Room-temperature conversion of ethane and the mechanism understanding over single iron atoms confined in graphene

• Published in: Journal of energy chemistry Vol. 36; pp. 47 - 50
• Main Authors: Wang, Suheng, Li, Haobo, He, Mengqi, Cui, Xiaoju, Hua, Lei, Li, Haiyang, Xiao, Jianping, Yu, Liang, Rajan, N. Pethan, Xie, Zhaoxiong, Deng, Dehui
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 01-09-2019
• Subjects: C–H activation; Ethane conversion; Graphene; Room-temperature reaction; Single iron atom; Single iron atom; C–H activation; Room-temperature reaction; Graphene; Ethane conversion
• ISSN: 2095-4956
• DOI: 10.1016/j.jechem.2019.04.003

The catalytic conversion of ethane to high value-added chemicals is significantly important for utilization of hydrocarbon resources. However, it is a great challenge due to the typically required high temperature (> 400 °C) conditions. Herein, a highly active catalytic conversion process of ethane at room temperature (25 °C) is reported on single iron atoms confined in graphene via the porphyrin-like N4-coordination structures. Combining with the operando time of flight mass spectrometer and density functional theory calculations, the reaction is identified as a radical mechanism, in which the C–H bonds of the same C atom are preferentially and sequentially activated, generating the value-added C2 chemicals, simultaneously avoiding the over-oxidation of the products to CO2. The in-situ formed O–FeN4–O structure at the single iron atom serves as the active center for the reaction and facilitates the formation of ethyl radicals. This work deepens the understanding of alkane C–H activation on the FeN4 center and provides the reference in development of efficient catalyst for selective oxidation of light alkane.
The single iron atoms confined in graphene with N4-coordination structures were used as a kind of efficient non-precious catalyst to convert ethane to high value-added C2 chemicals at room temperature along a radical mechanism. [Display omitted]