Amrita Singh-Morgan , Kim Trösch , Anna Weinfurter , Michael Inniger , Yuan-Zi Xu , Victor Mougel
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引用次数: 0
Abstract
The electrochemical synthesis of ammonia presents a promising pathway to decarbonize and electrify the production of the world’s second-largest commodity chemical. Among potential reactants, NOx gases stand out owing to their favorable thermodynamics, advantageous kinetics, and availability from both combustion emissions and nitrogen-fixation processes, such as plasma-induced atmospheric nitrogen oxidation. However, the typically low concentration of NOx in these sources poses significant challenges for electrochemical performance, particularly due to limitations in reactant mass transport. In this work, we report on the use of a porous nickel catalyst in a membrane electrode assembly (MEA) electrolyzer to enable the direct use of a dilute nitric oxide (NO) feed. The rational optimization of reactant mass transport led to the attainment of maximum values of NO-to-NH3 single-pass conversion of 93%, faradaic efficiency for ammonia of 92%, and ammonium production rate of 556 μmol/h⋅cm2.
期刊介绍:
Chem, affiliated with Cell as its sister journal, serves as a platform for groundbreaking research and illustrates how fundamental inquiries in chemistry and its related fields can contribute to addressing future global challenges. It was established in 2016, and is currently edited by Robert Eagling.