Investigation of the Structural Stability of Ion-Implanted Gd2Ti2-xSnxO7 Pyrochlore-Type Oxides by Glancing Angle X-ray Absorption Spectroscopy

被引:15
作者
Aluri, Esther Rani [1 ]
Hayes, John R. [1 ]
Walker, James D. S. [1 ]
Grosvenor, Andrew P. [1 ]
机构
[1] Univ Saskatchewan, Dept Chem, Saskatoon, SK S7N 5C9, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
3D TRANSITION-METALS; K-EDGE XANES; ELECTRONIC-STRUCTURE; 1ST-PRINCIPLES CALCULATION; INDUCED AMORPHIZATION; PHASE-TRANSFORMATION; STANNATE-PYROCHLORES; RADIATION TOLERANCE; NUCLEAR-WASTE; RE2TI2O7; RE;
D O I
10.1021/jp4095497
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
Rare-earth titanate and stannate pyrochlore-type oxides have been investigated in the past for the sequestration of nuclear waste elements because of their resistance to radiation-induced structural damage. In order to enhance this property, it is necessary to understand the effect of radioactive decay of the incorporated actinide elements on the local chemical environment. In this study, Gd2Ti2-xSnxO7 materials have been implanted with Au- ions to simulate radiation-induced structural damage. Glancing angle X-ray absorption near-edge spectroscopy (GA-XANES), glancing angle X-ray absorption fine structure (GA-EXAFS) analysis, and powder X-ray diffraction have been used to investigate changes in the local coordination environment of the metal atoms in the damaged surface layer. Examination of GA-XANES/EXAFS spectra from the implanted Gd2Ti2-xSnxO7 materials collected at various glancing angles allowed for an investigation of how the local coordination environment around the absorbing atoms changed at different depths in the damaged surface layer. This study has shown the usefulness of GA-XANES to the examination of ion-implanted materials and has suggested that Gd2Ti2-xSnxO7 becomes more susceptible to ion-beam-induced structural damage with increasing Sn concentration.
引用
收藏
页码:7910 / 7922
页数:13
相关论文
共 83 条
  • [1] Multiple-scattering approach to Sn L3-edge X-ray absorption near-edge structure (XANES) analyses for organic tin compounds
    Akatsuka, Takuya
    Ushiro, Mayuko
    Nagamatsu, Shin-ichi
    Takahashi, Yoshio
    Fujikawa, Takashi
    [J]. POLYHEDRON, 2008, 27 (14) : 3146 - 3150
  • [2] Aluri ER, 2013, PHYS CHEM CHEM PHYS, V15, P10477, DOI [10.1039/c3cp51250a, 10.1039/c3cρ51250a]
  • [3] An investigation of pyrochlore-type oxides (Yb2Ti2-xFexO7-δ) by XANES
    Aluri, Esther Rani
    Grosvenor, Andrew P.
    [J]. JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS, 2013, 74 (06) : 830 - 836
  • [4] Evolution of extraframework iron species in Fe silicalite 1. Effect of Fe content, activation temperature, and interaction with redox agents
    Berlier, G
    Spoto, G
    Bordiga, S
    Ricchiardi, G
    Fisicaro, P
    Zecchina, A
    Rossetti, I
    Selli, E
    Forni, L
    Giamello, E
    Lamberti, C
    [J]. JOURNAL OF CATALYSIS, 2002, 208 (01) : 64 - 82
  • [5] Investigating the Local Structure of Lanthanoid Hafnates Ln2Hf2O7 via Diffraction and Spectroscopy
    Blanchard, Peter E. R.
    Liu, Sam
    Kennedy, Brendan J.
    Ling, Chris D.
    Avdeev, Max
    Aitken, Jade B.
    Cowie, Bruce C. C.
    Tadich, Anton
    [J]. JOURNAL OF PHYSICAL CHEMISTRY C, 2013, 117 (05) : 2266 - 2273
  • [6] Bunker G., 2010, Introduction to XAFS, DOI DOI 10.1017/CBO9780511809194
  • [7] Pre-edge structure analysis of Ti K-edge polarized X-ray absorption spectra in TiO2 by full-potential XANES calculations
    Cabaret, D
    Joly, Y
    Renevier, H
    Natoli, CR
    [J]. JOURNAL OF SYNCHROTRON RADIATION, 1999, 6 : 258 - 260
  • [8] First-principles calculations of X-ray absorption spectra at the K-edge of 3d transition metals: an electronic structure analysis of the pre-edge
    Cabaret, Delphine
    Bordage, Amelie
    Juhin, Amelie
    Arfaoui, Mounir
    Gaudry, Emilie
    [J]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2010, 12 (21) : 5619 - 5633
  • [9] Carboni R, 2005, PHYS SCRIPTA, VT115, P986
  • [10] SYSTEMATICS OF THE PYROCHLORE STRUCTURE TYPE, IDEAL A2B2X6Y
    CHAKOUMAKOS, BC
    [J]. JOURNAL OF SOLID STATE CHEMISTRY, 1984, 53 (01) : 120 - 129