Active Area Research Articles

Aromatic carboxyl acid regulated nanoparticle deposition and passivation of tin oxide for high performance perovskite solar cells

The composition and nano particle agglomeration of hydrolyzed species in chemical bath deposition (CBD) plays a key role in obtaining efficient SnO2 film for high performance perovskite solar cells (PSCs). In this work, the aromatic acids with varied carboxyl groups were investigated to regulate the nano particle deposition and passivate the buried SnO2/perovskite interface. The quasi in-situ dynamic light scattering and Zeta potential results indicated that the nano particle agglomeration with trimesic acid (TMA) was significantly refined throughout the whole deposition process. The TMA-SnO2 achieved an ideal energy band alignment with perovskite and released the internal residual strain, promoting the growth and crystallization of the perovskite film due to the corrdination of carboxyl groups. As a result, the interface defects were effectively passivated with enhanced efficiency and stability. The small area device based on TMA-SnO2 obtained an efficiency of 25.07 %. The devices with an enlarged area of 1.4 cm2 and the 5x5 cm2 mini-module (active area 10.054 cm2) showed impressive PCEs of 23.93 % and 22.40 %, respectively. Furthermore, the unencapsulated devices exhibit enhanced long-term stability, maintaining 80 % and 90 % of the initial efficiencies under 80 ± 5°C thermal annealing in nitrogen for 1176 h and in air condition for 3224 h, respectively.

Evaluation and Upscaling of Impregnated La0.20Sr0.25Ca0.45TiO3 Fuel Electrodes for Solid Oxide Electrolysis Cells

Recent research into Rh and Ce0.80Gd0.20O1.90-impregnated La0.20Sr0.25Ca0.45TiO3 fuel electrodes for solid oxide fuel cells has demonstrated the high-stability of these material sets to a variety of harsh operating conditions at small scales (1 cm2 active area button cells), as well as commercial scales (100 cm2 cells) in short stacks (5 cells) and full micro-combined heat and power systems (60 cells). In this work, the authors present a comprehensive evaluation of the ability of these novel titanate-based materials to function as fuel electrodes in solid oxide electrolysis cells (SOECs). Short-term and durability testing of button cell scale SOECs highlighted the limited stability of lanthanum strontium manganite-based air electrodes, under CO2 and steam electrolysis conditions, with lanthanum strontium cobaltite ferrite-based air electrodes offering improved degradation characteristics. Upscaling of this optimized cell chemistry to a 16 cm2 active area SOEC and testing under CO2, CO2/H2O and H2O electrolysis conditions demonstrated encouraging performance over a period of ∼600 h, with stable co-electrolysis performance at ∼−7.5 A at 1.47 V for the first 100 h.

Examining the effects of the HIV-1 protein Tat and morphine on antiretroviral accumulation and distribution within the brain.

Despite combination antiretroviral therapy effectively suppressing HIV within the periphery, neuro-acquired HIV (neuroHIV) remains a significant problem and approximately half of people living with HIV will experience HIV-associated neurocognitive disorders (HAND). Concurrent opioid use exacerbates neuroHIV by promoting neuroinflammation, neuronal injury and synaptodendritic culling, viral replication, and potentially altering antiretroviral concentrations within the brain. The present study examined the effects of HIV and morphine co-exposure on the accumulation and spatial distribution of antiretroviral drugs across multiple regions within the brain in an HIV-1 Tat transgenic mouse model by using infrared-matrix-assisted laser desorption electrospray ionization mass spectrometry imaging (IR-MALDESI MSI). Morphine exposure uniquely decreased antiretroviral concentrations in anterior cerebral (primary motor and somatosensory) cortices, corpus collosum (anterior forceps), caudoputamen, nucleus accumbens, and posterior regions including the hippocampus, corpus callosum (main body), cerebral cortex (somatosensory and auditory cortices), thalamus, and hypothalamus. Interestingly, male mice experienced greater morphine-associated decreases in antiretroviral concentrations than females. The study also assessed whether changes in antiretroviral concentrations were linked with inflammation in astroglia, assessed through the measurement of astroglial activation using glial fibrillary acidic protein (GFAP) as a marker. Alterations in antiretroviral concentrations co-registering with areas of astroglial activation exhibited sex-specific treatment differences. This study highlights the intricate interplay between HIV, opioids, and antiretroviral drugs within the CNS, elucidating distinct regional and sex variations in responsiveness. Our findings emphasize the identification of vulnerabilities within the neural landscape and underscore the necessity of carefully monitoring opioid use to maintain the efficacy of antiretroviral therapies.

