4.8 Article

Fe single-atom catalysts with pre-organized coordination structure for efficient electrochemical nitrate reduction to ammonia

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 317, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2022.121750

Keywords

Single-atom catalysts; Metal-organic frameworks; Pre-organized structure; Electroreduction of nitrate to ammonia

Funding

  1. National Natural Science Foundation of China [22075108, 21905116, 21701168]
  2. Natural Science Foundation of Jiangsu Province [BK20190614]
  3. Postgraduate Research & Practice Innovation Program of Jiangsu Province [KYCX22_2321]
  4. School of Chemistry and Chemical Engineering, Henan Normal University
  5. Dalian high level talent innovation project [2019RQ063]
  6. Open project Foundation of State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences [20200021]
  7. Central Laboratory, School of Chemical and Material Engineering, Jiangnan University

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This study successfully improves the efficiency of electrochemical nitrate reduction reaction by tailoring the coordination structure of single atom catalysts, providing a new method for large-scale production of NH3.
Single atom catalysts (SAC) have the potential to achieve large-scale production of NH3 through electrochemical nitrate reduction reaction (NO3-RR). Tailoring the coordination structure of the SAC can effectively tune their electronic structure and thus promote their catalytic selectivity and activity. In this work, Fe SAC with unique FeN2O2 coordination was fabricated through direct pyrolysis of metal-organic frameworks that have preorganized FeN2O4 environment. Fe SAC exhibits both high faradaic efficiency (similar to 92%) and high ammonia yield rate (46 mg h(-1)- mg(cat)(-1)) in neutral electrolytes. Density functional theory calculations reveal that the O atoms in FeN2O2 can tune the d-band center of Fe and thus adjust the adsorption energies of the NO3RR intermediates. Compared to FeN4, FeN2O2 structure has higher conductivity and selectivity to NH3 and can spontaneously trigger the transformation of *NOH to N*, thus promoting the NO3-RR. This work provides a simple method to fabricate O, N-coordinated Fe SAC and may stimulate the flourishing development of asymmetric SAC for electrocatalysis.

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