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Lithium-ion capacitors (LICs) have attracted considerable interest because of their excellent power and energy densities. However, the development of LICs is limited by the low capacity of the cathode and the kinetics mismatch between the cathode and anode. In this work, mesoporous carbon materials (MCs) with uniform pore sizes were prepared using magnesium citrate as the raw material through a self-templating method. During the carbonization process, MgO nanoparticles generated from magnesium citrate act as a template, resulting in a more orderly pore structure. The resultant MCs demonstrate a high specific surface area of 1673 m2 g-1 and an abundance of small mesopores, which significantly accelerated ion migration within the electrolyte and expedited the formation of electric double layers. Benefiting from these advantages, the MCs cathode demonstrates a high reversible specific capacity, excellent cycling stability, and rate performance. The assembled MCs-based LIC provides a high energy density of 152.2 Wh kg-1 and a high power density of 14.3 kW kg-1. After 5000 cycles, a capacity retention rate of 80% at the current density of 1 A g-1 is obtained. These results highlight the excellent potential of MCs as a cathode material for LICs.

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Technologies associated with using concentrated energy flows are increasingly used in industry due to the need to manufacture products made of hard alloys and other difficult-to-process materials. This work is devoted to expanding knowledge about the processes accompanying the impact of laser pulses on material surfaces. The features of these processes are reflected in the acoustic emission signals, the parameters of which were used as a tool for understanding the accompanying phenomena. The influence of plasma formations above the material surface on self-oscillatory phenomena and the self-regulation process that affects pulse productivity were examined. The stability of plasma formation over time, its influence on the pulse performance, and changes in the heat flux power density were considered. Experimental data show the change in the power density transmitted by laser pulses to the surface when the focal plane is shifted. Experiments on the impact of laser pulses of different powers and durations on the surface of a hard alloy showed a relationship between the amplitude of acoustic emission and the pulse performance. This work shows the data content of acoustic emission signals and the possibility of expanding the research of concentrated energy flow technologies.

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Current research strives to create sustainable and ecofriendly organic electrode materials (OEMs) due to the rising concerns about traditional inorganic electrode materials that call for substantial resource consumption in battery manufacturing. However, OEMs often exhibit unbalanced performance, with high capacity conflicting with a long lifespan. Herein, a 2D fully conjugated covalent organic framework featuring abundant C═O and C═N groups (HTPT-COF) was strategically synthesized by coupling 2,3,7,8-tetraamino-1,4,6,9-tetraketone with hexaketocyclohexane octahydrate. It stabilizes the enriched active centers by an extended π-conjugated skeleton, thereby affording a high theoretical capacity in conjunction with potential structure stability. To further unlock the barriers of fast charge, the HTPT-COF was interwoven around highly conductive carbon nanotubes, creating a robust core-sheath heterostructure (HTPT-COF@CNT). Consequently, the crafted HTPT-COF@CNT achieves large reversible capacities of 507.7 mA h g-1, high-rate performance (247.8 mA h g-1 at 20.0 A g-1), and long-term durability (1000 cycles). Aiming to streamline the process and cut the cost of battery manufacturing, all-organic symmetric batteries were well fabricated using HTPT-COF@CNT as both cathode and anode, demonstrating high energy/power density (up to 191.7 W h kg-1 and 3800.3 W kg-1, respectively) and long-term stability over 1000 cycles. Such HTPT-COF@CNT represents a promising sustainable electrode that effectively addresses irreconcilable contradictions encountered by OEMs, boosting the development of advanced organic batteries with high capacity and cycling stability.

