<p><strong>Abstract.</strong> Fine&#8211;particle pollution associated with haze threatens human health, especially in the North China Plain, where extremely high PM<sub>2.5</sub> concentrations were frequently observed during winter. In this study, the WRF&#8211;Chem model coupled with an improved integrated process analysis scheme was used to investigate the formation and evolution mechanisms of a haze event happened over Beijing&#8211;Tianjin&#8211;Hebei (BTH) in December 2015, including examining the contributions of local emission and outside transport to the absolute PM<sub>2.5</sub> concentration in BTH, and the contributions of each detailed physical or chemical process to the variations in the PM<sub>2.5</sub> concentration. The influence mechanisms of aerosol radiative forcing (including aerosol direct and indirect effects) were also examined by using the process analysis. During the aerosol accumulation stage (December 20&#8211;22, Stage_1), the average near&#8211;surface PM<sub>2.5</sub> concentration in BTH was 250.0&#8201;&#181;g&#8201;m<sup>&#8722;3</sup>, which was contributed by local emission of 42.3&#8201;% and outside transport of 36.6&#8201;%. During the aerosol dispersion stage (December 23&#8211;27, Stage_2), the average concentration of PM<sub>2.5</sub> was 107.9&#8201;&#181;g&#8201;m<sup>&#8722;3</sup>. The contribution of local emission increased to 50.9&#8201;%, while the contribution of outside transport decreased to 24.3&#8201;%. The 24&#8211;h change (23:00LST minus 00:00LST) in the near&#8211;surface PM<sub>2.5</sub> concentration was +50.4&#8201;&#181;g&#8201;m<sup>&#8722;3</sup> during Stage_1 and &#8722;41.5&#8201;&#181;g&#8201;m<sup>&#8722;3</sup> during Stage_2. Contributions of aerosol chemistry process and vertical mixing process to the 24&#8211;h change were +43.8 (+17.9) &#181;g&#8201;m<sup>&#8722;3</sup> and &#8722;161.6 (&#8722;221.6) &#181;g&#8201;m<sup>&#8722;3</sup> for Stage_1 (Stage_2), respectively. Small differences in contributions from other processes were found between Stage_1 and Stage_2, such as advection process, cloud chemistry process, and so on. Therefore, the PM<sub>2.5</sub> increase over BTH during haze formation stage (Stage_1) was mainly attributed to strong production by aerosol chemistry process and weak removal by vertical mixing process. When aerosol radiative feedback was considered, the 24&#8211;h PM<sub>2.5</sub> increase was enhanced by 9.6 &#181;g&#8201;m<sup>&#8722;3</sup> during Stage_1, which could be mainly attributed to the contributions of vertical mixing process (+39.8&#8201;&#181;g&#8201;m<sup>&#8722;3</sup>), advection process (&#8722;38.6&#8201;&#181;g&#8201;m<sup>&#8722;3</sup>) and aerosol chemistry process (+5.1&#8201;&#181;g&#8201;m<sup>&#8722;3</sup>). The restrained vertical mixing could be the primary reason for the enhancement in near&#8211;surface PM<sub>2.5</sub> increase when aerosol radiative forcing was considered.</p>