Increase In Transition Temperature Research Articles

Fabrication of fire-retarded epoxy asphalt composites with compatibilization and toughening for road tunnel pavements

Although epoxy asphalt (EA) mixtures have been widely used for the pavement in tunnels, it was limited by its flammability, poor compatibility and low mechanical property. To solve the above problems, a compatibilized and toughening flame retardant (ESO-AA-DOPO) was prepared via the epoxidized soybean oil (ESO), arachidonic acid (AA) and 9,10-Dihydro-9-oxa-10-phosphaphenanthrene 10-oxide (DOPO). The presence of ESO-AA-DOPO significantly improved the flame retardancy, in which passing the UL-94 V-2 rating. The peak heat release rate (PHRR) reducing by 46.2 % for EA/40A-ESO-AA-DOPO composites comparing to that of pure EA. The analysis of char residue confirmed that the catalytic formation of dense and continuous char layer residue with good thermal oxidation stability originating from the ESO-AA-DOPO. The initial stage viscosity of ESO-AA-DOPO modified EA was lower than that of pure EA. Under the action of aliphatic epoxy resin and double bond, the molecular chain of epoxy resin presented a network structure, the base asphalt was divided into micelles, and the overall distribution of EA system was a 3D networks “sea-island”, which ensuring the increase in the glass transition temperature (Tg) of the EA system. The tensile strength and elongation at break of EA/40A-ESO-AA-DOPO composites were 123 % and 207 % higher than those of pure EA attributing to the improved compatibility and the formation of 3D networks “sea-island” structure.

Investigations of the adsorbed layer of polysulfone: Influence of the thickness of the adsorbed layer on the glass transition of thin films.

This work studies the influence of the adsorbed layer on the glass transition of thin films of polysulfone. Therefore, the growth kinetics of the irreversibly adsorbed layer of polysulfone on silicon substrates was first investigated using the solvent leaching approach, and the thickness of the remaining layer was measured with atomic force microscopy. Annealing conditions before leaching were varied in temperature and time (0-336h). The growth kinetics showed three distinct regions: a pre-growth step where it was assumed that phenyl rings align parallel to the substrate at the shortest annealing times, a linear growth region, and a crossover from linear to logarithmic growth observed at higher temperatures for the longest annealing times. No signs of desorption were observed, pointing to the formation of a strongly adsorbed layer. Second, the glass transition of thin polysulfone films was studied in dependence on the film thickness using spectroscopic ellipsometry. Three annealing conditions were compared: two with only a tightly bound layer formed in the linear growth regime and one with both tightly bound and loosely adsorbed layers formed in the logarithmic growth regime. The onset thickness and increase in the glass transition temperature increases with annealing time and temperature. These differences were attributed to the distinct conformations of the formed adsorbed layers.

Aramid-Reinforced UV Curable Adhesive Resins for Use As an Interlayer in Laminated Glass.

Colorless, transparent, and mechanically robust aramid polymers are synthesized from two diamine monomers with strong electron-withdrawing groups, using low-temperature solution condensation with diacid chloride. The aramids dissolved very well in the liquid acrylamide monomers. When N,N-dimethylacrylamide (DMA) is used as a reactive diluent, films with the desired features are produced from the hybrid aramid-DMA resins via ultraviolet (UV)curing. The hybrid films are colorless and transparent in the visible region and showed an increase in the glass transition temperature, tensile strength, and elastic modulus in proportion to the aramid content. Laminated glass is manufactured using the hybrid resin as an interlayer, which exhibits very strong adhesion between the two sheets of glass, is not easily broken by an external impact, and do not scatter fragments. Moreover, the laminated glass do not distort images and functioned very effectively in UV blocking, soundproofing, and suppressing changes in the ambient temperature. Heat treatment further improves the light transmittance and impact resistance of the laminated glass. Laminated glass specimens with various fluorescence colors are also manufactured. Aramid-reinforced films prepared using N,N-diethylacrylamide as a reactive diluent underwent thermally induced phase separation in a wet state, providing smart glass with a privacy protection function.

