Power Density Research Articles

Wind Energy Harvesting with Building-Integrated Ducted Openings: CFD Simulation and Neural Network Optimization

Building-integrated wind energy harvesting offers a promising local and decentralized energy generation solution, reducing transmission losses and infrastructure expenses. However, the complex urban wind patterns demand accurate aerodynamic optimization for optimal performance. This study seeks to optimize the geometric design of building-integrated ducted openings to maximize wind energy harvesting. The research aims to create a data-driven model predicting the openings' performance accurately, explore the inter-linked impacts of different geometrical variables, find optimal configurations across different building heights, and understand underlying aerodynamic mechanisms. The proposed design comprises a nozzle, throat, and diffuser. To increase power density, a data-driven design optimization method is employed. The optimization process involves determining the optimum opening height from the ground, along with five geometrical variables: inlet diameter, throat diameter, outlet diameter, nozzle length, and diffuser length. A comprehensive test matrix is developed using design of experiments (DoE) to build an artificial neural network (ANN) model. This neural network is developed using computational fluid dynamics (CFD) simulations validated with experimental data. Subsequently, a gradient-based global optimization method fine-tunes the neural network and identifies optimal designs for various heights. The research concludes that nozzle and diffuser opening angles within the range of 19° ≤ ΦNoz ≤ 23°and 7.5° ≤ ΦDif ≤ 8.2°, respectively, result in the optimal converging-diverging ducted opening geometry. This optimal opening can yield a power density increase of 31.5 to 35.5 times when compared to freestream flow and 17.5 to 22.4 times in comparison to cylindrical openings, depending on the opening location along the building height.

Effects of binder content on potato starch-derived porous carbon microspheres for high-performance supercapacitors

Potato starch-based carbon microspheres (PCMs) have successfully synthesized from potato starch by a simple strategy based on (NH4)2HPO4 and KOH activation. The PCMs presents a large specific surface area (SSA) of 2048 m2 g−1. The electrochemical behaviors of the PCMs with different binder content in 6 mol L−1 KOH were studied by impedance spectroscopy, cyclic voltammetry (CV), and galvanostatic charge-discharge (GCD). The results show that PCMs-85 (the binder content is 5 wt%) has a small equivalent series resistance (ESR), high specific capacitance, compacted density, and areal density. PCMs-85 exhibited good cycling durability of 100 % after 10,000 cycles at 1 A g−1 and delivered an energy density of 6.35 Wh L−1 and a volume power density of 167.38 W L−1. The corresponding capacitive performances of PCM-85-based symmetrical two-electrode supercapacitors are investigated in 6 mol L−1 KOH, 1 mol L−1 Na2SO4 and 1 mol L−1 TEA.BF4/AN electrolyte. The PCMs supercapacitor with 6 mol L−1 KOH electrolyte exhibits a mass-specific capacitance of 172 F g−1 with volumetric capacitances of 145 F cm−3 at 1 A g−1.

Highly durable perfluorosulfonic acid proton exchange membrane by combining inorganic free radical scavengers and organic antioxidants

In this work, a new type of complex was constructed by coordinating quercetin (QC) with cerium (Ce) ions. This complex was introduced into perfluorosulfonic acid resin (PFSA) to fabricate a proton exchange membrane. The coordination process prevented the formation of ion cross-links between cerium and sulfonic acid groups in PFSA, thereby keeping proton conductivity and fuel cell performance of membrane samples at a high level. Due to the insolubility of quercetin in water, its coordination with cerium minimized cerium migration, providing long-lasting resistance to free radicals. The effects of additives on PFSA membrane properties were investigated by measuring IEC, water uptake, swelling ratio, and proton conductivity. Fenton degradation experiments and membrane electrode assembly performance tests was conducted simultaneously. The results demonstrated that compared to the addition of quercetin or cerium alone, the use of QC-Ce increased the proton conductivity by 23.70% after 24-h Fenton degradation and lowered fluoride release by 58.29%. Meanwhile, the PFSA/QC-Ce composite membrane samples maintained an open circuit voltage of 0.935 V and a maximum power density of 668.15 mW cm−2 after 96 h of open circuit voltage hold testing.

