Aqueous solutions of lithium uranyl triperoxide, Li4[UO2(O2)3] (LiUT), were irradiated
with gamma rays at room temperature and found to form the uranyl peroxide
cage cluster, Li24[(UO2)(O2)(OH)]24 (Li–U24). Raman spectroscopy and 18O labeling were used to identify the Raman-active vibrations
of LiUT. With these assignments, the concentration of LiUT was tracked
as a function of radiation dose. A discrepancy between monomer removal
and cluster formation suggests that the reaction proceeds by the assembly
of an intermediate. Non-negative matrix factorization was used to
separate Raman spectra into components and resulted in the identification
of a unique intermediate species. Much of the conversion appears to
be driven by water radiolysis products, particularly the hydroxyl
radical. This differs from the 18O-labeled copper-catalyzed
formation of U24, which progresses at a steady rate with
no observation of intermediates. Li–U24 in solution
decomposes at high radiation doses resulting in a solid insoluble
product similar to Na-compreignacite, Na2(UO2)6O4(OH)6·7H2O,
which contains uranyl oxyhydroxy sheets.