MOF-derived 2D Co@C nanosheet membrane with enhanced catalytic activity: Mechanism and stability insights

Abstract

Two-dimensional (2D) metal-organic frameworks (MOFs) membranes have recently gained attention as novel material membranes for advanced oxidation processes (AOPs). Nonetheless, the susceptibility of 2D MOFs to reactive oxygen species (ROS) limits 2D MOF membranes’ effectiveness in AOPs. In this study, we introduce a novel approach, fabricating a 2D Co-MOF-derived nanosheet membrane (referred to as Co@C NS), assembled from pyrolyzed and exfoliated Co-MOF nanosheets, for the activation of peroxymonosulfate (PMS) in the removal of bisphenol A (BPA). Crucially, the synthesis process involves the pyrolysis of a carbon layer, serving as a protective barrier. This barrier effectively prevents the release of Co ions, ensuring the long-term structural and catalytic stability of the Co@C NS membrane. Notably, the membrane exhibits remarkable capabilities in discriminating between natural organic matter (NOM) and BPA through size exclusion, significantly mitigating the impact of NOM competition for ROS. Additionally, our study demonstrates an exceptional removal efficiency, achieving 100% BPA removal at an ultrahigh permeance of 1100 L m−2 h−1 bar−1, corresponding to an exceedingly short retention time of 0.14 s. Our mechanistic investigation reveals the involvement of singlet oxygen and sulfate radicals in the removal of BPA within the nanochannels, facilitated by the nanoconfinement effect. This study introduces valuable strategies for the development of 2D MOF-derived nanosheet membranes characterized by high catalytic activity and excellent stability, underlining their practical potential in AOP applications.