Engineering of Pt@Ni,N-doped graphene electrocatalyst based on recycled water bottles waste as an efficient cathode material for PEM fuel cells

Fuel cells (FCs) represent one of the most promising clean power sources. Their cost represents a considerable challenge to their widespread commercialization because of their sensitivity and the expensive cost of the employed platinum electrocatalysts. Accordingly, one feature of a fuel cell device that many interested parties are looking for is the engineering of catalysts with a low Pt content. Herewith, Pt supported on nickel loaded nitrogen-doped graphene (Pt@Ni,N-G) was synthesized through a simple pyrolysis process of mineral water bottles waste with urea and nickel metal at 800 °C followed by loading Pt in different proportions via a simple reduction method in aqueous solution at room temperature. The physicochemical and electrochemical properties of a promising Pt@Ni,N-G cathode electrocatalyst for polymer electrolyte membrane fuel cell (PEMFC) were characterized and evaluated using a number of specialized techniques. The results showed that the high Pt@Ni,N-G content enhanced the catalytic activity of the oxygen reduction reaction (ORR), with a specific activity of 3.13 mA cm−2 and a mass activity of 12.35 mA μg−1Pt at −0.1 V. A maximum power density of 87.8 mW cm−2 was achieved which is closest to that of commercial Pt/C. Designing Pt@Ni,N-G electrocatalysts by recycling waste bottles is not only expected to reduce the cost of fuel cells by ~30 % to raise the industry standard but also protect the environment and humanity from harmful pollutants.

Nickel-molybdenum bimetallic sulfide decorated biomass derived carbon support for high performance asymmetric supercapacitor application

Biomass - derived carbon electrode material with a porous structure is widely used in supercapacitor applications, which can improve electron transfer and shorter ion diffusion pathways. In this work, the garlic peel biomass carbon (GPBC), NiMo3S4(NMS) and garlic peel biomass carbon decorated with NiMo3S4 (GPBC/NMS) composite were prepared through a in situ two-step hydrothermal method. The synthesized materials were characterized by X-ray diffraction (XRD) and field emission scanning electron microscopy (FE-SEM), energy dispersive x-ray spectroscopy (EDS), Transmission electron microscopy techniques (TEM), Raman spectroscopy and Brunauer-Emmett-Teller (BET) techniques were used to analyze the structure, morphology and specific surface areas and X-ray photoelectron spectroscopy (XPS). The prepared bimetallic metal sulfide on a biomass - derived carbon namely the GPBC/NMS composite is used in supercapacitor application. The GPBC/NMS composite electrode exhibits good cycle performance with high specific capacity of 304C/g at current density of 1 A/g in a 3 M KOH electrolyte solution. The electrochemical performance of the GPBC/NMS//GPBC asymmetric supercapacitor device produces an excellent energy density 45.5 Wh kg−1 at a power density of 1125 W kg−1 in the 1.6 V operating potential window. The GPBC/NMS//GPBC also exhibits 93 % retention of its initial capacitance after the 10,000 GCD cycle performance. The above results demonstrate a new way of developing high performance electrode materials for energy storage applications.

The Symmetric Dual Inductor Hybrid Converter for Direct 48V-to-PoL Conversion

This work introduces the symmetric dual inductor hybrid (SDIH) dc-dc converter topology, which is suitable for large conversion ratios where regulation is required, such as direct 48 V to point-of-load (PoL) applications. A dickson-type switched capacitor network is used to effectively produce two interleaved PWM outputs with a greatly reduced voltage amplitude relative to the input voltage, allowing the subsequent magnetic volume to be reduced while retaining modest switching frequencies. Distinct from related variations, part count is significantly reduced while both even and odd order switched capacitor networks can be used with straightforward split-phase control; allowing either network type to achieve complete soft-charging of all flying capacitors. Additionally, charge flow is uniformly distributed through all elements, with equal capacitor and inductor values being preferred. Subsequently this topology is expected to simplify component selection, improve electrical and thermal performance, and reduce cost. Furthermore, analysis is presented that calculates precise phase durations without making small ripple assumptions, revealing up to a 75% timing error in cases where either inductor or capacitor ripple is ignored. Finally, a discrete prototype validates this analysis and demonstrates very high measured power densities of 1,029 W/in <inline-formula xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><tex-math notation="LaTeX">$^{3}$</tex-math></inline-formula> , 754 W/in <inline-formula xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><tex-math notation="LaTeX">$^{3}$</tex-math></inline-formula> , and 663 W/in <inline-formula xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink"><tex-math notation="LaTeX">$^{3}$</tex-math></inline-formula> for 48 V input and regulated output voltages of 3 V, 2 V, and 1 V, respectively, while switching at a frequency of 750 kHz.

