Search Results (3,515)

Poly(L-lactic acid) (PLLA) and poly(ε-caprolactone) (PCL), two biodegradable and biocompatible polymers that are commonly used for biomedical applications, are, respectively, the result of the ring-opening polymerization of LA and ε-CL, cyclic esters, which can be produced according to several mechanisms (cationic, monomer-activated cationic, anionic, and coordination-insertion), except for L-lactide, which is polymerized only by anionic, cationic, or coordination-insertion polymerization. A series of well-defined PLLA-b-PCL block copolymers have been obtained starting from the same PLLA homopolymer, having a molar mass of 2500 g·mol⁻¹, and being synthesized by coordination-insertion in the presence of tin octoate. PCL blocks were obtained via a cationic-activated monomer mechanism to limit transesterification reactions, and their molar masses varied from 1800 to 18,500 g·mol⁻¹. The physicochemical properties of the copolymers were determined by ¹H NMR, SEC, and DSC. Moreover, a series of nanoparticles (NPs) were prepared starting from these polyester-based copolymers by an emulsification/evaporation method. The sizes of the obtained NPs varied between 140 and 150 nm, as a function of the molar mass of the copolymers. Monomodal distribution curves with PDI values under 0.1 were obtained by Dynamic Light Scattering (DLS) and their spherical shape was confirmed by TEM. The increase in the temperature from 25 to 37 °C induced only a very slight decrease in the NP sizes. The results obtained in this preliminary study indicate that NPs have a temperature stability, allowing us to consider their use as drug-loaded nanocarriers for biomedical applications. Full article

Ultrathin titanium nitride (TiN) is a novel material platform for constructing active metasurfaces in the near-infrared region (NIR). Here, we realized tunable polarization-selective absorption by gating ultrathin TiN in an Ultrathin TiN Grating Metasurface (UTGM) and a gold resonator/TiN film Hybrid Metasurface (GTHM), respectively. The TM wave absorption (0.96) was much larger than that of the TE wave in the UTGM. When the carrier density decreased by 12%, the near-perfect TM absorption peak blue-shifted by 0.3 μm. Similarly, the linear dichroism (0.96) peak in GTHM blue-shifted by 0.12 μm when gating ultrathin TiN film. Active metasurfaces with tunable polarization-selective absorption have huge potential in dynamic integrated electro-optic devices in NIR. Full article

Nanostructured ferritic alloys (NFAs), such as oxide-dispersion strengthened (ODS) alloys, play a vital role in advanced fission and fusion reactors, offering superior properties when incorporating nanoparticles under irradiation. Despite their importance, the high cost of mass-producing NFAs through mechanical milling presents a challenge. This study delves into the microstructure-mechanical property correlations of three NFAs produced using a novel, cost-effective approach combining severe plastic deformation (SPD) with the continuous thermomechanical processing (CTMP) method. Analysis using scanning electron microscopy (SEM)-electron backscatter diffraction (EBSD) revealed nano-grain structures and phases, while scanning transmission electron microscopy (STEM)-energy dispersive X-ray spectroscopy (EDS) quantified the size and density of Ti-N, Y-O, and Cr-O fine particles. Atom probe tomography (APT) further confirmed the absence of finer Y-O particles and characterized the chemical composition of the particles, suggesting possible nitride dispersion strengthening. Correlation of microstructure and mechanical testing results revealed that CTMP alloys, despite having lower nanoparticle densities, exhibit strength and ductility comparable to mechanically milled ODS alloys, likely due to their fine grain structure. However, higher nanoparticle densities may be necessary to prevent cavity swelling under high-temperature irradiation and helium gas production. Further enhancements in uniform nanoparticle distribution and increased sink strength are recommended to mitigate cavity swelling, advancing their suitability for nuclear applications. Full article

The integration of perovskite materials in solar cells has garnered significant attention due to their exceptional photovoltaic properties. However, achieving a bandgap energy below 1.2 eV remains challenging, particularly for applications requiring infrared absorption, such as sub-cells in tandem solar cells and single-junction perovskite solar cells. In this study, we employed a doping strategy to engineer the bandgap and observed that the doping effects varied depending on the A-site cation. Specifically, we investigated the impact of bismuth (Bi³⁺) incorporation into perovskites with different A-site cations, such as cesium (Cs) and methylammonium (MA). Remarkably, Bi³⁺ doping in MA-based tin-lead perovskites enabled the fabrication of ultra-narrow bandgap films (~1 eV). Comprehensive characterization, including structural, optical, and electronic analyses, was conducted to elucidate the effects of Bi doping. Notably, 8% Bi-doped Sn-Pb perovskites demonstrated infrared absorption extending up to 1360 nm, an unprecedented range for ABX₃-type single halide perovskites. This work provides valuable insights into further narrowing the bandgap of halide perovskite materials, which is essential for their effective use in multi-junction tandem solar cell architectures. Full article

