Nitrogen-doped phosphorene for electrocatalytic ammonia synthesis
The rapid surface oxidation of phosphorene under ambient conditions is considered to be a serious issue for many applications, but is used here as a strategy to achieve efficient heteroatom doping. Highly crystalline nitrogen-doped phosphorene (N-phosphorene) is prepared using a combination of ball...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2020-08, Vol.8 (31), p.15875-15883 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The rapid surface oxidation of phosphorene under ambient conditions is considered to be a serious issue for many applications, but is used here as a strategy to achieve efficient heteroatom doping. Highly crystalline nitrogen-doped phosphorene (N-phosphorene) is prepared using a combination of ball milling and microwave techniques. The prepared N-doped phosphorene nanosheets showed outstanding electrocatalytic performance as a new type of non-metallic catalyst for nitrogen (N
2
) to ammonia (NH
3
) conversion, with an NH
3
yield rate and faradaic efficiency (FE) of up to 18.79 μg h
−1
mg
CAT
−1
and 21.51%, respectively, at a low overpotential (0 V)
versus
the reversible hydrogen electrode (RHE). Density functional theory calculations revealed that the high nitrogen reduction reaction (NRR) FEs originate from the increased hydrophobicity at the N and O doped phosphorene surfaces, which in turn hinders the competing hydrogen evolution reaction (HER) in an alkaline environment and promotes the NRR. This work not only introduces an efficient strategy to chemically functionalize 2D phosphorene, but also opens a new avenue in using N-doped phosphorene nanosheets as a metal-free catalyst.
A facile and efficient strategy to produce nitrogen-doped (N-doped) phosphorene nanosheets that can be used as an efficient metal-free catalyst for electrochemical ammonia synthesis under ambient conditions is presented. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d0ta03237a |