We studied the electrochemical synthesis
of NH3 on Fe–CuS/C
catalysts in an alkaline aqueous solution under ambient conditions.
The metal chalcogenide catalyst is active in the nitrogen reduction
reaction (NRR) for approximately 45 min with an NH3 production
yield of 16 μg h–1 cm–2 at
−0.4 V
RHE, while it decomposes
to CuO. The rapid degradation of the catalyst hinders the precise
investigation of the NH3 production activity in longer
time measurements. Herein, the electrochemical NH3 production
rate is enhanced with increased overpotentials when the degradation
effect is mitigated in the measurement, which was difficult to observe
in the NRR reports. In the Tafel analysis, the exchange current density,
heterogeneous rate constant, and transfer coefficient of the Fe–CuS/C
catalyst on the NRR were estimated. When the electrode degradation
is mitigated, one of the best NH3 production activities
among the reported metal sulfide electrochemical NRR catalysts is
obtained, which is 42 μg h–1 cm–2 at −0.6 VRHE.