Unique Stability Research Articles

Beyond volatility: Systemic resilience and risk mitigation in interconnected commodity markets

In today's interconnected commodity markets, understanding volatility spillover dynamics is crucial. This research builds on Diebold & Yilmaz (2012, 2014) to estimate System Resilience, a vital measure for investors and policymakers. By using connectedness-based estimates, a unique stability score for each system component is constructed and aggregated to estimate overall System Resilience. This concept is applied to three key commodity segments: Energy, Agriculture, and Metals. Results show that most commodities, especially bullion, maintain moderate stability, offering investment alternatives even during periods of heightened systemic risk. The study also examines rolling estimates of System Resilience to identify early warning signals through increased standard deviation in successive resilience series. Tipping points indicate critical slowdowns where recovery to a stable state is hindered. Findings suggest that apart from the Global Financial Crisis (GFC), commodity portfolios remain relatively stable. The implications are significant for energy policymakers, traders, and financial investors. Early detection of warning signals supports strategic risk management. This research contributes to academic discourse and provides actionable insights, highlighting the importance of early warning indicators in enhancing financial resilience in an ever-evolving market landscape. It underscores the value of foresight in navigating global financial stability.

Elucidating the effect of different divalent metals (Mn, Co, Cu, and Zn) on optical, photocatalytic degradation, reusability and ionizing radiation attenuation properties of lanthanum ferrite nanoparticles

Ferrite nanoparticles are promising materials in various fields due to their unique magnetic and chemical stability, remarkable utilization in photocatalytic degradation, and ionizing radiation attenuation properties. So, in the present work, M0.45La0.1Fe1.45O4 (M = Zn, Mn, Cu, and Co) ferrite nanoparticles (MLF nanoparticles) have been explored as a means for improving optical, photocatalytic degradation, reusability, and ionizing radiation attenuation properties. The obtained optical band gaps are 2.44 ± 0.01 eV, 2.20 ± 0.01 eV, 1.93 ± 0.01 eV and 1.70 ± 0.01 eV for the CuLF, ZnLF, CoLF, and MnLF, respectively. The optical band gaps of all the MLF nanoparticles lie within the visible range, indicating their potential as photocatalysts under visible light. The MnLF nanoferrite shows the best degrading efficiency at 97.29 % for methylene blue dye with outstanding stability and enhanced recyclability. In addition, according to the gamma-ray attenuation characteristics of the MLF nanoparticles, the sample ZnLF shows a promising ability for radiation attenuation due to its higher mass attenuation coefficient in comparison with the mass attenuation coefficient of the other MLF nanoparticles. Also, the ZnLF sample has the highest effective atomic number, and this is due to the high atomic number of Zn element in comparison with the other MLF nanoparticles.

Enhancing hydrogen evolution reaction efficiency with electrospun Ni-doped Zn(O,S) microfibers photocatalyst: A novel approach for sustainable energy conversion

This study presents Ni-doped Zn(O,S) microfibers as an effective photocatalyst for addressing global energy and environmental challenges by producing green hydrogen as a sustainable alternative to fossil fuels. In addition, the embedment of nanocatalyst into PVP fibers also mitigates the harmful of nanoparticle leaching. Ni-doped Zn(O,S) microfiber photocatalysts with varying Ni concentrations were effectively produced using a simple electrospinning technique, followed by annealing at 180 °C for 3 h. The optimized ZN-2.5 microfiber photocatalyst has achieved the highest hydrogen (H2) production rate of 648.2 μmmol g−1 h−1. ZN-2.5 has recorded 3240.5 μmmol g−1 of hydrogen generation rate after 5 h of illumination in addition to extraordinary stability up to 30 h. This work demonstrates the significant improvement of the overall photocatalytic H2 evolution reaction (HER) process over ZN-X catalysts via doping small amounts of Ni to the Zn(O,S) matrix. Ni doping increases the microfibers light absorbance ability, improves charge separation transfer, and minimizes the recombination rate of the photogenerated electron-hole pairs. Moreover, Ni-doped Zn(O,S) achieved unique stability up to 7 runs for photocatalytic H2 production. More oxygen vacancies are formed on the surface of the photocatalyst upon illumination thus showing elevating activity while recycling the photocatalyst. The reported photocatalysts in this paper are low-cost, earth-abundant, and environment-friendly which is encouraging to design more novel photocatalysts following the same trend.

Atomic-Scale Characterization of 180° Conductive Domain Walls in PbZr0.1Ti0.9O3.

