Search Results (5,933)

The efficient photocatalytic generation of hydrogen peroxide (H₂O₂) from pure water remains a formidable challenge, primarily due to the rapid recombination of photogenerated electron–hole pairs and insufficient redox potentials inherent in single-component photocatalysts. To address these issues, we designed and synthesized a heterojunction material comprising cadmium sulfide nanoparticles loaded on carbon spheres (CS@CdS). Under conditions utilizing pure water and ambient air, the CS@CdS composite achieves an H₂O₂ production rate of 1305 μmol·g⁻¹·h⁻¹, which is 3.1 and 3.6 times higher than that of pure CdS and CS, respectively, without the need for any sacrificial agents or external oxygen supply. Systematic characterization reveals that CS and CdS form a tightly coupled electronic interface, which significantly accelerates charge carrier separation and effectively prolongs the lifetime of photogenerated carriers, thereby boosting photocatalytic performance. Furthermore, the CS component extends the visible-light absorption range of the composite and functions as an electron acceptor to suppress charge recombination, collectively endowing CS@CdS with enhanced photocatalytic activity. Mechanistic studies indicate that H₂O₂ production over CS@CdS proceeds predominantly via a two-step single-electron oxygen reduction reaction (ORR) pathway. This work offers a viable strategy for constructing CS-based heterojunction photocatalysts for efficient H₂O₂ synthesis. Full article

Background: Acquired resistance to the third-generation EGFR tyrosine kinase inhibitor osimertinib, often mediated by EGFR triple mutations, poses a major clinical challenge in non-small cell lung cancer (NSCLC) treatment. Among these, some rare mutations, such as L858R/T790M/L792H and L858R/T790M/G796R, create steric hindrance that directly interferes with osimertinib binding, yet effective targeted therapeutic strategies for these specific mutations remain lacking. Cudratricusxanthone A (CTXA), a natural xanthone derivative isolated from Cudrania tricuspidata Bur., has demonstrated various pharmacological activities, but its effects against EGFR triple-mutant NSCLC have not been systematically investigated. Methods: Stable Ba/F3 and NIH/3T3 cell lines expressing EGFR L858R/T790M/L792H or L858R/T790M/G796R triple mutations were generated via electroporation. The antiproliferative effects of CTXA were evaluated by MTT/MTS assays, colony formation, and wound healing assays. Cell cycle distribution and apoptosis were analyzed by flow cytometry. Protein expression of EGFR signaling pathway components (p-EGFR, p-ERK, p-AKT, p-STAT3) and cell cycle regulators (Cyclin D1, CDK4) were examined by Western blotting. Molecular docking and 200 ns molecular dynamics simulations were performed to investigate the stability and binding modes of CTXA to the mutant EGFR kinase domains. Results: The successfully established triple-mutant cell lines exhibited high EGFR expression, IL-3-independent growth, and significant resistance to osimertinib. CTXA inhibited the proliferation of all triple-mutant cell lines in a time- and concentration-dependent manner, with 48 h IC₅₀ values ranging from 0.362 to 2.488 μM. Mechanistically, CTXA suppressed EGFR autophosphorylation and downregulated downstream p-ERK, p-AKT, and p-STAT3. CTXA induced G1 phase cell cycle arrest by downregulating Cyclin D1 and CDK4, significantly promoted apoptosis, and inhibited cell migration. Molecular docking revealed that while osimertinib binding was blocked by steric hindrance from His-792 or Arg-796, CTXA adapted to the mutated ATP-binding pockets through multiple hydrogen bonds and extensive hydrophobic interactions. Molecular dynamics simulations confirmed the stable binding of CTXA to both mutant EGFR proteins over the 200 ns simulations. Conclusions: This study demonstrates for the first time that the natural compound CTXA possesses antitumor efficacy against EGFR L858R/T790M/L792H and L858R/T790M/G796R mutants by regulating EGFR-ERK/AKT/STAT3 signaling. Our findings position CTXA as a promising lead compound for tackling this challenging form of acquired resistance and highlight the value of natural products in multi-target antitumor drug discovery. Full article