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The focus of the study in this article is analyzing the electrochemical properties of molybdenum disulfide on miscible poly(methyl methacrylate)-poly(lactic acid) blends for supercapacitors. The interaction between molybdenum disulfide and miscible poly(methyl methacrylate)-poly(lactic acid) blends, affinity toward water, surface morphology, and mechanical properties are inspected by Fourier transform infrared spectroscopy, water contact angle, scanning electron microscopy, and universal testing machine, respectively. Among the developed membranes, 0.75 wt% of molybdenum disulfide on poly(methyl methacrylate)-poly(lactic acid) shows better electrochemical performances. It exhibits a maximum specific capacitance of 255.5 F g-1 at a current density of 1.00 mA g-1, maximum energy density of 22.7 Wh kg-1, and maximum power density of 360 W kg-1. A cycle study reveals 92% capacitance retention after 2500 cycles. The designed supercapacitor device shows a maximum specific capacitance of 1240 µF g-1 at a current density of 0.5 µA g-1, maximum energy density of 43 µWh kg-1, and maximum power density of 700 µW kg-1. Flexible membranes of molybdenum disulfide are expected to be a potent combination for supercapacitor applications.

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Simple and scalable production of micro-supercapacitors (MSCs) is crucial to address the energy requirements of miniature electronics. Although significant advancements have been achieved in fabricating MSCs through solution-based printing techniques, the realization of high-performance MSCs remains a challenge. In this paper, graphene-based MSCs with a high power density were prepared through screen printing of aqueous conductive inks with appropriate rheological properties. High electrical conductivity (2.04 × 104 S∙m-1) and low equivalent series resistance (46.7 Ω) benefiting from the dense conductive network consisting of the mesoporous structure formed by graphene with carbon black dispersed as linkers, as well as the narrow finger width and interspace (200 µm) originating from the excellent printability, prompted the fully printed MSCs to deliver high capacitance (9.15 mF∙cm-2), energy density (1.30 µWh∙cm-2) and ultrahigh power density (89.9 mW∙cm-2). Notably, the resulting MSCs can effectively operate at scan rates up to 200 V∙s-1, which surpasses conventional supercapacitors by two orders of magnitude. In addition, the MSCs demonstrate excellent cycling stability (91.6% capacity retention and ~100% Coulombic efficiency after 10,000 cycles) and extraordinary mechanical properties (92.2% capacity retention after 5000 bending cycles), indicating their broad application prospects in flexible wearable/portable electronic systems.

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High power output and high conversion efficiency are crucial parameters for microbial fuel cells (MFCs). In our previous work, we worked with microfluidic MFCs to study fundamentals related to the power density of the MFCs, but nutrient consumption was limited to one side of the microchannel (the electrode layer) due to diffusion limitations. In this work, long-term experiments were conducted on a new four-electrode microfluidic MFC design, which grew Geobacter sulfurreducens biofilms on upward- and downward-facing electrodes in the microchannel. To our knowledge, this is the first study comparing electroactive biofilm (EAB) growth experiencing the influence of opposing gravitational fields. It was discovered that inoculation and growth of the EAB did not proceed as fast at the downward-facing anode, which we hypothesize to be due to gravity effects that negatively impacted bacterial settling on that surface. Rotating the device during the growth phase resulted in uniform and strong outputs from both sides, yielding individual power densities of 4.03 and 4.13 W m-2, which increased to nearly double when the top- and bottom-side electrodes were operated in parallel as a single four-electrode MFC. Similarly, acetate consumption could be doubled with the four electrodes operated in parallel.

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Post-COVID syndrome manifests with numerous neurological and cognitive symptoms, the precise origins of which are still not fully understood. As females and older adults are more susceptible to developing this condition, our study aimed to investigate how post-COVID syndrome alters intrinsic brain dynamics in older adults and whether biological sex and cognitive training might modulate these effects, with a specific focus on older females. The participants, aged between 60 and 75 years, were divided into three experimental groups: healthy old female, post-COVID old female and post-COVID old male. They underwent an adaptive task-switching training protocol. We analysed multiscale entropy and spectral power density of resting-state EEG data collected before and after the training to assess neural signal complexity and oscillatory power, respectively. We found no difference between post-COVID females and males before training, indicating that post-COVID similarly affected both sexes. However, cognitive training was effective only in post-COVID females and not in males, by modulating local neural processing capacity. This improvement was further evidenced by comparing healthy and post-COVID females, wherein the latter group showed increased finer timescale entropy (1-30 ms) and higher frequency band power (11-40 Hz) before training, but these differences disappeared following cognitive training. Our results suggest that in older adults with post-COVID syndrome, there is a pronounced shift from more global to local neural processing, potentially contributing to accelerated neural aging in this condition. However, cognitive training seems to offer a promising intervention method for modulating these changes in brain dynamics, especially among females.