Conductive domain walls (DWs) in ferroic materials have emerged as promising candidates for applications in nanoelectronics due to their unique properties such as high conductivity and nonvolatility. In this study, we investigate the atomic structure and conductivity of nominally neutral 180° DWs artificially created in an epitaxial thin film of tetragonal PbZr0.1Ti0.9O3. Using piezoresponse force microscopy and scanning transmission electron microscopy, we elucidate the complex structure of these 180° DWs and their coupling with ferroelastic domains, revealing that they exhibit a complex structure due to the strain-mediated interplay with the ferroelastic domains. Our results demonstrate that the 180° DWs conductivity is associated with the emergence of polar discontinuities, including the formation of tail-to-tail charged segments, which has been further confirmed by electron energy loss spectroscopy. Additionally, we investigated the long-term performance of these domain boundaries, demonstrating their unique mobility and structural stability. Our findings provide insights into the atomic-scale mechanisms that turn nominally neutral DWs into highly conductive channels, paving the way for their use in advanced nanoelectronic devices.

Exploring the reactivity of (hetero)aryl amides in the Chan‐Evans‐Lam reaction with arylalkenyl boron reagents

The unique reactivity and stability of enamides make them attractive reagents in organic synthesis. Herein, we investigated the reactivity of acetanilides and pyridyl acetamides in the formation of a C–N bond through a Chan‐Evans‐Lam reaction using arylalkenyl boron‐based reagents yielding a wide scope of N‐aryl enamides with an E configuration. The products obtained have been applied in the synthesis of N‐heterocycles, an important scaffold in several biologically active compounds, via sequential Heck reaction to prove the practical utility of the prepared N‐aryl enamides.

Two in One Gram Negative Antibacterial Agent and Organic Dye Photocatalyst from Green Synthesized Ocimum Sanctum-Based N and O Co-Doped Carbon Dot Silver Nanocomposite.

This study reports, successful synthesis of Oxygen(O) and Nitrogen(N) co-doped Ocimum Sanctum plant-based or tulsi carbon dots-silver nanoparticle nanocomposites (TCD-AgNP) for the development of an efficient, highly active, low-cost fingerprint antibacterial agent against gram-negative organisms and a highly efficient photocatalyst for the degradation of methylene blue (MB). Green synthesized, high quantum yield (47 %), intensely blue fluorescent, highly stable N and O co-doped TCDs from carbonization technique of tulsi leaves is achieved without any chemical treatment or surface fascination which could act as an efficient green reducing agent for the development green TCD-AgNP nanocomposites. The novelty and advantage of this study is the development of highly stable, blue fluorescent, high quantum yield (40 %) environmental -friendly TCD-AgNP nanocomposite through reduction method by using green TCDs. TCD-AgNP nanocomposites were synthesized by varying the concentrations of AgNO3 into a fixed amount of green TCDs. Spectrochemical characteristics of synthesized TCDs and TCD-AgNP nanocomposites were investigated through UV-Vis absorbance, Photoluminescence (PL) spectroscopy, Fourier transform infrared (FTIR), X-ray photoelectron spectroscopy (XPS) and Zeta potential measurements confirming excellent fluorescence, unique stability and effective O and N doping. High-resolution transmission electron microscopy (HR-TEM) images confirms that the synthesized TCDs and TCD-AgNP nanocomposites were spherical in shape with an average size of 6.3 nm and 11.5 nm respectively. The antibacterial studies proved that TCD-AgNP nanocomposites ware highly effective against Gram-negative (Serratia marcescens, E. coli, and Pseudomonas aeruginosa) microbial organisms and showed zones of inhibition 12, 9 and 18 mm as compared to streptomycin sulphate. Besides, TCD-AgNP nanocomposite was used as a photocatalyst for the degradation of MB (10 ppm) under sunlight irradiation for regular intervals of time at room temperature with a photodegradation efficiency of 95.63 % and a photocatalytic rate constant of 0.0195 min-1.

A Galerkin finite element method for the nonlinear strongly damped wave equation

In this work, we consider a Galerkin finite element method for solving a two-dimensional strongly damped nonlinear wave equation. Our purpose is to establish significant results about the unique solvability, stability and convergence of semidiscrete and fully discrete schemes. First, we prove the existence and uniqueness of the weak solution. Second, we show a priori bounds and convergence of the semidiscrete Galerkin scheme. Next, we propose a fully discrete method based on Cranck–Nicolson scheme to derive its unique solvability and stability. Our analysis includes rigorous proofs of optimal error estimates for this fully discrete scheme. Finally, we present computational experiments to illustrate the validity and accuracy of theoretical results. Overall, our study as well provides solid mathematical foundation for numerical solution and advances numerical methods for nonlinear wave equations. This offers new insights and techniques for the problem in question, thereby, contibuting to the field of numerical methods applied to partial differential equations.

