Search Results (793)

In this study, a hierarchically confined Pt/MnO₂–meso-Al₂O₃ catalyst with 0.5 wt% Pt loading was synthesized via a precipitation method using MnO₂ as a promoter and mesoporous Al₂O₃ (m-Al₂O₃) as a support, and its methane catalytic combustion performance and structure–activity relationship were systematically investigated. The results demonstrate that the 0.5 wt% Pt-loaded Pt-MnO₂/m-Al₂O₃ catalyst achieved 90% methane conversion at 236 °C. The enhanced performance is attributed to three synergistic mechanisms: (1) Pt doping induced lattice contraction in MnO₂ (XRD revealed a 0.03 Å reduction in the (001) interplanar spacing), which facilitated the formation of Mn³⁺–oxygen vacancy pairs (XPS indicated a Mn³⁺- content of 79.87%); (2) the MnPt₃O₆ interfacial structure (HAADF-STEM confirmed lattice spacings of 0.21 nm) accelerated oxygen species cycling, with the 0.5 wt% Pt-loaded catalyst for lattice oxygen desorption capacity (O₂-TPD) increasing by 54% compared to undoped samples; (3) the mesoporous m-Al₂O₃ carrier provided effective confinement, achieving a high specific surface area (27.6 m²/g) and sub-nanometer Pt dispersion (particle size < 2 nm). Under conditions of 1000 ppm CH₄ and a space velocity of 30,000 h⁻¹, the catalyst maintained a methane conversion rate of 98.2 ± 0.5% during continuous operation for 300 h. Post-cycling characterization revealed a stable crystalline structure (XRD full width at half maximum of 0.35° ± 0.02°) and grain size (15.5 ± 0.5 nm), confirming its robustness for industrial applications. This study provides theoretical and experimental foundations for the rational design of highly efficient catalysts for low-concentration methane elimination. For comparison, a Co-doped catalyst (1.0 wt% Co–MnO₂/Al₂O₃) was also prepared, which exhibited significantly lower activity (T₉₀ = 251 °C), underscoring the unique role of Pt in the confined architecture. This study provides theoretical and experimental foundations for the rational design of highly efficient catalysts for low-concentration methane elimination. Full article

Carbon nano-onions (CNOs) were synthesized at ambient conditions using the wick-pyrolysis technique with ghee as a precursor. A high-purity copper substrate produced unique CNOs, differing from those obtained with other metals. To purify the nanoparticles, they underwent treatment with a solvent mixture of acetone and deionized water or were pyrolyzed at 1000 °C under nitrogen without a catalyst. Various characterization techniques, including X-ray diffraction (XRD), Field Emission Scanning Electron Microscopy (FE-SEM), High-Resolution Transmission Electron Microscopy (HR-TEM), and Raman Spectroscopy, confirmed the successful formation of CNOs. Energy Dispersive Spectroscopy (EDS) and Elemental analysis (CHN) indicated the presence of oxygen in treated CNOs. X-ray photoelectron spectroscopy (XPS) revealed binding energies linked to C-O and C=O bonds. The average particle size was found to be 30–50 nm, with some agglomeration in pyrolyzed samples. A significant increase in surface area from 79.7 m²/g to 261.8 m²/g was observed, along with changes in pore radius and volume via Brunauer–Emmett–Teller (BET) analysis. Water contact angles on the CNO surface were measured at 125° and 138°, indicating hydrophobicity. Electrochemical tests on CNO-based composite electrodes yielded a specific capacitance of 109.7 F/g with 96% capacity retention over 5000 cycles. Full article

