TiO2 Nanoparticles Research Articles

Effect of Sm3+ activation on the optical properties and antibacterial activity of TiO2 nanoparticles

Effect of Sm3+ activation on the optical properties and antibacterial activity of TiO2 nanoparticles

Effects of seed coating with (titanium dioxide and selenium) nanoparticles on fenugreek (Trigonella foenum graecum L.) plant growth and antioxidant activity

Background: The fenugreek plant is a kind of herbaceous plant that resembles a clover. It is extensively used as a spice and condiment, as well as a medicinal plant. Studying the effect of seed coating on fenugreek is an important step to learn about the effects it imprints on plant growth and its antioxidant activity when its seeds are coated by nanoparticles of titanium and selenium. Methods: To study the effects of seed coating with Nanoparticles of Titanium dioxide at concentrations of (0, 100, 200, 300, and 400) ppm and selenium at concentrations of (0, 20, 40, 60, and 80) ppm on shoot length, number of leaves per plant, carbohydrate %, protein %, and antioxidant activity peroxidase %, single and two way interaction on fenugreek’s growth is taken into account. Treatments are designed as a properly randomized factorial experiment (5×5×3), with three replicates in a totally randomized design.Results: It was revealed that a single application of the previously mentioned ingredients had a significant impact on fenugreek growth and antioxidant activity, especially at high concentrations.Conclusions: Plant physiological properties were favorably influenced by seed coating with (Titanium dioxide and Selenium) nanoparticles. Based on the results of TiO2 NPs’ effect on seed germination and early seedling growth, it is possible that NPs aided in seed water absorption, increased seed ability to absorb and utilize efficiently, and activated and promoted hydrolytic enzymes in the seed antioxidant system.Keywords: Titanium dioxide; Selenium; Nanoparticles; Antioxidant activity; Fenugreek

Microbial Activity of TiO2 NPs via Two Phases Synthesized by The Sol-Gel Method

TiO2 titanium dioxide nano phases of anatase and rutile were controlled only by temperature control of the calcination process, which is a cheap technical technique, and were organized using a sol-gel process, which involved mixing titanium tetrachloride (TiCl4) with ethanol as starting materials, as well as heating at various temperatures (650, 850 ℃ ). The fundamental properties of the as-prepared nanomaterials were investigated using Fourier transform infrared spectra (FTIR). The antibacterial activity of TiO2 was next investigated using two strains of E. coli, Staphylococcus aureus, and Streptococcus bacteria. The TiO2 structure has a dominating phase of 650 °C in addition to rutile at 850 °C, with an average volume of crystalline (D) of 21.9 nm for the anatase phase and 30.41 nm for the rutile phase. According to XRD data, the spherical shape of the rutile phase is clearly evident in the TEM of TiO2 NPs, the tetragonal shape is clearly seen in the anatase, and the calcination process had a major effect on the crystal size. According to FTIR analysis, the majority of peaks are seen between 400 and 700 cm-1 as a result of bending and oscillation lengthening. The studies demonstrated that TiO2, in both protease and rutile forms, is a highly efficient antibacterial that can be used as a self-cleaning exterior to exterior surfaces (windows) as well as in bio-penetration places like hospitals and medical clinics.

Evaluation of some mechanical and optical properties of modified glass ionomer cement with TiO2 and SiO2 nanoparticles

BackgroundGlass ionomer cements with extended setting time and inferior mechanical properties present significant challenges for dentists in clinical practice. Thus, various alterations aimed to enhance their properties.Aim of the studyTo study the effect of adding TiO2 and SiO2 nanoparticles on properties of conventional glass ionomer cement.Methods2.5 wt% TiO2 and 2.5 wt% SiO2 were added to the glass ionomer cement (GC Gold Label Luting & Lining Cement, Japan). Microhardness, compressive strength, setting time and color changes were evaluated using Vickers hardness tester, Universal testing machine, Gillmore needle apparatus and spectrophotometer, respectively.ResultsData were analyzed using SPSS 18. Mean, SD, and confidence intervals were reported. Normality was checked using Kolmogorov–Smirnov test. The experimental group revealed a higher hardness value than the control group. Meanwhile, Compressive strength results revealed a higher value of the control group than experimental group. Setting time was longer for the experimental group, in the meantime no perceptible color change for the experimental group was recorded.ConclusionsAdding 2.5 wt% TiO2 and 2.5 wt% SiO2 to conventional glass ionomer had a positive effect on microhardness without affecting the perceptible color.

