What Dictates Rashba Splitting in 2D van der Waals Heterobilayers

Sunny Gupta; Boris I Yakobson

doi:10.1021/jacs.0c12809

What Dictates Rashba Splitting in 2D van der Waals Heterobilayers

J Am Chem Soc. 2021 Mar 10;143(9):3503-3508. doi: 10.1021/jacs.0c12809. Epub 2021 Feb 24.

Authors

Sunny Gupta¹, Boris I Yakobson^{1

2

3}

Affiliations

¹ Department of Materials Science and Nanoengineering, Rice University, Houston, Texas 77005, United States.
² Department of Chemistry, Rice University, Houston, Texas 77005, United States.
³ Smalley-Curl Institute for Nanoscale Science and Technology, Rice University, Houston, Texas 77005, United States.

PMID: 33625213
DOI: 10.1021/jacs.0c12809

Abstract

Rashba spin-orbit coupling enables electric control of spin states, promising enormous advances from conventional charge-based computing. Until now, a general scheme or a descriptor to find an optimal system with isolated spin states with large tunable splitting is still lacking. Here, based on first-principles calculations, we explore the microscopic physicochemical mechanism responsible for the Rashba effect in 2D van der Waals heterobilayers. We find that the difference in the Born effective charge of atoms at the interface can be used as a single-layer descriptor to predict heteropairs with large Rashba splitting, thus reducing the scaling factor in materials search. Moreover, we discover that for most 2D materials, the routinely used Rashba parameter α_R is not a good gauge of the effect's strength. From our general scheme, MoTe₂|Tl₂O and MoTe₂|PtS₂, with spin splitting above 120 meV, Rashba energy E_R = 94 meV, and wavenumber difference 2k₀ = 0.36 Å^-1 ("effective" α_R > 1 eVÅ), emerge as the best candidates for spin transistors at room temperature.