Tuning Main Group Element-based Metal-Organic Framework to Boost Electrocatalytic Nitrogen Reduction Under Ambient Conditions

Main group element-based materials are emerging catalysts for ammonia (NH3) production via a sustainable electrochemical nitrogen reduction reaction (N2RR) pathway under ambient conditions. However, their N2RR performances are less explored due to the limited active behavior and unclear mechanism. Here, an aluminum-based defective metal-organic framework (MOF), aluminum-fumarate (Al-Fum), is investigated. As a proof of concept, the pristine Al-Fum MOF is synthesized by the solvothermal reaction process, and the defect engineering method namely solvent-assisted linker exchange, is applied to create the defective Al sites. The defective Al sites play an important role in ensuring the N2RR activity for defective Al-Fum. It is found that only the defective Al-Fum enables stable and effective electrochemical N2RR, in terms of the highest production rate of 53.9 mu g(NH3) h(-1)mg(cat)(-1) (in 0.4 m K2SO4) and the Faradaic efficiency of 73.8% (in 0.1 m K2SO4) at -0.15 V vs reversible hydrogen electrode) under ambient conditions. Density functional theory calculations confirm that the N-2 activation can be achieved on the defective Al sites. Such sites also allow the subsequent protonation process via the alternating associative mechanism. This defect characteristic gives the main group Al-based MOFs the ability to serve as promising electrocatalysts for N2RR and other attractive applications.

Automated summary

Main group element-based materials, specifically aluminum-based defective metal-organic frameworks (MOFs), show promising capabilities as electrocatalysts for sustainable ammonia production via electrochemical nitrogen reduction reaction (N2RR) under ambient conditions. Defective aluminum sites in the aluminum-fumarate (Al-Fum) MOF play a crucial role in promoting N2RR activity. The defective Al-Fum exhibits stable and efficient electrochemical N2RR, with a high production rate of 53.9 μg(NH3) h(-1)mg(cat)(-1) and a Faradaic efficiency of 73.8% under ambient conditions.