“…It is well-known that the HDH of halogenated aromatic compounds occurs in the order of C–I > C–Br > C–Cl ≫ C–F, which is ascribed to the dissociation energy of the C–halogen bonds. , Although different transition metal catalysts such as Pd, Ni, Pt, Au, Rh, Ru, and Fe have been used in the HDH reaction, the success of the reaction is also dependent on the reducing sources. − Even bi- or trimetallic catalysts, either in alloys or in intermetallic forms, often show better performance than monometallic catalysts. − Efforts toward developing bimetallic catalysts for HDH have therefore been made. Supported bimetallic catalysts involving two coinage metals (Ag/Au), and in particular Pd/Fe have been prepared and employed in HDH reaction. − Poly(vinylidene fluoride)–alumina membrane-supported Pd/Fe nanocatalyst was used in the dechlorination of only monochloroacetic acid, Pd/Fe NPs impregnated with granular activated charcoal, and Pd/Fe bimetallic nanotubes, composed of Fe nanotubes as core coated with shell of Pd NPs, were studied for hydrodechlorination of only polychlorobiphenyls, or Pd/Fe bimetallic catalyst with micron sizes was employed specifically for the HDH of tetrabromo- or tetrachlorobisphenol A. , It is evident that the applicability of these supported catalytic systems has been often found to be limited and presumably stems from the fact that these catalytic systems do not comply with actual shape or facets, spatial distribution, and requisite proximity for interaction between two metals on the surface, among others, which could activate the reducing sources for further reactions.…”