Thermal Stability Research Articles

Forming performance and environmental impact of bamboo fiber reinforced polypropylene composites based on injection molding process for automobiles

AbstractTo explore the potential application of plant fiber reinforced composites for automotive component applications, this study prepared bamboo fiber (BF)/nano‐talc/polypropylene (PP) composites based on the injection molding process, comprehensively evaluated the effect of reinforcement materials on the forming properties of composites, including thermal performance, mechanical properties, water absorption, etc. Furthermore, taking a certain automotive injection molded interior part as the object, a life‐cycle assessment from production to the gate was conducted based on the real energy and material consumption during the composite preparation process. The results indicate that adding BF and talc powder increased the thermal stability, density, hardness, viscosity, and crystallinity of the composites while reducing the water contact angle on the surface. Surface‐modified BF and PP showed good compatibility. Talc powder exhibited good dispersibility in PP, and the synergistic effect of BF and talc powder effectively enhanced the composite performance. The tensile, flexural, and impact strength of the composites were improved by 40.64%, 51.48%, and 66.51%, respectively, compared with pure PP. The modulus of the composite increased nearly 2 times compared with pure PP. Additionally, the composite demonstrated good friction and wear properties. The environmental impact of the BF composite manufacturing process was significantly higher than that of pure PP. The substantial consumption of electricity, chemicals, and water resources in the extraction and modification processes of BF were the main factors. The findings of this study contribute to achieving green, high‐performance BF composite manufacturing and the expansion of its applications.Highlights Composites have a higher environmental impact compared to PP. BF and talc can synergistically enhance the performance of composites. BF shows good compatibility with PP. Composites exhibit good friction and wear characteristics.

Hierarchically N-doped porous carbon synthesized from 3D cellulose alcogel decorated by in-situ growth of ZIF-8 for high performance CO2 capture

The physical properties and chemical compositions of porous carbons are crucial factors in determining their effectiveness in adsorbing CO2. Cellulose-based porous carbon has emerged as an outstanding candidate adsorbent for CO2 capture. The research involved the creation of hierarchically nitrogen-doped porous carbon (HNC) using a 3D cellulose alcogel (CA) as substrate, which was prepared through a thermal introduced phase separation (TIPS) method combined with hydrolysis treatment. The plentiful functional groups of CA offered abundant growth sites for the introduction of ZIF-8 crystals. CA/ZIF-8 composite alcogel (CZA) with greater surface area and superior thermal stability compared to CA was successfully fabricated and used as precursor for the production of HNC. The important effects of microporosity and surface chemistry of HNC samples on CO2 capture were discussed in-depth. HNC-350–850 displayed a hierarchically porous structure with a large number of micropores and abundant N/O/Zn-doped functional groups, exhibiting high CO2 uptakes at 1 bar (3.56 mmol/g at 25 °C), good IAST CO2/N2 (15/85, V/V) selectivity of 16.31 at 25 °C, and outstanding regenerability with ∼100 % CO2 adsorption capacity retained after ten cycles. In the two-component CO2/N2 (15/85, V/V) competitive adsorption process, the maximum breakthrough periods for CO2 (433.1 s) is significantly longer than that of N2 (3.8 s). The CO2 breakthrough adsorption capacity reached 1.79 mmol/g at 25 °C and 1 bar with the separation coefficient of 45.8 for CO2 over N2. These results confirmed that HNC, in addition to having excellent CO2/N2 selectivity, demonstrated good feasibility for practical use. The green and practicable synthetic route described in this study is not only expected to offer novel adsorbents for high performance CO2 capture, but also provide a new theoretical foundation for the development of cellulose-based porous materials.

