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  • Spektor, KristinaESRF, France (author)

Na-Ni-H Phase Formation at High Pressures and High Temperatures: Hydrido Complexes [NiH5](3-) Versus the Perovskite NaNiH3

  • Article/chapterEnglish2020

Publisher, publication year, extent ...

  • 2020-04-08
  • AMER CHEMICAL SOC,2020
  • electronicrdacarrier

Numbers

  • LIBRIS-ID:oai:DiVA.org:liu-165956
  • https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-165956URI
  • https://doi.org/10.1021/acsomega.0c00239DOI
  • https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-181822URI

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  • Language:English
  • Summary in:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Funding Agencies|Swedish Research Council (VR)Swedish Research Council [2019-05551]; Swedish Government Strategic Research Area in Materials Science on Advanced Functional Materials at at Linkoping University (Faculty Grant SFO-Mat-LiU) [200900971]; Carl Tryggers Stiftelse (CTS) [16:198, 17:206]
  • The Na-Ni-H system was investigated by in situ synchrotron diffraction studies of reaction mixtures NaH-Ni-H-2 at around 5, 10, and 12 GPa. The existence of ternary hydrogen-rich hydrides with compositions Na3NiH5 and NaNiH3, where Ni attains the oxidation state II, is demonstrated. Upon heating at similar to 5 GPa, face-centered cubic (fcc) Na3NiH5 forms above 430 degrees C. Upon cooling, it undergoes a rapid and reversible phase transition at 330 degrees C to an orthorhombic (Cmcm) form. Upon pressure release, Na3NiH5 further transforms into its recoverable Pnma form whose structure was elucidated from synchrotron powder diffraction data, aided by first-principles density functional theory (DFT) calculations. Na3NiH5 features previously unknown square pyramidal 18- electron complexes NiH53-. In the high temperature fcc form, metal atoms are arranged as in the Heusler structure, and ab initio molecular dynamics simulations suggest that the complexes are dynamically disordered. The Heusler-type metal partial structure is essentially maintained in the low temperature Cmcm form, in which NiH53- complexes are ordered. It is considerably rearranged in the low pressure Pnma form. Experiments at 10 GPa showed an initial formation of fcc Na3NiH5 followed by the addition of the perovskite hydride NaNiH3, in which Ni(II) attains an octahedral environment by H atoms. NaNiH3 is recoverable at ambient pressures and represents the sole product of 12 GPa experiments. DFT calculations show that the decomposition of Na3NiH5 = NaNiH3 + 2 NaH is enthalpically favored at all pressures, suggesting that Na3NiH5 is metastable and its formation is kinetically favored. Ni-H bonding in metallic NaNiH3 is considered covalent, as in electron precise Na3NiH5, but delocalized in the polyanion [NiH3](-).

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  • Crichton, Wilson A.ESRF, France (author)
  • Filippov, StanislavStockholms universitet,Linköpings universitet,Teoretisk Fysik,Tekniska fakulteten,Stockholm Univ, Sweden,Institutionen för material- och miljökemi (MMK),Linköping University, Sweden(Swepub:liu)stafi86 (author)
  • Klarbring, JohanLinköpings universitet,Teoretisk Fysik,Tekniska fakulteten(Swepub:liu)johkl85 (author)
  • Simak, SergeyLinköpings universitet,Teoretisk Fysik,Tekniska fakulteten(Swepub:liu)sersi78 (author)
  • Fischer, AndreasAugsburg Univ, Germany (author)
  • Häussermann, UlrichStockholms universitet,Institutionen för material- och miljökemi (MMK),Stockholm Univ, Sweden(Swepub:su)ulrich (author)
  • ESRF, FranceTeoretisk Fysik (creator_code:org_t)

Related titles

  • In:ACS Omega: AMER CHEMICAL SOC5:15, s. 8730-87432470-1343

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