Optical excitation of single- and multi-mode magnetization precession in Fe-Ga nanolayers

We demonstrate a variety of precessional responses of the magnetization to ultrafast optical excitation in nanolayers of Galfenol (Fe,Ga), which is a ferromagnetic material with large saturation magnetization and enhanced magnetostriction. The particular properties of Galfenol, including cubic magnetic anisotropy and weak damping, allow us to detect up to 6 magnon modes in a 120nm layer, and a single mode with effective damping _eff = 0.005 and frequency up to 100 GHz in a 4- nm layer. This is the highest frequency observed to date in time-resolved experiments with metallic ferromagnets. We predict that detection of magnetisation precession approaching THz frequencies should be possible with Galfenol nanolayers

Breathing Current Domains in Globally Coupled Electrochemical Systems: A Comparison with a Semiconductor Model

Spatio-temporal bifurcations and complex dynamics in globally coupled intrinsically bistable electrochemical systems with an S-shaped current-voltage characteristic under galvanostatic control are studied theoretically on a one-dimensional domain. The results are compared with the dynamics and the bifurcation scenarios occurring in a closely related model which describes pattern formation in semiconductors. Under galvanostatic control both systems are unstable with respect to the formation of stationary large amplitude current domains. The current domains as well as the homogeneous steady state exhibit oscillatory instabilities for slow dynamics of the potential drop across the double layer, or across the semiconductor device, respectively. The interplay of the different instabilities leads to complex spatio-temporal behavior. We find breathing current domains and chaotic spatio-temporal dynamics in the electrochemical system. Comparing these findings with the results obtained earlier for the semiconductor system, we outline bifurcation scenarios leading to complex dynamics in globally coupled bistable systems with subcritical spatial bifurcations.Comment: 13 pages, 11 figures, 70 references, RevTex4 accepted by PRE http://pre.aps.or

Exploring the Bimodal Solar System via Sample Return from the Main Asteroid Belt: The Case for Revisiting Ceres

Abstract: Sample return from a main-belt asteroid has not yet been attempted, but appears technologically feasible. While the cost implications are significant, the scientific case for such a mission appears overwhelming. As suggested by the “Grand Tack” model, the structure of the main belt was likely forged during the earliest stages of Solar System evolution in response to migration of the giant planets. Returning samples from the main belt has the potential to test such planet migration models and the related geochemical and isotopic concept of a bimodal Solar System. Isotopic studies demonstrate distinct compositional differences between samples believed to be derived from the outer Solar System (CC or carbonaceous chondrite group) and those that are thought to be derived from the inner Solar System (NC or non-carbonaceous group). These two groups are separated on relevant isotopic variation diagrams by a clear compositional gap. The interface between these two regions appears to be broadly coincident with the present location of the asteroid belt, which contains material derived from both groups. The Hayabusa mission to near-Earth asteroid (NEA) (25143) Itokawa has shown what can be learned from a sample-return mission to an asteroid, even with a very small amount of sample. One scenario for main-belt sample return involves a spacecraft launching a projectile that strikes an object and flying through the debris cloud, which would potentially allow multiple bodies to be sampled if a number of projectiles are used on different asteroids. Another scenario is the more traditional method of landing on an asteroid to obtain the sample. A significant range of main-belt asteroids are available as targets for a sample-return mission and such a mission would represent a first step in mineralogically and isotopically mapping the asteroid belt. We argue that a sample-return mission to the asteroid belt does not necessarily have to return material from both the NC and CC groups to viably test the bimodal Solar System paradigm, as material from the NC group is already abundantly available for study. Instead, there is overwhelming evidence that we have a very incomplete suite of CC-related samples. Based on our analysis, we advocate a dedicated sample-return mission to the dwarf planet (1) Ceres as the best means of further exploring inherent Solar System variation. Ceres is an ice-rich world that may be a displaced trans-Neptunian object. We almost certainly do not have any meteorites that closely resemble material that would be brought back from Ceres. The rich heritage of data acquired by the Dawn mission makes a sample-return mission from Ceres logistically feasible at a realistic cost. No other potential main-belt target is capable of providing as much insight into the early Solar System as Ceres. Such a mission should be given the highest priority by the international scientific community

Amino acid composition, petrology, geochemistry, C-14 terrestrial age and oxygen isotopes of the Shi∫r 033 CR chondrite

