236 research outputs found
Origin of atomic clusters during ion sputtering
Previous studies have shown that the size distributions of small clusters ( n<=40 n = number of atoms/cluster) generated by sputtering obey an inverse power law with an exponent between -8 and -4. Here we report electron microscopy studies of the size distributions of larger clusters ( n>=500) sputtered by high-energy ion impacts. These new measurements also yield an inverse power law, but one with an exponent of -2 and one independent of sputtering yield, indicating that the large clusters are produced when shock waves, generated by subsurface displacement cascades, ablate the surface
A microscopic view of secondary ion formation
a b s t r a c t The formation of secondary ions in sputtering is described by combining classical molecular dynamics of the particle kinetics with simple analytical treatments modeling the transfer of kinetic into electronic excitation energy, the transport of excitation away from the point of its generation and the charge transfer between the solid and a sputtered particle. For the simplest case of a metal atom sputtered from a clean metal surface, the predictions of such a model are used to answer a few fundamental questions regarding the ion formation process. The results indicate that the transient local excitation of the bombarded solid plays a dominant role in determining the charge state of a sputtered atom. Moreover, we find that the assumption of a sputtered particle being emitted from an ideal, undisturbed surface with a constant emission velocity -a picture which forms the physical basis of nearly all published secondary ion formation models -is not generally justified
Mass-Transport Models with Multiple-Chipping Processes
We study mass-transport models with multiple-chipping processes. The rates of
these processes are dependent on the chip size and mass of the fragmenting
site. In this context, we consider k-chip moves (where k = 1, 2, 3, ....); and
combinations of 1-chip, 2-chip and 3-chip moves. The corresponding mean-field
(MF) equations are solved to obtain the steady-state probability distributions,
P (m) vs. m. We also undertake Monte Carlo (MC) simulations of these models.
The MC results are in excellent agreement with the corresponding MF results,
demonstrating that MF theory is exact for these models.Comment: 18 pages, 4 figures, To appear in European Physical Journal
HICS: Highly charged ion collisions with surfaces
The layout of a new instrument designed to study the interaction of highly
charged ions with surfaces, which consists of an ion source, a beamline
including charge separation and a target chamber, is presented here. By varying
the charge state and impact velocity of the projectiles separately, the
dissipation of potential and kinetic energy at or below the surface can be
studied independently. The target chamber offers the use of tunable
metal-insulator-metal devices as detectors for internal electronic excitation,
a timeof-flight system to study the impact induced particle emission and the
possibility to transfer samples in situ to a UHV scanning probe microscope.
Samples and detectors can be prepared in situ as well. As a first example data
on graphene layers on SrTiO3 which have been irradiated with Xe36+ are
presented.
Key words: highly charged ions, sputtering, AFM, grapheneComment: 4 pages, 4 figures, conference proceeding to 17th Internat. Workshop
for Ion Surf. Collision
Immune and Genetic Signatures of Breast Carcinomas Triggering Anti-Yo-Associated Paraneoplastic Cerebellar Degeneration
BACKGROUND AND OBJECTIVES: Paraneoplastic cerebellar degeneration (PCD) with anti-Yo antibodies is a cancer-related autoimmune disease directed against neural antigens expressed by tumor cells. A putative trigger of the immune tolerance breakdown is genetic alteration of Yo antigens. We aimed to identify the tumors' genetic and immune specificities involved in Yo-PCD pathogenesis. METHODS: Using clinicopathologic data, immunofluorescence (IF) imaging, and whole-transcriptome analysis, 22 breast cancers (BCs) associated with Yo-PCD were characterized in terms of oncologic characteristics, genetic alteration of Yo antigens, differential gene expression profiles, and morphofunctional specificities of their in situ antitumor immunity by comparing them with matched control BCs. RESULTS: Yo-PCD BCs were invasive carcinoma of no special type, which early metastasized to lymph nodes. They overexpressed human epidermal growth factor receptor 2 (HER2) but were hormone receptor negative. All Yo-PCD BCs carried at least 1 genetic alteration (variation or gain in copy number) on CDR2L, encoding the main Yo antigen that was found aberrantly overexpressed in Yo-PCD BCs. Analysis of the differentially expressed genes found 615 upregulated and 54 downregulated genes in Yo-PCD BCs compared with HER2-driven control BCs without PCD. Ontology enrichment analysis found significantly upregulated adaptive immune response pathways in Yo-PCD BCs. IF imaging confirmed an intense immune infiltration with an overwhelming predominance of immunoglobulin G-plasma cells. DISCUSSION: These data confirm the role of genetic alterations of Yo antigens in triggering the immune tolerance breakdown but also outline a specific biomolecular profile in Yo-PCD BCs, suggesting a cancer-specific pathogenesis
Cerebellar Ataxia With Anti-DNER Antibodies: Outcomes and Immunologic Features
BACKGROUND AND OBJECTIVES: There is no report on the long-term outcomes of ataxia with antibodies against Delta and Notch-like epidermal growth factor-related (DNER). We aimed to describe the clinical-immunologic features and long-term outcomes of patients with anti-DNER antibodies. METHODS: Patients tested positive for anti-DNER antibodies between 2000 and 2020 were identified retrospectively. In those with available samples, immunoglobulin G (IgG) subclass analysis, longitudinal cerebellum volumetry, human leukocyte antigen isotyping, and CSF proteomic analysis were performed. Rodent brain membrane fractionation and organotypic cerebellar slices were used to study DNER cell-surface expression and human IgG binding to the Purkinje cell surface. RESULTS: Twenty-eight patients were included (median age, 52 years, range 19-81): 23 of 28 (82.1%) were male and 23 of 28 (82.1%) had a hematologic malignancy. Most patients (27/28, 96.4%) had cerebellar ataxia; 16 of 28 (57.1%) had noncerebellar symptoms (cognitive impairment, neuropathy, and/or seizures), and 27 of 28 (96.4%) became moderately to severely disabled. Half of the patients (50%) improved, and 32.1% (9/28) had no or slight disability at the last visit (median, 26 months; range, 3-238). Good outcome significantly associated with younger age, milder clinical presentations, and less decrease of cerebellar gray matter volumes at follow-up. No human leukocyte antigen association was identified. Inflammation-related proteins were overexpressed in the patients' CSF. In the rodent brain, DNER was enriched in plasma membrane fractions. Patients' anti-DNER antibodies were predominantly IgG1/3 and bound live Purkinje cells in vitro. DISCUSSION: DNER ataxia is a treatable condition in which nearly a third of patients have a favorable outcome. DNER antibodies bind to the surface of Purkinje cells and are therefore potentially pathogenic, supporting the use of B-cell-targeting treatments
Elevated Expression of Osteopontin May Be Related to Adipose Tissue Macrophage Accumulation and Liver Steatosis in Morbid Obesity
OBJECTIVE—Osteopontin (OPN) plays an important role in the development of insulin resistance and liver complications in dietary murine models. We aimed to determine the expression pattern of OPN and its receptor CD44 in obese patients and mice according to insulin resistance and liver steatosis
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