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At least 1,045 records · Page 58

WIMP-like Dark Matter Without Thermalization At Freeze-Out

In the standard thermal relic scenario, dark matter remains in chemical equilibrium with the Standard Model radiation bath until freeze-out occurs at $T \sim m_X/20$, where $m_X$ is the dark matter mass. In this familiar class of models, the observed relic density is obtained for annihilation cross sections of order $σv \sim 10^{-26}$ cm$^3$/s. We show that comparable cross sections can naturally be realized in hidden-sector models in which the dark matter and Standard Model sectors decouple at a very high temperature, $T \gg m_X$, and subsequently evolve with separate thermal histories. Despite this decoupling, the two sectors have similar temperatures during freeze-out, leading to the usual thermal relic abundance. As a consequence, the coupling between the Standard Model and hidden sectors can be extremely small, potentially placing direct detection and collider signals far below foreseeable sensitivities.

Hooper, Dan [Wisconsin U., Madison] (ORCID:0009000↗

In situ cryogenic characterization of proton damage in thick p-channel skipper CCDs

Skipper charge-coupled devices (CCDs) are an offshoot of standard silicon pixel detectors and are capable of performing repeated non-destructive charge measurements, enabling deeply sub-electron readout noise. This capability has opened the door to single-photon counting from the near-infrared ($\sim$1.1 $μ$m) to the soft X-ray (several keV), making these devices strong candidates for future astronomical instruments operating in the photon-starved limit. Furthermore, the p-channel architecture used to fabricate Skipper CCDs on n-type silicon has been demonstrated to have an increased hardness to the intense radiation environment of space. Building upon previous irradiation campaigns on room-temperature sensors, here we describe the first radiation-hardness tests of p-channel skipper CCDs at their cryogenic operating temperatures. We assess the performance of the floating-gate output stage and global CCD parameters (charge transfer inefficiency, dark current, hot pixels, and charge traps). We find that these devices maintain excellent performance after displacement damage doses equivalent to ${\sim}$10 years at the Earth/Sun L2 Lagrange point, demonstrating for the first time that these sensors remain radiation-hard in realistic deep-space thermal and radiation environments.

Roach, Brandon M. [Chicago U., KICP] (ORCID:000000↗

Dark matter energy exchange in stars orbiting supermassive black holes

Stars on tight orbits around the supermassive black hole at the Galactic Center pass through regions where the dark matter~(DM) density may be strongly enhanced. We compute the orbit-averaged DM-induced energy exchange for S4714 as an example. It is a star on an exceptionally close and relativistic orbit around Sagittarius~A*. For a spiked dark matter profile, the exchange reaches the stellar luminosity at $σ_{χp} \sim 10^{-36}~\mathrm{cm}^2$ for MeV-GeV masses and $σ_{χe} \sim 5\times10^{-38}~\mathrm{cm}^2$ for sub-MeV masses, opening a new annihilation-free route toward dark-star phases. These cross sections lie within the range predicted by freeze-in scenarios and are consistent with cosmic-ray--boosted and solar-reflection dark matter constraints.

Meighen-Berger, Stephan A. [Iowa U.] (ORCID:000000↗

Developing a Digital Twin for SRF Cavity Assembly at Fermilab

When assembling Superconducting Radio Frequency (SRF) Cavities, maintaining an environment devoid of particulates like dust and other small particles is essential. If a single spec of dust enters the cavity a significant degradation of performance can occur. To avoid a cavity failure Fermilab assembles the SRF cavities within a ISO-4 (Class 10) environment. This environment though is still susceptible to foreign contaminants when technicians enter and new components are added to the cleanroom. To reduce the risk even more Fermilab has introduced a cobot manipulator into the cleanroom environment to speed up the assembly time which will reduce the time that the technicians operate in the cleanroom. But, this still leaves the potential of contaminants to enter the cleanroom if new components need to be tested within the cleanroom. This project aims to lay the groundwork to develop a Digital Twin environment of the cleanroom to aid in manufacturing processes and testing. In its simplest form, a digital twin is a bidirectional link between a physical system and its digital counterpart or twin. NVIDIA Isaac Sim is used as the digital twin foundation for the digital representation of the cleanroom, specifically for the UR16e assembly area. A simulated UR16e was used to validate the performance of Isaac Sim as a testing environment by comparing the tool center points (TCP) positional data between the simulated and digital representation of the UR16e. Due to a new vision based robotic assembly process being introduced to the cleanroom a digital representation of the physical camera was tested and validated to ensure that it will produce close to the same outcome as the physical environment. The TCP comparison results showed a peak translational error of approximately 0.1mm and rotational errors of up to 8 between the simulated and digital UR16es. While the camera validation performed with high repeatability across multiple runs, it still requires minor tuning before it can accurately replicate a physical camera.

