Journal
CELL REPORTS PHYSICAL SCIENCE
Volume 3, Issue 7, Pages -Publisher
CELL PRESS
DOI: 10.1016/j.xcrp.2022.100961
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Funding
- National Natural Science Foundation of China [52122308, 21905253, 51973200]
- China Postdoctoral Science Foundation [2020M682332, 2021T140614]
- Henan Postdoctoral Foundation [202003015]
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In this study, the researchers developed an electrocatalyst for efficient ammonia synthesis under ambient conditions. By decorating vertical NiCo2O4 pillars with boron-doped carbon dots (BCDs), they achieved a near 100% Faradaic efficiency (FE) for nitrate reduction to ammonia. The remarkable performance was attributed to the abundance of Lewis acid sites provided by the BCDs, which facilitated the adsorption of nitrate ions and suppressed the competitive hydrogen evolution reaction (HER).
Electrocatalytic nitrate reduction represents a very promising route for ammonia synthesis under ambient conditions. However, for most nitrate-to-ammonia electrocatalysts developed to date, the Faradaic efficiency (FE) to ammonia is modest due to the competitive hydrogen evolution reaction (HER). Here, we report that the decoration of vertically aligned NiCo2O4 pillars with boron-doped carbon dots (BCDs) enables electrocatalytic nitrate reduction to ammonia with similar to 100% FE. A BCDs/NiCo2O4/carbon cloth cathode delivers a NH3 production rate of 173.9 mu mol h(-1) cm(-2) at -0.55 V versus reversible hydrogen electrode (RHE). This state-of-the-art performance is linked to the BCDs, which provide an abundance of Lewis acid sites on the electrocatalyst surface for the adsorption of nitrate ions (simultaneously suppressing the competitive HER). This work reveals that highly selective NH3 electrosynthesis can be achieved under ambient conditions by regulating the surface acidity/basicity properties of metal-oxide-based catalysts, paving the way toward more sustainable NH3-production technologies.
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