Graphene and MXenes have emerged as promising materials for gas sensing applications due to their unique properties and superior performance. This review focuses on the fabrication techniques, applications, and sensing mechanisms of graphene and MXene-based composites in gas sensing. Gas sensors are crucial in various fields, including healthcare, environmental monitoring, and industrial safety, for detecting and monitoring gases such as hydrogen sulfide (H₂S), nitrogen dioxide (NO₂), and ammonia (NH₃). Conventional metal oxides like tin oxide (SnO₂) and zinc oxide (ZnO) have been widely used, but graphene and MXenes offer enhanced sensitivity, selectivity, and response times. Graphene-based sensors can detect low concentrations of gases like H₂S and NH₃, while functionalization can improve their gas-specific selectivity. MXenes, a new class of two-dimensional materials, exhibit high electrical conductivity and tunable surface chemistry, making them suitable for selective and sensitive detection of various gases, including VOCs and humidity. Other materials, such as metal-organic frameworks (MOFs) and conducting polymers, have also shown potential in gas sensing applications, which may be doped into graphene and MXene layers to improve the sensitivity of the sensors. Full article

The development of a suitable catalytic system for methane pyrolysis reactions requires a detailed investigation of the activation energy of C-H bonds on catalysts, as well as their stability against sintering and coke formation. In this work, both single-metal Ni atoms and small clusters of Ni atoms deposited on titanium nitride (TiN) plasmonic nanoparticles were characterized for the C-H bond activation of a methane pyrolysis reaction using ab initio spin-polarized density functional theory (DFT) calculations. The present work shows the complete reaction pathway, including energy barriers for C-H bond activation and dehydrogenated fragments, during the methane pyrolysis reaction on catalytic systems. Interestingly, the C-H bond activation barriers were low for both Ni single-atom and Ni-clusters, showing the energy barriers of ~1.10 eV and ~0.88 eV, respectively. Additionally, single-atom Ni-TiN showed weaker binding to adsorbates, and a net endothermic reaction pathway indicated that the single-atom Ni-TiN was expected to resist coke formation on its surface. However, these Ni single-atom catalysts can sinter, aggregate into a small cluster, and form a coke layer from the highly exothermic reaction pathway that the cluster takes despite the facile reaction pathway. Full article

Spontaneous vegetation within a managed green space is often regarded as unwelcoming and insignificant weeds. This perception is still deep-rooted among green-space managers and the general public worldwide; they are generally uncertain about the management needs after allowing these groups of flora to take root. The short-term growth dynamics of both spontaneous and planted vegetation should be analyzed, and a widely acceptable, feasible management plan to balance aesthetic and ecological functions should be formulated with the backing of data and analysis for such fast-growing flora in tropical and subtropical regions. A manicured, extensive green roof with only seven (two native, five exotic) plant species was transformed into a renaturalized biotope by replacing 15 native ferns and forb species over 15 months. After planting, a baseline plant survey was conducted, with 54 plant species representing spontaneous growth and 14 planted species alive (7 planted native species survived, plus 7 species planted prior to renaturalization revived). Three quarterly plant surveys recorded the cover-abundance of each species, and the growth dynamics of the planted and spontaneous plant species were evaluated over the first year of study. During each quarterly survey, the number of planted and spontaneous plant species remained stable (ranging from 14 to 16 species and 51 to 54 species, respectively), with a constant turnover of 11 to 12 die-out species and 11 to 12 newly colonized or revived species. Plant coverage of different plant forms fluctuated slightly (within 7%) in the quarterly surveys according to seasonal changes, except for ferns, which outperformed (12% increase in coverage in a year) all the other plant forms. The height of the planted vegetation fluctuated in a year, being shorter during the summer, while the height of spontaneous vegetation remained stable throughout the year, exhibiting resilience to scouring heat. The seasonal growth tendencies of both planted and spontaneous plants were illustrated in relation to their species ranks, and further hierarchical cluster analysis was conducted for the clustering of spontaneous species. Their differential growth patterns provided comprehensive information or supported decisions regarding plant selection and maintenance, which is a scientific novelty within this unexplored topic. Management recommendations based on the findings were suggested to fulfill both aesthetic and ecological needs. Species with stable and less stable growth patterns could be useful to meet maintenance efficiency and biodiversity enhancement needs, respectively. These findings provide insights to form guiding principles for choosing plant species for renaturalization projects. Full article

