Search Results (2,009)

Hydrogel scaffolds have emerged as pivotal materials in regenerative medicine due to their biocompatibility, tunable mechanical properties, and ability to mimic the extracellular matrix. However, conventional fabrication techniques often lack the precision required to create complex architectures, limiting their effectiveness in tissue engineering. This review explores advanced laser-based fabrication methods, such as two-photon polymerization, laser-induced forward transfer, selective laser sintering/melting, and laser direct writing, which offer unparalleled resolution and control over scaffold geometry. These techniques enable the production of intricate 3D structures tailored to specific clinical needs, from vascular networks to patient-specific implants. We analyze the principles, advantages, and limitations of each method, highlighting their biomedical applications and the challenges of scalability, material compatibility, and cost. By bridging the gap between laboratory research and clinical implementation, laser-based technologies hold significant promise for advancing personalized medicine and tissue regeneration. Full article

In this study, a dynamically tunable terahertz device based on a VO₂–graphene hybrid metasurface is proposed, which realizes the dual functions of ultra-wideband absorption and efficient transmission through VO₂ phase transformation. At 345 K (metallic state), the device attains an absorption efficiency exceeding 90% (average 97.06%) in the range of 2.25–6.07 THz (bandwidth 3.82 THz), showing excellent absorption performance. At 318 K (insulated state), the device achieves 67.66–69.51% transmittance in the 0.1–2.14 THz and 7.51–10 THz bands while maintaining a broadband absorption of 3.6–5.08 THz (an average of 81.99%). Compared with traditional devices, the design breaks through the performance limitations by integrating phase change material control with 2D materials. The patterned graphene design simplifies the fabrication process. System analysis reveals that the device is polarization-insensitive and tunable via graphene Fermi energy and relaxation time. The device’s excellent temperature response and wide angular stability provide a novel solution for terahertz switching, stealth technology, and sensing applications. Full article

Particle accelerators are powerful tools in fundamental research, medicine, and industry that provide high-energy beams that can be used to study matter and to enable advanced applications. The state-of-the-art particle accelerators are fundamentally constructed from superconducting radio-frequency (SRF) cavities, which act as resonant structures for the acceleration of charged particles. The performance of such cavities is governed by inherent superconducting material properties such as the transition temperature, critical fields, penetration depth, and other related parameters and material quality. For the last few decades, bulk niobium has been the preferred material for SRF cavities, enabling accelerating gradients on the order of ~50 MV/m; however, its intrinsic limitations, high cost, and complicated manufacturing have motivated the search for alternative strategies. Among these, sputter-deposited superconducting thin films offer a promising route to address these challenges by reducing costs, improving thermal stability, and providing access to numerous high-T_c superconductors. This review focuses on progress in sputtered superconducting materials for SRF applications, in particular Nb, NbN, NbTiN, Nb₃Sn, Nb₃Al, V₃Si, Mo–Re, and MgB₂. We review how deposition process parameters such as deposition pressure, substrate temperature, substrate bias, duty cycle, and reactive gas flow influence film microstructure, stoichiometry, and superconducting properties, and link these to RF performance. High-energy deposition techniques, such as HiPIMS, have enabled the deposition of dense Nb and nitride films with high transition temperatures and low surface resistance. In contrast, sputtering of Nb₃Sn offers tunable stoichiometry when compared to vapour diffusion. Relatively new material systems, such as Nb₃Al, V₃Si, Mo-Re, and MgB₂, are just a few of the possibilities offered, but challenges with impurity control, interface engineering, and cavity-scale uniformity will remain. We believe that future progress will depend upon energetic sputtering, multilayer architectures, and systematic demonstrations at the cavity scale. Full article

The prompt and reliable detection of NH₃ leakage at room temperature (RT) is considered important for safety assurance and sustainable production. Although chemiresistive NH₃ sensors feature low cost and structural simplicity, their practical application is hindered by high operating temperatures and inadequate selectivity. Metal–organic frameworks (MOFs) and their derivatives offer a promising approach to address these limitations. In this work, Ce-BDC precursors with tunable particle sizes and crystallinity were synthesized by adjusting the raw material concentration. Controlled pyrolysis yielded a series of CeO₂-C-X (X = 0.5, 1, 1.5, 2) materials with nanosized particles. Among them, the CeO₂-C-1 sensor delivered a high response of 82% toward NH₃ under 40% relative humidity at RT. Moreover, it possessed excellent selectivity, repeatability, and rapid response-recovery behavior compared with the other samples. CeO₂-C-1 also remained stable under varying oxygen and humidity conditions, demonstrating high applicability. The superior sensing properties may be attributed to its high specific surface area and optimized mesoporous structure, which facilitated efficient gas adsorption and reaction. These findings demonstrated that precise control of MOF precursors and the structure in CeO₂ nanomaterials was critical for achieving high-performance gas sensing and established Ce-MOF-derived CeO₂ as a promising sensing material for NH₃ detection at RT. Full article

