Abstract
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.
Original language | English |
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Article number | 1901024 |
Journal | Advanced Materials |
Volume | 31 |
Issue number | 36 |
DOIs | |
Publication status | Published - 1 Sept 2019 |
Externally published | Yes |
Keywords
- mesoporous
- nitrogen-doped carbon
- palladium
- semihydrogenation of acetylene
- single-atom catalysts