Non-stoichiometric high-entropy carbides (Nb_0.2Ta_0.2Ti_0.2W_0.2Zr_0.2)C_x (x = 0.71–0.85) nanoscale powders were prepared using oxides and carbon as raw materials via carbothermal reduction. The (Nb_0.2Ta_0.2Ti_0.2W_0.2Zr_0.2)C_0.73 synthesized at 1700 °C exhibited a grain size of approximately 400 nm, an oxygen content of 0.3 wt.%, and uniform nanoscale distribution of the five metal elements. After ball milling, (Nb_0.2Ta_0.2Ti_0.2W_0.2Zr_0.2)C_0.73 powder was sintered by spark plasma sintering to produce high-entropy ceramics with a relative density of 98.1% and an average particle size of about 5.3 μm. The Vickers hardness, nano-hardness, Young’s modulus, and fracture toughness were 17.6 GPa, 29.1 GPa, 514 GPa, and 5.3 MPa·m^1/2, respectively. The thermal conductivity of the ceramic at room-temperature was as low as 8.5 W/m·K. Full article

Micro- and nano-container-based self-healing coatings have emerged as a promising strategy for the long-term conservation of cultural heritage artifacts, including metals, stone, organic matter, and construction materials. These coatings incorporate microcapsules or nanocapsules with tailored shell and core materials, enabling autonomous release of healing agents or corrosion inhibitors in response to damage. For metallic artifacts, benzotriazole@mesoporous silica nanoparticles (BTA@MSN) microcapsules achieve selective pH-responsive release, reaching 77% at pH 9.0 and 42% at pH 5.0, effectively mitigating localized corrosion. Temperature-adaptive poly(methyl methacrylate-co-methacrylic acid) (PMMA-MA)/MgO microcapsules exhibit controlled rupture rates, with a 75% reduction at elevated temperatures, enhancing crack repair efficiency by approximately 5%. Organic artifacts, such as wooden or paper manuscripts, benefit from clove oil nanocapsules, which increase tensile strength by 43.5% and fracture toughness by 101.9%, with only 2.91% weight loss over 7 days compared to 33.1% for unencapsulated oil. Advanced fabrication methods—including microfluidics, Pickering emulsions, and multi-core systems—enable high encapsulation efficiency (up to 73.5%), uniform particle size, and repeatable healing. Multi-stimuli responsiveness (pH, temperature, light, magnetic fields) and biobased, environmentally friendly materials further enhance adaptability and sustainability. In this review, “self-healing” is defined broadly to include both physical crack repair and autonomous restoration of protective functions. Overall, self-healing micro/nanocapsule coatings provide a highly controllable, efficient, and durable solution for active heritage protection, representing a shift from passive to intelligent conservation strategies. Furthermore, a systematic comparison of different capsule systems is provided to clarify their respective advantages and limitations. Overall, hybrid systems exhibit the most balanced performance, while inorganic nanocontainers offer superior stability and controlled release, and polymeric capsules enable rapid healing but limited reusability. Full article

This work presents a comprehensive investigation of the thermal decomposition of nickel oxalate dihydrate as a precursor for the synthesis of porous NiO, with particular emphasis on microstructural formation and evolution. The transformations occurring at successive stages of the reaction were examined using SEM, TEM, N₂ adsorption, TG–DSC–MS, and in situ powder XRD, enabling the mechanisms of pore formation to be elucidated. The decomposition results in the formation of a porous pseudomorph composed of NiO nanoparticles with an average size of approximately 4 nm. This is the first time that the resulting microstructure has been shown to exhibit hierarchical, bimodal porous architecture. During dehydration, macropores are generated as a result of crystal fragmentation into blocks several hundred nanometers in size. Subsequent oxalate decomposition leads to the formation of mesoporous aggregates composed of nanometer-sized particles. The factors governing the parameters of the porous microstructure are analyzed. The resulting NiO, with its hierarchical pore structure, shows significant potential for applications in heterogeneous catalysis, gas sensing, and as electrodes for supercapacitors, lithium-ion batteries, and photoelectrochemical devices, as its macropores facilitate mass transport by reducing diffusion resistance while its mesopores provide a large accessible surface area for adsorption and catalytic reactions. Full article

