Long-term Stability Research Articles

Ag Nanoparticles Modified Sea Urchin-like W18O49 Microstructures for Sensitive Surface Enhanced Raman Spectroscopy Detection

Surface-enhanced Raman scattering (SERS) has gained significant attention in various fields, including biomedical diagnostics, environmental monitoring, and food safety. This technique offers many advantages such as label-free detection and the ability to detect analytes at low concentrations. In this study, we present a variety of tungsten oxide (W18O49) microstructures as solid SERS substrates using various solvents realized by a simple hydrothermal approach. Among them, the well-defined sea urchin-like W18O49 microstructures support greater light scattering and confinement to enhance the SERS signal when compared to other W18O49 structures. The surface of well-defined sea urchin-like W18O49 microstructures was then modified with uniformly distributed silver nanoparticles (Ag NPs). The combination of the unique morphology of the Ag and sea urchin-like W18O49 microstructures (W18O49@Ag) led to improved detection capabilities for analytes such as rhodamine 6G (R6G) and thiram molecules. The SERS enhancement factor (EF) of sea urchin-like W18O49@Ag microstructures was estimated to be as high as 1.53×106 with the lowest detectable concentrations of 1nM and 1μM for R6G and thiram, respectively. Thus, the well-defined sea urchin-like W18O49@Ag microstructures are excellent choice to replace the pure noble metal SERS substrates in the fields of rapid detection and trace analysis due to their high sensitivity, repeatability, and long-term stability.

Advancements in printed components for proton exchange membrane fuel cells: A comprehensive review

Proton Exchange Membranes (PEM) are a promising technology for fuel cells and electrolyzer cells, in line with societal goals for clean and sustainable fuel conversion and generation, respectively, in a vast field of applications. PEM fuel cell (PEMFC) technology has an important advantage for energy conversion applications, because it requires a lower operating temperature and is lighter and more compact than other technologies, which makes it ideal for portable and transportation applications. However, open issues remain to be addressed for PEMFC that hinder their widespread adoption, both on the technical side, such as too high operational temperature range, cell efficiency, and long-term stability, as well as on the industrial side with implementation issues, material and device component availability, and cost. PEM technology research usually focuses on the synthesis of novel materials such as non-noble metal catalysts and non-halogenated membranes. In parallel, developing high-throughput and cost-effective manufacturing methods for components, in particular Membrane Electrode Assembly (MEA), can also lift an important barrier to their mass production, thus contributing to the same goals and securing industrial provision. From this perspective, printing technologies such as spray coating, inkjet printing, and screen printing have emerged as promising approaches with the required precision and scalability. This review covers recent advancements and developments in advanced PEMFC technology manufacturing, with a focus on 2D printing methodologies to fabricate some or all of the MEA components. Leveraging these techniques as simplified large-area manufacturing methods for PEM technology can become a more viable and industrially attractive solution. This work presents a comparison study addressing the key progress indicators both in process and in characterization to build a working framework in which both scientists, engineers and manufacturers can collaborate toward the industrial implementation of this emergent field.

A facile and scalable fabrication procedure for PVDF-PDA/PEI/SiO2 hollow fiber composite ultrafiltration membranes: Integration of co-deposition and cross-linking

Polyvinylidene fluoride (PVDF) membranes, widely used for their stability, face limitations due to the hardly adjustable pore size in nanoscale and inherent hydrophobicity. To address this, we proposed a co-deposition method incorporating dopamine (DA), polyethyleneimine (PEI), and silicon dioxide (SiO2) nanoparticles with glutaraldehyde cross-linking for precise regulation of pore size and hydrophilicity in PVDF hollow fiber membranes. Notably, the pore diameter reduced from 119.0 ± 3.55 nm to 18.4 ± 0.36 nm, while the contact angle decreased from 107.7° to 40.9°. This simultaneous regulation led to a high-performance PDA/PEI/SiO2-PVDF hydrophilic ultrafiltration membrane with a rejection rate exceeding 99% for 20 nm nanoparticles in a long-term simulated separation experiment while achieving a significant protein permeability of 97% in BSA permeation experiments. Additionally, the membrane demonstrated exceptional long-term stability, offering a novel approach for tuning the performance of ultrafiltration/microfiltration membranes.

