Rubidium oxide is the chemical compound with the formula . Rubidium oxide is highly reactive towards water, and therefore it would not be expected to occur naturally. The rubidium content in minerals is often calculated and quoted in terms of . In reality, the rubidium is typically present as a component of (actually, an impurity in) silicate or aluminosilicate. A major source of rubidium is lepidolite, , wherein Rb sometimes replaces K.
is a yellow colored solid. The related species , and are colorless, pale-yellow, and orange, respectively.
The alkali metal oxides crystallise in the antifluorite structure. In the antifluorite motif, the positions of the anions and cations are reversed relative to their positions in CaF<sub>2</sub>, with rubidium ions 4-coordinate (tetrahedral) and oxide ions 8-coordinate (cubic).
Like other alkali metal oxides, Rb<sub>2</sub>O is a strong base. Thus, Rb<sub>2</sub>O reacts exothermically with water to form rubidium hydroxide.
So reactive is Rb<sub>2</sub>O toward water that it is considered hygroscopic. Upon heating, Rb<sub>2</sub>O reacts with hydrogen to rubidium hydroxide and rubidium hydride:
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 Rb<sub>2</sub>O does not entail oxidation of the metal but reduction of the anhydrous nitrate:
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:
Metallic Rb reacts with O<sub>2</sub>, as indicated by its tendency to rapidly tarnish in air. The tarnishing process is relatively colorful as it proceeds via bronze-colored Rb<sub>6</sub>O and copper-colored Rb<sub>9</sub>O<sub>2</sub>. The suboxides of rubidium that have been characterized by X-ray crystallography include Rb<sub>9</sub>O<sub>2</sub> and Rb<sub>6</sub>O, as well as the mixed Cs-Rb suboxides Cs<sub>11</sub>O<sub>3</sub>Rb<sub>n</sub> (n = 1, 2, 3).
The final product of oxygenation of Rb is principally RbO<sub>2</sub>, rubidium superoxide:
This superoxide can then be reduced to Rb<sub>2</sub>O using excess rubidium metal: