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Highly Selective Electrochemical Reduction of Dinitrogen to Ammonia at Ambient Temperature and Pressure over Iron Oxide Catalysts
Author(s) -
Cui Xiaoyang,
Tang Cheng,
Liu XiaoMeng,
Wang Chen,
Ma Wenjun,
Zhang Qiang
Publication year - 2018
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201800535
Subject(s) - catalysis , ammonia production , inorganic chemistry , chemistry , ammonia , electrochemistry , electrolyte , faraday efficiency , selective catalytic reduction , oxide , hematite , chronoamperometry , electrode , mineralogy , organic chemistry , cyclic voltammetry
The catalytic conversion of dinitrogen (N 2 ) into ammonia under ambient conditions represents one of the Holy Grails in sustainable chemistry. As a potential alternative to the Haber–Bosch process, the electrochemical reduction of N 2 to NH 3 is attractive owing to its renewability and flexibility, as well as its sustainability for producing and storing value‐added chemicals from the abundant feedstock of water and nitrogen on earth. However, owing to the kinetically complex and energetically challenging N 2 reduction reaction (NRR) process, NRR electrocatalysts with high catalytic activity and high selectivity are rare. In this contribution, as a proof‐of‐concept, we demonstrate that both the NH 3 yield and faradaic efficiency (FE) under ambient conditions can be improved by modification of the hematite nanostructure surface. Introducing more oxygen vacancies to the hematite surface renders an improved performance in NRR, which leads to an average NH 3 production rate of 0.46 μg h −1 cm −2 and an NH 3 FE of 6.04 % at −0.9 V vs. Ag/AgCl in 0.10 m KOH electrolyte. The durability of the electrochemical system was also investigated. A surprisingly high average NH 3 production rate of 1.45 μg h −1 cm −2 and a NH 3 FE of 8.28 % were achieved after the first 1 h chronoamperometry test. This is among the highest FEs reported so far for non‐precious‐metal catalysts that use a polymer‐electrolyte‐membrane cell and is much higher than the FE of precious‐metal catalysts (e.g., Ru/C) under comparable reaction conditions. However, the NH 3 yield and the FE dropped to 0.29 μg h −1 cm −2 and 2.74 %, respectively, after 16 h of chronoamperometry tests, which indicates poor durability of the system. Our results demonstrate the important role that the surface states of transition‐metal oxides have in promoting electrocatalytic NRR under ambient conditions. This work may spur interest towards the rational design of electrocatalysts as well as electrochemical systems for NRR, with emphasis on the issue of stability.