Distribution characteristics of TiO2 NPs in Daihai lake and their stability regulated by abiotic factors

Accurate detection and stability analysis of titanium dioxide (TiO2 NPs) in surface water are critical for ecological risk assessment. Quantitative analysis of TiO2 NPs in water and sediment of Daihai Lake was performed and their occurrence forms was characterized by TEM, XRD and FTIR. Further investigation into the impact of pH, ionic strength (IS) and dissolved organic matter (DOM) on the stability of TiO2 NPs was carried out, along with a correlation analysis between abiotic factors and TiO2 NPs concentration. Results showed that TiO2 NPs in water and sediment are 1.01 × 105 and 5.66 × 105 particles/mL in July 2023, respectively. After transformed in water sample from Daihai Lake, the hydrodynamic particle (HDD) of TiO2 NPs reach 600–700 nm, with reduced crystallinity and observable characteristic peaks of NaCl, which is related to the high concentration of NaCl in Daihai Lake. Structural defects and changes in surface properties of TiO2 NPs are introduced due to the adsorption of organic matter, leading to higher aggregation and sedimentation rates. Specifically, Ca2+ promote the sedimentation of TiO2 NPs more than Na+. Conversely, A/A0 increased to 0.80–0.94 from 0.64 after humic acid (HA) and fulvic acid (FA) added. Hydroxyl and carboxyl groups of FA enhanced steric hindrance and inhibited TiO2 NPs sedimentation. While a strong promotion effect on the sedimentation of TiO2 NPs is detected when 10 mmol/L Ca2+ coexisted with 10 mg/L HA, with 70% of the TiO2 NPs settled within 120 min. Additionally, the concentration of TiO2 NPs in Daihai Lake is significantly positively correlated with dissolved organic carbon (DOC) and humification index, which might be relate to the enhancement of TiO2 NPs stability of aromatic organic matter. And the high concentration of DOC will also lead to the stable existence of TiO2 NPs in water and exacerbate aquatic toxicity.

Green synthesis and characterization of TiO2 and Ag-doped TiO2 nanoparticles for photocatalytic and antimicrobial applications

TiO2 and Ag-doped TiO2 nanoparticles were synthesized using lemon grass plant leaf extract via a greener co-precipitation method. Plant biomolecules facilitated nanoparticle production, ensuring stability. Characterization involved XRD, FE-SEM, XPS, FT-IR, EDX, UV-DRS, HR-TEM and UV–Vis spectroscopy analyses, revealing tetragonal and cubic structures for TiO2 and Ag-TiO2, with average sizes of 11.96 and 41.8 nm, respectively. FT-IR confirmed characteristic bands, FE-SEM and HR-TEM analysis reveal that Ag-doped TiO2 nanoparticles primarily form irregular agglomerations, with interplanar spacings of 0.362 nm for the anatase (220) plane and 0.235 nm for the silver (111) plane and EDX determined elemental composition. UV–DRS calculated band gap values (3.3 eV for TiO2, 0.9 eV for Ag-TiO2). Photocatalytic performance against methylene blue dye under sunlight indicated higher degradation by Ag-TiO2 (96.96 %) than TiO2 (77.77 %). Antimicrobial testing showed superior activity of Ag-TiO2 over TiO2.

Mechanisms and Assessment of Genotoxicity of Metallic Engineered Nanomaterials in the Human Environment.