Metal oxide core–shell fibrous nanostructures are promising gas-sensitive materials for the detection of a wide variety of both reducing and oxidizing gases. In these structures, two dissimilar materials with different work functions are brought into contact to form a coaxial heterojunction. The influence of the shell material on the transportation of the electric charge carriers along these structures is still not very well understood. This is due to homo-, hetero- and metal/semiconductor junctions, which make it difficult to investigate the electric charge transfer using direct current methods. However, in order to improve the gas-sensing properties of these complex structures, it is necessary to first establish a good understanding of the electric charge transfer in ambient air. In this article, we present an impedance spectroscopy study of networked SnO₂/Ga₂O₃ core–shell nanobelts in ambient air. Tin dioxide nanobelts were grown directly on interdigitated gold electrodes, using the thermal sublimation method, via the vapor–liquid–solid (VLS) mechanism. Two forms of a gallium oxide shell of varying thickness were prepared via halide vapor-phase epitaxy (HVPE), and the impedance spectra were measured at 189–768 °C. The bulk resistance of the core–shell nanobelts was found to be reduced due to the formation of an electron accumulation layer in the SnO₂ core. At temperatures above 530 °C, the thermal reduction of SnO₂ and the associated decrease in its work function caused electrons to flow from the accumulation layer into the Ga₂O₃ shell, which resulted in an increase in bulk resistance. The junction resistance of said core–shell nanostructures was comparable to that of SnO₂ nanobelts, as both structures are likely connected through existing SnO₂/SnO₂ homojunctions comprising thin amorphous layers. Full article

This paper investigates TiN for its potential to enhance light-harvesting efficiency as an alternative material to Au for nanoscale plasmonic light trapping in thin-film solar cells. Using nanosphere lithography (NSL), plasmonic arrays of both Au and TiN are fabricated and characterized. Later, the fabricated TiN and Au arrays are integrated into a thin-film organic photovoltaic (OPV) device with a PBDB-T:ITIC-M bulk heterojunction (BHJ) active layer. A comparative study between these Au and TiN nanostructured arrays evaluates their fabrication process and plasmonic response, highlighting the advantages and disadvantages of TiN compared to a conventional plasmonic material such as Au. The effect of the fabricated arrays when integrated into an OPV is presented and compared to understand the viability of TiN. As one of the first experimental studies utilizing TiN arrays for the plasmonic enhancement of photovoltaics, the results offer valuable insight that can guide future applications and decisions in design. Full article

Tin dioxide (SnO₂) is a low-cost and high-capacity anode material for lithium-ion batteries, but the fast capacity fading significantly limits its practical applications. Current research efforts have focused on preparing sophisticated composite structures or optimizing functional binders, both of which increase material manufacturing costs. Herein, we utilize pristine and commercially available SnO₂ nanopowders and enhance their cycling performance by simply narrowing the potential range and optimizing electrolytes. Specifically, a narrower potential range (0–1 V) mitigates the capacity fading associated with the conversion reaction, whereas an ether-based electrolyte further suppresses the volume expansion related to the alloy reaction. Consequently, this SnO₂ anode delivers a promising battery performance, with a high capacity of ~650 mAhg⁻¹ and stable cycling for 100 cycles. Our work provides an alternative approach to developing high-capacity and long-cycling metal oxide anode materials. Full article

The aim of this work was to investigate the possibility of modifying the physical properties of indium tin oxide (ITO) layers by annealing them in different atmospheres and temperatures. Samples were annealed in vacuum, air, oxygen, nitrogen, carbon dioxide and a mixture of nitrogen with hydrogen (NHM) at temperatures from 200 °C to 400 °C. Annealing impact on the crystal structure, optical, electrical, thermal and thermoelectric properties was examined. It has been found from XRD measurements that for samples annealed in air, nitrogen and NHM at 400 °C, the In₂O₃/In₄Sn₃O₁₂ share ratio decreased, resulting in a significant increase of the In₄Sn₃O₁₂ phase. The annealing at the highest temperature in air and nitrogen resulted in larger grains and the mean grain size increase, while vacuum, NHM and carbon dioxide atmospheres caused the decrease in the mean grain size. The post-processing in vacuum and oxidizing atmospheres effected in a drop in optical bandgap and poor electrical properties. The carbon dioxide seems to be an optimal atmosphere to obtain good TE generator parameters—high ZT. The general conclusion is that annealing in different atmospheres allows for controlled changes in the structure and physical properties of ITO layers. Full article

