Operating Temperature Research Articles

Dynamically Confined Active Silver Nanoclusters with Ultrawide Operating Temperature Window in CO oxidation.

Supported metal nanoclusters are often highly active in many catalytic reactions but less stable particularly under harsh reaction conditions. Here, we demonstrate that this activity-stability trade-off can be efficiently broken through rational design of surrounding microenvironment of the supported nanocatalyst including gas adsorbate overlayer and underneath support surface chemistry. Our studies reveal that chemisorbed oxygen species on Ag surface and surface hydroxyl groups on oxide support, which are dynamically consumed during reaction but sustained by reaction environment (O2 and H2O vapor), drive spontaneous redispersion of Ag particles and stabilization of highly active Ag nanoclusters. Such a dynamic confinement effect from gas-catalyst-support interaction enables the Ag nanoclusters to exhibit complete catalytic oxidation of CO over a wide temperature window of 25 - 500 °C under dry conditions and 200 - 800 °C under wet conditions as well as remarkable stability at 300 °C over 1000 h.

Dynamically Confined Active Silver Nanoclusters with Ultrawide Operating Temperature Window in CO oxidation

Supported metal nanoclusters are often highly active in many catalytic reactions but less stable particularly under harsh reaction conditions. Here, we demonstrate that this activity‐stability trade‐off can be efficiently broken through rational design of surrounding microenvironment of the supported nanocatalyst including gas adsorbate overlayer and underneath support surface chemistry. Our studies reveal that chemisorbed oxygen species on Ag surface and surface hydroxyl groups on oxide support, which are dynamically consumed during reaction but sustained by reaction environment (O2 and H2O vapor), drive spontaneous redispersion of Ag particles and stabilization of highly active Ag nanoclusters. Such a dynamic confinement effect from gas‐catalyst‐support interaction enables the Ag nanoclusters to exhibit complete catalytic oxidation of CO over a wide temperature window of 25 ‐ 500 °C under dry conditions and 200 ‐ 800 °C under wet conditions as well as remarkable stability at 300 °C over 1000 h.

Optimization of Sr3NCl3-based perovskite solar cell performance through the comparison of different electron and hole transport layers

Strontium Nitride Trichloride (Sr3NCl3) is a promising absorber material for solar cells due to its unique structural, electrical, and optical properties. We conducted a thorough investigation to scrutinize the structural, optical, and electronic characteristics and the photovoltaic efficiency of double-heterojunction solar cells utilizing Sr3NCl3 absorbers. Various metals were evaluated for the front and rear contacts to determine the optimal metal-semiconductor interface, with the study determining that silver (Ag) is the most suitable option for the front contact and nickel (Ni) for the back contact. The PV performance of innovative Sr3NCl3 absorber-based cell structures was evaluated with two different Hole Transport Layers (HTLs), MASnBe3 and CBTS, alongside ZnO and WS2 serving as the transition metal dichalcogenide (TMD) Electron Transport Layers (ETLs). This investigation examined a range of factors, such as layer thickness, operational temperature, doping density, defect densities at both the interfaces and within the bulk, carrier generation and recombination rates, quantum efficiency (QE), series versus shunt resistance, absorption coefficient, and current density-voltage (J-V) characteristics, utilizing the SCAPS-1D simulator software. Fine-tuning of both two HTL and ETL revealed that the highest power conversion efficiency (PCE) of 27.34 % with JSC of 19.78 mA/cm2, fill factor (FF) of 88.84 %, and VOC of 1.56 V was achieved with MASnBe3 HTL and ZnO ETL, while the lowest PCE of 25.55 %, with JSC of 19.77 mA/cm2, FF of 89.07 %, and VOC of 1.45 V was obtained for CBTS HTL and WS2 ETL, respectively. These findings highlight the promising potential of Sr3NCl3 absorbers with ZnO as ETL and MASnBe3 as HTL for developing advanced perovskites heterostructure solar cells for enhanced performance in the future.

