Structure and chemical bonding in MgNi2H3 from combined high resolution synchrotron and neutron diffraction studies and ab initio electronic structure calculations. (1st October 2015)

• Record Type: Journal Article
• Authors: Yartys, V.A.; Antonov, V.E.; Chernyshov, D.; Crivello, J.-C.; Denys, R.V.; Fedotov, V.K.; Gupta, M.; Kulakov, V.I.; Latroche, M.; Sheptyakov, D.
• Is Part Of: Acta materialia. Volume 98(2015)
• Page Start: 416
• Page End: 422
• Publication Date: 2015-10-01
• Subjects: Metal hydrides -- Crystal structure -- High pressures -- Neutron diffraction -- DFT -- Phonon -- Magnesium -- Nickel; Materials -- Periodicals; Materials science -- Periodicals; Materials -- Mechanical properties -- Periodicals; Metallurgy -- Periodicals; Chemistry, Inorganic -- Periodicals; 620.112
• DOI: 10.1016/j.actamat.2015.07.053
• Languages: English
• ISSNs: 1359-6454

Abstract

Graphical abstract: In the orthorhombic crystal structure of MgNi2 D3, D atoms occupy Mg4 Ni2 octahedra and have a chair Ni4 configuration for the atoms located within the buckled Ni–H nets. DFT and phonon calculations showed that the Cmca structure of MgNi2 D3 is the most stable, both from the electronic structure and the lattice dynamic arguments. The stability of the Cmca crystal structure of MgNi2 H3 is enhanced by the formation of the directional Ni–H covalent bonds supplemented by the electron transfer from Mg to both Ni and H. Abstract: Our earlier study Yartys et al. (2015) showed that at high hydrogen pressures, hexagonal MgNi2 undergoes a hydrogen assisted phase transition into the orthorhombic MoSi2 -type structure. Here we report on a combined high resolution synchrotron and neutron diffraction investigation of the crystal structure of MgNi2 D3, and ab initio calculation of its electronic structure that revealed the nature of the metal–hydrogen bonding. The diffraction data (293 and 1.8 K) are well described with a Cmca unit cell with H atoms filling the deformed octahedra Mg4 Ni2 and the positions within the buckled nets –Ni–H–Ni–H– penetrating through the structure. DFT and phonon calculations showed that the Cmca structure of MgNi2 D3 is the most stable, both from the electronic structure and the lattice dynamical arguments. The Bader charge analysis indicates an electronic transfer from Mg (−1.59e − ) to Ni (+0.21e − ), H1 (+0.55e − ) and H2 (+0.31e − ). The phonon dispersion curves of MgNi2 H3 show positive frequencies, indicating that the structure is mechanically stable. The calculated gross heat of formation for the Cmca phase of MgNi2 H3 is −37.3 kJ/mol-H2, which makes it more stable by 3 kJ/mol-H2 than the prototype structures tested in Yartys et al. (2015). The stability of the Cmca crystal structure of MgNi2 H3 is enhanced by the formation of the directional Ni–H covalent bonds supplemented by the electron transfer from Mg to both Ni and H. The heat capacity as a function of temperature is obtained by phonon calculation in the quasi-harmonic approximation.