CO2 Methanation over Cobalt Nanoparticles Embedded in ZIF‐L–Derived Porous Carbon

Author:

Gholampour Nadia1ORCID,Zhao Yingrui1,Devred François1,Sassoye Capucine2,Casale Sandra3,Debecker Damien P.1ORCID

Affiliation:

1. Institute of Condensed Matter and Nanosciences (IMCN) Université catholique de Louvain (UCLouvain) Place Louis Pasteur1, Box L4.01. Ottignies-Louvain-la-Neuve, 09 1348 Louvain-la-Neuve Belgium

2. Laboratoire de Chimie de la Matière Condensée de Paris (LCMCP) UMR 7574 CNRS -Sorbonne Université, Campus Pierre et Marie Curie 4 Place Jussieu F-75005 Paris France

3. Laboratoire de Réactivité de Surface (LRS) UMR 7197 CNRS -Sorbonne Université, Campus Pierre et Marie Curie 4 Place Jussieu F-75005 Paris France

Abstract

AbstractCatalytic 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.

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference60 articles.

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