Assessing the effectiveness of “River Morphodynamic Corridors” for flood hazard mapping

In dynamic rivers the assessment of flood hazard related to geomorphological dynamics assumes crucial importance. Recently, some geomorphological approaches have been developed to assess channel dynamics in response to floods. In this study we explore the River Morphodynamic Corridors which include the current active channel and areas of the alluvial plain that may be (re)activated by channel dynamics during floods. In order to assess the effectiveness of such corridors for mapping flood hazard, we delineated the morphodynamic corridors along a river network of 74 km in the Cordevole River catchment (Italy) and compared the corridors with the channel changes that were triggered by a high-magnitude event (Vaia Storm) that hit the study area in October 2018. We observed that the morphodynamic corridors are capable to define areas where channel dynamics are most likely to occur and have proven satisfactorily effective in predicting channel widenings triggered by a severe flood. The results show that it is crucial to adopt different procedures for corridor delineation based on channel width, i.e., for small streams (width < 30 m) a more precautionary approach should be adopted that considers the entire alluvial plain as an area potentially affected by channel dynamics. The study highlighted an inherent limitation of the approach, since erosion that can affect valley slopes or fluvial terraces (i.e., widening of the alluvial plain) is not taken into account. This application represents the first validation of the River Morphodynamic Corridors approach through comparison with observed flood channel changes. Through this analysis, it can be inferred that, notwithstanding its relatively simple procedure, the approach allows a robust mapping and delineation of flood hazard due to river channel dynamics. The River Morphodynamic Corridors, when applied jointly with hydraulic model for assessing inundation processes, allow an overall assessment of flood hazard, particularly in dynamic river contexts.

Development of an efficient bifunctional electrocatalyst based on Co/CoSe2 nanoparticles embedded in N, Se co-doped carbon for AEMFC and rechargeable Zn-air battery

We suggest a hollow-structured N, Se dual-doped carbon framework embedded with Co/CoSe2 nanoparticles (Co/CoSe2@NSeC) as highly efficient bifunctional electrocatalyst for the oxygen reduction reaction (ORR) and oxygen evolution reaction (OER). The prepared electrocatalyst exhibits high electrochemical active surface area attributed to its unique hollow/porous structure and defective heteroatom doping sites. Furthermore, the strongly coupled heterojunction between Co and CoSe2 species not only provides abundant and highly active sites but also generates built-in electric field, thereby promoting electron transfer during the electrocatalytic reaction. Based on the above considerations, the prepared catalyst shows excellent bifunctional electrocatalytic performance. Leveraging the excellent ORR activity of Co/CoSe2@NSeC, alkaline exchange membrane fuel cells (AEMFC) with the Co/CoSe2@NSeC as air cathode exhibits high power density of 171.23 mW cm2. Furthermore, the rechargeable Zn-air battery employing the Co/CoSe2@NSeC shows high specific capacity (729.4 mAh gZn−1), peak power density (192.88 mW cm2), and sustained stability over 300 cycles.

An Audio-Visual Speech Separation Model Inspired by Cortico-Thalamo-Cortical Circuits.

