arXiv subjects

Ivan Blum

Publications and source records attributed to Ivan Blum.

6 recordsLinked to original sources

arXiv2025

Exploring mechanisms leading to composition errors in monazite (CePO4) analysed with atom probe tomography

Monazite (CePO4) is widely used in U-Th-Pb geochronology due to its reliable age determinations, although isotopic disturbances often require nanoscale investigation to better understand the mechanisms at play. Atom Probe Tomography (APT) offers unique capabilities for nanoscale chemical analysis and 3D atomic reconstruction but presents challenges for insulating materials such as CePO4, particularly due to oxygen loss during field evaporation. This study investigates the effects of laser wavelength, energy, metallic coatings and detection device on mass spectrum optimization and compositional accuracy in synthetic CePO4 samples. Results show that shorter laser wavelengths (260 nm) enhance peak resolution, particularly when combined with advanced reflectron configurations, as demonstrated with the LEAP 6000 XR. Chromium coatings further improve thermal dissipation and reduce noise levels. However, compositional measurements reveal systematic underestimation of oxygen and overestimation of P and Ce, likely influenced by preferential low-field element evaporation. These findings highlight the need to carefully tune experimental parameters to mitigate quantification biases and enhance the reliability of APT analyses for geological materials.

cond-mat.mtrl-sci↗

arXiv2025

Role of defects in atom probe analysis of sol-gel silica

Silicon dioxide is a suitable material to encapsulate proteins at room temperature so that they can be analysed at the atomic level using laser-assisted atom probe tomography (La-APT). To achieve this goal, in this study we show that UV and deep UV lasers can achieve a high success rate in La-APT of silica in terms of chemical resolution and three-dimensional image volume, with both lasers providing comparable results. Since the La-APT analyses are driven by photon absorption, in order to understand the mechanisms behind the enhanced absorption of UV light, we performed density functional theory calculations to model the electronic and optical properties of amorphous silica matrices generated using a Monte Carlo approach to structural optimisation. In particular, we have investigated the role of various defects introduced during sample preparation, such as substitutional and interstitial carbon, sodium and gallium ions, and hydrogen. Our results show that the presence of defects increases the absorption of silica in the UV and deep-UV range and thus improves the La-APT capabilities of the material. However, due to the low density of free charge carriers resulting from the absorption of laser energy by defects, deviations from the nominal chemical composition and suboptimal chemical resolution may occur, potentially limiting the optimal acquisition of APT mass spectra.

cond-mat.mtrl-sci↗

arXiv2024

Crystallographic dependence of Field Evaporation Energy Barrier in metals using Field Evaporation Energy Loss Spectroscopy mapping

Atom probe tomography data is composed of a list of coordinates of the reconstructed atoms in the probed volume. The elemental identity of each atom is derived from time-of-flight mass spectrometry, with no local energetic or chemical information readily available within the mass spectrum. Here, we used a new data processing technique referred to as field evaporation energy loss spectroscopy (FEELS), which analyses the tails of mass peaks. FEELS was used to extract critical energetic parameters that characterize the field evaporation process, which are related to the binding energy of atoms to the surface under intense electrostatic field and dependent of the path followed by the departing atoms during the field evaporation process. We focused our study on different pure face centered cubic metals (Al, Ni, Rh). We demonstrate that the energetic parameters extracted from mass spectra can be mapped in 2D with nanometric resolution. A dependence on the considered crystallographic planes is observed, with sets of planes of low Miller indices showing a lower sensitivity to the intensity of the electric field, which indicates a lower effective attachment energy. The temperature is also an important parameter in particular for Al, which we attribute to an energetic transition between two paths of field evaporation between 25K and 60K close to (002) pole at the specimen's surface. This paper shows that the complex information that can be retrieved from the measured energy loss of surface atoms is important both instrumentally and fundamentally.

cond-mat.mtrl-sci↗

arXiv2024

Evaporation of cations from non-conductive nano-samples using single-cycle THz pulses: an experimental and theoretical study

This study investigates the emission of cations from silica samples by single-cycle THz pulses, focusing on the influence of pulse polarity. Negative THz pulses were found to efficiently trigger the evaporation of cations from nanoneedles in amorphous silica samples compared to positive pulses. Conversely, this dependence on pulse polarity could not be found in samples with metallic behaviour such as LaB$_6$ and when multi-cycle pulses in different frequency ranges such as ultraviolet (UV) are used. First-principles simulations focus on silica under THz laser irradiation and show critical fields for ion evaporation of hydroxyl groups from Si(OH)$_4$, which serves as a model precursor molecule for the amorphous solid matrix. To explain our experimental results, we propose a simplified theoretical model that determines the role of the polarity of the THz pulse by taking into account the differences in electron mobility between silica and semi-metallic samples. The study explores the nonlinear microscopic mechanisms of atomic evaporation under external static and THz laser fields and clarifies the dynamics of THz-enhanced APT and related applications.

cond-mat.mtrl-sci↗

arXiv2020

An integral method for the calculation of the reduction in interfacial free energy due to interfacial segregation

A method based on the Gibbs' adsorption isotherm is developed to calculate the decrease in interfacial free energy resulting from solute segregation at an internal interface, built on measured concentration profiles. Utilizing atom-probe tomography (APT), we first measure a concentration profile of the relative interfacial excess of solute atoms across an interface. To accomplish this we utilize a new method based on J. W. Cahn's formalism for the calculation of the Gibbs interfacial excess. We also introduce a method to calculate the decrease in interfacial free energy that is caused by the segregating solute atoms. This method yields a discrete profile of the decrease in interfacial free energies, which takes into account the measured concentration profile and calculated Gibbsian excess profile. We demonstrate that this method can be used for both homo- and hetero-phase interfaces and takes into account the actual distribution of solute atoms across an interface as determined by APT. It is applied to the case of the semiconducting system PbTe-PbS 12 mol.%-Na 1 mol.%, where Na segregation at the PbS/PbTe interface is anticipated to reduce the interfacial free energy of the {100} facets. We also consider the case of the nickel-based Alloy 600, where B and Si segregation are suspected to impede inter-granular stress corrosion cracking (IGSCC) at homo- (GB) and hetero-phase metal carbide (M7C3) interfaces. The concentration profiles associated with internal interfaces are measured by APT using an ultraviolet (wavelength = 355 nm) laser to dissect nanotips on an atom-by-atom and atomic plane-by-plane basis.

cond-mat.mtrl-sci↗

arXiv2019

Unraveling the Metastability of C_n^{2+} (n=2-4) Clusters

Pure carbon clusters have received considerable attention for a long time. However, fundamental questions such as what the smallest stable carbon cluster dication is remain unclear. Here, we investigated the stability and fragmentation behavior of C_n^{2+} (n=2-4) dications using state-of-the-art atom probe tomography. These small doubly charged carbon cluster ions were produced by laser-pulsed field evaporation from a tungsten carbide field emitter. Correlation analysis of the fragments detected in coincidence reveals that they only decay to C_{n-1}^+ + C^+. During C_2^{2+} => C^+ + C^+, significant kinetic energy release (\approx 5.75-7.8 eV) is evidenced. Through advanced experimental data processing combined with \textit{ab initio} calculations and simulations, we show that the field evaporated diatomic ^12C_2^{2+} dications are either in a weakly bound ^3Π_u and ^3Σ_g^- state, quickly dissociating under the intense electric field, or in a deeply bound electronic ^5Σ_u^- state with lifetimes longer than 180 ps.

physics.atm-clus↗