Abstract
There are still not many meaningful alternatives to converting too-nitrogenated water into ammonia. This is mostly because it requires highly active and long-lasting catalysts. In this paper, we obtained a catalyst that meets these requirements by producing cobalt phosphide nanoparticles in a phosphorus-doped carbon matrix via an easy pyrolysis process. The composite was deposited onto carbon paper for the composite to better operate as an electrochemical material. A thorough structural and surface analysis confirmed that the CoP particles were embedded in the carbon matrix. This created a lot of reactive sites that made it easy for charges to move quickly through the material, which in turn created a lot of active sites that made it easy for charges to move quickly through the catalyst. As a result, the material produced ammonia at a rate of 0.5 mmol h-1 mgcat−1 and had a Faradaic efficiency of 86.18 % at −1.6 V vs. SCE. Computational research further indicated that the strong interaction between CoP and the doped carbon matrix makes it easier for important intermediates to stick to the surface, lowers the energy barrier for the rate-limiting phase, and effectively stops the competing hydrogen evolution pathway. These results suggest that the CoP-PC system is a strong and useful option for getting rid of nitrate pollution and making ammonia at the same time.
| Original language | English |
|---|---|
| Article number | 153249 |
| Journal | International Journal of Hydrogen Energy |
| Volume | 205 |
| DOIs | |
| Publication status | Published - 30 Jan 2026 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Free Keywords
- Ammonia
- CoP-PC composite
- Electrocatalysis
- Nitrate
ASJC Scopus subject areas
- Renewable Energy, Sustainability and the Environment
- Fuel Technology
- Condensed Matter Physics
- Energy Engineering and Power Technology
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