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Title: Survey of the class of isovalent antiperovskite alkaline-earth pnictide compounds

Abstract

The few reported members of the antiperovskite structure class $$Ae_3Pn_APn_B$$ of alkaline earth $(Ae = Ca$,Sr,Ba) pnictides $(Pn = N$,P,As,Sb,Bi) compounds are all based on the $$B$$-site anion $$Pn_B$$ = N. All fit can be categorized as narrow gap semiconductors, making them of interest for several reasons. Because chemical reasoning suggests that more members of this class may be stable, we provide here a density functional theory (DFT) based survey of this entire class of 3 x 5 x 5 compounds. We determine first the relative energetic stability of the distribution of pairs of $Pn$ ions in the $$A$$ and $$B$$ sites of the structure, finding that the $$B$$ site always favors the small pnictogen anion. The trends of the calculated energy gaps with $Ae$ cation and $Pn$ anions are determined, and we study effects of spin-orbit coupling as well as two types of gap corrections to the conventional DFT electronic spectrum. Because there have been suggestions that this class harbors topological insulating phases, we have given this possibility attention and found that energy gap corrections indicate the cubic structures will provide at most a few topological insulators. Structural instability is addressed by calculating phonon dispersion curves for a few compounds, with one outcome being that distorted structures should be investigated further for thermoelectric and topological character. Examples of the interplay between spin-orbit coupling and strain on the topological nature are provided. Finally, a case study of $$Ca_3BiP$$ including the effect of strain illustrates how a topological semimetal can be transformed into topological insulator and Dirac semimetal.

Authors:
 [1];  [1]
  1. Univ. of California, Davis, CA (United States). Dept. of Physics
Publication Date:
Research Org.:
Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States). National Energy Research Scientific Computing Center (NERSC)
Sponsoring Org.:
USDOE Office of Science (SC)
OSTI Identifier:
1544339
Alternate Identifier(s):
OSTI ID: 1415669
Grant/Contract Number:  
AC02-05CH11231
Resource Type:
Accepted Manuscript
Journal Name:
Physical Review B
Additional Journal Information:
Journal Volume: 97; Journal Issue: 3; Journal ID: ISSN 2469-9950
Publisher:
American Physical Society (APS)
Country of Publication:
United States
Language:
English
Subject:
75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY

Citation Formats

Goh, Wen Fong, and Pickett, Warren E. Survey of the class of isovalent antiperovskite alkaline-earth pnictide compounds. United States: N. p., 2018. Web. doi:10.1103/PhysRevB.97.035202.
Goh, Wen Fong, & Pickett, Warren E. Survey of the class of isovalent antiperovskite alkaline-earth pnictide compounds. United States. https://doi.org/10.1103/PhysRevB.97.035202
Goh, Wen Fong, and Pickett, Warren E. Thu . "Survey of the class of isovalent antiperovskite alkaline-earth pnictide compounds". United States. https://doi.org/10.1103/PhysRevB.97.035202. https://www.osti.gov/servlets/purl/1544339.
@article{osti_1544339,
title = {Survey of the class of isovalent antiperovskite alkaline-earth pnictide compounds},
author = {Goh, Wen Fong and Pickett, Warren E.},
abstractNote = {The few reported members of the antiperovskite structure class $Ae_3Pn_APn_B$ of alkaline earth $(Ae = Ca$,Sr,Ba) pnictides $(Pn = N$,P,As,Sb,Bi) compounds are all based on the $B$-site anion $Pn_B$ = N. All fit can be categorized as narrow gap semiconductors, making them of interest for several reasons. Because chemical reasoning suggests that more members of this class may be stable, we provide here a density functional theory (DFT) based survey of this entire class of 3 x 5 x 5 compounds. We determine first the relative energetic stability of the distribution of pairs of $Pn$ ions in the $A$ and $B$ sites of the structure, finding that the $B$ site always favors the small pnictogen anion. The trends of the calculated energy gaps with $Ae$ cation and $Pn$ anions are determined, and we study effects of spin-orbit coupling as well as two types of gap corrections to the conventional DFT electronic spectrum. Because there have been suggestions that this class harbors topological insulating phases, we have given this possibility attention and found that energy gap corrections indicate the cubic structures will provide at most a few topological insulators. Structural instability is addressed by calculating phonon dispersion curves for a few compounds, with one outcome being that distorted structures should be investigated further for thermoelectric and topological character. Examples of the interplay between spin-orbit coupling and strain on the topological nature are provided. Finally, a case study of $Ca_3BiP$ including the effect of strain illustrates how a topological semimetal can be transformed into topological insulator and Dirac semimetal.},
doi = {10.1103/PhysRevB.97.035202},
journal = {Physical Review B},
number = 3,
volume = 97,
place = {United States},
year = {Thu Jan 04 00:00:00 EST 2018},
month = {Thu Jan 04 00:00:00 EST 2018}
}

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Cited by: 20 works
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Figures / Tables:

FIG. 1 FIG. 1: (a) The antiperovskite structure of Ca3BiP with tetragonal compression along (001), the space group becomes $P$4/mmm. Ca2+ ions lie on two nonequivalent sites(blue and green). (b) Band structure and density of states of cubic Ca3BiP, without SOC. P 3p bands provide the lowest valence states, while Bi 6pmore » bands comprise the highest valence states. Ca 4s and 3d orbitals dominate the lower conduction states. The gap of 0.2 eV occurs at $Γ$, throughout the rest of the zone the gap is large.« less

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