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Comprehensive Summary: With the rapid development of solid‐state batteries, solid‐state polymer electrolytes (SPEs) have attracted widespread attention due to their excellent environmental friendliness, designability, and forming film ability. However, due to the limited conductive path of polymers, lithium‐ion diffusion kinetics are limited, and low ion conductivity is a huge challenge for SPEs in practical applications. This work provides a polyethylene oxide (PEO) based polymer electrolyte, which has multiple paths of ion diffusion caused by organic polymer framework of poly(hexaazatrinaphthalene) (PHATN). The unique porous channel, the specific surface characteristics, the coordination of ‐C=N‐ groups in PHATN with Li+, combined with the mobility of PEO segments, make the SPEs have a good ability to conduct Li+. Interestingly, the PHATN‐PEO/lithium bis(trifluoromethanesulfonyl) imide (LiTFSI) composite electrolytes exhibit excellent electrochemical properties. At room temperature, the conductivity of PHATN‐PEO electrolyte can reach 1.03 × 10–4 S·cm–1, which is greatly improved compared with 3.9 × 10–6 S·cm–1 of PEO. Delightedly, the lithium‐ion transference number of PHATN‐PEO electrolyte achieves 0.61, and the electrochemical window increases to 4.82 V. The LFP/1%PH‐PEO/Li solid‐state batteries show good electrochemical cycles. This work reveals an efficient stratagem for the design of polymer solid‐state electrolytes. [ABSTRACT FROM AUTHOR]

Comprehensive Summary: With the rapid development of solid‐state batteries, solid‐state polymer electrolytes (SPEs) have attracted widespread attention due to their excellent environmental friendliness, designability, and forming film ability. However, due to the limited conductive path of polymers, lithium‐ion diffusion kinetics are limited, and low ion conductivity is a huge challenge for SPEs in practical applications. This work provides a polyethylene oxide (PEO) based polymer electrolyte, which has multiple paths of ion diffusion caused by organic polymer framework of poly(hexaazatrinaphthalene) (PHATN). The unique porous channel, the specific surface characteristics, the coordination of ‐C=N‐ groups in PHATN with Li+, combined with the mobility of PEO segments, make the SPEs have a good ability to conduct Li+. Interestingly, the PHATN‐PEO/lithium bis(trifluoromethanesulfonyl) imide (LiTFSI) composite electrolytes exhibit excellent electrochemical properties. At room temperature, the conductivity of PHATN‐PEO electrolyte can reach 1.03 × 10–4 S·cm–1, which is greatly improved compared with 3.9 × 10–6 S·cm–1 of PEO. Delightedly, the lithium‐ion transference number of PHATN‐PEO electrolyte achieves 0.61, and the electrochemical window increases to 4.82 V. The LFP/1%PH‐PEO/Li solid‐state batteries show good electrochemical cycles. This work reveals an efficient stratagem for the design of polymer solid‐state electrolytes. [ABSTRACT FROM AUTHOR]

In all-solid lithium metal batteries, sulfide electrolytes offer superior ion conductivity. Nevertheless, they also confront significant challenges, such as the formation of internal dendrites and instability in lithium and humid air. In order to overcome these issues, a sulfide composite electrolyte has been prepared by mixing polyethylene oxide polymers with air-stable inorganic sulfide, Li4SnS4, which can achieve good chemical and electrochemical stability. Meanwhile, the introduced Li4SnS4 can facilitate the movement of Li+ ions in the composite electrolyte, which exhibits an elevated ion conductivity up to 2.55 × 10−5 S cm−1. [ABSTRACT FROM AUTHOR]

This study investigates the crystallization behavior of electrospun coaxial fibers composed of crystalline poly(ethylene oxide) (PEO) in the core and crystalline poly(L‐lactide) (PLLA) in the sheath. The influence of cold crystallization temperature and premelting temperature on the crystallization of PEO and PLLA is investigated. At a cold crystallization temperature of ≤60 °C, PLLA remained immobile. PEO crystallization is hard‐confined, leading to a low degree of crystallinity. At a cold crystallization temperature of >60 °C, PEO melted, whereas PLLA crystallized. An increase in cold crystallization temperature results in an increase in the crystallite size and crystallinity of PLLA. Furthermore, the melt crystallization behavior of PEO in the coaxial fibers is strongly influenced by its premelting temperature and crystallization temperature. A higher premelting temperature leads to enhanced interdiffusion between PEO and PLLA. This increased confinement results in a decrease in PEO's crystallizability. Additionally, premelting relaxes the PEO chains, causing a shift in crystal orientation from parallel to the fiber axis (observed in as‐electrospun fibers) to perpendicular to the fiber axis (observed in melt‐crystallized fibers). Moreover, at a low melt crystallization temperature, demixing between PEO and PLLA is observed. This, coupled with a higher degree of supercooling, leads to an increase in PEO's crystallizability. [ABSTRACT FROM AUTHOR]

Utilizing the solution casting technique, polymer nanocomposites (PNCs) films including polyethylene oxide and chitosan (PEO/CS) doped with titanium dioxide nanoparticles (TiO2 NPs) as nanoceramic were successfully synthesized. The study investigated how varying TiO2 nanoparticle concentrations influenced the structural, optical properties, and antibacterial activity of the polymeric matrix. XRD patterns revealed an increase in the amorphous nature of the polymer blend as the content of TiO2 NPs inside the PEO/CS blend grew. The FT-IR analysis confirmed the interaction between TiO2 NPs and the PEO/CS blend. This confirmation is attributed to the observed vibrational changes upon the incorporation of TiO2 dopant into the polymer matrix. The UV–visible spectrum aided in the determination of optical energy band gaps (both direct and indirect), showing reductions in both Egd and Egin with higher TiO2 concentrations. SEM highlighted the partial compatibility between PEO/CS and TiO2, while transmission electron microscopy depicted spherical TiO2 NPs with diameters ranging from approximately 9 to 25 nm. Antimicrobial assessments indicated heightened efficacy in all nanocomposite samples compared to the pure PEO/CS composite, with a linear correlation to the quantity of TiO2 nanoparticles present. These findings strongly suggest the potential of these nanocomposites for food packaging applications. [ABSTRACT FROM AUTHOR]

