt ion transfer in membrane systems with axial symmetry; in particular, we investigate an annular membrane disk in the form of a coupled system of Nernst–Planck–Poisson and Navier–Stokes equations in a cylindrical coordinate system. A hybrid numerical–analytical method for solving the boundary value problem is proposed, and a comparison of the results for the annular disk model obtained by the hybrid method and the independent finite element method is carried out. The areas of applicability of each of these methods are determined. The proposed model of an annular disk takes into account electroconvection, which is understood as the movement of an electrolyte solution under the action of an external electric field on an extended region of space charge formed at the solution–membrane boundary under the action of the same electric field. The main regularities and features of the occurrence and development of electroconvection associated with the electrical heterogeneity of the surface of the membrane disk of the annular membrane disk are determined; namely, it is shown that electroconvective vortices arise at the junction of the conductivity and non-conductivity regions at a certain ratio of the potential jump and angular velocity and flow down in the radial direction to the edge of the annular membrane. At a fixed potential jump greater than the limiting one, the formed electroconvective vortices gradually decrease with an increase in the angular velocity of rotation until they disappear. Conversely, at a fixed value of the angular velocity of rotation, electroconvective vortices arise at a certain potential jump, and with its subsequent increase gradually increase in size. Full article

For the interaction of angiotensin II (AngII) with AngII type 1 receptors (AT₁R), two potential proton hopping pathways have been identified, each associated with distinct physiological outcomes. The octapeptide AngII (Asp¹-Arg²-Val³-Tyr⁴-Ile⁵-His⁶-Pro⁷-Phe⁸) appears to form a charge relay system (CRS) in solution in which the C-terminal carboxylate abstracts a proton from the His⁶ imidazole group, which, in turn, abstracts a proton from the Tyr⁴ hydroxyl (OH) group, creating a tyrosinate anion. When AngII binds to the AT₁R, the CRS can be reconstituted with D281 of the receptor taking up the role of the Phe⁸ carboxylate in the tripartite interaction, whilst the Phe⁸ carboxylate forms a salt bridge with K199 of the receptor. As a consequence, the Tyr⁴ OH of AngII is positioned with accessibility to either the Phe⁸ carboxylate (bound to K199) or the His⁶ imidazole (activated by D281), thereby creating a potential gating mechanism for AT₁R receptor signaling. This study summarizes evidence based on structure activity data for various analogs wherein Tyr⁴ OH interaction with His⁶ imidazole (CRS formation) leads to G protein sequestration and vasoconstriction, whereas Tyr⁴ OH interaction with Phe⁸ carboxylate (bound to K199) engenders arrestin-mediated vasodilation and receptor desensitization. These findings, combined with quantum mechanical (semiempirical) calculations of CRS proton transfer presented herein, provide insights for the therapeutic targeting of angiotensin receptor blockers (sartans) and the development of second-generation drugs (bisartans). Full article

This study focuses on enhancing the photoelectrocatalytic (PEC) performance of LaFeO₃ photocathodes by incorporating Ag nanocrystals. LaFeO₃, a perovskite-type metal oxide semiconductor, has potential in PEC water splitting but suffers from fast charge carrier recombination. Ag nanoparticles are introduced due to their surface plasmon resonance (SPR) property and ability to form Schottky junctions with LaFeO₃. A series of Ag/LaFeO₃ materials are prepared using the molten salt method for LaFeO₃ synthesis and the direct reduction method for Ag loading. The results show that Ag nanoparticles are uniformly dispersed on LaFeO₃. The 3 mol% Ag/LaFeO₃ photocathode demonstrates a remarkable ninefold increase in photocurrent density (15 mA·cm⁻² at −0.2 V vs. RHE) compared to pure LaFeO₃ (1.7 mA·cm⁻²). The band gap of LaFeO₃ is reduced from 2.07 eV to 1.92 eV with 3 mol% Ag loading, and the charge transfer impedance is reduced by 77%, while the carrier concentration increases by 2.3 times. The novelty of this work lies in the comprehensive investigation of the interaction mechanisms between Ag nanoparticles and LaFeO₃, which lead to enhanced light absorption, improved charge separation, and increased electrochemical activity. The optimized Ag loading not only improves the photocatalytic efficiency but also enhances the stability of the photocathode. This work provides valuable insights into the interaction between Ag and LaFeO₃, and offers experimental and theoretical support for developing efficient photocatalytic materials for PEC water splitting. Full article

