Search Results (240)

Methane dry reforming (DRM) represents a promising route for the simultaneous valorization of CH₄ and CO₂ into syngas; however, conventional Ni-based catalysts suffer from rapid deactivation due to sintering and carbon deposition. In this work, we present a synergistically engineered Ni-based catalyst integrating hierarchical SiC confinement, Pd promotion via oleic-acid-assisted complexation, and MgO surface modification to overcome these challenges. Under optimized reaction conditions (CH₄/CO₂ = 1:1, 750 °C, GHSV = 36,000 mL g⁻¹ h⁻¹), the multifunctional NiPd/Si–xMg catalyst achieved steady-state conversions of 85% for CH₄ and 84% for CO₂, maintaining an H₂/CO ratio close to 1.0 over 100 h of continuous operation without noticeable deactivation. In contrast, the reference Ni/SiC and Ni/MgO catalysts exhibited initial conversions of 75–80% but declined by more than 50% within the same period, confirming the superior durability of the optimized system. Thermogravimetric analysis (TGA) revealed a drastic reduction in carbon deposition—from 119.0 mg C g⁻¹ for Ni/SiC to 81.4 mg C g⁻¹ for NiPd/Si-xMg—indicating enhanced coke resistance. Transmission electron microscopy (TEM) confirmed uniform Ni dispersion with an average particle size of 7.2 ± 1.8 nm, while H₂-TPR and CO₂-TPD analyses demonstrated improved reducibility and surface basicity. The combination of SiC confinement, Pd-induced hydrogen spillover, and MgO-mediated CO₂ activation effectively mitigated sintering and carbon accumulation, resulting in high activity, stability, and carbon tolerance. This integrated catalyst design provides a robust pathway toward industrially viable DRM systems for sustainable syngas production. Full article

Microplastics (MPs), defined as synthetic polymer particles ranging from 1 μm to 5 mm, originate from various sources, including synthetic textiles, tire wear, degraded plastic waste, etc. Their small size and chemical stability make them challenging to remove, collect and degrade, posing significant adverse effects to both ecosystems and human health. While efforts to develop sustainable alternatives and removal methods are ongoing, effective solutions remain limited. Catalytic degradation and upcycling present a promising route to mitigate MP pollution by enabling efficient breakdown into less harmful molecules and potential upcycling into valuable products with lower energy requirements. This review provides a comprehensive overview of recent advances in catalyst design and development specifically for MP degradation, highlighting photochemical, thermal, biological, electrochemical, and hybrid approaches. Key challenges, reaction mechanisms, and future directions are discussed, offering a timely reference for researchers in this emerging field. Full article

Non-precious catalysts for alkaline hydrogen evolution reaction (HER) face a fundamental multi-scale challenge: lack of synergy between electronic structure tuning for balancing H adsorption and water dissociation, active site stabilization for boosting intrinsic turnover frequency (TOF), and mass transport. Even Pt loses 2–3 orders of magnitude activity in alkaline media due to inefficient water dissociation, a synergistic gap unresolved by the Sabatier principle alone. Existing strategies only address isolated aspects: phase engineering optimizes electronic structure but not active site stability; heteroatom doping introduces defects unlinked to mass transport; and nanostructuring enhances mass transfer but not atomic-level activity. None of them address multi-scale mechanistic synergy. Herein, we design a hierarchically porous P-doped NiCo alloy (hpP-NiCo) with an aim of achieving this synergy via integrating α-FCC/ε-HCP phases, P-induced defects, and 3D porosity. The formed α/ε interface tunes the d-band center to balance H adsorption and water dissociation; and the doped P stabilizes metal-vacancy sites to boost TOF. In addition, porosity matches mass transport with active site accessibility. In 1 M KOH, hpP-NiCo reaches 1000 mA cm⁻² at 185 mV overpotential and has a Tafel slope of 43.1 mV dec⁻¹, corresponding to electrochemical desorption as the rate-limiting step and verifying Volmer acceleration. Moreover, it also exhibits bifunctional oxygen evolution reaction (OER), achieving 100 mA cm⁻² at potential of 1.55 V. This work establishes a mechanistic synergy model for non-precious HER catalysts. Full article

