Abstract

Nitrogen dioxide (NO2) is a toxic air pollutant, and efficient abatement technologies are important to mitigate the many associated health and environmental problems. Here, we report the reactive adsorption of NO2 in a redox−active metal–organic framework (MOF), MFM-300(V). Adsorption of NO2 induces the oxidation of V(III) to V(IV) centers in MFM-300(V), and this is accompanied by the reduction of adsorbed NO2 to NO and the release of water via deprotonation of the framework hydroxyl groups, as confirmed by synchrotron X-ray diffraction and various experimental techniques. The efficient packing of {NO2·N2O4}∞ chains in the pores of MFM-300(VIV) results in a high isothermal NO2 uptake of 13.0 mmol g–1 at 298 K and 1.0 bar and is retained for multiple adsorption–desorption cycles. This work will inspire the design of redox-active sorbents that exhibit reductive adsorption of NO2 for the elimination of air pollutants.

Highlights

  • Nitrogen dioxide (NO2) is a toxic air pollutant and efficient abatement technologies are important to mitigate the many associated health and environmental problems

  • We report the reactive adsorption of NO2 in a redox-active metal-organic framework (MOF), MFM-300(V)

  • Adsorption of NO2 induces the oxidation of V(III) to V(IV) centres in MFM300(V), and this is accompanied by the reduction of adsorbed NO2 to NO and the release of water via deprotonation of the framework hydroxyl groups, as confirmed by synchrotron X-ray diffraction and various experimental techniques

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Summary

Introduction

Nitrogen dioxide (NO2) is a toxic air pollutant and efficient abatement technologies are important to mitigate the many associated health and environmental problems. Adsorption of NO2 induces the oxidation of V(III) to V(IV) centres in MFM300(V), and this is accompanied by the reduction of adsorbed NO2 to NO and the release of water via deprotonation of the framework hydroxyl groups, as confirmed by synchrotron X-ray diffraction and various experimental techniques.

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