Engineered nanomaterials (ENMs) have a broad array of applications in agriculture, engineering, manufacturing, and medicine. Decades of toxicology research have demonstrated that ENMs can cause genotoxic effects on bacteria, mammalian cells, and animals. Some metallic ENMs (MENMs), e.g., metal or metal oxide nanoparticles TiO2 and CuO, induce genotoxicity via direct DNA damage and/or reactive oxygen species-mediated indirect DNA damage. There are various physical features of MENMs that may play an important role in promoting their genotoxicity, for example, size and chemical composition. For a valid genotoxicity assessment of MENMs, general considerations should be given to various factors, including, but not limited to, NM characterization, sample preparation, dosing selection, NM cellular uptake, and metabolic activation. The recommended in vitro genotoxicity assays of MENMs include hprt gene mutation assay, chromosomal aberration assay, and micronucleus assay. However, there are still knowledge gaps in understanding the mechanisms underlying the genotoxicity of MENMs. There are also a variety of challenges in the utilization and interpretation of the genotoxicity assessment assays of MENMs. In this review article, we provide mechanistic insights into the genotoxicity of MENMs in the human environment. We review advances in applying new endpoints, biomarkers, and methods to the genotoxicity assessments of MENMs. The guidance of the United States, the United Kingdom, and the European Union on the genotoxicity assessments of MENMs is also discussed.

Fabrication and characterization of a novel superhydrophobic cotton fabric with integrated 3D graphene-Ag/TiO2 aerogel for superior antibacterial performance, oil-water separation, and enhanced durability

This research delineates the pioneering development of a superhydrophobic cotton textile, ingeniously integrated with a three-dimensional graphene-Ag/TiO2 aerogel. The study meticulously details the fabrication process, structural characterization, and diverse industrial applications of this advanced textile. The fabric demonstrates exceptional hydrophobicity, evidenced by a water contact angle (WCA) of 161.8°. Scanning Electron Microscopy (SEM), X-ray Photoelectron Spectroscopy (XPS), X-ray Diffraction (XRD), Raman spectra, and Fourier Transform Infrared Spectroscopy (FTIR) substantiate the micromorphological and chemical alterations of the cotton surface, highlighting the successful reduction of graphene oxide (GO) and incorporation of polydimethylsiloxane (PDMS), TiO2, and Ag nanoparticles. The fabric’s antibacterial efficacy is rigorously established, boasting an impressive antibacterial rate that surpasses 99.99 % against E. coli and S. aureus. Additionally, the fabric demonstrates its capability to discern between oil and water with remarkable finesse, showcasing a separation efficiency that exceeds 98 %, even under extreme chemical conditions. The textile also exhibits excellent self-cleaning, washing, and chemical durability, alongside robust antistatic properties. Despite a marginal decrease in air permeability relative to raw cotton, the fabric’s multifunctional capabilities significantly compensate for this trade-off. The unique three-dimensional architecture of the hybrid graphene-Ag/TiO2 aerogel (AT-HGA) modified cotton marks a substantial advancement in bio-based material science, with broad potential applications in functional garments, medical textiles, and various industrial sectors.

A study on the influence of metal Ag, Cu, and Fe doping on the morphological, structural, and photocatalytic activity of TiO2 nanostructures

Metal-doped TiO2 nanoparticles (NPs) were elaborated by a sol–gel method using n-butoxide of titanium (IV) as precursors. The resulting NPs were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), Raman spectroscopy, and FTIR analysis. The SEM study shows the formation of a spheres-like structure. The EDX analysis proves the presence of Ag, Fe, and Cu on the doped TiO2 NPs. XRD and Raman spectroscopy analysis show that the doping inhibited the phase transformation and stabilized the anatase phase. The photocatalytic activity of prepared TiO2 NPs was evaluated in methylene blue (MB) photodegradation under UV irradiation. The results reveal that the doped TiO2 NPs were more efficient than undoped TiO2 NPs in the degradation of MB. The Cu-doped TiO2 NPs were found to be more efficient in this reaction with a degradation efficiency of about 92.31 % and a kinetic rate constant of about 10−2 min−1. The studies of the reactive species show that the holes are the main reactive species responsible for the photocatalytic oxidation of MB. Furthermore, the reusability studies showed that the photocatalysts are globally stable for the photodegradation of MB.