Imburgia, Joseph [Northern Illinois U.]↗

Cross-correlation of SPT-3G D1 CMB lensing and DES Y3 galaxy lensing

Measurements of the weak lensing of galaxies and of the cosmic microwave background (CMB) provide direct probes of the cosmic matter density field, but the two observables are sensitive to different spatial scales, redshift ranges, and survey systematics. Their cross-correlation thus enables consistency checks of the theoretical model and of potential systematics in either dataset. We present measurements of the cross-correlation between CMB lensing and cosmic shear over $\sim$1,300 deg$^2$ of the sky using the SPT-3G D1 CMB lensing maps and the Dark Energy Survey Year 3 (DES Y3) shear catalogs. For the first time, we measure this cross-correlation at high significance ($\sim 14σ$) when using a polarization-only CMB lensing reconstruction that is expected to be robust against biases induced by extragalactic foregrounds. We test a variety of other CMB lensing estimators that include temperature information and exhibit different tradeoffs between foreground biases and noise, as well as a shear sample that consists of blue, star-forming galaxies and has been shown to be less impacted by galaxy intrinsic alignments. Assuming $Λ$CDM and marginalizing over uncertainties in intrinsic alignments, baryonic feedback, and various nuisance parameters, we obtain a constraint on the amplitude of matter clustering $S_8 \equiv σ_8 \sqrt{Ω_m / 0.3} = 0.833^{+0.047}_{-0.061}$, consistent with both the primary CMB results from Planck and shear-only results from DES Y3. By combining our measurement with Planck, we find mild constraints on the astrophysical processes that impact the cross-correlation. We obtain a constraint on the intrinsic alignment amplitude of the DES sample that is competitive with that from shear-only analyses, and we find a lower limit on the strength of baryonic feedback.

Ouellette, A. [Illinois U., Urbana] (ORCID:0000000↗

Astrophysical Neutrino Sources as Colliders

High-energy neutrinos arise from processes at large center-of-mass energies, offering a window to test physics at comparable scales or beyond those accessible in collider experiments on Earth. Here, we present a recipe for extracting two-sided bounds on the inelastic $pp$ and $pγ$ cross sections from neutrino point-source data, by independently constraining every astrophysical input (cosmic-ray luminosities and target densities) through electromagnetic observations or theoretical arguments. The cross section is then the only remaining free parameter. Applying this framework to the IceCube associations with TXS~0506+056, NGC~1068, and the Galactic Plane, to a stacked population of eleven X-ray bright Seyfert galaxies, to the ultra-high-energy KM3NeT event KM3-230213A, and to projected observations of ultra-high-energy neutrinos, we obtain constraints that span center-of-mass energies from $\sqrt{s}\sim 1$ GeV to $\sim 10^{5}$ GeV, some of which are well beyond the reach of the LHC and, for the $pγ$ channel, beyond HERA. Several of these bounds are more stringent than unitarity limits.

Argüelles, Carlos A. [Harvard U.]↗

Probing the Cosmic Axion Background via Axion-Photon Conversion in Filaments

The cosmic axion background (CaB) is a hypothetical population of relativistic axions produced in the early universe. If the CaB is produced from dark matter decays, the axions in this population can convert to photons in the magnetic fields of cosmological filaments, resulting in an isotropic gamma ray background flux. We present new indirect detection constraints on the axion mass and axion-photon coupling, for GeV-TeV dark matter with a decay lifetime below $10^{30}$ sec, by comparing this flux against experimental data. We exclude significant parameter space for axion masses below $10^{-5}$~eV for a broad range of dark matter masses and lifetimes, assuming conservative filament magnetic field strengths ($\sim 1$ nG). For large filament fields ($\sim 100$ nG), our strategy also constrains a portion of the QCD-axion parameter space for TeV-scale dark matter masses.