Physics of Ferroelectric Wurtzite Al1−xScxN Thin Films

AbstractAl1−xScxN emerges as a revolutionary ferroelectric material within the III‐N family. It combines exceptional switchable polarization (80–165 µC cm−2), highly tunable coercive fields (1.5–6.5 MV cm−¹), and a wide bandgap (4.9–5.6 eV). Unlike conventional ferroelectrics, Al1−xScxN exhibits remarkable compatibility with both CMOS and III‐N technologies. It can be fabricated on plastic substrates at low temperatures, demonstrating excellent flexibility and biocompatibility. Remarkably, Al1−xScxN maintains superior performance in harsh environments due to its outstanding thermal stability (up to 1100 °C). These unique characteristics position Al1−xScxN as a highly promising candidate for a wide range of applications, including high‐performance memory, in‐memory computing, neuromorphic computing, and next‐generation wearable and implantable devices, particularly for operation in complex environments. Despite its potential, Al1−xScxN faces challenges such as high coercive fields, significant leakage currents, and limited polarization reversal cycle life. Addressing these challenges require a deeper understanding of the fundamental physics controlling Al1−xScxN films. This review explores the origins of Al1−xScxN's ferroelectricity and phase stability, delves into the fundamental theory of wurtzite ferroelectricity, investigates mechanisms for controlling spontaneous polarization and coercive fields, examines recent research progress in Al1−xScxN ferroelectric devices, and outlines future development directions for this exciting material.

A facile route derived solar selective nickel-cobalt oxide thin films via spraying process

Abstract This work focuses on understanding the role of annealing temperature on the solar selective performance of nickel-cobalt oxide thin films successfully sprayed onto Al substrates using the spray pyrolysis technique. The synthesized nickel-cobalt oxide thin films (~ 725± 20 nm thick) were post annealed at (400, 500 and 600) °C. The XRD and FESEM outcomes appeared high crystalline quality with crystal grains in the range of (27 – 52) nm and improved surface morphology for the sprayed thin films. The optical properties reflect solar absorptance ~ (85.2 %) and the thermal emittance ~ (4.45 %). The hardness and the Young’s modulus were (19.1 GPa) and (104 GPa) respectively. The aforementioned results are for the film annealed at 600 °C. The prepared and post annealed nickel-cobalt oxide thin films show band gap energies in the range of (1.15 – 1.38) eV. The nickel-cobalt oxide thin films also possess excellent thermal stability at higher temperature which makes them interesting candidate for solar absorbing and thermal collector applications.

Effective remediation of mercury (II) from aqueous solutions using CS-MnFe2O4-CoS-MWCNTs: Box-Behnken design optimization and adsorption isotherm, kinetics, and thermodynamics evaluation.

Mercury (Hg) is a hazardous heavy metal, non-biodegradable and toxic, posing a serious threat to aquatic life and human health. Therefore, the removal of Hg ions from contaminated water using effective and eco-friendly adsorbents is necessary. In the present study, three magnetic chitosan-based organic-inorganic nanocomposites, such as CS-MnFe2O4, CS-MnFe2O4-CoS, and CS-MnFe2O4-CoS-MWCNTs, were designed and constructed to investigate their capacity for adsorbing Hg ions from aqueous solutions. The physicochemical properties of prepared composites were characterized by various analyses. The BET analyses indicated their high surface area and porous structure, and the N2 adsorption-desorption showed that the modification of CS in three stages by MnFe2O4 and crosslinking reaction, CoS preparation, and MWCNT incorporation resulted in increased N2 adsorption. The XRD confirms the synthesis of MnFe2O4 and CoS in the CS matrix and also the distinct peaks of MWCNTs. The CS-MnFe2O4-CoS-MWCNTs showed acceptable thermal stability with 45% char yields and superparamagnetic properties with magnetic saturation (Ms) of 16 emu g-1. The interactive impacts of independent variables (pH, contact time, and adsorbent dosage) on the removal percentage of Hg(II) onto three prepared adsorbents, as well as the process optimization, were assessed by the Box-Behnken design. The optimum conditions were identified, and the data from the analysis of variance showed that the three independent factors (pH, contact time, and adsorbent dosage) significantly influenced the adsorption of Hg(II). The adsorption isotherm and thermodynamics analysis investigation showed that at low concentrations of Hg(II), the adsorption process was both endothermic and spontaneous for the studied adsorbents.