The rapid and precise detection of biomarkers and pathogens remains a critical challenge in clinical diagnostics. Traditional methodologies are frequently hindered by protracted workflows, complex sample preparation, and reliance on resource-intensive instrumentation. Acoustofluidics—the synergistic integration of acoustics and microfluidics—has emerged as a transformative solution for point-of-care testing (POCT). Bulk acoustic wave (BAW) and surface acoustic wave (SAW) technologies enable the contactless, label-free, and biocompatible manipulation of bioparticles across micro- and nanometer scales. This review critically examines recent advancements in BAW- and SAW-based acoustofluidic biosensors. We elucidate the fundamental principles governing distinct acoustic modes—including Quartz Crystal Microbalance (QCM), film bulk acoustic resonator (FBAR), and Solidly Mounted Resonator (SMR) for BAW and Rayleigh and Love waves for SAW—and evaluate their specific roles in liquid-phase sensing, particle sorting, and cellular focusing. Results show that integrating on-chip sample preparation accelerates diagnostic workflows, reducing assay times to under 10 min. Coupling acoustic manipulation with optical, mass-based, or electrochemical modalities effectively overcomes fundamental diffusion limits, achieving ultrasensitive, multimodal detection. We address translational challenges—acoustothermal heating, biofouling, and scalable integration. Following a discussion of clinical applications in oncology and infectious diseases, we map emerging trajectories, emphasizing AI-driven intelligent microfluidics, modular architectures, and flexible wearable platforms that will ultimately democratize continuous precision diagnostics. Full article

X-band copper resonating cavities are key components of future pulsed GHz normal-conductive multi-TeV accelerators. High electric field gradients are required for emerging applications; however, as gradients increase, components’ lifetime decreases, primarily due to radiofrequency (RF) breakdown. Coating technologies are being investigated in several laboratories to improve RF structure, performance and lifetime. To this end, we investigated the feasibility of fabricating nanometer-periodic Cu/Mo metallic multilayers on three-dimensional (3D) aluminum mandrels designed to replicate X-band copper resonating cavities. These nanometer-period multilayers are proposed to mitigate surface degradation due to electric breakdown at high accelerating gradients by stabilizing inner cavity surfaces against dislocation evolution and roughening caused by thermo-mechanical fatigue. High-Power Impulse Magnetron Sputtering (HiPIMS) in a bias-controlled dual closed-field magnetron configuration was employed to deposit alternating Mo and Cu nano-layers onto the 3D geometries. Given the complexity of HiPIMS technology, plasma pulse evolution was studied by combining time-resolved optical emission spectroscopy with electrical measurements of the pulse discharge. The influence of the process parameters, particularly the applied DC bias, on film growth was studied using non-destructive microprobe α-particle elastic backscattering spectrometry (µEBS) and scanning transmission electron microscopy (STEM). STEM and µEBS analyses confirmed that Mo layers with thicknesses of approximately 5–35 nm were successfully deposited repeatedly on thicker Cu layers (30–150 nm), preserving individual layer properties with minimal interdiffusion and alloying. The layers were deposited inside trenches with an aspect ratio of 5:1 representative of X-band irises. This technology, coupled with the replica process, could be applied to highly engineered nanostructured coatings for X-band cavity treatment in compact particle accelerator prototypes, as it may improve electrical breakdown lifetime under high accelerating fields, at least for degradation processes driven by the high mobility of copper dislocations. Full article

Cancer remains a major global health challenge, characterized by abnormal cell growth and metastasis. Current limitations of conventional therapies, particularly non-specific toxicity harming healthy cells, highlight the need for more targeted approaches. Nanotechnology offers a revolutionary solution, utilizing nanoparticles (NPs) for precise drug delivery to tumor sites while minimizing off-target effects. These nanometer-scale particles enable superior binding to cancer cell membranes, the tumor microenvironment, or nuclear receptors, facilitating significantly higher local concentrations of therapeutic agents. NPs, synthesized via physical, chemical, or biological methods, are categorized as organic (organic material-based) or inorganic (metallic particle-based). Key delivery mechanisms include the Enhanced Permeability and Retention (EPR) effect and Active Transport and Retention (ATR). This review specifically examines NP applications for the most prevalent cancers in the US (2025): breast, prostate, and lung. Gold and magnetic NPs show significant promise for early breast cancer detection. For lung cancer, polymeric NPs like PCL, PLA, and PLGA are effective carriers for peptides, proteins, and nucleic acids. BIND-014, a docetaxel-loaded NP formulation, represents an emerging strategy for prostate cancer. Clinically established examples include liposomal doxorubicin and albumin-bound paclitaxel. We comprehensively discuss the synthesis methods, delivery mechanisms, and the current landscape of NPs in research and clinical trials for these cancers. This analysis underscores the potential of nanotechnology to provide more effective and targeted therapeutic options for cancer patients in the future. A distinctive feature of this review is its comparative cancer-specific analysis of NP platforms in breast, prostate, and lung cancers. Unlike previous generalized reviews, this work integrates synthesis strategies, delivery mechanisms, translational challenges, and clinically relevant formulations to provide a bench-to-bedside perspective on the future of nanomedicine in oncology. Full article