This paper studies capacity planning for a wind–hydrogen integrated energy system under scenario-based uncertainty in wind generation, hydrogen demand, and electricity prices. The model is formulated as a two-stage stochastic program in which first-stage investment decisions are selected before uncertainty is realized and second-stage hourly operation is optimized for each representative scenario. The main methodological difficulty is that part of the first-stage hydrogen-storage investment cost may be available only through a non-analytical evaluator, such as supplier quotation logic, simulation software, or a data-driven estimator, while the operational recourse model remains linear. To address this setting, a hybrid heuristic–Benders framework, denoted as GSOA-Benders, is developed by coupling the General-Soldiers Optimization Algorithm for derivative-free first-stage search with Benders cuts generated from linear programming subproblems. The framework is not presented as a replacement for commercial solvers on explicit convex or mixed-integer models; rather, it is intended for cases where exact algebraic reformulation of the first-stage cost is unreliable or unavailable. In the black-box case study with 500 scenarios, the method converges in 35.86 s and obtains an investment plan expressed as $\mathbf{x}=[1,0.53,23.23,0]$, corresponding to wind-farm construction, a 0.53 MW electrolyzer, a 23.23 MWh hydrogen tank, and no fuel-cell investment. Additional discussion is provided on stability-gap interpretation, benchmark limitations, component lifetime assumptions, hydrogen losses, and environmental extensions. Full article

Reverse chemical looping pyrolysis (RCLPy) utilizes a reduced oxygen carrier to extract oxygen from the biomass feedstock during the pyrolysis stage and transfer it for the subsequent gasification stage. This decoupled mechanism enables efficient in situ utilization of oxygen and hydrogen inherent in the biomass to produce a hydrogen-rich syngas. In this work, Ca–Fe–Ni composite oxygen carriers for RCLPy were synthesized and their impact on the hydrogen production was investigated and optimized. The results demonstrate that the reduced Ca–Fe–Ni oxygen carrier exhibited both excellent deoxygenation and catalytic cracking capability, significantly promoting the generation of hydrogen and CO. Specifically, the reduced CaFeNi15 oxygen carrier decreases the CO₂ content in the pyrolysis gas from 40.4 vol.% without an oxygen carrier to 6.89 vol.% and with a hydrogen yield of 280.2 mL⸱g⁻¹ biomass and has a total hydrogen production of 318 mL⸱g⁻¹ biomass during the whole pyrolysis–gasification process. These findings underscore the advantages of the RCLPy process in utilizing inherent biomass hydrogen for high-purity syngas production. Future efforts should focus on developing oxygen carriers with enhanced long-term cyclic stability. Full article

Plasma-assisted ammonia (NH₃) decomposition is a promising strategy for hydrogen production. However, reactor geometry remains a key factor limiting its hydrogen yield per energy input (${\mathrm{Y}}_{{\mathrm{H}}_2}$). This study systematically investigates H₂ production in outer-dielectric (OD), inner-dielectric (ID), and double-dielectric (DD) coaxial DBD reactors. The results show that the ammonia decomposition performance of OD- and ID-coaxial DBDs is significantly higher than that of the DD-coaxial DBD. OD- and ID-coaxial DBDs generate abundant micro-discharge pulses, enabling effective discharge energy deposition at lower peak voltages. Consequently, the reduced electric fields E/N are maintained within the optimal kinetic window for NH₃ dissociation and H₂ production. Moreover, by balancing residence time and energy density, the 8 cm length electrode achieves a peak ${\mathrm{Y}}_{{\mathrm{H}}_2}$ of 1.22–1.24 gH₂/kWh in the OD-coaxial DBD. For the ID-coaxial DBD, a 1 mm dielectric thickness yields a maximum capacitance of 86 pF, achieving a peak ${\mathrm{Y}}_{{\mathrm{H}}_2}$ of ~1.35 gH₂/kWh at the optimum E/N. In contrast, the DD-coaxial DBD exhibits the lowest ${\mathrm{Y}}_{{\mathrm{H}}_2}$ (≤0.82 gH₂/kWh) with minimal temperature rise. This is caused by the reduced current pulse numbers and the deviation of E/N from the optimal range with elevated operating voltages. This work provides guidance for the optimization of DBD reactors in plasma-assisted NH₃ decomposition for efficient H₂ production. Full article

A novel citric acid-assisted in situ reduction method has been developed for the synthesis of bimetallic AuPd alloy nanoparticles supported on amine–phosphate-functionalized carbon nanotubes (AuPd/NH₂-P-CNTs). In this strategy, formic acid acts not only as the reducing agent for reducing metal precursors, but also as the hydrogen source for the subsequent catalytic dehydrogenation. The introduction of citric acid significantly accelerates the reduction kinetics and promotes the uniform formation of ultrafine AuPd nanoparticles (∼1.8 nm). As a result, the optimized Au_0.5Pd_0.5/NH₂-P-CNTs exhibit an extraordinary catalytic activity and 100% H₂ selectivity during hydrogen generation from FA with sodium formate as an additive, affording a remarkable initial turnover frequency of 5663.94 mol H₂ mol Pd⁻¹ h⁻¹ at 303 K. The experimental results reveal that the -NH₂ and -P functional groups on the support are crucial for stabilizing and uniformly dispersing the alloy nanoparticles. Furthermore, the enhanced reaction rate can be attributed to the strong metal–support interaction established between AuPd nanoparticles and -NH₂-P-CNT supports. This work provides a new perspective on the design of highly efficient Pd-based catalysts for hydrogen production from formic acid. Full article