PEDOT: PSS Doped Activated Biochar as a Novel Composite Material for Photocatalytic and Efficient Energy Storage Application

Herein, we report the synthesis of activated biochar from green algae and the effect of its doping on the structural, photocatalytic, and energy storage properties of PEDOT-PSS. The morphology of pure and doped samples was investigated with Fourier Transform Infrared Spectroscopy (FTIR), Atomic Force Microscopy (AFM), Brunauer–Emmett–Teller (BET) analysis, and thermogravimetric analysis (TGA). AFM results for PEDOT-PSS@6wt.% of BC indicate that the calculated average peak height, particle size, and roughness were 283 nm, 136 nm, and 71 nm, respectively. Adding biochar to PEDOT-PSS significantly improved the thermal stability of PEDOT-PSS up to 550 °C. The novel photocatalyst PEDOT-PSS@6wt.% BC improved photocatalytic performance by approximately 17% in Methylene Blue (MB) dye removal. The electrochemical performance in terms of supercapacitors for the synthesized samples was investigated using cyclic voltammetry (CV), galvanostatic charge–discharge (GCD), specific capacitance, stability, and electrochemical impedance spectra (EIS). PEDOT-PSS@6wt.% of BC as a novel electrode material in supercapacitors exhibits an initial specific capacitance of 1300 Fg−1. Moreover, the PEDOT-PSS@6wt.% of BC electrode shows excellent stability up to 1000 cycles of operation. The EIS studies suggest the presence of charge transfer resistance. Considering the economical biosynthesis and multifunctional features, the PEDOT-PSS@6wt.% of BC could potentially be used as a photocatalyst to remove organic dyes and supercapacitors in energy storage applications.

Temperature-irrelevant superhydrophobic polyimide–SiO2 aerogels with a confined shrinkage strategy for high-temperature thermal protection (>400 °C)

Polyimide (PI) aerogels often experience substantial volume shrinkage when exposed to temperatures above 200 °C. Furthermore, research regarding the hydrophobic characteristics of PI aerogels under high-temperature conditions is limited. Herein, a confined shrinkage strategy was proposed, and the PI–SiO2 aerogels were prepared with ultralow thermal shrinkage and high-temperature superhydrophobic properties. Micrometer-sized silica aerogel powders were used in this strategy as shrinkage inhibitors during the production of PI aerogels. The silica aerogel powders were then pulled together using the PI chain and braced to each other, limiting the shrinkage of the PI aerogel matrix attached to the powders. Results indicated that the prepared aerogel experienced a shrinkage of only 6.2 % after heat treatment at 400 °C for 1 h in a muffle furnace. The surface area of the sample decreased from 669 m2/g to 649 m2/g after heat treatment, revealing a reduction of only 2.7 %. Previous studies have never reported this remarkable thermal stability. Furthermore, the aerogel exhibited superhydrophobic properties with a water contact angle of 157.4° and a water rolling angle of approximately 0° at 300 °C due to its high surface roughness.

Photo-Crosslinked Polyurethane—Containing Gel Polymer Electrolytes via Free-Radical Polymerization Method

Using a novel technique, crosslinked gel polymer electrolytes (GPEs) designed for lithium-ion battery applications have been created. To form the photo crosslink via free-radical polymerization, a mixture of polyurethane acrylate (PUA), polyurethane methacrylate (PUMA), vinyl phosphonic acid (VPA), and bis[2-(methacryloyloxy)ethyl] phosphate (BMEP) was exposed to ultraviolet (UV) radiation during the fabrication process. The unique crosslinked configuration of the membrane increased its stability and made it suitable for use with liquid electrolytes. The resulting GPE has a much higher ionic conductivity (1.83 × 10−3 S cm−1) than the commercially available Celgrad2500 separator. A crosslinked structure formed by the hydrophilic properties of the PUA-PUMA blend and the higher phosphate content from BMEP reduced the leakage of the electrolyte solution while at the same time providing a greater capacity for liquid retention, significantly improving the mechanical and thermal stability of the membrane. GPP2 shows electrochemical stability up to 3.78 V. The coin cell that was assembled with a LiFePO4 cathode had remarkable cycling characteristics and generated a high reversible capacity of 149 mA h g−1 at 0.1 C. It also managed to maintain a consistent Coulombic efficiency of almost 100%. Furthermore, 91.5% of the original discharge capacity was maintained. However, the improved ionic conductivity, superior electrochemical performance, and high safety of GPEs hold great promise for the development of flexible energy storage systems in the future.