Synthesis of novel reactive flame retardant to improve fire resistance and mechanical properties in epoxy resin

A novel reactive flame-retardant (FR), phosphorus-modified tetraethylenepentamine (TEPA-m-MVP), was prepared via aza-Michael addition process, using dimethyl vinylphosphonate (MVP). TEPA-m-MVP was successfully covalently introduced into the structure of the epoxy system, into the epoxy resin matrix synthesised from tetraethylenepentamine (TEPA) and diglycidyl ether bisphenol A (DGEBA) reaction, leading to the development of a flame-retardant epoxy resin (FR-EP). The curing behaviour, mechanical properties, thermal stability and flame-retardant behaviour of FR-EP samples were investigated and compared to the behaviour of the neat epoxy resin (EP). FR-EPs showed an increase in glass transition temperature (Tg), from 120 to 147 °C upon integrating TEPA-m-MVP into the epoxy resin structure, while the value of the E modulus remained unaffected. Furthermore, FR-EP-2%P sample with the optimal P content, approximately 2 wt%, displayed excellent flame-retardant properties. In comparison to EP, total heat release (THR) and peak heat release rate (pHRR) for FR-EP-2%P decreased from 22.6 to 15.3 kJ.g−1 and from 1557 to 572 kW.m−2, respectively. In addition, an interesting impact of the crosslinking density of FR-EP samples on the fire behaviour was observed. This work presents a new strategy for the simultaneous modification of the flame retardancy and mechanical properties of epoxy systems.

Role of dislocations on martensitic transformation temperatures and microstructure: A molecular dynamics study

Microstructure and defects strongly affect martensitic transformations in metallic alloys. Significant progress has been made in understanding the atomic-level processes that control the role of grain boundaries and precipitates in these solid-to-solid phase transformations. Yet, the role of dislocations and their structures on martensitic transformation temperature and the resulting microstructure remains unclear. Therefore, we used large-scale molecular dynamics simulations to study the forward and reverse transformation of a martensitic material modeled after Ni63Al37 under cyclic thermal loading. The simulations reveal that dislocations in the austenite phase act as one-dimensional seeds for the martensite phase, which is present at temperatures significantly above the martensite start value. We find a reduction in the dislocation density during cyclic thermal loading, which results in the increase in martensite and austenite transition temperatures, in agreement with experiments. Importantly, we extracted a critical martensitic nuclei size for developing stable domains and found that relatively low dislocation densities are needed to grow independent martensitic variants resulting in a multi-domain structure.

Various Morphologies of Graphitic Carbon Nitride (g-C3N4) and Their Effect on the Thermomechanical Properties of Thermoset Epoxy Resin Composites.

This research aims to highlight the importance of diverse forms of graphitic carbon nitride (g-C3N4) as strengthening elements in epoxy composites. It explores the influence of three different forms of g-C3N4 and their concentrations on the mechanical properties of the epoxy composites. Various characterization techniques, such as scanning electron microscopy (SEM), dynamic light scattering (DLS), thermogravimetric analysis (TGA), and Fourier-transform infrared spectroscopy (FTIR), were utilized to comprehend the effects of g-C3N4 morphology and particle size on the physical and chemical characteristics of epoxy resin. Mechanical properties, such as tensile strength, strain, modulus, and fracture toughness, were determined for the composite samples. SEM analysis was performed to examine crack morphology in samples with different reinforcements. Findings indicate that optimal mechanical properties were achieved with a 0.5 wt% bulk g-C3N4 filler, enhancing tensile strength by 14%. SEM micrographs of fracture surfaces revealed a transition from brittle to rough morphology, suggesting increased toughness in the composites. While the TGA results showed no significant impact on degradation temperature, dynamic mechanical analysis demonstrated a 17% increase in glass transition temperature. Furthermore, the improvement in thermal breakdown up to 600 °C was attributed to reinforced covalent bonds between carbon and nitrogen, supported by FTIR results.