Performance and compensation method of first-order liquid crystal beam-steering system under continuous wave laser irradiation

The effects of laser irradiation thermal deposition on the performance degradation of liquid crystal (LC) devices in high-power laser systems are extremely vital. In this study, the first-order beam-steering system (FBS) was developed using a passive liquid crystal polarization grating (LCPG) and liquid crystal adjustable wave-plate (LCAW). The LCPG was prepared by holographic exposure technology, and the LCAW was prepared using the standard LC cell preparation process. We investigated the influences of diffraction efficiency of FBS under a 1070-nm continuous-wave (CW) laser irradiation. The energy is concentrated in the −1st order at first. When the half-wave retardation was reached, all the energy is concentrated in the +1st order (∼97 %), and the beam is deflected. Once the phase retardation decreases below the half-wave retardation, the energy gradually reconcentrates in the −1st order. When the LCAW fails, the diffraction the energy is refocused to the −1st order by the LCPG. The results indicated that both thermal deposition and driving voltage reduce the phase retardation of the LCAW, generating a variation of energy between in ±1st orders. By reducing the driving voltage, this half-wave retardation can be recovered under a certain half-wave voltage and laser power density, and the diffraction efficiency of the +1st order can be compensated to ∼97 %. If the reduced phase retardation is not less than half-wave, the FBS can still be modulated in high-power continuous lasers. Our research provides a reference for the development of beam-steering technology based on LC materials in high-power laser systems.

A sustainable solution: Conversion of distillers' grains waste into high-performance supercapacitor electrode materials for energy storage applications

The development of cost-effective biomass-derived carbon with good electrochemical properties is crucial for advancing energy storage devices sustainably. One feasible approach to producing supercapacitor electrode materials is the conversion of heteroatom-rich biomass waste into heteroatom self-doped hierarchical porous carbons with favorable electrochemical properties. In this study, distillers' grains with abundant crude fiber and protein were utilized as precursors to prepare N, S self-doped hierarchical porous carbon, which presents a high specific surface area of 3642.87 m2 g−1. The N, S doping could improve the interfacial wettability of electrode materials and enhance the pseudocapacitive effect of the materials. In three-electrode system, the carbon delivered a high capacitance of 347 F g−1 at 1 A g−1. Symmetrical capacitors assembled with PVA/KOH gel electrolytes delivered an ultrahigh energy density of 11.29 Wh kg−1 at a power density of 250 W kg−1. This strategy provides a practical, low-cost, and renewable design approach of carbon electrode for high-performance supercapacitors.

A regulatory power split strategy for energy management with battery and ultracapacitor

Electric vehicle batteries face fast degradation due to the high frequency of charging/discharging cycles and great peak power demands. Lifetime, continuity of supply and power density of these batteries affect the performance of electric vehicles (EVs). Hybrid energy storage systems (HESS) offers a feasible solution by incorporating other energy storage elements like ultra-capacitor (UC) along with battery. Their combination provides higher efficiency and better performance in terms energy/power density. UC can behave like a power buffer when the EV is accelerating and regenerating. The HESS needs a controller that can split the available power between different sub systems as per demand. This paper presents a regulatory control strategy useful in HESS with battery and UC for the speed regulation of a brushless DC (BLDC) motor using a 3-port bidirectional DC-DC converter. The regulatory control strategy monitors the state of charge (SOC) of UC and a fuzzy logic controller regulates the power flow between HESS and the motor. Simulation in MATLAB validates the efficacy of the strategy. Simulation results and hardware evaluation confirm that the regulatory control scheme is effective in splitting the available power according to the load demand and achieves better energy efficiency.

