Search Results (205)

Being a greenhouse gas, SF₆ has significant potential to cause global warming. No alternative gas has been found so far that meets the required criteria. Ongoing research has narrowed down the candidates to some relatively environmentally friendly elementary gases such as N₂, CO₂, and their mixtures with a small percentage of SF₆ (10–20%). Streamers are important and play a deterministic role in the breakdown phenomenon. The inception and growth of streamer discharge depend on the generation of free electrons. Various ionization sources, including field ionization, Auger release of electrons, photoionization, and electron detachment from negative ions, have been employed in dielectric media. In this work, field ionization is considered a free-electron generation mechanism for streamer initiation. In field ionization, neutral molecules produce free electrons when extremely high electric fields are present near the needle electrode. A 3D particle model with field ionization is then used to investigate positive streamer initiation in SF₆/N₂ and SF₆/CO₂ for different mixing ratios at 1 and 5 bar. It was observed that for both mixtures, the number and the apparent length of streamer branching decreased with increasing SF₆ concentration and were minimal at 100% SF₆. The number of branches and the apparent length of streamers were higher in the case of SF₆/CO₂ compared with SF₆/N₂ mixtures, indicating a higher ionization rate for the SF₆/CO₂ mixture. With increasing pressure, the branching and length of the streamers for both mixtures decreased significantly. Although the field-ionization model is only suitable for very high electric fields in the vicinity of the needle tip, its validity is still questionable for uniform fields and at lower pressures. Full article

The behavior of S and Cs during the alternate adsorption of each adsorbate on the Ni(100) surface is studied at room and elevated temperatures by means of low-energy electron diffraction (LEED), Auger electron spectroscopy (AES), thermal desorption spectroscopy (TDS) and work function (WF) measurements. For Cs deposition on the S-covered Ni(100) surface, the presence of sulfur increases the binding energy and the maximum amount of adsorbed cesium, as happens with other alkalis too. The first Cs overlayer is disordered, while the second strongly interacts with S with a tendency toward a Cs_xS_y surface compound formation. This interaction causes the gradual demetallization of the Cs overlayer with the increasing S coverage in the underlayer. When the Cs_xS_y stoicheometry is complete, however, subsequent Cs deposition forms an independent rather metallic overlayer. When the sulfated covers the surface, S(0.5ML)/Ni(100) is preheated to 1100 K, the S-Ni bond strengthens and S-Cs interaction correspondingly weakens to a degree that the S underlayer retains a periodic structure on the Ni substrate. This behavior indicates that the preheated S/Ni(100) surface is passivated to a degree against Cs with reduced mobility of sulfur adatoms. Differently, when S is adsorbed on the Cs-covered Ni(100) surface at room temperature, sulfur adatoms diffuse underneath the Cs overlayer to interact with the nickel substrate and form the same structural phases as on a clean surface. During that process, the sticking coefficient of sulfur remains constant regardless of the amount of pre-deposited cesium. The presence of Cs, however, increases the amount of S that can be deposited on the Ni substrate, probably in favor of the Cs_xS_y compound formation, which demetallizes the surface independent of the sequence of adsorption. Full article

Carbon nanotubes (CNTs) have remarkable mechanical, electrical, and thermal properties, making them highly attractive as foundational elements for advanced materials. However, translating their nanoscale potential into macroscale reliability and longevity requires a holistic design approach that integrates precise architectural control with robust damage mitigation strategies. This review presents a synergistic perspective on enhancing the durability of CNT-based systems by critically examining the interplay between molecular assembly, self-repair mechanisms, and the advanced characterization techniques required for their validation. We first establish how foundational architectural control—achieved through strategies like chemical functionalization, field-directed alignment, and dispersion—governs the ultimate performance of CNT materials. A significant focus is placed on advanced functionalization, such as fluorination, and its verification using high-powered spectroscopic tools, including X-ray photoelectron spectroscopy (XPS) and near-edge X-ray absorption fine structure (NEXAFS) spectroscopy. Subsequently, this manuscript delves into the mechanisms of self-repair, systematically analyzing both the intrinsic capacity of the carbon lattice to heal atomic-level defects and the extrinsic strategies that incorporate engineered healing agents into composites. This discussion is uniquely supplemented by an exploration of the experimental techniques, such as electron energy loss spectroscopy (EELS) and Auger electron spectroscopy (AES), that provide crucial evidence for irradiation-induced healing dynamics. Finally, we argue that a “characterization gap” has limited the field’s progress and highlight the critical role of techniques like in situ Raman spectroscopy for quantitatively monitoring healing efficiency at the molecular level. By identifying current challenges and future research frontiers, this review underscores that the creation of truly durable materials depends on an integrated understanding of how to build, repair, and precisely measure CNT-based systems. Full article