Hygrothermal effects on the durability of resin‐infused thermoplastic E‐glass fiber‐reinforced composites in marine environment

AbstractThis paper presents a comparative assessment of hygrothermal effects on the mechanical and thermomechanical properties of resin‐infused thermoplastic E‐glass fiber‐reinforced composites (FRC) in the marine environment. The thermoplastic FRCs were immersed in seawater at two different aging temperatures, that is, 35 and 70°C. The quasi‐static tests were conducted on unaged and aged FRCs, followed by scanning electron microscopy (SEM) to determine the effect of the marine environment on the mechanical properties and damage progression. The specimens immersed at 70°C showed a significant drop of 46.7%, 39.7%, 22.6%, and 16% in mechanical properties (tensile, compression, flexural, and ILSS) mainly due to plasticization, matrix cracking, and fiber/matrix debonding. The specimens immersed at 35°C showed a reduction in tensile, compressive, and flexural strength of 10%, 14.7% and 1.9% respectively, with no significant effect on ILSS. In addition, dynamic mechanical analysis (DMA) reveals that prolonged aging induces an increase in glass transition temperature due to polymerization reactions. This work is intended to reveal the effect of extreme marine environment on the resin‐infused thermoplastic FRC and to provide a useful reference for their potential structural applications in the marine industry.Highlights Influence of aging conditions on the long‐term performance of FRCs. Hygrothermal aging leads to an increase in the glass transition temperature. The marine environment degrades mechanical properties of FRCs by up to 50%. Matrix cracking and fiber‐matrix debonding evolved as dominant failure modes.

Characterization of Melt-Spun Recycled PA 6 Polymer by Adding ZnO Nanoparticles during the Extrusion Process.

With recent technological advances and the growing interest in environmentally friendly fiber production processes, the textile industry is increasingly turning to the spinning of filaments from recycled raw materials in the melt spinning process as the simplest method of chemical spinning of fibers. Such processes are more efficient because the desired active particles are melt-spun together with the polymer. The study investigates the melt spinning of recycled polyamide 6 (PA 6) fibers modified with zinc oxide nanoparticles (ZnO NPs) in concentrations ranging from 0.1 to 2.0 wt% of the polymer. The extrusion process was optimized under laboratory conditions. An analysis of the effectiveness of the nanoparticle distribution and chemical composition was performed using scanning electron microscopy (SEM) with energy-dispersive X-ray spectroscopy (EDS), differential scanning calorimetry (DSC), and Fourier transform infrared spectroscopy (FTIR). The results of the thermal analysis show an increase in the glass transition temperature of the extruded material from 50.97 °C (raw polymer) to 51.40 °C to 57.98 °C (polymer modified with ZnO NPs) and an increase in the crystallization point from 148.19 °C to a temperature between 175.61 °C and 178.16 °C, while the molar enthalpy (ΔHm) shows a decreasing trend from 65.66 Jg-1 (raw polymer) to 48.23 Jg-1 (PA 6 2.0% ZnO). The FTIR spectra indicate PA 6 polymer, with a characteristic peak at the wavelength 1466 cm-1, but pure ZnO and PA 6 blended with ZnO show a characteristic peak at 2322 cm-1. The distribution of nanoparticles on the fiber surface is more or less randomly distributed and the different size of NPs is visible. These results are confirmed by the EDS results, which show that different concentrations of Zn are present. The mechanical stability of the extruded polymer modified with NPs is not affected by the addition of ZnO NPs, although the overall results of strength (2.56-3.22 cN/tex) and modulus of elasticity of the polymer (28.83-49.90 cN/tex) are lower as there is no drawing process at this stage of the experiment, which certainly helps to increase the final strength of the fibers. The results indicate the potential of modification with ZnO NPs for further advances in sustainable fiber production.

