For laboratory use, RbOH is usually used in place of the oxide. RbOH can be purchased for ca.
US$5/g (2006). The hydroxide is more useful, less reactive toward atmospheric moisture, and less expensive than the oxide. As for most alkali metal oxides, the best synthesis of Rb2O does
not entail oxidation of the metal but reduction of the anhydrous nitrate: :10 Rb + 2 RbNO3 → 6 Rb2O + N2 Typical for alkali metal hydroxides, RbOH
cannot be dehydrated to the oxide. Instead, the hydroxide can be decomposed to the oxide (by reduction of the hydrogen ion) using Rb metal: :2 Rb + 2 RbOH → 2 Rb2O + H2 Metallic Rb reacts with O2, as indicated by its tendency to rapidly
tarnish in air. The tarnishing process is relatively colorful as it proceeds via bronze-colored Rb6O and copper-colored Rb9O2. The
suboxides of rubidium that have been characterized by
X-ray crystallography include Rb9O2 and Rb6O, as well as the mixed
Cs-Rb suboxides Cs11O3Rb
n (
n = 1, 2, 3). The final product of oxygenation of Rb is principally RbO2,
rubidium superoxide: :Rb + O2 → RbO2 This superoxide can then be reduced to Rb2O using excess rubidium metal: :3 Rb + RbO2 → 2 Rb2O ==References==