2015年5月
One-Dimensional Oxygen Diffusion Mechanism in Sr2ScGaO5 Electrolyte Explored by Neutron and Synchrotron Diffraction, O-17 NMR, and Density Functional Theory Calculations
JOURNAL OF PHYSICAL CHEMISTRY C
- 巻
- 119
- 号
- 21
- 開始ページ
- 11447
- 終了ページ
- 11458
- 記述言語
- 英語
- 掲載種別
- 研究論文(学術雑誌)
- DOI
- 10.1021/acs.jpcc.5b02173
- 出版者・発行元
- AMER CHEMICAL SOC
We investigated moderate-temperature oxygen diffusion mechanisms in Sr2ScGaO5 with Brownmillerite structure type. From oxygen isotope O-18-O-16 exchange experiments we determined that oxygen mobility sets in above 550 degrees C. Temperature-dependent neutron and X-ray (synchrotron) diffraction experiments allowed us to correlate the oxygen mobility with a subtle phase transition of the orthorhombic room-temperature structure with I2mb space group toward Imma, going along with a disorder of the (GaO4)(infinity)-tetrahedral chains. From lattice dynamical simulations we could clearly evidence that dynamic switching of the (GaO4)(infinity)-tetrahedral chains from its R to L configuration sets in at 600 degrees C, thus correlating oxygen diffusion with the dynamic disorder. Oxygen ion diffusion pathways are thus constrained along the one-dimensional oxygen vacancy channels, which is a different diffusion mechanism compared to that of the isostructural CaFeO2.5, where diffusion of the apical oxygen atoms into the vacant lattice sites are equally involved in the diffusion pathway. The proposed ordered room-temperature structure in I2mb is strongly supported by O-17, Sc-45, and Ga-71 NMR measurements, which indicate the presence of crystallographically unique sites and the absence of local disordering effects below the phase transition. The electric field gradient tensor components measured at the nuclear sites are found to be in excellent agreement with calculated values using the WIEN2k program. The oxygen site assignment has been independently confirmed by O-17{Sc-45} transfer of adiabatic populations double-resonance experiments.
- リンク情報
- ID情報
-
- DOI : 10.1021/acs.jpcc.5b02173
- ISSN : 1932-7447
- Web of Science ID : WOS:000355495600019