This study investigates the application of the vertical zone refining process to produce ultra-high-purity tin. Computational fluid dynamics (CFD) simulations were conducted using an Sn-1 wt.%Bi binary alloy to assess the effects of two key parameters—heater temperature and pulling rate—on Bi impurity segregation. The simulations revealed a dynamic evolution in molten zone height, characterized by an initial rapid rise, followed by a gradual increase and ending with a sharp decline. Despite these fluctuations, the lower solid–liquid interface consistently remained slightly convex. After nine zone passes, impurities accumulated at the top of the sample, with dual vortices forming a rhombus- or gate-shaped negative segregation zone. The simulations demonstrated that lower heater temperatures and slower pulling rates enhanced impurity segregation efficiency. Based on these results, experiments were performed using 6N-grade tin as the starting material. Glow discharge mass spectrometry (GDMS) analysis showed that the effective partition coefficients (k_eff) for impurities such as Ag, Pb, Co, Al, Bi, Cu, Fe, and Ni were significantly less than 1, while As was slightly below but very close to 1, and Sb was above 1. Under optimal conditions—405 °C heater temperature and a pulling rate of 5 μm/s—over 60% of impurities were removed after nine zone passes, approaching 6N9-grade purity. These findings provide valuable insights into optimizing the vertical zone refining process and demonstrate its potential for achieving 7N-grade ultra-high-purity tin. Full article

This study presents a comparative analysis of the corrosion resistance of nitrided layers on conventional Grade 2 titanium alloy and those produced by direct metal laser sintering (DMLS). Low-temperature glow-discharge nitriding of the tested materials was carried out using conventional glow-discharge nitriding (so-called nitriding at the cathode potential—TiN/CP) and with the use of an “active screen” (nitriding at the plasma potential—TiN/PP). The TiN + Ti₂N + Ti(N) layers were characterized by their microstructure, nanohardness profile distribution, surface topography, and corrosion resistance. The reduction in the cathodic sputtering phenomenon in the process using the active screen allowed the creation of surface layers that retained the topography of the base material. The parameters of the glow-discharge treatment led to grain growth in the printed substrates. This did not adversely affect corrosion resistance. The corrosion resistance of nitrided layers on the printed titanium alloy is only slightly lower than that of layers on the conventional Grade 2 alloy. Iron precipitates at grain boundaries facilitate increased nitrogen diffusion, resulting in reduced nitrogen concentration in the surface layer, slight changes in corrosion potential values, and increased nitrogen concentration in the Ti(N) diffusion layer. Full article

This study presents a hydrometallurgical process for the leaching and recovery of tin from waste-printed circuit boards (wPCBs). The process aims to separate and recover tin from filter dust produced during the crushing of wPCBs in a recycling facility. The separation of the metallic and non-metallic fractions was carried out by gravimetric separation. The metallic fraction consisted mainly of Cu (23.8%), Fe (17.8%), Sn (12.7%), Pb (6.3%), and Zn (3.4%). During the leaching tests, the effects of (a) HCl concentration (2, 4, 6 M), (b) pulp density (0.1, 0.2, 0.3 g/mL), and (c) the addition of NaCl (no addition, 1 M, 3 M) were investigated. All tests were conducted at an ambient temperature without agitation. A leaching efficiency of 78.2% was obtained during leaching with 6 M HCl and 0.3 g/mL pulp density, while 94.8% of tin was leached under the same conditions with the addition of 3 M NaCl. Tin was recovered from the pregnant solution by addition of 2 M NaOH at pH = 3.0, with an efficiency of 97.4%. The precipitate, despite being amorphous, was easily filtered and it consisted of 64.7% Sn and less than 2% of impurities. The proposed process consists of a leaching stage with 6 M HCl, 3 M NaCl, 0.3 g/mL pulp density, and a contact time of 24 h, and a recovery stage by chemical precipitation at pH = 3.0. The total tin recovery of the suggested process was 92.3%. Full article

Wide-bandgap tin oxide (${\mathrm{SnO}}_2$) thin-films are frequently used as an electron-transporting layers in perovskite solar cells due to their superior thermal and environmental stabilities. However, its crystallization by conventional thermal methods typically requires high temperatures and long periods of time. These post-processing conditions severely limit the choice of substrates and reduce the large-scale manufacturing capabilities. This work describes the intense-pulsed-light-induced crystallization of ${\mathrm{SnO}}_2$ thin-films using only 500 $\mathsf{\mu }\mathrm{s}$ of exposure time. The thin-films’ properties are investigated using both impedance spectroscopy and photoconductivity characteristic measurements. A Nyquist plot analysis establishes that the process parameters have a significant impact on the electronic and ionic behaviors of the ${\mathrm{SnO}}_2$ films. Most importantly, we demonstrate that light-induced crystallization yields improved topography and excellent electrical properties through enhanced charge transfer, improved interfacial morphology, and better ohmic contact compared to thermally annealed (TA) ${\mathrm{SnO}}_2$ films. Full article