This study demonstrates a molecular size-dependent strategy to regulate the network structure of poly(vinyl alcohol) (PVA) hydrogels using a series of saccharides with increasing molecular size—glucose, maltose, raffinose, soluble starch, and amylose. FTIR, XPS, XRD, and TG analyses reveal that increasing saccharide size shifts the network from plasticization to reinforcement, which is further confirmed by mechanical testing and rheological analysis. Small-molecule saccharides disrupt hydrogen bonds and enhance chain mobility, while macromolecular starches promote network regularity through strong hydrogen bonding and crystallization induction. This structural tunability ndows the resulting hydrogels with integrated functionalities: tensile strain increases from 640% to 1500%, self-healing efficiency reaches up to 90.6%, and high-fidelity electrocardiogram (ECG) signal acquisition is achieved with a signal-to-noise ratio of 39.84 dB, comparing favorably with commercial electrodes. This work establishes a structure–property relationship linking saccharide molecular size to network architecture and provides a versatile material platform for next-generation flexible wearable sensors and bioelectrodes. Full article

The production of green hydrogen via aqueous electrolysis of hydrogen sulfide (H₂S) holds significant potential to address challenges related to sustainable energy generation and environmental protection. The electrocatalytic splitting of water polluted with highly toxic H₂S is attractive for industrial applications because the process: (i) is less power-consuming than direct thermal H₂S decomposition; (ii) achieves high Faradaic efficiencies for hydrogen production; and (iii) yields elemental sulfur as an added-value by-product. This review covers a brief discussion on sulfide-containing water sources and electrochemical methods for hydrogen production from H₂S, specifically Direct, Indirect, and Electrochemical Membrane Reactor (EMR) systems. To become commercially and economically attractive, these approaches require improvements in electrolysis efficiency through the development of low-cost electrode materials that are resistant to sulfur poisoning and corrosion, while possessing high catalytic activity, enhanced stability, and durability. Early research focused on carbon-based materials combined with noble metal oxides, transition metal compounds, and related materials. Since their practical performance is limited, investigations have shifted toward nanostructured electrocatalysts with unique crystal structures and designs, which show significantly improved efficiency for H₂S electrolysis. This review highlights the potential of H₂S electrolysis for hydrogen production, giving special attention to recent advancements in electrode materials. Full article

Diamond-like carbon (DLC) coatings are increasingly explored as a practical route to enhance the surface performance of biomedical implants and tissue engineering scaffolds, particularly when combined with additive manufacturing. Rather than serving only as protective layers, DLC coatings allow for independent tuning of surface properties without modifying the bulk structure, which is especially relevant for complex 3D-printed components. This flexibility is often what makes them attractive for biomedical design. This review is structured around two main application areas: DLC coatings for prosthetic implants and DLC coatings for tissue engineering scaffolds. Within this context, the influence of DLC structure (e.g., sp²/sp³ bonding, hydrogen content, and doping) on mechanical, tribological, and biological behavior is discussed. Particular attention is given to additively manufactured metallic implants and porous scaffolds, where large surface area and internal architectures complicate coating uniformity and adhesion. Reports show that DLC coatings can improve corrosion resistance, reduce wear, and influence biological responses, such as antibacterial activity and cell interactions. Several challenges remain to be solved, especially in achieving uniform coating penetration in porous networks and in ensuring long-term stability under physiological conditions. The combination of additive manufacturing and DLC coatings has been shown to offer the potential to become an enabling technology for next-generation biomedical devices. Full article