The plasma electrolytic oxidation (PEO) technology was used to prepare ceramic coating on the surface of titanium alloy to prevent the galvanic corrosion of AH36/TC4(PEO). The results showed that after PEO treatment, ceramic coating with micropores was formed on the substrate surface. When the voltage was low, the pore size was small. With the increase of voltage, the thickness and the pore sizes of the coating increased. After PEO process, the average galvanic corrosion rate was reduced by 60%, and the number of pitting pits on the AH36 surface in the galvanic pair was reduced. The tensile strength and elongation of AH36 coupled with TC4(PEO) decreased by 4.0% and 11.9%, respectively. The contents of the corrosion products Fe2O3·H2O and FeO(OH) decreased, and the corrosion area of the tensile specimen was evidently reduced. Therefore, the PEO process can effectively reduce the galvanic corrosion susceptibility of AH36/TC4(PEO), alleviate the reduction degree of ductility and toughness of anode AH36, and enhance the corrosion resistance performance. [ABSTRACT FROM AUTHOR]

In the context of growing interest in phosphonic acid proton exchange membranes (PEMs) for fuel cell applications, we report on new PEMs containing low‐cost polyethylene oxide (PEO) covalently linked by siloxane bonds, SiOSi, to phosphonic acid (PA). Key chemistry in the formation of these membranes involves hydrolysis and condensation reactions of triethoxysilyl propyl capped PEO and pre‐hydrolyzed dimethyl phosphonatoethyltrimethoxysilane (DMPTMS) giving PEO‐Si2O3‐PA and cross‐linked chain PEO‐Si2O3‐PEO organosilsesquioxane components. The Si2O3 can enhance membrane thermal and mechanical properties. The membrane formulations were varied by (a) reagent ratios (b) PEO molecular weights or using polypropylene oxide (PPO) (c) incorporating chain extending groups methylene diphenyl diisocyanate (MDI) or hexamethylene diisocyanate (HDI). These variations provided five membrane families, one of which afforded a complete group of robust membranes with weight% x of PA, PAx in range PA0–PA33. These were studied using ATR‐FTIR, dry membrane water uptake capacity, ion exchange capacity (IEC), and conductivity from room temperature to 120°C at 100% relative humidity. Conductivity increased with PAx reaching 15 mS cm−1 at 120°C, activation energy 0.1 eV, for membrane PA33 for which thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), scanning electron microscopy (SEM), and energy dispersive X‐ray analysis (EDAX) are reported. A comparative performance of the five membrane families is presented. [ABSTRACT FROM AUTHOR]

The introduction of new sequencing approaches into clinical practice has radically changed the diagnostic approach to mitochondrial diseases, significantly improving the molecular definition rate in this group of neurogenetic disorders. At the same time, there have been no equal successes in the area of in-depth understanding of disease mechanisms and few innovative therapeutic approaches have been proposed recently. In this regard, the identification of the molecular basis of phenotypic variability in primary mitochondrial disorders represents a key aspect for deciphering disease mechanisms with important therapeutic implications. In this study, we present data from proteomic investigations in two subjects affected by mitochondrial disease characterized by a different clinical severity and associated with the same variant in the TWNK gene, encoding the mitochondrial DNA and RNA helicase with a specific role in the mtDNA replisome. Heterozygous pathogenic variants in this gene are associated with progressive external ophthalmoplegia and ptosis, usually with adult onset. The overall results suggest an imbalance in glucose metabolism and ROS production/regulation, with possible consequences on the phenotypic manifestations of the enrolled subjects. Although the data will need to be validated in a large cohort, proteomic investigations have proven to be a valid approach for a deep understanding of these neurometabolic disorders. [ABSTRACT FROM AUTHOR]

Despite their potential as next-generation energy storage devices, all-solid-state batteries (ASSBs) have not been widely developed because of the low ionic conductivity of solid electrolytes and the high interfacial impedance with electrodes. This study addressed these issues by enhancing the electrochemical properties through composition control. A composite solid electrolyte (CSE) was fabricated using Li6.5Ga0.2La2.95Rb0.05Zr2O12 (Ga–Rb-doped LLZO) and poly(ethylene oxide) (PEO) with various compositions. The results demonstrated high ionic conductivity and electrochemical stability when the weight ratio of Ga–Rb-doped LLZO to PEO was 6:4. These characteristics effectively mitigated Li dendrite formation and ensured excellent interfacial stability. Notably, LiFePO4/CSEs/Li full cells retained 92.3% of their initial capacity after 100 cycles at a 0.3 C rate. This study will promote the research and development of practical ASSBs incorporating LLZO solid electrolytes. [ABSTRACT FROM AUTHOR]

A liquid-repellent and corrosion resistant surface was fabricated on AZ31B Mg alloy by the usage of CeO 2 and TiO 2 nanoparticles (NPs), plasma electrolyte oxidation (PEO) method, and subsequent surface modification. The whole process included two main steps: a) applying PEO with CeO 2 –TiO 2 NPs on AZ31B and b) decreasing surface energy by using a fluorinating agent. Elements that were present on the surface were investigated by XRD and EDS analyses. Surface morphology and its roughness were scrutinized by FESEM images and AFM tests, respectively. Contact angles (CA) of water and some oils (Ethylene glycerol and Glycerol) on the prepared surface were measured. CAs of water and ethylene glycerol were reported at 175.6° and 151.4°, respectively. Also, the corrosion behavior of the prepared surface was assessed by EIS and potentiodynamic polarization analyses. Results showed that the corrosion rate of the neat AZ31B decreased noticeably from 127.78 to 0.027 mpy for superamphiphobic PEO-NPs AZ31B. The prepared sample showed high mechanical durability, which was scrutinized by water floatation, abrasive with grit SiC paper, adhesive tape peeling, and bending tests. After immersion of the sample in 5 wt% NaCl solution for various hours, results showed that the prepared sample had a noticeable corrosion resistance stability. [Display omitted] • A durable superamphiphobic surface was fabricated on AZ31B. • The prepared surface showed a remarkable water and oil repellency. • A prepared superamphiphobic surface promoted noticeably the corrosion resistance of AZ31B. • A superamphiphobic surface showed brilliant corrosion resistance stability and mechanical durability. [ABSTRACT FROM AUTHOR]