Review on Biomass Derived Activated Carbons as Electrochemical Electrode Material for Supercapacitor Device

Abstract: To face the challenge of the finite nature of fossil fuels and large energy crises across the globe, there is an urgent requirement for sustainable and renewable energy sources. Moreover, it is essential to focus on energy storage in order to meet the demand of future generations. Among various energy storage devices such as fuel cells, batteries, capacitors, supercapacitors, flywheels, etc., it is the supercapacitor device that has elicited extensive research interest recently because of prominent features like high power density, fast recharge capability, and long cycle life. The main objective of this article is to review the enhancement of the electrochemical performance of supercapacitor devices. The electrochemical properties of the supercapacitor device majorly depend on the electrode materials used, which include carbonaceous materials, metal oxides, and conducting polymers. In order to reduce energy shortages and environmental pressure, carbon materials derived from biomass/waste materials have been considered remarkable candidates for electrode materials with the advantages of high abundance, low cost, and environmental friendliness. This review shows the complied study of various methodologies for the preparation of activated carbons derived from different biomass residues such as plants, animals, and microorganisms, which have been investigated in the past few years as electrochemical electrode materials for supercapacitors. Further, ongoing challenges and potential improvements in this area for creating efficient energy storage devices are also discussed. The goal of this review article is to aid in the creation of new insights for energy storage applications of biomass-generated carbons that will lead to sustainable energy development.

Luminescent properties of Tm3+-activated phosphors with rosiaite structure

A series of solid solutions with compositions of La1-xTmxGa0.5Sb1.5O6 (x = 0.03, 0.05, 0.1) and La1-x-y-zTmxTbyDyzGa0.5Sb1.5O6 (x = 0.04, 0.07, 0.1; y = 0.04, 0.07, 0.1; z = 0.04, 0.04, 0.06) has been synthesized. It is shown that all the compounds have rosiaite structure (PbSb2O6, sp.gr. P-31m). Morphology, spectral-luminescent characteristics and color coordinates of the samples were studied. It was found that luminescence spectrum of thulium-activated samples recorded upon 351 nm excitation is typical for Tm3+ ions. At the same time, under excitation by radiation with λ = 457 nm and a power density of J = 4.7 kW/cm2, broadband thermal emission is observed, against which the bands corresponding to the 1G4→3H6, 1G4→3F4, 3F4→3H6 и 3H4→3H6 transitions of Tm3+ are detected. The luminescence spectra of the samples co-activated with Tm3+, Tb3+ and Dy3+are characterized by a relatively low intensity of the Tm3+ emission, which may be due to efficient energy transfer processes between Tb3+ and Dy3+ ions. A shift from the blue to the green color regions is observed in the color coordinates of the co-activated samples upon 351 nm excitation. Radiation with λ = 457 nm led to a shift in the emission colour to orange. Thus, it is shown that it is possible to create phosphors emitting in the blue, green and orange spectral regions by changing the wavelength of exciting radiation and activator composition for compounds with rosiaite structure.

Exploring the application of hydrazine hydrate in protonic ceramic fuel cells: Strategies and performance improvements

Hydrazine hydrate, characterized by its high hydrogen content and eco-friendliness, garners extensive attention in the field of fuels. Its high energy density and rapid decomposition capabilities render it a promising fuel option for Proton-Conductor Solid Oxide Fuel Cells (PCFCs). Given the unique properties of hydrazine hydrate, this study employs a dendritic porous anode structure to facilitate faster fuel transport. Additionally, the influence of operational temperature and concentration of hydrazine hydrate as fuel on cell performance is analyzed. An effective vapor management strategy is implemented to address its decomposition into water vapor, resulting in a significant 23.17 % increase in the maximum power density (MPD) of the cell. To further enhance the performance of hydrazine hydrate fuel in PCFCs, a Pt–Al spherical catalyst is integrated within the anode structure of the cell. This approach notably improves the cell performance, yielding an additional 14.98 % increase in MPD. This design not only augments the electrical output but also effectively mitigates the degradation of the interface between the anode and the electrolyte. These optimization measures significantly improve the lifespan and reliability of the cell. The outcomes of this study demonstrate the practical feasibility of using hydrazine hydrate as a fuel in PCFCs.

