Electrochemical Hydrogen Evolution Reaction Efficiently Catalyzed by Ru2 P Nanoparticles.
Yuan WangZong LiuHui LiuNian-Tzu SuenXu YuLigang FengPublished in: ChemSusChem (2018)
Developing alternatives to Pt catalysts is a prerequisite to cost-effectively produce hydrogen. Herein, we demonstrate Ru2 P nanoparticles (without any doping and modifications) as a highly efficient Pt-like catalyst for the hydrogen evolution reaction (HER) in different pH electrolytes. On transferring the hexagonal close-packed crystal structure of Ru to the orthorhombic structure of Ru2 P, a greatly improved catalytic activity and stability toward HER is found owing to Ru-P coordination. The electronic state change originates from the P-Ru bonding structures, which accounts for the HER activity improvement compared with Ru nanoparticles. Specifically, Ru2 P nanoparticles can drive 10 mA cm-2 at a very low overpotential of 55 mV, only 8 mV more than Pt/C in an acidic solution; and an extremely low overpotential of approximately 50 mV is needed in alkaline solution, about 20 mV less than the Pt/C catalyst. The Volmer-Tafel mechanism is indicated on Ru2 P nanoparticles with the typical Tafel slope of 30 mV dec-1 of Pt metal indicating a Pt-like catalytic ability. Ru2 P is more active in the Ru-P family as H atoms prefer to adsorb on Ru atoms rather than on the P element according to theoretical calculations. Considering the low price of Ru (20 % of Pt), anti-corrosion ability in the electrolyte, and the safe and reliable fabrication approach, the powder Ru2 P nanoparticles make an excellent HER catalyst with great promise for large-scale water electrolysis applications.