Synthesis of metal–organic framework ZIF-9-Mel and its application as an electrochemical modifier in Pb2+ detection

In this study, a selective electrochemical sensor was introduced for determination of lead ions based on a metal–organic framework (MOF)-melamine together with carbon black (CB) on the glassy carbon electrode (GCE). Herein, the zeolitic imidazolate framework-9-Mel (ZIF-9-Mel), which is a type of MOF, was synthesized and used as an electrode modifier. The interaction between Pb2+ and amine groups is conditioned by dative attachment, which causes the complexation of Pb2+-N through soft–soft interactions. To enhance the performance of the modified electrode, several parameters such as the pH of the buffer solution, the deposition potential, and the deposition time that affect response were optimized. Under optimized conditions (pH = 3, deposition time = 270 s, deposition potential = −0.7 V) the ZIF-9-Mel/CB/GCE sensor shows two linear ranges (0.5 nM–50 nM and 50 nM–1000 nM), low detection limit (0.16 nM), long-term stability, good repeatability and desirable reproducibility by differential pulse voltammetry (DPV) technique. To display the sensor ability for actual application, ZIF-9-Mel/CB/GCE was used for Pb2+ detection in lettuce and tomato samples with excellent results. According to the introduced method, MOFs are satisfactory materials for fabricating effective electrochemical sensors to detect Pb2+ ions simply and cost-effectively.

Reconstruction of Fe sacrifice protective layer enables highly effective CoP catalyst for hydrogen evolution reaction at high current density

Under the background of “Green hydrogen,” the method of hydrogen production through coupling water electrolysis with renewable energy has raised heightened demands for fundamental hydrogen evolution catalysts. Recently, CoP-based catalysts have attracted much attention due to their excellent HER activity. However, the self-reconfiguration behavior of CoP in actual operation seriously affects its long-term hydrogen evolution stability. Herein, an in-situ reconstructed Fe sacrificial protective layer is proposed to inhibit the complete conversion of CoP in alkaline HER process and improve the stability of CoP-based catalysts. Through this sacrificial strategy, nearly 80 % of CoP is retained, forming a new Co(OH)2/COP as the active interface of HER. As result, the catalyst can maintain hydrogen evolution at high current density for more than 10 days, and show excellent dynamic response in start-stop experiment. In an Anionic Exchange Membrane electrode cell, a fully hydrolyzed water AEM cell needs only 1.9 V to drive 1 A cm−2 current density.

Encapsulation and characterization of ω-3 medium- and long-chain triacylglycerols microencapsulated with different proteins as wall materials

In this study, ω-3 medium- and long-chain triacylglycerols (MLCTs) microcapsules with excellent performance were obtained using soy protein as the wall component to address the oxidation-related problems of MLCTs. Additionally, the effect of soy, whey, or pea proteins on microcapsules in terms of the changes in their structure and physicochemical properties was investigated. The results showed that the small particle size, low PDI (polydispersity index) and zeta potential, fast adsorption rate, and low interfacial tension of these protein-based samples fabricated through the O/W template method were conducive to maintaining the integrity of microcapsules during spray-drying. The microcapsules, characterized by a spherical shape, exhibited superior encapsulation efficiency of 94.56%, surpassing the findings of previous investigations. Overall, these microcapsules exhibited long-term storage stability and low controllable release rates, which could be utilized as carriers for liposoluble actives.

