Tunable electronic structure and topological properties of LnPn (Ln=Ce, Pr, Sm, Gd, Yb; Pn=Sb, Bi). Issue 1 (December 2018)

• Record Type: Journal Article
• Authors: Duan, Xu; Wu, Fan; Chen, Jia; Zhang, Peiran; Liu, Yang; Yuan, Huiqiu; Cao, Chao
• Is Part Of: Communications physics. Volume 1:Issue 1(2018)
• Page Start: 1
• Page End: 7
• Publication Date: 2018-12
• Subjects: Physics -- Periodicals; 530
• DOI: 10.1038/s42005-018-0074-8
• Languages: English
• ISSNs: 2399-3650

Abstract

Abstract Recently, the rare-earth monopnictide compounds LnPn have attracted considerable attention in condensed matter physics studies due to their possible topological properties. We have performed systematic first principles study of the electronic structure and band topology properties of LnPn (Ln=Ce, Pr, Sm, Gd, Yb; Pn=Sb, Bi). Assuming thef -electrons are well localized in these materials, both hybrid functional and modified Becke–Johnson calculations yield electronic structure in good agreement with experimental observations, while generalized gradient approximation calculations severely overestimate the band inversions. From Ce to Yb, a systematic reduction of band inversion with respect to the increasing Ln atomic number is observed, and $${\cal Z}_2$$ Z 2 for CePn and YbPn are [1;000] and [0;000], respectively. In both hybrid functional and modified Becke–Johns calculations, a topologically non-trivial to trivial transition is expected around SmSb for the antimonides and around DyBi for the bismuthides. Such variation is related with lanthanide contraction, but is different from simple pressure effects. Rare-earth monopnictide compounds have attracted attention for diverse physical properties such as low temperature antiferromagnetism. Here, the electronic structure of rare-earth monopnictide compounds is studied using density-functional based first-principles methods to identify the emergence of topological properties.