Poly(amidoamine) (PAMAM) dendrimers are widely recognized as versatile nanocarriers due to their tunable architecture and ability to associate with bioactive molecules. In this study, generation 3 PAMAM dendrimers functionalized with triphenylphosphonium (TPP) were employed to investigate the association of structurally related phenolic compounds—caffeic acid, p-coumaric acid, and cinnamic acid—through either covalent conjugation or non-covalent encapsulation. Physicochemical characterization by NMR, dynamic light scattering, and zeta potential measurements revealed the formation of supramolecular aggregates rather than isolated dendrimer units, with hydrodynamic diameters ranging from 127 to 260 nm and positive surface charge across all formulations. Encapsulation efficiencies determined by HPLC reached 93.8% for caffeic acid, 78.9% for p-coumaric acid, and 71% for cinnamic acid, indicating differential association behavior. Molecular dynamics simulations over 1 μs supported these findings, showing stronger and more stable interactions for polar antioxidants, particularly caffeic acid, driven by hydrogen bonding and electrostatic interactions, while cinnamic acid displayed preferential binding in more hydrophobic dendrimer regions. Radical scavenging assays (DPPH• and ABTS•+) demonstrated that all formulations retained antioxidant capacity, although dendrimer association modulated scavenging kinetics. In cellular assays under oxidative stress, free caffeic acid exhibited the strongest immediate reduction of intracellular reactive oxygen species, whereas dendrimer-associated systems showed reduced but significant activity, consistent with decreased solvent accessibility and slower release predicted by simulations. Overall, these results highlight a trade-off between molecular retention and immediate biological efficacy, demonstrating that the mode of association governs antioxidant accessibility and performance. This combined experimental and computational approach provides a mechanistic framework for the rational design of dendrimer-based delivery systems aimed at balancing stability and functional activity. Full article

With the increasing integration of transportation and energy systems, highway energy replenishment facilities are gradually evolving into hybrid refueling stations that integrate photovoltaic generation, energy storage, battery charging, and hydrogen refueling. However, due to differences in resource conditions across stations, independently operated hybrid refueling stations find it difficult to simultaneously improve overall economic performance and renewable energy utilization. To address this issue, this paper investigates the coordinated operation and distributed optimization of highway hybrid refueling stations. First, an inter-station hydrogen–carbon–green certificate trading framework is established, and a trading model for a cluster of hybrid refueling stations is then developed on this basis. Then, the inter-station trading problem is decomposed into two subproblems: symmetric trading volume determination and asymmetric Nash bargaining-based price determination. These two subproblems are solved in a distributed manner using the alternating direction method of multipliers. In addition, a hydrogen transportation model is developed to translate trading decisions into feasible transportation arrangements under highway network and hydrogen tube trailer scheduling constraints. Finally, the case study demonstrates that the proposed model enables multi-resource sharing among hybrid refueling stations, reduces the overall system cost by 21.30%, and achieves a fairer distribution of benefits among stations. Full article

Efficient, low-cost catalysts are required for on-demand H₂ generation from chemical hydrides. This study utilized piezoelectric poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) nanofibers (NFs) as a support to encapsulate bimetallic Co–Mo nanoparticles (NPs) for H₂ production via sodium borohydride (SBH) methanolysis. The PVDF-HFP membranes were synthesized through electrospinning, followed by in situ SBH reduction, which resulted in the uniform dispersion of amorphous Co–Mo NPs within the nanofibrous matrix. The optimized CoMo-0.2@PVDF-HFP membrane exhibited a hydrogen generation rate (HGR) of 1.9 × 10³ mL·min⁻¹·g⁻¹ (Co) at 298 K, indicating a 3.6-fold improvement relative to monometallic Co. Kinetic studies showed a nearly first-order relationship with catalyst dose and a nearly zero-order relationship with respect to SBH concentration, suggesting kinetics controlled by surface saturation. The activation energy (E_a) was determined to be 14.03 kJ·mol⁻¹. Moreover, the catalyst maintained over 80% of its original activity after five cycles. This enhanced performance is attributed to the combined effects of Co and Mo, the amorphous nature of the active sites, and the piezoelectric polarization of PVDF-HFP during mechanical stirring, which together improve charge transfer and reduce NP agglomeration. Full article

Decarbonizing air travel poses a major technological challenge, driven by the substantial power requirements of the drivetrain and the demanding weight and volume constraints of airborne systems. One promising avenue involves leveraging the high specific energy of hydrogen by designing compact, high-power fuel cell stacks to supply power for electric drivetrains. However, a key drawback of such propulsion architectures is the substantial heat generated within the fuel cells, which necessitates bulky and heavy thermal management systems to ensure safe and continuous operation. This study investigates a proposed air-based thermal management system, which operates by introducing pulsating heat pipes into the bipolar plates of a High-Temperature Polymer Electrolyte Membrane Fuel Cell (HT-PEM FC) stack. If proven to be feasible, heat pipe assisted air cooling may provide the benefit of reducing overall system complexity by decreasing the number of components in the thermal management system. To evaluate the thermal performance of the proposed system, a one-dimensional thermal model was initially developed in a previous study to describe the temperature distribution along the length of a heat pipe. Building upon this foundation, the present work extends the model by incorporating a two-dimensional Computational Fluid Dynamic (CFD) analysis to account for geometry-specific effects within the hexagonal design. Results indicate that the heat transfer from the hexagonal heat pipe geometry to the coolant air flow was marginally overestimated in previous analytical calculations. Revised heat transfer rates led to a shift in the predicted temperature distributions, resulting in the need for either increased external airflow, extended condenser sections, or reduced inlet temperatures to maintain target operating conditions. Although these adjustments may result in a slight increase in system mass and parasitic power consumption, the overall impact is limited, and the heat pipe-assisted air cooling approach remains theoretically feasible. Based on the results, design modifications are proposed and their impact on thermal performance is evaluated to address the challenges of heat rejection and temperature uniformity. A modification based on variation and optimization of PHP meander lengths was evaluated using the updated model and it significantly improved temperature homogeneity across the evaporator. Full article