This work focuses on the development of a composite polymer electrolyte (CPE) for all‐solid‐state lithium metal batteries (ASSLMBs), integrating LLTO nanofibers into a PEO (polyethylene oxide)‐PVDF‐HFP (poly(vinylidene fluoride‐cohexafluoropropylene)) matrix with LiClO4 as the lithium salt. The PEO has high ionic conductivity and flexibility, and the PVDF‐HFP has high mechanical strength and electrochemical stability. Therefore, the resulting composite has improved electrochemical performance and mechanical properties. Incorporating LLTO nanofibers enhances ionic conductivity due to the one‐dimensional ion transport pathways provided by the nanofibers while maintaining mechanical integrity and air stability, overcoming the challenges associated with conventional fillers. The prepared CPE demonstrates exceptional electrochemical stability up to 5.1 V versus Li/Li+, making it suitable for high‐voltage applications over traditional polymer electrolytes. The optimized CPE with 15 wt% LLTO provides the ionic conductivity of 1.1 × 10−5 S cm−1 at room temperature and reaches 1.46 × 10−4 S cm−1 at 80°C. The assembled LiNi1/3Mn1/3Co1/3PO4||PEO‐PVDF‐HFP‐LiClO₄‐LLTO||Li based 2032 coin cell worked in between 3 and 4.8 V versus Li/Li+ potential window without any electrolyte decomposition from 0.5 to 5 mV/s scan rates. Similarly, the fabricated LiFePO₄||PEO‐PVDF‐HFP (1:2)‐LiClO4‐LLTO (15 wt%)||Li cell provides an initial capacity of 149 mAh g−1 at 0.1 C and 85 mAh g−1 at 0.5 C, exploring its potential for lithium metal batteries. Overall, this work offers a promising pathway for developing advanced solid polymer electrolytes for next‐generation lithium metal batteries, which combine high ionic conductivity, excellent electrochemical performances, and robust mechanical properties. [ABSTRACT FROM AUTHOR]

Due to the need to develop methods that optimize the surface properties of lightweight alloys such as aluminum, titanium, and magnesium and align with contemporary requirements of the 21st century, such as enhanced environmental and sanitary efficiency, the plasma electrolytic oxidation (PEO) process stands out as a comprehensive solution. This process can develop oxide coatings on the mentioned alloys, which exhibit superior physical and chemical properties compared with conventional methods. Since 2010, research in this area has been conducted with real-world applications. Recent studies have adopted experimental design approaches to optimize parameters to reduce operational costs and make the technology more accessible. The present study conducted a comparative analysis between treatments performed by conventional methods and by plasma processes, highlighting the most promising results.

There is an increasing interest in the development of Mg alloys, both for industrial and biomedical applications, due to their favorable characteristics such as being lightweight and robust. However, the inadequate corrosion resistance and lack of antibacterial properties pose significant challenges in the industrial and biomedical applications, necessitating the implementation of advanced coating engineering techniques. Plasma electrolytic oxidation (PEO) has emerged as a preferred coating technique because of its distinctive properties and successful surface modification results. However, there is a continuous need for further enhancements to optimize the performance and functionalities of protective surface treatments. The integration of layered double hydroxide (LDH) into PEO coatings on Mg alloys presents a promising approach to bolstering protective properties. This thorough review delves into the latest developments in integrating LDH into PEO coatings for corrosion-related purposes. It particularly emphasizes the significant improvements in corrosion resistance, antibacterial effectiveness, and photocatalytic performance resulting from the incorporation of LDH into PEO coatings. The two key mechanisms that enhance the corrosion resistance of PEO coatings containing LDH are the anion exchangeability of the LDH structure and the pore-sealing effect. Moreover, the antibacterial activity of PEO coatings with LDH stemmed from the release of antibacterial agents stored within the LDH structure, alterations in pH levels, and the photothermal conversion property. Furthermore, by incorporating LDH into PEO coatings, new opportunities emerge for tackling environmental issues through boosted photocatalytic properties, especially in the realm of pollutant degradation.

Plasma electrolytic oxidation (PEO) coatings were developed on an additively manufactured Al10SiMg alloy pre-treated with hard anodizing (HA). The influence of α−Al2O3 particles incorporated during PEO was evaluated in terms of energy consumption, coating morphology, composition and wear behaviour. Combining a 20 μm-thick HA precursor and a PEO electrolyte with suspended α−Al2O3 particles resulted in the highest energy savings (∼60%). Wear volume loss measurements and wear track characterization revealed that the PEO coating with added particles (PEOP) outperformed the coating without particles and a conventional hard anodizing layer. This superiority was attributed to the partial sealing of the outer porous layer by the incorporated α−Al2O3 particles as well as the reduced SiO2 content and the formation of a W-rich tribolayer on the wear track surface.

In this study, we examined how current density, sodium phosphate concentration, and the addition of copper sulfate to the supporting electrolyte affect PEO coatings on pure titanium. The chemical composition, morphology, and optical behavior of PEO coatings were extensively analyzed using scanning electron microscopy (SEM), X-ray diffraction (XRD), and UV–Vis diffuse reflectance spectroscopy (DRS). With an increase in current density from 6 to 18 A/dm2, the coating's pore size enlarges and the rutile phase content within the coatings increases. The coating created at 12 A/dm2 shows the highest photocatalytic activity and triggers a unique three-stage behavior in the voltage-time diagram. Adding 4 g/l of CuSO 4 to the electrolyte resulted in the formation of an unwanted Cu-based precipitates, causing electrolyte instability. To stabilize it, potassium hydroxide was removed, and the base electrolyte concentration was adjusted. To address this issue, potassium hydroxide was eliminated from the supporting electrolyte. Subsequently, the concentration of the base electrolyte was optimized. Also, the synergistic influence of CuSO 4 addition (4 g/l) to the supporting electrolyte at different concentrations of 5, 10, and, 15 g/l of trisodium phosphate on PA was investigated. The superior photocatalytic performance of the optimum coating created in the electrolyte containing 5 g/l trisodium phosphate and 4 g/l CuSO 4 is attributed to its enhanced porous structure, along with the heterojunction between the anatase and rutile phases. These features significantly boost the available surface area and facilitate the efficient separation and transfer of photogenerated charge carriers. Ultimately, a mechanism for MB photodegradation was proposed based on the findings from Mott-Schottky analysis and DRS. [ABSTRACT FROM AUTHOR]

Inorganic‐organic hybrid solid electrolytes (HSEs) are an important category of electrolyte materials for solid‐state batterie. It is of interest and importance to investigate the influence of composition and content of inorganic fillers on the electrochemical performance of HSEs. In this paper, we fabricated HSEs using polyethylene oxide (PEO) as matrix and incorporating different inorganic powders as active fillers. A series of HSEs with different contents of Ga/Nb co‐substituted garnet oxide (Li6.35Ga0.15La3Zr1.8Nb0.2O12, GN‐LLZO) and Y‐doped Li29Zr9Nb3O40 (Li29.3Zr8.7Y0.3Nb3O40, 0.3Y‐LZNO) were carefully designed. The ionic conductivity of these PEO‐based HSEs were studied, and their performance in solid‐state lithium‐ion batteries with LiFePO4 (LFP) as cathode material and Li metal as anode were evaluated. The results showed that the HSE with addition content of inorganic powders, namely PEOLiTFSI@5 % GN‐LLZO +5 %0.3Y‐LZNO (noted as PL3) showed the optimized ionic conductivity of 2.9×10−4 S cm−1 at room temperature with an activation energy Ea of 0.21 eV. It has an electrochemical stability window of 4.65 V and ionic transfer number of 0.242. The addition of inorganic powders not only enhanced the ionic conductivities of PEO‐based HSEs, but also exhibited superior stability and interfacial compatibility with electrodes, leading to the improved cycle stability in the LFP/PL3/Li solid‐state battery configuration. [ABSTRACT FROM AUTHOR]