Rocha, Duncan [Chicago U., EFI; Chicago U., KICP]↗

Delineating the Impact of Transition‐Metal Crossover on Solid‐Electrolyte Interphase Formation with Ion Mass Spectrometry

Abstract Lithium‐metal batteries (LMB) employing cobalt‐free layered‐oxide cathodes are a sustainable path forward to achieving high energy densities, but these cathodes exhibit substantial transition‐metal dissolution during high‐voltage cycling. While transition‐metal crossover is recognized to disrupt solid‐electrolyte interphase (SEI) formation on graphite anodes, experimental evidence is necessary to demonstrate this for lithium‐metal anodes. In this work, advanced high‐resolution 3D chemical analysis is conducted with time‐of‐flight secondary‐ion mass spectrometry (TOF‐SIMS) to establish spatial correlations between the transition metals and electrolyte decomposition products found on cycled lithium‐metal anodes. Insights into the localization of various chemistries linked to crucial processes that define LMB performance, such as lithium deposition, SEI growth, and transition‐metal deposition are deduced from a precise elemental and spatial analysis of the SEI. Heterogenous transition‐metal deposition is found to perpetuate both heterogeneous SEI growth and lithium deposition on lithium‐metal anodes. These correlations are confirmed across various lithium‐metal anodes that are cycled with different cobalt‐free cathodes and electrolytes. An advanced electrolyte that is stable to higher voltages is shown to minimize transition‐metal crossover and its effects on lithium‐metal anodes. Overall, these results highlight the importance of maintaining uniform SEI coverage on lithium‐metal anodes, which is disrupted by transition‐metal crossover during operation at high voltages.

Chemistry↗

Impacts of Dissolved Ni 2+ on the Solid Electrolyte Interphase on a Graphite Anode

Transition metal (e.g. Ni) ions dissolved from layered-structured Ni-rich cathodes can migrate to the anode side and accelerate the failure of lithium-ion batteries. The investigations of the impact and distribution of Ni species on the solid electrolyte interphase (SEI) on the anode are crucial to understand the failure mechanism. Herein, we used time-of-flight secondary ion mass spectroscopy (TOF-SIMS) coupled with multivariate curve resolution (MCR) analysis to intuitively characterize the distribution of Ni species in the SEI. We find that the SEI on the graphite electrode using an EC-based electrolyte exhibits a multi-stratum structure. During accelerated aging of the LiNi 0.88 Co 0.08 Mn 0.04 O 2 /graphite full cell, the dissolution of Ni aggravates significantly upon cycling. A strong correlation between the dissolved-Ni and organic species in the SEI on graphite is illustrated. Here, the ion-exchange reaction between Ni 2+ and Li + ions in the SEI is demonstrated to be the main reason for the increase of SEI resistivity.

25 ENERGY STORAGE↗

Nanoweb Surface-Mounted Metal–Organic Framework Films with Tunable Amounts of Acid Sites as Tailored Catalysts

Metal–organic frameworks (MOFs) are a promising class of materials for many applications, due to their high chemical tunability and superb porosity. By growing MOFs as (thin-)films, additional properties and potential applications become available. In this work, copper (II) 1,3,5-benzenetricarboxylate (Cu-BTC) metal–organic framework (MOF) thin-films are reported, which were synthesized by spin-coating, resulting in “nanowebs”, that is, fiber-like structures. These surface-mounted MOFs (SURMOFs) were studied by using photoinduced force microscopy (PiFM) and time-of-flight secondary ion mass spectrometry (ToF-SIMS). The optimal concentration of precursors (10 mm ) was determined that resulted in chemically homogeneous, pure nanowebs. Furthermore, the morphology and (un)coordinated Cu sites in the web were tuned by varying the rotation speed of the spin-coating process. X-ray diffraction (XRD) analysis showed that rotation speeds ≥2000 rpm (with precursors in a water/ethanol solution) generate the catena-triaqua-μ-(1,3,5-benzenetricarboxylate)-copper(II), or Cu(BTC)(H 2 O) 3 coordination polymer. X-ray photoelectron spectroscopy (XPS) highlighted the strong decrease in number of (defective) Cu + sites, as the nanowebs mainly consist of coordinated Cu 2+ Lewis acid sites (LAS) and organic linker–linker, for example, hydrogen-bonding, interactions. Finally, the Lewis-acidic character of the Cu sites is illustrated by testing the films as catalysts in the isomerization of α-pinene oxide. The higher number of LAS (≥3000 rpm), result in higher campholenic aldehyde selectivity reaching up to 87.7 %. Furthermore, the strength of a combined micro- and spectroscopic approach in understanding the nature of MOF thin-films in a spatially resolved manner is highlighted.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Theoretical modeling of a bottom-raised oscillating surge wave energy converter structural loadings and power performances

