Crystal and Electronic Structures of A 2 NaIO 6 Periodate Double Perovskites (A = Sr, Ca, Ba): Candidate Wasteforms for I-129 Immobilization

• Published in: Inorganic chemistry Vol. 59; no. 24; pp. 18407 - 18419
• Main Authors: O'Sullivan, Sarah E, Montoya, Eduardo, Sun, Shi-Kuan, George, Jonathan, Kirk, Cameron, Dixon Wilkins, Malin C, Weck, Philippe F, Kim, Eunja, Knight, Kevin S, Hyatt, Neil C
• Format: Journal Article
• Language: English
• Published: United States 21.12.2020
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/acs.inorgchem.0c03044

The synthesis, structure, and thermal stability of the periodate double perovskites A NaIO (A= Ba, Sr, Ca) were investigated in the context of potential application for the immobilization of radioiodine. A combination of X-ray diffraction and neutron diffraction, Raman spectroscopy, and DFT simulations were applied to determine accurate crystal structures of these compounds and understand their relative stability. The compounds were found to exhibit rock-salt ordering of Na and I on the perovskite B-site; Ba NaIO was found to adopt the 3 aristotype structure, whereas Sr NaIO and Ca NaIO adopt the 2 / hettotype structure, characterized by cooperative octahedral tilting. DFT simulations determined the 3 and 2 / structures of Ba NaIO to be energetically degenerate at room temperature, whereas diffraction and spectroscopy data evidence only the presence of the 3 phase at room temperature, which may imply an incipient phase transition for this compound. The periodate double perovskites were found to exhibit remarkable thermal stability, with Ba NaIO only decomposing above 1050 °C in air, which is apparently the highest recorded decomposition temperature so far recorded for any iodine bearing compound. As such, these compounds offer some potential for application in the immobilization of iodine-129, from nuclear fuel reprocessing, with an iodine incorporation rate of 25-40 wt%. The synthesis of these compounds, elaborated here, is also compatible with both current conventional and future advanced processes for iodine recovery from the dissolver off-gas.