期刊
CHEMISTRY-A EUROPEAN JOURNAL
卷 24, 期 69, 页码 18494-18501出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201800535
关键词
ammonia; electrochemistry; hematite; nitrogen reduction; oxygen vacancies
资金
- National Key Research and Development Program [2016YFA0202500]
- National Natural Scientific Foundation of China [21676160, 21706146]
- China Postdoctoral Science Foundation [2016M600097]
- Tsinghua University Initiative Scientific Research Program
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 NH3 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 NH3 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 NH3 production rate of 0.46 mu g h(-1) cm(-2) and an NH3 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 NH3 production rate of 1.45 mu g h(-1) cm(-2) and a NH3 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 NH3 yield and the FE dropped to 0.29 mu g 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.
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