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Bipyridine-Confined Silver Single-Atom Catalysts Facilitate In-Plane C–O Coupling for Propylene Electrooxidation
The electrooxidation of propylene presents a promising route for the production of 1,2-propylene glycol (PG) under ambient conditions. However, the C–O coupling process remains a challenge owing to the high energy barrier. In this work, we developed a highly efficient electrocatalyst of bipyridine-c...
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Published in: | Nano letters 2024-02, Vol.24 (5), p.1801-1807 |
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container_end_page | 1807 |
container_issue | 5 |
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container_title | Nano letters |
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creator | Chi, Mingfang Zhao, Jiankang Ke, Jingwen Liu, Yan Wang, Ruyang Wang, Chuanhao Hung, Sung-Fu Lee, Tsung-Ju Geng, Zhigang Zeng, Jie |
description | The electrooxidation of propylene presents a promising route for the production of 1,2-propylene glycol (PG) under ambient conditions. However, the C–O coupling process remains a challenge owing to the high energy barrier. In this work, we developed a highly efficient electrocatalyst of bipyridine-confined Ag single atoms on UiO-bpy substrates (Ag SAs/UiO-bpy), which exposed two in-plane coordination vacancies during reaction for the co-adsorption of key intermediates. Detailed structure and electronic property analyses demonstrate that CH3CHCH2OH* and *OH could stably co-adsorb in a square planar configuration, which then accelerates the charge transfer between them. The combination of stable co-adsorption and efficient charge transfer facilitates the C–O coupling process, thus significantly lowering its energy barrier. At 2.4 V versus a reversible hydrogen electrode, Ag SAs/UiO-bpy achieved a record-high activity of 61.9 gPG m–2 h–1. Our work not only presents a robust electrocatalyst but also advances a new perspective on catalyst design for propylene electrooxidation. |
doi_str_mv | 10.1021/acs.nanolett.3c04978 |
format | article |
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However, the C–O coupling process remains a challenge owing to the high energy barrier. In this work, we developed a highly efficient electrocatalyst of bipyridine-confined Ag single atoms on UiO-bpy substrates (Ag SAs/UiO-bpy), which exposed two in-plane coordination vacancies during reaction for the co-adsorption of key intermediates. Detailed structure and electronic property analyses demonstrate that CH3CHCH2OH* and *OH could stably co-adsorb in a square planar configuration, which then accelerates the charge transfer between them. The combination of stable co-adsorption and efficient charge transfer facilitates the C–O coupling process, thus significantly lowering its energy barrier. At 2.4 V versus a reversible hydrogen electrode, Ag SAs/UiO-bpy achieved a record-high activity of 61.9 gPG m–2 h–1. 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title | Bipyridine-Confined Silver Single-Atom Catalysts Facilitate In-Plane C–O Coupling for Propylene Electrooxidation |
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