Immobilization of Xylanase on ZnO nanoparticles obtained by green synthesis from Eupatorium cannabinum L. and its application in enrichment of fruit juices

Juice production is one of the main components of the nutritional food industry. Therefore, improving fruit juice quality and preventing the formation of negative by-products is important for human health. The role of environmentally friendly, safe and economically more affordable green nanocarriers in improving the quality of fruit juice is increasing day by day. For this purpose, zinc oxide nanoparticles (ZnONPs) were prepared from the aqueous extract of the Eupatorium cannabinum L. using the green synthesis method. After immobilization, structural and morphological characterizations of the prepared ZnONPs and xylanase (Xyl)@ZnONPs were carried out, which confirmed that both the synthesis of ZnONPs and the immobilization of Xyl enzyme on ZnONPs were successfully carried out. The biochemical parameters of Xyl@ZnONPs such as optimum pH and temperature, kinetic parameters, thermal stability, reusability, and storage stability were investigated and compared with free Xyl. After immobilization, the optimum pH of free Xyl shifted from 5.0 to an alkaline pH of 8.0, while no change in the optimum temperature (70 °C) was observed for both enzymes. While the activation energy of free Xyl was 5.56 kJ/mol, it was found to be 7.27 kJ/mol for Xyl@ZnONPs. Xyl@ZnONPs outperformed free Xyl due to its long-term storage stability and reusability. Moreover, Xyl@ZnONPs retained 50 % of its activity after 5 reuses and 87 % of its activity after 4 weeks of storage at room temperature. In addition, a decrease in Km value and an increase in Vmax value were observed after immobilization, which means the increased catalytic activity of the Xyl@ZnONPs. As a result of re-using Xyl@ZnONPs in orange juice for 6 cycles, clarification yield of 66.43 % was obtained under optimized conditions. Overall, this study prepared a suitable, environmentally friendly, and robust carrier support for Xyl immobilization and developed a biocatalyst that will provide high performance in the industrial field.

Role of aloe vera based nanofluids for cool thermal energy storage system: A comparative study

The present experimental investigation incorporates the preparation of aloe vera gel-based phase change nanofluid (NFPCM) for a cool thermal energy storage (CTES) system. Two sets of NFPCMs were produced by adding graphene nanoplatelets (GNP) in deionized water and aloe vera gel (0.20 wt%, 0.40 wt%, and 0.60 wt%). The zeta potential analysis shows that the NFPCM with aloe vera gel is more stable even after 60 days from the preparation (−44 mV). The thermal conductivity of NFPCMs was analyzed through the transient hot wire method and the enhancement of 42 %, and 37.5 % were measured in the ice phase for NFPCMs with aloe vera gel and DI water (0.60 wt%) respectively at the heat transfer fluid temperature of −15 °C. The NFPCMs with aloe vera gel show that the addition of GNP prepended the peak melting temperature from −16 °C to −10.5 °C, which is due to the quick formation of nuclei as compared to NFPCMs with DI water. Additionally, a slight reduction in the latent heat of only 7 % was observed. The charging characteristics of NFPCMs were studied in a single spherical capsule at −8 °C. The maximum reduction in total charging time of 25 % was recorded for the aloe vera gel-based NFPCM with a maximum concentration of GNP (0.60 wt%). The green synthesis of aloe vera gel-based NFPCM exhibited noteworthy enhancements in thermophysical properties. Additionally, it was observed that the long-term stability of the NFPCM was achieved by excluding surfactants during the preparation process. The incorporation of graphene nanoplatelets (GNP) into aloe vera gel as the foundational phase change material (PCM) facilitates the partial charging of the CTES system with a reduced energy input.

Hierarchical Carbon Chain Network ‘Armor’ Escorts Long-term Cycling Stability for Vanadium Redox Flow Batteries

Nowadays, the bottleneck constraining the development of electrode materials for all-vanadium flow batteries lies in their poor performances at high current densities. Pertinently, we propose a high-stability hierarchical N and S co-doped carbon chain network ‘armor’ strategy to achieve long-term stability enhancement for electrodes. It is found that hierarchical carbon chain network can effectively enhance the voltage efficiency, energy efficiency, and long-term cycling stability for all-vanadium flow batteries. The modified electrode presents superior long-term stability over 1900 cycles, and the energy efficiency is maintained at about 80% at 180 mA cm-2. In addition, the energy efficiency can also reach over 70% at 320 mA cm-2, while at 280 mA cm-2 the modified electrode can circulate stably for over 800 turns. It is proved that the bridging effect of polydopamine facilitates the stable carbon chain network, and effectively regulates the N and S co-doping, further constructing the N and S co-doping sites to assemble electrochemical catalytic network. More importantly, the carbon chain network ‘armor’ design can effectively prevent electrode breakage. This work provides a reference way for the design of long-term stable electrodes, which is of great significance for advancing commercial applications of all-vanadium flow batteries.