Audio-visual approaches involving visual inputs have laid the foundation for recent progress in speech separation. However, the optimization of the concurrent usage of auditory and visual inputs is still an active research area. Inspired by the cortico-thalamo-cortical circuit, in which the sensory processing mechanisms of different modalities modulate one another via the non-lemniscal sensory thalamus, we propose a novel cortico-thalamo-cortical neural network (CTCNet) for audio-visual speech separation (AVSS). First, the CTCNet learns hierarchical auditory and visual representations in a bottom-up manner in separate auditory and visual subnetworks, mimicking the functions of the auditory and visual cortical areas. Then, inspired by the large number of connections between cortical regions and the thalamus, the model fuses the auditory and visual information in a thalamic subnetwork through top-down connections. Finally, the model transmits this fused information back to the auditory and visual subnetworks, and the above process is repeated several times. The results of experiments on three speech separation benchmark datasets show that CTCNet remarkably outperforms existing AVSS methods with considerably fewer parameters. These results suggest that mimicking the anatomical connectome of the mammalian brain has great potential for advancing the development of deep neural networks.

Building robust copper nanostructures via carbon coating derived from polydopamine for oxygen reduction reaction

This study explores the synthesis and electrocatalytic performance of copper-nitrogen-carbon composites formed by Cu single atoms/clusters embedded in nitrogen-doped carbon with Cu/Cu2O nanoparticles (Cu-X-NC) for the oxygen reduction reaction (ORR). The catalysts were synthesized using polydopamine as a carbon and nitrogen source via the solvothermal carbonization (STC) method, followed by pyrolysis and acid washing. The effect of solvothermal carbonization temperature (120, 150, and 180 ºC) on the structure and ORR activity was investigated. The physicochemical characterization showed that higher STC temperatures reduced the size of copper crystallites, slightly increased the formation of copper(I) oxide, and led to the creation of well-dispersed copper single atoms/clusters at 150°C. This optimal dispersion enhances the interaction between the copper single atoms and the reactants, leading to faster ORR kinetics, as demonstrated by the lower charge transfer resistance values in electrochemical impedance spectroscopy measurements. Additionally, the balance between micropore and mesopore structures at this temperature facilitates efficient mass transport, which is critical for achieving higher ORR activity. Moreover, accelerated stability tests showed excellent durability for Cu-150-NC, with negligible loss in onset potential after 10,000 cycles. The solvothermal process significantly increased the electrochemically active surface area (ECSA), with Cu-150-NC displaying the highest specific activity and mass activity per gram of copper, indicating superior performance. Overall, these findings underscore the importance of synthesis optimization and provide valuable insights for designing eco-friendly and high-performance copper catalysts for fuel cell applications.

Dual modification of cobalt silicate nanobelts by Co3O4 nanoparticles and phosphorization boosting oxygen evolution reaction properties

Oxygen evolution reaction (OER) process is the “bottleneck” of water splitting, and the low-cost and high-efficient OER catalysts are of great importance and attractive but they are still challenging. Herein, a dual modification strategy is developed to tune and enrich the structure of cobalt silicate (Co2SiO4) showing boosted OER properties. Cobalt oxide (Co3O4) decorated Co2SiO4 nanobelts, denoted as CS, is firstly prepared using a Co-based precursor by a facile hydrothermal reaction. Then, cobalt phosphide (CoP) nanoparticles are in-situ grown on CS (denoted as CS-P) by the phosphorization process, which provide many active sites and boost the surface reactivity. The experimental results and density function theory (DFT) calculations both reveal that the CoP on CS can improve the conductivity and ensure fast kinetics, thus leading to boost the OER properties of Co2SiO4. When the phosphorization temperature is at 400 °C (CS-P400), it gains the lowest overpotential of 297 mV, which is much lower than CS (340 mV) and Co2SiO4 (409 mV) at 10 mA·cm−2, and even superior to the state-of-the-art transition metal silicates. CS-P400 also achieves high electrochemical active surface area (ECSA) and small Tafel slope owing to its porous structures with large specific surface area and nanosheet-like structures which are good for exposing many active sites and favorable to the fast kinetics. This work not only provides a dual modification route to boost catalytic activity of Co2SiO4 (CS-P400), but also sheds light on a new avenue for developing highly dispersed CoP on silicates to boost OER performances.

