Bi₂WO₆-based heterojunction photocatalyst for antibiotic degradation has been a research hotspot, but its photocatalytic performance needs to be further improved. Therefore, 2D/2D P-doped g-C₃N₄/Bi₂WO₆ direct Z-scheme heterojunction photocatalysts with different composition ratios were prepared through three strategies of phosphorus (P) element doping, morphology regulation, and heterojunction, and the efficiency of its degradation of tetracycline hydrochloride (TC-HCl) under visible light was studied. Their structural, optical, and electronic properties were evaluated, and their photocatalytic efficiency for TC-HCl degradation was explored with a detailed assessment of the active species, degradation pathways, and effects of humic acid, different anions and cations, and water sources. The 30% P-doped g-C₃N₄/Bi₂WO₆ had the best photocatalytic performance for TC-HCl degradation. Its photocatalytic rate was 4.5-, 2.2-, and 1.9-times greater than that of g-C₃N₄, P-doped g-C₃N₄, and Bi₂WO₆, respectively. The improved photocatalytic efficiency was attributed to the synergistic effect of P doping and 2D/2D direct Z-scheme heterojunction construction. The stability and reusability of the 30% P-doped C₃N₄/Bi₂WO₆ were confirmed by cyclic degradation experiments. Radical scavenging experiments and electron spin resonance spectroscopy showed that the main active species were •O₂⁻ and h⁺. This work provides a new strategy for the preparation of direct Z-scheme heterojunction catalysts with high catalytic performance.