Here, this study presents theoretical formulations to evaluate the fundamental parameters and performance characteristics of a bottom-raised oscillating surge wave energy converter (OSWEC) device. Employing a flat plate assumption and potential flow formulation in elliptical coordinates, closed-form equations for the added mass, radiation damping, and excitation forces/torques in the relevant pitch-pitch and surge-pitch directions of motion are developed and used to calculate the system's response amplitude operator and the forces and moments acting on the foundation. The model is benchmarked against numerical simulations using WAMIT and WEC-Sim, showcasing excellent agreement. The sensitivity of plate thickness on the analytical hydrodynamic solutions is investigated over several thickness-to-width ratios ranging from 1:80 to 1:10. The results show that as the thickness of the benchmark OSWEC increases, the deviation of the analytical hydrodynamic coefficients from the numerical solutions grows from 3% to 25%. Differences in the excitation forces and torques, however, are contained within 12%. While the flat plate assumption is a limitation of the proposed analytical model, the error is within a reasonable margin for use in the design space exploration phase before a higher-fidelity (and thus more computationally expensive) model is employed. A parametric study demonstrates the ability of the analytical model to quickly sweep over a domain of OSWEC dimensions, illustrating the analytical model's utility in the early phases of design.

13 HYDRO ENERGY↗

Transformations of Ti-5Al-5V-5Cr-3Mo powder due to reuse in laser powder bed fusion: A surface analytical approach

Reactive Ti-5Al-5 V-5Cr-3Mo (Ti5553) alloy feedstock powder is used in laser powder-bed fusion (LPBF). Due to the large quantity of powder necessary for LPBF, powder is reused numerous times under oxidizing environments. Transformations to the powder’s native surface oxide may impact the LPBF process and lead to deviations from expected behavior of printed parts. In this work, we present a multimodal characterization of new and reused powder by combining X-ray photoelectron spectroscopy (XPS), time-of-flight secondary ion mass spectrometry (ToF-SIMS), and transmission electron microscopy (TEM) of focused ion beam (FIB)-prepared cross sections of individual powder particles to understand how the surface oxide composition changes, grows, and becomes hydroxylated and hydrated due to reuse. We show that the native oxide film of Ti5553 powder is a hydroxylated mixed oxide composed of TiO 2 and Al 2 O 3 that grows from 5.6 +/- 0.7 nm to 8.3 +/- 1.1 nm due to reuse. Al oxide regions of the surface oxide become more hydroxylated during reuse in comparison to Ti oxide regions. This indicates that an outer oxide of pure TiO 2 may enhance recyclability of Ti5553 powder while the presence of Al oxides may decrease recyclability. Further characterization of surface transformations due to recyclability may eliminate unnecessary variation in LPBF.

36 MATERIALS SCIENCE↗

Comprehensive insights into competitive oxidation/sulfidation reactions on binary ferritic alloys at high temperatures

Interpreting high-temperature corrosion induced by mixed-gas atmospheres is challenging due to the different contributions of oxidizing gases. In this work, a comprehensive study on the combined oxidation/sulfidation using label molecules is presented. Fe-Cr model alloys with 2 wt% and 9 wt% Cr were isothermally exposed using a volumetric mixture of 0.5%S 16 O 2 /27%H 2 18 O and 0.5%S 16 O 2 /7%H 2 18 O at 650 °C for 5 h and then characterized by secondary ion mass spectroscopy (SIMS). Additionally, the reactions were followed in-situ utilizing energy dispersive X-ray diffraction. The study showed that both S 16 O 2 and H 2 18 O contribute to the oxidation of the alloys but to different extents depending on the Cr-content.

36 MATERIALS SCIENCE↗

Large isotopic variability at the micron-scale in ‘Shuram’ excursion carbonates from South Australia

Ediacaran-aged (635–541 million years ago) marine sediments contain a large negative carbon isotope (δ 13 C) excursion, in which carbonate δ 13 C values reach -12‰ (VPDB). Known as the ‘Shuram’ excursion, many workers have interpreted this δ 13 C record as an unprecedented perturbation to the global carbon cycle, leading to speculation about a causal connection to the broadly contemporaneous rise of animal life. Others have interpreted the δ 13 C signal as a product of diagenesis, thereby minimizing its relevance for understanding the evolution of metazoans. In this work, we present SEM imaging and in-situ δ 13 C and δ 18 C values measured by secondary ion mass spectrometry (SIMS) to assess these competing hypotheses in the Wonoka Formation of South Australia. Our results from the minimum of the excursion show that rounded sedimentary grains of calcite have δ 13 C values between -12.8 to -10.6‰ and δ 18 C values between 17.8 to 15.5‰ (VPDB). Euhedral dolomite that appears to have grown unimpeded in open sedimentary pore spaces also is present. These early-stage dolomites are interpreted as early authigenic in origin and have δ 13 C values that reach +5‰, requiring a formation fluid with a substantially different δ 13 C composition from basin waters or bulk sediment. Together, these results provide little evidence for the hypothesis that a late diagenetic overprint has generated the ‘Shuram’ excursion in the Wonoka. Instead, they suggest the presence of a large carbon isotopic gradient in the surface environment, with shallow waters capable of precipitating carbonates with very low δ 13 C (down to 12‰) and deeper shelf and/or marine pore waters generating carbonates with positive carbon isotope values (up to +5‰). Because negative isotope excursions of similar magnitude are found in widely dispersed Ediacaran basins, it is likely that this gradient was characteristic of shelf environments of this period and that a still-unknown global process led to the ‘Shuram’ excursion in shallow water carbonates.

