Intermetallic phases in a recently developed Al-Li-Cu-Mg alloy have been investigated to understand their roles in the initiation and propagation processes of intergranular corrosion. Corrosion initiation involves trenching formation in the Al matrix
adjacent to the large particles of Al7Cu2(Fe, Mn) phases. These phases containing Li are electrochemically active and susceptible to self-dissolution via a de-alloying mechanism during corrosion process. The subsurface particles of Al7Cu2(Fe, Mn) and Al20Cu2Mn3 phases act as the internal cathodes for continuous corrosion propagation along the particle-matrix interface and the associated grain boundaries. Corrosion propagation along the particle-matrix interface was facilitated by the anodic dissolution of the surrounding Al matrix due to the micro-galvanic interaction with the cathodic intermetallic phases. In addition, T1 (Al2CuLi) precipitates and the isolated particles of Al7Cu2(Fe, Mn) and Al20Cu2Mn3 phases were dissolved along the path of corrosion propagation. The dissolved metal ions were redeposited through the network of crevice.
Charge exchange between highly charged ions and neutral atoms and molecules has been considered as one of the important mechanisms controlling soft X ray emissions in many astrophysical objects and environments. However, for modeling charge exchange
soft X ray emission, the data of n and l resolved state selective capture cross sections are often obtained by empirical and semiclassical theory calculations. With a newly built cold target recoil ion momentum spectroscopy (COLTRIMS) apparatus, we perform a series of measurements of the charge exchange of Ne(8,9)+ ions with He and H2 for collision energy ranging from 1 to 24.75 keV/u. n resolved state selective capture cross-sections are reported. By comparing the measured state selective capture cross sections to those calculated by the multichannel Landau Zener method (MCLZ), it is found that MCLZ calculations are in good agreement with the measurement for the dominant n capture for He target. Furthermore, by using nl resolved cross sections calculated by MCLZ and applying l distributions commonly used in the astrophysical literature to experimentally derived n resolved cross sections, we calculate the soft X ray emissions in the charge exchange between 4 keV/u Ne8+ and He by considering the radiative cascade from the excited Ne7+ ions. Reasonable agreement is found in comparison to the measurement for even and separable models, and MCLZ calculations give results in a better agreement.
Topological materials host fascinating low dimensional gapless states at the boundary. As a prominent example, helical topological edge states (TESs) of two-dimensional topological insulators (2DTIs) and their stacked three-dimensional (3D) equivalen
t, weak topological insulators (WTIs), have sparked research enthusiasm due to their potential application in the next generation of electronics/spintronics with low dissipation. Here, we propose layered superconducting material CaSn as a WTI with nontrivial Z2 as well as nodal line semimetal protected by crystalline non-symmorphic symmetry. Our systematic angle-resolved photoemission spectroscopy (ARPES) investigation on the electronic structure exhibits excellent agreement with the calculation. Furthermore, scanning tunnelling microscopy/spectroscopy (STM/STS) at the surface step edge shows signatures of the expected TES. These integrated evidences from ARPES, STM/STS measurement and corresponding ab initio calculation strongly support the existence of TES in the non-symmorphic nodal line semimetal CaSn, which may become a versatile material platform to realize multiple exotic electronic states as well as topological superconductivity.
Magnetocaloric effect (MCE), magnetization, specific heat, and magnetostriction measurements were performed in both pulsed and steady high magnetic fields to investigate the magnetocaloric properties of Heusler alloys Ni50-xCoxMn31.5Ga18.5 (x = 9 and
9.7). From direct MCE measurements for Ni41Co9Mn31.5Ga18.5 up to 56 T, a steep temperature drop was observed for magnetic-field-induced martensitic transformation (MFIMT), designated as inverse MCE. Remarkably, this inverse MCE is apparent not only with MFIMT, but also in the magnetic-field-induced austenite phase. Specific heat measurements under steady high magnetic fields revealed that the magnetic field variation of the electronic entropy plays a dominant role in the unconventional magnetocaloric properties of these materials. First-principles based calculations performed for Ni41Co9Mn31.5Ga18.5 and Ni45Co5Mn36.7In13.3 revealed that the magnetic-field-induced austenite phase of Ni41Co9Mn31.5Ga18.5 is more unstable than that of Ni45Co5Mn36.7In13.3 and that it is sensitive to slight tetragonal distortion. We conclude that the inverse MCE in the magnetic-field-induced austenite phase is realized by marked change in the electronic entropy through tetragonal distortion induced by the externally applied magnetic field.
The van der Waals ferromagnet Fe$_3$GeTe$_2$ has recently attracted extensive research attention due to its intertwined magnetic, electronic and topological properties. Here, using high-resolution angle-resolved photoemission spectroscopy, we systema
tically investigate the temperature evolution of the electronic structure of bulk Fe$_3$GeTe$_2$. We observe largely dispersive energy bands that are narrowed by a factor of 1.6 compared with ab-initio calculation. Upon heating towards the ferromagnetic transition near 225 K, we observe a massive reduction of quasiparticle coherence in a large energy range, which is attributed to the enhanced magnetic fluctuation in the system. Remarkably, the electron bands barely shift with increasing temperature, which deviates from the exchange splitting picture within the itinerant Stoner model. We argue that the local magnetic moments play a crucial role in the ferromagnetism of Fe$_3$GeTe$_2$, despite its strongly itinerant nature. Our results provide important insights into the electronic and magnetic properties of Fe$_3$GeTe$_2$ and shed light on the generic understanding of itinerant magnetism in correlated materials.