Numerical analysis on the fate and transport of TiO2 nanoparticles in fractured porous media: Addressing intrinsic heterogeneities in sorptive mass transfer

The aggregation and slow migration of nanoparticles in aqueous media have caused serious concerns about their fate and impacts in the subsurface environment. Anthropogenic release and distribution of TiO2 nanoparticles (TNP) have immense potential for surface adsorption, occlusion, impregnation, bioaccumulation, and phase partition into various environmental compartments, and the actual risks in their interactions are still unknown. In an attempt to realize the extent of source zone migration of TNP in a fracture-skin-matrix (F-S-M) medium, a numerical model is developed and analyzed for sensitivity of certain features of the flow field. In addition, the sorptive mass transfer is simulated under four characteristic scenarios with varying assumptions pertaining to the intrinsic heterogeneities. The simulation results highlight the non-selective regulatory role of the skin in providing temporary interfacial space for reversible adsorption between the fracture and the matrix as well as in retarding the desorption rate. A preferential detachment of TNP is observed to be favored by the enhanced properties of skin due to the similarity in diffusion and dispersion coefficients. Out of the four scenarios, the two-site model and two-step model simulated the dynamic pore-filling features of adsorption pertaining to the heterogeneities in TNP and F-S-M characteristics. The results demonstrate that the proposed numerical could fairly detect the transition between local equilibrium and dynamic adsorption-desorption cycles that would eventually determine the mass transfer limitations and the extent of elution of TNP along the flow.

Impact of Nano-TiO2 Combination with Biodiesel on Diesel Engine Performance and Emissions Under Fuel Magnetism Conditioning

AbstractProblems of atomization, spray, and lower output power are due to the biodiesel’s higher viscosity. All of these aim to encourage fuel magnetism and nanoparticles addition to reduce fuel consumption. Waste cooking oil was converted to methyl ester by transesterification. To make methyl ester blend, diesel and biodiesel were mixed at volume ratio of 20%. TiO2 nanoparticles were added to biodiesel blend B20 at doses of 25 and 50 mg/L. TEM and XRD were used to characterize the nanomaterials. A magnetic coil was placed before the fuel injector to apply a magnetic field on the line of fuel. South pole of the magnetic field is located near to the fuel line, whereas the north pole is located further away. To examine the impact of these nanomaterials with fuel magnetism on engine performance and emissions using WCO biodiesel mixture, an experimental test rig was built connected to diesel engine. During testing, diesel engine operates at 1500 rpm with load variation. The average increases in BTE were 1, 1.5, 3.5, 5.5, and 6.5% but the decreases in BSFC were 1.2, 2, 4, 5, and 6% for B20 + magnet, B20 + 25 TiO2, B20 + 25 TiO2 + magnet, B20 + 50 TiO2, and B20 + 50 TiO2 + magnet, respectively, at engine load range. The average drops in CO, NOx, and HC concentrations were 16, 22, and 33%, respectively, at load range for B20 + 50 TiO2 + magnet. To improve engine performance and reduce emissions, biodiesel blend B20 from waste cooking oil with nanoTiO2 concentration of 50 ppm under magnetic field effect was recommended as a substitute fuel in diesel engine.

Anthracite-Derived Porous Carbon@MoS2 Heterostructure for Elevated Lithium Storage Regulated by the Middle TiO2 Layer.

The rational design of MoS2/carbon composites have been widely used to improve the lithium storage capability. However, their deep applications remain a big challenge due to the slow electrochemical reaction kinetics of MoS2 and weak bonding between MoS2 and carbon substrates. In this work, anthracite-derived porous carbon (APC) is sequential coated by TiO2 nanoparticles and MoS2 nanosheets via a chemical activation and two-step hydrothermal method, forming the unique APC@TiO2@MoS2 ternary composite. The dynamic analysis, in-situ electrochemical impedance spectroscopy as well as theoretical calculation together demonstrate that this innovative design effectively improves the ion/electron transport behavior and alleviates the large volume expansion during cycles. Furthermore, the introduction of middle TiO2 layer in the composite significantly strengthens the mechanical stability of the entire electrode. As expected, the as-prepared APC@TiO2@MoS2 anode displays a high lithium storage capacity with a reversible capacity of 655.8 mAh g-1 after 150 cycles at 200 mA g-1, and robust cycle stability. Impressively, even at a high current density of 2 A g-1, the electrode maintains a superior reversible capacity of 597.7 mAh g-1 after 1100 cycles. This design highlights a feasibility for the development of low-cost anthracite-derived porous carbon-based electrodes.

