Engineering the Electronic Structures of Metal-Organic Framework Nanosheets via Synergistic Doping of Metal Ions and Counteranions for Efficient Water Oxidation

Metal-organic framework (MOF) nanosheets with attractive chemical and structural properties have been considered as prominent oxygen evolution reaction (OER) electrocatalysts, while the insufficient exposed active sites and low electrical conductivity of MOFs limit their electrocatalytic activity and further industrial applications. Herein, a unique strategy to remarkably boost electrocatalytic OER activity of one Ni-based MOF is developed by the simultaneous incorporation of Fe3+ ions and BF4- anions within its layer structure. The optimized electrocatalyst NiFe-MOF-BF4--0.3 NSs shows superior OER activity with a required ultralow overpotential of 237 mV at 10 mA cm(-2), a small Tafel slope of 41 mV dec(-1), and outstanding stability in an alkaline medium. The experimental and density functional theory (DFT) calculation results verify that the interactions between metal (M) ions and BF4- anions (defined as M...F, M = Ni or Fe) in this catalyst can adjust the adsorption abilities of oxygen intermediates and lower the free energy barrier of the potential-determining step by tailoring its electronic structure, thereby remarkably boosting its OER activity. This protocol provides new insights into surface and structure engineering of 2D MOFs, leading to greatly enhanced electrocatalytic OER performance.

Automated summary

This study developed a unique strategy to enhance the OER activity of Ni-based MOFs by the incorporation of Fe3+ ions and BF4- anions. The optimized NiFe-MOF-BF4-0.3 nanosheets exhibit superior OER activity and stability. Experimental and theoretical results demonstrate that the interactions between metal ions and BF4- anions play a crucial role in boosting the OER activity.