Full-spectrum solar water decomposition for hydrogen production via a concentrating photovoltaic-thermal power generator-solid oxide electrolysis cell system

This study introduces a novel solar-powered concentrating photovoltaic-thermal power generator-solid oxide electrolysis cell system designed to enhance hydrogen production efficiency by optimizing both electrical and thermal energy utilization. The system incorporates a thermal power generator to convert excess high-temperature thermal energy into electrical energy, addressing energy losses associated with high-temperature water electrolysis. Thermodynamic analysis shows that the integration of the thermal power generator improves energy and exergy efficiencies to 0.60 and 0.52, while lowering the optimal operating temperature to 1173 K. The system’s efficiency is sensitive to the proportion of electrical energy supplied by the thermal power generator, with an optimal range identified between 0.1 and 0.2. Higher temperatures improve hydrogen production and efficiency, but increased voltage negatively impacts thermodynamic efficiency. These findings demonstrate that the proposed system offers substantial improvements over conventional solar hydrogen production methods, making it a promising candidate for sustainable hydrogen production. Further research will focus on system integration, material costs, and scalability for commercial use.

Discovery of a novel binary azeotrope with positive synergistic insulation strength as eco-friendly SF6-alternative

Abstract Sulfur hexafluoride (SF6), as the arc extinguishing and insulating medium, is broadly applied in power equipment. While it is very essential to find an environmentally friendly substitute gas for SF6 due to its strong greenhouse effect. Although there are many potential alternatives, most have relatively high boiling points that cannot meet the minimum operating temperature of the power equipment. In the past, the liquefaction temperature of the mixture was reduced by mixing with buffer gases, such as CO2, N2, or dry air. But this method cannot take the insulation performance requirements of eco-friendly insulating gas into account. Therefore, given the current problems and challenges, a novel approach is presented to exploring new eco-friendly gases by incorporating the azeotropic theory. The liquefaction temperature of the gas mixture can be reduced simultaneously while the insulation strength is increased. In this approach, a theoretical prediction model E-PPR78 was introduced to predict the vapor-liquid equilibrium data and RC318 was found to exhibit azeotrope behavior with HFO-1336mzz(E) at 17%. Furthermore, the predicted vapor-liquid equilibrium data obtained were validated against cyclic-analytical experimental results, affirming the efficacy of the proposed model. Subsequently, to assess its insulation performance, breakdown tests were conducted under both AC and lightning impulse voltages, revealing significant positive synergistic effects in the gas mixture. The possible mechanisms of this positive synergistic effect were also discussed. This study offers an innovative way of tackling high boiling point issues plaguing eco-friendly gases. The findings may also enlighten the design of eco-friendly switchgear that utilizes HFO-1336mzz(E) mixtures to replace traditional SF6 gases.

Facile synthesis of green graphite-based (Ni/Cu/N) MOF composite for a methanol oxidation reaction

Recently, direct methanol fuel cells (DMFCs) have been regarded as the greatest energy-producing owing to their low operating temperature, high production rate of methanol, and low greenhouse gas emission. However, the energy conversion efficiency of the DMFCs is still unsatisfactory due to the slow kinetics of the fuel oxidation reaction. So, an economic electrocatalyst with high efficiency and good stability is still needed. Herein, low-cost nanocomposites of (Ni/Cu/N) MOF and palm pollen-derived G-graphite were prepared with different ratios namely, (1:1), (1:2), and (2:1) through a solvothermal reaction. The nanocomposites were characterized via X-ray diffraction (XRD), Scanning electron Microscopy (SEM), Fourier transform infrared (FTIR), Thermal gravimetric analysis (TGA), and, (Brunauer–Emmett–Teller) technique (BET). Electrodes have been tested as electro-catalysts for methanol-oxidation reaction (MOR) in a basic medium. As revealed from the cyclic voltammetry measurements, all electrodes exhibit a good response to MOR, being the nanocomposite with the ratio between (Ni/Cu/N) MOF and G-graphite (2:1) is the best with an oxidation peak current density of 55 mA/cm2 at a scan rate of 50 mV/s, with an onset potential of 0.35 V, and stability reaches 96 %. The electrochemical impedance spectroscopy (EIS) test showed that the ratio (2:1) has the lowest charge transfer resistance, RCT, of 5.21 Ω which confirms its higher electrochemical activity. This superior performance of the (Ni/Cu/N) MOF and G-graphite (2:1) over other reported MOF-based electrocatalysts is attributed to the synergistic effect of the (Ni/Cu/N) MOF electrocatalyst, wherein Ni and Cu provide redox electrocatalytic active sites for MOR while the G-graphite contributes towards the chemical stability and electrical conductivity of the electrode, respectively. The good activity and stability of the prepared electrodes suggest the potential use of these electrodes as electrocatalysts for MOR in direct methanol fuel cells (DMFCs).This study opens the venue for valorizing the natural wastes derived graphitic material as stable supporting material in Mof based composites electrodes for MOR.

