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Efficient interlayer confined nitrate reduction reaction and oxygen generation enabled by interlayer expansion
Electrochemically converting nitrate ions back to ammonia can not only eliminate water pollution but also obtain valuable ammonia without a serious carbon footprint, and is thus deemed as an efficient supplement to the traditional Haber-Bosch process. Currently reported catalysts can achieve a singl...
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Published in: | Nanoscale 2022-12, Vol.15 (1), p.24-214 |
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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: | Electrochemically converting nitrate ions back to ammonia can not only eliminate water pollution but also obtain valuable ammonia without a serious carbon footprint, and is thus deemed as an efficient supplement to the traditional Haber-Bosch process. Currently reported catalysts can achieve a single electrode reaction in the electrochemical nitrate reduction reaction. However, the bifunctionality of a single catalyst for both cathodic and anodic reactions has not yet been reported. Herein, we report Fe-doped layered α-Ni(OH)
2
with expanded interlayer spacing as an efficient bifunctional catalyst for the nitrate reduction reaction and oxygen evolution reaction. The expanded interlayer spacing facilitates
in situ
electrochemical potassium ion intercalation between layers.
In situ
Raman spectroscopy characterization confirms that both the nitrate reduction reaction and oxygen evolution reaction are confined between layers and are triggered by the accumulation of potassium ions. The obtained α-Ni
0.881
Fe
0.119
(OH)
2
nanosheets deliver an ammonia yield rate of 8.1 mol g
cat.
−1
h
−1
with a NO
3
−
-to-NH
3
faradaic efficiency of 97.5% at the cathode. The overpotential of oxygen generation at 10 mA cm
−2
is reduced to 254 mV at the anode. As a bifunctional catalyst in overall electrolysis, the current density of α-Ni
0.881
Fe
0.119
(OH)
2
reaches 24.8 mA cm
−2
at a voltage of 2.0 V and performs continuously for 50 h with a current retention of 80.2%.
The interlayer confined nitrate reduction reaction (NTRR) and oxygen evolution reaction (OER) were realized. The expanded interlayer spacing facilitates
in situ
K
+
intercalation. Fe-doped Ni(OH)
2
delivers excellent functionality in NTRR overall electrocatalysis. |
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ISSN: | 2040-3364 2040-3372 |
DOI: | 10.1039/d2nr05001c |