Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2023Collinear Rashba-Edelstein effect in nonmagnetic chiral materials9citations
  • 2022Transport signatures and the origin of non-collinear spin texturescitations

Places of action

Chart of shared publication
Jayaraj, Anooja
1 / 1 shared
Cerasoli, Frank T.
1 / 2 shared
Tenzin, Karma
1 / 2 shared
Nardelli, Marco Buongiorno
1 / 4 shared
Sławińska, Jagoda
1 / 12 shared
Chart of publication period
2023
2022

Co-Authors (by relevance)

  • Jayaraj, Anooja
  • Cerasoli, Frank T.
  • Tenzin, Karma
  • Nardelli, Marco Buongiorno
  • Sławińska, Jagoda
OrganizationsLocationPeople

article

Collinear Rashba-Edelstein effect in nonmagnetic chiral materials

  • Jayaraj, Anooja
  • Cerasoli, Frank T.
  • Tenzin, Karma
  • Roy, Arunesh
  • Nardelli, Marco Buongiorno
  • Sławińska, Jagoda
Abstract

Efficient generation and manipulation of spin signals in a given material without invoking external magnetism remain one of the challenges in spintronics. The spin Hall effect (SHE) and Rashba-Edelstein effect (REE) are well-known mechanisms to electrically generate spin accumulation in materials with strong spin-orbit coupling (SOC), but the exact role of the strength and type of SOC, especially in crystals with low symmetry, has yet to be explained. In this study, we investigate REE in three different families of nonmagnetic chiral materials, elemental semiconductors (Te and Se), metal silicides (FeSi and OsSi), and semimetal disilicides (<br/>TaSi<br/>2<br/> and <br/>NbSi<br/>2<br/>), using an approach based on density functional theory. By analyzing spin textures across the full Brillouin zones and comparing them with REE magnitudes calculated as a function of chemical potential, we link specific features in the electronic structure with the efficiency of the induced spin accumulation. Our findings show that magnitudes of REE can be increased by (i) the presence of one particular type of spin-orbit field, for example, Weyl-type SOC that yields a radial spin texture, (ii) high spin polarization of bands along one specific crystallographic direction, and (iii) low band velocities. By comparing materials possessing the same crystal structures but different strengths of SOC, we conclude that larger SOC may indirectly contribute to the enhancement of REE. It yields greater spin splitting of bands along specific crystallographic directions, which prevents canceling the contributions from the oppositely spin-polarized bands over wider energy regions and helps maintain larger REE magnitudes. Surprisingly, however, for some materials, the velocity of electronic states plays an even more important role in regulating the REE magnitudes than SOC. Additionally, these magnitudes are strongly influenced by changes in band topology. We believe that our results will be useful for designing spintronics devices and may aid further computational studies searching for efficient REE in materials with different symmetries and SOC strengths.

Topics
  • density
  • theory
  • semiconductor
  • strength
  • texture
  • density functional theory
  • silicide
  • spin polarization