Abstract
Electrochemical water splitting by electricity from the renewable power sources is one of the most promising pathways for green and sustainable hydrogen production. The key is to synthesize earth-abundant and noble-metal-free electrocatalysts with outstanding hydrogen evolution reaction (HER) activity and durability in wide-pH electrolytes by simple and cost-effective methods. Herein, we reported a one-step synthesis of uniform, ultrafine molybdenum carbide (Mo2C) and molybdenum nitride (Mo2N) hybrid [together as Mo2(CN)] inserted carbon nanosheets as efficient electrocatalyst for HER. The as-synthesized catalyst showed an excellent HER activity in acid medium, and even superior performance was obtained in the alkaline medium. The optimal Mo2(CN) annealed at 750 °C showed an overpotential of −80 mV at 10 mA cm−2 and a Tafel slope of 40 mV dec−1; the former strikingly outperforms commercial 20% Pt/C materials (−112 mV). Moreover, Mo2(CN) gave an onset voltage of −33 mV and overpotential of −202 mV at 100 mA cm−2 with merely a mass loading of 0.2 mg cm−2, which are, to date, among the best records for Mo-based catalysts in both media. The nanosheet structure providing large active area and quick charge transfer, and the synergistic effects between Mo2C and Mo2N toward HER are ascribed to the outstanding electrocatalytic activity according to the capacitive current and turnover frequency analysis. The remarkable catalytic activity and operational durability in wide pH ranges guarantee their potential for highly efficient hydrogen production.
| Original language | English |
|---|---|
| Pages (from-to) | 323-331 |
| Number of pages | 9 |
| Journal | Electrochimica Acta |
| Volume | 280 |
| DOIs | |
| State | Published - 1 Aug 2018 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- Electrochemical water splitting
- Hydrogen evolution reaction
- MoC
- Molybdenum nitride
- Noble-metal-free catalysts
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