Facile modification of TiO2 as S-Scheme multifunctional materials for environmental protection and energy-storage applications

This paper reports a simple one-step modification of commercial TiO2 with a conducting polytrimethoxyslilypropyl aniline (PTMSPA, a polyaniline derivative having silyl networks) to have multi-functional (photocatalytic, optical, pseudocapacitive, hydrophobic, porous, antibacterial, and electromagnetic interference shielding (EMI)) properties and demonstrates associated applications. We present the S-Scheme heterojunction (SHJ) formation between TiO2 and PTMSPA through band position alignments and designate the resultant TiO2 - TiO2- based SHJ multifunctional materials as MF-TSSM. The internal electric field that is generated at the interface facilitates the transportation of the photogenerated electron transfer . The XRD pattern of MF-TSSM exhibits mainly the peaks of anatase TiO2. The TEM image of MF-TSSM indicates that the TiO2 particles are spherical in shape with sizes showing variations in diameters ranging from 60 nm to 250 nm depending on the experimental conditions of preparation and TiO2 particles are homogeneously distributed within the PTMSPA matrix. The optical energy band gap of MF-TSSM is 1.60 eV, a much lower value than PTMSPA (3.02 eV), suggesting that the composite formation between TiO2 and PTMSPA. The contact angle of MF-TSSM is significantly increased to 47.1 ° from 8.0 of TiO2, informing the increase of hydrophobic characteristics. The rate constant (k) for methylene blue photodegradation was 0.030 min-1, and 0.010 min-1 for MF-TSSM and pristine TiO2, respectively, The MF-TSSM composite exhibits a higher specific capacitance value (28.7 F/g) than TMSPA (21.1 F/g). At a frequency of 0.42 THz, MF-TSSM and PTMSPA exhibit return loss features indicating good EMI shielding performance. The MF-TSSM has been tested against two different Gram-positive and Gram-negative bacterial strains. The nanoparticles were evaluated at doses of 10, 20, 40, and 80 µg/ml. The results indicated that Klebsiella pneumoniae demonstrated a greater zone of inhibition, ranging from 9 mm at 10 µg/ml to 23 mm at 80 µg/ml, indicating increased susceptibility. Pseudomonas aeruginosa exhibited reduced inhibition zones, ranging from 10 mm at 10 µg/ml to 14 mm at 80 µg/ml, indicating increased resistance. The excellent effectiveness of MF-TSSM against various Gram-positive and Gram-negative pathogenic bacteria is explained by the interaction between reactive oxygen species and the cellular components of the bacteria as well the electrostatic interaction arising between positive charges in TMSPA and negative charges in the cell components, resulting in notable cytotoxicity and damage to the bacterial cells. The research underscores the capability of these modified TiO₂ nanoparticles in addressing bacterial infections, with efficiency differing by bacterial strain.

Achieving superior hydrogen sorption kinetics of MgH2 by addition of Ni-doped TiO2 catalysts

MgH2 is a high-density hydrogen storage material but requires an efficient catalyst to improve its poor kinetics and reduce high operating temperature. TiO2 is a widely used photocatalyst for water splitting and hydrogen production, and has also demonstrated catalytic ability in the gas-solid reaction of MgH2. In this study, we synthesize the Ni-doped TiO2 nanoparticles, which significantly reduce the hydrogen absorption temperature down to subzero temperatures. The milled composite of MgH2 with 10 wt% Ti(5Ni)O2 can absorb 5.25 wt% H2 within 30 s at 25 °C, 4.30 wt% H2 within 50 s at 0 °C, and 3.94 wt% H2 within 50 s even at a low temperature of −30 °C. This composite can release 6.04 wt% of hydrogen in 3 min at 250 °C, and the dehydrogenation activation energy is reduced to 74.57±1.36 kJ/mol, a notable reduction in comparison to that observed in pure MgH2. This study demonstrates the potential of the modified TiO2 as an important kind of catalyst for solid-state hydrogen storage materials.

