Search Results (123)

Superhydrophobic micropillar surfaces, inspired by the lotus leaf, have been extensively studied over the past two decades for their self-cleaning, anti-friction, anti-icing, and anti-corrosion properties. In this study, we introduce a simple and effective method for introducing porosity into polydimethylsiloxane (PDMS) micropillar arrays using salt templating. We then evaluate the wetting behaviour of these surfaces before and after infusion with perfluoropolyether (PFPE) oil. Apparent contact angle and sliding angle were measured relative to a non-porous control surface. Across five porous variants, the contact angle decreased by approximately 5° (from 157° to 152° on average), while the sliding angle increased by about 3.5° (from 16.5° to 20° on average). Following PFPE infusion, the porous arrays exhibited reduced sliding angles while maintaining superhydrophobicity. These results indicate that introducing porosity slightly reduces water repellency and droplet mobility, whereas PFPE infusion restores mobility while preserving high water repellency. The change in wettability following PFPE infusion highlights the potential of these surfaces to function as robust, self-cleaning materials. Full article

Easy and rapid preparations of magnetic Co- and Pd-containing mesoporous carbons (IM1, IM2 and DM) from green phenolic resins, amphiphilic templates and metallic salts via two synthetic routes are reported. Catalysts IM1 and IM2 are prepared via an indirect method involving two steps, i.e., the preparation of Co-containing mesoporous carbons with different Co contents (2.5 and 12.5%) and the further introduction of Pd (2.3%) via impregnation using a solution of a Pd salt and a process of thermal reduction. The mesoporous carbon obtained contains two distinct crystalline metallic phases, i.e., Co particles of 5.0 nm (IM1) and Pd nanoparticles of ~1.3 nm (IM1), while the increase in Co content triggers higher Co particle sizes of 23 nm and Pd particle sizes of 1.3 and 6.8 nm (IM2). Differently, the catalyst DM is prepared via direct synthesis, in one step, including all precursors and both metal salts. This results in Pd₅₀-Co₅₀ nanoalloys of 6.5 nm uniformly dispersed in the carbon matrix. The reactivity and reusability of catalysts IM1, IM2 and DM were then ascertained in organic synthesis for hydrogenations of nitroarenes and enones. It turned out that no reactions were observed in the presence of the catalyst DM due to the presence of Co in Pd₅₀-Co₅₀, which deactivates the catalytic activity of Pd. Gratifyingly, catalysts IM1 and IM2 were very efficient for mild hydrogenations of both nitroarenes and enones using only 5 mequiv. of supported Pd in EtOH at room temperature. The smaller Pd particle sizes (1.3 nm) and the high surface-to-volume area are probably responsible for the high reactivity observed. Catalysts IM1 and IM2 can be recovered by application of an external magnetic field. However, a more efficient magnetic recovery of catalyst IM2 compared to IM1 was observed due to its higher Co content. Catalyst IM2 can be successfully reused at least seven times without a loss of efficiency. Finally, almost-Pd-free products can be obtained directly after reaction without any purification step, since the Pd leaching is very low (<0.1% of the initial amount), thus decreasing waste and increasing the reaction’s efficiency. Full article

Electrostriction is an intriguing behaviour of dielectric materials, characterized by stable electrostrain with minimal hysteresis. (Na_0.5Bi_0.5)TiO₃-based ceramics show promising electrostrictive behaviour, particularly the 0.90(Na_0.5Bi_0.5)TiO₃-0.08KNbO₃-0.02SrTiO₃ composition located near the morphotropic phase boundary between ferroelectric rhombohedral and relaxor pseudocubic phases. The templated grain growth method has been effectively used to control the grain orientation of NBT-based systems, thereby enhancing their electrical properties. In this study, texturing was introduced to 0.90(Na_0.5Bi_0.5)TiO₃-0.08KNbO₃-0.02SrTiO₃ ceramics through homoepitaxial NBT platelets prepared via a three-step molten salt/topochemical microcrystal conversion method. By adding 4 wt% of NBT platelets combined with optimized sintering conditions, textured ceramics were prepared exhibiting a high Lotgering factor of 83% with enhancement of strain (0.02%) and polarization (3 µC/cm²) at an electric field of 40 kV/cm, as well as stable dielectric permittivity between 130 and 300 °C. Moreover, the electrostrictive coefficient of textured ceramics increased by ~0.004 C²m⁻⁴ compared to that of untextured ceramics, confirming the improvement of the electrostrictive response. These results demonstrate that homoepitaxial templating effectively improves the electrical properties of NBT-KN-ST ceramics while preserving their electrostrictive nature, which offers a viable route for designing lead-free electrostrictive materials. Full article