Controlling the microstructure of electroless nickel coatings is crucial for optimizing the interfacial properties of carbon fibers. However, a systematic understanding of how dispersants can effectively leverage the refining effect of nanoparticles in composite plating systems remains lacking. This paper proposes the use of a composite dispersant, comprising polyethylene glycol (PEG) and sodium methylene bis-naphthalene sulfonate (NNO) at a 1:1 mass ratio, for nano-Al₂O₃ to achieve microstructure refinement of nickel coatings on carbon fiber surfaces. The results demonstrate that the composite dispersant modifies the surface state and dispersion stability of Al₂O₃ particles through synergistic adsorption, thereby regulating the nucleation and growth behavior of the Ni-P alloy. At an optimal composite dispersant concentration of 3 g/L, the coating exhibits the most compact structure, with Ni-P particle size refined to approximately 181 nm. The coating consists of two phases: crystalline Ni₃P and amorphous Ni-P. The dual adsorption effect of the dispersant—inhibiting Al₂O₃ agglomeration while improving the surface wettability of carbon fibers—is key to enhancing the refinement efficiency. Conversely, excessive dispersant addition leads to deteriorated coating quality. This study provides experimental evidence for understanding the multiphase interfacial interaction mechanism involving organic additives, nanoparticles, and metal deposition, and offers a novel strategy for controlling the surface functionalization of carbon fibers. Full article

CoFe₂O₄ nanoparticles were prepared using a hydrothermal method. All the studied samples were single-phase and were crystallized in a cubic Fd-3m structure. XRD and TEM analyses revealed that the particles had average sizes between 5 and 22 nm. It has been shown that, by using the PVP of different molecular masses, trends of growth and crystallization can be established, obtaining elongated 40 k, cubical 58 k, and rhomboidal 360 kg/mol nanoparticles. While using Ethylene glycol as solvent, the formation of separated “raspberry”-like nanostructures was revealed. The saturation magnetizations are somewhat smaller compared with crystalline CoFe₂O₄ saturation magnetization, but are high enough to have possible biomedical applications. FC and ZFC measurements show that the blocking temperature was around 100 K for the CF5 sample and around 20 K for the FC6 sample. The calculated anisotropy constants were between 7 and 10 kJ/m³, being close to previously reported values. The calculated blocking temperatures are in good agreement with experimental ones. The M_r/Ms ratio at room temperature was lower than 0.5, confirming the predominance of magnetostatic interactions. This paper serves as a good starting point for researchers seeking to synthesize a CoFe₂O₄ system with a desired size and growth tendency at the nanometer scale. Full article

