Speciation and unusual reactivity in PuO2+x

被引:45
|
作者
Conradson, SD
Begg, BD
Clark, DL
Den Auwer, C
Espinosa-Faller, FJ
Gordon, PL
Hess, NJ
Hess, R
Keogh, DW
Morales, LA
Neu, MP
Runde, W
Tait, CD
Veirs, DK
Villella, PM
机构
[1] Los Alamos Natl Lab, Los Alamos, NM 87545 USA
[2] Australian Nucl Sci & Technol Org, Menai, NSW 2234, Australia
[3] CEA Marcoule, F-30207 Bagnols Sur Ceze, France
[4] Pacific NW Natl Lab, Richland, WA 99352 USA
关键词
D O I
10.1021/ic026044l
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Pu L-3 XAFS measurements show that the excess oxygen in single phase PuO2+x occurs as oxo groups with Pu-O distances of 1.83-1.91 Angstrom. This distance and the energy of the edge (via comparison with a large number of related compounds) are more consistent with a Pu(IV/V) than a Pu(IV/VI) mixture. Analogous to Pu(IV) colloids, although the Pu-Pu pair distribution remains single site even when it shows substantial disorder, the Pu-O distribution can display a number of additional shells at specific distances up to 3.4 Angstrom even in high fired materials when no oxo groups are present, implying intrinsic H+/OH-(H2O). The number of oxo atoms increases when samples are equilibrated with humid air at ambient temperature, indicating that the Pu reactivity in this solid system differs notably from that of isolated complexes and demonstrating the importance of nanoscale cooperative phenomena and total free energy in determining its chemical properties.
引用
收藏
页码:3715 / 3717
页数:3
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