Magnetic reconnection is essential to release the flux rope during its ejection. The question remains: how does the magnetic reconnection change the flux rope structure? Following the original study of Qiu et al. (2007), we compare properties of ICME/MC flux ropes measured at 1 AU and properties of associated solar progenitors including flares, filaments, and CMEs. In particular, the magnetic field-line twist distribution within interplanetary magnetic flux ropes is systematically derived and examined. Our analysis shows that for most of these events, the amount of twisted flux per AU in MCs is comparable with the total reconnection flux on the Sun, and the sign of the MC helicity is consistent with the sign of helicity of the solar source region judged from the geometry of post-flare loops. Remarkably, we find that about one half of the 18 magnetic flux ropes, most of them being associated with erupting filaments, have a nearly uniform and relatively low twist distribution from the axis to the edge, and the majority of the other flux ropes exhibit very high twist near the axis, of up to 5 turns per AU, which decreases toward the edge. The flux ropes are therefore not linear force free. We also conduct detailed case studies showing the contrast of two events with distinct twist distribution in MCs as well as different flare and dimming characteristics in solar source regions, and discuss how reconnection geometry reflected in flare morphology may be related to the structure of the flux rope formed on the Sun.
Topotactic phase transformation enables structural transition without losing the crystalline symmetry of the parental phase and provides an effective platform for elucidating the redox reaction and oxygen diffusion within transition metal oxides. In addition, it enables tuning of the emergent physical properties of complex oxides, through strong interaction between the lattice and electronic degrees of freedom. In this communication, the electronic structure evolution of SrFeO epitaxial thin films is identified in real-time, during the progress of reversible topotactic phase transformation. Using real-time optical spectroscopy, the phase transition between the two structurally distinct phases (i.e., brownmillerite and perovskite) is quantitatively monitored, and a pressure-temperature phase diagram of the topotactic transformation is constructed for the first time. The transformation at relatively low temperatures is attributed to a markedly small difference in Gibbs free energy compared to the known similar class of materials to date. This study highlights the phase stability and reversibility of SrFeO thin films, which is highly relevant for energy and environmental applications exploiting the redox reactions.
Transition-metal oxides (TMOs) with brownmillerite (BM) structures possess one-dimensional oxygen vacancy channels (OVCs), which play a key role in realizing high ionic conduction at low temperatures. The controllability of the vacancy channel orientation, thus, possesses a great potential for practical applications and would provide a better visualization of the diffusion pathways of ions in TMOs. In this study, the orientations of the OVCs in BM-SrFeO are stabilized along two crystallographic directions of the epitaxial thin films. The distinctively orientated phases are found to be highly stable and exhibit a considerable difference in their electronic structures and optical properties, which could be understood in terms of orbital anisotropy. The control of the OVC orientation further leads to modifications in the hydrogenation of the BM-SrFeO thin films. The results demonstrate a strong correlation between crystallographic orientations, electronic structures, and ionic motion in the BM structure.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.