In this study, we present a novel high-thermal-conductivity-organosilicon potting adhesive developed for use in power modules. The adhesive is designed to enhance power modules’ thermal properties and mechanical strength, addressing the need for more efficient and reliable encapsulation materials in electronic applications. By optimizing the resin formulation, the adhesive exhibits improved tensile strength and elongation at break properties, making it particularly suitable for applications requiring high durability and resilience under thermal and mechanical stress. Herein, we propose a high-thermal-conductivity organosilicon electronic potting adhesive designed for power modules. The adhesive consists of two components: Component A and Component B. Component A is composed of a base polymer (0.5–10 parts), silicone resin (0.15–10 parts), plasticizer (0.5–5 parts), color paste (0.01–0.2 parts), thermally conductive filler (70–120 parts), filler treatment agent (2–8 parts), and a catalyst (0.1–2 parts). Component B includes a base polymer (0.5–10 parts), silicone resin (0.15–10 parts), plasticizer (0.5–5 parts), thermally conductive filler (70–120 parts), crosslinking agent (0.1–10 parts), chain extender (0.1–10 parts), and crosslinking inhibitor (0.01–1 part). The adhesive is designed to improve the tensile strength and elongation at break. These materials were engineered to facilitate easy repair and disassembly, ensuring cost-effective maintenance and reuse in power module systems. This work demonstrates the potential of the adhesive in advancing the performance and longevity of power electronics, providing valuable insights into its practical application for high-performance electronic devices. Full article

Dry reforming of methane and ethanol is a promising catalytic process for the conversion of carbon dioxide and hydrocarbon feedstocks into synthesis gas (H₂/CO), which serves as a key platform for the production of fuels and chemicals. Over the past decade, substantial progress has been achieved in the design of catalysts with enhanced activity and stability under the demanding conditions of these strongly endothermic reactions. This review summarizes the latest developments in catalyst systems for DRM and EDR, including Ni-based catalysts, perovskite-type oxides, MOF-derived materials, and high-entropy alloys. Particular attention is given to strategies for suppressing carbon deposition and preventing metal sintering, such as oxygen vacancy engineering in oxide supports, rare earth and transition metal doping, strong metal–support interactions, and morphological control via core–shell and mesoporous architectures. These approaches have been shown to improve coke resistance, maintain metal dispersion, and extend catalyst lifetimes. The review also highlights emerging concepts such as multifunctional hybrid systems and innovative synthesis methods. By consolidating recent findings, this work provides a comprehensive overview of current progress and future perspectives in catalyst development for DRM and EDR, offering valuable guidelines for the rational design of advanced catalytic materials. Full article

An overview of the Common Rail (CR) diesel engine challenges and of the promising state-of-the-art solutions for addressing them is provided. The different CR injector driving technologies have been compared, based on hydraulic, spray and engine performance for conventional diesel combustion. Various injection patterns, high injection pressures and nozzle design features are analyzed with reference to their advantages and disadvantages in addressing engine issues. The benefits of the statistically optimized engine calibrations have also been examined. With regard to the combustion strategy, the role of a CR engine in the implementation of low-temperature combustion (LTC) is reviewed, and the effect of the ECU calibration parameters of the injection on LTC steady-state and transition modes, as well as on an LTC domain, is illustrated. Moreover, the exploitation of LTC in the last generation of CR engines is discussed. The CR apparatus offers flexibility to optimize the engine calibration even for biofuels and e-fuels, which has gained interest in the last decade. The impact of the injection strategy on spray, ignition and combustion is discussed with reference to fuel consumption and emissions for both biodiesel and green diesel. Finally, the electrification of CR diesel engines is reviewed: the effects of electrically heated catalysts, electric supercharging, start and stop functionality and electrical auxiliaries on NO_x, CO₂, consumption and torque are analyzed. The feasibility of mild hybrid, strong hybrid and plug-in CR diesel powertrains is discussed. For the future, based on life cycle and manufacturing cost analyses, a roadmap for the automotive sector is outlined, highlighting the perspectives of the CR diesel engine for different applications. Full article

Photocatalytic nitrogen fixation under ambient conditions offers a sustainable alternative to the energy-intensive Haber–Bosch process, yet remains limited by the inertness of N≡N bonds and sluggish multi-electron/proton transfer kinetics. Nature’s nitrogenase enzymes, featuring the FeMo cofactor and ATP-driven electron cascades, inspire a new generation of artificial systems capable of mimicking their catalytic precision and selectivity. This review systematically summarizes recent advances in bio-inspired photocatalytic nitrogen reduction, focusing on six key strategies derived from enzymatic mechanisms: Fe–Mo–S active site reconstruction, hierarchical electron relay pathways, ATP-mimicking energy modules, defect-induced microenvironments, interfacial charge modulation, and spatial confinement engineering. While notable progress has been made in enhancing activity and selectivity, challenges remain in dynamic regulation, mechanistic elucidation, and system-level integration. Future efforts should prioritize operando characterization, adaptive interface design, and device-compatible catalyst platforms. By abstracting nature’s catalytic logic into synthetic architectures, biomimetic photocatalysis holds great promise for scalable, green ammonia production aligned with global decarbonization goals. Full article

