Structure Behavior Research Articles

Benchmarking luminescent properties of the arylvinylpyrimidine scaffold.

The exploration of the photophysical properties of push-pull molecules incorporating pyrimidine rings as electron-attracting moieties in their structure continues to be a fascinating area of investigation. A thorough examination of these properties not only contributes to fundamental knowledge but also provides crucial insights for the rational design of emissive materials in prospective applications. In this context, this work conducts an in-depth analysis of four families of 4,6-bis(arylvinyl)pyrimidines, evaluating the influence of substituents on both the aryl groups and position 2 of the pyrimidine ring. While previous research has primarily focused on solution studies, this work emphasizes the importance of examining solid-state photophysics. Through a multidisciplinary approach encompassing optical techniques, x-ray diffraction, and quantum chemical calculations, a comprehensive understanding of the structure-property relationships is achieved. This study underscores the intricate interplay between molecular structure, aggregation, and fluorescence behavior in pyrimidines, offering valuable insights with broader implications beyond academic realms.

The Effect of Steel Over Strength Ratio on Structure Behavior

Seismic design of steel building structures according to SNI 7860:2020 determining the necessary strength of structural members based on the expected yield stress, Ry.Fy, and the expected tensile stress, Rt.Fu. However, the values of Ry and Rt in SNI 7860:2020 are not yet based on the testing of steel products in Indonesia and are still based on the provisions in AISC 341-16. This research was conducted by collecting data on steel tensile test results to obtain the over-strength ratio and then modeling the steel frame building using the over-strength steel provisions of SNI 7860:2020 and based on the tensile test results to determine the difference in structural behavior. Based on the tensile test results, WF300 steel has a yield strength ratio (Ry) of 1.78, which is higher than the SNI specification of 1.5, and a tensile strength ratio (Rt) of 1.35, which is higher than the SNI specification of 1.2. Based on pushover analysis, the deviation value at the initial formation of the plastic hinge on Structure A1 (Ry=1.5) in the x-axis direction of 79.352 mm is smaller than Structure B1 (Ry=1.78) by 94.01 mm. This indicates that the plastic hinge of Structure A1 is formed earlier than Structure B1.

The Impact of the Final Sintering Temperature on the Microstructure and Dielectric Properties of Ba0.75Ca0.25TiO3 Perovskite Ceramics

Ba0.75Ca0.25TiO3 ceramics were successfully synthesized by a simple solid-state reaction method. This study examined the influence of sintering temperature on the structure, microstructure, dielectric properties and electrical behavior of the material. The XRD analysis reveals that the tetragonal phase (P4mm) is dominant in all the synthesized materials, with those sintered at T = 1400 °C and T = 1450 °C being single-phase, while others exhibit a minor orthorhombic phase (Pbnm). Higher sintering temperatures promoted better grain boundary formation and larger grain sizes. The electric permittivity increased with temperature up to T = 1400 °C, followed by a sharp decline at T = 1450 °C. Additionally, the Curie temperature decreased with increasing sintering temperature, indicating changes in phase transition characteristics. Thermal analysis showed that higher sintering temperatures led to sharper heat capacity peaks, while pyroelectric and thermally stimulated depolarization currents were maximized at T = 1400 °C due to oxygen vacancies. These findings highlight the significant impact of sintering temperature on the material’s structural and functional properties.

Shape Memory Polymer Foam Based on Nanofibrillar Composites of Polylactide/Polyamide

This paper presents the novel development of a shape memory polymer foam based on polymer–polymer nanocomposites. Herein, polylactide (PLA)/biosourced polyamide (PA) foams are fabricated by in situ fibrillation of polymer blends and a subsequent supercritical CO2 foaming technique. In this system, PLA serves as a shape memory polymer to endow this foam with a shape memory effect (SME), and in situ generated PA nanofibers are employed to reinforce the PLA cell walls and provide an additional permanent phase. A concentration of PA, 5 wt.%, was chosen to form an entangled nanofibrillar network. Foams of PLA/PA nanoblends with the same content of constituents were fabricated to reveal the effect of minor phase morphology on the cell structure and shape memory behavior of polymer foams. Profiting from the reinforcing effect of PA nanofibers, the PLA/PA nanocomposite foam exhibits smaller foam cells, a narrower cell size distribution and a comparable cell concentration than the PLA/PA nanoblend foam. In addition, PA nanofibers, unlike PA nanodroplets, favor the shape fixation ratio and recovery ratio and shorten the shape recovery time.