Rapid charge separation and transfer is the key scientific problem in photocatalysis. The construction of S-scheme heterojunction is one of the effective strategies to promote charge separation and maintain the strong redox properties. Herein, the NiO, K_0.2WO₃, and NiWO₄ ternary double S-scheme K_0.2WO₃/NiO/NiWO₄ heterojunction (W/NiO) was created by a one-step molten salt method. Ultraviolet-visible (UV-Vis) diffuse reflectance spectra, photoluminescence (PL) spectra, photoelectrochemistry tests, and other analyses revealed that the double S-scheme heterostructure broadened the spectral response range of NiO and promoted its separation of photocarriers. Compared with pristine NiO, the modified double S-scheme heterojunction enhanced the surface adsorption of water molecules and the accumulation of intermediate product of HCOO⁻, and optimized the CO₂ reduction system, realizing the improved CO yield of 373 μmol·g⁻¹·h⁻¹ in Ru(byp)₃²⁺/ethanolamine of CO₂ reduction system. This study indicates that double S-scheme heterojunction could facilitate efficient photogenerated charge transfer and separation, thereby achieving high activity and selectivity for CO₂ photoreduction. Our work provides a reference for the one-step construction of double S-scheme heterojunction. Full article

Pre-lithiation using Li–Si alloy-type additives is a promising technical approach to address the drawbacks of Si-based anodes, such as a low initial Coulombic efficiency (ICE) and inevitable capacity decay during cycling. However, its commercial application is limited by the air sensitivity of the highly reactive Li–Si alloys, which demands improved environmental stability. In this work, a protective membrane is constructed on Li₁₃Si₄ alloys using low-surface-energy paraffin and highly conductive carbon nanotubes through liquid-phase deposition, exhibiting enhanced hydrophobicity and improved Li⁺/e⁻ conductivity. The Li₁₃Si₄@Paraffin/carbon nanotubes (Li₁₃Si₄@P-CNTs) composite achieves a high pre-lithiation capacity of 970 mAh g⁻¹ and superb environmental stability, retaining 92.2% capacity after exposure to ambient air with 45% relative humidity. DFT calculations and in situ XRD measurements reveal that the paraffin-dominated coating membrane, featuring weak dipole–dipole interactions with water molecules, effectively reduces the moisture-induced oxidation kinetics of Li₁₃Si₄@P-CNTs in air. Electrochemical kinetic analysis and XPS depth profiling reveal the enhancement in charge transfer dynamics and surface Li⁺ transport kinetics (SEI rich in inorganic lithium salts) in P-SiO@C pre-lithiated by Li₁₃Si₄@P-CNTs pre-lithiation additives. Benefitting from pre-lithiation via Li₁₃Si₄@P-CNTs, the pre-lithiated SiO@C(P-SiO@C) delivers high ICE (103.7%), stable cycling performance (981 mAh g⁻¹ at 200 cycles) and superior rate performance (474.5 mAh g⁻¹ at 3C) in a half-cell system. The LFP||P-Gr pouch-type full cell exhibits a capacity retention of 83.2% (2500 cycles) and an energy density of 381 Wh kg⁻¹ after 2500 cycles. The Li₁₃Si₄@P-CNTs additives provide valuable design concepts for the development of pre-lithiation materials. Full article

This study demonstrates, for the first time, the formation of a hemiester of carbonic acid on self-assembled monolayers using voltammetric techniques and redox probes. A gold electrode (GE) was modified with 2-mercaptoethanol (ME) through self-assembly. With this modified electrode (GE-ME), a well-defined peak was observed by differential pulse voltammetry (DPV) for the negatively charged redox probe, ferricyanide/ferrocyanide, [Fe(CN)₆]³⁻/⁴⁻, in sodium acetate as an electrolyte adjusted to pH 8.2. In the presence of dissolved CO₂ in equilibrium with bicarbonate, there is a decrease in the ferrocyanide peak current with time (~30% in 60 min), attributed to the formation of hemiester 2-mercapto ethyl carbonate at the GE-ME/solution interface. Similarly, dissolved CO₂ and bicarbonate also affect the electrochemical impedance measurements by increasing resistance to the charge transfer process with time (elevation of Rct values), compatible with the formation of the hemiester. The addition of barium salt led to the displacement of the equilibrium towards BaCO₃ precipitation and consequent dissociation of the hemiester, attested by the recovery of the initial ferricyanide DPV signal. With the positively charged redox probe [Ru(NH₃)₆]²⁺, no decrease in the DPV peak was observed during the formation of the hemiester by reaction with bicarbonate. The repulsion of [Fe(CN)₆]³⁻, but not of [Ru(NH3)₆]²⁺, suggests that the formed species is the negatively charged 2-mercapto-ethyl carbonate, i.e., the hemiester with a dissociated proton. Due to the lack of a voltammetric signal from the hemiester itself, the formation of a self-assembled layer of thio-alcohol followed by the gradual formation of the corresponding carbonic acid hemiester allowed us to reach an elegant way of electrochemically demonstrating the formation of these species. Full article