Towards novel small-molecule inhibitors blocking PD-1/PD-L1 pathway: From explainable machine learning models to molecular dynamics simulation

Molecular design of small-molecule inhibitors targeting programmed cell death-1 (PD-1)/programmed cell death ligand-1 (PD-L1) pathway has been recognized as an active research area by the clinical success of cancer immunotherapy. In recent years, using machine learning (ML) methods to accelerate drug design have been confirmed. However, the black box character of ML methods makes model interpretation and ligands optimization obscured. Herein, five explainable ML models were constructed by integrating five ML models with the SHAP method, where these ML models were pretrained with >4000 molecules and their R2 ranged from 0.835 to 0.86 on test set. Subsequently, the explainable ML models were employed to identify the relationship between fragments and bio-activity of a small molecule inhibitor BMS-1166, leading to the modification of BMS-1166 into 60 novel compounds. After consensus docking and ADMET test, 3 small molecules (C27, C52 and C54) with better docking scores and lower toxicity than BMS-1166 were screened out further. Finally, the improved binding affinity of C27, C52 to the PD-L1 dimer was validated by the MD simulation. Overall, this work proposed an efficient protocol on the basis of explainable ML models for designing small-molecule inhibitors targeting PD-1/PD-L1 pathway in a rational way.

Hierarchical Nb@NbN core-shell-like nanocolumns for asymmetric supercapacitors

Transition metal nitrides (TMNs) are promising electrode materials for supercapacitors because of their high electrical conductivity and chemical stability. The rational design and facile synthesis of TMNs electrode materials with a unique nanostructure are the key to develop high-performance supercapacitors. Herein, we propose a two-step, binder-free, and eco-friendly approach utilizing magnetron sputtering at an oblique angle deposition configuration to fabricate hierarchical Nb@NbN core–shell-like nanocolumns for supercapacitors. This distinctive heterostructure not only creates lattice defects, increases active surface area, facilitates ion diffusion and charge transfer, but also optimizes the electronic structure and enhances the conductivity. As a result, the hierarchical Nb@NbN core–shell-like nanocolumn electrodes exhibit a high areal capacitance of 53.3 mF cm−2 at 1 mA cm−2 and an excellent capacitance retention of 93.5 % after 20,000 cycles, outperforming pristine NbN and the majority of previously reported TMNs electrodes. Moreover, the assembled Nb@NbN nanocolumns//VN thin films asymmetric supercapacitor device can deliver a maximum energy density of 49.8 mWh cm−3 and power density of 82 W cm−3. This work presents a facile and environmentally friendly strategy for the synthesis of TMNs core–shell-like nanocolumns, and further demonstrates their promising potential for use in supercapacitors.

Size-dependent Copper Nanoparticles Supported on Carbon Nanotubes with Balanced Cu+ and Cu0 Dual Sites for the Selective Hydrogenation of Ethylene Carbonate.

Cyclic carbonate hydrogenation offers an alternative for the efficient indirect CO2 utilization. In this study, a series of carbon nanotubes (CNTs) supported xCu/CNTs catalysts with different Cu loadings were fabricated using a convenient impregnation method, and exhibited excellent catalytic activity for the hydrogenation of ethylene carbonate to methanol and ethylene glycol. The structural and physicochemical properties revealed that acid treatment of CNTs resulted in plentiful oxygen-containing functional groups, providing sufficient anchoring sites for copper species. The calcination process conducted under an inert atmosphere resulted in the formation of ternary CuO, Cu2O, and Cu composites, enhancing the metal-support interaction and facilitating the formation of balanced Cu0 and Cu+ dual sites as well as high active surface area after reduction. Contributed to the synergetic effect of balanced Cu+ and Cu0 species proved by density functional theory calculation and the electron-rich CNTs surface, the 40Cu/CNTs catalyst achieved strengthened catalytic performance with methanol yield of 83%, ethylene glycol yield of 99% at ethylene carbonate conversion of >99%, and 150 h of long-term running stability. Consequently, CNTs supported Cu serve as efficient non-silica based catalyst for ester hydrogenation.