Hydrogels are hydrophilic, soft polymer networks with high water content and mechanical properties that are tunable; they are also biocompatible. Therefore, as biomaterials, they are of interest to modern medicine. In this review, the main applications of hydrogels in essential clinical applications are discussed. Chemical, physical, or hybrid crosslinking of either synthetic or natural polymers allow for the precise control of hydrogels’ physicochemical properties and their specific characteristics for certain applications, such as stimuli-responsiveness, drug retention and release, and biodegradability. Hydrogels are employed in gynecology to regenerate the endometrium, treat infections, and prevent pregnancy. They show promise in cardiology in myocardial infarction therapy through injectable scaffolds, patches in the heart, and medication delivery. In rheumatoid arthritis, hydrogels act as drug delivery systems, lubricants, scaffolds, and immunomodulators, ensuring effective local treatment. They are being developed, among other applications, as antimicrobial coatings for stents and radiotherapy barriers for urology. Ophthalmology benefits from the use of hydrogels in contact lenses, corneal bandages, and vitreous implants. They are used as materials for chemoembolization, tumor models, and drug delivery devices in cancer therapy, with wafers of Gliadel presently used in clinics. Applications in abdominal surgery include hydrogel-coated meshes for hernia repair or Janus-type hydrogels to prevent adhesions and aid tissue repair. Results from clinical and preclinical studies illustrate hydrogels’ diversity, though problems remain with mechanical stability, long-term safety, and mass production. Hydrogels are, in general, next-generation biomaterials for regenerative medicine, individualized treatment, and new treatment protocols. Full article

The exponential increase in environmental pollutants due to industrialization, urbanization, and agricultural intensification has underscored the urgent need for sensitive, selective, and real-time monitoring technologies. Among emerging analytical tools, organic fluorescent sensors have demonstrated exceptional potential for detecting a wide range of pollutants in water, air, and soil, with a limit of detection (LOD) in the pM–µM range. This review critically examines recent advances in organic fluorescent sensors, focusing on their photophysical properties, molecular structures, sensing mechanisms, and environmental applications. Key categories of organic sensors, including small molecules, polymeric materials, and nanoparticle-based systems, are discussed, highlighting their advantages, such as biocompatibility, tunability, and cost-effectiveness. Comparative insights into inorganic fluorescent sensors, including quantum dots, are also provided, emphasizing their superior photostability and wide operating range (in some cases from pg/mL up to mg/mL) but limited biodegradability and higher toxicity. The integration of nanomaterials and microfluidic systems is presented as a promising route for developing portable, on-site sensing platforms. Finally, the review outlines current challenges and future perspectives, suggesting that fluorescent sensors, particularly organic ones, represent a crucial strategy toward sustainable environmental monitoring and pollutant management. Full article

Yield stress and thixotropy are critical rheological properties for enabling successful 3D printing of magnetic colloidal systems. However, conventional magnetic colloids, typically composed of a single dispersed phase, exhibit insufficient rheological tunability for reliable 3D printing. In this study, we developed a novel magnetic colloidal system comprising a carrier liquid, magnetic nanoparticles, and organic modified bentonite. A direct-ink-writing 3D-printing platform was specifically designed and optimized for thixotropic materials, incorporating three distinct extruder head configurations. Through an in-depth rheological investigation and printing trials, quantitative analysis revealed that the printability of magnetic colloids is significantly affected by multiple factors, including magnetic field strength, pre-shear conditions, and printing speed. Furthermore, we successfully fabricated 3D architectures through the precise coordination of deposition paths and magnetic field modulation. This work offers initial support for the material’s future applications in soft robotics, in vivo therapeutic systems, and targeted drug delivery platforms. Full article

