催化作用
串联
硝酸盐
材料科学
尿素
Boosting(机器学习)
无机化学
分析化学(期刊)
化学工程
环境化学
化学
计算机科学
有机化学
工程类
机器学习
复合材料
作者
Wenyu Du,Zeyi Sun,Shiyao Shang,Kai Chen,Xing Yang,Ke Chu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-09-23
卷期号:18 (40): 27718-27726
被引量:36
标识
DOI:10.1021/acsnano.4c10187
摘要
Urea electrosynthesis by coelectrolysis of NO 3 – and CO 2 (UENC) holds enormous promise for sustainable urea production, while the efficient UENC process relies on the rational design of high-performance catalysts to facilitate the electrocatalytic C–N coupling efficiency and the hydrogenation reaction process. Herein, Fe single atoms supported on MoS 2 (Fe 1 /MoS 2 ) are developed as a highly effective and robust catalyst for UENC. Theoretical calculations and operando spectroscopic measurements reveal a tandem catalysis mechanism of the Fe 1 –S 3 motif and MoS 2 -edge to jointly promote the UENC process, where the Fe 1 –S 3 motif drives the early C–N coupling and subsequent *CO 2 NO 2 -to-*CO 2 NH 2 step. The generated *CO 2 NH 2 is then migrated from the Fe 1 –S 3 motif to the nearby MoS 2 -edge, which facilitates the *CO 2 NH 2 → *COOHNH 2 step for urea formation. Noticeably, Fe 1 /MoS 2 assembled in a flow cell reaches a maximum urea Faraday efficiency of 54.98% with a corresponding urea yield rate of 18.98 mmol h –1 g –1, performing at the top level among all of the UENC catalysts reported to date.
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