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Starch, lipids, and proteins are key macronutrients in starchy foods. Their interactions during processing can form starch-lipid-protein ternary complexes, significantly affecting food quality. Ultrasonic treatment, as a common processing method, is expected to regulate the quality of starchy foods by influencing the formation of ternary complexes. This study aimed to understand the effect of ultrasonic pretreatment on the formation of starch-lipid-protein ternary complexes using various types of starches. Wheat starch (WS), maize starch (MS), and potato starch (PS) were gelatinized and treated with ultrasound at various power densities (0-40 W/L) to form complexes with lauric acid (LA) and ß-lactoglobulin (ßLG), respectively. Ultrasound increased the amylose content of gelatinized WS, MS, and PS and shifted their chain length distribution towards the short chains. Results from Fourier transform infrared spectroscopy, laser confocal micro-Raman, X-ray diffraction, and differential scanning calorimetry showed that the largest amount of WS-LA-ßLG complexes was formed at the ultrasonic power density of 10 W/L, and MS-LA-ßLG and PS-LA-ßLG complexes at 20 W/L. Additionally, ultrasound enhanced the content of resistant starch (RS) in the starch-LA-ßLG complexes. The RS content increased from 14.12 % to 18.31 % for WS-LA-ßLG, and from 19.18 % and 20.69 % to 27.60 % and 28.63 % for MS-LA-ßLG and PS-LA-ßLG complexes, respectively. This study presents an approach for facilitating the formation of ternary complexes, contributing to the development of low-GI functional foods.

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Binary nanocomposite-based electrodes have been studied extensively in recent times owing to their multiple oxidation states, excellent physico-chemical features, and combined morphology, which are suitable for increasing the electrochemical performance of supercapacitors. The present work deals with Sb2O3-MoS2nanocomposites electrode for supercapacitor applications. The x-ray diffraction (XRD), Raman, scanning electron microscope (SEM), energy dispersive x-ray (EDX), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED) and x-ray photoelectron spectroscopy (XPS) characterizations have been studied to analyze the phase formation, vibrational modes, morphology, elemental composition and binding energies of the prepared Sb2O3-MoS2nanocomposites electrode material, as well as their electrochemical measurements such as cyclic voltammetry (CV), galvanostatic charge-discharge (GCD), and electrochemical impedance spectroscopy (EIS) have been analyzed. The developed Sb2O3-MoS2nanocomposites electrode provides a high specific capacitance of 454.3 F g-1at the current density of 1 A g-1. Further, the hybrid supercapacitor device has been constructed which shows 104.04 F g-1of specific capacitance at 2 A g-1and manifests a good energy density of 24.42 Wh kg-1at a power density of 1299.89 W kg-1. Additionally, the hybrid device Sb2O3-MoS2//AC exhibits a good capacitive retention of 90.6% and a coulombic efficiency of 100.45% at 10 A g-1over 8000 cycles.

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Transition metal sulfides are widely used in supercapacitor electrode materials and exhibit excellent performance because of their rich variety, low price, and high theoretical specific capacity. At present, the main methods to prepare transition metal sulfides include the hydrothermal method and the electrochemical method. In order to further improve their electrochemical performance, two aspects can be addressed. Firstly, by controllable synthesis of nanomaterials, porous structures and large surface areas can be achieved, thereby improving ion transport efficiency. Secondly, by combining transition metal sulfides with other energy storage materials, such as carbon materials and metal oxides, the synergy between different materials can be fully utilized. However, future research still needs to address some challenges. In order to guide further in-depth research, it is necessary to combine the current research-derived knowledge and propose a direction for future development of transition metal sulfide electrode materials.

