Abstract
The properties of Pt-Ni nanostructures were successfully controlled by employing different Pt precursors in the preparation of Pt-Ni nanocomposites, which were synthesized by a co-reducing Pt and Ni precursors. Pt-Ni nanostructures were obtained by leaching Ni species from the Pt-Ni nanocomposite. The use of H2PtCl6 as a precursor yielded aggregated small Pt particles, while [Pt(NH3)4]Cl 2 yielded large hollow Pt nanostructures. A possible mechanism leading to the morphological difference between the two structures was suggested. Owing to a higher electrochemically active surface area and a favorable surface structure, hollow Pt nanostructures from the [Pt(NH 3)4]Cl2 precursor showed significantly better performance in ammonia oxidation than the aggregated Pt particles resulting from the H2PtCl6 precursor.
| Original language | English |
|---|---|
| Pages (from-to) | 722-727 |
| Number of pages | 6 |
| Journal | Materials Chemistry and Physics |
| Volume | 147 |
| Issue number | 3 |
| DOIs | |
| State | Published - 2014.10.15 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Composite materials
- Electrochemical properties
- Electrochemical techniques
- Nanostructures
Quacquarelli Symonds(QS) Subject Topics
- Materials Science
- Physics & Astronomy
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