Search Results (1,245)

The construction sector faces the dual challenge of reducing energy consumption and mitigating the environmental burden of construction and demolition waste (CDW). Geopolymers offer a low-carbon alternative to Portland cement, yet their performance depends strongly on precursor composition. This study presents an extensive investigation of precursor chemistry, mechanical performance and phase composition, focusing on the partial substitution of ground granulated blast furnace slag (GGBFS) with mechanically activated CDW powder (15% and 30% by weight) alongside fly ash (FA). The oxide composition, amorphous content and particle size distribution were analyzed, using XRF, XRD and laser diffraction to evaluate the reactivity. Mortar samples were subsequently synthesized and tested for compressive and flexural strength, ultrasonic pulse velocity, density and porosity. The results demonstrate that while mechanically activated CDW incorporation decreases early strength compared with GGBFS-rich systems, compressive strengths above 45 MPa were attained at 28 days, with continuous improvement to >69 MPa for aged composites. The relationship between precursor chemistry, precursor sizes and mechanical performance highlights the feasibility of CDW valorization in geopolymer binders, contributing to energy efficiency, circular economy strategies and sustainable construction materials. Full article

Double complex salts (DCSs) of the composition [Co(NH₃)₆][Fe(CN)₆] are a promising precursor for the preparation of catalysts for the hydrogenation of carbon oxides (CO and CO₂) by Fischer–Tropsch synthesis. The specific surface area is an important parameter for catalysts. Our article investigates the influence of mechanochemical activation (MCA) on this DCS in order to determine the conditions for obtaining the largest specific surface area of the intermetallic compound, a product of the DCS thermolysis. In this work, the effect of MCA on the physicochemical properties of the DCS [Co(NH₃)₆][Fe(CN)₆] and the products of its thermal decomposition in an argon atmosphere were investigated. It was shown that MCA leads to partial reduction of Fe⁺³ to Fe⁺², changes in the coordination of ammonia, amorphization of the structure and a decrease in the thermal stability of DCS. Thermolysis at 650 °C of samples subjected to MCA for 10 min results in the formation of nanocrystalline intermetallic compound Co_0.5Fe_0.5. The results demonstrate the potential of using MCA to control the properties of functional materials based on DCS. Full article

Thermochromic VO₂ crystalline domains have been formed in amorphous nanocolumnar VO_x films by means of a low-temperature oxidation process. The oxidation of an amorphous film with [O]/[V] below 1.9 favors the formation of VO₂, V₃O₇, and V₂O₅ crystalline domains in the material for temperatures as low as 260 °C, while values above 1.9 lead to the sole formation of the V₂O₅ phase. It is found that the absorption of oxygen also causes a relevant film volume expansion that makes pores shrink. Under some specific conditions, low-temperature oxidation causes the near disappearance of the amorphous regions, clearly improving the overall transparency and optimizing the optical and electrical modulation capabilities associated with the presence of crystalline VO₂ domains. The best thermochromic performance was found when the original stoichiometry was [O]/[V] = 1.5 and the oxidation temperature was 280 °C. These conditions yield a relatively transparent coating in the visible range that presents an optical modulation in the near-infrared range of nearly 50% and a drop of electrical resistivity of more than two orders of magnitude, with a transition temperature of 50.3 °C. A tentative model based on the volume expansion experienced by the film upon oxidation is proposed, which links the structural/chemical features of the material and the formation of the crystalline domains at such relatively low temperatures. Full article