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Improving catalytic activity of cathode with noble metal-free catalysts can significantly establish microbial fuel cells (MFCs) as a sustainable and economically affordable technology. This investigation aimed to assess the viability of utilizing tri-metal ferrite (Co0.5Cu0.5 Bi0.1Fe1.9O4) as an oxygen reduction reaction (ORR) catalyst to enhance the performance of cathode in MFCs. Trimetallic ferrite was synthesized using a sol-gel auto-combustion process. Electrochemical evaluations were conducted to assess the efficacy of as-synthesized composite as an ORR catalyst, employing electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). This evaluation revealed that the impregnation of bismuth in the Co-Cu-ferrite structure improves the reduction current response and reduces the charge transfer resistance. Further experiments were conducted to test the performance of this catalyst in an MFC. The MFC with tri-metal ferrite catalyst generated a power density of 11.44 W/m3 with 21.4% coulombic efficiency (CE), which was found to be comparable with commercially available 10% Pt/C used as cathode catalyst in MFC (power density of 12.14 W/m3 and CE of 23.1%) and substantially greater than MFC having bare carbon felt cathode without any catalyst (power density of 2.49 W/m3 and CE of 7.39%). This exceptionally inexpensive ORR catalyst has adequate merit to replace commercial costlier platinum-based cathode catalysts for upscaling MFCs.

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Simultaneously achieving high-energy-density and high-power-density is a crucial yet challenging objective in the pursuit of commercialized power batteries. In this study, atomic layer deposition (ALD) is employed combined with a coordinated thermal treatment strategy to construct a densely packed, electron-ion dual conductor (EIC) protective coating on the surface of commercial LiNi0.5Co0.2Mn0.3O2 (NCM523) cathode material, further enhanced by gradient Al doping (Al@EIC-NCM523). The ultra-thin EIC effectively suppresses side reactions, thereby enhancing the stability of the cathode-electrolyte interphase (CEI) at high-voltages. The EIC's dual conduction capability provides a potent driving force for Li+ transport at the interface, promoting the formation of rapid ion deintercalation pathways within the Al@EIC-NCM523 bulk phase. Moreover, the strategic gradient doping of Al serves to anchor the atomic spacing of Ni and O within the structure of Al@EIC-NCM523, curbing irreversible phase transitions at high-voltages and preserving the integrity of its layered structure. Remarkably, Al@EIC-NCM523 displays an unprecedented rate capability (114.7 mAh g-1 at 20 C), and a sustained cycling performance (capacity retention of 74.72% after 800 cycles at 10 C) at 4.6 V. These findings demonstrate that the proposed EIC and doping strategy holds a significant promise for developing high-energy-density and high-power-density lithium-ion batteries (LIBs).

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A nanocomposite of multi-walled carbon nanotubes (MWCNTs) decorated with molybdenum dioxide (MoO2) nanoparticles is fabricated through the reduction of phosphomolybdic acid hydrate on functionalized MWCNTs in a hydrogen-argon (10%) atmosphere in a tube furnace. The MoO2/MWCNTs composite is proposed as an anodic modification material for microbial fuel cells (MFCs). MWCNTs have outstanding physical and chemical peculiarities, with functionalized MWCNTs having substantially large electroactive areas. In addition, combined with the exceptional properties of MoO2 nanoparticles, the synergistic advantages of functionalized MWCNTs and MoO2 nanoparticles give a MoO2/MWCNTs anode a large electroactive area, excellent electronic conductivity, enhanced extracellular electron transfer capacity, and improved nutrient transfer capability. Finally, the power harvesting of an MFC with the MoO2/MWCNTs anode is improved, with the MFC showing long-term repeatability of voltage and current density outputs. This exploratory research advances the fundamental application of anodic modification to MFCs, simultaneously providing valuable guidance for the use of carbon-based transition metal oxide nanomaterials in high-performance MFCs.

