摘要
Semihydrogenation of acetylene in the ethylene feed is a vital step for the industrial production of polyethylene. Despite their favorable reaction activity and ethylene selectivity, the Pd-based intermetallic compound and single-atom alloy catalysts still suffer from the limitation of atomic utilization derived from the partial exposure of active Pd atoms. Herein, a hard-template Lewis acid doping strategy is reported that can overcome the inefficient utilization of Pd atoms. In this strategy, N-coordinated isolated single-atomic Pd sites are fully embedded on the inner walls of mesoporous nitrogen-doped carbon foam nanospheres (ISA-Pd/MPNC). This synthetic strategy has been proved to be applicable to prepare other ISA-M/MPNC (M = Pt and Cu) materials. This ISA-Pd/MPNC catalyst with both high specific surface area (633.8 m2 g−1) and remarkably thin pore wall (1–2 nm) exhibits higher activity than that of its nonmesoporous counterpart (ISA-Pd/non-MPNC) catalyst by a factor of 4. This work presents an efficient way to tailor and optimize the catalytic activity and selectivity by atomic-scale design and structural control.
源语言 | 英语 |
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文章编号 | 1901024 |
期刊 | Advanced Materials |
卷 | 31 |
期 | 36 |
DOI | |
出版状态 | 已出版 - 1 9月 2019 |
已对外发布 | 是 |