This bioinformatic study provides a comprehensive theoretical assessment of oxalate-degrading enzymes in probiotics. Kidney stone disease is a common urological disorder with rising global incidence, largely driven by the precipitation of insoluble calcium oxalate salts. Current treatments—including thiazides, lithotripsy, or ultrasound fragmentation—often show variable outcomes and high recurrence rates. Here, we systematically assessed the oxalate-degrading potential of 38 probiotic species listed in the List of Cultures Available in Food (China National Health Commission) along with selected next-generation probiotics. Using BLASTp homology searches, we identified seven strains carrying both oxalyl-CoA decarboxylase (OXC) and formyl-CoA transferase (FRC) genes, one encoding oxalate decarboxylase (OXDC), and three harboring subunits of oxalate oxidoreductase (OOR). Additionally, seven species from international probiotic lists (EFSA QPS and AEProbio) were analyzed, among which two carry both OXC and FRC genes. We prioritized strains with the coupled OXC-FRC pathway or OOR enzymes, examined catalytic site conservation by multiple sequence alignment, and performed AlphaFold-based structural prediction with Template Modeling (TM)-align scoring. Species with TM-scores >0.8 exhibited highly conserved folds, suggesting functional oxalate degradation capacity. These findings provide theoretical guidance for identifying probiotic candidates with oxalate-degrading activity and establish a framework for developing next-generation functional probiotics to alleviate kidney stone disease. Full article

This study introduces novel experimental systems that facilitate the nucleation, growth, aggregation, and agglomeration of ionic salt solutions, leading to structurally and functionally distinctive crystal formations. Through evaporative crystallization in hanging drops—including layered binary solutions—a range of macroscopic agglomerates were produced, such as hollow spheroidal NaCl/NiSO₄ structures, octahedral NaCl films, pentagonally arranged CdSO₄ spherulites, and NH₄Cl dendritic shells. Additionally, NaCl spheroids were used as templates to fabricate carbon-based morphologies and colloidal photonic crystals with convex or concave geometries, which were subsequently analyzed optically. The study reveals that crystallization and self-assembly, whether independently or synergistically applied, can yield complex architectures with potential applications in advanced device manufacturing beyond conventional processing methods. Full article

This work demonstrates the potential of polydimethylsiloxane sponges for removing organic UV filter compounds such as octinoxate from aqueous solutions. The sponges were fabricated using simple templates made of hydrophilic fused or pressed particles (sugar or NaCl salt) with an approximate particle size of 0.4 mm. Among the prepared sponges, those templated with sugar cubes or coarse salt exhibited the highest adsorption capacity, effectively adsorbing up to 0.6% of their own mass in octinoxate. The PDMS sponges were fully regenerable, allowing for the complete removal of octinoxate without any detectable changes in their adsorption properties or dry weight. Due to their simple fabrication, ease of handling, ability to float, and reusability, PDMS sponges present an environmentally friendly and low-maintenance alternative to conventional filtration systems for the removal of octinoxate and potentially other UV filter compounds from environmental surface waters and recreational water bodies. Full article