In this work, the casting method was utilized to form the PEO/SnO2/ZrO2 nanocomposite to improve its structural and optical characteristics. The formation network path inside the polymeric matrix at the higher concentration of nanoparticles was confirmed by the optical microscope (OM). The nanocomposite of PEO/SnO2/ZrO2 has a higher absorbance in the UV region, which proved from the optical measurements that it can be used as an optoelectronic device. Increasing the concentration of SnO2 and ZrO2 NPs alters several properties. For example, the refractive index, optical conductivity, absorbance, extinction coefficient, and real and imaginary dielectric constants all increase, but the transmittance and energy optical band gap decrease. For the permitted and prohibited indirect transitions separately, the energy gap shrank from 3.68 eV to 3.4 eV and 3.66 eV to 3.35 eV, respectively. The narrowing of the energy band gap is very useful for many fields that work with optical devices. [ABSTRACT FROM AUTHOR]

Commercial pure titanium discs were subjected to sandblasting using varied treatment jet angles, and the samples were subsequently modified by plasma electrolytic oxidation to optimize both mechanical and electrochemical modifications. The coating morphology, real-time images, chemical composition, thickness, microhardness, roughness, and electrochemical behavior were characterized and investigated to research the microstructures and properties comprehensively. Research results demonstrate that an optimal jet angle in sandblasting led to improvements in coating topography, phases, and deposition, contributing to enhanced surface mechanical and anticorrosion performances. The further enhancement of the titania coating properties was attributed to the optimized hybrid electrochemical-mechanical-treatment. [ABSTRACT FROM AUTHOR]

This study provides a development of polymer electrolytes with an emphasis on their use in electrochemical devices. In present study we develop a new conducting carbon black (CB) powder dispersed into polyethylene oxide (PEO) polymer electrolyte using solution cast method. Various characterization techniques such as Impedance spectroscopy technique (EIS), Fourier transform infrared spectroscopy (FTIR), and Window stability (LSV) Linear sweep voltammetry has been studied in detail. The maximum ionic conductivity polymer electrolyte was at 0.05 wt%. of CB with σ value 1.20×10−5 S/cm. Finally the prepared CB dispersed polymer electrolyte using maximum conductivity sample is sandwiched between electrodes to fabricate an Electric double layer capacitor and Dye‐sensitized solar cell which show highest electrical capacity value of 68.5 F/gm at 5 mV/s respectively and 2.97 % efficiency shown by solar cell at 1 sun condition. [ABSTRACT FROM AUTHOR]

Due to the need to develop methods that optimize the surface properties of lightweight alloys such as aluminum, titanium, and magnesium and align with contemporary requirements of the 21st century, such as enhanced environmental and sanitary efficiency, the plasma electrolytic oxidation (PEO) process stands out as a comprehensive solution. This process can develop oxide coatings on the mentioned alloys, which exhibit superior physical and chemical properties compared with conventional methods. Since 2010, research in this area has been conducted with real-world applications. Recent studies have adopted experimental design approaches to optimize parameters to reduce operational costs and make the technology more accessible. The present study conducted a comparative analysis between treatments performed by conventional methods and by plasma processes, highlighting the most promising results. [ABSTRACT FROM AUTHOR]

• Modification of PEO coatings on Mg alloys by LDH offers a promising avenue for enhancing the protective properties of these materials. • Integration of LDH layers or nanoparticles into PEO coatings has demonstrated significant improvements in corrosion resistance. • Incorporation of LDH layers into PEO coatings significantly enhances their antibacterial and photocatalytic properties. There is an increasing interest in the development of Mg alloys, both for industrial and biomedical applications, due to their favorable characteristics such as being lightweight and robust. However, the inadequate corrosion resistance and lack of antibacterial properties pose significant challenges in the industrial and biomedical applications, necessitating the implementation of advanced coating engineering techniques. Plasma electrolytic oxidation (PEO) has emerged as a preferred coating technique because of its distinctive properties and successful surface modification results. However, there is a continuous need for further enhancements to optimize the performance and functionalities of protective surface treatments. The integration of layered double hydroxide (LDH) into PEO coatings on Mg alloys presents a promising approach to bolstering protective properties. This thorough review delves into the latest developments in integrating LDH into PEO coatings for corrosion-related purposes. It particularly emphasizes the significant improvements in corrosion resistance, antibacterial effectiveness, and photocatalytic performance resulting from the incorporation of LDH into PEO coatings. The two key mechanisms that enhance the corrosion resistance of PEO coatings containing LDH are the anion exchangeability of the LDH structure and the pore-sealing effect. Moreover, the antibacterial activity of PEO coatings with LDH stemmed from the release of antibacterial agents stored within the LDH structure, alterations in pH levels, and the photothermal conversion property. Furthermore, by incorporating LDH into PEO coatings, new opportunities emerge for tackling environmental issues through boosted photocatalytic properties, especially in the realm of pollutant degradation. [Display omitted] [ABSTRACT FROM AUTHOR]

Ti and its alloys have been vastly employed in the manufacturing of biomedical implants for orthopedy and dentistry, especially the Ti-6Al-4V alloy (wt%), which is the most-used Ti alloy worldwide. However, the ion release of Al and V in the long term has been related to harmful effects on the human body. In this scenario, surface modification strategies, such as plasma electrolytic oxidation (PEO), have often been performed in Ti alloys to match the clinical needs. This study evaluated the effect of electrical AC parameters on the surface of the commercial Ti-6Al-4V alloy immersed in ZrO2-rich electrolytic solution regarding the chemical, physical, structural, and topographical aspects. Then, the selected PEO-treated samples surpassed the electrochemical test in saline solution. The results indicated that the electrical AC parameters affect the duration and intensity of the oxidative reactions and plasma micro-discharge steps, resulting in porous and thick oxide layers. PEO treatment promoted bio-camouflage of the surface, enriching it with TiO2, ZrO2, and ZrTiO4 compounds and depleting it of Al and V. After screening the PEO-treated samples and their corrosion behavior, the results indicated that the porous ZrO2–TiO2 ceramic coatings in the Ti-6Al-4V alloy can be a viable alternative for the manufacturing of biomedical implants. [ABSTRACT FROM AUTHOR]

Studies on dissimilar materials joining have greatly increased, transitioning from temporary to permanent joining methods. The latter approach is more applicable due to the hybrid structure offering the best properties of the constituent materials, along with the development of new materials and manufacturing procedures. In this study, the AA2024-T3 alloy was treated with plasma electrolytic oxidation (PEO) and a thermoplastic composite/AA2024-T3 hybrid joint was manufactured using oxy-fuel welding (OFW). Morphological aspects, chemical compositions electrochemical and mechanical properties of hybrid composite joints were determined. The results indicated that the joint exhibits a uniform structure. The adhesion between the dissimilar materials reached a strength of 4.2 to 5.2 MPa, with cohesive bonding and without severe degradation of the thermoplastic matrix in some cases. It was observed that PEO treatment decreased the interface shear strength due to the high silicon content presence in the coating. The coatings effectively increased nobility and corrosion resistance, with corrosion rates ranging from 0.0087 to 0.018 mm/year.

