The Key Role of U28 in the Aqueous Self‐Assembly of Uranyl Peroxide Nanocages |
| |
| Authors: | Clément Falaise Dr May Nyman |
| |
| Affiliation: | Energy Frontier Research Center, Materials Science of Actinides, Department of Chemistry, Oregon State University, Corvallis, Oregon, United States |
| |
| Abstract: | For 11 years now, the structural diversity and aesthetic beauty of uranyl–peroxide capsules have fascinated researchers from the diverse fields of mineralogy, polyoxometalate chemistry, and nuclear fuel technologies. There is still much to be learned about the mechanisms of the self‐assembly process, and the role of solution parameters including pH, alkali template, temperature, time, and others. Here we have exploited the high solubility of the UO22+/H2O2/LiOH aqueous system to address the effect of the hydroxide concentration. Important techniques of this study are single‐crystal X‐ray diffraction, small‐angle X‐ray scattering, and Raman spectroscopy. Three key phases dominate the solution speciation as a function of time and the LiOH/UO22+ ratio: the uranyl–triperoxide monomer UO2(O2)3]4?and the two capsules (UO2)(O2)(OH)]2424?(U24) and (UO2)(O2)1.5]2828?(U28). When the LiOH/U ratio is around three, U28 forms rapidly and this cluster can be isolated in high yield and purity. This result was most surprising and challenges the hypothesis that alkali templating is the most important determinant in the cluster geometry. Moreover, analogous experiments with KOH, NH4OH, and TEAOH (TEA=tetraethylammonium) also rapidly yield U28, which suggests that U28 is the kinetically favored species. Complete mapping of the pH–time phase space reveals only a narrow window of the U28 dominance, which is why it was previously overlooked as an important kinetic species in this chemical system, as well as others with different counterions. |
| |
| Keywords: | cations cluster compounds self-assembly small-angle x-ray scattering uranium |
|
|