Aims. Our aim is to determine the distance of the UV outflow components from the central source, their abundances and total column density, and the mechanism responsible for their observed absorption variability. Methods. We studied the UV spectra
acquired during the campaign as well as from three previous epochs (2002-2010). Our main analysis tools are ionic column-density extraction techniques and photoionization models (both equilibrium and time-dependent models) based on the code Cloudy. Results. For component 1 (at -600 km/s) our findings include the following: metallicity that is roughly twice solar; a simple model based on a fixed total column-density absorber, reacting to changes in ionizing illumination that matches the different ionic column densities derived from four spectroscopic epochs spanning 13 years; and a distance of R=6+2.5-1.5 pc from the central source. Component 2 (at -1430 km/s) has shallow troughs and is at a much larger R. For component 3 (at -1880 km/s) our findings include: a similar metallicity to component 1; a photoionization-based model can explain the major features of its complicated absorption trough variability and an upper limit of 60 or 150 pc on R. This upper limit is consistent and complementary to the X-ray derived lower limit of 12 or 31 pc for R. The total column density of the UV phase is roughly 1% and 0.1% of the lower and upper ionization components of the warm absorber, respectively. Conclusions. The NGC 7469 outflow shows super-solar metallicity similar to the outflow in Mrk 279, carbon and nitrogen are twice and four times more abundant than their solar values, respectively. Similar to the NGC 5548 case, a simple model can explain the physical characteristics and the variability observed in the outflow.
Magnetic topological quantum materials (TQMs) provide a fertile ground for the emergence of fascinating topological magneto-electric effects. Recently, the discovery of intrinsic antiferromagnetic (AFM) topological insulator MnBi2Te4 that could reali
ze quantized anomalous Hall effect and axion insulator phase ignited intensive study on this family of TQM compounds. Here, we investigated the AFM compound MnBi4Te7 where Bi2Te3 and MnBi2Te4 layers alternate to form a superlattice. Using spatial- and angle-resolved photoemission spectroscopy, we identified ubiquitous (albeit termination dependent) topological electronic structures from both Bi2Te3 and MnBi2Te4 terminations. Unexpectedly, while the bulk bands show strong temperature dependence correlated with the AFM transition, the topological surface states show little temperature dependence and remain gapless across the AFM transition. The detailed electronic structure of MnBi4Te7 and its temperature evolution, together with the results of its sister compound MnBi2Te4, will not only help understand the exotic properties of this family of magnetic TQMs, but also guide the design for possible applications.
Topological quantum materials coupled with magnetism can provide a platform for realizing rich exotic physical phenomena, including quantum anomalous Hall effect, axion electrodynamics and Majorana fermions. However, these unusual effects typically r
equire extreme experimental conditions such as ultralow temperature or sophisticate material growth and fabrication. Recently, new intrinsic magnetic topological insulators were proposed in MnBi2Te4-family compounds - on which rich topological effects could be realized under much relaxed experimental conditions. However, despite the exciting progresses, the detailed electronic structures observed in this family of compounds remain controversial up to date. Here, combining the use of synchrotron and laser light sources, we carried out comprehensive and high resolution angle-resolved photoemission spectroscopy studies on MnBi2Te4, and clearly identified its topological electronic structures including the characteristic gapless topological surface states. In addition, the temperature evolution of the energy bands clearly reveals their interplay with the magnetic phase transition by showing interesting differences for the bulk and surface states, respectively. The identification of the detailed electronic structures of MnBi2Te4 will not only help understand its exotic properties, but also pave the way for the design and realization of novel phenomena and applications.
We report first precision mass measurements of the $1/2^-$ isomeric and $9/2^+$ ground states of $^{101}$In. The determined isomeric excitation energy continues a smooth trend of odd-$A$ indium isotopes up to the immediate vicinity of $N=50$ magic nu
mber. This trend can be confirmed by dedicated shell model calculations only if the neutron configuration mixing is considered. We find that the single particle energies are different for different states of the same isotope. The presented configuration-dependent shell evolution, type II shell evolution, in odd-$A$ nuclei is discussed for the first time. Our results will facilitate future studies of single-particle neutron states.
Isochronous mass spectrometry has been applied in the storage ring CSRe to measure the masses of the neutron-rich $^{operatorname{52-54}}$Sc and $^{54,56}$Ti nuclei. The new mass excess values $ME$($^{52}$Sc) $=$ $-40525(65)$ keV, $ME$($^{53}$Sc) $=$
$-38910(80)$ keV, and $ME$($^{54}$Sc) $=$ $-34485(360)$ keV, deviate from the Atomic Mass Evaluation 2012 by 2.3$sigma$, 2.8$sigma$, and 1.7$sigma$, respectively. These large deviations significantly change the systematics of the two-neutron separation energies of scandium isotopes. The empirical shell gap extracted from our new experimental results shows a significant subshell closure at $N = 32$ in scandium, with a similar magnitude as in calcium. Moreover, we present $ab$ $initio$ calculations using the valence-space in-medium similarity renormalization group based on two- and three-nucleon interactions from chiral effective field theory. The theoretical results confirm the existence of a substantial $N = 32$ shell gap in Sc and Ca with a decreasing trend towards lighter isotones, thus providing a consistent picture of the evolution of the $N = 32$ magic number from the $pf$ into the $sd$ shell.
