Hydrogen incorporation into SiO 2 films grown by low-pressure chemical vapor deposition (CVD) from SiH 4 /O 2 mixtures is investigated by means of infrared spectroscopy (IRS), nuclear magnetic resonance (NMR), elastic recoil detection analysis (ERDA), X-ray photoemission spectroscopy (XPS), and nuclear reaction analysis (NRA). We find that hydrogen atoms are preferentially bonded to O atoms, forming bulk SiOH groups, either isolated or clustered, and H 2 O groups, with a minor incorporation of SiH groups, as well as geminal and surface isolated SiOH groups. The proportion of clustered SiOH groups decreases upon increasing the deposition temperature, which has been attributed to the faster dehydroxylation reactions and higher surface mobility of the hydrogenated species involved in the film growth. Using a novel method based on the combination of NRA and ERDA, we verify quantitatively that the predominance of O-H over Si-H bonding implies a slight overstoichiometric character (O/Si atomic ratio > 2) that is accentuated with increasing OH concentration.