CoCorrole‐Functionalized PCN‐222 for Carbon Monoxide Selective Adsorption

Author:

Loze Margerie1,Brandès Stéphane1ORCID,Fleurat‐Lessard Paul1ORCID,Desbois Nicolas1ORCID,Blondeau‐Patissier Virginie2ORCID,Gros Claude P.1ORCID,André Laurie1ORCID

Affiliation:

1. Institut de Chimie Moléculaire de l'Université de Bourgogne, ICMUB, UMR CNRS 6302 Université de Bourgogne 9, Avenue Alain Savary, BP 47870 21078 Dijon Cedex France

2. Institut FEMTO-ST, UMR CNRS 6174 Université de Franche-Comté 26, chemin de l'épitaphe 25030 Besançon Cedex France

Abstract

AbstractThe high risk of CO poisoning justifies the need for indoor air quality control and warning systems based on the detection of low concentrations (ppm‐ppb) of CO. Cobalt corrole complexes selectively bind CO vs. O2, CO2, N2, opening new fields of applications. By combining the CO chemisorption properties of cobalt corroles with the known sorption capacity of MOFs, we hope to obtain high performance sensing materials for CO detection. In addition, the exposed metal sites of MOFs lead to CO2 physisorption, allowing the co‐detection of CO and CO2. In this work, PCN‐222, a stable Zr‐based MOF made from Ni(TCPP) with natural vacancies, has been used as a porous matrix for the grafting of electron‐poor metallocorroles. The materials were characterized by powder XRD, SEM and optical microscopy, BET analyses and gas adsorption measurements at 298 K. No degradation of the crystalline structure of PCN‐222 was observed. At 1 atm, the adsorbed CO(g) volumes measured for the best materials were 12.15 cm3 g−1 and 14.01 cm3 g−1 for CoCorr2@PCN‐222 and CoCorr3@PCN‐222 respectively, and both materials exhibited high CO chemisorption and selectivity against O2, N2, and CO2 at low pressure due to the highest energy of the chemisorption process vs physisorption.

Funder

Université de Bourgogne

Conseil régional de Bourgogne-Franche-Comté

European Commission

Publisher

Wiley

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