Summary, Future, and Challenges of Fluoride‐Ion Batteries

Due to the limitations of lithium‐ion batteries (LIBs), there is an urgent need to explore alternative energy storage technologies. However, the high‐energy density of fluoride‐ion batteries (FIBs) has attracted widespread attention as a potential successor to LIBs. FIBs are emerging as a low‐cost, safe, and versatile energy storage solution, with a broad operating temperature range. With continuous efforts from researchers, significant progress has been made in the field of FIBs. Nevertheless, compared to traditional batteries, research on FIBs remains limited, and many challenges and unexplored avenues persist. This article elucidates the principles of FIBs, summarizes the materials for both cathodes and anodes, discusses electrolytes, and addresses existing issues. It also outlines future directions and potential applications of FIBs. As it is continued to innovate and explore, FIBs hold promise for revolutionizing energy storage technology, offering enhanced performance, safety, and sustainability.

Construction of CuCoCe ternary catalyst via a porous organic polymer template approach for efficient CO-PROX with wide operating temperature window

Preferential CO oxidation (CO-PROX) is a promising approach for removing trace CO from hydrogen-rich streams, effectively preventing Pt anode poisoning in proton-exchange membrane fuel cells (PEMFCs). To effectively eliminate CO within the PEMFC operating temperature range, catalysts must exhibit high CO conversion and O2 selectivity. Expanding the operating temperature window of these catalysts is crucial. This study presents the synthesis of a CuCoCe ternary catalyst (CuCo/Ce-P) using an imidazole-functionalized porous organic polymer as a sacrificial template. Compared to the CuCoCe ternary catalyst prepared without a template (CuCo/Ce), CuCo/Ce-P exhibits significantly enhanced catalytic activity, with a T50 reduction from 85 °C to 55 °C and an expanded operating temperature window of approximately 40 ℃. Characterization results indicate that the imidazole-functionalized porous organic polymer facilitates improved dispersion of active species by anchoring metal ions through electron-rich groups, enhances intermetallic interactions, promotes electron transfer, and significantly improves the oxygen-deficient capacity of the CuCoCe ternary catalyst. Consequently, the catalyst exhibits a greater number of active interfaces, leading to enhanced catalytic activity and a wider operating temperature window.

Copper‐infused zinc porphyrin supramolecular polymersomes for triple synergistic combat against wound bacterial biofilm infections

AbstractBacterial biofilm infections (BBI) on wound surfaces and implants pose a significant clinical challenge due to the impermeable nature of biofilms and obstacles in tissue repair. Traditional photothermal therapy (PTT) or chemodynamic therapy (CDT), whether used alone or in combination, often causes damage to surrounding normal tissues from high operating temperatures or elevated levels of reactive oxygen species, leading to unsatisfactory anti‐biofilm effects. This study introduces a novel copper ions loaded zinc porphyrin polymer vesicle (Cu‐PPS) that employs a triple synergistic approach involving PTT, CDT, and bacterial cuproptosis‐like death (BCD). Cu‐PPS exhibits exceptional photothermal efficiency of 51.06%, promoting the release of copper ions under photothermal stimulation, enhancing CDT and BCD effectiveness, and facilitating mature biofilm clearance and tissue repair. This approach achieves a bactericidal rate exceeding 99% and an anti‐biofilm rate of 93.32% in vitro and also excellent efficacy in treating BBI in vivo. This study presents an innovative therapeutic strategy for combating biofilm infections, addressing the challenges encountered in the clinical management of BBI.