Insights into the photocatalytic process of surface-platinized hierarchical anatase TiO2 nanoparticles by in-situ DRIFT analysis

BackgroundEnvironmental remediation researchers are challenged to unravel the mechanisms of dual-responsive photocatalysts for degrading pollutants in both liquid and gas phases. This study aims to provide comprehensive insights into the photocatalytic processes employed by surface-platinized hierarchical anatase TiO2 nanoparticles. The investigation includes an in-depth analysis of the associated mechanism through in-situ DRIFT analysis. MethodsUtilizing surfactant-assisted surface platinized TiO2 samples synthesized through soft-template and chemical reduction techniques, this study investigated their efficacy in the degradation of crystal violet dye (10 ppm) under irradiation from a 380.8 W mercury-xenon lamp. The photooxidation of gas-phase ethanol was subsequently examined using the DRIFT technique. Significant findingsThe Pt-deposited C-TiO2 nanoparticles exhibited an impressive photocatalytic dye degradation efficiency of 87.07 %, surpassing the performance of other synthesized catalysts. To elucidate the mechanism behind this enhancement, an in-situ DRIFT analysis was conducted using the photo-oxidation of ethanol. The enhanced efficiency can be attributed to the incorporation of Pt metal, which serves as an electron collector in the n-type TiO2 semiconductor, thereby prolonging electron lifetime. Additionally, the pivotal role of hydroxyl radicals and holes in generating intermediates was thoroughly examined through DRIFT analysis, providing comprehensive insights into the photocatalytic reaction and the reactive intermediate species involved.

Acetylacetonate-modified TiO2 nanoparticles coated on the carbon felt as the negative electrode of vanadium redox flow battery for reducing HER and enhancing V3+/V2+ redox reactions

The occurrence of the hydrogen evolution reaction (HER) on the surface of the carbon-based negative electrode of the vanadium redox flow battery (VRFB) causes high charge transfer resistance (RCT) for the desired V3+/V2+ redox reaction leading to irreversible capacity loss. To this effect, we have synthesized acetylacetonate-modified TiO2 (SGTA) and unmodified TiO2 (SGT) coating colloidal solutions as electrocatalysts for enhanced V3+/V2+ redox reaction on the carbon-felt negative electrodes of VRFB. The SGTA particles exhibit significantly higher homogeneity with sizes of ≤15 nm, in comparison to the severely aggregated SGT particles with diameters of ∼23–75 nm in colloidal solution. When coated on the pristine carbon felt (P-CF), the surface morphology of the SGTA@CF electrode exhibits relatively dense, uniformly coated particles, in comparison to the sparse, non-even coating of aggregated particles on the SGT@CF electrode surface. Consequently, the charge transfer for V3+ → V2+ reduction reaction and charge storage capacity are determined to be in the order SGTA@CF > SGT@CF > P-CF, confirming that the competitive and irreversible HER was higher on the surface of non-evenly coated fibers and bare carbon felt, respectively.

Eco-friendly synthesis and applications of graphene-titanium dioxide nanocomposites for pollutant degradation and energy storage

An innovative, eco-friendly method has been developed to synthesize reduced graphene oxide (rGO) sheets using orange peel extract. Following this, TiO2 nanoparticles are anchored to the rGO sheets through a hydrothermal process, resulting in an rGO/TiO2 nanocomposite (GTO/NC). This study utilized standard characterization techniques to confirm the formation of GTO/NC-1 and GTO/NC-2. Comparative analysis demonstrated that orange peel extract exhibits reducing capabilities compared to other natural reducers. The resulting GTO/NC-1 and GTO/NC-2, specifically GTO/NC-2, enhanced catalytic performance in degrading methyl orange a prevalent organic pollutant in various industrial applications. This nanocomposite achieved a turnover frequency of 0.003 mg MO/mg catalyst/min and displayed remarkable durability, enduring 3.0 cycles with robust first-order rate constants of 0.0193 min−1. Additionally, the electrochemical properties of GTO/NC-1 and GTO/NC-2 as electrode materials were assessed, revealing a specific capacitance of 320.0 Fg−1 at a current density of 1.0 Ag−1 and maintaining about 86.8 % of its initial capacitance after various charge–discharge cycles. These properties highlight the potential of GTO/NC-1 and GTO/NC-2 as both efficient catalysts for environmental remediation and durable materials for energy storage applications, offering substantial benefits for sustainable technology solutions.

Lasing from Doubly Degenerate Bound States in the Continuum.