Both organic matter and iron oxide (FeO) dynamics pose key roles in soil cadmium (Cd) bioavailability. However, the microbially driven transformation of soil organic matter and FeO and their linkages to Cd fractions remain unclear under reductive soil disinfestation (RSD) with different organic sources, which limits our mechanistic understanding of Cd immobilization by RSD. To address this gap, we conducted a 45 day microcosm experiment using a paddy soil contaminated with 22.8 mg/kg Cd. Six treatments were established: untreated control (CK), waterlogged (WF), and RSD-amended soils with 0.7% or 2.1% wheat straw (LWD, HWD) or soybean meal (LSD, HSD). We systematically assessed soil Cd fractionation, organic carbon and FeO concentrations, and bacterial community structure, aiming to clarify differences in Cd immobilization efficiency and the underlying mechanisms between wheat straw and soybean meal. For strongly extractable Cd, wheat straw RSD reduced the soil Cd concentrations from 6.02 mg/kg to 4.32 mg/kg (28.2%), whereas soybean meal RSD achieved a maximum reduction to 2.26 mg/kg (62.5%). Additionally, the soil mobility factor of Cd decreased from 44.6% (CK) to 39.2% (HWD) and 32.5% (HSD), while the distribution index increased from 58.5% (CK) to 62.2% (HWD) and 66.8% (HSD). Notably, the HWD treatment increased soil total organic carbon, humus, and humic acid concentrations by 34.8%, 24.6%, and 28.3%, respectively. Regarding amorphous FeO, their concentrations increased by 19.1% and 33.3% relative to CK. RSD treatments significantly altered soil C/N ratios (5.91–12.5). The higher C/N ratios associated with wheat straw stimulated r-strategist bacteria (e.g., Firmicutes, Bacteroidetes), which promoted carbohydrate degradation and fermentation, thereby enhancing the accumulation of humic substances. In contrast, the lower C/N ratios of soybean meal increased dissolved organic carbon and activated iron-reducing bacteria (FeRB; e.g., Anaeromyxobacter, Clostridium), driving iron reduction and amorphous iron oxide formation. PLS-PM analysis confirmed that wheat straw RSD immobilized Cd primarily through humification, whereas soybean meal RSD relied on FeRB-mediated FeO amorphization. These findings suggest that Cd immobilization in soil under RSD may be regulated by microbially mediated organic matter transformation and iron oxide dynamics, which was affected by organic materials of different C/N ratios. Full article

We present a rapid, energy-efficient, and ecofriendly route for the synthesis of alkaline earth titanate perovskites—CaTiO₃, SrTiO₃, and BaTiO₃—using an affordable, commercially available CO₂ laser engraver, commonly found in makerspaces and small-scale workshops. The method involves direct laser irradiation of compacted pellets composed of low-cost, abundant, and non-toxic precursors: TiO₂ and alkaline earth carbonates (CaCO₃, SrCO₃, BaCO₃). CaTiO₃ and BaTiO₃ were synthesized with phase purities exceeding 97%, eliminating the need for conventional high-temperature furnaces or prolonged thermal treatments. X-ray diffraction (XRD) coupled with Rietveld refinement confirmed the formation of orthorhombic CaTiO₃ (Pbnm), cubic SrTiO₃ (Pm3⁻m), and tetragonal BaTiO₃ (P4mm). Raman spectroscopy independently corroborated the perovskite structures, revealing vibrational fingerprints consistent with the expected crystal symmetries and Ti–O bonding environments. All samples contained only small amounts of unreacted anatase TiO₂, while BaTiO₃ exhibited a partially amorphous fraction, attributed to the sluggish crystallization kinetics of the Ba–Ti system and the rapid quenching inherent to laser processing. Transmission electron microscopy (TEM) revealed nanoparticles with average sizes of 50–150 nm, indicative of localized melting followed by ultrafast solidification. This solvent-free, low-energy, and highly accessible approach, enabled by widely available desktop laser systems, demonstrates exceptional simplicity, scalability, and sustainability. It offers a compelling alternative to conventional ceramic processing, with broad potential for the fabrication of functional oxides in applications ranging from electronics to photocatalysis. Full article

This study investigated the effects of incorporating rice husk ash (RHA) as a partial replacement for cement on the properties of concrete. To determine the optimal replacement level, RHA was used to replace cement in varying proportions, ranging from 0% to 25% in 5% increments. The mix with 0% RHA served as the control. The properties evaluated included setting time, density, and compressive strength. The results revealed that blending RHA with cement increased the initial setting time. This was attributed to the lower calcium oxide (CaO₂) content of RHA, which slows early-age hydration reactions. Conversely, the final setting time was reduced due to the pozzolanic activity of RHA, which enhances later-stage reactions. Additionally, the inclusion of RHA resulted in a decrease in concrete density, owing to its lower specific gravity and bulk density compared to Portland cement. Despite this, RHA-modified specimens exhibited higher compressive strengths than the control specimens. This strength enhancement was linked to the formation of additional calcium–silicate–hydrate (C-S-H) gel due to the pozzolanic reaction between amorphous silica in RHA and calcium hydroxide (CaOH) from hydration reaction. The gel fills concrete voids at the microstructural level, producing a denser and more compact concrete matrix. Based on the balance between strength and durability, the optimal RHA replacement level was identified as 10%. Full article