Characterization of manufacturing material and carbon nanohybrid for renewable energy and storage systems

Scientists are exploring advanced energy alternatives to compete with rising fossil fuel consumption and CO2 emissions due to population growth and technological advancements. Supercapacitors are highly efficient systems for storing energy due to their specific capacitance and power density, meeting modern energy storage demands. Perovskite and carbon-based materials have emerged as the most effective materials in this respect. In this work, SrSnO3/rGO nanohybrid is chosen as the supercapacitor electrode material for the very first time and a range of characterization techniques are employed to ascertain the structural and textural characteristics of the composite. The physicochemical properties of the SrSnO3 included rGO are shown to have a greater surface area, excellent electrical conductivity and a lower resistance. It is demonstrated that the rGO improved quicker ion diffusion channels for the increased redox performance in the SrSnO3/rGO nanohybrid. Additionally at 1 A/g, the SrSnO3/rGO nanohybrid has an elevated specific capacitance of 1385 F/g along with energy and power density of 66 Wh/kg and 293 W/kg, respectively in a three-electrode system. During the two electrode observations, the revealed Cs of SrSnO3/rGO nanohybrid was 122 F/g at 1 A/g with 66 Wh/kg and 293 W/kg of energy density and power density, respectively. The SrSnO3/rGO nanohybrid has exceptional functionality, as demonstrated by its 65 h stability examination via chronoamperometry and a modest drop in its CV polarization curve area after the 5000th cycle of the CV stability analysis. These evaluated results point to the nanohybrid's promising future.

Synergistic effect of co-sputtered tungsten-titanium nitride as electrode material for efficient hybrid supercapacitors

The dawn of bimetallic transition metal nitrides has attracted considerable interest as battery grade electrode material for potential energy storage applications. In addition, it is essential to investigate binder-free processes to improve the performance of the fabricated electrodes. In this study, binder-free tungsten‑titanium nitrides (W-TiN) are deposited through RF/DC magnetron co-sputtering onto the conducting nickel foam (NF). SEM, EDX and X-ray diffraction are exploited to investigate surface morphology, elemental composition, and structural properties of sputtered materials. The W-TiN electrodes are characterized through electrochemical investigation in half-cell configuration. The tested W-TiN electrode is further utilized with activated carbon (AC) electrode to develop hybrid supercapacitor device W-TiN//AC. The hybrid device revealed a maximum energy density (Es) of 88.8 Wh/kg and power density (Ps) 1700 W /kg. To further understand the mechanism of hybrid devices, the capacitive and diffusive contributions are computed using linear and quadradic models. This study provides a new direction to integrate co-sputtered binder-free electrode materials and devices for large scale production of advanced hybrid energy storage devices.

Laser-Scribed Battery Electrodes for Ultrafast Zinc-Ion Energy Storage.

Aqueous Zn batteries are promising for large-scale energy storage applications but are plagued by the lack of high-performance cathode materials that enable high specific capacity, ultrafast charging, and outstanding cycling stability. In this work, we design a laser-scribed nano-vanadium oxide (LNVO) cathode that can simultaneously achieve these properties. Our material stores charge through Faradaic redox reactions on/near the surface at fast rates owing to the small grain size (2-6nm) of vanadium oxide and interpenetrating three-dimensional (3D) graphene network, displaying a surface-controlled capacity contribution (90%-98%). Multiple characterization techniques unambiguously reveal that zinc and hydronium ions co-insert with minimal LNVO lattice change upon cycling. As a result, we demonstrate that a high specific capacity of 553 mAh g-1 can be achieved by the LNVO/Zn system at 0.1 A g-1 , and an impressive 264 mAh g-1 capacity can be retained at 100 A g-1 with a 10 s charge/discharge cycle, showing excellent rate capability. The LNVO/Zn is also capable of reaching >90% capacity retention after 3,000 cycles at a high rate of 30 A g-1, as well as achieving both high energy (369Wh kg-1) and power densities (56,306W kg-1). Moreover, the LNVO cathode retains its excellent cycling performance when integrated into quasi-solid-state pouch cells, further demonstrating mechanical stability and its potential for practical application in wearable and grid-scale applications. This article is protected by copyright. All rights reserved.