The ethanol oxidation reaction (EOR) is a key process for direct ethanol fuel cells (DEFCs), offering a high-energy-density and carbon-neutral pathway for sustainable energy conversion. However, the practical implementation of DEFCs is significantly hindered by the EOR due to its sluggish kinetics, complex multi-electron transfer pathways, and severe catalyst poisoning by carbonaceous intermediates. This review provides a comprehensive and mechanistically grounded overview of recent advances in EOR electrocatalysts, with a particular emphasis on the structure–activity relationships of noble metals (Pt, Pd, Rh, Au) and non-noble metals. The effects of catalyst composition, surface structure, and electronic configuration on C–C bond cleavage efficiency, product selectivity (C1 vs. C2), and CO tolerance are critically evaluated. Special attention is given to the mechanistic distinctions among different metal systems, highlighting how these factors influence reaction pathways and catalytic behavior. Key performance-enhancing strategies—including alloying, nanostructuring, surface defect engineering, and support interactions—are systematically discussed, with mechanistic insights supported by in situ characterization and theoretical modeling. Finally, this review identifies major challenges and emerging opportunities, outlining rational design principles for next-generation EOR catalysts that integrate high activity, durability, and scalability for real-world DEFC applications. Full article

Despite the immense potential in environmental remediation, the translation of magnetic nanomaterials (MNMs) from laboratory innovations to practical, field-scale applications remains hindered by significant technical and environmental challenges. This is particularly evident in soil environments—which are inherently more complex than aquatic systems and have received comparatively less research attention. Beginning with an outline of the fundamental properties that make iron-based MNMs effective as adsorbents and catalysts for heavy metals and organic pollutants, this review systematically examines their core contaminant removal mechanisms. These include adsorption, catalytic degradation (e.g., via Fenton-like reactions), and magnetic recovery. However, the practical implementation of MNMs is constrained by several key limitations, such as particle agglomeration, oxidative instability, and reduced efficacy in multi-pollutant systems. More critically, major uncertainties persist regarding their long-term environmental fate and biocompatibility. In light of these challenges, we propose that future efforts should prioritize the rational design of stable, selective, and intelligent MNMs through advanced surface engineering and interdisciplinary collaboration. Full article

This review covers the current state, challenges, and future directions of catalytic combustion technologies for mitigating fugitive methane emissions from the fossil fuel industry. Methane, a potent greenhouse gas, is released from diverse sources, including natural gas production, oil operations, coal mining, and natural gas engines. The paper details the primary emission sources, and addresses the technical difficulties associated with dilute and variable methane streams such as ventilation air methane (VAM) from underground coal mines and low-concentration leaks from oil and gas infrastructure. Catalytic combustion is a useful abatement solution due to its ability to destruct methane in lean and challenging conditions at lower temperatures than conventional combustion, thereby minimizing secondary pollutant formation such as NO_X. The review surveys the key catalyst classes, including precious metals, transition metal oxides, hexa-aluminates, and perovskites, and underscores the crucial role of reactor internals, comparing packed beds, monoliths, and open-cell foams in terms of activity, mass transfer, and pressure drop. The paper discusses advanced reactor designs, including flow-reversal and other recuperative systems, modelling approaches, and the promise of advanced manufacturing for next-generation catalytic devices. The review highlights the research needs for catalyst durability, reactor integration, and real-world deployment to enable reliable methane abatement. Full article

The persistent release of synthetic dyes such as methylene blue (MB) into aquatic environments poses a significant ecological hazard due to their chemical stability and toxicity. In recent years, the application of engineered composite photocatalysts has emerged as a potent solution for efficient dye degradation under visible and UV light. This review comprehensively summarizes various advanced composites, including carbon-based, metal-doped, and heterojunction materials, tailored for MB degradation. Notably, composites such as TiO₂/C-550, WS₂/GO/Au, and MOF-derived α-Fe₂O₃/ZnO achieved near-complete degradation (>99%) within 30–150 min, while others, like ZnO/JSAC-COO⁻ and Ag/TiO₂/CNT, displayed enhanced charge separation and stability over five consecutive cycles. Band gap engineering (ranging from 1.7 eV to 3.2 eV) and reactive oxygen species (·OH, ·O₂⁻) generation were key to their photocatalytic performance. This review compares the structural attributes, synthetic strategies, and degradation kinetics across systems, highlighting the synergistic role of co-catalysts, surface area, and electron mobility. This work offers systematic insight into the state-of-the-art composite photocatalysts and provides a comparative framework to guide future material design for wastewater treatment applications. Full article

