Abstract
Urea oxidation is an important process for hydrogen production using living catalysts with nickel components. In this study, iridium-doped manganese nickel oxide was prepared with a reflux procedure on carbon black (Ir@MnNiO/C) at 120 ℃ for 24 h and was annealed in an air atmosphere at 500 ℃ for 2 h. The chemical composition and morphology of Ir@MnNiO/C was investigated by X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM). The electrocatalytic activity with Ir@MnNiO/C catalysts for urea oxidation in alkaline KOH with urea electrolyte confirmed that Ir@MnNiO/C exhibited a significant redox capacity and a superior charge-transfer conversion. This catalyst showed enhanced urea oxidation and oxygen evolution reaction values, with potentials of 1.42 V and 1.27 V (vs. Ag/AgCl) at a current density of 10 mA cm−2, respectively. Ir@MnNiO/C as both the cathode and anode required cell voltages of 2.0 V and 1.86 V, respectively, at 10 mA cm−2 to function as a full cell electrolyzer for water and urea splitting in alkaline electrolytes. In the field of renewable energy generation, these findings provide an effective framework for useful and well-balanced noble and non-noble metal electrocatalysts.
| Original language | English |
|---|---|
| Article number | 164492 |
| Journal | Applied Surface Science |
| Volume | 715 |
| DOIs | |
| State | Published - 2026.01.15 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Hydrogen evolution reaction
- Iridium manganese nickel oxide
- Overall water splitting
- Oxygen evolution reaction
- Urea oxidation reaction
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