Hydrogen generation of single alloy Pd/Pt quantum dots over Co3O4 nanoparticles via the hydrolysis of sodium borohydride at room temperature

Abstract

AbstractTo satisfy global energy demands and decrease the level of atmospheric greenhouse gases, alternative clean energy sources are required. Hydrogen is one of the most promising clean energy sources due to its high chemical energy density and near-zero greenhouse gas emissions. A single alloyed phase of Pd/Pt nanoclusters as quantum dots (QDs) was prepared and loaded over Co3O4 nanoparticles with a low loading percentage (1 wt.%) for hydrogen generation from the hydrolysis of NaBH4 at room temperature. L-glutathione (SG) was used as a capping ligand. It was found that the single alloy catalyst (Pd0.5–Pt0.5)n(SG)m/Co3O4 caused a significant enhancement in hydrogen generation in comparison to the monometallic clusters (Pdn(SG)m and Ptn(SG)m). Moreover, the Pd/Pt alloy showed a positive synergistic effect compared to the physical mixture of Pd and Pt clusters (1:1) over Co3O4. The QDs alloy and monometallic Pd and Pt clusters exhibited well-dispersed particle size in ~ 1 nm. The (Pd0.5–Pt0.5)n(SG)m)/Co3O4 catalyst offers a high hydrogen generation rate (HGR) of 8333 mL min− 1 g− 1 at room temperature. The synergistic effect of Pd and Pt atoms in the nanoclusters alloy is the key point beyond this high activity, plus the prepared clusters' unique atomic packing structure and electronic properties. The effect of the NaBH4 concentration, catalyst amount, and reaction temperature (25–60 °C) were investigated, where HGR reaches 50 L min− 1 g− 1 at 60 °C under the same reaction conditions. The prepared catalysts were analyzed by UV–Vis, TGA, HR-TEM, XRD, and N2 adsorption/desorption techniques. The charge state of the Pd and Pt in monometallic and alloy nanoclusters is zero, as confirmed by X-ray photoelectron spectroscopy analysis. The catalysts showed high recyclability efficiency for at least five cycles due to the high leaching resistance of the alloy nanoclusters within the Co3O4 host. The prepared catalysts are highly efficient for energy-based applications.