High-temperature superconductivity of boron-carbon clathrates at ambient pressure

被引:13
作者
Li, Junda [1 ]
Yue, Jincheng [1 ]
Guo, Siqi [1 ]
Zhang, Ao [2 ]
Zhu, Li [3 ]
Song, Hao [1 ]
Liu, Zhao [1 ]
Liu, Yanhui [1 ]
Cui, Tian [1 ,4 ]
机构
[1] Ningbo Univ, Inst High Pressure Phys, Sch Phys Sci & Technol, Ningbo 315211, Peoples R China
[2] Southeast Univ, Sch Phys, Nanjing 211189, Peoples R China
[3] Rutgers State Univ, Dept Phys, Newark, NJ 07102 USA
[4] Jilin Univ, Coll Phys, State Key Lab Superhard Mat, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
ATOMIC SCREENING CONSTANTS; CRYSTAL-STRUCTURE; LANTHANUM; HYDRIDE; REGION;
D O I
10.1103/PhysRevB.109.144509
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The successful synthesis of the carbon-boron clathrate SrB 3 C 3 under high-pressure conditions of 50 GPa opens up a new possibility for exploring high-temperature superconductors at ambient pressure. Based on the first-principle calculation, we designed a class of LaH 10 -like clathrate compounds Fm 3 m - X B 2 C 8 ( X = K, Rb, Cs, Sr, Ba, Ga, In, Tl, Sn, Pb, and Bi) and investigate their physical properties and potential superconductivities. Our calculations reveal that the dynamic stability of Fm 3 m - X B 2 C 8 at ambient pressure is determined by the degree of compatibility between the host metal X and the carbon-boron sublattices. Especially, p orbitals of the p -region metals can enhance the interaction of the guest atoms with B -C cages, which results in maintaining these clathrates as dynamically stable. Moreover, altering the oxidation states of the guest atoms can adjust the electronic density of states near the Fermi surface, which in turn affects the superconducting transition temperatures ( T c 's) of these compounds. Herein, when filled with + 1 oxidation state metals, the T c 's of X B 2 C 8 ( X = K, Rb, Cs, Ga, In, and Tl) all exceed the liquid-nitrogen boiling point of 77 K and the T c of TlB 2 C 8 is expected to reach 96 K at ambient pressure, which is the highest among the studied carbon-boron compounds.
引用
收藏
页数:8
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