Deep-Eutectic-Solvent-Decorated Metal-Organic Framework for Food and Environmental Sample Preparation.

Deep eutectic solvent (DES) is distinguished by its unique solvent properties, chemical stability, and eco-friendly nature, which are pivotal in a spectrum of chemical processes. It enhances the sample preparation process by increasing efficiency and minimizing the environmental impact. Metal-organic frameworks (MOFs), which are porous structures formed through coordination bonds between metal ions and organic ligands, are defined by their adjustable pore dimensions, extensive surface areas, and customizable architectures. The integration of DES within MOF to create DES@MOF capitalizes on the beneficial attributes of both materials, augmenting MOFs' stability and versatility while providing a multifunctional carrier for DES. This composite material is both highly stable and readily tunable, establishing it as a leading contender for applications in sample preparation for food and environmental samples. This comprehensive review explores the application of DES-decorated MOF in food and environmental sample preparation and highlights the expansive potential of DES@MOF in diverse fields. We provide a detailed analysis of the characteristics of DES@MOF and its individual components, methods for decorating MOFs with DES, the advantages of these composite materials in sample pretreatment, and their specific applications in food safety and environmental monitoring. DESs are employed to modify MOFs, offering a multitude of benefits that can substantially improve the overall performance and applicability of MOFs. The review also discusses current challenges and future directions in this field, offering valuable insights for further research and development. The synergistic effects of DES and MOFs offer new opportunities for applications in food safety and other areas, leading to the development of more efficient, sensitive, and environmentally friendly analytical methods. This collaboration paves the way for sustainable technologies and innovative solutions to complex challenges.

Photothermally Active Quantum Dots in Cancer Imaging and Therapeutics: Nanotheranostics Perspective.

Cancer is becoming a global threat, as the cancerous cells manipulate themselves frequently, resulting in mutants and more abnormalities. Early-stage and real-time detection of cancer biomarkers can provide insight into designing cost-effective diagnostic and therapeutic modalities. Nanoparticle and quantum dot (QD)-based approaches have been recognized as clinically relevant methods to detect disease biomarkers at the molecular level. Over decades, as an emergent noninvasive approach, photothermal therapy has evolved to eradicate cancer. Moreover, various structures, viz., nanoparticles, clusters, quantum dots, etc., have been tested as bioimaging and photothermal agents to identify tumor cells selectively. Among them, QDs have been recognized as versatile probes. They have attracted enormous attention for imaging and therapeutic applications due to their unique colloidal stability, optical and physicochemical properties, biocompatibility, easy surface conjugation, scalable production, etc. However, a few critical concerns of QDs, viz., precise engineering for molecular imaging and sensing, selective interaction with the biological system, and their associated toxicity, restrict their potential intervention in curing cancer and are yet to be explored. According to the U.S. Food and Drug Administration (FDA), there is no specific regulation for the approval of nanomedicines. Therefore, these nanomedicines undergo the traditional drug, biological, and device approval process. However, the market survey of QDs is increasing, and their prospects in translational nanomedicine are very promising. From this perspective, we discuss the importance of QDs for imaging, sensing, and therapeutic usage pertinent to cancer, especially in its early stages. Moreover, we also discuss the rapidly growing translational view of QDs. The long-term safety studies and cellular interaction of these QDs could enhance their visibility and bring photothermally active QDs to the clinical stage and concurrently to FDA approval.

