Abstract
One-dimensional (1D) metal-coated Pd structures are efficient catalysts for the ethanol electro-oxidation and promising strategy for minimizing the Pd-loading toward commercialization of direct ethanol fuel cells (DEFCs). Herein, the decorated and core-shell architectures of a novel Pd coating on Ag nanowires (PdAg-NWs) are controllable by a two-step polyol method based on the galvanic replacement reaction. The integration of uniform shell with a low Pd concentration and partial hollow structure onto 1D PdAg-NWs exhibits the highest efficiency for ethanol oxidation reaction (EOR) in alkaline solution. In comparison with Pd nanoparticles (PdNPs/C), the PdAgNWs/C performes 11 times superior EOR activity, and the onset potential shifts 80 mV negatively. The presence of Ag in PdAg-NWs enhances the absorption capacity of ethanol molecules and hydroxyl ions on the active sites, and improves the catalyst tolerance to CO-like intermediates, making them a potential anodic catalyst for DEFCs.
Original language | English |
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Pages (from-to) | 3909-3921 |
Number of pages | 13 |
Journal | International Journal of Hydrogen Energy |
Volume | 46 |
Issue number | 5 |
Early online date | 2020 |
DOIs | |
Publication status | Published - 19 Jan 2021 |
MoE publication type | A1 Journal article-refereed |
Keywords
- PdAg nanowire
- Low Pd-loading
- Core-shell
- Direct ethanol fuel cells
- Electrochemical durability
- CO poisoning tolerance