Interstitial oxygen in oxygen-stoichiometric apatites

被引:107
作者
León-Reina, L
Losilla, ER
Martínez-Lara, M
Bruque, S
Llobet, A
Sheptyakov, DV
Aranda, MAG
机构
[1] Univ Malaga, Dept Quim Inorgan, E-29071 Malaga, Spain
[2] Los Alamos Natl Lab, Manuel Lujan Jr Neutron Scattering Ctr, Los Alamos, NM 87545 USA
[3] ETH, Neutron Scattering Lab, CH-5232 Villigen, Switzerland
[4] PSI, CH-5232 Villigen, Switzerland
关键词
D O I
10.1039/b503374h
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
Several oxy-apatite materials La10-xSrx( TO4)(6)O3-0.5x ( T = Ge, Si; (10-x) = 9.00, 8.80, 8.65 and 8.00) and La-9.33( Si1-xGexO4)(6)O-2( x = 0, 0.5, 0.67) have been prepared as highly crystalline phases. The impedance study showed that all samples are oxide ion conductors. However, bulk conductivities changed by more than 2 orders of magnitude at a given temperature for some compositions. A thorough study on the oxygen sublattices for oxygen-stoichiometric oxy-apatites has been carried out. Constant-wavelength neutron powder diffraction data have been collected for La-9.33( SiO4)(6)O-2. Time-of-flight neutron data have been collected for La-9.33(Si0.5Ge0.5O4)(6)O-2, La8Sr2(SiO4)(6)O-2 and La8Sr2(GeO4)(6)O-2. The room-temperature structures have been derived from joint Rietveld refinements of neutron and laboratory X-ray powder diffraction data. High temperature structures have been obtained only from Rietveld refinements of neutron powder diffraction data. The refinements show that La-9.33( SiO4)(6)O-2 and La-9.33(Si0.5Ge0.5O4)(6)O-2 contain interstitial oxygen, associated to vacancies at the oxygen channels. The amount of interstitial oxygen is negligible in La8Sr2( SiO4)(6)O-2 and La8Sr2(GeO4)(6)O-2. Hence, the novelty of this work is to explain the high oxide conductivity of the lanthanum-deficient samples which it is due to the presence of interstitial oxygens. Lanthanum stoichiometric samples do not have interstitial oxygens and, so, their conductivities are much lower.
引用
收藏
页码:2489 / 2498
页数:10
相关论文
共 47 条
[41]   Single-crystal growth and structure determination of a new oxide apatite, NaLa9(GeO4)6O2 [J].
Takahashi, M ;
Uematsu, K ;
Ye, ZG ;
Sato, M .
JOURNAL OF SOLID STATE CHEMISTRY, 1998, 139 (02) :304-309
[42]   Sensing properties of an oxygen sensor using BaCe0.8Gd0.2O3-α ceramics as electrolytes [J].
Taniguchi, N ;
Yasumoto, E ;
Nakagiri, Y ;
Gamo, T .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1998, 145 (05) :1744-1748
[43]   Preparation and characterisation of apatite-type lanthanum silicates by a sol-gel process [J].
Tao, SW ;
Irvine, JTS .
MATERIALS RESEARCH BULLETIN, 2001, 36 (7-8) :1245-1258
[44]   Effect of Ba and Bi doping on the synthesis and sintering of Ge-based apatite phases [J].
Tolchard, JR ;
Sansom, JEH ;
Slater, PR ;
Islam, MS .
JOURNAL OF SOLID STATE ELECTROCHEMISTRY, 2004, 8 (09) :668-673
[45]   Defect chemistry and oxygen ion migration in the apatite-type materials La9.33Si6O26 and La8Sr2Si6O26 [J].
Tolchard, JR ;
Islam, MS ;
Slater, PR .
JOURNAL OF MATERIALS CHEMISTRY, 2003, 13 (08) :1956-1961
[46]   Characterisation of (CeO2)0.8(GdO1.5)0.2 synthesised using various techniques [J].
Torrens, RS ;
Sammes, NM ;
Tompsett, GA .
SOLID STATE IONICS, 1998, 111 (1-2) :9-15
[47]   Structural derivation and crystal chemistry of apatites [J].
White, TJ ;
Dong, ZL .
ACTA CRYSTALLOGRAPHICA SECTION B-STRUCTURAL SCIENCE CRYSTAL ENGINEERING AND MATERIALS, 2003, 59 :1-16