Aerosol mass spectrometry was used to characterize submicron aerosols before and after aging in a Gothenburg Potential Aerosol Mass (Go:PAM) reactor at two suburban sites in China, one in northern China at Changping (CP), Beijing, and a second in southern China at Hong Kong (HK). Organic aerosol (OA) dominated in the ambient nonrefractory particulate matter <1 μm (NR‐PM₁) for both CP (42–71%) and HK (43–61%), with a large contribution from secondary OA factors that were semivolatile oxygenated (SVOOA) and low‐volatility oxygenated (LVOOA). Under constant OH exposure, OA enhancement (78–98%) dominated the NR‐PM₁ mass increment at both sites, while nitrate was enhanced the most among the inorganic species (7–9%). Overall, the CP site exhibited higher OA oxidation potential and more enhancement of SVOOA than LVOOA (7.5 vs. 2.7 μg/m³), but the reverse was observed in HK (0.8 vs. 2.6 μg/m³). In CP, more enhancement of the less oxygenated SVOOA suggests that aerosol aging was more sensitive to the abundant locally emitted primary OA and volatile organic compound precursors. On the contrary, the more formation of the highly oxidized LVOOA in HK indicates that aerosol aging mainly escalated the degree of oxygenation of OA as ambient aerosol was already quite aged and there was a lack of volatile organic compound precursors. The comparative measurements using the same oxidation system reveal distinct key factors and mechanisms that influence secondary aerosol formation in two suburban locations in China, providing scientific insights to assist formulation of location‐specific mitigation measures of secondary pollution.