Coastal blue carbon ecosystems (traditional types such as mangroves, salt marshes, and seagrass meadows; emerging types such as tidal flats and mariculture) play pivotal roles in capturing and storing atmospheric carbon dioxide. Reliable assessment of the spatial and temporal variation and the carbon storage potential holds immense promise for mitigating climate change. Although previous field surveys and regional assessments have improved the understanding of individual habitats, most studies remain site-specific and short-term; comprehensive, multi-decadal assessments that integrate all major coastal blue carbon systems at the national scale are still scarce for China. In this study, we integrated 30 m Landsat imagery (1992–2022), processed on Google Earth Engine with a random forest classifier; province-specific, literature-derived carbon density data with quantified uncertainty (mean ± standard deviation); and the InVEST model to track coastal China’s mangroves, salt marshes, tidal flats, and mariculture to quantify their associated carbon stocks. Then the GeoDetector was applied to distinguish the natural and anthropogenic drivers of carbon stock change. Results showed rapid and divergent land use change over the past three decades, with mariculture expanded by 44%, becoming the dominant blue carbon land use; whereas tidal flats declined by 39%, mangroves and salt marshes exhibited fluctuating upward trends. National blue carbon stock rose markedly from 74 Mt C in 1992 to 194 Mt C in 2022, with Liaoning, Shandong, and Fujian holding the largest provincial stock; Jiangsu and Guangdong showed higher increasing trends. The Normalized Difference Vegetation Index (NDVI) was the primary driver of spatial variability in carbon stock change (q = 0.63), followed by precipitation and temperature. Synergistic interactions were also detected, e.g., NDVI and precipitation, enhancing the effects beyond those of single factors, which indicates that a wetter climate may boost NDVI’s carbon sequestration. These findings highlight the urgency of strengthening ecological red lines, scaling climate-smart restoration of mangroves and salt marshes, and promoting low-impact mariculture. Our workflow and driver diagnostics provide a transferable template for blue carbon monitoring and evidence-based coastal management frameworks. Full article

This study presents the development of a TiO₂ nanowire-based electrochemical sensor for the selective and sensitive detection of hydrogen peroxide (H₂O₂) under neutral pH conditions, with a particular focus on its application in analyzing plant stress. The sensor exhibited a linear detection range of 0–0.5 mM, a sensitivity of 0.0393 mA · mM⁻¹, and a detection limit of 2.8 μM in phosphate-buffered saline solution (PBS, pH 7.4). This work’s main novelty lies in the systematic investigation of the relationship between TiO₂ nanostructure morphology, which is controlled by hydrothermal synthesis parameters, and the resulting sensor performance. Interference studies confirmed excellent selectivity in the presence of common electroactive species found in plant samples, such as NaCl, KNO₃, glucose, citric acid, and ascorbic acid. Real sample analysis using barley plant extracts grown under salt stress and treated with Fe₃O₄ nanoparticles confirmed the sensor’s applicability in complex biological matrices, enabling accurate quantification of endogenously produced H₂O₂. Endogenous H₂O₂ concentrations were found to range from near-zero levels in control and Fe₃O₄-only treated plants, to elevated levels of up to 0.36 mM in salt-stressed samples. These levels decreased to 0.25 and 0.15 mM upon Fe₃O₄ nanoparticle treatment, indicating a dose-dependent mitigation of stress. This finding was supported by genome template stability (GTS) analysis, which revealed improved DNA integrity in Fe₃O₄-treated plants. This study takes an integrated approach, combining the development of a nanostructured sensor with physiological and molecular stress assessment. The urgent need for tools to detect stress at an early stage and manage oxidative stress in sustainable agriculture underscores its relevance. Full article

This study investigates the use of a salt template to synthesize mesoporous bioactive glass (MBG). Different salts were used as hard templates to create pores in the glass structure to investigate the possibility of using acid-soluble salt templates and to understand the properties of glass synthesized without thermal treatment. The MBGs were synthesized in a TRIS buffer solution at a pH of 9.5 to allow hydrolysis of the metal oxide precursors. The glass was then washed with mild acid to remove the template. After the samples were washed, some were subjected to thermal treatment, while others were not to investigate the impact of thermal treatment on the structure of the MBG. The successful synthesis of MBG was confirmed by X-ray diffraction, Fourier-transfer infrared spectroscopy, scanning emission scanning microscope, and nitrogen adsorption–desorption analysis. This synthesized MBG had a large surface area, pore volume, pore size, and high drug loading efficiency. MBG synthesized without thermal treatment had slower degradation over the test period, but higher loading efficiency and slower drug release, making it appropriate for applications requiring long-term drug delivery while maintaining its bioactivity. Full article