In this study, the AA1100 aluminum alloy underwent the plasma electrolytic oxidation (PEO) process to enhance its adhesion to a thermoplastic composite of polyetherimide (PEI) reinforced with glass fiber, following ASTM D1002:10 standards. A 23 factorial design was employed, varying three parameters in the oxidation process: immersion time, applied electric potential, and electrolyte concentration (Na2B4O7). The joining of aluminum and thermoplastic composite samples was achieved through oxy-fuel welding (OFW), using oxygen and acetylene gases. For the characterization of the joined samples, a universal tensile testing machine was utilized with a displacement speed of 1.5 mm/min. The analysis of the oxide coating involved scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and Fourier transform infrared spectroscopy (FT-IR). Through variance analysis, it was determined that the statistical model encompasses approximately 80% of the variability in the adhesion process between materials. An improvement of up to 104% in adhesion between the materials was observed with the process, indicating an effective bond due to the presence of the thermoplastic matrix in the treated aluminum sample. This improvement is attributed to the morphology of the oxide coating, resembling corals, with micro-pores and recesses that facilitated mechanical anchoring.

Poly(methyl methacrylate)/polyethylene oxide (PMMA/PEO)/Ni1-xZnxFe2-2xMn2xO4 blends of various composition were formed using coprecipitation and casting techniques. X-ray diffraction (XRD) analysis was performed on the blends and fillers. High-resolution transmission electron microscopy technique revealed that the fillers had a crystallite size of 15–25 nm. The impact of Ni1-xZnxFe2-2xMn2xO4 loading on the light absorbance, transmission, reflectance, refractive index and extinction coefficient and the dielectric constant, energy loss functions, and optical conductivity of PMMA/PEO blend was examined. The absorbance of the PMMA/PEO blend increased irregularly as it was loaded with the nanocomposite samples, and it peaked at x = 0.25. The transmittance reduced to a minimum value (28–58%) as the blend was doped with x=0.25. The PMMA/PEO blended polymer's direct and indirect band gaps were 5.02 and 4.74 eV, respectively. As the blend was loaded with NiFe2O4 alone, they reached their minimum values (direct/indirect: 4.94/4.66 eV). Depending on the amounts of Zn and Mn ions in the NiFe2O4 doped PMMA/PEO blends, the various blends displayed a blue-violet color on their chromaticity diagram. The electrical dielectric constant, electric modulus, ac conductivity and energy density of the different blends depended on the amount of Zn and Mn ions added in the NiFe2O4 matrix. [ABSTRACT FROM AUTHOR]

In this study, the AA1100 aluminum alloy underwent the plasma electrolytic oxidation (PEO) process to enhance its adhesion to a thermoplastic composite of polyetherimide (PEI) reinforced with glass fiber, following ASTM D1002:10 standards. A 23 factorial design was employed, varying three parameters in the oxidation process: immersion time, applied electric potential, and electrolyte concentration (Na2B4O7). The joining of aluminum and thermoplastic composite samples was achieved through oxy-fuel welding (OFW), using oxygen and acetylene gases. For the characterization of the joined samples, a universal tensile testing machine was utilized with a displacement speed of 1.5 mm/min. The analysis of the oxide coating involved scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), and Fourier transform infrared spectroscopy (FT-IR). Through variance analysis, it was determined that the statistical model encompasses approximately 80% of the variability in the adhesion process between materials. An improvement of up to 104% in adhesion between the materials was observed with the process, indicating an effective bond due to the presence of the thermoplastic matrix in the treated aluminum sample. This improvement is attributed to the morphology of the oxide coating, resembling corals, with micro-pores and recesses that facilitated mechanical anchoring. [ABSTRACT FROM AUTHOR]

Utilizing low-molecular weight polyethylene oxide (L-PEO) for SPE using free-solvent casting technique presented a challenge in terms of electrochemical properties and formability issues. In this study, TEMPO-oxidized NC is utilized as a reinforcing agent to increase free volume and segmental motion of a solid-state L-PEO composite, which allows Li+ ion transport and prevents mechanical instability. During the breaking-forming process of Li–O bonds, ion transport occurs at a 40 EO/Li molar ratio, which is stabilized by NC structural network via intrachain or interchain hooping. The ion transport of the SPE-C electrolyte membrane fullfill Arrhenius behavior with increasing ionic conductivity. [ABSTRACT FROM AUTHOR]

All-solid-state battery (ASSB) technology is a new energy system that reduces the safety concerns and improves the battery performance of conventional lithium-ion batteries (LIB). The increasing demand for such new energy systems makes the transition from laboratory scale production of ASSB components to larger scale essential. Therefore, this study investigates the dry extrusion of poly(ethylene oxide):lithium bis (trifluoromethylsulfonyl)imide (PEO:LiTFSI) all-solid-state electrolytes at a ratio of 20:1 (EO:Li). We investigated the influence of different extruder setups on the product quality. For this purpose, different screw designs consisting of conveying, kneading and mixing elements are evaluated. To do so, a completely dry and solvent-free production of PEO:LiTFSI electrolytes using a co-rotating, intermeshing, twin-screw extruder under an inert condition was successfully carried out. The experiments showed that the screw design consisting of kneading elements gives the best results in terms of process stability and homogeneous mixing of the electrolyte components. Electrochemical impedance spectroscopy was used to determine the lithium-ion conductivity. All electrolytes produced had an ionic conductivity (σionic) of (1.1–1.8) × 10−4 S cm−1 at 80 °C. [ABSTRACT FROM AUTHOR]

