Plasma-assisted atomic layer deposition ͑ALD͒ of metal oxide films is increasingly gaining interest, however, the underlying reaction mechanisms have rarely been addressed. In this work, a case study is presented for the plasma-assisted ALD process of Al 2 O 3 based on Al͑CH 3 ͒ 3 dosing and O 2 plasma exposure. A complementary set of time-resolved in situ diagnostics was employed, including spectroscopic ellipsometry, quartz crystal microbalance, mass spectrometry, and optical emission spectroscopy. The saturation of the Al͑CH 3 ͒ 3 adsorption reactions was investigated, as well as the reaction products created during both the precursor dosing and the plasma exposure step. The generality of the observations was cross-checked on a second commercial ALD reactor. The main observations are as follows: ͑i͒ during the precursor dosing, the Al͑CH 3 ͒ 3 predominantly binds bifunctionally to the surface at 70°C through a reaction in which H is abstracted from the surface and CH 4 is released into the gas phase; ͑ii͒ during the plasma exposure, O radicals in the plasma are consumed at the surface by combustionlike reactions with the surface −CH 3 ligands, producing mainly H 2 O, CO 2 , and CO; ͑iii͒ small gas phase densities of CH 4 and higher hydrocarbons ͑C 2 H x ͒ are also present during the O 2 plasma exposure step indicating complementary surface reactions including a secondary thermal ALD-like reaction by the H 2 O produced at the surface; ͑iv͒ the plasma and its optical emission are strongly affected by the surface reaction products released in the plasma. In the latter respect, optical emission spectroscopy proved to be a valuable tool to study the surface reaction products during the plasma exposure as well as the saturation of the surface reactions. The implications of the experimental observations are addressed and it is discussed that the reaction mechanisms are generic for plasma-assisted ALD processes based on metal organic precursors and O 2 plasma as oxidant source.