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Novel Interstitial Mg–TM (TM = Ti, Zr, Hf, V, Nb and Ta) Hydrides with an FCC Structure and CaNiH3 with a Perovskite Structure

Sato, Toyoto, 1978- (författare)
Stockholms universitet,Institutionen för fysikalisk kemi, oorganisk kemi och strukturkemi
Noréus, Dag, Professor (preses)
Stockholms universitet,Institutionen för fysikalisk kemi, oorganisk kemi och strukturkemi
Hauback, Bjørn C., Professor (opponent)
Institute for Energy Technology
 (creator_code:org_t)
ISBN 9171552723
Stockholm : Institutionen för fysikalisk kemi, oorganisk kemi och strukturkemi, 2006
Engelska 52 s.
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)
Abstract Ämnesord
Stäng  
  • This thesis is focused on structural investigations of novel interstitial ternary alkaline-earth–transition metal hydrides formed by immiscible metals that are held together by the presence of hydrogen atoms. The contents are divided in two parts: Metastable Mg-based hydrides, in which transition-metal additives improve hydrogen storage properties; and a new Ca–Ni hydride, CaNiH3, with a perovskite structure, in which hydrogen enables a Ca:Ni =1:1 ratio although no such alloy composition exists.New ternary Mg-based hydride with an additive of either Ti, Zr, Hf, V, Nb or Ta were synthesized in a high-pressure anvil cell at 4–8 GPa and 600 ºC. All hydrides had an FCC metal atom structure with an axis of about 4.8 Å. This corresponds to an assumed high-pressure MgH2 phase that is stable at a pressure above 3.6 GPa (P. Vajeeston, P. Ravindran, A. Kjekshus, H. Fjellvåg, Phys. Rev. Lett. 89 (2002) 175506). Ordering of the metal atoms in the lattice leads to a doubling of the FCC unit cell all axis, and the metal atom structure of the hydrides (excluding Zr doped hydride) can be described by the Ca7Ge-type structure. Hydrogen atom arrangements at two tetrahedral sites were found from a powder X-ray diffraction pattern obtained with synchrotron radiation. One of the tetrahedral sites coordinates one TM atom and three Mg atoms, and the other coordinates four Mg atoms.CaNiH3 crystallizes with a cubic unit cell: a = 3.544(1) Å, V = 44.51(4) Å3 and Z = 1 in space group Pm-3m (No. 221). The hydrogen positions were determined from CaNiD3, using powder neutron diffraction, and the hydride was of an ideal perovskite ABH3 type. It was stabilized by a polyanionic framework of [NiH3]2- counterbalanced by Ca2+ cations. Total-energy calculations of the electronic structure showed that the hydride was a metallic conductor due to a half-filled Ni-H antibonding eg band.

Ämnesord

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)

Nyckelord

Metal hydrides
Mg-based hydrides
a new Ca-Ni hydride
Chemistry
Kemi

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