This study evaluates the effectiveness of a silica preceramic polymer for joining and coating Plasma Electrolytic Oxidated (PEO) aluminum components at temperatures below 200 °C. PEO aluminum slabs were coated and joined with a silica precursor polymer (Durazane1800, Merck, Darmstadt, Germany), both with and without the addition of 48 wt% silica nanoparticles, and cured at 180 °C for 4 h in air. Thermogravimetric analysis assessed the curing process and thermal stability, while X-ray diffraction confirmed the polymer's conversion to amorphous silica after heating at 1200 °C. Resistance to humid environments was tested by soaking coated samples in tap water for a week, with no mass variation observed. Mechanical testing through tensile mode and tensile lap tests showed that adding 48 wt% silica nanoparticles significantly improved joint cohesion and nearly quadrupled mechanical strength. Fracture surfaces were examined using Field Emission Scanning Electron Microscopy, and composition analysis was performed with Energy Dispersion X-ray Spectroscopy. Crack detection was conducted using Computer Tomography with an in situ bending test setup to obtain the mechanical resistance of the PEO coating. The results indicate that the silica preceramic polymer is suitable for joining and coating PEO aluminum components, with silica nanoparticles enhancing mechanical strength and providing excellent thermal stability and resistance to humidity. [ABSTRACT FROM AUTHOR]

The present study investigates the influence of organic acids, added to the electrolytic solution, on the structure, morphology, and corrosion behaviour of plasma electrolytic oxidation (PEO) coatings produced on titanium grade 2. Particular attention is paid to the role of functional groups in the modification of the oxide's properties. For this reason, all three selected acids, namely glutaric, glutamic, and tartaric acid, display two carboxylic groups, thus they interact with the substrate material mainly through –COO− adsorption. However, glutamic acid also has an amine group, while tartaric acid has two hydroxyl groups. The presence of such additional functional groups is found to impact the formation of the PEO coatings. According to scanning electron microscopy (SEM) analyses, the number of defects and their dimension increase with an increasing number of active groups present in the organic molecules. Then, when glutaric acid with only two carboxyl groups, is employed as an additive, smaller pores are produced. The dimension of defects increases when glutamic and tartaric acid are used. X-ray diffraction (XRD) testing demonstrates that rutile and anatase are present in all the coatings and that when using tartaric acid, a relatively high level of amorphism is reached. The electrochemical and corrosion behaviours are evaluated by potentiodynamic polarization (PDP) and electrochemical impedance spectroscopy (EIS) performed in a heated sulphuric acid solution. It is found that all types of coatings provide protection against corrosion, with oxides produced using glutamic acid showing the lowest corrosion current density (0.58 mA·m−2) and low corrosion rate (1.02 μm·y−1). [ABSTRACT FROM AUTHOR]

In a solid-state dye-sensitized solar cell, a fast-ion conducting (σ25°C > 10−4 S cm−1) solid redox mediator (SRM; electrolyte) helps in fast dye regeneration and back-electron transfer inhibition. In this work, we synthesized solid Co2+/3+ redox mediators using a [(1 − x)succinonitrile: x poly(ethylene oxide)] matrix, LiX, Co(tris-2,2′-bipyridine)3(bis(trifluoromethyl) sulfonylimide)2, and Co(tris-2,2′-bipyridine)3(bis(trifluoromethyl) sulfonylimide)3 via the solution-cast method, and the results were compared with those of their acetonitrile-based liquid counterparts. The notation x is a weight fraction (=0, 0.5, and 1), and X represents an anion. The anion was either bis(trifluoromethyl) sulfonylimide [TFSI−; ionic size, 0.79 nm] or trifluoromethanesulfonate [Triflate−; ionic size, 0.44 nm]. The delocalized electrons and a low value of lattice energy for the anions made the lithium salts highly dissociable in the matrix. The electrolytes exhibited σ25°C ≈ 2.1 × 10−3 (1.5 × 10−3), 7.2 × 10−4 (3.1 × 10−4), and 9.7 × 10−7 (6.3 × 10−7) S cm−1 for x = 0, 0.5, and 1, respectively, with X = TFSI− (Triflate−) ions. The log σ–T−1 plot portrayed a linear curve for x = 0 and 1, and a downward curve for x = 0.5. The electrical transport study showed σ(TFSI−) > σ(Triflate−), with lower activation energy for TFSI− ions. The anionic effect increased from x = 0 to 1. This effect was explained using conventional techniques, such as Fourier transform infrared spectroscopy (FT-IR), X-ray diffractometry (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), UV–visible spectroscopy (UV-vis), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). [ABSTRACT FROM AUTHOR]

In this study, to reactivate the oxide film and to secure biocompatibility, plasma electrolytic oxidation (PEO) treatment and hydroxyapatite (HA) deposition via mechanical coating (MC) processes were investigated. This experimental approach involved subjecting the Ti–6Al–4V alloy specimens to PEO treatment, followed by MC with HA powder for different hours as HA has the potential to increase bioactivity and surface characteristics due to its chemical composition and structural properties similar to natural bone. Therefore, the study aimed to examine the effects of MC with HA powder for 0, 1, 3, 5, 7, and 9 h on PEO-coated Ti–6Al–4V alloy discs for analyzing the surface characterization, phase analysis, surface roughness, wettability, adhesion strength, hardness, corrosion behavior, and cell proliferation properties for dental implant use. The findings demonstrate that prolonged HA milling enhances the substrate's mechanical strength, corrosion resistance, and adhesion properties. The presence of prominent anatase and HA peaks, particularly in the 5 MC-PEO, 7MC-PEO, and 9 MC-PEO samples, validates the synergistic impact of the PEO oxide layer and HA milling, resulting in outstanding corrosion resistance and biocompatibility. Cell culture analysis reveals a positive correlation between increased milling time and enhanced cell proliferation, particularly towards small-sized HA particles. [Display omitted] [ABSTRACT FROM AUTHOR]

Studies on dissimilar materials joining have greatly increased, transitioning from temporary to permanent joining methods. The latter approach is more applicable due to the hybrid structure offering the best properties of the constituent materials, along with the development of new materials and manufacturing procedures. In this study, the AA2024-T3 alloy was treated with plasma electrolytic oxidation (PEO) and a thermoplastic composite/AA2024-T3 hybrid joint was manufactured using oxy-fuel welding (OFW). Morphological aspects, chemical compositions electrochemical and mechanical properties of hybrid composite joints were determined. The results indicated that the joint exhibits a uniform structure. The adhesion between the dissimilar materials reached a strength of 4.2 to 5.2 MPa, with cohesive bonding and without severe degradation of the thermoplastic matrix in some cases. It was observed that PEO treatment decreased the interface shear strength due to the high silicon content presence in the coating. The coatings effectively increased nobility and corrosion resistance, with corrosion rates ranging from 0.0087 to 0.018 mm/year. [ABSTRACT FROM AUTHOR]