Fabrication of carbon nanotube neuromorphic thin film transistor arrays and their applications for flexible olfactory-visual multisensory synergy recognition

Abstract Artificial multisensory devices play a key role for the human-computer interaction in the field of artificial intelligence (AI). In this work, we have designed and constructed a novel olfactory-visual bimodal neuromorphic carbon nanotube thin film transistor (TFT) arrays for artificial olfactory-visual multisensory synergy recognition with the ultralow single-pulse power consumption of 25 aJ, employing semiconducting single-walled carbon nanotubes (sc-SWCNTs) as channel materials and gas sensitive materials, and poly[[4,8-bis[5-(2-ethylhexyl)-2-thienyl]benzo[1,2-b:4,5-b0]dithiophene-2,6-diyl]-2,5-thiophenediyl-[5,7-bis(2-ethylhexyl)-4,8-dioxo-4H,8H-benzo[1,2-c:4,5-c0]dithio-phene-1,3-diyl]] (PBDB-T) as the photosensitive material. It is noted that it is the first time to realize the simulation of olfactory and visual senses (from 280 nm to 650 nm) with the wide operating temperature range (0-150 °C) in a single SWCNT TFT device and successfully simulate the recovery of olfactory senses after COVID-19 by olfactory-visual synergy. Furthermore, our SWCNT neuromorphic TFT devices with high Ion/Ioff ratio (up to 106) at a low operating voltage (-2-0.5 V) can mimic not only the basic biological synaptic functions of olfaction and vision (such as paired-pulse facilitation, short-term plasticity, and long-term plasticity), but also optical wireless communication by Morse code. The proposed multisensory, broadband light-responsive, low-power synaptic devices provide great potential for developing AI robots to face complex external environments.

Hybrid nanofluid flow over a vertical plate through porous medium in a conducting and chemically reacting field with radiation absorption and variable suction

This research investigates the flow of an electrically conductive hybrid nanofluid across a porous plate that is in motion and experiencing temperature and velocity slip. In addition, the impacts of radiation absorption and variable suction are included. The heat transfer phenomena have been investigated using a hybrid nanofluid consisting of distilled water, brass, and cobalt. The behavior of the hybrid nanofluid is determined by the Tiwari-Das model. The graphs are drawn with the help of MATLAB software. It is noticed that compared to Cu3Zn2−TiO2 hybrid nanofluid, C−TiO2 with distilled water exhibits the optimum heat transfer by 5.72 % for fixed values of S and R. The temperature reaches at its maximum at y = 0.4520. Remarkably, the maximum improvement of 42.9547 % is noted for Ra=0.8,ϕ1=ϕ2=0.02,S=0.2,h2=0.5. The addition of brass and cobalt nanoparticles to a base fluid may considerably lower its operational temperature. The hybrid nanofluid composed of carbon-titanium oxide shows the greatest increase in heat transmission, but the hybrid nanofluid made of brass titanium-oxide indicates just a modest improvement. The buoyancy forces enhance the growth of both the momentum and thermal boundary layers. As the Cu3Zn2−Co hybrid nanofluid acts as a coolant, which can be used in the cooling of the battery.

Two-dimensional p-n heterojunctions of black phosphorus nanosheet-sensitized α-MoO3 nanoflake for low-temperature chemiresistive NH3 recognition

Of diverse NH3 gas-detection strategies applied in the fields of individual healthcare and industrial production, chemiresistive gas sensors gain the most popularity owing to the superior merits of low cost, convenient signal processing and high sensitivity. However, severe challenges still exist such as elevated operation temperature (>200 °C), limited sensitivity and unsatisfactory selectivity especially under low-concentration and high-humidity conditions. To overcome these hindrances, a sensing layer of black phosphorus nanosheets (BP)-modified α-MoO3 nanoflakes was prepared in this work. After subtle optimization of ingredient composition and operation temperature, the composite sensor S2 could recognize NH3 gas with the concentration spanning from 0.4 to 25 ppm at 40 °C. In particular, a larger mean response (27 % vs. ∼ 2.3 %) with a response/recovery speed of 275/388 s toward 10 ppm NH3 and lower detection of limit (LoD, 0.4 ppm vs. 10 ppm) was achieved with respect to pure BP counterpart. In addition, excellent repeatability, selectivity, long-term stability and humidity-tolerant features were demonstrated for Sensor S2. The improved sensing performance after α-MoO3 incorporation was primarily ascribed to abundant p-n heterojunctions, excellent conductivity of BP and hydrophilic MoO3 that mitigated the water corrosion effect on susceptible BP nanosheets. This work offers an alternative strategy for sensitive and low-temperature NH3 detection, and well cater for the demanding requirements of high sensitivity and low-power consumption in the field of novel gas sensors applicable in the future Internet of Things and exhaled breath-oriented medical diagnosis.

