Raman and infrared spectra of five uranyl oxyhydroxide hydrates, becquerelite, billietite, curite, schoepite and vandendriesscheite, are reported. The observed bands are attributed to the (UO 2 ) 2+ stretching and bending vibrations, U-OH bending vibrations and H 2 O and (OH) − stretching, bending and libration modes. The U-O bond lengths in uranyls and the O-H· · ·O bond lengths are calculated from the wavenumbers assigned to the stretching vibrations. They are close to the values inferred and/or predicted from the X-ray single-crystal structure. The complex hydrogen-bonding network arrangement was proved in the structures of all the minerals studied. This hydrogen bonding contributes to the stability of these uranyl minerals.