The hybrid nanomaterials doped organic polymer can be considered as a promising nanosystems to apply in various optical and electronics fields. In present work, the nanocomposites films based on polyethylene oxide(PEO) filled by silicon nitride(Si3N4) and cerium oxide(CeO2) nanostrucures were synthesized to employ in numerous advanced electronics and optical approaches. The PEO/Si3N4/CeO2 nanocomposites have unusual characteristics compared of other nanocomposites included exceptional optical characteristics, inexpensive, superior chemical and physical properties. The optical and structural characteristics of PEO/Si3N4/CeO2 nanocomposites are investigated. Results indicated the absorbance of PEO was rise of 53% in the wavelength(λ)=320 nm (UV-spectrum) while its increased of 23% in the λ=520 nm (VIS-spectrum) and 22.3% in the λ=720 nm (NIR-spectrum) when the Si3N4/CeO2 NPs content reached of 7.6 wt.%. The transmittance decreased of 64% at λ=320 nm and its reduced of 19.9% at λ=720 nm, these results make the PEO/Si3N4/CeO2 nanocomposites are important and promising nanomaterials for optical and electronics fields. The energy gap was decreased from 4.2 eV to 2.3 eV with increasing Si3N4/CeO2 NPs content to 7.6 wt.%. The other optical factors of PEO enhanced among boosting Si3N4/CeO2 NPs content. Finally, the attained results demonstrated the PEO/Si3N4/CeO2 nanocomposites are promising nanostructures and important key for development of optical and nanoelectronics applications. [ABSTRACT FROM AUTHOR]

The corrosion problem of Mg alloy limits its application in many engineering fields. Plasma electrolytic oxidation (PEO) is an economical and eco-friendly technology that can create a dense oxide layer on Mg alloy, offering a solution to the corrosion issue. This research summarizes the use of PEO technology in developing corrosion-resistant coatings for Mg alloys and examines the growth mode and corrosion process of PEO coatings. It is concluded that current efforts to enhance the corrosion resistance of PEO coatings on Mg alloys can be categorized into two approaches: improving the internal structure of the coating and enhancing the phase composition. This includes optimizing coating thickness, roughness, and density; repairing micropores and cracks; and introducing corrosion-resistant compounds by doping. Micropores and cracks are identified as vulnerable points for corrosion, and sealing is an effective strategy to address this. By modifying the phase composition of the coating, corrosion occurrence can be minimized, significantly boosting the corrosion resistance of Mg alloys. Finally, future challenges and potential advancements in corrosion-resistant PEO coatings for Mg alloys are discussed. [ABSTRACT FROM AUTHOR]

The use of Mg‐based biomaterials with a number of their advantageous properties are overshadowed by uncontrollable metal corrosion. Moreover, the use of implants goes alongside with the threat of pathogens‐associated complications. In this study, PEO coated Mg biomaterial loaded with antibacterial Ag(I) and Cu(II) complexes is produced and tested to meet both appropriate protective characteristics as well as sufficient level of antibacterial activity. To achieve a suitable level of anticorrosion protection phosphate and fluoride‐phosphate electrolytes are used in the PEO process. Investigation of the surface thickness and morphology done by means of cross‐section analysis and scanning electron microscopy (SEM), as well as electrochemical impedance spectroscopy (EIS) assay show precedence of the fluoride containing PEO coating and make it the material of choice for further modification with Ag(I) and Cu(II) complexes. The presence of the complexes on the PEO surface is confirmed by energy dispersive X‐ray spectroscopy (EDX). X‐ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM) and glow discharge optical emission spectroscopy (GDOES) are used to estimate the complexes' chemical state and depth of penetration in the coating surface. Based on the results of antibacterial assay, the modified coatings are found to be active against both Gram‐positive and Gram‐negative bacteria. [ABSTRACT FROM AUTHOR]

This work introduces the synthesis of hybrid polymer electrolytes based on polyethylene oxide (PEO) and electrolyte solution bis(trifluoromethane)sulfonimide lithium salt/ionic liquid 1-ethyl-3-methyl-imidazolium bis(trifluoromethylsulfonyl)imide (LiTFSI/EMIMTFSI) with in situ produced and dispersed silica particles by the sol–gel method. Conventional preparation of solid polymer electrolytes was followed by desolvation of lithium salt in a polymer matrix of PEO, which, in some cases, additionally contains plasticizers. This one-pot synthesis is an alternative route for fabricating a solid polymer electrolyte for solid-state batteries. The presence of TFSI- reduces the crystallinity of the PEO matrix (plasticizing effect), increases the dissociation and solubility of LiTFSI in the PEO matrix because of a highly delocalized charge distribution, and reveals excellent thermal, chemical, and electrochemical stability. Tetraethylorthosilicate (TEOS) was chosen due to the slow reaction rate, with the addition of (3-glycidyoxypropyl)trimethoxysilane (GLYMO), which contributes to the formation of a silica network. FTIR studies confirmed the interactions between the silica, the polymer salt, and EMIMTFSI. Impedance spectroscopy measurements were performed in a wide range of temperatures from 25 to 70 °C. The electrochemical performance was explored by assembling electrolytes in LiCoO2 (LCO), NMC(811), and LiFePO4 (LFP) coin half-cells. The HPEf15 shows a discharge capacity of 143 mA/g for NMC(811) at 0.1 C, 134 mA/g for LCO, and 139 mA/g for LFP half-cells at 0.1 C and 55 °C. The LFP half-cell with a discharge capacity of 135 mA/g at 0.1 C (safety potential range of 2.8 to 3.8) obtained a cyclability of 97.5% at 55 °C after 100 cycles. Such a type of electrolyte with high safety and good electrochemical performance provides a potential approach for developing a safer lithium-ion battery. [ABSTRACT FROM AUTHOR]

Objective: Mitochondrial myopathy without extraocular muscles involvement (MiMy) represents a distinct form of mitochondrial disorder predominantly affecting proximal/distal or axial muscles, with its phenotypic, genotypic features, and long-term prognosis poorly understood. Methods: A cross-sectional study conducted at a national diagnostic center for mitochondrial disease involved 47 MiMy patients, from a cohort of 643 mitochondrial disease cases followed up at Qilu Hospital from January 1, 2000, to January 1, 2021. We compared the clinical, pathological, and genetic features of MiMy to progressive external ophthalmoplegia (PEO) and mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) patients. Results: MiMy patients demonstrated a more pronounced muscle involvement syndrome, with lower 6MWT scores, higher FSS, and lower BMI compared to PEO and MELAS patients. Serum levels of creatinine kinase (CK), lactate, and growth and differentiation factor 15 (GDF15) were substantially elevated in MiMy patients. Nearly a third (31.9%) displayed signs of subclinical peripheral neuropathy, mostly axonal neuropathy. Muscle biopsies revealed that cytochrome c oxidase strong (COX-s) ragged-red fibers (RRFs) were a typical pathological feature in MiMy patients. Genetic analysis predominantly revealed mtDNA point pathogenic variants (59.6%) and less frequently single (12.8%) or multiple (4.2%) mtDNA deletions. During the follow-up, a majority (76.1%) of MiMy patients experienced stabilization or improvement after therapeutic intervention. Conclusions: This study provides a comprehensive profile of MiMy through a large patient cohort, elucidating its unique clinical, genetic, and pathological features. These findings offer significant insights into the diagnostic and therapeutic management of MiMy, ultimately aiming to ameliorate patient outcomes and enhance the quality of life. [ABSTRACT FROM AUTHOR]