Enhanced Electrocatalytic Performance of Novel d-Ti3CN@CdSe Nanocomposite for Efficient Water Splitting: Achieving Low Overpotential and High Stability

The escalating global demand for clean and sustainable energy has ignited significant interest in hydrogen production through water splitting. A major challenge in this pursuit is the development of efficient and cost-effective electrocatalysts for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). Here, we present the synthesis of a novel two-dimensional d-Ti3CN @CdSe nanocomposite, designed as a high-performance electrocatalyst for overall water splitting. Synthesized via hydrothermal methods, the nanocomposite was characterized using advanced characterization techniques viz. Raman spectroscopy, XRD, XPS, and SEM/EDS. Electrochemical evaluations demonstrate that the d-Ti3CN @CdSe nanocomposite significantly enhances catalytic performance compared to its individual components, achieving a low overpotential of 232 mV for HER at 10 mA cm−2 and reducing the OER overpotential from 498.3 mV for d-Ti3CN MXene to 382.2 mV in the nanocomposite at 30 mA cm−2. Additionally, it exhibits excellent stability, retaining about 75.37% of its current density after 36 h of continuous operation. This remarkable performance is attributed to the synergistic interactions between CdSe nanoparticles and Ti3CN MXene layers, which prevent restacking, increase the electrochemically active surface area, and enhance charge transfer efficiency. These features position the d-Ti3CN @CdSe nanocomposite as a promising candidate for scalable and sustainable water-splitting applications.

High-performance porous 3D Ni skeleton electrodes for the oxygen evolution reaction

A key component of green hydrogen production technologies is the fabrication of large-scale porous transport layer (PTL) for use in anion electrolyte membrane water electrolysers (AEMWEs). One strategy to achieve that goal is to manufacture Ni-based 3D electrode skeletons that can be further catalyzed to achieve high current densities at low overpotentials. In the present work, shock-wave induced spray (SWIS) and cold spray (CS) deposition techniques were used to prepare 20 cm2 Ni-based electrode skeletons. In our experimental conditions, the porosity of coatings prepared using the SWIS deposition system and Ni powders with particle sizes D50 = 32 and 75 μm never exceeded 28%. Higher porosity could only be achieved using the CS deposition system and a spheroidal Ni–Al powder, whose particles consist of an aluminum core encapsulated in a nickel shell. After Al leaching in an alkaline solution, the resulting electrodes showed good mechanical and structural integrity with up to 41% porosity. The electrochemical active surface area of the most porous electrodes is a factor of 2100 larger than a polished Ni plate, and it has superaerophobic properties with a captive air bubble contact angle of 151°. During 1 h of electrolysis, the overpotential at 100 mA cm−2 of the most active leached Ni–Al cold spray deposited electrode was 330 mV, compared to 380 mV for a Ni foam electrode.

Heterobimetallic Synergism in Triple-Redox 2D Framework for Largely Boosted Water Oxidation and Flanked Carboxylic-Acid-Triggered Unconventional Tandem Catalysis.

A fish-bone-shaped and thermochemically stable 2D metal-organic framework (MOF) with multimodal active center-decked pore-wall is devised. Redox-active [Co2(COO)4] node and thiazolo[5,4-d]thiazole functionalization benefit this mixed-ligand MOF exhibiting electrochemical water oxidation with 375mV overpotential at 10mA cm-2 current density and 78mV per dec Tafel slope in alkaline medium. Pair of oppositely oriented carboxylic acids aids postmetalation with transition metal ions to engineer heterobimetallic materials. Notably, overpotential of Ni2+ grafted triple-redox composite reduces to 270mV with twofold declined Tafel slope than the parent MOF, ranking among the best-reported values, and outperforming majority of related catalysts. Significantly, turnover frequency and charge transfer resistance display 35.5 and 1.4-fold upsurge, respectively, with much uplifted chronopotentiometric stability and increase active surface area owing to synergistic Co(II)-Ni(II) coupling. The simultaneous presence of ─COOH and nitrogen-rich moieties renders this hydrogen-bonded MOF as acid-base synergistic catalyst for recyclable deacetalization-Knoevenagel reaction with >99% product yield under solvent-free mild condition. Besides control experiments, unique role of ─COOH as hydrogen-bond donor site in substrate activation is validated from comparing the performances of molecular-shearing approach-derived structurally similar unfunctionalized MOF, and the heterobimetallic composite. To the best of tandem Knoevenagel condensation, larger-sized acetal exhibits poor yield of α,β-unsaturated dicyanides, and demonstrates pore-fitting-mediated size-selectivity.