Temperature-responsive solvation enabled by dipole-dipole interactions towards wide-temperature sodium-ion batteries

Rechargeable batteries with high durability over wide temperature is needed in aerospace and submarine fields. Unfortunately, Current battery technologies suffer from limited operating temperatures due to the rapid performance decay at extreme temperatures. A major challenge for wide-temperature electrolyte design lies in restricting the parasitic reactions at elevated temperatures while improving the reaction kinetics at low temperatures. Here, we demonstrate a temperature-adaptive electrolyte design by regulating the dipole-dipole interactions at various temperatures to simultaneously address the issues at both elevated and subzero temperatures. This approach prevents electrolyte degradation while endowing it with the ability to undergo adaptive changes as temperature varies. Such electrolyte favors to form solvation structure with high thermal stability with rising temperatures and transits to one that prevents salt precipitation at lower temperatures. This ensures stably within a wide temperature range of ‒60 −55 °C. This temperature-adaptive electrolyte opens an avenue for wide-temperature electrolyte design, highlighting the significance of dipole-dipole interactions in regulating solvation structures.

Processes of Metal Oxides Catalyst on Conversion of Spent Coffee Grounds into Rich-Synthesis Gas by Gasification

Spent coffee grounds (SCGs), a waste product of the coffee industry, present a significant untapped resource for fuel production. This study aims to optimize the gasification of SCG using various metal catalysts (NiO, MnO2, Al2O3, and Fe2O3) to maximize syngas yield. SCG samples were gasified at different temperatures (800 °C, 900 °C, 1000 °C) and analyzed using Scanning Electron Microscopy (SEM), Thermogravimetric Analysis (TG-DTA), and Fourier Transform Infrared (FTIR) spectroscopy to evaluate catalyst performance and reaction mechanisms. The findings indicated that utilizing mixing techniques for physical contact to introduce catalysts led to a uniform distribution of catalyst particles throughout the sample. The decomposition rate of the gasification experiment after adding the catalyst was 24% faster than that of the pure SCGs. In the gasification experiment, the MnO2 catalyst showed the highest CO production, which was 71% higher than that of NiO under the same conditions. At this temperature, MnO2 generated around 171% more CO than at 800 °C, surpassing the yields observed with other catalysts. The study concludes that Mn emerged as the most promising catalyst, significantly improving both CO and CH4 yields. Selecting the appropriate metal catalyst and optimizing operational temperatures are crucial for enhancing the efficiency of SCG gasification.

Modeling and Performance Analysis of Solid Oxide Fuel Cell Power Generation System for Hypersonic Vehicles

Advanced airborne power generation technology represents one of the most effective solutions for meeting the electricity requirements of hypersonic vehicles during long-endurance flights. This paper proposes a power generation system that integrates a high-temperature fuel cell to tackle the challenges associated with power generation in the hypersonic field, utilizing techniques such as inlet pressurization, autothermal reforming, and anode recirculation. Firstly, the power generation system is modeled modularly. Secondly, the influence of key parameters on the system’s performance is analyzed. Thirdly, the performance of the power generation system under the design conditions is simulated and evaluated. Finally, the weight distribution and exergy loss of the system’s components under the design conditions are calculated. The results indicate that the system’s electrical efficiency increases with fuel utilization, decreases with rising current density and steam-to-carbon ratio (SCR), and initially increases before declining with increasing fuel cell operating temperature. Under the design conditions, the system’s power output is 48.08 kW, with an electrical efficiency of 51.77%. The total weight of the power generation system is 77.09 kg, with the fuel cell comprising 69.60% of this weight, resulting in a power density of 0.62 kW/kg. The exergy efficiency of the system is 55.86%, with the solid oxide fuel cell (SOFC) exhibiting the highest exergy loss, while the mixer demonstrates the greatest exergy efficiency. This study supports the application of high-temperature fuel cells in the hypersonic field.

