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Lithium-ion batteries are superior energy storage devices that are widely utilized in various fields, from electric cars to small portable electric devices. However, their susceptibility to thermal runaway necessitates improvements in battery case materials to improve their safety. This study used electrochemical analyses, including open-circuit potential (OCP), potentiodynamic polarization, and critical pitting temperature (CPT) analyses, to investigate the corrosion resistance of super duplex stainless steel (SAF 2507) applied to battery cases in relation to post-weld heat treatment (PWHT) time. The microstructure during the manufacture, laser welding, and PWHT was analyzed using field-emission scanning electron microscopy, X-ray diffraction, and electron backscatter diffraction, and the chemical composition was analyzed using dispersive X-ray spectroscopy and electron probe micro-analysis. The PWHT increased the volume fraction of austenite from 5% to 50% over 3 min at 1200 °C; this increased the OCP from −0.21 V to +0.03 V, and increased the CPT from 56 °C to 73 °C. The PWHT effectively improved the corrosion resistance, laying the groundwork for utilizing SAF 2507 in battery case materials. But the alloy segregation and heterogeneous grain morphology after PWHT needs improvement. [ABSTRACT FROM AUTHOR]

High-entropy alloys (HEAs), a relatively new class of materials, have attracted significant attention in materials science owing to their unique properties and potential applications. High entropy stabilizes the phase of a solid solution over a wide range of chemical compositions, yielding unique properties superior to those of conventional alloys. Therefore, this study analyzed the microstructure and electrochemical behavior of HEAs (Cantor) to evaluate their corrosion resistance, according to their manufacturing process (casting, cold rolling, and annealing). The microstructural morphologies and sizes were analyzed using electron backscatter diffraction. The electrochemical behavior was examined using open circuit potential measurements, electrochemical impedance spectroscopy, potentiodynamic polarization tests, and critical pitting temperature measurements using a potentiostat. The casting process formed a nonuniform microstructure (average grain size = 19 μm). The cold rolling process caused the formation of fine grains (size = 4 μm). A uniform microstructure (grain size > 151 μm) was formed after heat treatment. The corrosion resistance of the HEAs was determined from the passivation layer formed by Cr oxidation. These microstructural differences resulted in variations in the electrochemical behavior. Microstructural and electrochemical analyses are crucial because HEAs have diverse potential applications. Therefore, this study contributes to future improvements in HEA manufacturing processes. [ABSTRACT FROM AUTHOR]

Li-ion batteries used in portable electronic devices and electric vehicles require high safety standards, necessitating the use of high-performance structural materials for battery casings. Super duplex stainless steel (SDSS) is a structural material suitable for portable electronic products owing to its excellent strength and corrosion resistance. SDSS AISI2507 was used to construct a Li-ion battery casing, a Ag coating was applied via physical vapor deposition (PVD) after the heat treatment of AISI2507 with or without a secondary phase, and the coating thickness was controlled by varying the PVD time. The thickness of the Ag coating layer increased proportionally with time, thereby enhancing the electrical conductivity. The structure and coating behavior were confirmed using FE-SEM, XRD, and GDS. The secondary phase was crystallized by the segregation of the alloy and formed a BCC structure. The FCC lattice structure exhibited excellent coating behavior on the austenite (FCC structure) of AISI2507. Conversely, the secondary phase exhibited low adhesion owing to differences in composition and crystal structure. However, the Ag coating layer on AISI2507 exhibited excellent electrical conductivity, outperforming conventional Ni-plated Li-ion battery casings comprising AISI304. However, the precipitation of the secondary phase must be controlled, as the formation of the secondary phase acts as a factor that decreases electrical conductivity from 58.8 to 53.6 (ICAS) %. The excellent performance of Ag-coated AISI2507 makes it suitable for the fabrication of enhanced Li-ion battery casings. [ABSTRACT FROM AUTHOR]

Super duplex stainless steel (SDSS) is a suitable structural material for various engineering applications due to its outstanding strength and corrosion resistance. In particular, its high-temperature strength can enhance the safety of electronic products and cars. SDSS AISI2507, known for its excellent strength and high corrosion resistance, was analyzed for its microstructure and electrochemical behavior at the ignition temperature of Li-ion batteries, 700 °C. At 700 °C, AISI2507 exhibited secondary phase precipitation values of 1% and 8% after 5 and 10 h, respectively. Secondary phase precipitation was initiated by the expansion of austenite, forming sigma, chi, and CrN phases. The electrochemical behavior varied with the fraction of secondary phases. Secondary phase precipitation reduced the potential (From −0.25 V to −0.31 V) and increased the current density (From 8 × 10−6 A/cm2 to 3 × 10−6 A/cm2) owing to galvanic corrosion by sigma and chi. As the fraction of secondary phases increased (From 0.0% to 8.1%), the open circuit potential decreased (From −0.25 V to −0.32 V). Secondary phase precipitation is a crucial factor in reducing the corrosion resistance of SDSS AISI2507 and occurs after 1 h of exposure at 700 °C. [ABSTRACT FROM AUTHOR]