Printed flexible solid-state microsupercapacitor with highly-stable aqueous cobalt-based inks

Cobalt-based nanomaterials are among the most noticed candidates for manufacturing supercapacitive electrodes. Inkjet-printing is an emerging technique for fabricating miniaturized devices. In this work, highly flexible microsupercapacitors (MSCs) are manufactured, using a pseudocapacitive (C = 900 F‌ g−1 at 1 A g−1) Co-oxide-hydroxide water-based and ultra-stable (up to 12 months) ink on paper. The synthesized capacitive active material consists of cobalt-oxide nanocubes and cobalt-hydroxide hexagonal nanoflakes. Conductive (Rs = 13 Ω/□) silver nanowire networks serve as current collectors, and the morphology of cobalt oxide-hydroxide structures and the developed ink features, allow for printing well-detailed and homogeneous patterns. The inkjet-printed symmetric and asymmetric devices show notable areal specific capacitances of 35.68 mF cm−2 and 23.60 mF cm−2 at a current density of 0.1 mA cm−2, respectively. The asymmetric devices deliver impressive energy and power densities of 2.76 μW h cm−2 (4.10 W h kg−1) and 646 μW cm−2 (959 W kg−1), respectively. A thorough study on the cyclic and mechanical stability of the flexible devices resulted in perfect capacitance maintenance of 94.3 % after 10,000 charge and discharge cycles and retention of over 80 % even after 1000 cycles of successive bending and folding. The extensive study of capacitance retention following folding under various obtuse and reflex angles, which can be regarded as an important step toward characterizing flexible devices suitable for being utilized in wearable electronics, is carried out for the first time to the best of our knowledge. The findings of this study clearly illustrate the prospects of using the inkjet-printing technique to fabricate high-performance MSC devices appropriate for integration with flexible and wearable electronics.

Integrating Aperiodic 3D Porous Electrodes into 3D Batteries through Spray‐Deposited Polymer Electrolytes

AbstractDue to their exceptional energy and power densities, 3D micro‐batteries emerge as highly promising candidates for miniaturized power sources. However, fabricating a complete and uniform electrolyte/separator membrane to separate 3D electrodes in assembled 3D batteries remains a significant challenge. Herein, the study presents a straightforward approach to preparing 3D electrolyte membranes via a modified spray‐deposition method. This 3D electrolyte membrane effectively isolates the 3D porous LiFePO4 cathode from the Li anode with a ionic conductivity of 9.6 × 10−4 S cm−1, facilitating the creation of an integrated aperiodic 3D battery. The 3D battery exhibits a specific capacity of up to 8.8 mAh cm−2 (29.1 mWh cm−2) and attains a maximum power density of 12.7 mW cm−2. The characteristic time is 0.17 s for 3D battery while 0.73 s for traditional 2D batteries. The enhanced rate performance with thick electrode is primarily attributed to the reduced ionic diffusion pathway. These results represent the highest peak power and energy density among all reported aperiodic 3D batteries. The utilization of spray‐deposited electrolytes for 3D electrode separation promises significant advancements in developing 3D batteries and demonstrates great potentials for practical applications.