Synergistic effects of β-Cyclodextrin derivative inclusion complexes with favipiravir to enhance solubility and antiviral efficacy against Herpes Simplex virus type 1 (HSV-1)

In this study, the formation of β-cyclodextrin derivatives (β-Cyclodextrin; β-CD, Hydroxypropyl-β-Cyclodextrin; Hβ-CD, and Sulfobutylether-β-Cyclodextrin; Sβ-CD) inclusion complexes with favipiravir (FPR) was confirmed using various spectroscopic and analytical techniques. These complexes were shown to enhance FPR solubility and antiviral activity against herpes simplex virus type 1 (HSV-1). UV–visible and fluorescence spectroscopy revealed a continuous increase in FPR absorbance and fluorescence intensity with increasing β-CD concentrations, indicating the successful formation of 1:1 inclusion complexes. The prepared β-CD solid complexes were characterized using FTIR, XRD, FESEM, and TGA-DSC, which highlighted significant surface properties, morphological changes, and improved thermal stability. Phase solubility studies demonstrated enhanced FPR solubility in the presence of the β-CDs, with stability constants (Ks) following the order: Hβ-CD (694.8 M−1) > Sβ-CD (418.4 M−1) > β-CD (364.3 M−1). In-vitro release studies showed that the Hβ-CD complex achieved a higher cumulative release of 90.16 ± 1.94 % over 90 min compared to free FPR (25.32 ± 0.29 %), attributed to its greater solubility. Molecular docking provided insights into the interaction mechanisms, revealing higher binding affinities and stability for FPR with β-CD. In-vitro antiviral assays against HSV-1 demonstrated significant viral titer reductions for free FPR with β-CDs, with Hβ-CD outperforming others due to its rapid release profile after 96 h of incubation, confirming its potential for improved antiviral formulations. The cytotoxic effects of FPR and its β-CDs inclusion complexes were evaluated on Vero cells using an MTT assay over 96 h, showing reduced cytotoxicity for the inclusion complexes compared to free FPR. Additionally, cellular uptake studies revealed that β-CDs inclusion complexes conjugated with DAPI and FITC exhibited greater intensity within Vero cells compared to free FPR.

Flame retardant polyurethane foam prepared from compatible blends of ammonium ligninsulfonate-based and zinc alginate

Abstract Zinc alginate (ZnAlg) was prepared and subsequently employed to modify ammonium ligninsulfonate-based polyurethane foams (PUFs). A range of analytical techniques, including thermogravimetry, integral programmed decomposition temperature, activation energy, smoke density, cone calorimetry and scanning electron microscopy, were employed to characterise the modified PUFs. The results demonstrated that the PUFA15Z5 (15 % ammonium lignin sulfonate and 5 g ZnAlg) with the lowest mass loss exhibited the second-highest sample decomposition temperature (T50 %), second-highest peak temperature (TMAX2), IPDT and activation energy. Furthermore, the PUFA15Z5 sample exhibited the smallest smoke density (23.11) and the highest light transmittance (67.11 %). The peak heat release rate, total heat release, smoke production rate, total smoke release and four fire risk assessment indicators of the PUFA15Z5 were the lowest, while its carbon residue was the densest. The results demonstrated that the PUFA15Z5 exhibited the most favourable thermal stability, flame retardant properties and the lowest smoke toxicity. These findings provided a valuable reference for subsequent biomass-based flame retardant modified polyurethane foams (PUFs).

The effect of silane‐modified carbon black and nano‐silica, individually and in combination, on the performance of ethylene–propylene–diene monomer rubber