A super-polishing procedure was performed on the Al₂O₃ (0001) surface for epitaxial purposes. The roughness of the final polished surface was measured to be 0.16 nm using atomic force microscopy and X-ray reflectivity techniques. After heat treatment at 130 °C, results from low-energy electron diffraction and Auger energy spectroscopy indicated that the top surface was well ordered and clean, rendering it suitable for epitaxial growth. The successful growth of a GaN thin film on an Al₂O₃ (0001) substrate was confirmed by the hk-circle scan in XRD and the presence of a sharp peak in the rocking curve of the GaN (0002) Bragg peak. These findings indicate that the top surface of the substrate is conducive to epitaxial growth. Full article

A potential field of study for improving the efficiency of next-generation photovoltaic devices hot carriers in perovskite solar cells is investigated in this review paper. Considering their relevance to hot carrier dynamics, the paper thoroughly studies metal halide perovskites’ essential characteristics and topologies. We review important aspects like carrier excitation, exciton binding energy, phonon coupling, carrier excitation, thermalization, and hot hole and hot electron dynamics. We investigate, in particular, the significance of relaxation mechanisms, including thermalization and the Auger heating effect. Moreover, the bottleneck effect and defect management are discussed with an eye on their impact on device performance and carrier behaviour. A review of experimental methods for their use in investigating hot carrier dynamics, primarily transient photovoltage measurements, is included. Utilizing this thorough investigation, we hope to provide an insightful analysis of the difficulties and techniques for reducing the effect of hot carriers in perovskite solar cells and optimizing their performance. Full article

Multidrug resistance (MDR) represents a major obstacle to successful chemotherapy and, due to overlapping defense mechanisms, such as enhanced DNA repair and the evasion of apoptosis, can also be associated with radioresistance. In this study, we investigated whether MDR breast cancer cells (MCF-7/CMF) exhibit reduced susceptibility to radiation-induced DNA fragmentation compared to their non-resistant parental counterpart (MCF-7). Using a nucleosome-based ELISA, we quantified the chromatin fragmentation in MCF-7 and MCF-7/CMF cells following their exposure to four radiopharmaceuticals: [^99mTc]pertechnetate, [¹³¹I]NaI (sodium iodide), [¹²⁵I]NaI, and the DNA-incorporating compound [¹²⁵I]iododeoxyuridine ([¹²⁵I]IdU). Each radioactive preparation was assessed across a range of activity concentrations, using a two-way ANOVA. For [^99mTc]pertechnetate and [¹³¹I]NaI, significantly higher DNA fragmentation was observed in the sensitive cell line, whereas [¹²⁵I]NaI showed no significant difference between the two phenotypes. In contrast to the other radiopharmaceuticals, [¹²⁵I]IdU induced greater fragmentation in resistant cells. This finding was supported by the statistical analysis (a 63.7% increase) and visualized in the corresponding dose–response plots. These results highlight the critical role of the intranuclear enrichment of Auger emitters and support further development of radiopharmaceuticals in accordance with this principle. Our data suggest that radiotoxicity is governed not by linear energy transfer (LET) alone, but, fundamentally, by the spatial proximity of the radionuclide to the DNA. Targeting tumor cell DNA with precision radiotherapeutics may, therefore, offer a rational strategy to overcome MDR in breast cancer. Full article

The current effect of passive devices is crucial for device testing. The current effect of a suspended graphene pressure sensor in the range of 0–2 mA is studied in this paper. The results show that the resistance of graphene films and the piezoresistive effect of devices exhibit stable performance within the current threshold range of 400 μA and 300 μA, respectively. Auger electron spectroscopy and Raman spectroscopy tests indicate that the resistance of graphene increases first and then decreases at high current intensity, resulting from the electrostatic adsorption of oxygen atoms in the initial phase of electrification and the Joule-induced desorption in the later phase. This study presents guiding significance for the electrical testing of suspended graphene devices. Full article

This paper presents a comprehensive review of recent advancements in radionuclide-labeled biomaterials for cancer therapy, with a particular focus on the characteristics, production methods, and labeling techniques of α-particle, β-particle, and Auger electron-based radiotherapy. It explores innovative strategies for targeted delivery systems and highlights the advantages of theranostics and combination therapies. The application of radionuclide-labeled biomaterials in various cancer types, including prostate cancer, breast cancer, neuroendocrine tumors, gliomas, and melanoma, is systematically summarized. Furthermore, the article critically examines current technological bottlenecks and challenges in clinical translation, while proposing future directions such as AI-assisted dose optimization and multimodal combination therapies. This review provides essential theoretical foundations and practical insights to facilitate the clinical translation of radionuclide-labeled biomaterials. Full article

