催化作用
双金属片
石墨烯
化学
星团(航天器)
协同催化
密度泛函理论
氨生产
选择性
电催化剂
组合化学
过渡金属
纳米技术
材料科学
计算化学
电化学
物理化学
有机化学
电极
计算机科学
程序设计语言
作者
Shuo Wang,Tingting Zhao,Li‐Kai Yan
出处
期刊:Catalysts
[MDPI AG]
日期:2023-05-11
卷期号:13 (5): 869-869
被引量:11
标识
DOI:10.3390/catal13050869
摘要
Electrocatalytic nitrogen reduction reaction (NRR) can realize the green production of ammonia while developing electrocatalysts with high selectivity and ability is still an ongoing challenge. Two-dimensional (2D) graphitic carbon nitride (CN) frameworks can provide abundant hollow sites for stably anchoring several transition metal (TM) atoms to facilitate single-cluster catalysis, promising to overcome the problems of low activity and poor selectivity in the process of ammonia synthesis. Herein, extensive density functional theory (DFT) calculations were performed to investigate the feasibility of six bimetallic triatomic clusters FexMoy (x = 1, 2; x + y = 3) supported on C6N6, C2N, and N-doped porous graphene (NG) as NRR electrocatalysts. Through a systematic screening strategy, we found that the Fe2Mo–NG possesses the highest activity with a limiting potential of –0.36 V through the enzymatic mechanism and could be the promising catalyst for NH3 synthesis. The Fe2Mo moiety in Fe2Mo–NG moderately regulates the electron transfer between reaction intermediates and NG, which is ascribed to enhanced performance. This work accelerates the rational design of catalysts in the field of NRR and contributes to broadening the understanding of cluster catalysis.
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