Adjacent-Ligand Tuning of Atomically Precise Cu-Pd Sites Enables Efficient Methanol Electrooxidation with a CO-Free Pathway.

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Tác giả: Zhengbo Chen, Yuhai Dou, Yuanlong Qin, Dingsheng Wang, Guo Wang, Kedi Yu, Zechao Zhuang

Ngôn ngữ: eng

Ký hiệu phân loại:

Thông tin xuất bản: Germany : Angewandte Chemie (International ed. in English) , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 633529

Whether the catalyst can realize the non-CO pathway is the key to greatly improve the catalytic activity and stability of methanol oxidation reaction (MOR). It is feasible to optimize the reaction path selectivity by modifying organic ligands and constructing single-atom systems. At the same time, heterogeneous metal nanosheets with atomic thickness have been shown to significantly enhance the catalytic activity of materials due to their ultra-high exposure of active sites and synergistic effects. Herein, we synthesize an ultra-thin heterogeneous alloy metallene with organic ligand-modified surface Cu single atom by one-pot wet chemical method, and further construct an efficient Cu-Pd active sites. The prepared octanoic acid ligand modified PdCu single-atom alloys metallene (SAA OA-Cu-Pdene) shows excellent catalytic activity and stability, with mass activity up to 5.64 A mg
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