Tuning of Structural Transition Pressure and Electronic Properties of Alkaline Earth Chalcogenides by Isoelectronic Substitution

被引:5
作者
Nag, Abhinav [1 ]
Kumari, Anuja [1 ]
Kumar, Jagdish [1 ]
机构
[1] Cent Univ Himachal Pradesh, Dept Phys & Astron Sci, Shahpur, India
关键词
Dirac point; band structure; spin-orbit interaction; equation of state; alkaline earth chalcogenides; density functional theory; TOPOLOGICAL DIRAC SEMIMETAL; BAND-STRUCTURE CALCULATIONS; ELASTIC PROPERTIES; CALCIUM CHALCOGENIDES; INDUCED METALLIZATION; AB-INITIO; EQUATION; STATE; SRSE; 1ST-PRINCIPLES;
D O I
10.1007/s11664-020-08196-6
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
CaTe exhibits Dirac-like linear dispersion in a simple cubic CsCl-type structure which is stable above pressure of 33 GPa. In the present paper, we have studied all the alkaline earth metal chalcogenides to check for the possibility of a structural transition pressure (P-s) below 33 GPa and also exhibiting Dirac-like linear dispersions as in CaTe. Our results show that a larger cation or anion increases the unit cell volume and lowers the P-s and vice versa. Although the P-s can be lowered by isoelectronic substitution, the Dirac-like electronic band dispersion around P-s is exhibited only by SrTe at 17 GPa which is almost half the P-s for CaTe. Interestingly, our study finds that in absence of spin-orbit interaction all studied alkaline chalcogenides exhibit Dirac-like dispersions at pressures ranging from 17 GPa for SrTe to 650 GPa for CaS, whereas a few retain Dirac-like dispersion even under the effect of spin-orbit interaction.
引用
收藏
页码:4773 / 4784
页数:12
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