High-Performance Methanol Oxidation via Ni12-Metal8/CNF Catalyst for Fuel Cell Applications

In this work, non-precious electrocatalysts were synthesized using the electrospinning technique. Ni12M8/CNF (M = Cd, Co, and Cu) catalysts were successfully prepared in a fixed ratio to withstand the optimum transition metal co-catalyst in addition to the role of CNFs as support in ion-charge movement through the catalyst surface. The prepared catalysts were physically studied by XRD, SEM, and TEM. The electrochemical activity was verified using different fuel concentrations, different sweeping scan rates, and electrochemical impedance. Ni12Cu8/CNFs showed the highest electrochemical activity reaching 152 mA/cm2 through different methanol concentrations. The outstanding performance is attributed to the large active surface area provided by carbon nanofibrous that eases the charge carrier transfer through the untrapped surface of the catalyst. The electrochemical tests suggest that Ni12Cu8/CNFs have the lowest ohmic impedance resistance ensuring the highest efficiency of the designed catalyst. The obtained results serve as an efficient catalyst for direct methanol electrooxidation reactions and suggest a possible application of a low-cost, easily accessible, and large surface area established via the preparing method.

Enhancing rhamnolipid production via immobilized Pseudomonas stutzeri lipase: A comparative study

Rhamnolipids (RLs) are widely studied biosurfactants with significant industrial potential in cosmetics, pharmaceuticals, and bioremediation due to their excellent surface activity, emulsifying properties and bioactive characteristics. However, high production costs impede their mass production. This study investigates the immobilization of Pseudomonas stutzeri lipase (PSL) on various supports to enhance RL synthesis efficiency, focusing on yield and regioselectivity in the enzymatic synthesis of 4-O-lauroylrhamnose by the transesterification of rhamnose with vinyl laurate. Three immobilization methods were compared: covalent binding, adsorption on Celite, and adsorption on hydrophobic supports. The immobilization efficiency varied depending on the method used, with the lowest observed for adsorption on Celite (56 %), followed by covalent immobilization on Sepabeads (EC-EP/S 78 % and EC-EP/L 70 %), and the highest for adsorption on hydrophobic supports (83–97 %, with EC-OD being the best at 97 %). For the enzymatic synthesis of 4-O-lauroylrhamnose, covalent immobilization on Sepabeads™ EC-EP yielded low conversions due to restricted conformational freedom of the enzyme. Celite® 545 adsorption resulted in moderate conversion rates, limited by the electrostatic interactions restricting enzyme activity. The most promising results were obtained with hydrophobic supports, particularly Purolite® ECR8806F, achieving nearly complete conversion and maintaining high regioselectivity at the 4-position of rhamnose in both THF and the green solvent 2-methyltetrahydrofuran (2-MeTHF). The study highlights the critical role of support hydrophobicity and active surface area in the immobilized enzyme performance. PSL immobilized on Purolite® ECR8806F demonstrated significant potential for sustainable RLs production, showing excellent reusability, stability and productivity across multiple reaction cycles. This study presents a significant advancement in RLs production by optimizing PSL immobilization and reaction conditions, facilitating the way for more cost-effective and sustainable industrial applications.

Applicability of Graphene Oxide Interlayers in PEMs for Reducing Crossover in Electrochemical Acetone Hydrogenation Reactors

Reactant and product crossover is challenging for proton exchange membrane (PEM)-based electrochemical systems, as it leads to efficiency losses and safety issues. Blocking interlayers can reduce the permeability of PEMs. In this work, a reduction in organic crossover by up to 55% is reached by implementing graphene oxide (GO) flakes in a Nafion membrane for application in an acetone hydrogenation reactor. Additionally, the GO-membrane’s hydrogen crossover is reduced significantly. Those effects are accompanied by an up to 12% increased OCV and scale with the GO interlayer loading. The performance of the MEAs containing GO composite membranes is slightly reduced. This performance loss is traced back to an increased high-frequency resistance (HFR) of the GO composite membranes, the effect of an additional interface resistance resulting from the GO interlayer, and manufacturing-dependent variations in the electrochemically active surface area. Impedance analysis suggests a rearrangement of the GO flakes during operation, reflected by a decreasing HFR and interfacial resistance of the blocking interlayer after the net 15 h lasting electrochemical test protocol. This observation is supported by transmission electron microscopy, which shows structural variations in the GO interlayer at EoT. Nonetheless, the reduction in organic and hydrogen crossover is maintained at EoT.

