羧化
材料科学
催化作用
金属有机骨架
多孔性
产量(工程)
纳米颗粒
纳米技术
化学工程
化学
有机化学
复合材料
吸附
工程类
作者
Jialin Shi,Lina Zhang,Nannan Sun,Deng Hu,Qun Shen,Fang Mao,Qiang Gao,Wei Wei
标识
DOI:10.1021/acsami.9b07991
摘要
Metal–organic frameworks (MOFs) are promising hosts for catalytic active sites due to their adjustable porosity and framework chemistry. Strategies to improve synergistic effects between the installed sites and the parent MOF are highly desired. Herein, a facile and rapid method for the preparation of x Ag@ZIF-8 materials was reported. The materials were systematically characterized and used as catalysts for carboxylation of terminal alkynes via direct insertion of CO 2 to the C(sp)–H bond (CTA CO2 ). It was found that the integrity of the ZIF-8 structure could be retained upon Ag loading, but short-range crystalline ordering was modified. Two types Ag species could be installed, namely, highly dispersed Ag(I) in the backbone (Ag HD ) and aggregated Ag(0) nanoparticles on the outer surface (Ag NP ). The Ag NP sites are highly effective for the activation of terminal alkynes due to its high accessibility, while the Ag HD -modified ZIF-8 framework worked as a CO 2 reservoir with enhanced affinity. Combination of these factors translated to high activity in the CTA CO2 process, the measured turnover frequency and time yield are among the highest among most heterogeneous catalysts.
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