This paper provides a systematic review of the latest advancements in metal-organic frameworks (MOFs) and covalent organic frameworks (COFs) for electrocatalytic carbon dioxide reduction. Both materials exhibit high specific surface areas, tunable pore structures, and abundant active sites. MOFs enhance CO₂ conversion efficiency through improved conductivity, optimized stability, and selective regulation—including bimetallic synergy, pulse potential strategies, and tandem catalysis. COFs achieve efficient catalysis through precise design of single or multi-metal active sites, optimization of framework conjugation, and photo/electro-synergistic systems. Both types of materials demonstrate excellent selectivity toward high-value-added products (CO, formic acid, C₂⁺ hydrocarbons), but they still face challenges such as insufficient stability, short operational lifespan, high scaling-up costs, and poor electrolyte compatibility. Future research should integrate in situ characterization with machine learning to deepen mechanistic understanding and advance practical applications. Full article

Strong coupling between plasmons and excitons in two-dimensional materials offers a powerful route for manipulating light–matter interactions at the nanoscale, with potential applications in quantum optics, nanophotonics, and polaritonic devices. Here, we design and numerically investigate a low-loss coupling platform composed of a silver nanocuboid dimer and monolayer of WS₂ using finite-difference time-domain (FDTD) simulations. The dimer supports a subradiant bonding plasmonic mode with a linewidth as narrow as 60 meV. This ultralow-loss feature enables strong coupling with monolayer WS₂ at relatively low coupling strengths. FDTD simulations combined with the coupled oscillator model reveal a Rabi splitting of ~60 meV and characteristic anticrossing behavior in the dispersion relations. Importantly, we propose and demonstrate two independent tuning mechanisms—loss engineering through nanocuboid tilt and coupling-strength modulation through the number of WS₂ layers—that enable transitions between weak and strong coupling regimes. This work provides a low-loss and tunable plasmonic platform for studying and controlling strong light–matter interactions in plasmon-two-dimensional material systems, with potential for room-temperature quantum and optoelectronic devices. Full article

Cobalt-doped iron disulfide (FeS₂) thin films were synthesized via chemical bath deposition (CBD) followed by annealing at 450 °C, yielding phase-pure pyrite structures with multifunctional properties. A deposition temperature of 95 °C is critical for promoting Co incorporation, suppressing sulphur vacancies, and achieving structural stabilization of the film. After annealing, the dendritic morphologies transformed into compact quasi-spherical nanoparticles (~100 nm), which enhanced the crystallinity and optoelectronic performance of the films. The films exhibited strong absorption (>50%) in the visible and near-infrared regions and tunable direct bandgaps (1.14 to 0.96 eV, within the optimal range for single-junction solar cells. Electrical characterization revealed a fourth-order increase in conductivity after annealing (up to 4.78 Ω⁻¹ cm⁻¹) and confirmed stable p-type behavior associated with Co²⁺-induced acceptor states and defect passivation. These results demonstrate that CBD enabled the fabrication of Co-doped FeS₂ thin films with synergistic structural, electrical, and optical properties. The integration of earth-abundant elements and tunable electronic properties makes these films promising absorber materials for the next-generation photovoltaic devices. Full article

We report combined scanning probe microscopy and electrical measurements to investigate local electronic transport in reduced graphene oxide (rGO) devices. We demonstrate that quantum transport in these materials can be significantly tuned by the electrostatic potential applied with a conducting atomic force microscope (AFM) tip. Scanning gate microscopy (SGM) reveals a clear p-type response in which local gating modulates the source–drain current, while scanning impedance microscopy (SIM) indicates corresponding shifts of the Fermi level under different gating conditions. The observed transport behavior arises from the combined effects of AFM tip-induced Fermi-level shifts and defect-mediated scattering. These results show that resonant scattering associated with impurities or structural defects plays a central role and highlight the strong influence of local electrostatic potentials on rGO conduction. Consistent with this electrostatic control, the device also exhibits chemical gating and sensing: during exposure to electron-withdrawing molecules (acetone), the source–drain current increases reversibly and returns to baseline upon purging with air. Repeated cycles over 15 min show reproducible amplitudes and recovery. Using a simple transport model, we estimate an increase of about $40\%$ in carrier density during exposure, consistent with p-type doping by electron-accepting analytes. These findings link nanoscale electrostatic control to macroscopic sensing performance, advancing the understanding of charge transport in rGO and underscoring its promise for nanoscale electronics, flexible chemical sensors, and tunable optoelectronic devices. Full article

