摘要
Developing highly active and stable electrocatalysts for practical proton exchange membrane water electrolyzers (PEMWEs) operating at industry-relevant current densities remains a significant challenge. In particular, the hydrogen evolution reaction (HER) at ampere-level current densities leads to the rapid consumption of interfacial protons, resulting in sluggish kinetics. Herein, a strategy is proposed to reduce the proton transfer energy barriers and improve the HER kinetics at high current densities by anchoring tri-lacunary Keggin-type polyoxometalates (POMs) on Pt. The lacunary POMs clusters function as proton pumps, increasing the connectivity of hydrogen bond networks and enabling proton transfer via a proton-coupled electron transfer mechanism. In addition, an unconventional Tafel step mediated by short-pathway hydrogen spillover from POMs clusters to Pt active sites is also created. As a result, an ultra-high mass activity of 782.94 A·mg Pt −1 and remarkable durability over 6000 h at a current density of 2000 mA·cm −2 can be simultaneously achieved in a practical PEMWE with an ultralow Pt loading mass of 4.2 µg Pt ·cm −2 . The strategy provides new opportunities in developing next-generation low-Pt electrocatalysts for PEMWE applications.
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