Solid-state electrolytes are currently receiving increasing interest due to their high mechanical strength and chemical stability for safe battery construction. However, their poor ion conduction and unclear conduction mechanism need further improvement and exploration. This study focuses on a hybrid solid-state electrolyte containing MOF-based scaffolds, using metal salts as the conductor. In this paper, we employ an ion substitution strategy to manipulate the scaffold structure at the lattice level by replacing hydrogen with larger alkali cations. The research systematically presents how changes in the lattice affect the physical and chemical properties of MOFs and emphasizes the role of scaffold–salt interactions in the evolution of ion conduction. The results reveal that long range-ordered structural distortion can enhance permittivity at 1 Hz, from 58 ohms to more than 10 M ohms, which can boost ion pairs dissociation and improve the transference number from 4.7% to 22.6%. Defects in the lattice can help stabilize the intermediate state in the charge transfer process and lower the corresponding impedance from 2.6 MΩ to 559 Ω. Full article

Confronting escalating challenges in energy security and environmental sustainability has intensified interest in renewable sources for fuels and chemicals. Among the most promising alternatives, sugars derived from biomass are emerging as a cornerstone in advancing an environmentally sustainable economy. Within this framework, the development of sunlight-driven carbohydrate oxidation is of significant interest, as it enables the production of a broad spectrum of high-value, bio-sourced chemicals through eco-friendly processes. Gold nanoparticles (Au NPs) immobilized on inorganic supports have demonstrated considerable potential in this area, although the methodology still requires further exploration. In this study, we explored the selective oxidation of glucose into the corresponding gluconic acid salt in presence of a novel Au/Ni-Al-Zr-layered double hydroxide (LDH) photocatalyst under standardized A.M. 1.5 G light illumination. To optimize the photocatalytic conditions, an experimental plan is herein proposed, highlighting the critical influences of both catalyst loading and pH. In optimal conditions, the Au catalyst demonstrated a high efficiency, achieving 87% glucose conversion and 100% selectivity towards gluconic acid in only 90 min. By means of long-pass filters to select the incident light energy to the photocatalytic reactor, we evidenced that the charge transfer processes were occurring from the Ni-Al-Zr LDH support to the gold nanoparticles, thus opening new directions towards further photocatalyst modifications. This work underlines the potential of Au/LDH materials for sunlight-driven photocatalysis and provides a pathway for the sustainable production of high-value chemicals from renewable biomass sources. Full article

This article proposes various new approximate analytical solutions of the boundary value problem for the non-stationary system of Nernst–Planck–Poisson (NPP) equations in the diffusion layer of an ideally selective ion-exchange membrane at overlimiting current densities. As is known, the diffusion layer in the general case consists of a space charge region and a region of local electroneutrality. The proposed analytical solutions of the boundary value problems for the non-stationary system of Nernst–Planck–Poisson equations are based on the derivation of a new singularly perturbed nonlinear partial differential equation for the potential in the space charge region (SCR). This equation can be reduced to a singularly perturbed inhomogeneous Burgers equation, which, by the Hopf–Cole transformation, is reduced to an inhomogeneous singularly perturbed linear equation of parabolic type. Inside the extended SCR, there is a sufficiently accurate analytical approximation to the solution of the original boundary value problem. The electroneutrality region has a curvilinear boundary with the SCR, and with an unknown boundary condition on it. The article proposes a solution to this problem. The new analytical solution methods developed in the article can be used to study non-stationary boundary value problems of salt ion transfer in membrane systems. The new analytical solution methods developed in the article can be used to study non-stationary boundary value problems of salt ion transport in membrane systems. Full article

