催化作用
杂原子
产量(工程)
化学
氨
Atom(片上系统)
磷
氮原子
氮气
氨生产
钴
无机化学
材料科学
有机化学
戒指(化学)
冶金
嵌入式系统
计算机科学
作者
Jiacheng Li,Miao Li,Ning An,Shuo Zhang,Qinan Song,Yilin Yang,Jing Li,Xiang Liu
标识
DOI:10.1073/pnas.2123450119
摘要
Efficient n = O bond activation is crucial for the catalytic reduction of nitrogen compounds, which is highly affected by the construction of active centers. In this study, n = O bond activation was achieved by a single-atom catalyst (SAC) with phosphorus anchored on a Co active center to form intermediate N-species for further hydrogenation and reduction. Unique phosphorus-doped discontinuous active sites exhibit better n = O activation performance than conventional N-cooperated single-atom sites, with a high Faradic efficiency of 92.0% and a maximum ammonia yield rate of 433.3 μg NH4·h-1·cm-2. This approach of constructing environmental sites through heteroatom modification significantly improves atom efficiency and will guide the design of future functional SACs with wide-ranging applications.
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