High-entropy ceramic (HEC) thin films generally refer to multi-component solid solutions composed of multiple metallic and non-metallic elements, existing in forms such as carbides, nitrides, and borides. Benefiting from the high-entropy effect, lattice distortion, sluggish diffusion, and cocktail effect of high-entropy systems, HEC thin films form simple amorphous or nanocrystalline structures while exhibiting high hardness/elastic modulus, excellent tribological properties, and thermal stability. Although the mixing entropy increases with the number of elements in the system, a higher number of elements does not guarantee improved performance. In addition to system configuration, the regulation of preparation methods and processes is also a key factor in enhancing performance. Arc ion plating (AIP) has emerged as one of the mainstream techniques for fabricating high-entropy ceramic (HEC) thin films, which is attributed to its high ionization efficiency, flexible multi-target configuration, precise control over process parameters, and high deposition rate. Through rational design of the compositional system and optimization of key process parameters—such as the substrate bias voltage, gas flow rates, and arc current—HEC thin films with high hardness/toughness, wear resistance, high-temperature oxidation resistance, and electrochemical performance can be fabricated, and several of these properties can even be simultaneously achieved. Against the backdrop of AIP deposition, this review focuses on discussions grounded in the thermodynamic principles of high-entropy systems. It systematically discusses how process parameters influence the microstructure and, consequently, the mechanical, tribological, electrochemical, and high-temperature oxidation behaviors of HEC thin films under various complex service conditions. Finally, the review outlines prospective research directions for advancing the AIP-based synthesis of high-entropy ceramic coatings. Full article

In the last few years, Thin Film Transistors (TFTs) based on materials such as amorphous Indium–Gallium–Zinc Oxide (a-IGZO) have gained interest in large-area and low-cost electronics due to their high carrier mobility, high on/off current ratio, low off-state current, and steep subthreshold slope. These characteristics make IGZO TFTs suitable for radio-frequency identification (RFID) tags, analog-to-digital converters (ADCs), logic circuits, sensors, and analog components, including operational amplifiers (OPAMPs). This work presents the implementation and characterization of an OPAMP based on n-type a-IGZO TFTs fabricated on glass substrate. Two previously reported design strategies were integrated: a positive feedback network to increase the output impedance and a topology to enhance the transconductance of the driver transistors, both in the differential input stage. A gain of 26 dB, a bandwidth of 2.4 kHz, a gain–bandwidth product (GBWP) of 48 kHz, and a phase margin of 64° were obtained, which confirms the reliability of the design and the fabrication process. Full article

Hydrogenated tetrahedral amorphous carbon (ta-C:H) thin films were modified using 266 nm picosecond laser pulses to investigate structural transformations at low and moderate fluences. Nitrogen-doped hydrogenated tetrahedral amorphous carbon layers 20–40 nm thick were deposited on silicon (Si) and silicon dioxide on silicon (SiO₂/Si) substrates and irradiated with picosecond pulses at 0.5–1.6 J cm⁻² using a raster-scanned beam. Structural changes in morphology, composition, and bonding were evaluated via optical microscopy, atomic force microscopy (AFM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. Even below 1.0 J cm⁻², localized color shifts and slight swelling indicated early structural rearrangements without significant material removal. Above 1.0–1.2 J cm⁻², the films were largely ablated, although a persistent 3–6 nm carbon layer remained on both substrate types. XPS showed an increase in sp²-bonded carbon by roughly 15%–20% in optimally modified regions, and Raman spectroscopy revealed defect-activated D-bands and the formation of multilayer defective graphene or reduced-graphene-oxide-like flakes at ablation boundaries. These results indicate that picosecond ultraviolet irradiation enables controllable graphitization and thinning of ta-C:H films while maintaining uniform processing over centimeter-scale areas, providing a route to thin, conductive, partially graphitized carbon coatings for optical and electronic applications. Full article