We have analyzed Shi∫r 033, a CR chondrite from the Omani desert, using several different analytical techniques designed to study the degree of terrestrial alteration of this meteorite and also its petrologic classification. Bulk chemical analyses (including organic carbon and mean total H2O content) are consistent with a CR classification. Additionally, oxygen isotope analysis on a bulk sample indicates that Shi∫r 033 is of type CR2. Amino acid analysis using liquid chromatography with UV fluorescence detection (HPLC-FD) and liquid chromatography-time of flight-mass spectrometry (LC-ToF-MS) show that the absolute and the relative amino acid content of Shi∫r 033 is distinct from other carbonaceous chondrites. Oxygen isotope analysis of a phyllosilicate-rich dark inclusion shows that this inclusion is closer to CV3 or CO3 chondrites. The effects of terrestrial weathering in Shi∫r 033 are evident from the dark inclusion carbon isotopic data, bulk chemistry (through the elevated concentrations of Sr and Ba), and amino acid data, which suggests extensive amino acid contamination of the meteorite from the fall site soil. Nevertheless, Shi∫r 033 contains a small fraction of indigenous components, as indicated by the presence of the extraterrestrial amino acid α-aminoisobutyric acid (AIB) that was not detected in the Shi∫r soils. Finally, the terrestrial age of Shi∫r 033 was determined and is discussed in the context of high levels of contamination

Sublimation extraction coupled with gas chromatography-mass spectrometry: A new technique for future in situ analyses of purines and pyrimidines on Mars

International audienceWe have developed a sublimation technique coupled with chemical derivatization and gas chromatography mass spectrometry (GC-MS) to detect nucleobases and other volatile organic compounds derived from bacteria in Mars analog materials. To demonstrate this technique, a sample of serpentine inoculated with Escherichia coli (E coli) cells was heated to 500 degrees C for several seconds under Martian ambient pressure. The sublimate was collected on a cold finger, then derivatized and analyzed by GC-MS. We found that adenine, cytosine, thymine and uracil were the most abundant molecules detected in the sublimed E coli extract by GC-MS. In addition, nucleobases were also detected in sublimed extracts of a deep-sea sediment sample, seawater, and soil collected from the Atacama Desert in Chile after heating the samples under the same conditions. Our results indicate that nucleobases can be easily isolated directly from natural samples using sublimation and then detected by GC-MS after chemical derivatization. The sublimation-based extraction technique is one approach that should be considered for use by future in situ instruments designed to detect organic compounds relevant to life in the Martian regolith

Molecular distribution and 13C isotope composition of volatile organic compounds in the Murchison and Sutter's Mill carbonaceous chondrites

Volatile organic compounds (VOCs) are carbon-containing chemicals that may evaporate rapidly at room temperature and standard pressure. Such organic compounds can be preserved inside carbonaceous chondrite matrices. However, unlike meteoritic soluble organic matter (SOM) and insoluble organic matter (IOM), VOCs are typically lost (at least in part) during sample processing (meteorite crushing) and exposure to terrestrial atmosphere and/or solvents. Like SOM and IOM, VOCs can provide valuable insights into the chemical inventory of the meteorite parent body and even the presolar cloud from which our solar system formed, as well as the composition and processes that occurred during the early formation of our solar system and the asteroidal stage. Thus, in this work, we designed and built an instrument that allowed us to access the VOCs present in samples of the carbonaceous chondrites Murchison and Sutter's Mill after mineral disaggregation by means of freeze–thaw cycling. We simultaneously evaluated the abundances and compound-specific 13C-distributions of the volatiles evolving after meteorite powdering at ~20, 60, and 100°C. Carbon monoxide (CO) and methane (CH4) were released from these meteorites as the most abundant VOCs. They were combusted together for analysis and showed positive δ13C values, indicative of their extraterrestrial origins. Carbon dioxide (CO2) was also an abundant VOC in both meteorites, and its isotopic values suggest that it was mainly formed from dissolved carbonates in the samples. We also detected aldehydes, ketones, and aromatic compounds in low amounts. Contrary to Murchison, which mostly yielded VOCs with positive δ13C values, Sutter's Mill yielded VOCs with negative δ13C values. The less enriched 13C isotope composition of the VOCs detected in Sutter's Mill suggest that they are either terrestrial contaminants, such as VOCs in compressed gas dusters and common laboratory solvents, or compounds disconnected from interstellar sources and/or formed through parent body processing. Understanding the relative abundances and determining the molecular distributions and isotopic compositions of free meteoritic VOCs are key in assessing their extraterrestrial origins and those of chondritic SOM and IOM. Our newly developed technique will be valuable in the study of the samples brought to the Earth from carbonaceous asteroid Bennu by NASA's OSIRIS-REx mission. © 2024 The Authors. Meteoritics & Planetary Science published by Wiley Periodicals LLC on behalf of The Meteoritical Society. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.Open access articleThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at [email protected]