Experimental characterisation and visualisation of a novel two-phase flexible heat transfer device

The importance of passive Flexible Heat Transfer Device (FHTD) in electronic cooling or space applications lies in their ability to provide efficient, reliable, and adaptable thermal management solutions. Heat transfer enhancement studies pertaining to FHTD developed to meet the thermal management demands of futuristic flexible electronic devices are presented in the current work. The possibility of extending the heat transport limit of FHTD beyond 24 W by limiting the maximum operating temperature to 60 °C is discussed. The superior performance of FHTD at varying heat loads from 5 W to 40 W at 45°and 90°bending angles is brought out compared with existing heat transfer devices like Flexible Heat Pipe (FHP) and copper thermal straps. The performance is reported in thermal resistance and equivalent thermal conductivity. A commercial dielectric liquid is used as a working fluid in FHTD to enhance the heat transfer limit employing phase change. The evaporator and condenser sections of the flexible section are made transparent to visualise the boiling and condensation phenomenon. Under steady-state operation at a 45°bending angle, The FHTD demonstrates a minimum thermal resistance of 0.73 K/W and a peak effective thermal conductivity of 8172 W/m K. The heat transfer coefficient ranges from 200 to 700 W/m2 K, consistent with values reported for heat pipes in the literature. Additionally, the study explores the impact of modifying the external surface texture to create more nucleation sites, thereby enhancing the performance of the FHTD. The results show that the laser-textured surface on the heat pipe condenser effectively reduces the onset of nucleate boiling for dielectric fluid by 3.5 °C and decreases the maximum temperature of the evaporator by 4.5 °C. The present work dictates the fundamental baseline for possible design choices of futuristic passive flexible heat transfer devices.

Deep oxidation of NO via catalytic ozonation

ABSTRACT In addition to selective catalytic reduction (SCR) and selective non-catalytic reduction (SNCR) which are available to remove NOx from flue gas, oxidation method is receiving more and more attention because this method makes it possible to remove NOx and SO2 from flue gas simultaneously by wet scrubbing. O3 as a strong oxidant has a high oxidation capacity and it can oxide NO to N2O5 which has a higher water solubility compared with NO2. However, it needs a long reaction time and the escape of unreacted ozone may cause secondary pollution. In this study, FeMnCo/Al2O3 catalyst and FeMnCe/Al2O3 catalyst were prepared and applied to enhance the deep oxidation of NOx with ozone and reduce O3 slip. Effects of various operating parameters such as O3/NO ratio, gas residence time and operating temperature were evaluated and the results demonstrate that N2O5 began to generate when O3/NO ratio was higher than 1.0 and increased with increasing O3/NO ratio. Little residual O3 was formed in the presence of catalyst while 350 ppm O3 was measured at the outlet gas when O3/NO ratio was controlled at 2.0. The N2O5 conversion efficiency increased with increasing gas residence time, operating temperature and the highest N2O5 conversion efficiency was achieved at 100°C. Furthermore, the conversion efficiency remained around 90% during 20 h operation over FeMnCe/Al2O3 catalyst with an O3/NO ratio of 1.73, a gas residence time of 1.2 s, and a temperature of 100°C. On the other hand, the N2O5 conversion efficiency remained around 80% during 3 h operation over FeMnCo/Al2O3 catalyst. Overall, FeMnCe/Al2O3 catalyst reveals good potential for deep oxidation of NO by O3 and can be further developed as a viable catalyst for reducing NO emission from industries.