This study investigates amorphous anodized porous TiO₂ (a-TiO₂) as a substrate for iridium-based oxygen evolution catalysts. The substrates were prepared via anodization of Ti foil in a glycerol-based solution for 15 min @ 60 V. Nickel was subsequently electrodeposited to act both as a conductive and sacrificial layer for the galvanic deposition of iridium from an Ir(IV) chloro-complex solution. Electrochemical anodization resulted in a uniform IrO_x layer on the a-TiO₂ substrate, featuring Ir aggregates ~250 nm in size and an Ir:Ni atomic ratio of ca. 7, as determined by EDS analysis. The quantity of Ni determined by ICP-MS bulk analysis indicated that Ni resided also within the porous matrix. Varying the Ni deposition charge density (q_Ni) revealed that an intermediate loading (1463 mC cm⁻²) provided the best balance between Ir accessibility during the galvanic replacement step and electronic continuity. The optimized IrO_x/Ir-Ni/a-TiO₂ electrode achieved excellent OER performance (η = 344 mV @ 10 mA cm⁻²; 1.68 mA μg_Ir⁻¹ @ η = 300 mV) at an ultra-low Ir loading of 2.15 μg_Ir cm⁻² and demonstrated good short-term stability, with only a 20 mV potential increase over 4 h of continuous operation at 5.5 mA cm⁻². Overall, this strategy offers a scalable pathway for producing efficient OER electrodes with minimal noble metal loading. Full article

Amorphous indium-gallium-zinc-oxide (a-IGZO) thin-film transistors (TFTs) have emerged as promising candidates for next-generation large-area and low-power electronics due to their high mobility, low leakage current, and compatibility with low-temperature fabrication on flexible or transparent substrates. In this work, we report the fabrication of bottom-gate a-IGZO NMOS TFTs using HfO₂ as high-k gate dielectric and Mo top contacts. The devices were electrically characterized through capacitance–voltage (C–V) and current–voltage (I–V) measurements, from which key parameters were extracted. Based on these transistors, we designed, fabricated, and characterized inverters employing four different load configurations: resistive, diode, depletion, and pseudo-CMOS. A comparative analysis was performed in terms of voltage transfer characteristics (VTCs), gain, and noise margins, highlighting that depletion-load inverters offer the highest gain and robust noise margins. Finally, a two-channel multiplexer was designed and fabricated. The multiplexer was characterized under both square and sinusoidal input signals up to 1 kHz, demonstrating correct channel selection and robust switching behavior. These results confirm the potential of a-IGZO TFT-based circuits as building blocks for low-power and high-reliability digital and mixed-signal electronics. Full article

This study evaluated the surface functionalization of a non-equiatomic TiZrNbTaMo high-entropy alloy (HEA) by micro-arc oxidation (MAO) in Cu-rich electrolytes to tailor its performance for biomedical implants. The Cu content was varied, and the resulting coatings were investigated for their morphology, phase constitution, chemical structure, wettability, and cytocompatibility. X-ray diffraction (XRD) measurements of the substrate indicated a body-centered cubic (BCC) matrix with minor HCP features, while the MAO-treated samples depicted amorphous halo with sparse reflections assignable to CaCO₃, CaO, and CaPO₄. Chemical spectroscopic analyses identified the presence of stable oxides (TiO₂, ZrO₂, Nb₂O₅, Ta₂O₅, MoO₃) and the successful incorporation of bioactive elements (Ca, P, Mg) together with traces of Cu, mainly as Cu₂O. MAO treatment increased surface roughness and rendered a hydrophilic behavior, which are features typically favorable to osseointegration process. In vitro cytotoxic assays with MC3T3-E1 cells (24 h) showed that Cu addition did not induce harmful effects, maintaining or improving cell viability and adhesion compared to the controls. Collectively, MAO in Cu-rich electrolyte yielded porous, bioactive, and Cu-incorporated oxide coatings on TiZrNbTaMo HEA, preserving cytocompatibility and supporting their potential for biomedical applications like orthopedic implants and bone-fixation devices. Full article

