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Aromatic compounds are abundant in urban and industrial environments and potentially serve as one of the primary precursors for new particle formation (NPF). Pi-pi stacking is a distinctive weak interaction observed between aromatic compounds. Aromatic oxygenated organic molecules (AOOM) are key products of atmospheric oxidation of aromatic compounds; however, the role of pi-pi stacking in their involvement in atmospheric new particle formation (NPF) remains unclear. This study used quantum chemical calculations to reveal the nucleation mechanism of AOOM through pi-pi stacking and hydrogen bonding. The results indicate that the contribution of pi-pi stacking to nucleation in aromatic compounds is primarily determined by the stacking area. For aromatic hydrocarbons with 1–2 phenyl groups, the Gibbs free energy (ΔG) of dimolecular clusters formed solely by pi-pi stacking is positive. In contrast, for polycyclic aromatic hydrocarbons with three or more phenyl groups, the ΔG of these clusters decreases significantly and becomes negative. Single-phenyl AOOM primarily participates in the NPF process through hydrogen bonding with sulfuric acid molecules. In this work, an explanation is provided for observations and laboratory findings of the appearance of aromatic-ring-retaining species in nanoparticles. The discovery of pi-pi stacking also completes the variety of atmospheric nucleation weak interactions. The oxidation and nucleation mechanisms of aromatic compounds should be reassessed, considering the effects of pi-pi stacking, especially polycyclic aromatic hydrocarbons. These findings have important implications for sustainable urban air-quality management. By clarifying the role of pi-pi stacking, particularly in polycyclic aromatic hydrocarbons, this study may improve predictions of new particle formation, refine secondary organic aerosol modeling, and inform targeted emission-control policies to protect public health and mitigate climate impacts.
Deng et al. (Wed,) studied this question.