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Nitrate (NO3−), which is mainly oxidized from NO2 by the OH radical (OH·) and O3 in the atmosphere, is a major component of inorganic aerosols. However, the contributions of the OH· and O3 pathways to NO3− in urban aerosols and the influence of air pollution to both pathways remain unclear. Oxygen isotopes of NO3− were measured for PM2.5 in Beijing in 2014. The Δ17O‐NO3− values (17.0–32.8‰) were significantly higher in winter (27.2 ± 3.6‰) than in summer (24.2 ± 1.3‰). By estimating contributions of O3 to the NOx cycle, the Δ17O values of NO3− endmembers produced via the NO2 + OH· (P1), NO3· + DMS/HC (P2), and N2O5 hydrolysis (P3) pathways were calculated for each observation. The contributions of the three pathways (P1: 32 ± 10%, P2: 34 ± 10%, and P3: 34 ± 20% annually) were calculated using the Stable Isotope Analysis in R model. We found that NO3− formation was dominated by the O3 oxidation pathways (P2 + P3; 68 ± 23% annually, 73 ± 21% in spring, 59 ± 23% in summer, 75 ± 20% in autumn, and 69 ± 22% in winter). Moreover, PM2.5, NO2, and NO3− pollution decreased the importance of the OH· pathway relative to the O3 pathways for NO3− production. However, O3 pollution increased the importance of the OH· pathway relative to the O3 pathways for NO3− production. These results provided a comprehensive analysis on the oxygen isotope records in particulate NO3− for understanding the relative importance of major oxidation pathways of NO2. Atmospheric pollution substantially influenced the pathways of NO2 oxidation to NO3− in city environments.

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