Research on Graphitic Carbon Nitride (g-C3N4) prepared by template-based method and its photocatalytic properties

Abstract. The Graphitic Carbon Nitride (g-C3N4), a non-metallic polymer photocatalytic material, has a wide range of raw materials and a simple preparation process. Due to its unique electronic structure and excellent photocatalytic performance, g-C3N4 has attracted wide attention in the field of environmental purification and energy conversion in recent years. However, g-C3N4 faces a lot of challenges, including a wide band gap, many interlayer defects, and poor interlayer electron transport. Nevertheless, its unique semiconductor structure and chemical stability still provide the possibility to explore the effect of its piezoelectric properties on photocatalysis, which paves the way for a novel approach to environmentally friendly hydrogen production. Therefore, the paper delves into the application of different template methods in the preparation of g-C3N4 by reviewing the related literature, and analyzes the role of different template materials in the preparation. In addition, in this paper, the photocatalytic properties of g-C3N4 are explored, which are mainly reflected in the photocatalytic water separation performance and photocatalytic degradation of organic dyes. It is found that the g-C3N4 shows great potential in the fields of photocatalytic water decomposition for hydrogen production and degradation of organic pollutants due to its unique band gap, nontoxicity, low cost and wide range of sources. Future research should continue to explore more kinds of template materials and their preparation processes, with the aim of realizing further enhancement of the performance of g-C3N4 photocatalysts and promoting their practical applications in the fields of environment and energy.

The Removal and Mitigation Effects of Biochar on Microplastics in Water and Soils: Application and Mechanism Analysis

Due to their widespread distribution, microplastics (MPs) are endangering the soil ecological environment system, causing water pollution and altering the soil’s physicochemical and microbiological features. Because of its unique pore structure and strong stability, biochar is widely used as an adsorbent. However, the effects of MP–biochar interactions in water and soil environment are still unclear. This review outlines the application and mechanism of biochar as an adsorbent in a water environment for the removal of MPs. Also, biochar serves as remediation material for MPs in soils as it mitigates the adverse effects of MPs on soil properties, enzyme activities and soil microbial community. It was found that woody biochar had the highest yield and was more effective in adsorbing MPs. Further research should focus on the combined effects of biochar and MPs, the environmental risks of biochar, the modification of biochar application of MP-removal technologies, the characterization of MP properties, the remediation of combined contamination of MPs and other pollutants, and the transportation of MPs.

Magnetic Anisotropic Effects in Charged Aza[10]annulene Analogs with a Non-planar Carbon Framework.

Classically, aromaticity portrays the unique stability and peculiar reactivities of cyclic planar conjugated systems with (4n+2) π electrons. Understanding the electronic environments in new chemical frameworks through experimental and theoretical validation is central to this ever-expanding theme in chemical science. Such investigations in curved π-surfaces have special significance as they can unravel the variations when the planarity requirement is slightly lifted. In this report, we discuss the synthesis,spectroscopicand theoretical studies involving a new group of cyclazine analogs having a charged aza[10]annulene periphery, centrally locked through a sp3 carbon. Magnetic anisotropic effects arising from electron delocalization through its curved π-surface were mapped through a specific set of chemical groups introduced through this sp3 carbon. The nucleus-independent chemical shift calculations revealed negative chemical shift values, indicating the aromatic nature of the aza[10] annulene rim. This is corroborated by a clockwise diatropic ring current, evident from anisotropy-induced current density analysis. Variations in the chemical shift of NMR signals in these systems were also computationally examined through isotropic chemical shielding surface analysis.

A kinetic and mechanistic study of the self-reaction between two propargyl radicals.

The propargyl radical plays a critical role in various chemical processes, including hydrocarbon combustion, flame synthesis, and interstellar chemistry. Its unique stability arises from the delocalization of π-electrons, allowing it to participate in a wide range of reactions despite being a radical. The self-reaction of propargyl radicals is a fundamental step in synthesizing polycyclic aromatic hydrocarbons. In this work, therefore, a computational study into the C3H3 + C3H3 potential energy surface has been carefully characterized. The calculated results indicate that the reaction can occur by H-abstraction or addition of two propargyl radicals together. The H-abstraction mechanism can create the products P3 (H2CCC + H3CCCH) and P4 (H2CCCH2 + HCCCH) but the energy barriers of the two H-abstraction channels are very high (from 12 to 22kcal/mol). In contrast, the addition mechanism of two propargyl radicals forming the intermediates (I1, I5, I12) and the bimolecular products (P1, P2, P7, P11, P12) are dominant. Among the bimolecular products, the P11 (C6H4 + H2) product is the most energetically favorable, and the channel leading to this product is also the most preferred path compared to all other paths throughout the PES. The calculated enthalpy changes of various reaction paths in this study are in good agreement with the available literature data, indicating that the CCSD(T) method is suitable for the title reaction. The overall rate constant of the reaction depends on both temperature and pressure, reducing with temperature but rising with pressure. The calculated results agree closely with the available experimental values ​​and previous calculated data. Thus, it can be affirmed that in addition to the CASPT2 method as applied in the study of Georgievskii et al. (Phys. Chem. Chem. Phys., 2007, 9, 4259-4268), the CCSD(T) method is also very good for the self-reaction of two propargyl radicals. The M06-2X and CCSD(T) methods with the aug-cc-pVTZ basis set were used to optimize and calculate single-point energies for all species of the reaction. The bimolecular rate constants of the dominant reaction paths were predicted in the temperature and pressure ranges of 300-1800K and 0 - 76,000Torr, respectively, using the VTST and RRKM models with Eckart tunneling correction for the H-shift steps.

