Abstract
Electroreduction of nitrate to ammonia provides an interesting pathway for wastewater treatment and valorization. Cu-based catalysts are active for the conversion of NO3 - to NO2 - but suffer from an inefficient hydrogenation process of NO2 -. Herein, CuxO/N-doped graphdiyne (CuxO/N-GDY) with pyridine N configuration are in situ prepared in one pot. Benefiting from the synergistic effect of pyridinic N in GDY and CuxO, the prepared CuxO/N-GDY tested in a commercial H-cell achieved a faradaic efficiency of 85% toward NH3 at -0.5V versus RHE with a production rate of 340µmolh-1mgcat -1 in 0.1M KNO3. When integrating the CuxO/N-GDY in an anion exchange membrane flow electrolyzer, a maximum Faradaic efficiency of 89% is achieved at a voltage of 2.3V and the production rate is 1680µmol h-1mgcat -1 at 3.3V in 0.1M KNO3 at room temperature. Operation at 40°C further promoted the overall reaction kinetics of NO3 - to NH3, but penalized its selectivity with respect to hydrogen evolution reaction. The high selectivity and production rate in this device configuration demonstrate its potential for industrial application.
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