摘要
Thermocatalytic ammonia decomposition for hydrogen production is regarded as an effective strategy to tackle the challenges of hydrogen storage and transport. Most current strategies focus on the adsorption-evolution mechanism to balance kinetic barriers in rate-determining steps, thereby reducing reaction temperature. Herein, we report a strategy to promote the kinetics of ammonia decomposition by altering the reaction pathway through lattice nitrogen mediation. The results indicate that using a nitrogen-containing graphene-like g-C3N4 as the support, the ammonia decomposition efficiency and hydrogen production rate are improved by 72.11 % and 80.11 mmol gcat-1 min-1, respectively, compared to nitrogen-free graphene as the support (5 wt% Ru/Gr-AR), under conditions of only 20 mg catalyst, 500 °C, and a gas hourly space velocity (GHSV) of 18,000 mL gcat-1 h-1. Under these conditions, the hydrogen production rate (99.45 mmol gcat-1 min-1) is significantly higher than that of previously reported Ru-based catalysts, and a 100-hour test further confirms its excellent stability. In addition, by proposing a nitrogen-cycle pathway model for ammonia decomposition potentially mediated by lattice nitrogen, we can not only provide a plausible explanation for the enhanced catalytic activity of nitrogenous catalyst, but also provide important guidance for the design of new catalysts.
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