Elevating Nonlinear Optical Response through d-electron Modulation in Metal-Organic Frameworks.

Electronic structure and excited state behavior is of pronounced influence on regulation of nonlinear optical (NLO) response. Herein, a serials of transition metal ions bearing different d-electron numbers were in situ coordinated within porphyrinic metal-organic frameworks (MOFs), creating NLO-responsive M-metal (metal = Fe, Co, Ni, Cu, and Zn) frameworks. It demonstrated that the NLO properties can be optimized with the increased occupancy of the d-shell, which enhances the degree of delocalization. Specifically, the full-filled (d10) electron configuration of Zn2+ stabilizes the electronic structure, combination with π-π* local excitation character of M-Zn, promoting charge transfer process and resulting in outstanding NLO properties. Moreover, parameters related to the nonlinear process (β, n2, Imχ(3), Reχ(3) and χ(3)) of M-Zn are calculated to be higher than those of other materials, consistent with theoretical calculations. This work paves the way for NLO modulation based on electronic analysis and provides a promising approach for constructing high-performance NLO materials.

Numerical Modeling of Soil and Structure Behavior for Tunneling in Different Types of Soil

This note studies the correlation between surface and tunnel volume loss in various types of dry soil via finite element method. The effect of small strain stiffness, the buoyancy effect of soil, and tunnel overburden depth are considered in the 2D tunneling model. The results show that both surface volume loss ratio and settlement trough width parameter in the empirical solution can be expressed as a linear equation of tunnel volume loss ratio for 1D overburden shallow tunnels. Furthermore, the surface volume loss ratio can be presented as a non-linear polynomial equation of overburden depth and tunnel volume loss ratio in a 3D space, and this equation holds in different types of soil. The ranges of required fitting parameters and upper and lower bounding surfaces are suggested for various types of soil. Knowledge of this correlation between surface and tunnel volume loss is valuable, as it can be employed in practice for preliminary tunnel design in the absence of tunneling induced maximum ground settlement.

The interaction between beta-ionone and 2-hydroxypropyl-beta-cyclodextrin during the formation of the inclusion complex

As an aroma material, beta-ionone also has a range of pharmacological activities. To solve its problems such as low bioavailability, water-immiscibility, thermo-instability, and volatility, beta-ionone was successfully encapsulated in 2-hydroxypropyl-beta-cyclodextrin (HP-beta-CD) in our previous work. However, the structure of the product, the interaction between beta-ionone and HP-beta-CD, and the mechanism of action were not clear. In this paper, in order to gain a more profound understanding of the structure and chemical behavior of beta-ionone-HP-beta-CD inclusion complex, the interaction between beta-ionone and HP-beta-CD was investigated by molecular simulation. The optimized structures, binding energy, deformation energy, charge transfer, frontier orbital energy gap, chemical hardness, chemical potential, and electrophilicity index were obtained. In the complex, beta-ionone denotes electrons to HP-beta-CD and carries a positive charge. The negative chemical potential of inclusion complex indicates that complex process is spontaneous. The complex shows a relatively higher reactivity and electrophilicity than beta-ionone and HP-beta-CD.

Effect of CHAPS on the selective synthesis of (S)-n-octyl ibuprofen ester in AOT reverse micelle catalyzed by lipase

CHAPS (3-[(3-cholamidopropyl) dimethylammonio]-1-propane sulfonate), a biocompatible zwitterionic surfactant derived from bile salt, has attracted great attention due to its distinct molecular structure and aggregation behavior. Addition of a low level of CHAPS to AOT (sodium bis(2-ethylhexyl) sulfosuccinate) reverse micelles has been found to be able to enhance the catalytic activity of the solubilized lipase. In this study, the effect of CHAPS on the lipase-catalyzed selective synthesis of (S)-n-octyl ibuprofen ester was investigated in AOT reverse micelles at 37 °C. The results demonstrate that the presence of CHAPS in AOT reverse micelle enhances both the yield and the enantiomeric excess (ee) value of (S)-n-octyl ibuprofen ester, especially at low water content. With 8 mM CHAPS in AOT reverse micelle ([AOT] = 100 mM, [H2O]/[AOT] = 12, pH = 7.0), a 48-hour yield of 34.2 % could be obtained, which is approximately twice that without CHAPS. In addition, the ee value of the product is increased from 89.1 % to 98.2 %. To understand the mechanism of the CHAPS effect, dynamic light scattering, fluorescence emission spectroscopy and Fourier transform infrared spectroscopy techniques were used to characterize the size of the reverse micelle, the conformation of the solubilized lipase and the activity of the bulk water in the reverse micelle. It reveals that at low water content, the addition of CHAPS enlarges the size of AOT reverse micelle, stabilizes the lipase conformation and reduces the nucleophilicity of bulk water in AOT reverse micelle. The synergistic effect of the aforementioned factors results in the improvement of the enzymatic synthesis of the ester. The above research provides scientific support for the lipase-based preparation of chiral acids/alcohols in the reverse micellar system.

