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Dag Noréus

Publications and source records attributed to Dag Noréus.

4 recordsLinked to original sources

Reaction of hydrogen gas with C60 at elevated pressure and temperature: hydrogenation and cage fragmentation.

Products of the reaction of C(60) with H(2) gas have been monitored by high-resolution atmospheric pressure photoionization Fourier transform ion cyclotron resonance mass spectrometry (APPI FT-ICR MS), X-ray diffraction, and IR spectroscopy as a function of hydrogenation period. Samples were synthesized at 673 K and 120 bar hydrogen pressure for hydrogenation periods between 300 and 5000 min, resulting in the formation of hydrofullerene mixtures with hydrogen content ranging from 1.6 to 5.3 wt %. Highly reduced C(60)H(x) (x > 36-40) and products of their fragmentation were identified in these samples by APPI FT-ICR MS. A sharp change in structure was observed for samples with at least 5.0 wt % of hydrogen. Low-mass (300-500 Da) hydrogenation products not observed by prior field desorption (FD) FT-ICR MS were detected by APPI FT-ICR MS and their elemental compositions obtained for the first time. Synthetic and analytical fragmentation pathways are discussed.

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Polyanionic hydrides from polar intermetallics AeE2 (Ae = Ca, Sr, Ba; E = Al, Ga, In).

The hydrogenation behavior of the polar intermetallic systems AeE2 (Ae = Ca, Sr, Ba; E = Al, Ga, In) has been investigated systematically and afforded the new hydrides SrGa2H2 and BaGa2H2. The structure of these hydrides was characterized by X-ray powder diffraction and neutron diffraction of the corresponding deuterides. Both compounds are isostructural to previously discovered SrAl2H2 (space group P3m1, Z = 1, SrGa2H2/D2: a = 4.4010(4)/4.3932(8) A, c = 4.7109(4)/4.699(1) A; BaGa2H2/D2: a = 4.5334(6)/4.5286(5) A, c = 4.9069(9)/4.8991(9) A). The three hydrides SrAl2H2, SrGa2H2, and BaGa2H2 decompose at around 300 degrees C at atmospheric pressure. First-principles electronic structure calculations reveal that H is unambiguously part of a two-dimensional polyanion [E2H2]2- in which each E atom is tetrahedrally coordinated by three additional E atoms and H. The compounds AeE2H2 are classified as polyanionic hydrides. The peculiar feature of polyanionic hydrides is the incorporation of H in a polymeric anion where it acts as a terminating ligand. Polyanionic hydrides provide unprecedented arrangements with both E-E and E-H bonds. The hydrogenation of AeE2 to AeE2H2 takes place at low reaction temperatures (around 200 degrees C), which suggests that the polyanion of the polar intermetallics ([E2]2-) is employed as precursor.

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Bonding and stability of the hydrogen storage material Mg(2)NiH(4).

Structural stability and bonding properties of the hydrogen storage material Mg(2)NiH(4) (monoclinic, C2/c, Z = 8) were investigated and compared to those of Ba(2)PdH(4) (orthorhombic, Pnma, Z = 8) using ab initio density functional calculations. Both compounds belong to the family of complex transition metal hydrides. Their crystal structures contain discrete tetrahedral 18 electron complexes T(0)H(4)(4-) (T = Ni, Pd). However, the bonding situation in the two systems was found to be quite different. For Ba(2)PdH(4), the electronic density of states mirrors perfectly the molecular states of the complex PdH(4)(4-), whereas for Mg(2)NiH(4) a clear relation between molecular states of TH(4)(4-) and the density of states of the solid-state compound is missing. Differences in bonding of Ba(2)PdH(4) and Mg(2)NiH(4) originate in the different strength of the T-H interactions (Pd[bond]H interactions are considerably stronger than Ni[bond]H ones) and in the different strength of the interaction between the alkaline-earth metal component and H (Ba[bond]H interactions are substantially weaker than Mg[bond]H ones). To lower the hydrogen desorption temperature of Mg(2)NiH(4), it is suggested to destabilize this compound by introducing defects in the counterion matrix surrounding the tetrahedral Ni(0)H(4)(4-) complexes. This might be achieved by substituting Mg for Al.

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