AbstractThis study assesses the effectiveness of a specially developed surface‐modified carbon black, both on its own and in combination with nano‐silica, as a hybrid filler for ethylene–propylene–diene monomer (EPDM) rubber compounds. The modification process, which included treatment with a silane coupling agent, resulted in enhanced curing characteristics. The ∆Torque values for compounds incorporating the modified carbon black exceeded those of other formulations by 25.85%. Scanning electron microscopy (SEM) analysis demonstrated improved filler dispersion and better compatibility between rubber and filler due to the surface modification. The silane‐modified carbon black showed considerable enhancements in mechanical properties, particularly in tear resistance, with increases in tensile and tear strength of 22.46% and 34.86%, respectively, following surface treatment. Dynamic mechanical analysis (DMA) indicated the influence of both surface modification and filler type, revealing that the combination of modified carbon black and nano‐silica achieved a reduction in rolling resistance of 20.41% and enhanced ice and wet grip performance by 7.95%. Additionally, modified carbon black displayed varying effects on the glass transition temperature. Thermal gravimetric analysis (TGA) confirmed that the thermal stability of the compounds was consistent, while solvent resistance improved with surface modification, as shown by swelling ratios. Thermodynamic analysis indicated that the surface modification of carbon black positively influences the elasticity and chain mobility of the rubber compounds studied. In conclusion, the careful selection and optimization of filler materials and their modifications are essential for customizing the properties of rubber compounds to satisfy specific performance criteria and applications.Highlights Promising EPDM compounds were prepared with Silane‐Modified CB and Nano‐Silica. Silane‐modified CB effectively improved the curing properties of the EPDM compound. The ΔTorque and cross‐link density of modified CB/EPDM show the highest value. Modified CB/Nano‐Silica/EPDM exhibited significant improvement in tear strength. Modified CB/Nano‐silica/EPDM have lower rolling resistance and higher wet grip.

Sodium-Poor, Hydroxyl-Rich, Defective Na2Ti3O7 Prepared by γ-Irradiation and Its Enhanced Proton Conductivity.

The use of γ-irradiation to tailor the physicochemical properties of materials is not widely applied to layered alkali metal oxides. Herein, we show that γ-irradiation (up to 400 kGy) of Na2Ti3O7 leads to a sodium-poor, hydroxyl-rich analogue where the layered structure, plate-like morphology, and textural properties are preserved. The deintercalation of sodium ions modifies the Ti-O bond lengths and expands the unit cell; the latter is supported by density functional theory (DFT) calculations. 23Na solid-state NMR suggests the transport of the symmetric, 7-fold Na2 sites to an intermediate environment, which is closer to the asymmetric, 9-fold Na1 sites. An 8 wt % mass loss (1.4 mol water/mol titanate) is observed, indicating an increased concentration of protons/hydroxyls. These hydroxyl groups (i.e., lattice protons) possess higher thermal stability than solely surface-adsorbed ones in the nonirradiated sample. At 200-400 kGy, the proton conduction (50 °C and ∼70% RH) of ∼10-6 S·cm-1 is 1 order of magnitude larger than that in the nonirradiated sample; the relaxation time decreases from 30 to 2-6 μs with γ-irradiation. The γ-dose dependence of dielectric loss is also present and analyzed using the Jonscher universal power law, indicating the low-frequency dispersion behavior characteristics of high charge densities.

Digging Its Own Site: Linear Coordination Stabilizes a Pt1/Fe2O3 Single-Atom Catalyst.

Determining the local coordination of the active site is a prerequisite for the reliable modeling of single-atom catalysts (SACs). Obtaining such information is difficult on powder-based systems and much emphasis is placed on density functional theory computations based on idealized low-index surfaces of the support. In this work, we investigate how Pt atoms bind to the (11̅02) facet of α-Fe2O3; a common support material in SACs. Using a combination of scanning tunneling microscopy, X-ray photoelectron spectroscopy, and an extensive computational evolutionary search, we find that Pt atoms significantly reconfigure the support lattice to facilitate a pseudolinear coordination to surface oxygen atoms. Despite breaking three surface Fe-O bonds, this geometry is favored by 0.84 eV over the best configuration involving an unperturbed support. We suggest that the linear O-Pt-O configuration is common in reactive Pt-based SAC systems because it balances thermal stability with the ability to adsorb reactants from the gas phase. Moreover, we conclude that extensive structural searches are necessary to determine realistic active site geometries in single-atom catalysis.