Aging behaviour and mechanical characterisation of maltenes and asphaltenes

The analysis of bitumen is challenging due to its complex and ever-changing chemical composition. Fractionation techniques based on solubility and polarity properties facilitate the examination process, shedding more light on composition, structure and aging behaviour. However, these separation experiments are often performed post-aging, making it difficult to understand the behaviour and mechanical properties of individual subfractions. Hence, the focus of this study was to separate maltenes and asphaltenes in large quantities and age them at various temperatures (80, 130 and 180°C), followed by analysis with chemical and mechanical methods. Results showed that both maltenes and asphaltenes display viscoelastic properties: maltenes are more viscous, while asphaltenes are more elastic compared to the base binder. Maltenes aged at 180°C became extremely stiff with a nearly temperature-independent phase angle, while asphaltenes aged at 130°C exhibited the stiffest and most elastic behaviour. Decomposition of sulfoxides at high temperatures was observed for both fractions, while additional decarboxylation occurred in the asphaltenes. During the aging of the maltenes, a significant amount of asphaltenes were formed, which most likely originated from both the aromatics and resins fraction. Furthermore, no major discrepancies between oxidation products in bitumen and in the maltenes were detected, indicating that asphaltenes might not crucially influence the qualitative aging process. This study demonstrated a possible approach for obtaining bituminous subfractions in large quantities, allowing for a detailed analysis of their mechanical and aging properties.

Properties of Sn-Doped PBZT Ferroelectric Ceramics Sintered by Hot-Pressing Method.

This work investigated the structure, microstructure, and ferroelectric and dielectric behavior of (Pb0.97Ba0.03)(Zr0.98Ti0.02)1-xSnxO3 (PBZT_xSn) solid solution with variable tin content in the range x = 0.00-0.08. Synthesis was carried out using the powder calcination method, and sintering was carried out using the hot-pressing method. For all the PBZT_xSn samples at room temperature, X-ray diffractograms confirmed the presence of an orthorhombic (OR) crystal structure with space group Pnnm, and the microstructure is characterized by densely packed and properly shaped grains with an average size of 1.36 µm to 1.73 µm. At room temperature, PBZT_xSn materials have low permittivity values ε' ranging from 265 to 275, whereas, at the ferroelectric-paraelectric phase transition temperature (RE-C), the permittivity is high (from 8923 to 12,141). The increase in the tin dopant in PBZT_xSn lowers permittivity and dielectric loss and changes the scope of occurrence of phase transitions. The occurring dispersion of the dielectric constant and dielectric loss at low frequencies, related to the Maxwell-Wagner behavior, decreases with increasing tin content in the composition of PBZT_xSn. Temperature studies of the dielectric and ferroelectric properties revealed anomalies related to the phase transitions occurring in the PBZT_xSn material. With increasing temperature in PBZT_xSn, phase transitions occur from orthorhombic (OR) to rhombohedral (RE) and cubic (C). The cooling cycle shifts the temperatures of the phase transitions towards lower temperatures. The test results were confirmed by XRD Rietveld analysis at different temperatures. The beneficial dielectric and ferroelectric properties suggest that the PBZT_xSn materials are suitable for micromechatronic applications as pulse capacitors or actuator elements.

