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Preparation of Ru-doped Cu-based catalysts for enhanced electrochemical ammonia synthesis from efficient electrocatalytic nitrate reduction
Ammonia (NH 3 ) is not only an essential feedstock for fertilizer, but also deemed as a potential hydrogen carrier. Worldwide industrial-scale NH 3 synthesis relies heavily on the Haber-Bosch process, which involves harsh operation under reaction conditions. In addition, nitrate is prevalent in grou...
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Published in: | Catalysis science & technology 2023-10, Vol.13 (21), p.6313-632 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Ammonia (NH
3
) is not only an essential feedstock for fertilizer, but also deemed as a potential hydrogen carrier. Worldwide industrial-scale NH
3
synthesis relies heavily on the Haber-Bosch process, which involves harsh operation under reaction conditions. In addition, nitrate is prevalent in groundwater and surface water, causing serious pollution. Electrocatalytic nitrate reduction reaction (NITRR), a sustainable ammonia synthesis technique, is the most promising alternative to the traditional Haber-Bosch process. We combined the noble metal Ru by impregnation based on Cu-based materials that can inhibit the HER to prepare Cu/Cu
2
O/RuO
2
@C composites. Surprisingly, the NH
3
yield of Cu/Cu
2
O/RuO
2
@C composites prepared by the NITRR reached 209.44 μmol cm
−2
h
−1
and 82.40% Faraday efficiency at −0.6 V (
vs.
RHE). Such a high reduction activity is attributed to the synergistic effect between Ru heteroatoms and the Cu-based material. In addition, Cu/Cu
2
O/RuO
2
@C exhibited good cycling stability and repeatability. This work highlights the potential importance of electrocatalyst design, contributing to research and exploration of related materials.
Cu/Cu
2
O/RuO
2
@C composites prepared by the NITRR reached an NH
3
yield of 209.44 μmol cm
−2
h
−1
and 82.40% Faraday efficiency at −0.6 V (
vs.
RHE). |
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ISSN: | 2044-4753 2044-4761 |
DOI: | 10.1039/d3cy01072d |