| Autor: |
Fan Jing, Bao Kuo, Duan De-Fang, Wang Lian-Cheng, Liu Bing-Bing, Cui Tian |
| Předmět: |
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| Zdroj: |
Chinese Physics B; Aug2012, Vol. 21 Issue 8, p1-9, 9p |
| Abstrakt: |
The previously proposed theoretical and experimental structures, bond characterization, and compressibility of Mg(BH4)2 in a pressure range from 0 to 10 GPa are studied by ab initio density-functional calculations. It is found that the ambient pressure phases of meta-stable I41=amd and unstable P-3m1 proposed recently are extra stable and cannot decompose under high pressure. Enthalpy calculation indicates that the ground state of F222 structure proposed by Zhou et al. [2009 Phys. Rev. B 79 212102] will transfer to I41=amd at 0.7 GPa, and then to a P-3m1 structure at 6.3 GPa. The experimental P6122 structure (-phase) transfers to I41=amd at 1.2 GPa. Furthermore, both I41=amd and P-3m1 can exist as high volumetric hydrogen density phases at low pressure. Their theoretical volumetric hydrogen densities reach 146.351 g H2/L and 134.028 g H2/L at ambient pressure, respectively. The calculated phonon dispersion curve shows that the I41=amd phase is dynamically stable in a pressure range from 0 to 4 GPa and the P-3m1 phase is stable at pressures higher than 1 GPa. So the I41=amd phase may be synthesized under high pressure and retained to ambient pressure. Energy band structures show that they are both always ionic crystalline and insulating with a band-gap of about 5 eV in this pressure range. In addition, they each have an anisotropic compressibility. The c axis of these structures is easy to compress. Especially, the c axis and volume of P-3m1 phase are extraordinarily compressible, showing that compression along the c axis can increase the volumetric hydrogen content for both I41=amd and P-3m1 structures. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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