Affiliation:
1. Key Laboratory of Materials Physics and Anhui Key Laboratory of Nanomaterials and Nanotechnology Institute of Solid State Physics HFIPS Chinese Academy of Sciences Hefei 230031 China
2. University of Science and Technology of China Hefei 230026 China
3. Centre for Catalysis and Clean Energy Griffith University Gold Coast Campus Gold Coast QLD 4222 Australia
Abstract
AbstractTo date, the excellent mass‐catalytic activities of Pt single‐atoms catalysts (Pt‐SACs) toward hydrogen evolution reaction (HER) are categorically confirmed; however, their high current density performance remains a challenge for practical applications. Here, a binder‐free approach is exemplified to fabricate self‐standing superhydrophilic‐superaerphobic Pt‐SACs cathodes by directly anchoring Pt‐SAs via Pt‐NxC4‐x coordination bonds to the structurally‐integrated 3D nitrogen‐doped carbon tubes (N‐CTs) array grid (denoted as Pt@N‐CTs). The 3D Pt@N‐CTs cathode with optimal Pt‐SACs loading is capable of operating at a high current density of 1000 mA cm−2 with an ultralow overpotential of 157.9 mV with remarkable long‐term stability over 11 days at 500 mA cm−2. The 3D super‐wettable free‐standing Pt@N‐CTs possess interconnected vertical and lateral N‐CTs with hierarchical‐sized open channels, which facilitates the mass transfer. The binder‐free immobilization adding to the large surface area and 3D‐interconnected open channels endow Pt@N‐CTs cathodes with high accessible active sites, electrical conductivity, and structural stability that maximize the utilization efficiency of Pt‐SAs to achieve ampere‐level current density HER at low overpotentials.
Funder
National Natural Science Foundation of China
Cited by
1 articles.
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