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The expanding agricultural practices rely on carbon- and energy-intensive Bosch–Meiser processes for urea synthesis. Alternatively, electrochemical coupling of CO 2 and N 2 is emerging as a sustainable approach. Unfortunately, the high energy barrier for N 2 and CO 2 cracking for C–N bond coupling limits the urea synthesis efficiency. Herein, we have electrodeposited Bi on Cu foil via triple pulse voltage, and the fabricated Bi(0.01 V)@Cu electrode demonstrates a high yield rate of 646 μg h –1 mg –1 cat. of urea with 70.7% Faradaic efficiency at −0.45 V vs RHE. The isotopic labeling experiments assert that the produced urea is solely from the dissolved CO 2 and N 2 gases. More importantly, we have utilized in situ electrochemical Raman spectroscopy and Fourier transform infrared (FTIR) measurements to monitor the real-time formation of urea, further supported by a microelectrochemical approach using a Pt-microelectrode and the results were verified by density functional theory (DFT) analysis. Moving a step forward, plant growth and flowering upon addition of extracted urea have been demonstrated for practical application.
Kaur et al. (Fri,) studied this question.