Impact of Carbonization Temperature on the Structure and Li Deposition Behavior of 3D Dual Metal Carbon Fibers

Li deposition within lithiophilic–lithiophobic metal carbon fibers is influenced by several structural factors, including electrical conductivity, surface‐bound functional groups, particle size and distribution of the lithiophilic–lithiophobic components, which are significantly affected by the carbonization temperature. To gain a deeper understanding of how these different parameters affect the Li deposition behavior, a detailed analysis of Ag and Cu containing carbon fibers at carbonization temperatures from 500 to 1000 °C is performed. At lower carbonization temperatures, the fibers exhibit an unordered carbon structure with a high concentration of heteroatoms and a lithiophilic–lithiophobic gradient. However, the high electrical resistance at these temperatures impedes Li‐ion interaction with the fibers, leading to the formation of mossy and dead Li. In contrast, higher carbonization temperatures result in the removal of heteroatoms and a more ordered carbon structure. The agglomeration of Cu and Ag particles at these temperatures disrupts the lithiophilic–lithiophobic gradient, causing concentrated Li deposition on top of the fibers. A threshold temperature of 700 °C has been identified for achieving homogeneous Li deposition. At this temperature, the lithiophilic–lithiophobic gradient still exists, and the more ordered carbon structure enhances Li‐ion interaction with the fibers, resulting in stable Li deposition for over 1100 h.

Nitrogen Centered Radicals in Visible-Light Promoted Reactions

Nitrogen Centered Radicals (NCR) are known in literature since the first years of 1900, but only with the spread of photoredox catalysis, and in particular visible light-mediated radical processes, nitrogen radical chemistry became more accessible generating these kinds of radicals in situ employing mild conditions. In fact, unlike their carbon counterpart, nitrogen radicals have not historically spread in academia or industry due to a lack of an efficient strategy to produce them. Nowadays, NCR are more established, and this graphical review illustrates the key publications from the literature categorized them by both the type of NCR and the type of reaction. In fact, nitrogen radicals can be divided in four different categories according to their electronical configuration, orbital structure and chemical behaviour. The reactivity of all these radicals can be summarized into four main classes: they are mostly exploited into intramolecular cyclization; intramolecular hydrogen atom abstraction; Norrish type-I fragmentation and intermolecular addition to π systems.

A comprehensive theoretical scheme for understanding the core structure and the mechanical behavior of basal dislocations with solute atmosphere in Mg alloys

The basal dislocations play a key role in the deformation of hexagonal Mg alloys. However, its core structure and mechanical behavior have thus far not yet been understood adequately, largely owing to the fact that the basal dislocation, often decorated with segregated solute atmosphere and dissociated into two partials, cannot be modeled accurately. Significant discrepancies exist between theoretically calculated and experimentally observed structures for these dissociated dislocations. Here we present a comprehensive theoretical scheme to model them in the Mg alloys with alloying elements of Y, Zn, Al and Li, respectively. Firstly, solute–dislocation interactions were computed by appropriate first-principles calculations. Secondly, the statistic solute concentration at a dislocation is estimated by a Fermi–Dirac distribution. Finally, all these effects on dislocations are integrated into an improved two-dimensional Peierls–Nabarro model to predict their core structures and mechanical behaviors in Mg alloys. It is shown that although Zn, Al and Li atoms have little effect on basal dislocations, Y atoms can largely increase their dissociated width. Furthermore, when it moves from its ground state configuration, the dissociated dislocation can further be widened, such that its dissociated widths in a Mg–0.8Y (at%) alloy at 300 K can reach 12–36 nm, in rather good agreement with the experimentally observed values of 20–30 nm. Besides, the Peierls and yield stresses of Mg alloys shall increase with increasing added solute concentration, while they are decreased drastically with increasing the temperature from 300 to 800 K, but with the Mg-Y alloy as somewhat exception, which is again consistent with experimental observations.

Hydrogel Electrolyte with Regulated Water Activity and Hydrogen Bond Network for Ultra‐Stable Zinc Electrode

