电合成
氨生产
催化作用
质子耦合电子转移
氨
质子
电子转移
电化学
化学
动力学
电极
无机化学
化学工程
物理化学
物理
有机化学
工程类
量子力学
作者
Suxian Xu,Yong Zhu,Zhibing Wen,Shengming Yu,Zeyu Teng,Guoquan Liu,Hua Gao,Ran Zhao,Licheng Sun,Fei Li
出处
期刊:Chem catalysis
[Elsevier]
日期:2023-09-01
卷期号:3 (9): 100751-100751
被引量:3
标识
DOI:10.1016/j.checat.2023.100751
摘要
The electrochemical nitrate reduction reaction (eNO3RR) is an appealing technology for converting environmentally toxic NO3− to ammonia (NH3). This approach was usually obstructed by the multi-proton/electron involved process. Here, we report a catalyst with Ru single atoms supported on Co3O4 (Ru SAs-Co3O4). The as-developed Ru SAs-Co3O4 catalyst shows a remarkable NH3-evolving activity with a faradic efficiency of 94.92% ± 4.02% at the potential of −0.2 V (vs. RHE) and a generation rate of 1,843.45 ± 57.14 μmol h−1 cm−2 at the potential of −0.5 V. Further investigations revealed that the Ru SAs play a dual role in simultaneously accelerating the proton transfer and modulating the d-electron structures of the neighboring Co sites, which led to a lower energy barrier of the rate-determining step. Eventually, by combining the eNO3RR and electrosynthesis of 5,5′-azotetrazolate at a two-electrode system, an energy-saving NH3 synthesis, while simultaneously producing value-added chemicals, was successfully achieved.
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