To probe the properties of single atoms is a challenging task, especially from the experimental standpoint, due to sensitivity limits. Nevertheless, it is sometimes possible to achieve this by making corresponding choices and adjustments to the experimental technique and sample under investigation. In the present case, the absolute value of the electronic charge the Fe atoms acquire when they are adsorbed on the surface of aluminum oxide α-Al₂O₃(0001) was measured by a set of surface-sensitive techniques: low-energy ion scattering (LEIS), Auger electron spectroscopy (AES), low-energy electron diffraction (LEED), and work function (WF) measurements, in combination with density functional theory (DFT) calculations. The main focus was the submonolayer coverage of Fe atoms in situ deposited on the well-ordered stoichiometric α-Al₂O₃(0001) 7 nm thick film formed on a Mo(110) crystal face. An analysis of the evolution of the Fe LVV Auger triplet upon variation of the Fe coverage shows that there is electronic charge transfer from Fe to alumina and that its value gradually decreases as the Fe coverage grows. The same trend is also predicted by the DFT results. Extrapolation of the experimental Fe charge value versus coverage plot yields an estimated value of a single Fe atom adsorbed on α-Al₂O₃(0001) of 0.98e (electron charge units), which is in reasonable agreement with the calculated value (+1.15e). The knowledge of this value and the possibility of its adjustment may be important points for the development and tuning of modern sub-nanometer-scale technologies of diverse applied relevance and can contribute to a more complete justification and selection of the corresponding theoretical models. Full article

Vanadium and oxygen form a complex system of vanadium oxides with multiple phases and mixed valency, increasing the difficulty of characterization. In this work, amorphous vanadium oxide thin films with mixed valence states were fabricated by atomic layer deposition, and then post-annealing was conducted for crystalline films. For the surface analysis of this mixed-valence system, X-ray photoelectron spectroscopy (XPS) and Auger electron spectroscopy (AES) were employed. However, XPS is only able to quasi-quantitatively determine the surface-proximity oxidation states. To account for the inadequacy of surface-sensitive XPS and AES techniques, a surface oxidation model (SOM) was proposed for the ellipsometric modeling of the mixed-valence system. Furthermore, by conducting air thermal oxidation (ATO) experiments, the four sets of fitting parameters of SOM were decreased to three, lowering the system complexity. This study is expected to help with the analysis of vanadium oxide mixed-valence systems and other multivalent metal oxide systems. Full article

Ultrathin NiO films, ranging from 1 to 16 monolayers (ML) in thickness, have been stabilized via reactive molecular beam epitaxy on the (001) surface of a metastable body-centered cubic (BCC) Ni film. Low-energy electron diffraction (LEED) confirms that NiO grows as a crystalline film, exposing the (001) surface. Auger electron spectroscopy (AES) reveals a slight oxygen excess compared to a perfectly stoichiometric NiO film. Scanning tunneling microscopy (STM) shows that at low coverages the film exhibits atomically flat terraces, while at higher coverage a “wedding cake” morphology emerges. Scanning tunneling spectroscopy (STS) reveals a thickness-dependent evolution of the electronic band gap, which increases from 0.8 eV at 3 ML to 3.5 eV at 16 ML. The center of the band gap is approximately 0.2 eV above the Fermi level, indicating that NiO is p-doped. Full article

Auger electrons are low-energy, high-linear-energy-transfer particles that deposit their energy over nanometers distances. Their biological impact depends heavily on where the radionuclide is localized within the cell. To verify the hypothesis that the cell membrane may be a better molecular target than the cytoplasm in Auger electron therapy, we investigated whether the radiotoxicity of ^99mTc varied depending on its location in the cell. The behavior of peptide radiopharmaceuticals ^99mTc-TECANT-1 targeted the cell membrane was compared with ^99mTc-TEKTROTYD directed to the cytoplasm. Our findings confirmed that ^99mTc-TECANT-1 displayed greater binding to AR-42-J cells than ^99mTc-TEKTROTYD. Additionally, it was demonstrated that the receptor agonist ^99mTc-TEKTROTYD is localized in more than 90% of the cytoplasm, while ^99mTc-TECANT-1 is found in 60–80% of the cell membrane. When evaluating cell survival using the MTS assay, we observed that toxicity was significantly higher when ^99mTc was targeted to the membrane compared to the cytoplasm. This indicates that, for ^99mTc, as with ¹⁶¹Tb, the membrane is a more sensitive target for Auger electrons than the cytoplasm. Our results also suggest that receptor antagonists labelled with therapeutic doses of ^99mTc may be effective in treating certain cancers. However, further detailed studies, particularly dosimetric investigations, are necessary to validate these findings. Full article