Enzymes are highly selective and efficient biological catalysts that play a critical role in modern industrial biocatalysis. Their ability to operate under mild conditions and reduce environmental impact makes them ideal alternatives to conventional chemical catalysts. This review provides a comprehensive overview of advances in enzyme-based catalysis, focusing on enzyme classification, engineering strategies, and industrial applications. The six major enzyme classes—hydrolases, oxidoreductases, transferases, lyases, isomerases, and ligases—are discussed in the context of their catalytic roles across sectors such as pharmaceuticals, food processing, textiles, biofuels, and environmental remediation. Recent developments in protein engineering, including directed evolution, rational design, and computational modeling, have significantly enhanced enzyme performance, stability, and substrate specificity. Emerging tools such as machine learning and synthetic biology are accelerating the discovery and optimization of novel enzymes. Progress in enzyme immobilization techniques and reactor design has further improved process scalability, reusability, and operational robustness. Enzyme sourcing has expanded from traditional microbial and plant origins to extremophiles, metagenomic libraries, and recombinant systems. These advances support the integration of enzymes into green chemistry and circular economy frameworks. Despite challenges such as enzyme deactivation and cost barriers, innovative solutions continue to emerge. Enzymes are increasingly enabling cleaner, safer, and more efficient production pathways across industries, supporting the global shift toward sustainable and circular manufacturing. Full article

Transition metal dichalcogenides (TMSs), exemplified by molybdenum disulfide (MoS₂), exhibit significant potential as alternatives to noble metals (e.g., Pt) for the hydrogen evolution reaction (HER). However, conventional synthesis methods of MoS_x often suffer from active site loss, harsh reaction conditions, or undesirable oxidation, limiting their practical applicability. The development of MoS_x with high-density active sites remains a formidable challenge. Herein, we propose a novel strategy employing [Mo₃S₁₃]²⁻ clusters as precursors to construct three-dimensional amorphous MoS_x nanosheets through optimized hydrothermal and solvent evaporation-induced self-assembly approaches. Comprehensive characterization confirms the material’s unique amorphous lamellar structure, featuring preserved [Mo₃S₁₃]²⁻ units and engineered interlayer dislocations that facilitate enhanced electron transfer and active site exposure. This work not only establishes [Mo₃S₁₃]²⁻ clusters as effective building blocks for high-performance MoS_x catalysts, but also provides a scalable and environmentally benign synthesis route for the large-scale production of such nanostructured a-MoS_x. Our findings facilitate the rational design of non-noble HER catalysts via structural engineering, with broad implications for energy conversion technologies. Full article

High-temperature proton exchange membrane fuel cells (HT-PEMFCs) offer distinct advantages over their low-temperature counterparts. However, their commercial viability is significantly hampered by durability challenges stemming from electrocatalyst support degradation in the corrosive phosphoric acid environment. This review provides a comprehensive analysis of advanced strategies to overcome this critical durability issue. Two main research directions are explored. The first involves engineering more robust carbon-based materials, including graphitized carbons, carbon nanostructures (nanotubes and graphene), and heteroatom-doped carbons, which enhance stability by modifying the carbon’s intrinsic structure and surface chemistry. The second direction focuses on replacing carbon entirely with intrinsically stable non-carbonaceous materials. These include metal oxides (e.g., TiO₂, SnO₂), transition metal carbides (e.g., WC, TiC), and nitrides (e.g., Nb₄N₅). For these non-carbon materials, a key focus is on overcoming their typically low electronic conductivity through strategies such as doping and the formation of multi-component composites. The analysis benchmarks the performance and durability of these advanced supports, concluding that rationally designed composite materials, which combine the strengths of different material classes, represent the most promising path toward developing next-generation, long-lasting catalysts for HT-PEMFCs. Full article

Virtual Reality (VR) has emerged as a transformative tool in higher education, enabling immersive and interactive learning environments that support the assimilation of complex concepts, hands-on training, and innovative pedagogical practices. This systematic literature review analyzes studies published between 2020 and 2025 that examined the integration of VR in higher education and its connection with the United Nations Sustainable Development Goals (SDGs). Following the PRISMA guidelines, twelve studies were selected from the Web of Science and Scopus databases and assessed using predefined quality criteria. The findings highlight the predominance of mixed-methods approaches, with applications spanning diverse disciplines such as engineering, medical sciences, architecture, teacher training, and sustainability. The results emphasize VR’s potential to enhance student motivation, engagement, and digital competencies, while also contributing to Quality Education (SDG 4), along with other SDGs such as Good Health and Well-Being (SDG 3), Affordable and Clean Energy (SDG 7), Decent Work and Economic Growth (SDG 8), Reducing Inequalities (SDG 10), Sustainable Cities and Communities (SDG 11), and Climate Action (SDG 13). However, persistent challenges include high implementation costs, limited accessibility and teacher training, lack of standardization, and small short-term study designs. This review underscores the need for broader, longitudinal, and interdisciplinary research that integrates underrepresented SDGs and addresses inclusivity, equity, and long-term effectiveness, consolidating VR as a catalyst for innovation and sustainable development in higher education. Full article