Effect of yeast protein on reduced‐fat ice cream: Sensory quality, rheological behaviour, thermal properties and fat destabilisation

This study prepared six different ice creams to investigate the effect of yeast protein (YP) on their sensory, rheological, thermal properties and fat destabilisation. Results indicated that YP could improve sensory quality, flow and viscoelastic properties. The thermal property was also positively influenced by YP with a significant decrease in frozen water percentage and an increase in glass transition temperature (P < 0.05). Additionally, the particle size and confocal laser scanning microscopy results illustrated that YP could moderately promote the fat aggregate percentage and size. Overall, YP could serve as a fat replacer to produce reduced‐fat ice cream.

Kinetics of Plasticized Poly(vinyl chloride) Thermal Degradation, Induction, Autocatalysis, Glass Transition, Diffusion

AbstractKinetics of non‐oxidative thermal degradation of poly(vinyl chloride) (PVC) plasticized with di(2‐ethylhexyl)phthalate and epoxidized linseed oil (ELO) were studied using differential scanning calorimetry. PVC thermal degradation autocatalyzed by forming HCl is delayed in the presence of acid scavenging ELO. Direct HCl elimination rates during steady state degradation (induction period) were almost independent on ELO concentration, with rate constants ranging from ≈3.2×10−6 s−1 at 463 K to ≈7.0×10−5 s−1 at 503 K. Activation energy of HCl elimination increased with glass transition temperature (Tg) increase from 136.0 kJ mol−1 at Tg=260.3 K to 141.9 kJ mol−1at Tg=274.2 K. Diffusion coefficients of HCl diffusion in plasticized PVC deduced using Williams‐Landel‐Ferry equation were of the order of 10−4 cm2 sec−1. Calculated activation energy of HCl diffusion in plasticized PVC was ≈30 kJ mol−1. The rate constants of PVC autocatalytic degradation were derived from the experimental data (for the 1st time) using Šesták‐Berggren approach and ranged from 3.2×10−2 sec−1 at 503 K to 4.4×10−3 sec−1 at 463 K. Autocatalysis activation energies ranged from 70.4 kJ mol−1 to 85.1 kJ mol−1 and increased with increase of glass transition temperature. It was established that PVC degradation kinetics was not controlled by HCl diffusion. Compensation effect was observed for initial and catalyzed PVC degradation.

Infrared emission properties of VO2 films fabricated with different oxygen flow ratios

Infrared (IR) camouflage materials are widely used to realize thermal camouflage by adjusting the IR emissivity (ε) of the target object. However, ε modulation without an external energy supply is still a great challenge. Self-regulating VO2 films with different IR emission properties are investigated by adjusting the oxygen flow ratio (O2%) and film thickness. The ε of VO2 films changes before and after the phase transition, and the Δε (the difference of ε before and after the phase transition) of films is different under different O2%, and the maximum Δε can reach 0.49. In addition, the difference temperature (ΔTIR) between the actual temperature (TA: the surface temperature of a standard silicon wafer measured by IR camera, which represents the actual temperature of VO2 samples.) and the IR trapping temperature (TIR: the temperature of VO2 samples measured by IR camera.) is greater than 35 °C after the phase transition. With the range of 1.6 %–2.2 % O2, the IR emission transition temperature (Tε-MIT) and hysteretic width (ΔTε-MIT) increase with increasing O2%. The thickness of the VO2 film affects the IR emission characteristics. The VO2 film is suitable for thermal camouflage materials and for IR anticounterfeiting.

Aging of a Poly(vinyl acetate)-Based White Glue and Its Durability in Contemporary Artworks.