This study develops a one-pot anodic templating electrodeposition strategy using dual-cation-crosslinking and interpenetrating networks, coupled with pulsed electrical signals, to fabricate a vessel-mimetic multilayered tubular hydrogel. Typically, the anodic electrodeposition is performed in a mixture of sodium alginate (SA) and carboxymethyl chitosan (CMC), with the ethylenediaminetetraacetic acid calcium disodium salt hydrate (EDTA·Na₂Ca) incorporated to provide a secondary ionic crosslinker (i.e., Ca²⁺) and modulate the cascade reaction diffusion process. The copper wire electrodes serve as templates for electrochemical oxidation and enable a copper ion (i.e., Cu²⁺)-induced tubular hydrogel coating formation, while pulsed electric fields regulate layer-by-layer deposition. The dual-cation-crosslinked interpenetrating hydrogels (CMC/SA-Cu/Ca) exhibit rapid growth rates and tailored mechanical strength, along with excellent antibacterial performance. By integrating the unique pulsed electro-fabrication with biomimetic self-assembly, this study addresses challenges in vessel-mimicking structural complexity and mechanical compatibility. The approach enables scalable production of customizable multilayered hydrogels for artificial vessel grafts, smart wound dressings, and bioengineered organ interfaces, demonstrating broad biomedical potential. Full article

The incorporation of MAX phase interface layers into silicon carbide (SiC) composites has been shown to significantly enhance mechanical properties, particularly under irradiation conditions. However, conventional Ti-based MAX phases suffer from thermal instability and tend to decompose at high temperatures. In this work, an Sc₂SnC coating was successfully synthesized onto the surface of SiC fibers (SiC_f) via an in situ reaction between metals and pyrolytic carbon (PyC) in a molten salt environment. The PyC layer, pre-deposited by chemical vapor deposition (CVD), served as both a carbon source and a structural template. Characterization by SEM, XRD, and Raman spectroscopy confirmed the formation of Sc₂SnC coatings with a distinctive hexagonal flake-like morphology, accompanied by an internal ScC_x intermediate layer. By turning the Sc-to-Sn ratio in the molten salt, coatings with varied morphologies were achieved. ScC_x was identified as a critical intermediate phase in the synthesis process. The formation of numerous defects during the reaction enhanced element diffusion, resulting in preferential growth orientations and diverse grain structures in the Sc₂SnC coating. Full article

With the depletion of solid lithium ore, extracting lithium from salt lake brine has become a critical focus for future endeavors. A four-step method was used to synthesize high-purity H_1.6Mn_1.6O₄ for extracting Li⁺. Porous cubic Mn₂O₃ was hydrothermally synthesized with carbon spheres and surfactants as templates. Then, it was converted to LiMnO₂ by calcining with Li₂CO₃. After roasting and acid pickling, H_1.6Mn_1.6O₄ was successfully synthesized. The impacts of calcination temperature, Li/Mn molar ratio and glucose addition on LiMnO₂ composition, loss percentage of dissolved Mn in precursor, and the adsorption characteristics of the lithium ion sieve were studied. Glucose inhibited the formation of LiMn₂O₄ and promoted the formation of pure LiMnO₂. The resulting precursor without impurities showed porous structure. After acid pickling, H_1.6Mn_1.6O₄ showed a high-adsorption performance and excellent cycle performance. After five cycles, adsorption capacity remained above 30 mg/g, and the loss percentage of dissolved Mn stabilized at about 1%. The Li⁺–H⁺ exchange conformed to pseudo-second-order adsorption dynamics and the Langmuir adsorption isotherm equation, indicating that the adsorption process can be classified as monolayer chemical adsorption. Full article

