Breaking the inactivity of MXenes to drive Ampere-level selective oxygen evolution reaction in seawater

Abstract

The limited activity and stability of conventional anodes in seawater have posed a significant obstacle to sustainable green hydrogen production directly from seawater via electrolysis. To address these challenges, we engineered Ti3C2Tx-MXene by incorporating iron and boron into its matrix (tagged FBT) for selective oxygen evolution reaction (OER). Positioning B underneath the top layer induces charge disparity on the Fe-sites, which influences the subsequent growth of the ZIF-67 metal-organic framework (MOF) on the MXene surface through Fe-O-Co ionic bonds. DFT calculations reveal a favorable binding energy of −2.30 eV at the heterointerface for ZIF-67 adsorption to the surface of FBT via O-Co bond, a shortened bond length of 1.94 Å, confirming the formation of ionic bonds. These ionic bonds tune the active sites for an enhanced and selective OER over chlorine evolution reaction (CER), preventing active Fe species' leaching and ensuring stability at >1.56 A cm−2 in 6 M alkaline seawater over 370 hours. Further, FBT and ZIF-67/FBT require low overpotentials of 521.2 and 508 mV, respectively, to deliver 1 A cm−2 in 6 M alkaline seawater. Our findings demonstrate a robust strategy to significantly expand the potential of MXenes from simple conductive substrates to efficient OER catalysts for seawater splitting and beyond.