Efficient Ammonia Synthesis from Nitrate Catalyzed by Au/Cu with Enhanced Adsorption Ability. Issue 4 (17th January 2023)
- Record Type:
- Journal Article
- Title:
- Efficient Ammonia Synthesis from Nitrate Catalyzed by Au/Cu with Enhanced Adsorption Ability. Issue 4 (17th January 2023)
- Main Title:
- Efficient Ammonia Synthesis from Nitrate Catalyzed by Au/Cu with Enhanced Adsorption Ability
- Authors:
- Bi, Bo
Dong, An-Qi
Shi, Miao-Miao
Sun, Xue-Feng
Li, Hong-Rui
Kang, Xia
Gao, Rui
Meng, Zhe
Chen, Ze-Yu
Xu, Tong-Wen
Yan, Jun-Min
Jiang, Qing - Abstract:
- Abstract : The traditional method for synthesizing NH3 is the Haber–Bosch process which results in high‐fuel consumption and environmental pollution. Therefore, ecofriendly electrochemical synthesis of NH3 through nitrate (NO3 − ) reduction is a good choice. Herein, an integral Au/Cu electrode to catalyze NO3 − reduction to NH3 is introduced. The catalyst exhibits not only the highest NH3 yield rate (73.4 mg h −1 cm −2 ) up to now but also a very high Faradaic efficiency of 98.02% at −0.7 V at room temperature. It is commonly believed that the transformation of NO3 − to nitrite (NO2 − ) is an obstacle to the NH3 generation from NO3 − reduction. Surprisingly, unlike most of the other catalysts, Au/Cu exhibits better activity for NO3 − reduction than that for NO2 − reduction. Based on the detailed experimental and density functional theory calculations, the excellent performance of Au/Cu for selective NO3 − reduction lies in the enhanced adsorption capabilities of Au/Cu to NO3 − in the alkaline environment and the lower energy barriers of the electrochemical reduction reaction. Abstract : An integral Au/Cu foam electrode realizes the high NH3 yield rate (73.4 mg h −1 cm −2 and Faradaic efficiency (98.02%) from NO3 − electroreduction. The small addition of Au can induce structural relaxation and electron transfer at the interface, thus increasing the adsorption ability of Au/Cu, while displaying a superior performance for electrochemical NO3− reduction reaction (eNO3 RR) thanAbstract : The traditional method for synthesizing NH3 is the Haber–Bosch process which results in high‐fuel consumption and environmental pollution. Therefore, ecofriendly electrochemical synthesis of NH3 through nitrate (NO3 − ) reduction is a good choice. Herein, an integral Au/Cu electrode to catalyze NO3 − reduction to NH3 is introduced. The catalyst exhibits not only the highest NH3 yield rate (73.4 mg h −1 cm −2 ) up to now but also a very high Faradaic efficiency of 98.02% at −0.7 V at room temperature. It is commonly believed that the transformation of NO3 − to nitrite (NO2 − ) is an obstacle to the NH3 generation from NO3 − reduction. Surprisingly, unlike most of the other catalysts, Au/Cu exhibits better activity for NO3 − reduction than that for NO2 − reduction. Based on the detailed experimental and density functional theory calculations, the excellent performance of Au/Cu for selective NO3 − reduction lies in the enhanced adsorption capabilities of Au/Cu to NO3 − in the alkaline environment and the lower energy barriers of the electrochemical reduction reaction. Abstract : An integral Au/Cu foam electrode realizes the high NH3 yield rate (73.4 mg h −1 cm −2 and Faradaic efficiency (98.02%) from NO3 − electroreduction. The small addition of Au can induce structural relaxation and electron transfer at the interface, thus increasing the adsorption ability of Au/Cu, while displaying a superior performance for electrochemical NO3− reduction reaction (eNO3 RR) than that for eNO2 RR. … (more)
- Is Part Of:
- Small structures. Volume 4:Issue 4(2023)
- Journal:
- Small structures
- Issue:
- Volume 4:Issue 4(2023)
- Issue Display:
- Volume 4, Issue 4 (2023)
- Year:
- 2023
- Volume:
- 4
- Issue:
- 4
- Issue Sort Value:
- 2023-0004-0004-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2023-01-17
- Subjects:
- adsorption ability -- ammonia synthesis -- Au/Cu -- catalysts -- nitrate/nitrite reduction reactions
Chemistry -- Periodicals
Science -- Periodicals
Engineering -- Periodicals
505 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
https://onlinelibrary.wiley.com/journal/26884062 ↗ - DOI:
- 10.1002/sstr.202200308 ↗
- Languages:
- English
- ISSNs:
- 2688-4062
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8310.159000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 26884.xml