Facile Synthesis of Bis-Diphenylphosphine Oxide as a Flame Retardant for Epoxy Resins

A phosphorus-containing compound, (oxybis(4,1-phenylene))bis(phenylphosphine oxide) (ODDPO), was successfully synthesized and used as a flame retardant for epoxy resin (EP). The results demonstrated that EP/ODDPO, containing 1.2 wt% phosphorus, achieved a vertical burning V-0 rating, with a limited oxygen index value of 29.2%, indicating excellent flame retardancy. Comprehensive evaluations revealed that ODDPO exhibited both gas-phase and condensed-phase flame-retardant effects on EP, with a particularly notable barrier effect. In addition, the incorporation of ODDPO had a minimal negative impact on the glass transition temperature (Tg) and thermal stability of the EP matrix. Compared to unmodified EP (EP-0), the Tg value and initial decomposition temperature of EP/ODDPO-1.2 decreased by only 7.6 °C and 10.0 °C, respectively. Moreover, the introduction of ODDPO significantly improved the hydrophobicity and water absorption resistance of epoxy materials, which is attributed to ODDPO’s rigidity and symmetric structure, reducing water molecule permeation. Furthermore, the dielectric properties of ODDPO-modified EP samples were strengthened compared to EP-0, due to the ODDPO’s symmetric structure reducing the polarity of the matrix. The above results indicated that ODDPO serves as an excellent flame retardant while enhancing other properties of the EP matrix, thereby contributing to the preparation and application of high-performance epoxy materials.

Effect of silane coupling agent on mechanical properties, flame retardancy, and ceramifiable behavior of ceramifiable flame‐retardant silicone rubber composite

AbstractIn order to improve the dispersibility of inorganic fillers and enhance its ceramifiable flame‐retardant efficiency, the ceramifiable flame‐retardant silicone rubber composites were prepared using glass powder, zinc borate, ammonium polyphosphate, mica powder, platinum catalyst as ceramifiable flame‐retardant agent, and various silane coupling agents as interfacial modifier. The micromorphology, mechanical properties, flame retardancy, thermal stability, and combustion behavior of ceramifiable flame‐retardant silicone rubber composites, as well as the flexural strength of the corresponding ceramics generated after pyrolysis of the composites were examined. The results reveal that the inclusion of silane coupling agents improves the dispersibility of ceramifiable flame‐retardant agents substantially. The mechanical properties, flame retardancy, thermal stability, and combustion behavior of ceramifiable flame‐retardant silicone rubber composites are all improved. When compared to a composite without a silane coupling agent, the tensile strength of the composite can be improved by up to 1.9 times. Only 0.5phr silane coupling agent is required to raise the vertical combustion rating from V‐1 to V‐0, and the composite with 3 phr KH570 has a LOI value of 38.6. Meanwhile, the heat release rate of the composite is reduced to a certain extent, and the time to ignition and residue are dramatically enhanced after the addition of silane coupling agent in the cone calorimetry test. Moreover, flexural strength of the corresponding ceramics generated after pyrolysis of the composites rapidly increases with increasing silane coupling agent content, which can reach to 24.7 MPa with addition of 3 phr KH570.

Preparation of alkyl microporous organic network-based capillary column for an efficient gas chromatographic separation of position isomers.

The large surface area, excellent thermal stability and easy modification make microporous organic networks (MONs) good candidates in the field of gas chromatography (GC). Due to the limited species and highly conjugated networks of MONs, their applications are still in infancy and restricted. To accelerate their developments and to enrich their types in GC, here we report the first example of synthesizing alkyl MON and its capillary column for GC separation of position isomers. Linear 1,8-dibromooctane is used as the alkyl monomer instead of traditional aromatic ones to construct novel alkyl MON to decrease the inherent conjugated characteristic of MONs. The alkyl MON exhibits good thermal stability (up to 350°C), large surface area (1173m2g-1), and non-polar character, allowing good resolution for alkanes, alkyl benzenes, alcohols, ketones, and diverse position isomers, including dichlorobenzene, trichlorobenzene, bromotoluene, nitrotoluene, methylbenzaldehyde, and ionone with the limits of detection (0.003mgmL-1) and limits of quantitation of (0.10mgmL-1). The in situ growth-prepared alkyl MON column demonstrates remarkable duration time and precisions for the retention relative standard deviations, (RSDs%, intra-day, n=7), 0.06%-0.53% (intra-day, n=7), and 2.87%-10.59% (column-to-column, n=3). In addition, the fabricated alkyl MON-coated capillary column offers better resolution than three commercial GC columns for the resolution of methylbenzaldehyde, bromotoluene, and chlorotoluene isomers. This work reveals the practicability for synthesizing alkyl MONs and demonstrates their prospects for position isomers separation.

