High-Rate, High-Selectivity Electrochemical Oxidation of Ammonia to Nitrite with a Silver-Based Catalyst
Thi Mung Vu, Sam Johnston, Darcy Simondson, Cuong K. Nguyen, Tam D. Nguyen, Daniel Van Zeil, Rosalie K. Hocking, Douglas R. MacFarlane, Alexandr N. Simonov
Abstract
Effective operation of electrocatalysts for the ammonia oxidation reaction (AOR) is typically constrained by poisoning, rapid corrosion, and low Faradaic efficiencies (FEs). Aiming to address these challenges, we present herein a robust silver oxide (AgO x ) catalyst generated by in situ anodic electrodeposition from a solution of Tollen’s reagent ([Ag(NH 3 ) 2 ]OH). When tested in 1 M KOH and 0.1 M NH 3 at 1.1 V vs standard hydrogen electrode, AgO x catalyzes the AOR to nitrite at an FE of 70 ± 6% and a yield rate of 42 ± 7 nmol s –1 cm –2, on a time scale of 33 h, which is the highest performance reported so far. Our data suggest that the mechanism of the AgO x -catalyzed AOR is defined by pH, with the strongly alkaline conditions (>0.1 M KOH) favoring the heterogeneous electrocatalytic pathway producing nitrite. In turn, operation at <0.1 M KOH promotes the formation of N 2 via a homogeneous reaction mediated by the Ag 3+/2+ redox couple. Electrochemical and physical characterization, including by in situ X-ray absorption and Raman spectroscopy, suggests that the active sites within AgO x promoting nitrite production are Ag 3+ -based.