During the marine transport of liquid hydrogen, heat ingress leads to the generation of boil-off gas (BOG), which increases the pressure in the liquid hydrogen storage tanks. Effective BOG management is therefore essential to ensure tank safety and minimize hydrogen loss. This study develops a cryogenic compression recovery and storage system for BOG generated during the marine transport of 160,000 m³ liquid hydrogen. The core process involves compressing a portion of the BOG and subsequently utilizing the BOG’s inherent cold energy to cool the compressed hydrogen, ultimately enabling the storage of the final cryogenic compressed hydrogen product. ASPEN-PLUS software was employed to analyze the proposed system’s specific energy consumption (SEC) and ψ (hydrogen density/SEC) for producing cryogenic compressed hydrogen (CcH₂) across a temperature range of 53 to 110 K and a pressure range of 40 to 100 MPa. Seven optimal sets of state parameters were identified for the cryogenic compressed hydrogen product. Based on a specified optimal parameter set of 80 K and 50 MPa, a simulation of the proposed system’s performance yielded a SEC of 2.25 kWh/kg CcH₂ and an exergy efficiency of 87.88% with BOG feed at 53 K and 0.1 MPa, along with the exergy loss and exergy efficiency for each component. Compared to a BOG re-liquefaction system and a MRJT CcH₂ system under identical conditions, the proposed system achieves 31.81% and 64.9% reduction, respectively, in SEC and 17.32% and 94.6% improvement, respectively, in exergy efficiency. Furthermore, the effects of feed temperature and cryogenic compressed hydrogen product mass flow rate on the proposed system’s SEC and exergy efficiency were investigated. Full article

Models are described for calculating the crack initiation times for Alloy 600 and Type 304 SS in PWR and BWR primary coolant circuits, respectively. In PWRs, initiation is defined in terms of the grain boundary oxidation concept of Scott and Le Calvar, whereas in BWRs, cracks are envisioned to nucleate from corrosion pits. In contrast, in BWRs, we envision cracks to nucleate from corrosion pits, with the difference in the two systems being primarily due to electrochemical factors. Thus, in BWR primary coolant and the absence of hydrogen water chemistry (HWC), the oxidizing conditions due to the radiolytic production of H₂O₂ cause the ECP to be significantly more positive than the critical pitting potential. Accordingly, the nucleation and growth of pits due to passivity breakdown and the establishment of differential aeration between the pit nucleus’s internal and external environments, which results in growth of pits to the critical size necessary to satisfy the Kondo criteria for transition of a pit into a crack, is judged to be a realistic scenario. Contrariwise, in PWR primary coolant, the ECP is so negative [≈−1.0 V_she] due to the large amount of pressurizing H₂ present in the circuit [20–60 cm³(STP)/kg H₂O] that the nucleation and growth of pits is not possible. However, Totsuka and Smialowska found that MA Alloy 600 suffers hydrogen-induced cracking (HIC) at an ECP < −0.85 V_she, demonstrating that, in service with a high hydrogen concentration, brittle fractures will occur. The initiation sites were not identified. The crack initiation models for Alloy 600 in PWRs and Type 304 SS in BWRs reproduce the effects of the following independent variables: applied stress, temperature, cold work, grain boundary segregations, water chemistry, pH, and electrochemical potential. The origins of the observed scatter in experimentally measured crack initiation times are discussed, and the challenges of developing a more general crack initiation model (GCIM) are identified. From a mathematical viewpoint, the most significant challenge arises from the nested distributions involving the many parameters and expressions within the GCIM that are either distributed because of an imprecise definition or because some experimentally determined input parameters are experimentally scattered. Additionally, the evolution of semi-elliptical surface cracks resulting from the electrochemical crack length (ECL) being shorter than the classical mechanical crack length (MCL) must be incorporated if the GCIM is to find utility in the water-cooled nuclear power industry where semi-elliptical surface cracks are normally observed. Full article