The sodium/proton exchanger NHA2, also known as SLC9B2, is important for insulin secretion, renal blood pressure regulation, and electrolyte retention. Recent structures of bison NHA2 has revealed its unique 14-transmembrane helix architecture, which is different from SLC9A/NHE members made up from 13-TM helices. Sodium/proton exchangers are functional homodimers, and the additional N-terminal helix in NHA2 was found to alter homodimer assembly. Here, we present the cryo-electron microscopy structures of apo human NHA2 in complex with a Fab fragment and also with the inhibitor phloretin bound at 2.8 and 2.9 Å resolution, respectively. We show how phosphatidic acid (PA) lipids bind to the homodimer interface of NHA2 on the extracellular side, which we propose has a regulatory role linked to cell volume regulation. The ion binding site of human NHA2 has a salt bridge interaction between the ion binding aspartate D278 and R432, an interaction previously broken in the bison NHA2 structure, and these differences suggest a possible ion coupling mechanism. Lastly, the human NHA2 structure in complex with phloretin offers a template for structure-guided drug design, potentially leading to the development of more selective and potent NHA2 inhibitors. Full article

Significant research has focused on cost–effective, highly active, and exceptionally stable non–noble metal electrocatalysts (NNMEs) to boost the performance of the oxygen reduction reaction (ORR). Of note, the development of design and synthesis of Fe–N–C electrocatalysts is essential but remains challenging. Herein, the Fe and N co–doped porous carbon material with a yolk–shell (YS) structure, termed SA–H₂TPyP@PDA–Fe (900), was fabricated by self–assembly of metal–free porphyrin as a yolk and polymerization of dopamine as a shell with an addition of iron salts, followed by the high–temperature pyrolysis and acid–leaching. As a result, active sites, like FeN₄ and N–doped C, within rich porous YS carbon structures, play an important role for ORR in an alkaline media. The SA–H₂TPyP@PDA–Fe (900) electrocatalyst shows positive ORR performances than those of SA–H₂TPyP (900) and SA–H₂TPyP@PDA (900), indicating the dominating function of the YS carbon structure decorated with Fe–based species. This efficient route of template–free–induced preparation of the YS structure discovers the design and synthesis of NNMEs for ORR. Full article

Nb-Sn, V-Sn mixed-metal oxides and Nb-Si, V-Si metal oxide–silicas were successfully synthesized through a “soft” templating method, in which appropriate amounts of metal salts (either niobium(V) chloride, or vanadium(IV) oxide sulfate hydrate or tin(II) chloride dihydrate) or tetraethyl orthosilicate (TEOS) were mixed with hexadecyltrimethylammonium chloride (HDTA) or sodium dodecyl sulfate (SDS) solutions to obtain a new series of mesoporous oxides, followed by calcination at different temperatures. As-obtained samples were characterized by SEM, TEM, XRD, and UV-Vis spectra techniques. The photocatalytic activities of the samples were evaluated by degradation of methyl orange II (MO) under simulated sunlight irradiation. The effects of metal species and calcination temperature on the physicochemical characteristic and photocatalytic activity of the samples were investigated in detail. The results indicated that, compared to pure oxides, mixed-metal oxide showed superior photocatalytic performance for the degradation of MO. A maximum photocatalytic discoloration rate of 97.3% (with MO initial concentration of 0.6·10⁻⁴ mol/dm³) was achieved in 300 min with the NbSiOx material, which was much higher than that of Degussa P25 under the same conditions. Additionally, the samples were tested in the photochemical oxidation process, i.e., advanced oxidation processes (AOPs) to treat the commercial non-ionic surfactant: propylene oxide ethylene oxide polymer mono(nonylphenyl) ether (N8P7, PCC Rokita). A maximum of 99.9% photochemical degradation was achieved in 30 min with the NbSiOx material. Full article