Self-assembled ordered AuNRs-modified electrodes for simultaneous determination of dopamine and topotecan with improved data reproducibility.

Gold nanomaterials have been widely explored in electrochemical sensors due to their high catalytic property and good stability in multi-medium. In this paper, the reproducibility of the signal among batches of gold nanorods (AuNRs)-modified electrodes was investigated to improve the data stabilization and repeatability. Ordered and random self-assembled AuNRs-modified electrodes were used as electrochemical sensors for the simultaneous determination of dopamine (DA) and topotecan (TPC), with the aim of obtaining an improved signal stability in batches of electrodes and realizing the simultaneous determination of both substances. The morphology and structure of the assemblies were analyzed and characterized by UV-Vis spectra, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray powder diffraction (XRD). Electrochemical studies showed that the ordered AuNRs/ITO electrodes have excellent signal reproducibility among several individuals due to the homogeneous mass transfer in the ordered arrangement of the AuNRs. Under the optimized conditions, the simultaneous detection results of DA and TPC showed good linearity in the ranges 1.75-45 μM and 1.5-40 μM, and the detection limits of DA and TPC were 0.06 μM and 0.17 μM, respectively. The results showed that the prepared ordered AuNR/ITO electrode had high sensitivity, long-term stability, and reproducibility for the simultaneous determination of DA and TPC, and it was expected to be applicable for real sample testing.

Constructing Two-Dimensional Heterostructure Channels with Engineered Biomembrane and Graphene for Precise Scandium Sieving.

The special properties of rare earth elements have effectively broadened their application fields. How to accurately recognize and efficiently separate target rare earth ions with similar radii and chemical properties remains a formidable challenge. Here, we constructed precise two-dimensional (2D) heterogeneous channels using engineered E. coli membranes between graphene oxidse (GO) layers. The difference in binding ability and corresponding conformational change between Lanmodulin (LanM) and rare earth ions in the heterogeneous channel allow for precisely recognizing and sieving of scandium ions (Sc3+). The engineered E. coli membranes not only can protect the integrity of structure and functionality of LanM, the rich lipids and sugars but also help the E. coli membranes closely tile on the GO nanosheets through interaction, preventing swelling and controlling interlayer spacing accurately down to the sub-nanometer. Apparently, the 2D heterogeneous channels showcase excellent selectivity for trivalent ions (SFFe 3+ /Sc 3+≈3), especially for Sc3+ ions in rare earth elements with a high selectivity (SFCe/Sc≈167, SFLa/Sc≈103). The long-term stability and tensile strain tests verify the membrane's outstanding stability. Thus, this simple, efficient, and cost-effective work provides a suggestion for constructing two-dimensional interlayer heterogeneous channels for precise sieving, and the valuable strategy is proposed for the efficient extraction of Sc. This article is protected by copyright. All rights reserved.

Variant-Localized High-Concentration Electrolyte without Phase Separation for Low-Temperature Batteries.

Dual-ion batteries (DIBs) present great application potential in low-temperature energy storage scenarios due to their unique dual-ion working mechanism. However, at low temperatures, the insufficient electrochemical oxidation stability of electrolytes and depressed interfacial compatibility impair the DIB performance. Here, we design a variant-localized high-concentration solvation structure for universal low-temperature electrolytes (ν-LHCE) without the phase separation via introducing an extremely weak-solvating solvent with low energy levels. The unique solvation structure gives the ν-LHCE enhanced electrochemical oxidation stability. Meanwhile, the extremely weak-solvating solvent can competitively participate in the Li+-solvated coordination, which improves the Li+ transfer kinetics and boosts the formation of robust interphases.Thus, the ν-LHCE electrolyte not only has a good high-voltage stability of >5.5 V and proper Li+ transference number of 0.51 but also shows high ionic conductivities of 1 mS/cm at low temperatures. Consequently, the ν-LHCE electrolyte enables different types of batteries to achieve excellent long-term cycling stability and good rate capability at both room and low temperatures. Especially, the capacity retentions of the DIB are 77.7% and 51.6 %, at -40 oC and -60 oC, respectively, indicating great potential for low- andtemperature energy storage applications, such as polar exploration,emergency communication equipment, and energy storage station in cold regions.