TiO₂:Eu³⁺ nanoparticles with varying europium concentrations were successfully synthesized via a one-pot sol–gel approach using a molecular heterometallic single-source precursor (SSP) Eu-Ti. For comparison, nanomaterials with similar europium levels were also produced by impregnating europium salts onto the same TiO₂ substrate. All the nanomaterials were thoroughly characterized using Eu elemental analysis, powder X-ray diffraction (XRD), scanning (SEM), transmission (TEM), scanning transmission electron microscopy (STEM), Brunauer–Emmett–Teller (BET) analysis, thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, and photoluminescence (PL). This low-temperature synthesis yielded crystalline powders, and calcination at 400 °C was performed to remove surface organic impurities, enabling a precise comparison of the final nanomaterials. While both preparation methods produced materials with similarly dispersed and localized dopants on the TiO₂ surface, photoluminescence studies revealed that the SSP-derived nanomaterials exhibited significantly superior electro-optical properties. This enhanced efficiency is attributed to the co-hydrolysis of both reactants, which facilitates an optimized interface between the crystalline TiO₂ core and the dopant-rich amorphous surface, thereby enabling far more effective charge transfer than that achieved by impregnation. Full article

In order to improve the electrochemical activity and discharge performance of aluminum–air batteries and to reduce self-corrosion of the anode, an SLM-manufactured aluminum alloy was employed as the anode of the Al-air battery, and the influence of PAAS and ZnO inhibitors taken separately or together on the self-corrosion rate and discharge performance of the Al-air battery in a 4 M NaOH solution were investigated. The experimental result indicated that the effect of a composite corrosion inhibitor was stronger than that of a single corrosion inhibitor. The addition of the compound inhibitor not only promoted the activation of the anode but also formed a more stable composite protective film on the surface of the anode, which effectively slowed down the self-corrosion and improved the utilization rate of the anode. In NaOH/PAAS/ZnO electrolytes, the dissolution of the Al6061 alloy was mainly controlled by the diffusion of the electric charge in the corrosion products or the zinc salt deposition layer. Meanwhile, for the Al-air battery, the discharge voltage, specific capacity, and specific energy increased by 21.74%, 26.72%, and 54.20%, respectively. In addition, the inhibition mechanism of the composite corrosion inhibitor was also expounded. The excellent discharge performance was due to the addition of the composite corrosion inhibitor, which promoted the charge transfer of the anode reaction, improved the anode’s activity, and promoted the uniform corrosion of the anode. This study provides ideas for the application of aluminum–air batteries in the field of new energy. Full article

As the core of modern energy technology, lithium-ion batteries (LIBs) have been widely integrated into many key areas, especially in the automotive industry, particularly represented by electric vehicles (EVs). The spread of LIBs has contributed to the sustainable development of societies, especially in the promotion of green transportation. However, the high demand for battery performance and safety in these fields has made the high viscosity, volatility, and potential leakage inherent in traditional organic liquid electrolytes a constraint on their further expansion. Especially at low temperature, the increased viscosity of the electrolyte, reduced solubility of lithium salts, crystallization or solidification of the electrolyte, increased resistance to charge transfer due to interfacial by-products, and short-circuiting due to the growth of anode lithium dendrites all affect the performance and safety of LIBs. Therefore, improving the safety performance of LIBs under low-temperature environments has become a focus of current research. This paper primarily reviews the progress made in utilizing different types of electrolytes in LIBs to enhance safety and optimize low temperature performance and discusses the current research progress as well as the future development direction of the field. Full article

Graphitic carbon nitride (g-C₃N₄) is a promising material for photocatalytic applications. However, it suffers from poor visible-light absorption and a high recombination rate of photogenerated electron–hole pairs. Here, Co/La@g-C₃N₄ with enhanced photocatalytic activity was prepared by co-doping Co and La into g-C₃N₄ via a facile one-pot synthesis. Co/La@g-C₃N₄ displayed better performance, achieving 94% tetracycline (TC) removal within 40 min, as compared with g-C₃N₄ (BCN, 65%). It also demonstrated promising performance in degrading other pollutants, which was ~2–4-fold greater relative to BCN. The improved photocatalytic activity of Co/La@g-C₃N₄ was associated with improved photogenerated charge separation, reduced charge transfer resistance, a built-in electric field arising from the p-n-p heterojunction, and the synergistic effect of ternary components for the separation and transfer of the photogenerated charge carriers. Superoxide radicals are suggested to be the most notable reactive species responsible for the photocatalytic reaction. Environmental factors, including the pollutant concentration, catalyst dosage, solution pH, inorganic salts, water matrices, and mixture with dyes, were considered in the photocatalytic reactions. Co/La@g-C₃N₄ showed good reusability for five cycles of the photocatalytic degradation of TC. The facile one-pot co-doping of Co and La in g-C₃N₄ formed a p-n-p heterojunction with boosted photocatalytic activity for the highly efficient removal of TC from various water matrices. Full article