AbstractQuasi‐solid‐state zinc‐ion batteries (QZIBs) have attracted wide attention due to their excellent dimensional stability and high safety. However, poor ion conduction capabilities, severe dendrite growth, and rampant side reactions still hinder their commercialization. The regulation of the solvation structure of Zn2+ is considered to be an effective method to address these issues. Herein, a hydrogel electrolyte with a regulated solvation structure (HE‐RS) is designed via the combination of tetramethyl urea (TMU) additive and polyvinyl alcohol (PVA) matrix. The hydrophilic ─C═O group of TMU exhibits strong affinity with the PVA chains, improving the mechanical strength of the PVA matrix. The ─N(CH3)2 groups at both ends of TMU exhibit strong hydrophobic characteristics, which leads to local hydrophobicity and decreased water activity. Additionally, abundant oxygen‐containing (electronegative) groups on both PVA and TUM can adsorb Zn2+ and provide sites for Zn2+ transference. Benefiting from these merits, Zn2+ solvation structure and deposition behavior are regulated. Consequently, the Zn||Zn symmetric cell with HE‐RS exhibits a stable cycling life exceeding 2000 h. Moreover, the HE‐RS‐based Zn||NH4V4O10 cell exhibits a capacity retention of 96.4% after 1000 cycles at 2 A g−1.

Bi2O2.33/Bi4O5I2-heterojunction photocatalysts for adsorption and visible light-driven degradation of pharmaceutical pollutants

This study introduces the innovative Bi4O5I2/Bi2O2.33 heterojunction for diclofenac (DF) degradation. Pharmaceutical pollutants, especially DF, pose significant threats to water sources, necessitating efficient treatment methods. Bi2O2.33, renowned for its unique ferromagnetic properties, emerges as a promising photocatalyst for pollutant degradation. Bi4O5I2, known for strong visible light absorption and stability, holds potential for environmental applications. Interestingly, the inclusion of titanium dioxide (TiO2) in the composite catalysts significantly influences their observed ferromagnetic properties, as revealed by Electron Paramagnetic Resonance (EPR) spectroscopy, by influencing the interactions within the Bi4O5I2/Bi2O2.33 heterojunction and influencing its structure, morphology, and spin behavior. This interaction results in enhanced EPR and Ferromagnetic Resonance (FMR) signals, indicating intriguing spin interactions, polarization effects, charge transfers, surface dynamics, and stabilized magnetic domains. While the enhanced ferromagnetism holds promise for efficient charge separation and potential applications in environmental remediation, the expected boost in visible light-driven activity was not fully realized. This limitation is attributed to TiO2 inherent inability to directly absorb visible light, hindering its utilization for enhanced photocatalysis within the heterojunction. Nevertheless, these findings elucidate the multifaceted role of TiO2 in modulating the magnetic properties of these catalysts, offering valuable insights for future advancements in the design of advanced photocatalysts for effective environmental remediation.

Efficient sealing of cemented sheath: An oil-responsive self-healing latex with toughness enhancement for cement composites

The integrity of the cemented sheath is important to the safe exploration of oil and gas resources. Sealing failure of cement sheath will result in formation fluid channeling and pressure carryover in the annulus. The both toughening and oil-responsive self-healing latex (TOS) was prepared to achieve efficient sealing of cemented sheath, and prolong its service life. The structure and oil swelling behavior of TOS, its toughening and self-healing effects on hardened cement paste (HCP) were analyzed by comprehensive characterizations. Results demonstrated that TOS possessed excellent stability and an oil swelling rate of 1235 %. Cement specimens by curing 28d containing 8 % TOS exhibited a 27.8 % increase in flexural strength, a 48.7 % reduction in elasticity modulus and a 33.8 % reduction in brittleness coefficient. The addition of TOS can effectively improve the toughness of cement. The average pore size of specimens containing 8 % TOS admixture decreased to 9.17 nm. This indicates that TOS enhanced the structural density of cement materials. The crack about 103μm in the cracking specimens with 8 % TOS was almost healed, and the corresponding permeability was reduced 99.1 % after curing in oil. Adsorption and film formation of TOS can resist the cracking of cement sheath, and the oil swelling expansion of film in cement matrix can repair the cracked structure.

Study on theoretical model and actual deformation of weft-knitted transfer loop based on particle constraint