Preparation and Characterization of Nanofiber Coatings on Bone Implants for Localized Antimicrobial Activity Based on Sustained Ion Release and Shape-Preserving Design

Titanium (Ti), as a hard tissue implant, is facing a big challenge for rapid and stable osseointegration owing to its intrinsic bio-inertness. Meanwile, surface-related infection is also a serious threat. In this study, large-scale quasi-vertically aligned sodium titanate nanowire (SNW) arrayed coatings incorporated with bioactive Cu2+ ions were fabricated through a compound process involving acid etching, hydrothermal treatment (HT), and ion exchange (IE). A novel coating based on sustained ion release and a shape-preserving design is successfully obtained. Cu2+ substituted Na+ in sodium titanate lattice to generate Cu-doped SNW (CNW), which maintains the micro-structure and phase components of the original SNW, and can be efficiently released from the structure by immersing them in physiological saline (PS) solutions, ensuring superior long-term structural stability. The synergistic effects of the acid etching, bidirectional cogrowth, and solution-strengthening mechanisms endow the coating with higher bonding strengths. In vitro antibacterial tests demonstrated that the CNW coatings exhibited effective good antibacterial properties against both Gram-positive and Gram-negative bacteria based on the continuous slow release of copper ions. This is an exciting attempt to achieve topographic, hydrophilic, and antibacterial activation of metal implants, demonstrating a paradigm for the activation of coatings without dissolution and providing new insights into insoluble ceramic-coated implants with high bonding strengths.

Precise Helium Sieving from Hydrogen Using Fluorine-Decorated Carbon Hollow Fiber Membranes.

Separating helium (He) and hydrogen (H2), two gases that are extremely similar in molecularsize and condensation properties, presents a formidable challenge in the helium industry. The development of membranes capable of precisely differentiating between these gases is crucial for achieving large-scale, energy-efficient He/H2 separation. However, the limited selectivity of current membranes has hindered their practical application. In this study, we propose a novel approach to overcome this challenge by engineering submicroporous membranes through the fluorination of partially carbonized hollow fibers. We demonstrate that the fluorine substitution on the inner rim of the micropore walls within the carbon hollow fibers enables tunability of the microporous architecture. Furthermore, it enhances interactions between H2 molecules and the micropore walls through the polarization and hydrogen bonding induced by C-F bonds, resulting in simultaneous improvements in both He/H2 diffusivity and solubility selectivities. The fluorinated HFM-550-F-1min membrane exhibits exceptional mixed-gas separation performance, with a binary mixed-gas He/H2 selectivity of 10.5 and a ternary mixed-gas He/(H2+CO2) selectivity of 20.8, at 40 bar feed pressure and 35 oC, surpassing all previously reported polymer-based gas separation membranes, and remarkable plasticization resistance and long-term continuous stability over 30 days.

In Situ Characterizations of the Dynamics of Cathode Electrolyte Interfaces at Different Current Densities.