While extensive research has focused on understanding the degradation mechanisms of Poly(vinyl acetate) (PVAC) paint under different environmental conditions, limited attention has been paid to the long-term stability of PVAC-based white glues, especially when used in artworks. This study investigates the accelerated degradation, under simulated photoaging, and isothermal treatment of a commercial PVAC-based white glue considered representative of this class of materials used in contemporary artworks to predict its durability and assess its behavior in art objects. Through accelerated aging experiments and comparison with natural aging observed in artworks, the study reveals the formation of chromophores and the release of plasticizers as key processes; in particular, the progressive darkening was considered an early indicator of degradation processes, before structural changes could be detected by FTIR or NMR spectroscopies. The plasticizer loss induces an increase in glass transition temperature, from 7 °C to temperatures higher than room temperature, affecting the adhesive's cohesive strength and contributing to the detachment of materials in artworks. The findings underscore the importance of preventive conservation measures to mitigate degradation issues in PVAC-based artworks.

Effect of cobalt doping on the structural, magnetic, optical, and electronic properties of LiFeCr4O8

Cobalt doping's influence on the structural, magnetic, and electronic properties of the double spinel LiFeCr4O8 was systematically investigated. Rietveld refinement revealed a consistent increase in lattice parameter a and unit cell volume with cobalt incorporation. Magnetic susceptibility measurements indicated three distinct transitions: an increase in the ferrimagnetic transition temperature (TN), a decrease in the magnetostructural transition temperature (TMS), and an increase in the spin gap transition by cobalt doping. Through diffuse reflectance spectroscopy the direct optical band gap (Eog) was obtained with values of 1.169 eV, 1.303 eV, 1.396 eV, and 1.230 eV for x = 0.0, 0.1, 0.2, and 0.5, respectively. The observed increase in Eog with cobalt doping suggests a widening of the band gap, which could be beneficial for optoelectronic applications. By means of X-ray photoelectron spectroscopy (XPS) the core levels of Li 1s, Co 3p, Fe 3p, Cr 3p, Fe 2p, Cr 2p, and O 1s were identified. XPS valence band (VB) analysis revealed a decreasing intensity at binding energy BE = 0 eV with respect to x = 0.0. Density functional theory calculations with Hubbard U correction (DFT + U) confirmed a ferrimagnetic semiconductor behavior with a direct electronic band gap (Eeg) of 1.085 eV.

Formulations based on pullulan and a derivative as coating material for the food sector

Carboxymethylated derivatives of pullulan (PU) were synthesized and evaluated as coating for the postharvest preservation of blueberries. Carboxymethylpullulan was obtained by etherification reaction with the substitution degrees of 0.52, 0.34, and 0.26 for CMP1, CMP2, and CMP3 respectively. Infrared spectroscopy and nuclear magnetic resonance results showed characteristic signals of the carbonyl group belonging to the carboxymethyl group. Thermal analysis showed that CMP1, CMP2, and CMP3 derivatives presented thermal stability values of 209.91 C, 214.73 C, and 225.52 °C, respectively, and were lower with respect to PU with Td of 238.84 °C. Furthermore, an increase in the glass transition temperature due to carboxymethylation was determined. The chemical modification decreased the contact angle with respect to PU (71.34°) with values for CMP1, CMP2, and CMP3 of 39.89°, 53.72° and 60.61°, respectively. The carboxymethylation also increased the water vapor permeability and mechanical properties of the films. In addition, it was found that the CMP molecules affected the optical properties. The application of CMP-based coatings reduced the mass loss and ripening rate of blueberries compared to native pullulan, therefore, packaging from CMP molecules could be used as a coating capable of delaying ripening and extending the shelf life of fruits.

Stress-induced changes in magnetite: insights from a numerical analysis of the Verwey transition

