Promotion of Ammonia Electrooxidation on Pt nanoparticles by Nickel Oxide Support
| Autor: | Xiaoyu Cui, Anis Allagui, Nalin I. Andersen, Alexey Serov, Spyridon Ntais, Zhenzhen Lu, Emily Cossar, Aaron Roy, Plamen Atanassov, Elena A. Baranova |
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| Rok vydání: | 2016 |
| Předmět: |
Tafel equation
Chemistry General Chemical Engineering Nickel oxide Inorganic chemistry Non-blocking I/O Oxide 02 engineering and technology Chronoamperometry 010402 general chemistry 021001 nanoscience & nanotechnology 01 natural sciences 0104 chemical sciences Catalysis chemistry.chemical_compound Physisorption Electrochemistry Cyclic voltammetry 0210 nano-technology |
| Zdroj: | Electrochimica Acta. 222:1455-1463 |
| ISSN: | 0013-4686 |
| Popis: | In this study Pt nanoparticles supported on NiO, MnO 2 , and on carbon black were prepared and tested for the ammonia electrooxidation reaction (AmER) in alkaline media. The morphology and structure of the catalysts were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), x-ray diffraction (XRD), nitrogen physisorption, and their surface properties were studied using synchrotron radiation photoelectron spectroscopy (SRPES). Cyclic voltammetry, chronoamperometry and Tafel plots were used to study the electrochemical behavior of ammonia on Pt/metal oxide catalysts. Pt/NiO showed the highest current density and the lowest onset potential for AmER (-0.48 V vs. Hg/HgO) which increased in the order E onset (Pt/NiO) onset (Pt/MnO 2 ) onset (Pt/C). The reaction kinetic order with respect to the concentration of ammonia is close to zero, indicating fast surface adsorption of ammonia in agreement with previous studies on polycrystalline Pt electrodes, whereas the apparent Tafel slopes were found higher (56 − 69 mV dec −1 ) than previously reported values for Pt (39 mV dec −1 ). Our results show that the nature of the support strongly influences the size and electronic properties of the Pt nanoparticles, and as a result their electrocatalytic activity for AmER. |
| Databáze: | OpenAIRE |
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