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Measuring postural control in an upright standing position is the standard method. However, this diagnostic method has floor or ceiling effects and its implementation is only possible to a limited extent. Assessing postural control directly on the trunk in a sitting position and consideration of the results in the spectrum in conjunction with an AI-supported evaluation could represent an alternative diagnostic method quantifying neuromuscular control. In a prospective cross-sectional study, 188 subjects aged between 18 and 60 years were recruited and divided into two groups: "LowBackPain" vs. "Healthy". Subsequently, measurements of postural control in a seated position were carried out for 60 s using a modified balance board. A spectrum per trail was calculated using the measured CoP tracks in the range from 0.01 to 10 Hz. Various algorithms for data classification and prediction of these classes were tested for the parameter combination with the highest proven static influence on the parameter pain. The best results were found in a frequency spectrum of 0.001 Hz and greater than 1 Hz. After transforming the track from the time domain to the image domain for representation as power density, the influence of pain was highly significant (effect size 0.9). The link between pain and gender (p = 0.015) and pain and height (p = 0.012) also demonstrated significant results. The assessment of postural control in a seated position allows differentiation between "LowBackPain" and "Healthy" subjects. Using the AI algorithm of neural networks, the data set can be correctly differentiated into "LowBackPain" and "Healthy" with a probability of 81%.

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Aqueous aluminum ion batteries (AAIBs) possess the advantages of high safety, cost-effectiveness, eco-friendliness and high theoretical capacity. However, the Al2O3 film on the Al anode surface, a natural physical barrier to the plating of hydrated aluminum ions, is a key factor in the decomposition of the aqueous electrolyte and the severe hydrogen precipitation reaction. To circumvent the obnoxious Al anode, a proof-of-concept of an anode-free AAIB is first proposed, in which Al2TiO5, as a cathode pre-aluminum additive (Al source), can replenish Al loss by over cycling. The Al-Cu alloy layer, formed by plating Al on the Cu foil surface during the charge process, possesses a reversible electrochemical property and is paired with a polyaniline (cathode) to stimulate the battery to exhibit high initial discharge capacity (175 mAh g-1), high power density (≈410 Wh L-1) and ultra-long cycle life (4000 cycles) with the capacity retention of ≈60% after 1000 cycles. This work will act as a primer to ignite the enormous prospective researches on the anode-free aqueous Al ion batteries.

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Water evaporation-induced electricity generators (WEGs) have drawn widespread attention in the field of hydrovoltaic technology, which can convert atmospheric thermal energy into sustainable electric power. However, it is restricted in the wide application of WEGs due to the low power output, complex fabrication process, and high cost. Herein, we present a simple and effective approach to fabricate TiO2-carbon black film-based WEGs (TC-WEGs). A single TC-WEG device can sustainably output an open-circuit voltage of 1.9 V and a maximum power density of 40.9 µW/cm2. Moreover, it has been shown that TC-WEGs exhibit stable electrical energy output when operating in seawater, which can yield a short-circuit current of 1.2 µA. The superior electricity generation performance can be attributed to the intrinsic characteristics of the TC-WEGs, including hydrophilicity, porous structure, and electrical conductivity. This work provides an important reference for the constant harvesting of clean energy.

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The objective of this study is to perform an analysis to determine the most suitable type of wind turbine that can be installed at a specific location for electricity generation, using annual measurements of wind characteristics and meteorological parameters. Wind potential analysis has shown that the analyzed location is suitable for the development of a wind farm. The analysis was carried out for six different types of wind turbines, with a power ranging from 1.5 to 3.0 MW and a hub height set at 80 m. Wind power potential was assessed using the Weibull analysis. The values of the scale coefficient c were determined, and a large monthly variation was observed, with values ranging from 1.92 to 8.36 m/s and an annual value of 4.95 m/s. Monthly values for the shape coefficient k varied between 0.86 and 1.53, with an annual value of 1.07. Additionally, the capacity factor of the turbines was determined, ranging from 17.75 to 22.22%. The Vestas turbine, with a nominal power of 2 MW and a capacity factor of 22.22%, proved to be the most efficient wind turbine for the specific conditions of the location. The quantity of greenhouse gas emissions that will be reduced if this type of turbine is implemented was also calculated, considering the average CO2 emission intensity factor (kg CO2/kWh) of the national electricity system.