SUMMARY Magnetic susceptibility behaviour around the Verwey transition of magnetite (≈125 K) is known to be sensitive to stress, composition and oxidation. From the isotropic point (≈130 K) to room temperature, decreasing magnetic susceptibility indicates an increase in magnetocrystalline anisotropy. In this study, we present a model which numerically analyses low-temperature magnetic susceptibility curves (80–280 K) of an experimentally shocked (up to 30 GPa) and later heated (973 K) magnetite ore. To quantify variations of the transition shape caused by both shock and heating, the model statistically describes local variations in the Verwey transition temperature within bulk magnetite. For the description, Voigt profiles are used, which indicate variations between a Gaussian and a Lorentzian character. These changes are generally interpreted as variations in the degree of correlation between observed events, that is between local transition temperatures in the model. Shock pressures exceeding the Hugoniot elastic limit of magnetite ($ \ge $5 GPa) cause an increase in transition width and Verwey transition temperature, which is partially recovered by heat treatment. Above the Verwey transition temperature, susceptibility variations related to the magnetocrystalline anisotropy are described with an exponential approach. The room temperature magnetic susceptibility relative to the maximum near the isotropic point is reduced after shock, which is related to grain size reduction. Since significant oxidation and cation substitution can be excluded for the studied samples, variations are only attributed to changes in elastic strain associated with shock-induced deformation and annealing due to heat treatment. The shocked magnetite shows a high correlation between local transition temperatures which is reduced by heat treatment. The model allows a quantitative description of low-temperature magnetic susceptibility curves of experimentally shocked and subsequently heat-treated polycrystalline magnetite around the Verwey transition temperature. The curves are accurately reproduced within the experimental uncertainties. Further applications for analysing magnetite-bearing rocks seem possible if model parameters, such as for oxidation are included into the model.

Phase transformation behavior and shape memory effect of nickel-titanium shape memory alloy using the magnetic field assisted wire electrical discharge machining

Nickel-titanium shape memory alloy (NiTi-SMA) can restore its original shape after deformation, making it show great application in the fields of biomedicine, aerospace, etc. The wire electrical discharge machining (WEDM) has the advantage of machining micro and complex structures, which can greatly promote the application of NiTi-SMA. However, there are issues such as heat affected layer (HAL) on the surface of WEDM, which can affect the functionality of NiTi-SMA. Therefore, when using WEDM to NiTi-SMA, more attention should be paid to the functional changes after machining. This article primarily examine is the impact of peak current and pulse on time on the phase transformation behavior, shape memory effect, and mechanical properties of NiTi-SMA during WEDM, and introduces into the magnetic field assisted (MFA) process to improve the machining performance of NiTi-SMA. The results indicate that the HAL formed on the surface of NiTi-SMA is primarily composed of the irreversible phase transformation of B2 austenite. This layer induces a hardening effect, resulting in an increase in the phase transition temperature and a decrease in the phase transition energy (∆HM-A), as a result, the martensitic phase transformation behavior is suppressed. When the peak current and pulse on time increase, the surface quality of the NiTi-SMA processed decreases. The thickness of the HAL and microhardness increase, causing an increase in the phase transition temperature of the NiTi-SMA processed samples. Additionally, the transformation energy ∆HM-A, shape recovery rate, and mechanical properties decrease, and after recovery, more surface cracks appear and show larger extensions. MFA-WEDM can improve the surface quality of NiTi-SMA processing, reduce the thickness of the HAL, and effectively enhance the phase transformation temperature and energy ∆HM-A of the NiTi-SMA processed samples. With a magnetic field strength of 0.45 T, the tensile shape recovery rates of 98%, 94.4%, and 91.0% were achieved at 2%, 5%, and 8% strain, respectively. This represents an improvement of 8.9% compared to the maximum shape recovery rate with conventional WEDM. At the same time, it also inhibits the generation and propagation of surface cracks after deformation recovery. Additionally, MFA-WEDM improves the mechanical properties of NiTi-SMA, and reduces the thickness of the brittle fracture region by 49.7% compared to conventional WEDM. Therefore, MFA-WEDM can effectively enhance the shape memory effect of NiTi-SMA. However, it is important to avoid excessive peak currents and pulse on time to achieve optimal shape memory functionality.