Recent Progress in Free Radical Transformations of Allenamides.

Allenamides are special allenes, and the unique reactivity, selectivity (both stereoselective and regionally selective) and stability of allenamides have been widely studied. In this review, the development of the free radical transformation of allenamides over the last few years will be summarized. This review discusses in detail in three parts: intermolecular radical addition to C- X (X = N, S, O, Se) bonds, metal salt mediated cyclization of allenamides, and photocatalytic cyclization of allenamides. In addition, reasonable details of the mechanisms are provided for the vast majority of these transformations.

Physical properties and biological investigations of polycaprolactone filled with zinc oxide/hematite nanoparticles to meet biomedical application

The biological properties of metal oxides offer great potential for the development of advanced biomaterials in the field of therapy. In this study, zinc oxide, hematite, and Polycaprolactone (PCL) were used to fabricate polymeric nano-composites (NCs) with the aim of addressing medical needs. The incorporation of hematite and zinc oxide into the NCs was driven by their unique light absorption properties and stability, making them promising optical constituents. The structure and size analysis of the NCs have been performed using XRD, FTIR, and FESEM techniques. Morphologically, the introduction of inorganic components led to changes in the porous structure of the NCs, resulting in a reduction in pore size. Additionally, UV–Vis spectroscopy revealed a shift in the absorption edge along the x-axis. For the binary composition PCL-ZnO, the absorption edge started at 4.35 eV, while for the PCL-ZnO-30 % Fe2O3 NC, it decreased to 1.5 eV. The results demonstrated that the NC exhibited 100 % cell viability when exposed to a concentration of 156.25 μg/ml, and even exceeded 100 % (120.7 %) when exposed to a concentration of 2.4 μg/ml. These findings suggest the potential of the PCL-ZnO-30 % Fe2O3 NC for medical applications, highlighting its favorable biocompatibility. As a result, the examined NCs are a potentially useful composition for medical applications.

Survey of Chemical Unfolding Complexity as a Unique Stability Assessment Assay for Monoclonal Antibodies

Seventy-two intentionally sequence-diverse antibody variable regions were selected, expressed as IgG1 antibodies, and evaluated by chemical unfolding to survey the complexities of denaturant induced unfolding behavior. A two-transition fit well described the curves and uncovered a wide range of sensitivities to denaturant. Four general types of unfolding curves were observed: balanced traces (each transition responsible for half of the total unfolding transition), low-unfolding traces (first transition is a majority of the unfolding curve), high-unfolding traces (the second transition is the majority of the unfolding curve), and coincident traces (the two transitions are found close to each other, approximating a single transition).The complexity of the data from this survey indicates that focusing on the first inflection point or fitting a single transition model is likely an over-simplistic method for measuring stability by the chemical unfolding assay. Additionally, other conformational assays, such as thermal and low pH unfolding, showed no correlation with the chemical unfolding results, indicating that each of these assays provide alternate information on the different pathways of antibody conformational stability. These results provide a basis for beginning to better connect unfolding behavior to other physical phenotypic behaviors and production process behaviors.

Development of Polymer Composite Membrane Electrolytes in Alkaline Zn/MnO2, Al/MnO2, Zinc/Air, and Al/Air Electrochemical Cells.