The demand for Li-ion batteries has increased because of their extensive use in vehicles and portable electronic devices. This increasing demand implies greater interaction between batteries and humans, making safety a paramount concern. Although traditional batteries are fabricated using Al, recent efforts to enhance safety have led to the adoption of AISI304. The strength and corrosion resistance of AISI304 are greater than those of Al; however, issues such as stress-induced phase transformation and low high-temperature strength have been observed during processing. Duplex stainless steel SAF2507, which is characterized by a dual-phase structure consisting of austenite and ferrite, exhibits excellent strength and corrosion resistance. Although SAF2507 demonstrated outstanding high-temperature strength up to 700 °C, it precipitated a secondary phase. The precipitation of this secondary phase, believed to be caused by the precipitation of the carbides of Cr and Mo, has been extensively studied. Research on the precipitation of the secondary phase near 1000 °C has been conducted owing to the annealing temperature (1100 °C) of the SAF2507 solution. The secondary phase precipitates at approximately 1000 °C because of slow cooling rates. However, few studies have been conducted on the precipitation of the secondary phase at approximately 700 °C. This study analyzed the precipitation behavior of the secondary phase at 700 °C when SAF2507 was applied and assessed its safety during heat generation in Li-ion batteries. The precipitation behavior was analyzed using field emission scanning electron microscopy for morphology, energy-dispersive X-ray spectroscopy for composition, and X-ray diffraction for phase identification. [ABSTRACT FROM AUTHOR]

The development of Li-ion battery cases requires superior electrical conductivity, strength, and corrosion resistance for both cathode and anode to enhance safety and performance. Among the various battery case materials, super duplex stainless steel (SDSS), which is composed of austenite and ferrite as two-phase stainless steel, exhibits outstanding strength and corrosion resistance. However, stainless steel, which is an iron-based material, tends to have lower electrical conductivity. Nevertheless, nickel-plating SDSS can achieve excellent electrical conductivity, making it suitable for Li-ion battery cases. Therefore, this study analysed the plating behaviour of SDSS plates after nickel plating to leverage their exceptional strength and corrosion resistance. Electroless Ni plating was performed to analyse the plating behaviour, and the plating behaviour was studied with reference to different plating durations. Heat treatment was conducted at 1000 °C for one hour, followed by cooling at 50 °C/s. Post-heat treatment, the analysis of phases was executed using FE-SEM, EDS, and EPMA. Electroless Ni plating was performed at 60–300 s. The plating duration after the heat treatment was up to 300 s, and the behaviour of the materials was observed using FE-SEM. The phase analysis concerning different plating durations was conducted using XRD. Post-heat treatment, the precipitated secondary phases in SAF2507 were identified as Sigma, Chi, and CrN, approximating a 13% distribution. During the electroless Ni plating, the secondary phase exhibited a plating rate equivalent to that of ferrite, entirely plating at around 180 s. Further increments in plating time displayed growth of the plating layer from the austenite direction towards the ferrite, accompanied by a reduced influence from the substrate. Despite the differences in composition, both the secondary phase and austenite demonstrated comparable plating rates, showing that electroless Ni plating on SDSS was primarily influenced by the substrate, a finding which was primarily confirmed through phase analysis. [ABSTRACT FROM AUTHOR]

Electroanalytical and optical techniques are widely used in the development of nanomaterials-based sensor platforms. These techniques have a quick response, high sensitivity, and selectivity. Electroanalytical and optical techniques are widely used in the development of nanomaterial-based sensor platforms. These sensors must be able to detect biomarkers, pathogens, toxins, and pharmaceuticals in biological matrices associated with cardiovascular disease, cancer, and neurodegenerative diseases. Considering these pathophysiologies, numerous investigations have been undertaken to develop sensors for early diagnosis and treatment, utilizing nanomaterials such as quantum dots. Graphene quantum dots (GQDs), which are ideally nanometer-sized graphene fragments, have recently received increased attention due to their excellent physicochemical properties such as fast electron mobility, photostability, water solubility, biocompatibility, high specific surface area, and nontoxicity. Apart from the properties mentioned above, GQDs provide π–π interactions, electrostatic, and covalent interactions with an analyte, and ease of synthesis as well as the ability to combine with other nanomaterials, which have enabled their use in various sensing platforms. This review summarizes recent advances in GQDs-based nanocomposites for sensor applications, with a focus on electroanalytical and optical techniques, as well as current challenges and future prospects. [ABSTRACT FROM AUTHOR]

The O and N gas ions (O3+, O+, N2+, and N4+) were implanted on the glassy carbon surface employing the electron cyclotron resonance ion source, which were characterized using electrochemical and surface analysis methods. The modified electrode was examined for the catalytic oxidation of bioorganic molecules including dopamine, where the O+ ion implanted GC revealed the best catalytic performance. The XPS and Raman results represented that the ion implantation made enrichment in graphite nanocrystalline structure with edge plane, showing the enhanced electrochemical activity. It showed excellent performance for dopamine detection without significant interferences between 50.0 nM and 400.0 μM with the detection limit of 10.0±2.5 nM (95 % confidence level). The reliability of proposed electrode was evaluated by the real urine sample analysis. [ABSTRACT FROM AUTHOR]

We report an optimized multi-step chemical vapor deposition process for growing MoS2 thin films. This process enables large-area processing, film patterning simply by using shadow masks, and precise control of the final thickness by changing the initial thickness of the first step of MoO3 film deposition. The structural characterization of the MoS2 films is performed with transmission electron microscopy and X-ray diffraction as a function of film thickness. MoS2 film with a thickness of 3 nm possesses a highly crystalline structure with a spacing of 0.62 nm. The crystallinity and orientation of the films are degraded with increased film thickness. Careful analysis by time-of-flight secondary ion mass spectroscopy reveals that a film with a thickness of 9 nm is not completely sulfurized, and unreacted MoO3 is left at the bottom of the film. These fundamental analyses coincide with the thickness dependence of thin-film transistor (TFT) performance. A TFT with the optimal film thickness of 3 nm achieves high performance, namely a carrier mobility of 0.57 cm2 V−1 s−1 and an on/off ratio of ~ 102. [ABSTRACT FROM AUTHOR]