Organic Waste for Bioelectricity Generation in Microbial Fuel Cells: Effects of Feed Physicochemical Characteristics

Food waste (FW), piggery waste (PW), and activated sludge (AS) were investigated as potential organic feeds for bioelectricity generation in laboratory-scale microbial fuel cells (MFCs). The MFCs fed by FW gained the highest maximum power density at 7.25 W/m3, followed by those fed by PW at 3.86 W/m3 and AS at 1.54 W/m3. The tCOD removal in the FW-, PW-, and AS-MFCs reached 76.9%, 63.9%, and 55.22%, respectively, within a 30-day retention time. Food waste, which resulted in the highest power density and tCOD removal, was selected for a series of following tests to investigate the effects of some physicochemical properties of organic feed on the performance of MFCs. The effect of feed particle size was tested with three controlled size ranges (i.e., 3, 1, and &lt;1 mm) in MFCs. A smaller feed particle size provided a higher power density of 7.25 W/m3 and a tCOD removal of 76.9% compared to the MFCs fed with organic waste with a larger particle size. An increment in feed moisture from 70% to 90% improved the maximum power density from 7.2 to 8.5 W/m3, with a 17.5% enhancement, and improved the tCOD removal from 75.8% to 83.3%, with a 10.0% enhancement. A moderate C/N ratio of approximately 30/1 maximized the power density and COD removal (7.25 W/m3 and 81.73%) in the MFCs compared to C/N ratios of 20/1 (4.0 W/m3 and 64.14%) and 45/1 (4.38 W/m3 and 71.34%).

Numerical and Thermodynamic Analysis of the Effect of Operating Temperature in Methane-Fueled SOFC

This study examines the thermodynamic and numerical analyses of a methane-fed solid oxide fuel cell (SOFC) over a temperature range varying between 873 K and 1273 K. These analyses were conducted to investigate and compare the performance of the SOFC under various operating conditions in detail. As part of the thermodynamic analysis, important parameters such as cell voltage, power density, exergy destruction, entropy generation, thermal efficiency, and exergy efficiency were calculated. These calculations were used to conduct energy and exergy analyses of the cell. According to the findings, an increase in operating temperature led to a significant improvement in performance. At the initial conditions where the SOFC operated at a temperature of 1073 K and a current density of 9000 A/m2, it was observed that when the temperature increased by 200 K while keeping the current density constant, the power density increased by a factor of 1.90 compared to the initial state, and the thermal efficiency increased by a factor of 1.45. Under a constant current density, the voltage and power density values were 1.0081 V, 1.0543 V, 2337.13 W/m2, and 2554.72 W/m2 at operating temperatures of 1073 K and 1273 K, respectively. Under a current density of 4500 A/m2, the entropy generation in the cell was determined to be 29.48 kW/K at 973 K and 23.68 kW/K at 1173 K operating temperatures. The maximum exergy efficiency of the SOFC was calculated to be 41.67% at a working temperature of 1273 K and a current density of 1500 A/m2. This study is anticipated to be highly significant, as it examines the impact of temperature variation on exergy analysis in SOFC, validating both numerical and theoretical results, thus providing a crucial roadmap for determining optimized operating conditions.

Quantitative analysis of laser-generated ultrasonic wave characteristics and their correlation with grain size in polycrystalline materials

Abstract The quantitative relationship between nanosecond pulsed laser parameters and the characteristics of laser-generated ultrasonic waves in polycrystalline materials was evaluated. The high energy of the pulsed laser with a large irradiation spot simultaneously generated ultrasonic longitudinal and shear waves at the epicenter under the slight ablation regime. An optimized denoising technique based on wavelet thresholding and variational mode decomposition was applied to reduce noise in shear waves with a low signal-to-noise ratio. An approach for characterizing grain size was proposed using spectral center frequency ratio (SCFR) based on time-frequency analysis. The results have demonstrated that the generation regime of ultrasonic waves is not solely determined by the laser power density; even at high power densities, a high energy with a large spot can generate an ultrasonic waveform dominated by the thermoelastic effect. It is ascribed to the intensification of the thermoelastic effect with the proportional increase in laser irradiation spot area for a given laser power density. Furthermore, both longitudinal and shear wave SCFRs are linearly related to grain size in polycrystalline materials; however, the shear wave SCFR is more sensitive to finer-grained materials. This study holds great significance for evaluating metal material properties using laser ultrasound.