Strontium doping in mullite-type bismuth aluminate: a vacancy investigation using neutrons, photons and electrons

被引:20
作者
Gesing, Thorsten M. [1 ,2 ]
Schowalter, Marco
Weidenthaler, Claudia [3 ]
Murshed, M. Mangir
Nenert, Gwilherm [4 ]
Mendive, Cecilia B. [5 ]
Curti, Mariano [5 ]
Rosenauer, Andreas
Buhl, J. -Christian [2 ]
Schneider, Hartmut [1 ,6 ]
Fischer, Reinhard X. [1 ]
机构
[1] Univ Bremen, Geowissensch FB5, D-28359 Bremen, Germany
[2] Leibniz Univ Hannover, D-30167 Hannover, Germany
[3] Max Planck Inst Kohlenforsch, D-45470 Mulheim, Germany
[4] Inst Max Von Laue Paul Langevin, F-38042 Grenoble 9, France
[5] Univ Nacl Mar del Plata, Dept Quim, Mar Del Plata, Buenos Aires, Argentina
[6] Univ Cologne, D-50939 Cologne, Germany
关键词
OXIDE-ION CONDUCTIVITY; SOLID-STATE NMR; ELECTRICAL-PROPERTIES; POWDER DIFFRACTION; BI2AL4O9; CERAMICS;
D O I
10.1039/c2jm33208f
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report on strontium doped dibismuth-nonaoxoaluminate(III) produced at 1023 K. Partial substitution of bismuth by strontium in the structure yields oxygen vacancies for charge balance. Introducing oxygen vacancies rearranged the associated Al2O7 double-tetrahedra forming "Al3O10" tri-clusters which were identified by multi-quantum Al-27 MAS NMR. Both STEM-EDX and XPS showed homogeneous distribution of strontium in the bulk and on the surface, respectively. Moreover, XPS confirms the valence state of bismuth after doping. The orientations of bismuth 6s(2) lone electron pairs were calculated using DFT methods. The amount of strontium in the crystal structure was further confirmed from the decomposition product SrAl12O19 formed during the temperature-dependent X-ray powder diffraction. The structural proof was carried out by refining the structure of (Bi0.94Sr0.06)(2)Al4O8.94 from powder neutron and X-ray diffraction data. Rietveld refinements clearly showed the under occupation of one oxygen site and the shift of two aluminum atoms from the double-tetrahedra to two tri-cluster sites.
引用
收藏
页码:18814 / 18823
页数:10
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