酸性媒体におけるオペランド活性化とHER強化のための電気化学的置換法由来のCuOₓ-Pt/Cu界面
Pracheta Trivedi1, Sandeep Yadav1, Neha Clare Minj1
1Laboratory for Electrocatalysis and Energy, Department of Chemistry, Indian Institute of Technology, Kanpur 208 016, Uttar Pradesh, India. ananths@iitk.ac.in.
Abstract:
This work presents an interesting and easy galvanic displacement strategy for the synthesis of self-supported Pt-Cu heterointerfaces optimized for the hydrogen evolution reaction (HER) in acidic media. By galvanically replacing surface copper with Pt2+ ions, we achieve a unique CuOx-Pt/Cu interface, which undergoes dynamic in situ activation during the HER to form a Pt-Cu2O/Cu heterostructure, in which Pt is present in trace amounts. This transformation significantly enhanced the electrocatalytic HER requiring just 38 mV and 76 mV as overpotentials for 10 and 100 mA cm-2, respectively, outperforming bulk Pt foil. The synergistic interplay between Pt, Cu2O, and Cu is believed to have delivered superior charge transfer and active-site stabilization, while the self-supporting architecture improves catalyst durability and accessibility. Our approach demonstrates scalable, cost-efficient catalyst fabrication that maximizes Pt utilization while minimizing Pt consumption, providing a promising pathway toward next-generation HER electrocatalysts for efficient green hydrogen production under acidic conditions with ultralow Pt content.
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