The non‐destructive ultrasonic technique is a great employ for knowing the solute–solvent interaction in the polymer blend. By the ultrasonic velocity and attenuation evaluation, the visco‐elastic behaviors of the polymer solution have been assessed and compared with the results of conventional dynamic mechanical analysis. In the present research work, a comprehensive ultrasonic investigation of molecular interaction in a polymeric mixture of Poly (ethylene oxide) PEO and dimethyformamide (DMF) at 333 K has been executed by using the information provided by the literature. For this purpose, ultrasonic waves of two different frequencies such as 2 and 5 MHz have been implemented. Several acoustical parameters such as adiabatic compressibility, acoustic impedance, relaxation time, and ultrasonic attenuation coefficient (훼/푓2) are explored. Thermodynamic parameters like relative association and intermolecular free path length are also estimated. The evaluated values have been associated with the previous experimental results. The non‐ideal approach of the solution is analyzed and discussed in detail. [ABSTRACT FROM AUTHOR]

The Nd:TiO2 PEO coatings were formed in a phosphate-based electrolyte with the addition of Nd2O3 under the current density of 150, 200, 250 and 300 mA/cm2. SEM results showed that the micropores decreased on quantity and increased on scale with the increasing current density. AFM results revealed that the roughness of the coatings increased with the increasing current density. Phase and composition analysis showed that the Nd:TiO2 coatings were mainly composed of anatase and rutile phase. And the anatase phase content has reached the maximum value at the current density of 250 mA/cm2. XPS results indicated that Ti2p spin-orbit components of the Nd:TiO2 coatings are shifted towards higher binding energy, compared with the pure TiO2 coating, suggesting that some of the Nd3+ ions are combined with TiO2 lattice and led to dislocation. Photocatalytic test showed that the photocatalytic activity of Nd:TiO2 coatings varied in the same pattern with the anatase content variation in Nd:TiO2 coatings. The photocatalytic experiment results show that the photocatalytic activity of Nd:TiO2 coatings can be greatly enhanced with moderate amount of Nd3+. However, excessive amount of Nd3+ does not have an effective impact on the photoctalytic activity improvement. [ABSTRACT FROM AUTHOR]

This work aims to fabricate of SiC (silicon carbide)/SrTiO3 (strontium titanate) nanomaterials doped PMMA (polymethyl methacrylate)/ PEO (polyethylene oxide) to utilize in many electronics and optics nanodevices. The structural and optical properties of (PMMA-PEO/SiC-SrTiO3) nanostructures were investigated. The SEM and OM confirmed that good distribution of SiC-SrTiO3 NPs inside the matrix of PMMA-PEO. The results of optical properties for (PMMA-PEO/SiC-SrTiO3) nanostructures showed that the absorbance (A) enhanced of 47.5% at UV-spectra (λ = 300 nm) and 54.9% at visible- spectra (λ = 500 nm) and 61.4% at NIR-λ=800nm when the ratio of SiC /SrTiO3 NPs reached of 6.4 wt.%. These results make them as potential nanostructures to apply in optical and renewable energy fields. The energy gap reduced for allowed transition from 3.6 eV to 2.2 eV and from 3.1 eV to 1.5 eV for forbidden transition. The optical parameters of (PMMA-PEO) blend improved with rising in the SiC-SrTiO3 NPs concentrations, this performance made the (PMMA-PEO/SiC-SrTiO3) are suitable for several optics and nanoelectronics fields. Finally, the results of structural and optical characteristics indicated to the (PMMA–PEO/SiC-SrTiO3) nanostructures may be applied in various nanoelectronics devices. [ABSTRACT FROM AUTHOR]

Plasma electrolytic oxidation (PEO) was carried out on SLM-produced AlSi10Mg alloy using various corrosion inhibitor additives. The study investigated the effects of these additives on microstructural evolution, phase composition, and corrosion behavior by comparing the functionalized coating to a standard base silicate PEO one. The results revealed that, in most cases, the additives significantly altered the coatings' thickness, density, and adherence, leading to improved corrosion resistance due to an enhanced barrier effect over electrolyte penetration. Long-term immersion electrochemical impedance spectroscopy (EIS) tests proved the additives’ corrosion inhibitor capability, as they all were able to enhance coating stability.

[Display omitted] • Cationic surfactant CTAB was used to improve the dispersion of LLZTO with PEO. • CTAB modified electrolyte have better organic–inorganic interface contact. • CTAB modified electrolyte show higher interfacial stability and ionic conductivity. • CTAB modified electrolyte exhibit better rate capability and cycling stability. The garnet-type solid electrolyte Li 6.4 La 3 Zr 1.4 Ta 0.6 O 12 (LLZTO) was modified with a cationic surfactant Cetyltrimethylammonium Bromide (CTAB) to improve the dispersion of LLZTO inorganic particles in Poly (ethylene oxide) (PEO) electrolyte (PEO-LLZTO@CTAB) by a liquid phase casting method. During fabrication, the cationic modifier CTAB is uniformly adsorbed on the surface of LLZTO particles, which can effectively reduce their surface energy and lead to a thin CTAB surface coating layer. This fabricated PEO-LLZTO@CTAB can avoid the aggregation of LLZTO particles in the composite solid-state electrolyte (CSSE) and improve the interfacial contact at the PEO/LLZTO interface, thus reducing the overall resistance of PEO-LLZTO@CTAB/Li half-cell and inhibiting the dendrite growth during cycling. The all-solid-state batteries (ASSBs) with LiFePO 4 (LFP) as the cathode, PEO-LLZTO@CTAB as the electrolyte and Li as the anode exhibit a high initial discharge capacity of 146.6 mAh-g−1, excellent rate performance and high-capacity retention of 91.0 % after 300 cycles at 0.2 C multiplier and 60 °C within the voltage range of 2.7–4.0 V. [ABSTRACT FROM AUTHOR]