Applied Catalysis2022,Vol.31310.DOI:10.1016/j.apcatb.2022.121463

Atomically dispersed lewis acid sites meet poly(ionic liquid)s networks for solvent-free and co-catalyst-free conversion of CO2 to cyclic carbonates

Huaitao Peng Qiuju Zhang Yinming Wang
Applied Catalysis2022,Vol.31310.DOI:10.1016/j.apcatb.2022.121463

Atomically dispersed lewis acid sites meet poly(ionic liquid)s networks for solvent-free and co-catalyst-free conversion of CO2 to cyclic carbonates

Huaitao Peng 1Qiuju Zhang 2Yinming Wang2
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作者信息

  • 1. National Center for International Research on Photoelectric and Energy Materials, School of Materials and Energy, Yunnan University, Kunming 650091, PR China
  • 2. Key Laboratory of Advanced Fuel Cells and Electrolyzers Technology of Zhejiang Province, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo, Zhejiang 315201, PR China
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Abstract

The rational integration of multiple functional units into heterogeneous materials to improve catalytic performance is highly desirable for CO2 value-added processes. Herein, a catalyst composed of porous carbon matrix with atomically dispersed Lewis acid sites (i.e., AIO5 motifs) and imidazolium-based poly(ionic liquid)s (denoted as PILs@Al-O-C) was fabricated. Compared with pure Al-O-C or PILs, the optimized PILs@Al-O-C exhibits superior catalytic performance (>90% yield) towards cycloaddition reaction of CO2 and epoxides in the absence of solvent and co-catalyst. The enhanced activity of PILs@Al-O-C is attributed to the synergistic effect among the uniform N sites (Lewis base sites) and abundant bromide anions (nucleophilic agents) in the PILs network, as well as the atomically dispersed Al sites (Lewis acid sites) in the Al-O-C matrix. This work provides an advanced PILs@Al-O-C catalyst for constructing a neat catalytic system towards CO2 fixation.

Key words

Atomically-dispersed Lewis acid sites/Poly(ionic liquid)s/Carbon-based catalysts/CO2 cycloaddition

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出版年

2022
Applied Catalysis

Applied Catalysis

ISSN:0926-3373
被引量22
参考文献量64
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