This paper reports on the novel composite membrane electrolytes used in Zn/MnO2, Al/MnO2, Al/air, and zinc/air electrochemical devices. The composite membranes were made using poly(vinyl alcohol), poly(acrylic acid), and a sulfonated polypropylene/polyethylene separator to enhance the electrochemical characteristics and dimensional stability of the solid electrolyte membranes. The ionic conductivity was improved significantly by the amount of acrylic acid incorporated into the polymer systems. In general, the ionic conductivity was also enhanced gradually as the testing temperature increased from 20 to 80 °C. Porous zinc gel electrodes and pure aluminum plates were used as the anodes, while porous carbon air electrodes or porous MnO2 electrodes were used as the cathodes. The cyclic voltammetry properties and electrochemical impedance characteristics were investigated to evaluate the cell behavior and electrochemical properties of these prototype cells. The results showed that these prototype cells had a low bulk resistance, a high cell power density, and a unique device stability. The Al/MnO2 cell achieved a density of 110 mW cm-2 at the designated current density for the discharge tests, while the other cells also exhibited good values in the range of 70-100 mW cm-2. Furthermore, the Zn/air cell consisting of the PVA/PAA = 10:5 composite membrane revealed an excellent discharge capacity of 1507 mAh. This represented a very high anode utilization of 95.7% at the C/10 rate.

Recent Advances in Scandium(III) Triflate Catalysis: A Review

AbstractOver the past three decades, triflate salts have emerged as crucial Lewis acid catalysts in organic synthesis, playing a significant role in cyclization, C−H bond functionalization, and various other reactions. Among these, rare‐earth triflates have garnered attention due to their water compatibility, environmental friendliness, noncorrosive nature, and reusability. In particular, scandium(III) triflate [Sc(OTf)3] stands out as a water‐resistant Lewis acid with remarkable catalytic activity in aqueous environments. Unlike typical Lewis acids such as AlCl3, BF3, and SnCl4, which are decomposed or deactivated by water, Sc(OTf)3 remains stable and effective. Its exceptional Lewis acidity, resilience against hydrolysis, and recyclability make it a prominent green catalyst. The unique stability of Sc(OTf)3 in water is attributed to the smaller size of scandium ions (Sc3+), enhancing its catalytic efficiency. Sc(OTf)3 has a longstanding history in organic synthesis, facilitating a wide range of reactions including aldol, Michael, allylation, Friedel‐Crafts acylations, Diels‐Alder, Mannich, cycloadditions (including cyclopropanation), and cascade reactions. The increasing utilization of Sc(OTf)3 over the past decade underscores the necessity for updated insights. This review provides a concise overview of the versatility of Sc(OTf)3 as a catalyst, focusing on developments from 2017 to 2024.

Si-Linked Glycomimetics through a Stereoselective Silicon Transfer and Anion Addition.

We report a synthesis of silicon-linked glycomimetics, demonstrating unique structural properties and metabolic stability due to the inertness of the C-Si bond. Our method focuses on the stereoselective transfer of silicon and anion addition, revealing that chirality at the silicon atom can be controlled through kinetic resolution. This approach allows for the selective generation of 1,2-cis and 1,2-trans isomers via the manipulation of C2-protected silicon ethers and nucleophilic opening of glycal epoxides. We achieved high selectivity at the anomeric carbon and expanded the scope to include various saccharides and substituted silanes. Our findings indicate that silicon transfer occurs intramolecularly and is influenced by the nature of the counterion and reaction conditions. Additionally, chiral silanes produced through our method hold promise for medicinal chemistry applications, addressing significant gaps in the synthesis and utility of glycomimetics. This work opens new avenues for the development of bioactive silicon-based molecules.

Comparative Study of Deflector Configurations under Variable Vertical Angle of Incidence and Wind Speed through Transient 3D CFD Modeling of Savonius Turbine

The demand for clean and sustainable energy has led to the exploration of innovative technologies for renewable energy generation. The Savonius turbine has emerged as a promising solution for harnessing wind energy in urban environments due to its unique design, simplicity, structural stability, and ability to capture wind energy from any direction. However, the efficiency of Savonius turbines poses a challenge that affects their overall performance. Extensive research efforts have been dedicated to enhancing their efficiency and optimizing their performance in urban settings. For instance, an axisymmetric omnidirectional deflector (AOD) was introduced to improve performance in all wind directions. Despite these advancements, the effect of wind incident angles on Savonius turbine performance has not been thoroughly investigated. This study aims to fill this knowledge gap by examining the performance of standard Savonius configurations (STD) compared to the basic configuration of the deflector (AOD1) and to the optimized one (AOD2) under different wind incident angles and wind speeds. One key finding was the consistent superior performance of this AOD2 configuration across all incident angles and wind speeds. It consistently outperformed the other configurations, demonstrating its potential as an optimized configuration for wind turbine applications. For instance, at an incident angle of 0°, the power coefficient of the configuration of AOD2 was 61% more than the STD configuration. This ratio rose to 88% at an incident angle of 20° and 125% at an incident angle of 40°.