In complex electromagnetic environments, traditional static absorbers struggle to meet dynamic control requirements. Tunable absorbers based on metasurfaces have emerged as a research hotspot due to their ability to flexibly control electromagnetic wave properties. This paper provides a systematic review of research progress in tunable absorbers across the microwave, terahertz, and infrared bands, with a focus on analyzing the physical mechanisms, material systems, and performance characteristics of five dynamic control methods: electrical control, magnetic control, optical control, temperature control, and mechanical control. Electrical control achieves rapid response through materials such as graphene and varactor diodes; magnetic control utilizes ferrites and other materials for stable tuning; optical control relies on photosensitive materials for ultrafast switching; temperature control employs phase-change materials for large-range reversible regulation; and mechanical control expands tuning freedom through structural deformation. Research indicates that multi-band compatibility faces challenges due to differences in structural scale and physical mechanisms, necessitating the integration of emerging materials and synergistic control strategies. This paper summarizes the core performance metrics and typical applications of absorbers across various bands and outlines future development directions such as multi-field synergistic control and low-power design, providing theoretical references and technical pathways for the development of intelligent tunable absorber devices. Full article

Microfluidic methods are powerful platforms for synthesizing advanced functional materials because they allow for precise control of microscale reaction environments. Microfluidics manipulates reactants in lab-on-a-chip systems to enable the fabrication of highly uniform materials with tunable properties, which are crucial for drug delivery, diagnostics, catalysis, and nanomaterial design. This review emphasizes recent progress in microfluidic technologies for synthesizing functional materials, with a focus on polymeric, hydrogel, lipid-based, and inorganic particles. Microfluidics provides exceptional control over the size, morphology, composition, and surface chemistry of materials, thereby enhancing their performance through uniformity, tunability, hierarchical structuring, and on-chip functionalization. Our review provides novel insights by linking material design strategies with fabrication methods tailored to biomedical applications. We also discuss emerging trends, such as AI-driven optimization, automation, and sustainable microfluidic practices, offering a practical and forward-looking perspective. As the field advances toward robust, standardized, and user-friendly platforms, microfluidics has the potential to increase industrial adoption and enable on-demand solutions in nanotechnology and personalized medicine. Full article

This study introduces an efficient, all-aqueous emulsion-templating strategy for fabricating highly tunable yeast immobilization carriers with superior biocatalytic performance. Utilizing cellulose nanocrystals (CNCs) to stabilize dextran/polyethylene glycol (Dex/PEG) water-in-water emulsions, an architecture-controlled void is obtained by crosslinking the PEG-rich phase with variable concentrations of polyethylene glycol diacrylate (PEGDA) (10–25 wt%). This approach successfully yielded macroporous networks, enabling precise tuning of void diameters from 10.4 to 6.6 μm and interconnected pores from 2.2 to 1.4 μm. The optimally designed carrier, synthesized with 15 wt% PEGDA, featured 9.6 μm voids and robust mechanical strength (0.82 MPa), and facilitated highly efficient yeast encapsulation (~100%). The immobilized yeast demonstrated exceptional fermentation activity, remarkable storage stability (maintaining > 95% productivity after 4 weeks), and high reusability (85% activity retention after seven cycles). These enhancements are attributed to the material’s excellent water retention capacity and the provision of a stable microenvironment. This green and straightforward method represents a significant advance in industrial cell immobilization, offering unparalleled operational stability, protection, and design flexibility. Full article

Intrinsically stretchable polymer ionic conductors (PICs) hold significant application prospects in fields such as flexible sensors, energy storage devices, and wearable electronic devices, serving as promising solutions to prevent mechanical failure in flexible electronics. However, the development of PICs is hindered by an inherent trade-off between mechanical robust and electrical properties. Cellulose, renowned for its high mechanical strength, tunable chemical groups, abundant resources, excellent biocompatibility, and remarkable recyclability and biodegradability, offers a powerful strategy to decouple and enhance mechanical and electrical properties. This review presents recent advances in cellulose-based polymer ionic conductors (CPICs), which exhibit exceptional design versatility for flexible electrodes and strain sensors. We systematically discuss optimization strategies to improve their mechanical properties, electrical conductivity, and environmental stability while analyzing the key factors such as sensitivity, gauge factor, strain range, response time, and cyclic stability, where strain sensing refers to a technique that converts tiny deformations (i.e., strain) of materials or structures under external forces into measurable physical signals (e.g., electrical signals) for real-time monitoring of their deformation degree or stress state. Full article