摘要
A rapid solvent-free microwave-assisted strategy was developed to fabricate Pt- and Ni-modified Co(OH)2catalysts for alkaline hydrogen evolution. Among them, Ni-Pt@Co(OH)2, prepared via sequential Ni-first then Pt loading, exhibited the best performance. Structural analyses confirmed uniform Pt dispersion with dominant Pt(111) facets, while ICP-MS showed reduced Pt usage compared to Pt@Co(OH)2. Electrochemical measurements in 1.0 M KOH revealed an overpotential of 71 mV at 10 mA·cm−2, comparable to Pt/C, and a mass activity 4–6.5 times higher across 25–75 mV. EIS demonstrated lower charge-transfer resistance, and stability tests showed negligible degradation after 3000 CV cycles and 11 h continuous operation. The outstanding performance arises from enhanced Pt utilization, abundant conductive sites, and strong Ni-Pt interfacial synergy, highlighting Ni-Pt@Co(OH)2as a promising catalyst for efficient alkaline HER with reduced Pt consumption.
危险品化学品经营许可证(带存储)