The molten salt reactor is a fourth-generation nuclear power plant considered a long-term eco-friendly energy source with high efficiency and the potential for green hydrogen production. The selection of alloys for such reactors, which can operate for more than 30 years, is a primary concern because of corrosion by high-temperature molten salt. In this study, three Fe- and Ni-based alloys were selected as structural material candidates. Corrosion immersion tests were conducted in NaCl–KCl molten salt for 48 h at 800 °C and 40% RH conditions in an air environment. In the absence of moisture and oxygen removal, ClNaK salt-induced damage was observed in the investigated alloys. The corrosion behavior of the alloys was characterized using various techniques, including scanning electron microscopy, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and Auger electron spectroscopy. The results show that the corrosion process can be explained by salt-induced surface damage, internal ion migration, and depletion to the surface. The corrosion rate is high in SS316L (16Cr-Fe), N10003 (7Cr-Ni), and C-276 (16Cr-Ni), in decreasing order. Based on the corrosion penetration, ion elution, and interfacial diffusion results, C-276 and N10003 are good candidates for structural materials for MSRs. Therefore, Ni-based alloys with high Cr content minimize surface damage and ion depletion in unpurified molten salt environments. This indicates that Ni-based alloys with high Cr content exhibit highly corrosion resistance. Full article

Objective: This review provides an overview of the current knowledge regarding the mechanisms of action of AGuIX, a clinical-stage theranostic nano-radiosensitizer composed of gadolinium. It covers the steps following the administration, from the internalization in tumor cells to the interaction with X-rays and the subsequent physical, chemical, biological, and immunological events. Results: After intravenous injection, AGuIX accumulates in tumors through the enhanced permeability and retention (EPR) effect, and its specific retention properties allow its persistence in tumors for several days. At the cellular level, the nanomedicine is internalized by endocytic processes and mainly located in the cytoplasm, especially in lysosomes. AGuIX enhances the effects of radiotherapy (RT) at several levels, starting from radiation–matter interactions to a chemical stage of reactive oxygen species (ROS) production, followed by a cascade of biological events leading to tumor cell death and immune response. Indeed, AGuIX induces a local increase in radiation dose deposition through the emission of Auger electrons, leading to a subsequent increase in ROS generation. AGuIX also impacts RT-induced biological mechanisms, including DNA damage and cell death mechanisms such as apoptosis, autophagic cell death, and ferroptosis. Last, the combination of AGuIX and RT stimulates an antitumor immune response through the induction of immunogenic cell death (ICD), the activation of dendritic and T cells, and the reprogramming of tumor-associated macrophages (TAMs) into a pro-inflammatory phenotype. Conclusions: AGuIX is a clinical-stage nanoparticle (NP) intravenously administered with pan-cancer potential due to its specific biodistribution properties and a strong ability to amplify RT-induced mechanisms. Full article

Global disparities in cancer prevention, detection, and treatment demand a unified international effort to reduce the disease’s burden and improve outcomes. Despite advances in chemotherapy and radiotherapy, many tumors remain resistant to these treatments. Gold nanoparticles (AuNPs) have shown promise as radiosensitizers, enhancing the effectiveness of low-energy X-rays by emitting Auger electrons that cause localized cellular damage. In this study, spherical AuNPs of 5 nm and 10 nm were characterized and tested on various cell lines, including malignant breast cells (MCF-7), non-malignant cells (CHO-K1 and MCF-10A), and human lymphocytes. Cells were treated with AuNPs and irradiated with attenuated 6 megavoltage (MV) X-rays or p(66)/Be neutron radiation to assess DNA double-strand break (DSB) damage, cell viability, and cell cycle progression. The combination of AuNPs and neutron radiation induced higher levels of γ-H2AX foci and micronucleus formation compared to treatments with AuNPs or X-ray radiation alone. AuNPs alone reduced cellular kinetics and increased the accumulation of cells in the G2/M phase, suggesting a block of cell cycle progression. For cell proliferation, significant effects were only observed at the concentration of 50 μg/mL of AuNPs, while lower concentrations had no inhibitory effect. Further research is needed to quantify internalized AuNPs and correlate their concentration with the observed cellular effects to unravel the biological mechanisms of their radioenhancement. Full article