High-performance dielectric materials that can be processed at ultra-low temperatures are essential for next-generation LTCC technologies and compact RF–microwave components. In this work, a multicomponent Bi–Fe–Nb oxide system was synthesized using a modified citrate sol–gel method and thermally treated at only 400 °C to investigate its structural evolution and dielectric behavior. XRD and Raman analysis revealed the coexistence of a well-crystallized BiOCl phase embedded within a partially amorphous Bi–Fe–Nb–O matrix. SEM and EDS mapping confirmed the presence of two distinct microstructural regions, reflecting differences in local composition and crystallization kinetics. Microwave measurements at 2.7 and 5.0 GHz showed low dielectric losses and a stable dielectric response. Impedance spectroscopy in the RF range revealed strong Maxwell–Wagner polarization at low frequencies and thermally activated relaxation evidenced by the temperature shift in the modulus and impedance peaks. Arrhenius analysis of the relaxation frequencies yielded similar activation energies from both modulus and impedance formalisms, indicating a single underlying relaxation mechanism. Equivalent-circuit fitting confirmed non-Debye behavior, with nearly temperature-independent capacitance and decreasing resistance consistent with thermally activated conduction. These results demonstrate that the Bi–Fe–Nb system exhibits promising dielectric stability and functional behavior even when processed at exceptionally low temperatures. Full article

Sewer corrosion driven by sulfur metabolism threatens infrastructure durability. Current study examined the effect of conductive lining materials on microbial communities and sulfide control under simulated sewer conditions. Three lab-scale reactors (3.5 L total volume, 2.1 L working volume) were prepared with amorphous carbon (SAN-EARTH) and magnetite-black (MTB) linings, while a Portland cement reactor with no coating served as the control. Each reactor was operated for 120 days at room temperature and fed with artificial wastewater. The working volume consisted of 1.4 L of synthetic wastewater mixed with 0.7 L of sewage sludge used as the inoculum source. Sulfate, sulfide, hydrogen sulfide, nitrogen species, pH, and organic carbon were monitored, and microbial dynamics were analyzed via 16S rRNA sequencing and functional annotation. SAN-EARTH and MTB reactors completely suppressed sulfide and hydrogen sulfide, while Portland cement showed the highest accumulation. Both conductive linings maintained alkaline conditions (pH 9.0–10.5), favoring sulfide oxidation. Microbial analysis revealed enrichment of sulfur-oxidizing bacteria (Thiobacillus sp.) and electroactive taxa (Geobacter sp.), alongside syntrophic interactions involving Aminobacterium and Jeotgalibaca. These findings indicate that conductive lining materials reshape microbial communities and sulfur metabolism, offering a promising strategy to mitigate sulfide-driven sewer corrosion. Full article

The construction sector faces pressure to decarbonise while addressing rising resource demands and agricultural waste. Ordinary Portland cement (OPC) is a major CO₂ emitter, yet biomass residues are often open-burned or landfilled. This study explores corncob ash (CCA) as a sustainable supplementary cementitious material (SCM), examining how calcination conditions influence pozzolanic potential and support circular economy and climate goals, which have not been adequately explored in literature. Ten CCA samples were produced via open-air burning (2–3.5 h) and electric-furnace calcination (400–1000 °C, 2 h), alongside a reference OPC. Mass yield, colour, XRD, XRF, LOI, and LOD were analysed within a process–structure–property–performance–sustainability framework. CCA produced in a 400–700 °C furnace window consistently achieved high amorphous contents (typically ≥80%) and combined pozzolanic oxides (SiO₂ + Al₂O₃ + Fe₂O₃) above the 70% ASTM C618 threshold, with 700 °C for 2 h emerging as an optimal condition. At 1000 °C, extensive crystallisation reduced the expected reactivity despite high total silica. Extended open-air burning (3–3.5 h) yielded chemically acceptable but more variable ashes, with lower amorphous content and higher alkalis than furnace-processed CCA. Simple industrial ecology calculations indicate that valorising a fraction of global CC residues and deploying optimally processed CCA at only 20% OPC replacement could displace 180 million tonnes CC waste and clinker avoidance on the order of 5–6 Mt CO₂ per year, while reducing uncontrolled residue burning and primary raw material extraction. The study provides an experimentally validated calcination window and quality indicators for producing reactive CCA, alongside a clear link from laboratory processing to clinker substitution, circular resource use, and alignment with SDGs 9, 12, and 13. The findings establish a materials science foundation for standardised CCA production protocols and future life cycle and performance evaluations of low-carbon CCA binders. Full article