To enhance the dechlorination reactivity of millimetric sponge iron (s-Fe(0)), a facile one-pot method was used to decorate s-Fe(0) with Ag(+) ions under ambient conditions. The results recorded by X-ray diffraction patterns, X-ray photoelectron spectra and high-resolution transmission electron microscopy demonstrated that the growth of Ag(0) was dominated primarily by (111) plane with a mean length of ∼20 nm. The roles of Ag(0) loading, catalyst dosage, particle size, initial pH and contaminant concentration were assessed during the removal of pentachlorophenol (PCP). Catalyst recyclability was also studied. The results revealed that 3-5mm s-Fe(0) particles with 5 wt% Ag(0) loading exhibited the best performance with a dose of 3.0 g per 60 mL PCP solution. In addition, the dechlorination of PCP followed two-step, pseudo-first-order reaction kinetics, and Ag(0)-s-Fe(0) was advantageous compared with bimetals of nanoscale zero-valent iron, iron power and iron flakes. The dechlorination mechanism of PCP over Ag(0)-s-Fe(0) was attributed to the surface Ag(0) decoration, which catalyzed the formation of reactive hydrogen atoms for indirect reaction, and the direct electron transfer via Fe-Ag(0) galvanic cells for direct reaction. This suggests that Ag-based bimetals of s-Fe(0) have great potential in the pretreatment of organic halogen compounds in aqueous solution.