Neodymium oxide-based hybrid phase few-layer MoS2 nanocomposite as high-performance symmetric supercapacitor electrode

The two-dimensional layered materials (for example MoS2) are potential electrodes for supercapacitors with their excellent lamellar structure, high surface area, mechanical flexibility, and potential redox activity. However, due to restacking of chemical structure and low electrical conductivity of the pure MoS2 electrodes are prevented for energy storage applications. Therefore the electrodes are made up of a composite by a mixture of MoS2 and rare-earth metals significantly addressing these issues with improved electrical conductivity, large electrochemical active surface, and shorter ion-diffusion kinetics. In the present study, the MoS2 and MoS2/Nd2O3 composite were synthesized by hydrothermal method. The structural phase identification of prepared samples was accomplished by using an X-ray diffractometer (XRD) and Raman spectra. Furthermore, TEM reveals changes in the shape of nanosheets and interlayer spacing. The GCD of symmetric MoS2/Nd2O3 composite electrodes displayed remarkable charging/discharging performance, with increased stability and rate capability. The MoS2/Nd2O3 composite shows utmost Csp of 2528.18 Fg-1 at 1 Ag-1. In addition, the CV and GCD studies suggest that the electrodes exhibit pseudocapacitive behavior and excellent energy density(E) of 191 Wh kg-1 at 1474.1 W kg-1 power density(P) in 1M H2SO4. The supercapacitor device made up of MoS2/Nd2O3 composite shows greater performance in practical LED glowing applications. Therefore, the composites make advancements in energy storage devices like batteries and supercapbatteries due to their excellent energy storage, high electrochemically active surface area, and stability.

Estimating adolescent mental health in the general population: current challenges and opportunities.

Adolescence is a period of change and increased mental health difficulties, which are important for lifetime outcomes. Adolescent mental health is therefore an active research area, with large samples often drawing on self-report general measures (ie, not disorder-specific or focused on a narrow outcome). We argue that these measures have a key role in our understanding of issues such as prevalence, antecedents, prevention, and intervention, however, measurement has been given little attention and high-quality measures do not tend to be available or used. We offer insights into historical and psychometric challenges that have contributed to current problems and highlight the implications of relying on poor measures, which at their worst can be biased and unethical. We make recommendations for research and practice on selecting measures and improving the evidence base and make a call to action to reject low-quality measurement in this field.

Assembly and operation optimization of proton exchange membrane water electrolyzer for performance enhancement

Abstract Proton exchange membrane water electrolysis (PEMWE) for hydrogen production possesses wide-ranging and rapid dynamic response capabilities, offering promising applications in the consumption of new energy sources and the dynamic balancing of power grids with a high proportion of renewable energy. The assembly and operating conditions of PEMWE significantly affect its performance. Therefore, thoroughly studying and understanding the influence of PEMWE’s assembly and operating conditions on water electrolysis performance are crucial for enhancing PEMWE’s performance and promoting its applications. In this research, the influence of installation preload torque, feedwater flow rate, and operating temperature on the performance of the electrolyzer, including the electrochemical active specific surface area (ECSA), high-frequency resistance (HFR) and various types of polarizations (including activation polarization, ohmic polarization, and mass transfer polarization) during the operation of the electrolyzer, were detailedly investigated. The results showed that the optimal preload torque and operating temperature for the electrolyzer were 3 Nm and 80°C. Under these conditions, an optimized PEMWE performance would be achieved by ensuring that the feedwater flow rate exceeded the water consumption during electrolysis.