摘要
Hydrogen generation from electrical water splitting has become a greatly increasing requirement for energy systems, however, highly effective and durable electrocatalysts towards universal-pH hydrogen evolution reaction (HER) remain a big challenge. Herein, we design and synthesize ruthenium di-phosphide (RuP 2 ) confined in carbon layers (RuP 2 -C) with a unique yolk-shell structure (RuP 2 -C@RuP 2 -C) from MOF . As expected, it not only exceeds the HER activity of Pt catalysts, with very tiny overpotentials at 10 mA cm −2 (9 and 17 mV in 1.0 M KOH and 0.5 M H 2 SO 4 , individually), but also has high stability. Besides, it also exhibits a low overpotential (40 mV) close to Pt catalysts and high stability in 1.0 M PBS, indicating that RuP 2 -C@RuP 2 -C (RPC@RPC) owns outstanding HER performance at all pH values. Density functional theory (DFT) calculation results further unravel that the P-site on the surface of RPC@RPC possesses low hydrogen adsorption energy, beneficial for boosting the HER activity.
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