The oxidation of metals at low temperatures is important not only from a fundamental point of view but also from technological relevance. Recent research has demonstrated that the nanoscale oxidation of metals such as Zr can be significantly altered during photon radiation. While there have been some experimental results to this effect, there are still no quantitative models to explain the enhancement in oxidation and the resulting self-limiting oxide thickness in the presence of radiation. In this paper, we report a detailed theoretical and numerical study of UV light-enhanced low-temperature metal oxidation. This model takes into consideration oxygen adsorption and desorption at the oxide/gas interface, ionic currents within the growing oxides enhanced by the UV-induced high-field migration, as well as electronic tunnel current in the metal-oxide-oxygen systems. Compared to the low tunnel electronic current in natural oxidation ͑without UV light͒, the tunnel electronic current due to excitation in the UV-lightenhanced oxidation process is dramatically larger than the thermionic electron current, leading to an increased oxide thickness. In addition, the model is utilized to calculate the self-limiting oxide thickness as a function of temperature with and without UV radiation, including the effect of oxygen partial pressure. Our numerical calculations indicate trends consistent with reported experimental results.Low-temperature metal oxidation is an important area of research not only from a fundamental point of view to understand mechanisms of metal oxidation but also due to the technological importance of nanoscale oxides. Examples include the use of nanometer thick metal oxides such as MgO and Al 2 O 3 as tunnel barriers in spin tunnel junction devices, 1,2 HfO 2 and ZrO 2 as alternate gate dielectrics in advanced transistor devices, 3-5 and Ta 2 O 5 in corrosion-resistant coatings. 6,7 In such cases, it is extremely important to understand the rate of oxidation and how it can be controlled precisely to enable stoichiometric oxide formation. The thickness of natural oxides at room temperature is typically of the order of 1-3 nm. 8,9 It has recently been demonstrated that oxidation of metals under UV light can dramatically enhance the rate of oxidation and also lead to high-quality dielectrics that can be used in nanoelectronic devices. 10-12 While there is limited experimental data on the initial oxidation rates of different metals under UV radiation, 13,14 there are presently no theoretical models to explain this process quantitatively. Progress in modeling low-temperature oxidation of metals is less pronounced compared to the understanding of intermediate-and high-temperature oxidation regimes. A brief description of some of the original oxidation models discussing lowtemperature oxide growth are described below.1. Wagner theory. 15 The model presented a quantitative description of the oxidation mechanism by linear equations for charged defects through ionic solids. The conclusion is L ϰ ͱ t, where L is the ...