Electrocatalytically Active Fe‐(O‐C2)4 Single‐Atom Sites for Efficient Reduction of Nitrogen to Ammonia. Issue 32 (27th May 2020)

• Record Type: Journal Article
• Authors: Zhang, Shengbo; Jin, Meng; Shi, Tongfei; Han, Miaomiao; Sun, Qiao; Lin, Yue; Ding, Zhenhua; Zheng, Li Rong; Wang, Guozhong; Zhang, Yunxia; Zhang, Haimin; Zhao, Huijun
• Is Part Of: Angewandte Chemie international edition. Volume 59:Issue 32(2020)
• Page Start: 13423
• Page End: 13429
• Publication Date: 2020-05-27
• Subjects: ammonia -- electrocatalysis -- nitrogen reduction -- single-atom catalysts; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.202005930
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: Single‐atom catalysts have demonstrated their superiority over other types of catalysts for various reactions. However, the reported nitrogen reduction reaction single‐atom electrocatalysts for the nitrogen reduction reaction exclusively utilize metal–nitrogen or metal–carbon coordination configurations as catalytic active sites. Here, we report a Fe single‐atom electrocatalyst supported on low‐cost, nitrogen‐free lignocellulose‐derived carbon. The extended X‐ray absorption fine structure spectra confirm that Fe atoms are anchored to the support via the Fe‐(O‐C2 )4 coordination configuration. Density functional theory calculations identify Fe‐(O‐C2 )4 as the active site for the nitrogen reduction reaction. An electrode consisting of the electrocatalyst loaded on carbon cloth can afford a NH3 yield rate and faradaic efficiency of 32.1 μg h −1 mgcat. −1 (5350 μg h −1 mgFe −1 ) and 29.3 %, respectively. An exceptional NH3 yield rate of 307.7 μg h −1 mgcat. −1 (51 283 μg h −1 mgFe −1 ) with a near record faradaic efficiency of 51.0 % can be achieved with the electrocatalyst immobilized on a glassy carbon electrode. Abstract : Effects of distribution on performance : A single‐atom Fe electrocatalyst supported on nitrogen‐free lignocellulose‐derived graphitic carbon with Fe‐(O‐C2 )4 active sites was synthesized and exceptional catalytic activity for N2 reduction to NH3 was demonstrated. The results indicate that the performance of a given catalyst is strongly influenced by factors other than its intrinsic electrocatalytic activity.