Abstract In order to derive the structural properties and deformation behavior of the weft-knitted transfer fabric, a multilayer spring-mass geometric circle model with weft-knitted transfer loop is provided in conjunction with the fabric samples’ image. Eight type-value points were utilized to control the transfer loop’s morphological structure. Connections between the type-value points and the particle system were established. Non-uniform rational B spline curves and texture mapping were utilized to create the three-dimensional impression of the weft-knitted transfer loop. By measuring the offset of the type-value points in conjunction, the actual deformation of the weft-knitted transfer fabric was determined. Utilizing a cylindrical envelope box for collision detection, the possible unreasonable interpenetration phenomenon in the simulation was solved, and thus a stable weft-knitted transfer loop structure was obtained. Using Microsoft Visual Studio and C#, the deformation of the weft-knitted transfer fabric was simulated, the simulated weft-knitted transfer fabric’s deformation pattern accurately depicts the fabric’s three-dimensional structure and deformation behavior while also matching the structural characteristics of the fabric sample. The findings demonstrate that the theoretical structural model of weft-knitted transfer fabric constructed can accurately represent the loop’s structure, and the actual deformation of the simulated weft-knitted transfer fabric is consistent with the deformation characteristics of the fabric sample. Weft-knitted transfer fabric’s deformation behavior may be effectively reflected by the multilayer spring-mass geometric circle model, allowing for the modeling of the fabric’s morphology and 3D structure.

Effects of chemical etching on surface structure and tribological behavior of silicate substrates

Abstract This study investigated the effect of chemical etching on the surface structure and tribological behavior of silicate substrates. Silicate surfaces were etched using a mixture of nitric acid (HNO3) and ammonium bifluoride (NH4HF2) for durations ranging from 1 to 60 min. The etched surfaces were characterized using optical microscopy, scanning electron microscopy, surface profilometry, water contact angle measurements, and UV–vis spectroscopy to evaluate the changes in surface morphology, roughness, wettability, and optical properties. Tribological performance was assessed using reciprocating ball-on-plate friction tests. The results showed that increasing the etching time resulted in the formation of microscale surface features, increased surface roughness, enhanced hydrophilicity, and reduced optical transmittance. The average friction coefficient decreased with an increase in the etching time up to 30 min, beyond which a slight increase was observed. The 1-minute etched specimen exhibited the best wear resistance with the narrowest wear track and the least material removal. The improved tribological performance was attributed to the formation of a stable transfer film, reduced real contact area, and entrapment of wear debris. This study highlights the potential of chemical etching as a technique to tailor the surface structure and tribological properties of silicate materials for various applications.

Understanding of formation, gastrointestinal breakdown, and application of whey protein emulsion gels: Insights from intermolecular interactions.

Whey protein emulsion gel is an ideal model food for revealing how the multilength scale food structures affect food digestion, as their structure and mechanical properties can be precisely manipulated by controlling the type and intensity of intermolecular interactions between protein molecules. However, there are still significant understanding gaps among intermolecular interactions, protein aggregation and gelation, emulsion gel formation, gel breakdown in the gastrointestinal tract (GIT), and the practical use of whey protein emulsion gels, which limits their GIT-targeted applications. In this regard, the relationship between the structure and digestion behavior of heat-set whey protein emulsion gels is reviewed and discussed mainly from the following aspects: (1) structural characteristics of whey protein molecules; (2) how different types of intermolecular interactions influence heat-induced aggregation and gelation of whey protein in the aqueous solutions and the oil-in-water emulsions, and the mechanical properties of the final gels; (3) functions of the mouth, the stomach, and the small intestine in processing of solid foods, and how different types of intermolecular interactions influence the breakdown properties of heat-set whey protein emulsion gels in GIT (i.e., their respective role in controlling gel digestion). Finally, the implications of knowledge derived from the formation and gastrointestinal breakdown of heat-set whey protein emulsion gels for developing controlled delivery vehicles, human satiety enhancers, and sensory modifiers are highlighted.

First-principles calculations of self-defects on the structural, electronic, and optical properties of BaXO3 (X = Ti, Zr, and Hf) perovskite oxide materials

This study utilizes computational simulations to examine the properties of BaXO3 (X = Ti, Zr, and Hf) perovskite oxide materials with self-defects, including vacancy and interstitial. The investigation focuses on their crystal structure, electronic characteristics, and optical behavior. The results show that the pristine BaTiO3, BaZrO3, and BaHfO3 exhibit p-type semiconductor behavior with varying band gaps. The electronic properties are primarily governed by the orbitals of oxygen and transition metal elements, suggesting potential for precise control of electron transport. Introduction of self-defects enhances the magnetization, making them suitable for magnetic applications. Moreover, these materials demonstrate promising optical properties for energy conversion and storage in the visible light and ultraviolet regions. We expected that these findings offer valuable insights for further research on perovskite oxide materials and their applications, particularly regarding the influence of self-defects during the fabrication process.