We investigate the chemical composition of organic light-absorbing components, also known as brown carbon (BrC) chromophores, formed in a proxy of anthropogenic secondary organic aerosol generated from the photooxidation of naphthalene (-SOA) in the absence and presence of NO. High-performance liquid chromatography equipped with a photodiode array detector and electrospray ionization high-resolution mass spectrometer is employed to characterize -SOA and its BrC components. We provide molecular-level insights into the chemical composition and optical properties of individual -SOA components and investigate their BrC relevance. This work reveals the formation of strongly absorbing nitro-aromatic chromophores under high-NO conditions and describes their degradation during atmospheric aging. NO addition enhanced the light absorption of -SOA while reducing wavelength-dependence, as seen by the mass absorption coefficient (MAC) and absorption Ångström exponent (AAE). Optical parameters of -SOA generated under low- and high-NO conditions showed a range of values from MAC ∼ 0.12 m g and AAE ∼ 8.87 (low-NO) to MAC ∼ 0.19 m g and AAE ∼ 7.59 (high-NO), consistent with "very weak" and "weak" BrC optical classes, respectively. The weak-BrC class is commonly attributed to biomass smoldering emissions, which appear to have optical properties comparable with the -SOA. Molecular chromophores contributing to naphthalene BrC absorption were identified with substantial nitro-aromatics, indicating that these species may be used as source-specific markers of BrC related to the anthropogenic emissions.

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http://dx.doi.org/10.1021/acs.est.1c03135DOI Listing

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