LiNi0.8Mn0.1Co0.1O2 with high nickel content plays a critical role in enabling lithium metal batteries (LMBs) to achieve high specific energy density, making them a prominent choice for electric vehicles (EVs). However, ensuring the long-term cycling stability of the cathode electrolyte interfaces (CEIs), particularly at fast-charge conditions, remains an unsolved challenge. The decay mechanism associated with CEIs and electrolytes in LMB at high current densities is still not fully understood. To address this issue, in situ Fourier transform infrared (FTIR) is employed to observe the dynamic process of formation/disappearance/regeneration of CEIs during charge and discharge cycles. These dynamic processes further exacerbate the instability of CEIs as current density increases, leading to rupture and dissolution of CEIs and subsequent deterioration in battery performance because of continuous electrolyte reactions. Additionally, the dynamic changes occurring within individual components of CEIs at different cycling stages and various current densities are also discussed. The results demonstrate that excellent capacity retention at small current density is attributed to enrichment of inorganic compounds (Li2CO3, LiF, etc.) and rendering better stability and smaller expansion of CEIs. The key to achieving excellent electrochemical performance at high current densities lies on protecting CEIs, mainly inorganic components.

A Slightly Expanded Graphite Anode with High Capacity Enabled By Stable Lithium-Ion/Metal Hybrid Storage.

Integrating lithium-ion and metal storage mechanisms to improve the capacity of graphite anode holds the potential to boost the energy density of lithium-ion batteries. However, this approach, typically plating lithium metal onto traditional graphite anodes, faces challenges of safety risks of severe lithium dendrite growth and short circuits due to restricted lithium metal accommodation space and unstable lithium plating in commercial carbonate electrolytes. Herein, a slightly expanded spherical graphite anode is developed with a precisely adjustable expanded structure to accommodate metallic lithium, achieving a well-balanced state of high capacity and stable lithium-ion/metal storage in commercial carbonate electrolytes. This structure also enables fast kinetics of both Li intercalation/de-intercalation and plating/stripping. With a total anode capacity of 1.5 times higher (558mAhg-1) than graphite, the full cell coupled with a high-loading LiNi0.8Co0.1Mn0.1O2 cathode (13mgcm-2) under a low N/P ratio (≈1.15) achieves long-term cycling stability (75% of capacity after 200 cycles, in contrast to the fast battery failure after 50 cycles with spherical graphite anode). Furthermore, the capacity of the full cell also reaches a low capacity decay rate of 0.05% per cycle at 0.2C under the low temperature of -20°C.

Self-powered stable high-performance UV–Vis–NIR broadband photodetector based on PVP-Cobalt@Carbon nanofibers/n-GaAs heterojunction

The self-powered PVP-Co@C nanofibers/n-GaAs heterojunction photodetector (HJPD) was fabricated by electrospinning of the nanofibers onto GaAs. An excellent rectification ratio of 6.60 × 106 was obtained from I–V measurements of the device in the dark. The I–V measurements of the fabricated device under 365 nm, 395 nm and 850 nm lights, as well as I–V measurements in visible light depending on the light intensity, were performed. The HJPD demonstrated excellent photodetection performance in terms of a good responsivity of ∼225 mA W−1 (at −1.72 V) and at zero bias, an impressive detectivity of 6.28 × 1012 Jones, and a high on/off ratio of 8.38 × 105, all at 365 nm wavelength. In addition, the maximum external quantum efficiency and NPDR values were 3495% (V = −1.72 V) and 2.60 × 1010 W−1 (V = 0.0 V), respectively, while the minimum NEP value was ∼10−14 W.Hz−1/2 for 365 nm at V = 0.V volts. The HJPD also exhibited good long-term stability in air after 30 d without any encapsulation.

Reduced-Dimensionality Al Nanocrystals: Nanowires, Nanobars, and Nanomoustaches.

Aluminum nanocrystals created by catalyst-driven colloidal synthesis support excellent plasmonic properties, due to their high level of elemental purity, monocrystallinity, and controlled size and shape. Reduction in the rate of nanocrystal growth enables the synthesis of highly anisotropic Al nanowires, nanobars, and singly twinned "nanomoustaches". Electron energy loss spectroscopy was used to study the plasmonic properties of these nanocrystals, spanning the broad energy range needed to map their plasmonic modes. The coupling between these nanocrystals and other plasmonic metal nanostructures, specifically Ag nanocubes and Au films of controlled nanoscale thickness, was investigated. Al nanocrystals show excellent long-term stability under atmospheric conditions, providing a practical alternative to coinage metal-based nanowires in assembled nanoscale devices.

