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嵌入铁的石墨烯上甲烷吸附和C─H键活化的理论研究:外电场的影响。

Theoretical study of methane adsorption and C─H bond activation over Fe-embedded graphene: Effect of external electric field.

作者信息

Ketrat Sombat, Maihom Thana, Treesukul Piti, Boekfa Bundet, Limtrakul Jumras

机构信息

School of Information Science and Technology (IST), Vidyasirimedhi Institute of Science and Technology, Rayong, 21210, Thailand.

Department of Chemistry, Faculty of Liberal Arts and Science, Kasetsart University, Kamphaeng Saen Campus, Nakhon Pathom, 73140, Thailand.

出版信息

J Comput Chem. 2019 Dec 15;40(32):2819-2826. doi: 10.1002/jcc.26058. Epub 2019 Aug 31.

Abstract

The effect of an external electric field (EF) on the methane adsorption and its activation on iron-embedded graphene (Fe-GPs) are investigated by using the M06-L density functional method. The EF is applied in the perpendicular direction to the graphene in the range of -0.015 to +0.015 a.u. with the interval of 0.005 a.u. The effects of EF on the adsorption, transition state and product complexes of the methane activation reaction are revealed. The binding energies of methane on Fe site in Fe-GPs are increased from -12.9 to -15.3, -18.1 and -21.5 kcal/mol for the negative EF of -0.005, -0.010 and -0.015, respectively. By applying positive EF, the activation barriers for methane activation are reduced in range of 3-8 kcal/mol (around 12-31%) and the reaction energies are more exothermic. The positive EF kinetically favors the reaction compared to the system without EF. The adsorption and activation of methane on Fe-GPs can be easily tuned by adjusting the external electric field for various applications. © 2019 Wiley Periodicals, Inc.

摘要

采用M06-L密度泛函方法研究了外部电场(EF)对甲烷在嵌入铁的石墨烯(Fe-GPs)上吸附及其活化的影响。电场在垂直于石墨烯的方向上施加,范围为-0.015至+0.015 a.u.,间隔为0.005 a.u.。揭示了电场对甲烷活化反应的吸附、过渡态和产物络合物的影响。对于-0.005、-0.010和-0.015的负电场,甲烷在Fe-GPs上Fe位点的结合能分别从-12.9增加到-15.3、-18.1和-21.5 kcal/mol。施加正电场时,甲烷活化的活化能垒降低了3-8 kcal/mol(约12-31%),反应能量更放热。与无电场的体系相比,正电场在动力学上有利于反应。通过调节外部电场,甲烷在Fe-GPs上的吸附和活化可轻松调整,以用于各种应用。© 2019威利期刊公司

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