This paper reports dual-mode vortex lasing with a topological charge of -2 via doubly degenerate bound states in the continuum. We patterned a photonic crystal slab with hexagonal TiO2 nanoparticles arranged in a hexagonal lattice to support doubly degenerate bound states in the continuum at the Γ point, and the finite array was truncated to have a square boundary. Because emission from bound states in the continuum at the Γ point is forbidden, lasing emerges at off-Γ points, where the double degeneracy is lifted, resulting in two lasing peaks close in wavelength. The coherence time of vortex lasing is about 1.4 ps under pulsed pumping with a width of 75 fs. Polarization- and angle-resolved spectral measurements reveal that the two lasing peaks show orthogonal polarization states.

Optimising Nanoparticle Dispersion Time for Enhanced Thermomechanical Properties in DGEBA-Based Shape Memory Polymer Composites

Shape-memory polymers (SMPs) are smart materials that can change shape upon an external stimulus. This phenomenon is called the shape memory effect (SME), which is caused by entropy change due to rapid molecular motion in the polymer segments. Due to the inherently weak thermomechanical properties, use of SMPs is limited in many engineering applications. Therefore, SMPs are often reinforced with fibres and nanoparticles (NPs). NPs offered greater flexibility due to their superior physical, chemical, electrical, mechanical, and thermal properties. However, the homogeneous distribution of NPs is crucial for composition’s stability and enhancement of the base material’s properties. Among the different techniques used for dispersing NPs, ultrasonic irradiation has shown excellent emulsifying and crushing performance. The sonication process is essential for mitigating agglomerates; however, prolonged sonication time probably increases epoxy temperature, micro-bubbles, cavitation, breaking apart molecules and finally degrading the epoxy resin performances. This paper provides critical insight of nanoparticle dispersion into diglycidyl ether of bisphenol A epoxies (DGEBA). DGEBA epoxy resin was added to TiO2 NPs and sonicated for 60 min with 5 min intervals while the temperature of epoxy was maintained below 60oC by using a water cooling throughout the sonication process. The process parameters such as amplitude, mode, epoxy volume and the weight percentage of NPs were kept constant. After each sonication step, Fourier-transform infrared spectroscopy (FTIR) was performed using Thermo Scientific™ and analysed through OMNIC™ Professional quantitation software. In accordance with FTIR results, until 30 min of the sonication, DGEBA resin was not degraded. In order to confirm the performances and the reinforcing effect of NPs, thermo-mechanical and shape memory properties were compared with the neat specimen. The outcomes of this research have suggested quick guidance to find optimum NP dispersion time for DGEBA resins, which has been hardly studied before.

Preparation of TiO2 nanoparticles decorated porous carbon via a pseudo co-templating strategy and their application as substrates for high performance cathode of Li[sbnd]S batteries

Lithium‑sulfur batteries (LSBs) with a high theoretical specific capacity are considered as one of the most promising energy storage devices for next-generation. However, issues such as the insulation of pristine sulfur, the shuttle effect of polysulfides (LiPSs), and the volume change of sulfur cathode during cycling hinder their commercial applications. In this work, composite microspheres of TiO2@p-C consisting of porous carbon decorated with TiO2 nanoparticles, have been designed and synthesized aiming to confine and trap the polysulfides inside the porous substrates and to improve the kinetics of the electrochemical reaction therein. TiO2 particles with size of a few nanometers are prepared by a tetraethyl ammonium hydroxide assisted sol-gel method. Composite microspheres of TiO2@p-C are created through spray drying technique using chitosan as carbon source, and nanoparticles of SiO2 with TiO2 as co-template while selectively etching of the former. The confinement effects via the pores in the TiO2@p-C microspheres and the affinity between the polar TiO2 moieties and the polysulfide species work synergistically, alleviating the effusion of the polysulfides and promoting the conversion reaction of them as well. As a result, the shuttle effect of polysulfides can be inhibited obviously. Significantly, the S@TiO2@p-C-2 composite cathode exhibits excellent cyclic performance of 1263 mAh g−1 at 0.2C and maintains still a discharge capacity of 809 mAh g−1 after 100 charge and discharge cycles. At a current density of 2C, it still delivers an outstanding specific capacity of 772 mAh g−1. In the case of high sulfur load up to 90 wt%, the discharge capacity of S@TiO2@p-C-2 composite electrode could still maintain at 469.5 mAh g−1 after 100 cycles under current density of 0.2C.