Titanium dioxide (TiO₂) has evolved from a conventional photocatalyst into a sophisticated nano-platform that bridges environmental sustainability and biomedicine. This paper proposes a unified interfacial redox design framework that links the electronic-structure engineering of the TiO₂ with the spatial control of its reactive oxygen species (ROS). In the environmental sector, we highlight advances in photocatalytic detoxification, such as the cleavage of organophosphates via Ag-modified TiO₂, driven by doping and metal–support interactions. In the biomedical domain, TiO₂ is framed as an active bio-interface capable of coordinative protein binding. We specifically examine the “moonlighting” protein dihydrolipoamide dehydrogenase (DLDH) as a model for stable, oriented biofunctionalization. By integrating RGD-targeting motifs, these hybrid systems enable integrin-directed, localized photodynamic effects. We further address critical toxicological considerations, emphasizing that TiO₂ behavior is context-dependent and governed by particle size, crystallinity, and surface state. By synthesizing insights from catalysis and redox biology, this manuscript outlines principles for the rational design of safer, application-specific TiO₂ technologies. This convergence supports a transition from non-selective oxidation toward predictable, spatially confined redox outcomes in both complex environmental matrices and physiological systems. This review outlines key mechanistic insights and proposes design principles for controlled and context-dependent TiO₂ activity. Full article

Deep shale gas reservoirs in the southern Sichuan Basin (Weiyuan area) exhibit strong heterogeneity and complex pore-fracture networks. Traditional reservoir evaluation methods struggle to accurately capture their microscale pore characteristics and fracability, thereby restricting efficient development and precise sweet spot prediction. Therefore, integrating digital core technology with geological analysis is essential to systematically quantify key reservoir parameters, including microscale pore structure, mineral composition, and brittleness characteristics. To clarify the controlling factors of high-quality deep shale gas reservoirs in the Weiyuan area and assess their exploration and development potential, we performed digital core analysis at micron to nanometer scales. Three-dimensional digital core models of representative deep shale gas wells were constructed. Integrating mineral composition, geochemical characteristics, and pore space features, we discuss the geological conditions for deep shale gas accumulation and the fracability of horizontal wells, and we delineate favorable shale reservoir zones. The results show that digital core technology enables quantitative and visual characterization of each sublayer of the Longmaxi Formation shale reservoir, including mineral types, laminae types, pore-throat structures, and organic matter distribution. From the Long 11-1 sublayer to the Long 11-4 sublayer, the pore-throat radius, total pore volume, total throat volume, connected pore-throat percentage, and coordination number all gradually decrease. In the eastern Weiyuan area, the siliceous components in deep shale gas reservoirs at the base of the Longmaxi Formation are primarily of both biogenic and terrigenous origin. Due to local variations in the sedimentary environment, terrigenous input contributes significantly to the total siliceous content in this region. Although the Long 11-1 sublayer of the Longmaxi Formation is lithologically classified as mud shale, its particle size and mineral composition more closely resemble those of clayey siltstone or argillaceous sandstone, suggesting considerable potential for reservoir space development. Typical wells in the eastern Weiyuan area exhibit distinct lithological characteristics, including coarser grain sizes, stronger hydrodynamic conditions during deposition, and abundant terrigenous clastic supply. The rigid framework formed by silt- to sand-sized particles effectively mitigates compaction, thereby facilitating the preservation of intergranular pores and microfractures. High organic matter abundance, appropriate thermal maturity, and a considerable thickness of high-quality shale ensured sufficient hydrocarbon supply. The main types of natural fractures are intergranular and grain-edge fractures formed by differences in sedimentary grain size, and bedding-parallel fractures generated by hydrocarbon generation overpressure. Based on reservoir mineral composition, pore characteristics, areal porosity, and pore size distribution identified via digital core analysis, the bottom 0–3 m of the Long 11-1 sublayer is determined to be the optimal target interval. By delineating the microscopic characteristics of the shale reservoir and predicting rock mechanical parameters, a fracability evaluation index was established from digital core simulations. This guides the selection of target layers in deep shale gas reservoirs and optimizes hydraulic fracturing design. Full article