PLS‐guided Mutant Recombination to Improve the Stability of Bovine Enterokinases Obtained by Directed Evolution

Activity and thermostability are critical yet challenging to improve simultaneously in enzymes. Using directed evolution, we previously identified bovine enterokinase (EKL) variants with enhanced soluble expression and thermal stability. Partial least squares (PLS) analysis of 321 EKL variants revealed the impact of individual mutations and identified neutral or detrimental mutations in top‐performing variants. Leveraging PLS rankings, we created new variants with fewer mutations and enhanced stability. Most original and PLS‐guided variants exhibited an activity‐stability trade‐off. However, two new triple‐ and quadruple‐mutants improved both activity and stability, surpassing the trade‐off limit. Recombining PLS‐guided mutations likely eliminated neutral or harmful mutations, enhancing stability. MD simulations linked residue‐specific dynamics with stability, pinpointing critical structural regions near aggregation‐prone areas. Our findings validate PLS as a potent strategy to enhance enzyme properties, complementing directed evolution.

Synergic Effects of Ordered Mesoporous Bifunctional Ionic Liquid: A Recyclable Catalyst to Access Chemoselective N-Protected Indoline-2,3-dione Analogous

SBA-15 and organic ionic liquid were incorporated in a post-grafting technique for generating a bifunctional ionic liquid embedded mesoporous SBA-15. The prepared heterogeneous catalyst was employed for the first time to synthesize N-alkylated indoline-2,3-dione at mild conditions to afford excellent yields in a short reaction time. The synthesized DABCOIL@SBA-15 catalyst was meticulously characterized by various techniques, such as FT-IR, solid-state 13C NMR, solid-state 29Si NMR, small-angle X-ray diffraction (XRD), and N2 adsorption–desorption. Further, the morphological behavior of the catalyst was studied by SEM and TEM. The thermal stability and number of active sites were determined by thermogravimetric analysis (TGA). The Hammett equation was used to analyze the synergetic effect of the catalyst and substituent effects on the N-alkylated products of 5-substituted isatin derivatives, which resulted in a negative slope. This negative slope indicates a positive charge in the transition state. Notably, the DABCOIL@SBA-15 catalyst demonstrated its practicality by being reused for seven cycles with consistently high catalytic activity.

Enhancing the Performance of Nanocrystalline SnO2 for Solar Cells through Photonic Curing Using Impedance Spectroscopy Analysis

Wide-bandgap tin oxide (SnO2) 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 SnO2 thin-films using only 500 μs 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 SnO2 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) SnO2 films.

AC poling of high Qm and low acoustic impedance Pb(Mg1/3Nb2/3)O3-Pb(Zr,Ti)O3 single crystals produced by a solid state crystal growth

Abstract The AC poling cycle dependence of Mn-doped Pb(Mg1/3Nb2/3)O3-0.3Pb(Zr.Ti)O3 (PMN-0.3PZT) single crystals (SC) produced via the solid-state crystal growth (SSCG) method was investigated. The piezoelectric strain and charge constants, d33 ＝ 1130 pC/N, g33 = 42.7 x 10-3 Vm/N, and mechanical quality factor Qm = 800 were obtained under conditions of 1 Hz, bipolar sine wave, 7.5 kV/cm electric field, and 6000 cycles.
In contrast to the conventional Bridgman process SC, the low-density and high Qm SSCG SC necessitates a substantial number of AC cycles due to the presence of pores within the SC.
In addition, the ACP SC showed a 13°C increase in the phase change temperature Trt compared to the DC-poled SC. This information of ACP SSCG SCs with improved thermal stability, low acoustic impedance, and enhanced receiving efficiency attributable to high g33 offers new insight into high-frequency ultrasonic devices.