Optimizing Indoor Comfort and Energy Efficiency using Right-Angled Triangular Responsive Facades in Cairo, Egypt

Building energy consumption has been rapidly increasing in recent years due to several factors such as climate change and global population growth. Besides, the majority of buildings are not designed with the consideration of the alteration of the severe conditions of the external surrounding environment, which affects the indoor environment negatively. As a result, excessive HVAC systems are utilized in order to maintain the indoor environment and achieve the indoor human comfort. Thus, large amounts of energy are being consumed and the rates of the energy consumption are increasing rapidly. Responsive architecture is considered as one of the solutions that architects, and façade designers use in order to block the excessive solar radiation and direct natural light and thus enhance the indoor comfort zone. However, the majority of the façade’s pattern designs are not following specific guidelines. This study contributes to the field by identifying an optimal right-angled triangular façade design that effectively enhances indoor thermal comfort, reduces solar radiation, and minimizes energy consumption, thereby providing a practical solution for improving building performance in response to climate change and urban growth challenges. This article will study four different façade pattern cases, which are common in the rotational movement, façade orientation and pattern dimensions; however, they differ in the orientation of the axes of movement. The four-façade pattern proposals will be investigated through simulating the solar radiation, consumed cooling energy and the indoor operative temperature during the maximum solar exposure day. A comparative analysis will be conducted between the results in order to highlight the most efficient right-angled triangular pattern that can be used on the south façade in Cairo, Egypt in order enhance the indoor thermal comfort, enhance the energy consumption rates, reduce the solar radiation and improve the building performance.

Sol-Gel Pt-VO2 Films as Selective Chemoresistive and Optical H2 Gas Sensors.

In this work, VO2 (M1/R) thin films were exploited as H2 gas sensors. A flat film morphology, obtained by furnace annealing, was compared with a laser-induced nanostructured one. The combination of the environmentally friendly sol-gel approach with the ultrafast laser crystallization allows for significant reductions in energy consumption and related emissions during the fabrication of VO2 sensors. By decorating the sensors' surface with Pt nanoparticles (NPs), the sensor response was enhanced exploiting the hydrogen spillover effect. The Pt/VO2 sensors, tested at operating temperatures between 20 and 200 °C and for concentration of H2 from few ppm to 50000 ppm, offered a dual chemoresistive and optical sensing mode. Low operating temperatures of 150 °C were achieved, along with a detection limit as low as 2 ppm and a perfect baseline recovery. Both sensors guaranteed specific selectivity toward H2, without response to NO2 or humidity, and long-term stability over 500 h. The H2 sensing mechanism, for both the monoclinic and rutile VO2 phases, was investigated through in operando X-ray Diffraction and in situ X-ray Photoelectron Spectroscopy tests. The interaction was found to be based on the reversible formation of HxVO2 bronze, along with the reversible variations in the oxidation state of V.

Thermodynamics-driven metabolic and microbial preference for lactate methanization at different operational temperatures

Lactate-dominant organic acids released from acidified feedstocks inhibit anaerobic digestion processes, which can result in decreased biomethane (CH4) yield or even complete process failure. Herein, this study focus on exploring the effects of temperature (35 °C, 38 °C, 41 °C, 44 °C, 47 °C, 50 °C, and 55 °C) on the thermodynamics of microbial communities to assess the thermodynamics or microbial flora in driving the concurrent bioreactions involved in organic acid degradation. The findings revealed a prevalence of species such as Syntrophaceticus schinkii, DTU014, and Methanosarcina at 38 °C-44 °C. These species are known for their abilities in propionate and butyrate degradations, acetate oxidation, and methanation, respectively. Conversely, at thermophilic temperatures (47 °C, 50 °C, and 55 °C), this study observed higher abundance of thermophilic microorganisms like Defluviitoga and Methanoculleus, although these organisms are adapted to higher temperatures, their lactate utilization and methane production were less efficient than mesophilic species. Despite higher ΔG values for lactate, propionate, and butyrate degradation at 38 °C–44 °C compared with thermophilic temperatures, the relative abundance of functional enzymes (specifically, propionate and butyrate degrading enzymes) was found to be marginally higher than 47 °C–55 °C. As a result, 41 °C–44 °C induced remarkable thermodynamic effects that not only facilitated organic acid degradation but also promoted subsequent methanation, indicating the suitability of these temperatures for the methanation of biowaste acidified by lactate. Overall, this study provides insight into the temperature-dependent response of organic acid degradation, specifically focusing on the mechanisms involved in overcoming energy barriers, shaping the microbial flora, and ultimately improving the efficiency and stability of anaerobic digestion, especially for lactate-acidified feedstock.