Metal oxide semiconductors are widely used in photocatalysis for the sustainable synthesis of fine chemicals and fuels. However, the mechanisms and the actual catalytically active species involved in these photocatalytic processes are not yet fully understood. Herein, we reveal that the addition of certain amines can effectively accelerate the photocatalytic atom transfer radical addition (ATRA) reaction by stabilizing a soluble Bi‐species formed through a reaction between Bi2O3 and diethyl bromomalonate using either N, N‐dimethylformamide (DMF) or dimethyl sulfoxide (DMSO) as a solvent. Moreover, thermodynamic calculations revealed that N, N, N’, N’‐tetramethylethylenediamine (TMEDA), and DMF yield the most stable complexes [(κ2‐TMEDA)2BiBr3], ultimately accelerating the formation of the targeted ATRA product.