催化作用
甲烷化
碳化
钴
咪唑酯
纳米颗粒
沸石咪唑盐骨架
化学工程
碳纤维
材料科学
氢
多孔性
多相催化
金属有机骨架
化学
无机化学
纳米技术
吸附
有机化学
复合材料
复合数
工程类
作者
Nadia Gholampour,Yingrui Zhao,François Devred,Capucine Sassoye,Sandra Casale,Damien P. Debecker
标识
DOI:10.1002/cctc.202201338
摘要
Catalytic hydrogenation of CO2 into CH4 is an effective method to convert waste CO2 and green hydrogen into clean fuel on a large scale. However, the viability of such process largely relies on the development of highly active heterogeneous catalysts. Here, a tailored methanation catalyst, Co nanoparticles immobilized into a highly porous N-doped carbon matrix, is prepared by the carbonization of a cobalt-based layered zeolitic imidazolate framework (ZIF−L) material under an argon atmosphere. This catalyst displays a specific activity of 22.3 molCH4/gcat.min at 350 °C, significantly outperforming a similar catalyst derived from the more conventional ZIF-67 (11.7 molCH4/gcat.min). This is explained by the stabilization of small Co nanoparticles (∼20 nm) and by the presence of abundant medium-strength basic sites related to the nitrogen doping in the catalyst prepared from ZIF−L. Notably, the new catalyst shows high stability; no deactivation is observed up to 60 hours on stream.
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