Literature DB >> 22691062

Probing cation and vacancy ordering in the dry and hydrated yttrium-substituted BaSnO3 perovskite by NMR spectroscopy and first principles calculations: implications for proton mobility.

Lucienne Buannic1, Frédéric Blanc, Derek S Middlemiss, Clare P Grey.   

Abstract

Hydrated BaSn(1-x)Y(x)O(3-x/2) is a protonic conductor that, unlike many other related perovskites, shows high conductivity even at high substitution levels. A joint multinuclear NMR spectroscopy and density functional theory (total energy and GIPAW NMR calculations) investigation of BaSn(1-x)Y(x)O(3-x/2) (0.10 ≤ x ≤ 0.50) was performed to investigate cation ordering and the location of the oxygen vacancies in the dry material. The DFT energetics show that Y doping on the Sn site is favored over doping on the Ba site. The (119)Sn chemical shifts are sensitive to the number of neighboring Sn and Y cations, an experimental observation that is supported by the GIPAW calculations and that allows clustering to be monitored: Y substitution on the Sn sublattice is close to random up to x = 0.20, while at higher substitution levels, Y-O-Y linkages are avoided, leading, at x = 0.50, to strict Y-O-Sn alternation of B-site cations. These results are confirmed by the absence of a "Y-O-Y" (17)O resonance and supported by the (17)O NMR shift calculations. Although resonances due to six-coordinate Y cations were observed by (89)Y NMR, the agreement between the experimental and calculated shifts was poor. Five-coordinate Sn and Y sites (i.e., sites next to the vacancy) were observed by (119)Sn and (89)Y NMR, respectively, these sites disappearing on hydration. More five-coordinated Sn than five-coordinated Y sites are seen, even at x = 0.50, which is ascribed to the presence of residual Sn-O-Sn defects in the cation-ordered material and their ability to accommodate O vacancies. High-temperature (119)Sn NMR reveals that the O ions are mobile above 400 °C, oxygen mobility being required to hydrate these materials. The high protonic mobility, even in the high Y-content materials, is ascribed to the Y-O-Sn cation ordering, which prevents proton trapping on the more basic Y-O-Y sites.

Entities:  

Year:  2012        PMID: 22691062     DOI: 10.1021/ja304712v

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  3 in total

1.  Crystal structure and proton conductivity of BaSn0.6Sc0.4O3-δ : insights from neutron powder diffraction and solid-state NMR spectroscopy.

Authors:  Francis G Kinyanjui; Stefan T Norberg; Christopher S Knee; Istaq Ahmed; Stephen Hull; Lucienne Buannic; Ivan Hung; Zhehong Gan; Frédéric Blanc; Clare P Grey; Sten G Eriksson
Journal:  J Mater Chem A Mater       Date:  2016-03-16

2.  Joint Experimental and Computational 17O and 1H Solid State NMR Study of Ba2In2O4(OH)2 Structure and Dynamics.

Authors:  Rıza Dervişoğlu; Derek S Middlemiss; Frédéric Blanc; Yueh-Lin Lee; Dane Morgan; Clare P Grey
Journal:  Chem Mater       Date:  2015-05-01       Impact factor: 9.811

3.  On the origin of high ionic conductivity in Na-doped SrSiO3.

Authors:  Po-Hsiu Chien; Youngseok Jee; Chen Huang; Riza Dervişoğlu; Ivan Hung; Zhehong Gan; Kevin Huang; Yan-Yan Hu
Journal:  Chem Sci       Date:  2016-02-17       Impact factor: 9.825

  3 in total

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