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论文类型：期刊论文

第一作者：Wang, Tongtong

合写作者：Song, Xuedan,Luo, Qunxing,Yang, Xiaodong,Chong, Siying,Zhang, Jie,Ji, Min

发表时间：2018-09-01

发表刊物：MICROPOROUS AND MESOPOROUS MATERIALS

收录刊物：SCIE、EI

卷号：267

页面范围：84-92

ISSN号：1387-1811

关键字：Metal-organic frameworks; CO2 chemisorption; Acid-base synergetic; Ionic liquid; DFT calculations

摘要：In terms of 'green chemistry' and 'atom economy', the cycloaddition of CO2 to yield cyclic carbonate without any additive is an eco-friendly way to utilize CO2. Unfortunately, the low CO2 capture quantity of common catalysts limited its catalytic efficiency. Herein, a novel acid-base bifunctional catalyst was successfully prepared by immobilizing ionic liquid on MIL-101-NH2 (IL/MIL-101-NH2) and tested for propylene carbonate (PC) rapid and facile synthesis from CO2 and propylene oxide (PO). The synergetic interaction between Lewis base with strong CO2 chemical capture capacity and Bronsted acid with strong hydrogen bond donor leads to the high catalytic efficiency of IL/MIL-101-NH2 for carbonate synthesis from CO2 and PO without any additive. The immobilization mode between MIL-101-NH2 and IL is energetically supported by the density functional theory (DFT) calculations. This design idea of specific catalyst and the acid-base synergetic strategy provides new insights into the design of powerful catalyst systems for the CO2 conversion.