A lightweight composite that simultaneously exhibits high strength and excellent thermal insulation is of great interest for thermal protection applications. In this study, dimensionally stable needled quartz fiber felt-reinforced phenolic aerogel composites were prepared using vacuum impregnation, sol–gel, and ambient pressure drying. The composites exhibit a multiscale porous structure formed by interconnected nanometer polymer skeletons and micronscale fibers. By regulating the thermoplastic phenolic resin concentration in the precursor solution, the pore structure of the material was refined; the average particle diameter reduced from 99.76 nm to 38.91 nm, and the average pore diameter decreased from 216.79 nm to 49.53 nm. At a phenolic resin concentration of 25%, the composite exhibits outstanding thermal insulation and mechanical properties: a low thermal conductivity of 0.0646 W·m⁻¹·K⁻¹ at room temperature, with a mere 19.5 °C temperature rise on the sample backside after 1800 s heating at 200 °C, and compressive strengths of 7.70 MPa in the XY-direction and 3.87 MPa in the Z-direction (at 10% strain). X-ray micro-CT characterized the internal structural evolution during loading, revealing a failure mechanism dominated by fiber buckling. Theoretical models and experimental data were used to analyze and quantify the contribution rates of gas and solid heat conduction in NQF/PR aerogel composites, with solid conduction accounting for over 80%. Combined with microstructural evolution, the mechanism for the high thermal insulation efficiency of NQF/PR aerogel composites was elucidated. This study prepared NQF/PR aerogel composites with promising application potential. By systematically evaluating their compressive behavior and quantifying the respective contributions of gas and solid conduction, this work provides a methodological framework to guide the rational design of similar aerogel composites. Full article

In micro-opto-electro-mechanical systems (MOEMS), the micro-optical cavity plays a pivotal role. As performance requirements for MOEMS devices continue to rise, these cavities must achieve higher performance levels while simultaneously reducing their physical footprint. However, existing high-precision micro-optical cavities face challenges such as high process sensitivity and conflicting trade-offs between dynamic range and precision. To address these issues, piezoelectric thin-film actuators present a viable solution due to their high precision, stroke flexibility, electromagnetic interference resistance, and structural scalability. This study proposes a piezoelectric thin-film actuator based on the $d_{33}$ mode. The device adopts an island-circular structure that integrates a lead zirconate titanate (PZT) piezoelectric film with metal electrodes. By employing particle swarm optimization (PSO) to enhance displacement output and anti-gravity capabilities, the actuator achieves displacement outputs below 100 nm within a compact form factor while maintaining nanometer-level resolution. Simulation and experimental results confirm a first-order natural frequency of approximately 5.8 kHz, along with a reasonable linear displacement response across a 4–6 V drive voltage range. Furthermore, the device demonstrates functionality within a Fabry–Pérot (F-P) microcavity system, enabling active optical path length modulation through precise cavity tuning. This research provides an effective approach to enhancing the dynamic performance and process compatibility of micro-optical cavity devices, advancing the development of next-generation MOEMS systems. Full article

Transition metal oxides (TMOs) have been recognized as highly prospective anode materials for lithium-ion batteries (LIBs) due to their low cost, high capacity, and distinctive lithiation mechanisms. Nevertheless, their practical adoption is constrained by significant volume changes during lithiation/delithiation, inferior electrical conductivity, severe particle agglomeration, unsatisfactory cycling stability, and limited rate performance. In an effort to mitigate these flaws, we developed a tactic employing a zeolitic imidazolate framework (ZIF) as the self-sacrificing template and tuning the Co/Fe/Ni ratio with a ZIF framework to prepare an innovative trimetallic metal–organic framework (MOF)-derived CoNiO₂/NiCo₂O₄/NiFe₂O₄ compound (CFNO422) with nano/micro hierarchical architecture. The nano/micro hierarchical structure effectively accommodates volume changes, alleviates structural stress, and offers copious active sites for lithium storage. More importantly, the synergistic interaction among multiple component oxides promotes richer redox reactions and enhances electronic conductivity. Benefiting from the structural compatibility and composition, CFNO422 delivers an outstanding reversible capacity (1301.3 mAh g⁻¹ up to 120 cycles at 0.2 A g⁻¹), enhanced rate capability (614.3 mAh g⁻¹ even at 2.0 A g⁻¹), and exceptional cycling stability (527.4 mAh g⁻¹ over 600 cycles at 1.0 A g⁻¹). This research proposes a versatile synthesis for MOF-derived polymetallic oxides as anode materials, opening a new avenue for advanced energy storage. Full article