4D printed shape memory bismaleimide resin with high storage modulus and low shrinkage rate via second-stage curing

In recent years, the field of shape memory materials with active deformation capabilities has experienced rapid development. However, bismaleimide, as a widely used structural material in the aerospace industry, has been neglected in the field of shape memory. This work designed a UV-crosslinked network with 1-vinyl-2-pyrrolidone monomer, and prepared 4D printed smart structures based on shape memory bismaleimide resin through UV-assisted DIW printing. 4D printed semi-interpenetrating network polymer materials were obtained through a two-stage UV-thermal curing process, resulted in an increase in the material's glass transition temperature to a maximum of 187.4 °C. The storage modulus was improved to 5229 MPa. More important, we achieved a lowest shrinkage rate (0.21 %) of 4D printed polymer. The composite sandwich structure with electrical-driven shape memory performance was printed by double-sided printing of bismaleimide resin on conductive carbon fabric. 4D printed composite structure realizes in-situ self-blocking secondary curing, deformation process after curing. This significant progress provides a promising prospect for remote controllable and precise driving in the aerospace field.

Inserting intermolecular hydrogen bonds to achieve dimensional regulation and phase transition temperature enhancement

Organic-inorganic hybrid materials have become potential candidates in fields of light emitting diodes (LEDs), mechanical switches, energy conversion due to their excellent magneto-opto-electronic properties. Further improving the performance of materials is a prerequisite for achieving their commercial application. Currently, many effective strategies have been proposed and validated to enhance the properties of materials, but both simultaneously realizing the improvement phase transition temperature and dimensional regulation of materials remains a huge challenge. Here, we successfully synthesized two hybrid materials, (pyrrolidinium)PbI3 (Com-1) and (3-hydroxypyrrolium)6Pb5I16 (Com-2). In this work, the strategy of inserting intermolecular hydrogen bonds cleverly achieves a significant increase in phase transition temperature (ΔT = 81 K) and dimensional regulation (1D to 2D). Moreover, semiconductor properties of two compounds are investigated to be direct bandgap semiconductor. In short, inserting intermolecular hydrogen bonds between molecules is an effective strategy to improve physical performance.

Dimerized Nonfused Electron Acceptor Based on a Thieno[3,4-c]pyrrole-4,6-dione Core for Organic Solar Cells.

In this work, the first dimerized nonfused electron acceptor (NFEA), based on thieno[3,4-c]pyrrole-4,6-dione as the core, has been designed and synthesized. The dimerized acceptor and its single counterpart exhibit similar energy levels but different absorption spectra due to their distinct aggregation behavior. The dimerized acceptor-based organic solar cells (OSCs) demonstrate a higher power conversion efficiency of 11.05%, accompanied by enhanced thermal stability. This improvement is attributed to the enhancement of the short-circuit current density and fill factor, along with an increase in the glass transition temperature. Characterizations of exciton dynamics and film morphology reveal that a dimerized acceptor-based device possesses an enhanced exciton dissociation efficiency and a well-established charge transport pathway, explaining its improved photovoltaic performance. All these results indicate that the dimerized NFEA as a promising candidate can achieve efficiency-stability-cost balance in OSCs.

Correlation of thermal and electrical properties of silver germanophosphate glasses with their structural analysis by Raman and NMR spectroscopy

In present study glasses of the system Ag2O-GeO2-P2O5 were studied in the compositional series (50−x)Ag2O-xGeO2-50P2O5 with x = 0−40 mol%. Ag2O substitution by GeO2 results in a significant increase of both glass transition temperature, Tg, and crystallization temperature, Tc, up to 628 °C (Tg) and 851 °C (Tc) at x = 40 mol% GeO2. The glass structure was investigated from the analysis of 31P MAS NMR and Raman spectra. Both methods show transformation of phosphate glass network formed mainly by Q2 units to germanate-phosphate network formed by Q1xGe and Q21Ge phosphate units and germanate units. Raman spectra, in addition, reveal evolution of P‒O‒P linkages to P‒O‒Ge and Ge‒O‒Ge linkages through the glass series. DC conductivity trend upon GeO2 addition showed non-monotonic behaviour, which is related to structural changes in the glass-network.