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Nickel copper cobalt oxide (NiCuCoO) ternary metal oxide nanoparticles were synthesized by employing the hydrothermal method. NiCuCoO electrode demonstrates a specified capacity of 596 C g-1 at 1 A g-1, high capacitance retaining of 99% even if 1000 sequences at the density of current 10 A g-1, and significant extended cyclic strength over 1000 sequences. The gathered asymmetric supercapacitor (ASC) tool via NiCuCoO as the cathode and activated carbon as anode materials achieve a specified capacity of 168 C g-1 at a current density of 1 Ag-1, an excellent capacity retaining of 95% even later than 5000 sequences at a density of current 10 A g-1. The fabricated device exhibits a high density of energy and power is 96 Wh kg-1 and 841 W kg-1. The prepared material confirms an excellent capacitance routine, so this work represents for a next-generation energy storage device.

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The microbial desalination cell (MDC) is a bio-electrochemical system that exhibits the ability to oxidize organic compounds, produce energy, and decrease the saline concentrations within the desalination chamber. The selective removal of ions from the desalination chamber is significantly influenced by the anion and cation exchange membranes. In this study, a three-chamber microbial desalination cell was developed to treat seawater using a synthesize Fe3O4 magnetite nanoparticle (MNP)-modified anode. The impact of different performance parameters, such as temperature, pH, and concentrations of NPs, has been investigated in order to assess the performance of three-chamber MDCs in terms of energy recovery and salt removal. The evaluation criteria of the system included multiple factors such as chemical oxygen demand (COD), Coulombic efficiency (CE), desalination efficiency, as well as system aspects including voltage generation and power density. The highest COD% removal efficiency was 74% at 37 °C, pH = 7, and 30 g/L salt concentration with an optimized NPs concentration of 2.0 mg/cm2 impregnated on anode. The maximum Coulombic efficiency was 10.3% with the maximum power density of 4.3 W/m3. The effect of the nanoparticle concentration impregnated on the anode was clarified by the primary factor of analysis. This research has revealed consistent patterns in the enhancement of voltage generation, COD, and Coulombic efficiencies when incorporating higher concentrations of nanoparticles on the anode at a certain point.

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Melamine-based metal-organic frameworks (MOFs) for high-performance supercapacitor applications are described in this paper. Melamine (Me) is employed as an organic linker, and three metal ions cobalt, nickel, and iron (Co, Ni, Fe) are used ascentral metal ions to manufacture the desired MOF materials (Co-Me, Ni-Me, and Fe-Me). While melamine is an inexpensive organic linker for creating MOF materials, homogenous molecular structures can be difficult to produce. The most effective technique for expanding the molecular structures of MOFs through suitable experimental optimization is used in this work. The MOFs materials are characterized using standard techniques. The kinetics of the materials' reactions are investigated using attenuated total reflectance. X-ray photoelectron spectroscopy (XPS), powder X-ray diffraction (P-XRD), Fourier transform infrared (ATR-FT-IR) spectroscopy, and Brunauer-Emmett-Teller (BET) studies verified the development of the MOFs structure. The surface morphology of the produced materials is investigated using field emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HR-TEM), and atomic force microscopy (AFM). The elements found in MOFs are studied via XPS analysis, energy dispersive X-ray diffraction (EDX), mapping, and mapping. The materials' absorption characteristics were examined by the use of UV-visible absorption spectroscopy. The thermal stability of the materials is examined by thermogravimetric analysis (TGA); these materials are more stable, according to the findings, even at high temperatures. The electrochemical investigation determines the specific capacitance of the materials. The specific capacitance of Co-Me, Ni-Me, and Fe-Me in 3 M KOH electrolyte is 1267.36, 803.22, and 507.59F/g @ 1 A-1, according to the three-electrode arrangement. The two-electrode device maximizes power and energy density by using an asymmetrical supercapacitor in a 3 M KOH electrolyte. The power and energy densities of Co-Me, Ni-Me, and Fe-Me are 3650.63, 2813.21, and 6210.45 W kg-1, and 68.43, 46.32, and 42.2 Wh kg-1, respectively. According to the materials stability test, the MOFs are highly stable after 10,000 cycles. Preliminary results suggest that the materials are suitable for usage in high-end supercapacitor uses.