58 GEOSCIENCES↗

Submicron Sodium Banding in Cultured Planktic Foraminifera Shells

The calcite shells, or tests, of foraminifera provide a window into Earth history because they are well preserved in marine sediments and contain useful geochemical proxies for paleoceanography. Previous observations of diurnal heterogeneity in proxies like Mg/Ca demonstrate a complex relationship between environmental conditions and test composition. The definitive causes for this diurnal banding and the potential impact for proxy interpretation in systems other than Mg/Ca have yet to be determined. Here we use time-of-flight secondary ion mass spectrometry (ToF-SIMS), a chemical and isotope mapping technique with a spatial resolution of 300 nm, to show that Na banding is a consistent feature in the tests of cultured Orbulina universa, a species of planktic foraminifer. This banding occurs in two distinct forms: (1) sharp Na bands associated with embedded organic sheets and (2) regular, thicker, but lower-amplitude Na bands that are found throughout the test. In Orbulina bilobata, a morphotype of O. universa that develops a second partial spherical chamber attached to the primary sphere, we use the first type of banding to show that a second organic sheet is used as a template to form this second chamber. Thus, sodium banding links test geochemistry with foraminiferal growth models, allowing us to explain the pattern and timing of chamber formation as well as a specific type of geochemical banding in foraminifera. Furthermore, the magnitude, timing, and coherency between Na and Mg bands can help constrain mechanistic explanations for geochemical banding in foraminifera in general.

paleoclimate, Foraminifera, biomineralization, pal↗

Microstructural, mechanical and optical properties research of a carbon ion-irradiated Y 2 SiO 5 crystal

Ion irradiation has been a popular method to modify properties of different kinds of materials. Ion-irradiated crystals have been studied for years, but the effects on microstructure and optical properties during irradiation process are still controversial. In this study, we used 6 MeV C ions with a fluence of 1 × 10 15 ion/cm 2 irradiated Y 2 SiO 5 (YSO) crystal at room temperature, and discussed the influence of C ion irradiation on the microstructure, mechanical and optical properties of YSO crystal by Rutherford backscattering/channeling analyzes (RBS/C), X-ray diffraction patterns (XRD), Raman, nano-indentation test, transmission and absorption spectroscopy, the prism coupling and the end-facet coupling experiments. We also used the secondary ion mass spectrometry (SIMS) to analyze the elements distribution along sputtering depth. Finally, 6 MeV C ions with a fluence of 1 × 10 15 ion/cm 2 irradiated caused the deformation of YSO structure and also influenced the spectral properties and lattice vibrations.

46 INSTRUMENTATION RELATED TO NUCLEAR SCIENCE AND ↗

Evolution of aqSOA from the Air–Liquid Interfacial Photochemistry of Glyoxal and Hydroxyl Radicals

The effect of photochemical reaction time on glyoxal and hydrogen peroxide at the aqueous surface is investigated using in situ time-of-flights Secondary ion mass spectrometry (ToF-SIMS) enabled by a system for analysis at the liquid vacuum interface (SALVI) microreactor. Carboxylic acids (i.e., glyoxylic acid, oxalic acid, malonic acid, tartaric acid) are observed in the initial reactions (i.e., < 3 h.), more oligomers, cluster ions, and water clusters formed in the long ultraviolet (UV) aging period (i.e., = 3 h). Our results provide the direct evidence that water clusters could promote proton transfer and facilitate the formation of oligomers and cluster ions in the aqeous environment as photochemical aging continues. Furthermore, new chemical reaction pathways are proposed to expand existing understanding. The temporal evolution shows that oxidation products such as carboxylic acids reach a maximum in 1 h, whereas oligomer yields peak in 3 to 4 h. Glyoxal not only undergoes oxidation to form carboxylic acids (mainly occurred in the aging time less than 3 h), but also takes part in radical reactions, hemiacetal, oligomerization, polymerization, esterification, and anhydride reactions to form higher molecular weight species. Our in situ findings verify that the air-liquid interfacial reactions are important pathways for aqueous secondary organic aerosol (aqSOA) formation.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