Water-mediated Recycling of Gold, Palladium, and Platinum Using Semimetallic TiS2 and TaS2 Nanosheets

The intensive and irreplaceable consumption of precious metals (PMs) including Au, Pd, and Pt in the electronic and catalysis industries, coupled with their scarcity in the earth’s crust, demand innovative recycling solutions for PM sustainability ^1-8 . However, efforts to recycle PMs from leachates of their waste are frustrated by an unsatisfactory extraction capacity at low concentrations and remain predominantly focused on gold, leaving other PMs unexplored ^9-13 . We report the ultrahigh reductive recycling of PM ions and their simultaneous aqueous-phase deposition on semimetallic transition metal dichalcogenides (TMD) of TiS ₂ and TaS ₂ nanosheets _. Notably, TiS ₂ shows unprecedented high extraction capacities of ~8 g/g, 2.3 g/g, and 1.15 g/g for Au, Pd, and Pt ions, respectively, and the adsorbed PM ions directly transformed into nanoparticles deposited on the nanosheets. Mechanistic studies reveal that water-mediated electron donation from the sulfur site of the semimetallic TiS ₂ and TaS ₂ nanosheets is responsible for the ultrahigh extraction capacity, with a single TiS ₂ molecule donating more than 13 electrons to gold ions. This electron transfer is mediated by the formation of sulfur-oxygen species during water dissociation. We further demonstrate the selective and complete recovery of Au, Pd, and Pt from real-world waste streams including electronic waste, spent catalysts, and automotive catalytic converters.