Assembling lanthanide-transition metal clusters on TiO2 for photocatalytic nitrogen fixation

Ammonia synthesis using light with low energy consumption offers an effective solution for energy saving and environmental protection. Herein, an abundant oxygen vacancy photocatalyst was synthesized via the integration of lanthanide-transition metal (4f-3d) clusters Ln(52)Ni(56) on the TiO2 surface. The investigation of photocatalytic nitrogen fixation showed that Ln(52)Ni(56) not only acts as a tool to improve charge separation but also enriches oxygen vacancies. Multiple synergies resulted in a photocatalytic nitrogen fixation efficiency of up to 800 mu mol h(-1) g(-1) with the direct utilization of nitrogen and water without any sacrificial agents or co-catalysts. Electron paramagnetic resonance spectroscopy was conducted to investigate the mechanism of oxygen vacancy inactivation and recovery. This study provides a reference for the construction of a photochemical nitrogen fixation catalyst driven by defect engineering.

Automated summary

In this study, an abundant oxygen vacancy photocatalyst was synthesized through defect engineering, showing high photocatalytic nitrogen fixation efficiency with direct utilization of nitrogen and water, without any sacrificial agents or co-catalysts. The mechanism of oxygen vacancy was investigated by electron paramagnetic resonance spectroscopy.