4.6 Article

Electro-synthesis of Ammonia from Dilute Nitric Oxide on a Gas Diffusion Electrode

Journal

ACS ENERGY LETTERS
Volume 7, Issue 3, Pages 958-965

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsenergylett.1c02552

Keywords

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Funding

  1. Energy Efficiency & Resources Core Technology Program of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) - Ministry of Trade, Industry & Energy, Republic of Korea [20193410100210, N02210008]
  2. Basic Science Research Program of the National Research Foundation of Korea - Ministry of Science and ICT, Republic of Korea [NRF-2021R1A2C2007823]
  3. Ulsan National Institute of Science and Technology [1.210102.01]
  4. Korea Evaluation Institute of Industrial Technology (KEIT) [20193410100210] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  5. National Research Foundation of Korea [4199990614407] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The electrochemical conversion of nitric oxide (NO) to ammonia (NH3) offers a sustainable route to transform air pollutants into value-added chemicals. By incorporating nanoscale zero-valent iron into a gas diffusion electrode (GDE), a high NH3 production rate and efficiency can be achieved. Controlling the proton concentration in the electrolyte further accelerates the NH3 production rate.
The electrochemical conversion of nitric oxide (NO) to ammonia (NH3) provides a sustainable route to transform an air pollutant into a value-added chemical. However, the development of NO electroreduction remains hindered by the poor solubility in aqueous electrolytes, requiring the use of concentrated NO. Here, we report a dilute NO reduction using a gas diffusion electrode (GDE) to circumvent the mass transport issue. Through the incorporation of nanoscale zero-valent iron into carbon black on the GDE, 96% NH3 Faradaic efficiency was achieved with 1% NO, and the computational calculations revealed that the Fe catalyzed the breaking of the N-O bond in the H-2 NO intermediate. The NH3 production rate was accelerated by controlling the concentration of protons in the electrolyte and reached 1239 mu mol cm(-2) h(-1) with 10% NO. Our findings show that the gas-phase electrolysis of dilute NO can offer a practical option for upcycling the waste nitrogen.

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