Technical Aspects and Outcome of Multi-Staged and Single-Staged Thoracoabdominal Fenestrated Endovascular Aortic Repair.

In some cases of endovascular thoracoabdominal or juxtarenal aortic aneurysm repair, a thoracic endograft in combination with a fenestrated renovisceral device may be needed in order to create a sufficient proximal landing zone. This study aimed to evaluate the technical aspects and postoperative morbidity of a single- or 2-stage approach. Eighty-seven consecutive patients undergoing thoracic endovascular aortic repair (TEVAR) in combination with elective fenestrated repair (fenestrated endovascular aortic repair [FEVAR]; fenestrated Anaconda device) from 2015 to 2022 were included in this retrospective bicentric study. Underlying pathologies, aortic morphology, technical details, and postoperative morbidity were recorded. Single-staged ("1S," n=61) and 2-staged ("2S," n=26) interventions were compared. Indications were thoracoabdominal aneurysms (TAAAs) (Crawford I-IV) (n=56, 64%) and juxtarenal aneurysms (n=31, 36%). In 2S, the proportion of TAAA was higher than in 1S (2S: 77%, 1S: 59%; p=0.001). In 2S, the covered length of the descending aorta was longer (1S: 128±60 mm, 2S: 202±64 mm; p=0.003). Temporary aneurysm sack perfusion (TASP) was established in 11 (18%) of 1S and 1 (4%) of 2S patients (p=0.079), as well as cerebrospinal fluid (CSF) drainage catheter in 48 (79%) of 1S and 19 (73%) of 2S. The rate of spinal cord ischemia (SCI) and the severity of SCI were not different in both groups, with a total of 3 cases of persisting paraplegia. The rate of access complications was higher in 2S (n=6, 23%) than in 1S (n=4, 7%; p=0.027). Postoperative 30 day morbidity did not significantly differ in both groups and neither did 30 day mortality (4.6% in 1S vs 3.8% in 2S; p=0.083). The combination of TEVAR and FEVAR using a fenestrated endograft is feasible and safe. Aortic morphology does not change significantly after endovascular repair. A single-staged strategy is feasible with excellent results, especially in Crawford IV, Crawford V, or juxtarenal aneurysms. Two-staged repair is recommended in cases with long aortic coverage and a higher American Society of Anesthesiologists (ASA) class. Follow-up data are needed to evaluate the long-term stability of the TEVAR/FEVAR interconnection. Our study has revealed the safety and efficacy of the combination of TEVAR and FEVAR in the treatment of TAAAs and juxtarenal aneurysms with compromised supravisceral landing zones. A single-staged concept is not necessary in all cases. Staged procedures may reduce postoperative morbidity in cases with long aortic coverage and higher ASA class.

Analysis of Current Research in the Field of Sustainable Employment Based on Latent Dirichlet Allocation

In the current context of sluggish global economic recovery, widening regional disparities, and little room for policy error, the global employment situation is unprecedentedly severe. Therefore, research on sustainable employment is critical. In this study, we utilized a Latent Dirichlet Allocation (LDA) topic modeling approach to identify four central topics within the realm of sustainable employment: “Career Sustainability and Employee Development”, “Socio-Economic Dynamics and Strategies for Sustainable Employment”, “Study on Age, Health, and Sustainable Workforce in the Labor Market”, and “Research on the Impact of Workplace Interventions and Psychological Health Support”. The findings revealed the multidimensional, complex nature of sustainable employment issues. This study expands the theoretical horizon of sustainable employment and proposes multidimensional strategic suggestions for practical applications, including regularly assessing and updating organizations’ leadership styles and employee development strategies, offering customized career development programs and skill training, and formulating inclusive employment policies and supportive workplace environments in order to enhance employee job satisfaction and overall well-being, thereby effectively improving the practical outcomes of sustainable employment and bringing about long-term stability and positive impacts on the labor market. These results provide essential theoretical and practical contributions for policymakers, organizational leaders, and anyone seeking sustainable employment.