产量(工程)
电化学
傅里叶变换红外光谱
尿素
法拉第效率
拉曼光谱
电极
分析化学(期刊)
材料科学
化学
无机化学
冶金
化学工程
物理化学
有机化学
光学
物理
工程类
作者
Sukhjot Kaur,Kalpana Garg,Divyani Gupta,Alankar Kafle,Dharmender Dharmender,Vivekanand Shukla,Rajeev Ahuja,Tharamani C. Nagaiah
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-12-13
卷期号:10 (1): 85-93
被引量:17
标识
DOI:10.1021/acsenergylett.4c02823
摘要
The expanding agricultural practices rely on carbon- and energy-intensive Bosch–Meiser processes for urea synthesis. Alternatively, electrochemical coupling of CO2 and N2 is emerging as a sustainable approach. Unfortunately, the high energy barrier for N2 and CO2 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–1cat. 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 CO2 and N2 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.
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